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Skogeng LP, Blévin P, Breivik K, Bustnes JO, Eulaers I, Sagerup K, Krogseth IS. Investigating the impact of climate change on PCB-153 exposure in Arctic seabirds with the nested exposure model. ENVIRONMENTAL SCIENCE. PROCESSES & IMPACTS 2025; 27:1317-1330. [PMID: 40208668 DOI: 10.1039/d4em00584h] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 04/11/2025]
Abstract
At the same time Arctic ecosystems experiences rapid climate change, at a rate four times faster than the global average, they remain burdened by long-range transported pollution, notably with legacy polychlorinated biphenyls (PCBs). The present study investigates the potential impact of climate change on seabird exposure to PCB-153 using the established Nested Exposure Model (NEM), here expanded with three seabird species, i.e. common eider (Somateria mollissima), black-legged kittiwake (Rissa tridactyla) and glaucous gull (Larus hyperboreus), as well as the filter feeder blue mussel (Mytulis edulis). The model's performance was evaluated using empirical time trends of the seabird species in Kongsfjorden, Svalbard, and using tissue concentrations from filter feeders along the northern Norwegian coast. NEM successfully replicated empirical PCB-153 concentrations, confirming its ability to simulate PCB-153 bioaccumulation in the studied seabird species within an order of magnitude. Based on global PCB-153 emission estimates, simulations run until the year 2100 predicted seabird blood concentrations 99% lower than in year 2000. Model scenarios with climate change-induced altered dietary composition and lipid dynamics showed to have minimal impact on future PCB-153 exposure, compared to temporal changes in primary emissions of PCB-153. The present study suggests the potential of mechanistic modelling in assessing POP exposure in Arctic seabirds within a multiple stressor context.
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Affiliation(s)
- Lovise Pedersen Skogeng
- The Climate and Environmental Research Institute - NILU, Tromsø, Norway
- Department of Arctic and Marine Biology, UiT - Arctic University of Norway, Tromsø, Norway.
| | - Pierre Blévin
- Environmental Impacts, Akvaplan-niva, Tromsø, Norway
| | - Knut Breivik
- The Climate and Environmental Research Institute - NILU, Tromsø, Norway
- Department of Chemistry, University of Oslo, Oslo, Norway
| | | | - Igor Eulaers
- Pollution and Marine Mammals, Norwegian Polar Institute, Tromsø, Norway
| | - Kjetil Sagerup
- Environmental Impacts, Akvaplan-niva, Tromsø, Norway
- Nowegian Institute for Nature Research, Tromsø, Norway
| | - Ingjerd Sunde Krogseth
- The Climate and Environmental Research Institute - NILU, Tromsø, Norway
- Department of Arctic and Marine Biology, UiT - Arctic University of Norway, Tromsø, Norway.
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2
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Karanam SK, Nagvishnu K, Uppala PK, Edhi S, Varri SR. Crimean-Congo hemorrhagic fever: Pathogenesis, transmission and public health challenges. World J Virol 2025; 14:100003. [PMID: 40134837 PMCID: PMC11612873 DOI: 10.5501/wjv.v14.i1.100003] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 08/05/2024] [Revised: 10/11/2024] [Accepted: 11/05/2024] [Indexed: 11/28/2024] Open
Abstract
The dangerous Crimean-Congo hemorrhagic fever virus (CCHFV), an encapsulated negative-sense RNA virus of the family Nairoviridae, is transmitted from person to person via ticks. With a case fatality rate between 10% to 40%, the most common ways that the disease may spread to humans are via tick bites or coming into touch with infected animals' blood or tissues. Furthermore, the transfer of bodily fluids between individuals is another potential route of infection. There is a wide range of symptoms experienced by patients throughout each stage, from myalgia and fever to extreme bruising and excess bleeding. Tick management measures include minimising the spread of ticks from one species to another and from people to animals via the use of protective clothing, repellents, and proper animal handling. In order to prevent the spread of illness, healthcare workers must adhere to stringent protocols. Despite the lack of an authorised vaccine, the main components of treatment now consist of preventative measures and supportive care, which may include the antiviral medicine ribavirin. We still don't know very much about the virus's mechanisms, even though advances in molecular virology and animal models have improved our understanding of the pathogenesis of CCHFV. A critical need for vaccination that is both safe and effective, as well as for quick diagnosis and efficient treatments to lessen the disease's impact in areas where it is most prevalent. Important steps towards lowering Crimean-Congo hemorrhagic fever mortality and morbidity rates were to anticipatethe future availability of immunoglobulin products.
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Affiliation(s)
- Sita Kumari Karanam
- Department of Pharmaceutical Biotechnology, Maharajah’s College of Pharmacy, Vizianagaram 535002, Andhra Pradesh, India
| | - Kandra Nagvishnu
- Department of Pharmacology, Santhiram Medical College and General Hospital, Nandyal 518501, Andhra Pradesh, India
| | - Praveen Kumar Uppala
- Department of Pharmacology, Maharajah's College of Pharmacy, Vizianagaram 535002, Andhra Pradesh, India
| | - Sandhya Edhi
- Department of Pharmacy, Maharajah's College of Pharmacy, Vizianagaram 535002, Andhra Pradesh, India
| | - Srinivasa Rao Varri
- Department of Pharmaceutical Analysis, Maharajah's College of Pharmacy, Vizianagaram 535002, Andhra Pradesh, India
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Kesic R, Elliott JE, Lee SL, Elliott KH. Legacy and emergent contaminants in glaucous-winged gull eggs from Canada's Pacific coast: Spatial distribution, temporal trends, and risks for human consumers. ENVIRONMENTAL POLLUTION (BARKING, ESSEX : 1987) 2024; 363:125099. [PMID: 39393758 DOI: 10.1016/j.envpol.2024.125099] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 07/26/2024] [Revised: 09/30/2024] [Accepted: 10/08/2024] [Indexed: 10/13/2024]
Abstract
Using glaucous-winged gull (Larus glaucescens) eggs from Canada's Pacific coast, we investigated spatial and temporal trends (2008-2022) of a suite of legacy and emergent contaminants, including 16 perfluoroalkyl substances (PFAS), 15 polybrominated diphenyl ethers (PBDEs), 7 alternative halogenated flame retardants (AHFRs), total mercury (THg), as well as stable isotopes of carbon (δ13C) and nitrogen (δ15N) to control for diet. Legacy organochlorines (OCs) were also measured in eggs in 2020 for a preliminary human health risk assessment (HHRA). Between 2008 and 2022, glaucous-winged gull eggs from more urban-influenced colonies (Mandarte Island) were up to ∼2x more contaminated with PFAS, PBDEs, AHFRs, and THg than eggs from the offshore colony (Cleland Island), suggesting different source regions and dietary exposures. Concentrations of Σ15PBDEs declined linearly among colonies (p < 0.001), consistent with several North American phase-outs and regulatory restrictions dating back to the early/mid 2000s. Conversely, temporal trends for PFOS, Σ12PFCAs, Σ7AHFRs, and THg were characterized by a combination of second-order declines and non-linear increases in recent years. After correcting THg for dietary shifts using δ15N, THg concentrations followed a U-shaped trend at Mandarte and Cleland Islands, while those at Mitlenatch Island remained relatively constant over time. Increasing trends for some contaminants coincided with both an increase in δ13C and δ15N. For the HHRA, all gull eggs collected in 2020 had hazard quotients (HQs) < 0.2, indicating no foreseeable risk or harm for First Nations consumers for certain contaminants. Our findings indicate that spatio-temporal trends of persistent contaminants in Pacific glaucous-winged gull eggs are influenced by a combination of factors, including the impact of regulations on anthropogenic emissions, coupled with changes in foraging behaviour and food-web structure.
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Affiliation(s)
- Robert Kesic
- Environment and Climate Change Canada, Wildlife Research Division, Delta, British Columbia, Canada.
| | - John E Elliott
- Environment and Climate Change Canada, Wildlife Research Division, Delta, British Columbia, Canada.
| | - Sandi L Lee
- Environment and Climate Change Canada, Wildlife Research Division, Delta, British Columbia, Canada.
| | - Kyle H Elliott
- Department of Natural Resource Sciences, McGill University, Sainte Anne-de-Bellevue, Quebec, H3A 0G4, Canada.
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4
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Aune AA, Gabrielsen GW, Ellis HI, Jenssen BM. Triiodothyronine (T 3), but not resting metabolic rate correlates positively with per- and polyfluoroalkyl substances (PFAS) in Arctic terns. ENVIRONMENTAL RESEARCH 2024; 263:120200. [PMID: 39427944 DOI: 10.1016/j.envres.2024.120200] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 04/09/2024] [Revised: 10/17/2024] [Accepted: 10/18/2024] [Indexed: 10/22/2024]
Abstract
In Arctic seabirds, positive correlations between per- and polyfluoroalkyl substances (PFAS) and thyroid hormones (THs) and resting metabolic rate (RMR) have been documented. Herein we investigated levels and patterns of PFAS in Arctic terns (Sterna paradisaea) nesting in Kongsfjorden, Svalbard (Norway), and if circulating concentrations of PFAS correlated with their circulating concentrations of TH, and the RMR of the birds. The hypothesis was that there will be positive correlations between PFAS, TH, and RMR, indicating that PFAS-induced increases in plasma THs could be responsible for the increased RMR. The dominating PFAS in the terns were perfluorooctane sulfonate (PFOS), perfluoroundecanoate (PFUnDA) and perfluorotridecanoate (PFTrDA). The PFAS pattern was similar to what has been found in other seabirds in Kongsfjorden. There were positive correlations between several PFAS and total triiodothyronine (TT3) concentrations in the terns. When sex was accounted for there were significant correlations in female terns, but not in males. There were no correlations between PFAS and RMR or between TT3 and RMR. This indicates that there is no link between a PFAS-induced increase in plasma TT3 concentrations and a resultant increased RMR. The positive associations between blood PFAS concentrations and plasma TT3 concentrations may be a passive association, as both PFAS and T3 bind to thyroid hormone binding proteins (THBP). We recommend that interrelationships between circulating concentrations of PFAS, THs and THBP are investigated further to identify the role of PFAS as TH disrupting chemicals and chemicals that may affect the RMR in birds.
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Affiliation(s)
- Aslak Arnesson Aune
- Department of Biology, Norwegian University of Science and Technology, NO-7491, Trondheim, Norway.
| | | | - Hugh I Ellis
- Department of Biology, University of San Diego, San Diego, CA, 92110, USA
| | - Bjorn Munro Jenssen
- Department of Biology, Norwegian University of Science and Technology, NO-7491, Trondheim, Norway; Department of Arctic Technology, University Centre in Svalbard, P.O. Box 156 N-9171 Longyearbyen, Norway.
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Humann-Guilleminot S, Blévin P, Gabrielsen GW, Herzke D, Nikiforov VA, Jouanneau W, Moe B, Parenteau C, Helfenstein F, Chastel O. PFAS Exposure is Associated with a Lower Spermatic Quality in an Arctic Seabird. ENVIRONMENTAL SCIENCE & TECHNOLOGY 2024; 58:19617-19626. [PMID: 39441666 PMCID: PMC11542889 DOI: 10.1021/acs.est.4c04495] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Subscribe] [Scholar Register] [Received: 05/06/2024] [Revised: 10/16/2024] [Accepted: 10/16/2024] [Indexed: 10/25/2024]
Abstract
Several studies have reported an increasing occurrence of poly- and perfluorinated alkyl substances (PFASs) in Arctic wildlife tissues, raising concerns due to their resistance to degradation. While some research has explored PFAS's physiological effects on birds, their impact on reproductive functions, particularly sperm quality, remains underexplored. This study aims to assess (1) potential association between PFAS concentrations in blood and sperm quality in black-legged kittiwakes (Rissa tridactyla), focusing on the percentage of abnormal spermatozoa, sperm velocity, percentage of sperm motility, and morphology; and (2) examine the association of plasma levels of testosterone, corticosterone, and luteinizing hormone with both PFAS concentrations and sperm quality parameters to assess possible endocrine disrupting pathways. Our findings reveal a positive correlation between the concentration of longer-chain perfluoroalkyl carboxylates (PFCA; C11-C14) in blood and the percentage of abnormal sperm in kittiwakes. Additionally, we observed that two other PFAS (i.e., PFOSlin and PFNA), distinct from those associated with sperm abnormalities, were positively correlated with the stress hormone corticosterone. These findings emphasize the potentially harmful substance-specific effects of long-chain PFCAs on seabirds and the need for further research into the impact of pollutants on sperm quality as a potential additional detrimental effect on birds.
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Affiliation(s)
- Ségolène Humann-Guilleminot
- Department
of Environmental Science, Radboud Institute for Biological and Environmental
Sciences (RIBES), Faculty of Science, Radboud
University, Nijmegen 6500, the Netherlands
- Laboratory
of Evolutionary Ecophysiology, Institute of Biology, University of Neuchâtel, Neuchâtel 2000, Switzerland
| | - Pierre Blévin
- Centre
d’Etudes Biologiques de Chizé, UMR 7372 CNRS - Université de La Rochelle, Villiers-en-Bois 79360, France
- Akvaplan
niva AS, Fram Centre, Tromsø NO-9296, Norway
| | | | - Dorte Herzke
- Norwegian
Institute for Air Research, Fram Centre, Tromsø NO-9296, Norway
| | | | - William Jouanneau
- Centre
d’Etudes Biologiques de Chizé, UMR 7372 CNRS - Université de La Rochelle, Villiers-en-Bois 79360, France
| | - Børge Moe
- Norwegian
Institute for Nature Research, Trondheim NO-7034, Norway
| | - Charline Parenteau
- Centre
d’Etudes Biologiques de Chizé, UMR 7372 CNRS - Université de La Rochelle, Villiers-en-Bois 79360, France
| | - Fabrice Helfenstein
- Laboratory
of Evolutionary Ecophysiology, Institute of Biology, University of Neuchâtel, Neuchâtel 2000, Switzerland
- Norwegian
Institute for Nature Research, Trondheim NO-7034, Norway
- Department
of Clinical Research, University of Bern, Bern 3010, Switzerland
| | - Olivier Chastel
- Centre
d’Etudes Biologiques de Chizé, UMR 7372 CNRS - Université de La Rochelle, Villiers-en-Bois 79360, France
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Matos DM, Ramos JA, Brandão ALC, Baptista F, Rodrigues I, Fernandes JO, Batista de Carvalho LAE, Marques MPM, Cunha SC, Antunes S, Paiva VH. Influence of paternal factors on plastic ingestion and brominated chemical exposure in East Tropical Atlantic Procellariid chicks. THE SCIENCE OF THE TOTAL ENVIRONMENT 2024; 945:173815. [PMID: 38857804 DOI: 10.1016/j.scitotenv.2024.173815] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 02/09/2024] [Revised: 06/04/2024] [Accepted: 06/04/2024] [Indexed: 06/12/2024]
Abstract
The presence of plastic debris and organo-brominated compounds in the marine environment poses a concern to wildlife. Plastic can absorb and release chemical compounds, making their ingestion potentially harmful, while chemical compounds have become omnipresent, with a tendency to bioaccumulate in the food web. Seabirds are often used as indicators of marine plastic pollution, yet studies on the exposure of tropical communities to plastic contamination are still scarce. In this study we monitored the amounts of plastics in faeces and organo-brominated compounds ingested/assimilated in feathers by adults and chicks of Cape Verde shearwaters and Bulwer's petrels from Cabo Verde. Anthropogenic pollutants, polybrominated diphenyl ethers (PBDEs), and naturally generated methoxylated-PBDEs (MeO-PBDEs) were among the probed compounds. The frequency of plastic debris ingestion was similar in both species' adults and chicks, although, the characteristics of the ingested plastic differed. Frequency and number of microplastics increased throughout the nestling season for chicks from both species. All species and age groups showed the presence of PBDEs and MeO-PBDEs. Among PBDEs, Bulwer's petrels exhibited higher concentrations than Cape Verde shearwaters, and chicks had higher concentration profiles than adults. Specifically, Bulwer's petrel chicks showed higher concentrations than Cape Verde shearwater chicks. On the contrary, Cape Verde shearwater adults exhibited higher occurrence and concentrations of MeO-PBDEs when compared to Cape Verde shearwater chicks. We found no effect of plastic loadings or loadings of organohalogen contaminants on body condition or size, although harmful effects may be hidden or reveal themselves in a medium- to long-term. Feather samples from both adults and chicks were shown to be useful for comparing intraspecific contamination levels and appear suitable for the long-term assessment of organohalogen contaminants in seabirds. Species-specific foraging and feeding strategies are likely the drivers of the observed variation in organochlorine contamination burdens among seabird species.
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Affiliation(s)
- Diana M Matos
- University of Coimbra, MARE - Marine and Environmental Sciences Centre/ARNET - Aquatic Research Network, Department of Life Sciences, Calçada Martim de Freitas, 3000-456 Coimbra, Portugal.
| | - J A Ramos
- University of Coimbra, MARE - Marine and Environmental Sciences Centre/ARNET - Aquatic Research Network, Department of Life Sciences, Calçada Martim de Freitas, 3000-456 Coimbra, Portugal
| | - A L C Brandão
- University of Coimbra, Molecular Physical-Chemistry R&D Unit, Department of Chemistry, 3004-535 Coimbra, Portugal
| | - Francisca Baptista
- University of Coimbra, MARE - Marine and Environmental Sciences Centre/ARNET - Aquatic Research Network, Department of Life Sciences, Calçada Martim de Freitas, 3000-456 Coimbra, Portugal
| | - Isabel Rodrigues
- Biosfera Cabo Verde, Sul do Cemitério, Rua 5 - Caixa Postal 233, São Vicente, Cabo Verde
| | - J O Fernandes
- LAQV/REQUIMTE, Laboratório de Bromatologia e Hidrologia, Faculdade de Farmácia, Universidade do Porto, Rua de Jorge Viterbo Ferreira 228, 4050-313 Porto, Portugal
| | - L A E Batista de Carvalho
- University of Coimbra, Molecular Physical-Chemistry R&D Unit, Department of Chemistry, 3004-535 Coimbra, Portugal
| | - M P M Marques
- University of Coimbra, Molecular Physical-Chemistry R&D Unit, Department of Chemistry, 3004-535 Coimbra, Portugal; University of Coimbra, Department of Life Sciences, Calçada Martim de Freitas, 3000-456 Coimbra, Portugal
| | - S C Cunha
- LAQV/REQUIMTE, Laboratório de Bromatologia e Hidrologia, Faculdade de Farmácia, Universidade do Porto, Rua de Jorge Viterbo Ferreira 228, 4050-313 Porto, Portugal
| | - Stefan Antunes
- Biosfera Cabo Verde, Sul do Cemitério, Rua 5 - Caixa Postal 233, São Vicente, Cabo Verde
| | - V H Paiva
- University of Coimbra, MARE - Marine and Environmental Sciences Centre/ARNET - Aquatic Research Network, Department of Life Sciences, Calçada Martim de Freitas, 3000-456 Coimbra, Portugal
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Ricolfi L, Taylor MD, Yang Y, Lagisz M, Nakagawa S. Maternal transfer of per- and polyfluoroalkyl substances (PFAS) in wild birds: A systematic review and meta-analysis. CHEMOSPHERE 2024; 361:142346. [PMID: 38759804 DOI: 10.1016/j.chemosphere.2024.142346] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 03/13/2024] [Revised: 05/07/2024] [Accepted: 05/14/2024] [Indexed: 05/19/2024]
Abstract
Per- and polyfluoroalkyl substances (PFAS) are synthetic chemicals widely used in consumer products. PFAS can accumulate in animal tissues, resulting in biomagnification and adverse effects on wildlife, such as reproductive impairment. In bird species, PFAS are transferred from mothers to eggs along with essential nutrients and may affect embryo development. However, the extent of maternal PFAS transfer across different species and compounds remains poorly understood. Here, we conducted a systematic review and meta-analysis to quantify maternal PFAS transfer in wild birds and investigate potential sources of variation. We tested the moderating effects of compounds' physicochemical properties and biological traits of studied birds. The dataset included 505 measurements of PFAS concentration and 371 effect sizes derived from 13 studies on 16 bird species and 25 compounds. Overall, across all studies and species, we found a 41% higher concentration of PFAS in offspring than in mothers. Specifically, contaminants were concentrated in the yolk, longer and heavier compounds showed preferential transfer, larger clutch size was associated with decreased PFAS transfer and a higher transfer rate was shown in species with piscivorous and opportunistic/diverse diets. A validation assessment showed good robustness of the overall meta-analytic result. Given the crucial role of birds in maintaining ecological balance, this research article has relevant implications for modelling the impacts of PFAS on wildlife, ecosystems, and human health.
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Affiliation(s)
- Lorenzo Ricolfi
- Evolution and Ecology Research Centre, School of Biological, Earth and Environmental Sciences, University of New South Wales Sydney, Sydney, NSW, 2052, Australia.
| | - Matthew D Taylor
- Evolution and Ecology Research Centre, School of Biological, Earth and Environmental Sciences, University of New South Wales Sydney, Sydney, NSW, 2052, Australia; Port Stephens Fisheries Institute, New South Wales Department of Primary Industries, Nelson Bay, Australia; Queensland Alliance for Environmental Health Sciences, Faculty of Health and Behavioural Sciences, The University of Queensland, Brisbane, Australia.
| | - Yefeng Yang
- Evolution and Ecology Research Centre, School of Biological, Earth and Environmental Sciences, University of New South Wales Sydney, Sydney, NSW, 2052, Australia.
| | - Malgorzata Lagisz
- Evolution and Ecology Research Centre, School of Biological, Earth and Environmental Sciences, University of New South Wales Sydney, Sydney, NSW, 2052, Australia.
| | - Shinichi Nakagawa
- Evolution and Ecology Research Centre, School of Biological, Earth and Environmental Sciences, University of New South Wales Sydney, Sydney, NSW, 2052, Australia.
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Guan KL, Luo XJ, Zhu CH, Chen X, Chen PP, Guo J, Hu KQ, Zeng YH, Mai BX. Tissue-Specific Distribution and Maternal Transfer of Persistent Organic Halogenated Pollutants in Frogs. ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY 2024; 43:1557-1568. [PMID: 38695729 DOI: 10.1002/etc.5882] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Subscribe] [Scholar Register] [Received: 12/05/2023] [Revised: 01/21/2024] [Accepted: 04/01/2024] [Indexed: 06/27/2024]
Abstract
Persistent organic pollutants pose a great threat to amphibian populations, but information on the bioaccumulation of contaminants in amphibians remains scarce. To examine the tissue distribution and maternal transfer of organic halogenated pollutants (OHPs) in frogs, seven types of tissues from black-spotted frog (muscle, liver, kidney, stomach, intestine, heart, and egg) were collected from an e-waste-polluted area in South China. Among the seven frog tissues, median total OHP concentrations of 2.3 to 9.7 μg/g lipid weight were found (in 31 polychlorinated biphenyl [PCB] individuals and 15 polybrominated diphenyl ether [PBDE], dechlorane plus [syn-DP and anti-DP], bexabromobenzene [HBB], polybrominated biphenyl] PBB153 and -209], and decabromodiphenyl ethane [DBDPE] individuals). Sex-specific differences in contaminant concentration and compound compositions were observed among the frog tissues, and eggs had a significantly higher contaminant burden on the whole body of female frogs. In addition, a significant sex difference in the concentration ratios of other tissues to the liver was observed in most tissues except for muscle. These results suggest that egg production may involve the mobilization of other maternal tissues besides muscle, which resulted in the sex-specific distribution. Different parental tissues had similar maternal transfer mechanisms; factors other than lipophilicity (e.g., molecular size and proteinophilic characteristics) could influence the maternal transfer of OHPs in frogs. Environ Toxicol Chem 2024;43:1557-1568. © 2024 SETAC.
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Affiliation(s)
- Ke-Lan Guan
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China
- University of Chinese Academy of Sciences, Beijing, China
| | - Xiao-Jun Luo
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China
| | - Chu-Hong Zhu
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China
- University of Chinese Academy of Sciences, Beijing, China
| | - Xi Chen
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China
- University of Chinese Academy of Sciences, Beijing, China
| | - Peng-Peng Chen
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China
- University of Chinese Academy of Sciences, Beijing, China
| | - Jian Guo
- Guangdong University of Petrochemical Technology, Maoming, China
| | - Ke-Qi Hu
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China
| | - Yan-Hong Zeng
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China
| | - Bi-Xian Mai
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China
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9
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Sun G, Du X, Wu Y, Yin G, Chen L, Liu X, Zhou Y, Qiu Y, Lin T. Novel and legacy brominated flame retardants in snakes and frogs: Tissue distribution, biomagnification, and maternal transfer. THE SCIENCE OF THE TOTAL ENVIRONMENT 2023; 896:165194. [PMID: 37391149 DOI: 10.1016/j.scitotenv.2023.165194] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 04/18/2023] [Revised: 06/26/2023] [Accepted: 06/26/2023] [Indexed: 07/02/2023]
Abstract
Although many studies have examined polybrominated diphenyl ethers (PBDEs) and novel brominated flame retardants (NBFRs) in biota, information on the bioaccumulation characteristics of NBFRs from field works is limited. This study investigated the tissue-specific exposure to PBDEs and NBFRs in two reptilian (short-tailed mamushi and red-backed rat snake) and one amphibian species (black-spotted frog) prevalent in the Yangtze River Delta, China. The levels of ΣPBDEs and ΣNBFRs ranged from 4.4-250 and 2.9-22 ng/g lipid weight for snakes respectively and 2.9-120 and 7.1-97 ng/g lipid weight for frogs respectively. BDE-209, BDE-154, and BDE-47 were three major PBDE congeners while decabromodiphenylethane (DBDPE) dominated in NBFRs. Tissue burdens indicated that snake adipose was the major storage site of PBDEs and NBFRs. The biomagnification factors (BMFs) estimated from black-spotted frog to red-backed rat snake indicated the biomagnification of penta- to nona-BDE congeners (BMFs 1.1-4.0) but the lack of biomagnification of other BDE and all NBFR congeners (BMFs 0.16-0.78). Mother to egg transfer of PBDEs and NBFRs evaluated in frogs showed that maternal transfer efficiency was positively related to chemical lipophilicity. This is the first field study on the tissue distribution of NBFRs in reptiles and amphibians and the maternal transfer behavior of 5 major NBFRs. The results underline the bioaccumulation potential of alternative NBFRs.
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Affiliation(s)
- Guanzhen Sun
- College of Marine Ecology and Environment, Shanghai Ocean University, Shanghai 201306, China
| | - Xinyu Du
- College of Marine Ecology and Environment, Shanghai Ocean University, Shanghai 201306, China; State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China.
| | - Yan Wu
- Key Laboratory of Geographic Information Science (Ministry of Education), School of Geographic Sciences, East China Normal University, Shanghai 200241, China
| | - Ge Yin
- Shimadzu (China) Co., LTD, Shanghai 200233, China
| | - Luting Chen
- SUEZ (Shanghai) Investment Co., LTD, Shanghai 200070, China
| | - Xiaojun Liu
- Université de technologie de Compiègne, ESCOM, TIMR (Integrated Transformations of Renewable Matter), Centre de recherches Royallieu - CS 60 319, 60 203 Compiègne Cedex, France
| | - Yihui Zhou
- State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China
| | - Yanling Qiu
- State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China
| | - Tian Lin
- College of Marine Ecology and Environment, Shanghai Ocean University, Shanghai 201306, China
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10
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Jouanneau W, Léandri-Breton DJ, Herzke D, Moe B, Nikiforov VA, Pallud M, Parenteau C, Gabrielsen GW, Chastel O. Does contaminant exposure disrupt maternal hormones deposition? A study on per- and polyfluoroalkyl substances in an Arctic seabird. THE SCIENCE OF THE TOTAL ENVIRONMENT 2023; 868:161413. [PMID: 36621503 DOI: 10.1016/j.scitotenv.2023.161413] [Citation(s) in RCA: 1] [Impact Index Per Article: 0.5] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 09/18/2022] [Revised: 12/09/2022] [Accepted: 01/02/2023] [Indexed: 06/17/2023]
Abstract
Maternal effects are thought to be essential tools for females to modulate offspring development. The selective deposition of avian maternal hormones could therefore allow females to strategically adjust the phenotype of their offspring to the environmental situation encountered. However, at the time of egg formation, several contaminants are also transferred to the egg, including per- and polyfluoroalkyl substances (PFAS) which are ubiquitous organic contaminants with endocrine disrupting properties. It is, however, unknown if they can disrupt maternal hormone deposition. In this study we explored relationships between female PFAS burden and maternal deposition in the eggs of steroids (dihydrotestosterone, androstenedione and testosterone), glucocorticoids (corticosterone) and thyroid hormones (triiodothyronine and thyroxine) in a population of the Arctic-breeding black-legged kittiwake (Rissa tridactyla). Egg yolk hormone levels were unrelated to female hormone plasma levels. Second-laid eggs had significantly lower concentrations of androstenedione than first-laid eggs. Triiodothyronine yolk levels were decreasing with increasing egg mass but increasing with increasing females' body condition. Testosterone was the only transferred yolk hormone correlated to maternal PFAS burden: specifically, we found a positive correlation between testosterone in yolks and circulating maternal perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDcA) and perfluoroundecanoic acid (PFUnA) in first-laid eggs. This correlative study provides a first insight into the potential of some long-chain perfluoroalkyl acids to disrupt maternal hormones deposition in eggs and raises the question about the consequences of increased testosterone deposition on the developing embryo.
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Affiliation(s)
- William Jouanneau
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS - La Rochelle Université, 17031 La Rochelle, France; Norwegian Polar Institute, Fram Centre, NO-9296 Tromsø, Norway.
| | - Don-Jean Léandri-Breton
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS - La Rochelle Université, 17031 La Rochelle, France; Department of Natural Resource Sciences, McGill University, Ste Anne-de-Bellevue, QC H9X 3V9, Canada
| | - Dorte Herzke
- NILU - Norwegian Institute for Air Research, Fram Centre, NO-9296 Tromsø, Norway
| | - Børge Moe
- NINA - Norwegian Institute for Nature Research, NO-7485 Trondheim, Norway
| | - Vladimir A Nikiforov
- NILU - Norwegian Institute for Air Research, Fram Centre, NO-9296 Tromsø, Norway
| | - Marie Pallud
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS - La Rochelle Université, 17031 La Rochelle, France
| | - Charline Parenteau
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS - La Rochelle Université, 17031 La Rochelle, France
| | | | - Olivier Chastel
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS - La Rochelle Université, 17031 La Rochelle, France
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11
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Elliott JE, Kesic R, Lee SL, Elliott KH. Temporal trends (1968-2019) of legacy persistent organic pollutants (POPs) in seabird eggs from the northeast Pacific: Is it finally twilight for old POPs? THE SCIENCE OF THE TOTAL ENVIRONMENT 2023; 858:160084. [PMID: 36368377 DOI: 10.1016/j.scitotenv.2022.160084] [Citation(s) in RCA: 2] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 08/12/2022] [Revised: 11/03/2022] [Accepted: 11/05/2022] [Indexed: 06/16/2023]
Abstract
Legacy persistent organic pollutants (POPs), such as organochlorine pesticides (OCs) and polychlorinated biphenyls (PCBs), are known to persist in the marine environment; however, whether concentrations of these POPs have decreased or stabilized from Canada's Pacific coast in recent years is unclear. Here, we examined temporal trends of various legacy POPs in the eggs of five seabird species; two cormorants (Nannopterum auritum and Urile pelagicus), an auklet (Cerorhinca monocerata), a murrelet (Synthliboramphus antiquus), and a storm-petrel (Hydrobates leucorhous), sampled 1968 to 2019 from 23 colonies along the Pacific coast of British Columbia, Canada. The contaminant profile in the eggs of all species and sampling years was dominated by ΣPCBs, followed by ΣDDT (mostly p,p'-DDE), ΣHCH (β-HCH), ΣCHLOR (oxychlordane), and ΣCBz (HCB). ΣOC and ΣPCB concentrations were generally higher in double-crested cormorant eggs than in the other four species. The majority of legacy POPs are either significantly declining (e.g. p,p'-DDE, HCB, HE, oxychlordane, ΣPCBs) or showing no directional change over time (ΣMirex) in the eggs of our monitoring species. Contaminants such as α-HCH, cis- and trans-chlordane, p,p'-DDT, dieldrin, and octachlorostyrene also showed evidence of downward trends, largely influenced by non-detect values during more recent sampling periods. Increasing trends were observed for β-HCH in the eggs of some species; however, mean concentrations eventually returned to early 2000 levels by the end of the study period. Although bulk δ15N and δ13C egg values varied interannually, compound-specific amino acid analyses suggested no major changes in trophic position or baseline food web signature. Temporal trends observed here were comparable to those found in other seabird species and pelagic food webs. As most legacy POPs in our data set were at very low levels in recent years, we support the general consensus that it is indeed the twilight years for old POPs, and we attribute these declines largely to voluntary regulations and international restrictions on the production and use of these compounds, and thus their release into the marine environment.
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Affiliation(s)
- John E Elliott
- Environment and Climate Change Canada, Ecotoxicology & Wildlife Health Division, 5421 Robertson Rd, Delta, British Columbia, Canada.
| | - Robert Kesic
- Environment and Climate Change Canada, Ecotoxicology & Wildlife Health Division, 5421 Robertson Rd, Delta, British Columbia, Canada.
| | - Sandi L Lee
- Environment and Climate Change Canada, Ecotoxicology & Wildlife Health Division, 5421 Robertson Rd, Delta, British Columbia, Canada.
| | - Kyle H Elliott
- Department of Natural Resource Sciences, McGill University, Sainte Anne-de-Bellevue, Montreal, Quebec, Canada.
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12
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Zhou Y, Fu J, Wang M, Guo Y, Yang L, Han J, Zhou B. Parental and transgenerational impairments of thyroid endocrine system in zebrafish by 2,4,6-tribromophenol. J Environ Sci (China) 2023; 124:291-299. [PMID: 36182138 DOI: 10.1016/j.jes.2021.09.022] [Citation(s) in RCA: 6] [Impact Index Per Article: 3.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/17/2021] [Revised: 09/16/2021] [Accepted: 09/17/2021] [Indexed: 06/16/2023]
Abstract
Many environmental contaminants could be transmitted from parents and generate impairments to their progeny. The 2,4,6-tribromophenol (TBP), a novel brominated flame retardant which has been frequently detected in various organisms, was supposed to be bioaccumulated and intergenerational transmitted in human beings. Previous studies revealed that TBP could disrupt thyroid endocrine system in zebrafish larvae. However, there is no available data regarding the parental and transgenerational toxicity of this contaminant. Thus, in this study adult zebrafish were exposed to environmental contaminated levels of TBP for 60 days to investigate the parental and transgenerational impairments on thyroid endocrine system. Chemical analysis verified the bioaccumulation of TBP in tested organs of parents (concentration: liver>gonads>brain) and its transmission into eggs. For adults, increased thyroid hormones, disturbed transcriptions of related genes and histopathological changes in thyroid follicles indicate obvious thyroid endocrine disruptions. Transgenerational effects are indicated by the increased thyroid hormones both in eggs (maternal source) and in developed larvae (newly synthesized), as well as disrupted transcriptional profiles of key genes in HPT axis. The overall results suggest that the accumulated TBP could be transmitted from parent to offspring and generate thyroid endocrine disruptions in both generations.
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Affiliation(s)
- Yuxi Zhou
- State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China; University of Chinese Academy of Sciences, Beijing 100049, China
| | - Juanjuan Fu
- State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China; University of Chinese Academy of Sciences, Beijing 100049, China
| | - Min Wang
- State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
| | - Yongyong Guo
- State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
| | - Lihua Yang
- State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
| | - Jian Han
- State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China.
| | - Bingsheng Zhou
- State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
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13
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Bellot P, Brischoux F, Fritsch C, Goutte A, Alliot F, Rocchi S, Angelier F. Evidence of environmental transfer of tebuconazole to the eggs in the house sparrow (Passer domesticus): An experimental study. CHEMOSPHERE 2022; 308:136469. [PMID: 36116623 DOI: 10.1016/j.chemosphere.2022.136469] [Citation(s) in RCA: 10] [Impact Index Per Article: 3.3] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 07/01/2022] [Revised: 09/10/2022] [Accepted: 09/12/2022] [Indexed: 06/15/2023]
Abstract
Triazole compounds are among the most widely used fungicides in agroecosystems to protect crops from potential fungal diseases. Many farmland birds spend a significant part of their life cycle in agroecosystems, which may chronically expose them to pesticides. We experimentally tested whether exposure to environmental concentrations of tebuconazole could induce a contamination of the eggs in an agroecosystem sentinel species, the house sparrow (Passer domesticus). Wild-caught adult sparrows were maintained in captivity and exposed (exposed group) or not (control group) for seven months to tebuconazole through drinking water. Eggs were opportunistically collected for the determination of tebuconazole concentration by Liquid Chromatography coupled to tandem Mass Spectrometry in eggs. We found that eggs from exposed parents all contained tebuconazole with a mean concentration of 1.52 ng g-1 dry weight. In eggs from control parents, the tebuconazole concentration was below the limit of quantification (0.23 ng g-1 dry weight) for 11 out of 13 eggs. Thus, our study demonstrates for the first time that environmental exposure of female birds to tebuconazole can translate into egg contamination by this fungicide.
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Affiliation(s)
- Pauline Bellot
- Centre D'Etudes Biologiques de Chizé, CNRS-La Rochelle Université, UMR 7372, 79360, Villiers en Bois, France.
| | - François Brischoux
- Centre D'Etudes Biologiques de Chizé, CNRS-La Rochelle Université, UMR 7372, 79360, Villiers en Bois, France
| | - Clémentine Fritsch
- Laboratoire Chrono-Environnement, UMR 6249 CNRS / Université Bourgogne Franche-Comté, 25000, Besançon, France
| | - Aurélie Goutte
- École Pratique des Hautes Études, PSL Research University, UMR 7619 METIS, Sorbonne Université- CNRS, Paris, France
| | - Fabrice Alliot
- École Pratique des Hautes Études, PSL Research University, UMR 7619 METIS, Sorbonne Université- CNRS, Paris, France
| | - Steffi Rocchi
- Laboratoire Chrono-Environnement, UMR 6249 CNRS / Université Bourgogne Franche-Comté, 25000, Besançon, France; Service de Parasitologie-Mycologie, CHU Jean Minjoz, 25000, Besançon, France
| | - Frédéric Angelier
- Centre D'Etudes Biologiques de Chizé, CNRS-La Rochelle Université, UMR 7372, 79360, Villiers en Bois, France
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14
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Jouanneau W, Léandri-Breton DJ, Corbeau A, Herzke D, Moe B, Nikiforov VA, Gabrielsen GW, Chastel O. A Bad Start in Life? Maternal Transfer of Legacy and Emerging Poly- and Perfluoroalkyl Substances to Eggs in an Arctic Seabird. ENVIRONMENTAL SCIENCE & TECHNOLOGY 2022; 56:6091-6102. [PMID: 34874166 DOI: 10.1021/acs.est.1c03773] [Citation(s) in RCA: 38] [Impact Index Per Article: 12.7] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 06/13/2023]
Abstract
In birds, maternal transfer is a major exposure route for several contaminants, including poly- and perfluoroalkyl substances (PFAS). Little is known, however, about the extent of the transfer of the different PFAS compounds to the eggs, especially for alternative fluorinated compounds. In the present study, we measured legacy and emerging PFAS, including Gen-X, ADONA, and F-53B, in the plasma of prelaying black-legged kittiwake females breeding in Svalbard and the yolk of their eggs. We aimed to (1) describe the contaminant levels and patterns in both females and eggs, and (2) investigate the maternal transfer, that is, biological variables and the relationship between the females and their eggs for each compound. Contamination of both females and eggs were dominated by linPFOS then PFUnA or PFTriA. We notably found 7:3 fluorotelomer carboxylic acid─a precursor of long-chain carboxylates─in 84% of the egg yolks, and provide the first documented finding of ADONA in wildlife. Emerging compounds were all below the detection limit in female plasma. There was a linear association between females and eggs for most of the PFAS. Analyses of maternal transfer ratios in females and eggs suggest that the transfer is increasing with PFAS carbon chain length, therefore the longest chain perfluoroalkyl carboxylic acids (PFCAs) were preferentially transferred to the eggs. The mean ∑PFAS in the second-laid eggs was 73% of that in the first-laid eggs. Additional effort on assessing the outcome of maternal transfers on avian development physiology is essential, especially for PFCAs and emerging fluorinated compounds which are under-represented in experimental studies.
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Affiliation(s)
- William Jouanneau
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS - La Rochelle Université, 17031 La Rochelle, France
- Norwegian Polar Institute, Fram Centre, NO-9296 Tromsø, Norway
| | - Don-Jean Léandri-Breton
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS - La Rochelle Université, 17031 La Rochelle, France
- Department of Natural Resource Sciences, McGill University, Ste Anne-de-Bellevue, Quebec H9X 3 V9, Canada
| | - Alexandre Corbeau
- ECOBIO (Ecosystèmes, biodiversité, évolution), UMR 6553 CNRS - Université de Rennes, 35000 Rennes, France
| | - Dorte Herzke
- NILU - Norwegian Institute for Air Research, Fram Centre, NO-9296 Tromsø, Norway
| | - Børge Moe
- NINA - Norwegian Institute for Nature Research, NO-7485 Trondheim, Norway
| | - Vladimir A Nikiforov
- NILU - Norwegian Institute for Air Research, Fram Centre, NO-9296 Tromsø, Norway
| | | | - Olivier Chastel
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS - La Rochelle Université, 17031 La Rochelle, France
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15
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Ding Y, Zheng X, Yu L, Lu R, Wu X, Luo X, Mai B. Occurrence and Distribution of Persistent Organic Pollutants (POPs) in Amphibian Species: Implications from Biomagnification Factors Based on Quantitative Fatty Acid Signature Analysis. ENVIRONMENTAL SCIENCE & TECHNOLOGY 2022; 56:3117-3126. [PMID: 35113557 DOI: 10.1021/acs.est.1c07416] [Citation(s) in RCA: 19] [Impact Index Per Article: 6.3] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 06/14/2023]
Abstract
Contaminants pose a great threat to amphibian populations, but the bioaccumulation and distribution of contaminants in amphibians are still unclear. Polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) had median concentrations of 468-3560 ng/g lipid weight (lw) and 206-2720 ng/g lw in the muscle of amphibians, respectively. BDE 209 was the predominant PBDE congener, while CBs 118, 138, 153, and 180 were the main PCB congeners. The diet compositions of amphibians were estimated by quantitative fatty acid signature analysis (QFASA). Dragonfly contributed the most to the diet of amphibians. Biomagnification factors (BMFs) based on quantitative amphibian/insect relationships showed more credible results than BMFs based on amphibian/each insect or amphibian/combined prey relationships. BMFs derived from QFASA declined with log KOW from 5 to 6.5 and then showed a parabolic relationship with log KOW greater than 6.5. BMFs of PCBs were significantly influenced by the elimination capacity of PCBs in amphibians. Less-hydrophobic PCBs preferentially accumulated in the skin than in muscle, which was probably due to the dermal exposure of less-hydrophobic PCBs for amphibians. The biomagnification and distribution of contaminants may be affected by multiple exposure pathways and the toxicokinetics of contaminants in various life stages of amphibians.
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Affiliation(s)
- Yang Ding
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China
| | - Xiaobo Zheng
- College of Resources and Environment, South China Agricultural University, Guangzhou 510642, China
| | - Lehuan Yu
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China
- School of Biology and Food Engineering, Guangdong University of Education, Guangzhou 510303, China
| | - Ruifeng Lu
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China
| | - Xiaodan Wu
- College of Resources and Environment, South China Agricultural University, Guangzhou 510642, China
| | - Xiaojun Luo
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China
- CAS Center for Excellence in Deep Earth Science, Guangzhou 510640, China
| | - Bixian Mai
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China
- CAS Center for Excellence in Deep Earth Science, Guangzhou 510640, China
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16
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Ángel-Moreno Briones Á, Hernández-Guzmán FA, González-Armas R, Galván-Magaña F, Marmolejo-Rodríguez AJ, Sánchez-González A, Ramírez-Álvarez N. Organochlorine pesticides in immature scalloped hammerheads Sphyrna lewini from the western coast of the Gulf of California, Mexico: Bioaccumulation patterns and human exposure. THE SCIENCE OF THE TOTAL ENVIRONMENT 2022; 806:151369. [PMID: 34740652 DOI: 10.1016/j.scitotenv.2021.151369] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.7] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 06/30/2021] [Revised: 10/26/2021] [Accepted: 10/28/2021] [Indexed: 06/13/2023]
Abstract
Despite the intensive use of organochlorine pesticides (OCPs) in the proximity of the Gulf of California, there is no information regarding their levels in predatory shark species, which could be exposed to relatively high concentrations. In this area, neonates and juveniles of the critically endangered scalloped hammerhead Sphyrna lewini are caught for consumption, so the examination of the accumulation of OCPs is necessary for future conservation, as well as to assess the exposure to humans. Levels and accumulation patterns of 29 OCPs were analyzed in the liver and muscle of 20 immature scalloped hammerheads. Twenty-three compounds were detected in liver and 17 OCPs were found in muscle. In the latter tissue, only p,p'-DDE presented concentrations above the detection limit in all samples (0.59 ± 0.21 ng/g w.w.), while in the liver, DDTs were also the main group of pesticides (215 ± 317 ng/g w.w.), followed by ∑Chlordanes > ∑Chlorobenzenes > Mirex > HCBD > Others. One of the two analyzed neonates presented high concentrations of OCPs in the liver (1830 ng/g w.w.), attributed to a bioamplification process. No differences in accumulation of OCPs were found between juveniles of both sexes, where an increase in the concentration of various compounds related with size and age was observed. Additionally, juveniles under 2 years of age may undergo a growth dilution process. Our results suggest that the consumption of this species does not imply risks to human health (chronic or carcinogenic effects) associated with OCPs. Likewise, we recommend further monitoring due to the possible recent inputs of some OCPs (e.g. dicofol, median of ratio o, p'-DDT/p, p'-DDT = 0.7) into the environment.
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Affiliation(s)
- Ángela Ángel-Moreno Briones
- Instituto Politécnico Nacional, Centro Interdisciplinario de Ciencias Marinas, Av. IPN s/n, La Paz, Baja California Sur C. P. 23096, Mexico
| | - Félix Augusto Hernández-Guzmán
- Instituto de Investigaciones Oceanológicas, Universidad Autónoma de Baja California, Carretera Transpeninsular Ensenada-Tijuana 3917, Ensenada, Baja California C. P. 22860, Mexico
| | - Rogelio González-Armas
- Instituto Politécnico Nacional, Centro Interdisciplinario de Ciencias Marinas, Av. IPN s/n, La Paz, Baja California Sur C. P. 23096, Mexico
| | - Felipe Galván-Magaña
- Instituto Politécnico Nacional, Centro Interdisciplinario de Ciencias Marinas, Av. IPN s/n, La Paz, Baja California Sur C. P. 23096, Mexico
| | - Ana Judith Marmolejo-Rodríguez
- Instituto Politécnico Nacional, Centro Interdisciplinario de Ciencias Marinas, Av. IPN s/n, La Paz, Baja California Sur C. P. 23096, Mexico
| | - Alberto Sánchez-González
- Instituto Politécnico Nacional, Centro Interdisciplinario de Ciencias Marinas, Av. IPN s/n, La Paz, Baja California Sur C. P. 23096, Mexico
| | - Nancy Ramírez-Álvarez
- Instituto de Investigaciones Oceanológicas, Universidad Autónoma de Baja California, Carretera Transpeninsular Ensenada-Tijuana 3917, Ensenada, Baja California C. P. 22860, Mexico.
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17
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Allen SF, Ellis F, Mitchell C, Wang X, Boogert NJ, Lin CY, Clokey J, Thomas KV, Blount JD. Phthalate diversity in eggs and associations with oxidative stress in the European herring gull (Larus argentatus). MARINE POLLUTION BULLETIN 2021; 169:112564. [PMID: 34148634 DOI: 10.1016/j.marpolbul.2021.112564] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.5] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 03/08/2021] [Revised: 05/18/2021] [Accepted: 05/25/2021] [Indexed: 06/12/2023]
Abstract
Phthalates are plastic-derived contaminants that are ubiquitous in natural environments and function as pro-oxidants. The extent to which phthalates bioaccumulate in wild animals and associations with oxidative stress are poorly understood. Here, we describe relationships between maternally-derived phthalates, lipid peroxidation (malondialdehyde, MDA) and the dietary antioxidant α-tocopherol in eggs of European herring gulls (Larus argentatus) in Cornwall, UK. Up to six phthalate parent compounds and four phthalate metabolites were detected. Egg concentrations of MDA were positively associated with dicyclohexyl phthalate (DCHP) and negatively associated with α-tocopherol, suggesting that DCHP is associated with oxidative stress in gulls. The consequences of phthalate exposure in ovo for offspring development warrants study.
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Affiliation(s)
- Simon F Allen
- Centre for Ecology and Conservation, College of Life & Environmental Sciences, University of Exeter, Penryn, Cornwall TR10 9FE, UK
| | - Francesca Ellis
- Centre for Ecology and Conservation, College of Life & Environmental Sciences, University of Exeter, Penryn, Cornwall TR10 9FE, UK
| | - Christopher Mitchell
- Centre for Ecology and Conservation, College of Life & Environmental Sciences, University of Exeter, Penryn, Cornwall TR10 9FE, UK
| | - Xianyu Wang
- Queensland Alliance for Environmental Health Sciences, The University of Queensland, 20 Cornwall Street, Woolloongabba, Queensland 4102, Australia
| | - Neeltje J Boogert
- Centre for Ecology and Conservation, College of Life & Environmental Sciences, University of Exeter, Penryn, Cornwall TR10 9FE, UK
| | - Chun-Yin Lin
- Queensland Alliance for Environmental Health Sciences, The University of Queensland, 20 Cornwall Street, Woolloongabba, Queensland 4102, Australia
| | - Joseph Clokey
- Queensland Alliance for Environmental Health Sciences, The University of Queensland, 20 Cornwall Street, Woolloongabba, Queensland 4102, Australia
| | - Kevin V Thomas
- Queensland Alliance for Environmental Health Sciences, The University of Queensland, 20 Cornwall Street, Woolloongabba, Queensland 4102, Australia
| | - Jonathan D Blount
- Centre for Ecology and Conservation, College of Life & Environmental Sciences, University of Exeter, Penryn, Cornwall TR10 9FE, UK.
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18
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Knudtzon NC, Thorstensen H, Ruus A, Helberg M, Bæk K, Enge EK, Borgå K. Maternal transfer and occurrence of siloxanes, chlorinated paraffins, metals, PFAS and legacy POPs in herring gulls (Larus argentatus) of different urban influence. ENVIRONMENT INTERNATIONAL 2021; 152:106478. [PMID: 33770583 DOI: 10.1016/j.envint.2021.106478] [Citation(s) in RCA: 17] [Impact Index Per Article: 4.3] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 11/24/2020] [Revised: 01/29/2021] [Accepted: 02/20/2021] [Indexed: 06/12/2023]
Abstract
Urban herring gulls (Larus argentatus) are exposed to contaminants from aquatic, terrestrial and anthropogenic sources. We aim to assess if differences in urbanisation affect ecological niche and contaminant concentrations in female herring gulls. Furthermore, we investigated maternal transfer from mothers to eggs for all the target compounds, including chlorinated paraffins (CPs) and cyclic volatile methyl siloxane (cVMSs), which to our knowledge have not been assessed in herring gulls previously. We compare concentrations of legacy and emerging contaminants and metals in blood and eggs between two herring gull colonies located 51 km apart, in the urban influenced Norwegian Oslofjord. While both colonies are within an urbanised area, the inner fjord is more so, as it is surrounded by Oslo, the capital and largest city in Norway Stable isotopes of carbon and nitrogen indicated a more marine ecological niche in the outer than the inner fjord colony, although with overlap. Persistent organic pollutant (POP) concentrations were similar in the inner and outer fjord colonies, while the short-chained chlorinated paraffins (SCCP), which are recently added to the Stockholm convention and contaminants of emerging concern (CECs) varied, with higher concentrations of SCCP and the cVMS decamethylcyclopentasiloxane (D5) in females and eggs of the inner fjord colony. Per- and polyfluorinated substances (PFAS) concentrations were higher in the outer fjord colony, likely linked to releases from a point-source (airport and waste management facility with open access to food waste). In blood, chlorinated paraffins contributed most the total lipophilic contaminants (inner: 78%, outer: 56%), while polychlorinated biphenyls (PCBs) were the most abundant lipophilic contaminants in eggs (inner: 62%, outer: 46%). Dechloranes and brominated flame retardants (BFRs) were detected in few samples. Maternal transfer, assessed by egg to blood ratios, of cVMSs were similar to the POPs with mean log ratio 0.39 (D5), while it was lower for SCCPs, with log ratios-0.77. Our results indicate comparable POP exposure of the herring gulls in the inner and outer Oslofjord, likely due to overlap in ecological niches between the colonies and wide distribution of POPs. The differences between the colonies in concentrations of PFAS, cVMS and CPs shows that point source exposures and urban influence may be more important than ecological niche for these compounds.
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Affiliation(s)
- Nina C Knudtzon
- Department of Biosciences, University of Oslo, Blindernveien 31, 0316 Oslo, Norway
| | - Helene Thorstensen
- Department of Biosciences, University of Oslo, Blindernveien 31, 0316 Oslo, Norway
| | - Anders Ruus
- Department of Biosciences, University of Oslo, Blindernveien 31, 0316 Oslo, Norway; Norwegian Institute for Water Research, Gaustadalleen 21, 0349 Oslo, Norway
| | - Morten Helberg
- Department of Biosciences, University of Oslo, Blindernveien 31, 0316 Oslo, Norway; Østfold University College, B R A Veien 4, 1757 Halden, Norway
| | - Kine Bæk
- Norwegian Institute for Water Research, Gaustadalleen 21, 0349 Oslo, Norway
| | - Ellen K Enge
- Norwegian Institute for Air Research, Instituttveien 18, 2007 Kjeller, Norway
| | - Katrine Borgå
- Department of Biosciences, University of Oslo, Blindernveien 31, 0316 Oslo, Norway.
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Sebastiano M, Jouanneau W, Blévin P, Angelier F, Parenteau C, Gernigon J, Lemesle JC, Robin F, Pardon P, Budzinski H, Labadie P, Chastel O. High levels of fluoroalkyl substances and potential disruption of thyroid hormones in three gull species from South Western France. THE SCIENCE OF THE TOTAL ENVIRONMENT 2021; 765:144611. [PMID: 33385816 DOI: 10.1016/j.scitotenv.2020.144611] [Citation(s) in RCA: 22] [Impact Index Per Article: 5.5] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 09/30/2020] [Revised: 12/08/2020] [Accepted: 12/16/2020] [Indexed: 06/12/2023]
Abstract
Per- and poly-fluoroalkyl substances (PFAS) raised increasing concerns over the past years due to their persistence and global distribution. Understanding their occurrence in the environment and their disruptive effect on the physiology of humans and wildlife remains a major challenge in ecotoxicological studies. Here, we investigate the occurrence of several carboxylic and sulfonic PFAS in 105 individuals of three seabird species (27 great black-backed gull Larus marinus; 44 lesser black-backed gull Larus fuscus graellsii; and 34 European herring gull Larus argentatus) from South western France. We further estimated the relationship between plasma concentrations of PFAS and i) the body condition of the birds and ii) plasma concentrations of thyroid hormone triiodothyronine (TT3). We found that great and lesser black-backed gulls from South Western France are exposed to PFAS levels comparable to highly contaminated species from other geographical areas, although major emission sources (i.e. related to industrial activities) are absent in the region. We additionally found that PFAS are negatively associated with the body condition of the birds in two of the studied species, and that these results are sex-dependent. Finally, we found positive associations between exposure to PFAS and TT3 in the great black-backed gull, suggesting a potential disrupting mechanism of PFAS exposure. Although only three years of data have been collected, we investigated PFAS trend over the study period, and found that great black-backed gulls document an increasing trend of plasma PFAS concentration from 2016 to 2018. Because PFAS might have detrimental effects on birds, French seabird populations should be monitored since an increase of PFAS exposure may impact on population viability both in the short- and long-term.
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Affiliation(s)
- M Sebastiano
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Univ. La Rochelle, France.
| | - W Jouanneau
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Univ. La Rochelle, France
| | - P Blévin
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Univ. La Rochelle, France; Akvaplan-niva AS, Fram Centre, NO-9296 Tromsø, Norway
| | - F Angelier
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Univ. La Rochelle, France
| | - C Parenteau
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Univ. La Rochelle, France
| | - J Gernigon
- Réserve Naturelle de Lilleau des Niges, 17880, France
| | - J C Lemesle
- Réserve Naturelle de Lilleau des Niges, 17880, France
| | - F Robin
- Réserve Naturelle de Lilleau des Niges, 17880, France; Ligue pour la Protection des Oiseaux (LPO), 17300 Rochefort, France
| | - P Pardon
- Univ. Bordeaux, CNRS, EPOC, EPHE, UMR 5805, F-33600 Pessac, France
| | - H Budzinski
- Univ. Bordeaux, CNRS, EPOC, EPHE, UMR 5805, F-33600 Pessac, France
| | - P Labadie
- Univ. Bordeaux, CNRS, EPOC, EPHE, UMR 5805, F-33600 Pessac, France
| | - O Chastel
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Univ. La Rochelle, France
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20
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Hu C, Shui B, Yang X, Wang L, Dong J, Zhang X. Trophic transfer of heavy metals through aquatic food web in a seagrass ecosystem of Swan Lagoon, China. THE SCIENCE OF THE TOTAL ENVIRONMENT 2021; 762:143139. [PMID: 33138994 DOI: 10.1016/j.scitotenv.2020.143139] [Citation(s) in RCA: 28] [Impact Index Per Article: 7.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 06/16/2020] [Revised: 10/11/2020] [Accepted: 10/13/2020] [Indexed: 06/11/2023]
Abstract
The Swan Lagoon is a national nature reserve and an important spawning ground in China. In this study, we evaluated the concentration of heavy metals (Cd, Cr, Cu, Pb, and Zn) in different aquatic organisms (aquatic plants, crustaceans, mollusks, and fish), in order to examine their trophic transfer in food web. The results showed that the concentrations of Cd, Cu, Pb, and Zn were considerably higher in mollusks, whereas Cr concentrations were significantly higher in aquatic plants than in mollusks, crustaceans, and fish (p < 0.01). Heavy metals exhibit different patterns of trophic transfer in food web. Cd, Cr, Cu, and Pb tended to be efficiently biodiluted with increasing trophic levels in food web (trophic magnification factor, TMF < 1; p < 0.05). The concentration of Zn increased with increasing trophic level; however, it exhibited a TMF of only 1.03, and was not significantly correlated with δ15N (p > 0.05), indicating neither biomagnification or biodilution in the food web.
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Affiliation(s)
- Chengye Hu
- Fishery College, Zhejiang Ocean University, Zhoushan 316022, China
| | - Bonian Shui
- Fishery College, Zhejiang Ocean University, Zhoushan 316022, China
| | - Xiaolong Yang
- National Marine Environmental Monitoring Center, State Oceanic Administration, Dalian 116023, China
| | - Linlong Wang
- The Key Laboratory of Mariculture, Ministry of Education, Ocean University of China, Qingdao 266003, China
| | - Jianyu Dong
- The Key Laboratory of Mariculture, Ministry of Education, Ocean University of China, Qingdao 266003, China
| | - Xiumei Zhang
- Fishery College, Zhejiang Ocean University, Zhoushan 316022, China; Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China.
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21
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Parolini M, Cappelli F, De Felice B, Possenti CD, Rubolini D, Valsecchi S, Polesello S. Within- and Among-Clutch Variation of Yolk Perfluoroalkyl Acids in a Seabird from the Northern Adriatic Sea. ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY 2021; 40:744-753. [PMID: 32833265 DOI: 10.1002/etc.4833] [Citation(s) in RCA: 10] [Impact Index Per Article: 2.5] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 05/07/2020] [Revised: 06/10/2020] [Accepted: 07/23/2020] [Indexed: 06/11/2023]
Abstract
Perfluoroalkyl substances (PFAS) are surface-active agents used in diverse industrial and commercial applications. They contaminate both freshwater and marine ecosystems, are highly persistent, and accumulate through trophic transfer. Seabirds are exposed to environmental contaminants due to their high trophic position in food webs and relatively long lifespan. We measured levels of 10 perfluoroalkyl acids (PFAAs) in egg yolks of yellow-legged gulls (Larus michahellis) breeding in the northern Adriatic Sea (Northeast Italy). We examined variations in PFAAs within clutches (between eggs of different laying order) and among clutches. Perfluorooctane sulfonate (PFOS) was the most abundant yolk PFAA (mean = 42.0 ng/g wet wt), followed by perfluorooctanoic acid (PFOA; 3.8 ng/g wet wt) and perfluorododecanoic acid (PFDoDa; 2.8 ng/g wet wt). The ∑PFAAs averaged 57.4 ng/g wet weight, ranging between 26.5 and 115.0 ng/g wet weight. The PFAA levels varied substantially among clutches (0.29-0.79 of the total variation), whereas the effects of laying order were considerably weaker (0.01-0.13). Egg-laying order effects were detected for ∑PFAAs, PFOS, perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), perfluoroundecanoic acid (PFUnA), and PFDoDa, whereby the last-laid eggs exhibited lower PFAA concentrations than early-laid eggs. Our results indicate that seagulls from the northern Adriatic basin deposit measurable amounts of PFAAs in their eggs. The large among-clutches differences in PFAAs suggest that exposure of yellow-legged gull females to these compounds is highly variable. Environ Toxicol Chem 2021;40:744-753. © 2020 SETAC.
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Affiliation(s)
- Marco Parolini
- Department of Environmental Science and Policy, University of Milan, Milan, Italy
| | - Francesca Cappelli
- Water Research Institute, National Research Council of Italy, Brugherio, Monza and Brianza, Italy
- Department of Science and High Technology, University of Insubria, Como, Italy
| | - Beatrice De Felice
- Department of Environmental Science and Policy, University of Milan, Milan, Italy
| | | | - Diego Rubolini
- Department of Environmental Science and Policy, University of Milan, Milan, Italy
| | - Sara Valsecchi
- Water Research Institute, National Research Council of Italy, Brugherio, Monza and Brianza, Italy
| | - Stefano Polesello
- Water Research Institute, National Research Council of Italy, Brugherio, Monza and Brianza, Italy
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Thorstensen H, Ruus A, Helberg M, Baek K, Enge EK, Borgå K. Common Eider and Herring Gull as Contaminant Indicators of Different Ecological Niches of an Urban Fjord System. INTEGRATED ENVIRONMENTAL ASSESSMENT AND MANAGEMENT 2021; 17:422-433. [PMID: 32926521 DOI: 10.1002/ieam.4340] [Citation(s) in RCA: 1] [Impact Index Per Article: 0.3] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 03/31/2019] [Revised: 06/11/2020] [Accepted: 09/11/2020] [Indexed: 06/11/2023]
Abstract
Seabirds like gulls are common indicators in contaminant monitoring. The herring gull (Larus argentatus) is a generalist with a broad range of dietary sources, possibly introducing a weakness in its representativeness of aquatic contamination. To investigate the herring gull as an indicator of contamination in an urban-influenced fjord, the Norwegian Oslofjord, we compared concentrations of a range of lipophilic and protein-associated organohalogen contaminants (OHCs), Hg, and dietary markers in blood (n = 15), and eggs (n = 15) between the herring gull and the strict marine-feeding common eider (Somateria mollissima) in the breeding period of May 2017. Dietary markers showed that the herring gull was less representative of the marine food web than the common eider. We found higher concentrations of lipophilic OHCs (wet weight and lipid weight) and Hg (dry weight) in the blood of common eider (mean ± SE ∑PCB = 210 ± 126 ng/g ww, 60 600 ± 28 300 ng/g lw; mean Hg = 4.94 ± 0.438 ng/g dw) than of the herring gull (mean ± SE ∑PCB = 19.0 ± 15.6 ng/g ww, 1210 ± 1510 ng/g lw; mean Hg = 4.26 ± 0.438 ng/g dw). Eggs gave opposite results; higher wet weight and lipid weight OHC concentrations in the herring gull (mean ± SE ∑PCB = 257 ± 203 ng/g ww, 3240 ± 2610 ng/g lw) than the common eider (mean ± SE ∑PCB = 18.2 ± 20.8 ng/g ww, 101 ± 121 ng/g lw), resulting in higher OHC maternal transfer ratios in gulls than eiders. We suggest that the matrix differences are due to fasting during incubation in the common eider. We suggest that in urban areas, herring gull might not be representative as an indicator of marine contamination but rather urban contaminant exposure. The common eider is a better indicator of marine pollution in the Oslofjord. The results are influenced by the matrix choice, as breeding strategy affects lipid dynamics regarding the transfer of lipids and contaminants to eggs and remobilization of contaminants from lipids to blood during incubation, when blood is drawn from the mother. Our results illustrate the benefit of a multispecies approach for a thorough picture of contaminant status in urban marine ecosystems. Integr Environ Assess Manag 2021;17:422-433. © 2020 The Authors. Integrated Environmental Assessment and Management published by Wiley Periodicals LLC on behalf of Society of Environmental Toxicology & Chemistry (SETAC).
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Affiliation(s)
| | - Anders Ruus
- Department of Biosciences, University of Oslo, Oslo, Norway
- Section for Marine Pollution, Norwegian Institute for Water Research, Oslo, Norway
| | - Morten Helberg
- Department of Teacher Education, Østfold University College, Halden, Norway
| | - Kine Baek
- Section for Marine Pollution, Norwegian Institute for Water Research, Oslo, Norway
| | - Ellen Katrin Enge
- Department of Environmental Chemistry, Norwegian Institute for Air Research, Kjeller, Norway
| | - Katrine Borgå
- Department of Biosciences, University of Oslo, Oslo, Norway
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23
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Piña-Ortiz A, Ceyca-Contreras JP, Covantes-Rosales CE, Betancourt-Lozano M, Castillo-Guerrero JA. Temporal and sex-based variation in organochlorine pesticide levels in the blue-footed booby in two coastal colonies of Sinaloa, Mexico. MARINE POLLUTION BULLETIN 2021; 164:112050. [PMID: 33515824 DOI: 10.1016/j.marpolbul.2021.112050] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.5] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 07/11/2020] [Revised: 12/31/2020] [Accepted: 01/02/2021] [Indexed: 06/12/2023]
Abstract
The temporal, inter-site, and sex-based variation of 19 organochlorine pesticides (OCPs) in blood plasma samples collected from blue-footed boobies of two islands in Sinaloa, Mexico, was evaluated. The effect of OCPs was evaluated with the heterophil/lymphocyte ratio, micronucleated erythrocyte frequency, and scaled mass index. The OCP-group levels decreased as the breeding season progressed, and interannual (but not inter-colony) differences were detected. Intra-annual variation in OCP levels seemed to reflect run-off inputs, although other environmental processes may better explain the variation between years. Sex-based differences in OCP levels were likely related to ecological and physiological processes linked to breeding (e.g., egg-laying and use of lipid reserves). No correlations between OCP-group levels and biomarkers were detected. Small pelagic fishes are the main prey sources of blue-footed boobies and the targets of regional industrial fisheries, and thus blue-footed booby OCP levels could reflect ecosystem health and indicate potential risks for human consumers.
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Affiliation(s)
- Alberto Piña-Ortiz
- Unidad Mazatlán en Acuicultura y Manejo Ambiental, Centro de Investigación en Alimentación y Desarrollo A.C., Av. Sábalo-Cerritos s/n, Estero del Yugo, Mazatlán, Sinaloa CP82100, Mexico.
| | - Juan Pablo Ceyca-Contreras
- Unidad Mazatlán en Acuicultura y Manejo Ambiental, Centro de Investigación en Alimentación y Desarrollo A.C., Av. Sábalo-Cerritos s/n, Estero del Yugo, Mazatlán, Sinaloa CP82100, Mexico; Laboratorio de Ornitología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León, Ciudad Universitaria, San Nicolás de los Garza, Nuevo León CP66450, Mexico.
| | - Carlos Eduardo Covantes-Rosales
- Unidad Mazatlán en Acuicultura y Manejo Ambiental, Centro de Investigación en Alimentación y Desarrollo A.C., Av. Sábalo-Cerritos s/n, Estero del Yugo, Mazatlán, Sinaloa CP82100, Mexico.
| | - Miguel Betancourt-Lozano
- Unidad Mazatlán en Acuicultura y Manejo Ambiental, Centro de Investigación en Alimentación y Desarrollo A.C., Av. Sábalo-Cerritos s/n, Estero del Yugo, Mazatlán, Sinaloa CP82100, Mexico.
| | - José Alfredo Castillo-Guerrero
- Departamento de Estudios para el Desarrollo Sustentable de la Zona Costera, Centro Universitario de la Costa Sur, Universidad de Guadalajara, Gómez Farías 82, San Patricio-Melaque, Municipio de Cihuatlán, Jalisco CP48980, Mexico.
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24
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Li ZR, Luo XJ, Lin L, Zeng YH, Mai BX. Effect of laying sequence and selection of maternal tissues in assessment of maternal transfer of organohalogenated contaminants during chicken egg formation: A pilot study. ENVIRONMENTAL POLLUTION (BARKING, ESSEX : 1987) 2021; 270:116157. [PMID: 33321435 DOI: 10.1016/j.envpol.2020.116157] [Citation(s) in RCA: 8] [Impact Index Per Article: 2.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 07/01/2020] [Revised: 11/19/2020] [Accepted: 11/23/2020] [Indexed: 06/12/2023]
Abstract
Many studies have reported maternal transfer of organic contaminants in oviparous species, with inconsonant results. Egg-laying sequence and selected maternal tissues may impact on assessment of potential maternal transfer of contaminants. Here, this hypothesis was verified by exposing chickens (Gallus domesticus) to polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), and dechlorane plus (DPs). Concentrations in eggs laid during exposure exhibited periodic fluctuations (conforming to egg-laying cycles) and a decreasing trend during depuration. Fluctuation patterns of DPs and BDE209 differed from those of other compounds. The PBDE congener profiles in eggs were dominated by BDE209 during exposure and by BDE100 and 153 during depuration. The abundance of PCB congener (CB138) which is recalcitrant to metabolism increased with laying sequence. Maternal transfer potential was negatively correlated (P = 0.0014, R2 = 0.7874) to the log KOW of chemicals (log KOW >7) when the muscle, heart, lung, or stomach was used. No correlations were found when the liver, fat, kidneys, or intestine was used (log KOW >7), although DPs and BDE209 showed the highest maternal transfer potential. Different fluctuation patterns of DPs and BDE209 in eggs and increased abundance of BDE209 in eggs laid in the initial egg-laying period imply that the liver, fat, kidney, or intestinal tissues could be more appropriate in assessing maternal transfer of the target analytes.
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Affiliation(s)
- Zong-Rui Li
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, 510640, China; State Environmental Protection Key Laboratory of Environmental Pollution Health Risk Assessment, South China Institute of Environmental Sciences, Ministry of Ecology and Environment, Guangzhou, 510655, China; University of Chinese Academy of Sciences, Beijing, 100049, China
| | - Xiao-Jun Luo
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, 510640, China.
| | - Lan Lin
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, 510640, China; University of Chinese Academy of Sciences, Beijing, 100049, China
| | - Yan-Hong Zeng
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, 510640, China
| | - Bi-Xian Mai
- State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Resources Utilization and Protection, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, 510640, China
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25
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Carravieri A, Warner NA, Herzke D, Brault-Favrou M, Tarroux A, Fort J, Bustamante P, Descamps S. Trophic and fitness correlates of mercury and organochlorine compound residues in egg-laying Antarctic petrels. ENVIRONMENTAL RESEARCH 2021; 193:110518. [PMID: 33245882 DOI: 10.1016/j.envres.2020.110518] [Citation(s) in RCA: 13] [Impact Index Per Article: 3.3] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 10/14/2020] [Revised: 11/18/2020] [Accepted: 11/19/2020] [Indexed: 06/11/2023]
Abstract
Understanding the drivers and effects of exposure to contaminants such as mercury (Hg) and organochlorine compounds (OCs) in Antarctic wildlife is still limited. Yet, Hg and OCs have known physiological and fitness effects in animals, with consequences on their populations. Here we measured total Hg (a proxy of methyl-Hg) in blood cells and feathers, and 12 OCs (seven polychlorinated biphenyls, PCBs, and five organochlorine pesticides, OCPs) in plasma of 30 breeding female Antarctic petrels Thalassoica antarctica from one of the largest colonies in Antarctica (Svarthamaren, Dronning Maud Land). This colony is declining and there is poor documentation on the potential role played by contaminants on individual physiology and fitness. Carbon (δ13C) and nitrogen (δ15N) stable isotope values measured in the females' blood cells and feathers served as proxies of their feeding ecology during the pre-laying (austral spring) and moulting (winter) periods, respectively. We document feather Hg concentrations (mean ± SD, 2.41 ± 0.83 μg g-1 dry weight, dw) for the first time in this species. Blood cell Hg concentrations (1.38 ± 0.43 μg g-1 dw) were almost twice as high as those reported in a recent study, and increased with pre-laying trophic position (blood cell δ15N). Moulting trophic ecology did not predict blood Hg concentrations. PCB concentrations were very low (Σ7PCBs, 0.35 ± 0.31 ng g-1 wet weight, ww). Among OCPs, HCB (1.02 ± 0.36 ng g-1 ww) and p, p'-DDE (1.02 ± 1.49 ng g-1 ww) residues were comparable to those of ecologically-similar polar seabirds, while Mirex residues (0.72 ± 0.35 ng g-1 ww) were higher. PCB and OCP concentrations showed no clear relationship with pre-laying or moulting feeding ecology, indicating that other factors overcome dietary drivers. OC residues were inversely related to body condition, suggesting stronger release of OCs into the circulation of egg-laying females upon depletion of their lipid reserves. Egg volume, hatching success, chick body condition and survival were not related to maternal Hg or OC concentrations. Legacy contaminant exposure does not seem to represent a threat for the breeding fraction of this population over the short term. Yet, exposure to contaminants, especially Mirex, and other concurring environmental stressors should be monitored over the long-term in this declining population.
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Affiliation(s)
- Alice Carravieri
- Littoral Environnement et Sociétés (LIENSs), UMR 7266 CNRS- La Rochelle Université, 2 Rue Olympe de Gouges, La Rochelle, 17000, France.
| | - Nicholas A Warner
- NILU-Norwegian Institute for Air Research, Fram Centre, Tromsø, NO-9296, Norway; UiT-The Arctic University of Norway, Department of Arctic and Marine Biology, Hansine Hansens veg 18, Tromsø, 9037, Norway
| | - Dorte Herzke
- NILU-Norwegian Institute for Air Research, Fram Centre, Tromsø, NO-9296, Norway; UiT-The Arctic University of Norway, Department of Arctic and Marine Biology, Hansine Hansens veg 18, Tromsø, 9037, Norway
| | - Maud Brault-Favrou
- Littoral Environnement et Sociétés (LIENSs), UMR 7266 CNRS- La Rochelle Université, 2 Rue Olympe de Gouges, La Rochelle, 17000, France
| | - Arnaud Tarroux
- NINA-Norwegian Institute for Nature Research, Fram Centre, Tromsø, NO-9296, Norway
| | - Jérôme Fort
- Littoral Environnement et Sociétés (LIENSs), UMR 7266 CNRS- La Rochelle Université, 2 Rue Olympe de Gouges, La Rochelle, 17000, France
| | - Paco Bustamante
- Littoral Environnement et Sociétés (LIENSs), UMR 7266 CNRS- La Rochelle Université, 2 Rue Olympe de Gouges, La Rochelle, 17000, France; Institut Universitaire de France (IUF), 1 Rue Descartes, Paris, 75005, France
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Sorais M, Spiegel O, Mazerolle MJ, Giroux JF, Verreault J. Gulls foraging in landfills: Does atmospheric exposure to halogenated flame retardants result in bioaccumulation? ENVIRONMENT INTERNATIONAL 2021; 147:106369. [PMID: 33418198 DOI: 10.1016/j.envint.2020.106369] [Citation(s) in RCA: 11] [Impact Index Per Article: 2.8] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 10/01/2020] [Revised: 12/18/2020] [Accepted: 12/23/2020] [Indexed: 06/12/2023]
Abstract
Several bird species have adapted to foraging in landfills, although these sites are known to represent significant sources of emissions of toxic semi-volatile chemicals including the halogenated flame retardants (HFRs) (e.g., polybrominated diphenyl ethers (PBDEs) and emerging compounds). The objective of this study was to investigate the association between atmospheric exposure to PBDEs and selected emerging HFRs and their bioaccumulation in landfill-foraging birds. We determined HFR concentrations in liver of 58 GPS-tagged ring-billed gulls (Larus delawarensis) breeding in a colony near Montreal (Canada) as well as their atmospheric exposure determined using a miniature bird-borne passive air sampler. PBDE mixtures were the most abundant HFRs determined in passive air samplers (daily exposure rates of ∑9PentaBDE: 47.4 ± 6.5 pg/day; DecaBDE: 36.0 ± 6.3 pg/day, and ∑3OctaBDE: 3.4 ± 0.5 pg/day) and liver (∑9PentaBDE: 68.1 ± 8.9 ng/g ww; DecaBDE: 52.3 ± 8.1 ng/g ww, and ∑3OctaBDE: 12.8 ± 2.1 ng/g ww), and their concentrations increased with the presence probability of gulls in landfills. We found a spatial relationship between the local sources of atmospheric exposure to PBDEs and the sites associated with greatest PBDE concentrations in liver. Specifically, the atmospheric exposure index was correlated with the bioaccumulation index (Pearson r for ∑9PentaBDE: r = 0.63, p < 0.001; DecaBDE: r = 0.66, p < 0.001, and ∑3OctaBDE: r = 0.42, p < 0.001). However, we found no correlation at the individual level between daily exposure rates of HFRs in passive air samplers and their liver concentrations. This suggests that complex exposure pathways combined with toxicokinetic factors shaped HFR profiles in gull liver, potentially confounding the relationships with atmospheric exposure.
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Affiliation(s)
- Manon Sorais
- Centre de recherche en toxicologie de l'environnement (TOXEN), Département des sciences biologiques, Université du Québec à Montréal, P.O. Box 8888, Succursale Centre-ville, Montreal, QC H3C 3P8, Canada
| | - Orr Spiegel
- School of Zoology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel
| | - Marc J Mazerolle
- Centre d'Étude de la Forêt (CEF), Département des sciences du bois et de la forêt, Université Laval, Quebec City, QC G1V 0A6, Canada
| | - Jean-François Giroux
- Groupe de recherche en écologie comportementale et animale (GRECA), Département des sciences biologiques, Université du Québec à Montréal, P.O. Box 8888, Succursale Centre-Ville, Montreal, QC H3C 3P8, Canada
| | - Jonathan Verreault
- Centre de recherche en toxicologie de l'environnement (TOXEN), Département des sciences biologiques, Université du Québec à Montréal, P.O. Box 8888, Succursale Centre-ville, Montreal, QC H3C 3P8, Canada.
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Sebastiano M, Angelier F, Blévin P, Ribout C, Sagerup K, Descamps S, Herzke D, Moe B, Barbraud C, Bustnes JO, Gabrielsen GW, Chastel O. Exposure to PFAS is Associated with Telomere Length Dynamics and Demographic Responses of an Arctic Top Predator. ENVIRONMENTAL SCIENCE & TECHNOLOGY 2020; 54:10217-10226. [PMID: 32696640 DOI: 10.1021/acs.est.0c03099] [Citation(s) in RCA: 25] [Impact Index Per Article: 5.0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 06/11/2023]
Abstract
Environmental factors that can influence telomeres are diverse, but the association between telomeres and exposure to environmental contaminants is yet to be elucidated. To date, prior studies have focused on legacy persistent chlorinated pollutants (POPs), while the effects of poly- and perfluoroalkyl substances (PFAS) have been poorly documented. Here, we investigated the associations among PFAS congeners, absolute telomere length (cross-sectional approach), and telomere dynamics (rate of telomere length change over time, longitudinal approach) in one of the most contaminated arctic top predators, the glaucous gull Larus hyperboreus from Svalbard. We further estimated the effect of PFAS on apparent survival rates and re-sighting probabilities using a 10-year capture/recapture dataset (2010-2019). We found that birds exposed to higher concentrations of perfluorononadecanoate (PFNA) (median of 1565 pg/mL of ww in males and 1370 pg/mL of ww in females) and perfluorotetradecanoate (PFTeDA) (median of 370 pg/mL of ww in males and 210 pg/mL of ww in females) showed the slowest rate of telomere shortening. We also found that high blood concentrations of perfluorooctanoate (PFOA) (median of 120 pg/mL of ww in males and 150 pg/mL of ww in females) and perfluorohexanesulfonate (PFHxS) (median of 495 pg/mL of ww in males and 395 pg/mL of ww in females) were positively associated with higher re-sighting probabilities and apparent survival in males but not in females. Our work is the first to report an association between single PFAS compounds and telomeres, and the first to link PFAS exposure with survival probabilities, suggesting that the effect of PFAS exposure might be more tied to the type of compound rather than the total concentration of PFAS.
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Affiliation(s)
- Manrico Sebastiano
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Univ., 79360 La Rochelle, France
| | - Frédéric Angelier
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Univ., 79360 La Rochelle, France
| | - Pierre Blévin
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Univ., 79360 La Rochelle, France
- Akvaplan-niva AS, Fram Centre, NO-9296 Tromsø, Norway
| | - Cécile Ribout
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Univ., 79360 La Rochelle, France
| | | | | | - Dorte Herzke
- Norwegian Institute for Air Research, NILU, Fram Centre, NO-9296 Tromsø, Norway
| | - Børge Moe
- Norwegian Institute for Nature Research, NINA, Høgskoleringen 9, NO-7034 Trondheim, Norway
| | - Christophe Barbraud
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Univ., 79360 La Rochelle, France
| | - Jan Ove Bustnes
- Norwegian Institute for Nature Research, NINA, Fram Centre, NO-9296 Tromsø, Norway
| | | | - Olivier Chastel
- Centre d'Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Univ., 79360 La Rochelle, France
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Smythe TA, Mattioli LC, Letcher RJ. Distribution behaviour in body compartments and in ovo transfer of flame retardants in North American Great Lakes herring gulls. ENVIRONMENTAL POLLUTION (BARKING, ESSEX : 1987) 2020; 262:114306. [PMID: 32163809 DOI: 10.1016/j.envpol.2020.114306] [Citation(s) in RCA: 13] [Impact Index Per Article: 2.6] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 01/21/2020] [Revised: 02/28/2020] [Accepted: 02/29/2020] [Indexed: 06/10/2023]
Abstract
Polybrominated diphenyl ethers (PBDEs) and other halogenated flame retardants (HFRs) continue to be an environmental concern. In the Laurentian Great Lakes, herring gulls (Larus argentatus) are an important wildlife sentinel species, although very little information is available regarding the body distribution (limited to e.g. liver and blood) of these contaminants and in relation to depuration via in ovo transfer. Maternal transfer rates and distribution were presently determined in six body compartments from eight female, Great Lakes herring gulls and separate egg compartments from their entire clutch. Among the 25 PBDEs and 23 non-PBDE HFRs assessed, only six PBDE congeners (BDE-47/99/100/153/154/209), hexabromocyclododecane (HBCDD), and Dechlorane Plus (syn- and anti-DDC-CO) were frequently detectable and quantifiable. Σ6BDE concentrations were an order of magnitude greater than non-PBDE HFR concentrations, and were greatest in the adipose (9641 ± 2436 ng/g ww), followed by egg yolk (699 ± 139 ng/g ww) > muscle (332 ± 545 ng/g ww) > liver (221 ± 65 ng/g ww) > plasma (85.4 ± 20.4 ng/g ww) > brain (54.6 ± 10.6 ng/g ww) > red blood cells (RBCs; 23.5 ± 5.6 ng/g ww) > albumen (7.3 ± 1.3 ng/g ww). Σ2DDC-CO and HBCDD were frequently below the method limit of quantification in the brain, RBCs, plasma, and albumen. Additionally, novel methoxylated-polybrominated diphenoxybenzene contaminants were detected and quantified in herring gull tissues and eggs. The primary difference in PBDE congener profiles was the resistance of both BDE-153 and -154 towards accumulation in the brain, and a corresponding increase in BDE-209 accumulation, which may suggest congener-specific differences in crossing the blood-brain barrier in herring gulls. Maternal transfer rates of PBDEs and non-PBDE HFRs were low (∼4.7 and ∼2.9 % respectively), suggesting that in ovo transfer is not a significant mode of depuration for these compounds.
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Affiliation(s)
- Tristan A Smythe
- Ecotoxicology and Wildlife Health Division, Wildlife and Landscape Science Directorate, Environment and Climate Change Canada, National Wildlife Research Centre, 1125 Colonel By Drive, Carleton University, Ottawa, ON, K1A 0H3, Canada; Department of Chemistry, Carleton University, Ottawa, ON, K1S 5B6, Canada
| | - Lisa C Mattioli
- Ecotoxicology and Wildlife Health Division, Wildlife and Landscape Science Directorate, Environment and Climate Change Canada, National Wildlife Research Centre, 1125 Colonel By Drive, Carleton University, Ottawa, ON, K1A 0H3, Canada
| | - Robert J Letcher
- Ecotoxicology and Wildlife Health Division, Wildlife and Landscape Science Directorate, Environment and Climate Change Canada, National Wildlife Research Centre, 1125 Colonel By Drive, Carleton University, Ottawa, ON, K1A 0H3, Canada; Department of Chemistry, Carleton University, Ottawa, ON, K1S 5B6, Canada.
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29
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Lee J, Lee SY, Chung D, Park KW, Shim K, Lee J, Park JH. Utilization of black-tailed gull (Larus crassirostris) eggs for monitoring of mercury levels in coastal areas of South Korea: Preliminary study. THE SCIENCE OF THE TOTAL ENVIRONMENT 2020; 713:136578. [PMID: 31955089 DOI: 10.1016/j.scitotenv.2020.136578] [Citation(s) in RCA: 5] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 10/13/2019] [Revised: 11/26/2019] [Accepted: 01/06/2020] [Indexed: 06/10/2023]
Abstract
Studies on the monitoring of mercury accumulation using high trophic-level predators of the marine ecosystem have been scarce in South Korea. In this study, we compared the mercury concentrations of the eggs of the black-tailed gulls, a higher-order predator, breeding in two coastal areas. Breeding sites with varying mercury concentrations in land-origin freshwater fish and freshwater and marine sediments were selected in the southeastern (Hongdo Island) and western (Baengnyeongdo Island) seas. The 5-year mean total mercury concentration in eggs collected during the breeding seasons from 2012 to 2016 was higher in those collected from Hongdo than in those collected from Baengnyeongdo. This difference in mercury concentration in eggs was observed for each year. In addition, the total mercury concentration in eggs was consistently higher on Hongdo, which also had higher mercury pollution, than on Baengnyeongdo Island. These results support the suitability of black-tailed gull eggs for monitoring of mercury pollution.
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Affiliation(s)
- Jangho Lee
- Natural Environment Research Division, National Institute of Environmental Research, 42, Hwangyeong-ro, Seo-gu, Incheon 22689, Republic of Korea.
| | - Soo Yong Lee
- Natural Environment Research Division, National Institute of Environmental Research, 42, Hwangyeong-ro, Seo-gu, Incheon 22689, Republic of Korea.
| | - David Chung
- Natural Environment Research Division, National Institute of Environmental Research, 42, Hwangyeong-ro, Seo-gu, Incheon 22689, Republic of Korea.
| | - Ki-Wan Park
- Natural Environment Research Division, National Institute of Environmental Research, 42, Hwangyeong-ro, Seo-gu, Incheon 22689, Republic of Korea.
| | - Kyuyoung Shim
- Natural Environment Research Division, National Institute of Environmental Research, 42, Hwangyeong-ro, Seo-gu, Incheon 22689, Republic of Korea.
| | - Jongchun Lee
- Indoor Environment and Noise Research Division, National Institute of Environmental Research, 42, Hwangyeong-ro, Seo-gu, Incheon 22689, Republic of Korea.
| | - Jong-Hyouk Park
- Measurement and Analysis Division, Jeonbuk Regional Environment Office, 120, Anjeon-ro, Deokjin-gu, Jeonju-si, Jeollabuk-do 54872, Republic of Korea.
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30
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Quinn LP, Roos C, Pieters R, Polder A, Bouwman H. Brominated flame retardants in wild bird eggs from the industrialised heartland of South Africa. AFRICAN ZOOLOGY 2020. [DOI: 10.1080/15627020.2019.1671895] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.4] [Reference Citation Analysis] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 01/25/2023]
Affiliation(s)
- LP Quinn
- National Metrology Institute of South Africa, Lynnwood, South Africa
| | - C Roos
- Unit of Environmental Sciences and Management, North-West University, Potchefstroom, South Africa
| | - R Pieters
- Unit of Environmental Sciences and Management, North-West University, Potchefstroom, South Africa
| | - A Polder
- Unit of Environmental Sciences and Management, North-West University, Potchefstroom, South Africa
- Department of Food Safety and Infection Biology, Norwegian University of Life Sciences, Norway
| | - H Bouwman
- Unit of Environmental Sciences and Management, North-West University, Potchefstroom, South Africa
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31
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Nilsen FM, Rainwater TR, Wilkinson PM, Brunell AM, Lowers RH, Bowden JA, Guillette LJ, Long SE, Schock TB. Examining maternal and environmental transfer of mercury into American alligator eggs. ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY 2020; 189:110057. [PMID: 31835046 PMCID: PMC11005113 DOI: 10.1016/j.ecoenv.2019.110057] [Citation(s) in RCA: 14] [Impact Index Per Article: 2.8] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Subscribe] [Scholar Register] [Received: 09/03/2019] [Revised: 12/02/2019] [Accepted: 12/05/2019] [Indexed: 06/10/2023]
Abstract
American alligators are exposed to mercury (Hg) throughout their natural range and may maternally transfer Hg into their eggs. Wildlife species are highly sensitive to Hg toxicity during embryonic development and neonatal life, and information on Hg transfer into eggs is critical when attempting to understand the effects of Hg exposure on developing oviparous organisms. To examine Hg transfer in alligators, the objectives of the present study were to 1) determine Hg concentrations in yolk (embryonic and neonatal food source) from wild alligator eggs collected from three locations - Yawkey Wildlife Center SC (YWC), Lake Apopka FL (LA), and Lake Woodruff FL (LW); 2) examine the relationship between THg concentrations in wild alligator nest material and egg yolk at Merritt Island National Wildlife Refuge, FL; 3) examine the Hg concentrations in wild maternal female alligators (blood) and the THg in corresponding egg yolks and embryos across three nesting seasons at a single location (YWC), and evaluate the relationship between nesting female THg concentrations (blood) and their estimated age and number of nesting years (YWC); and 4) assess the transfer of biologically-relevant Hg concentrations (based on Hg measured in maternal female blood) into embryos using an egg-dosing experiment. Mean total Hg (THg) concentrations observed at each site were 26.3 ng/g ± 11.0 ng/g (YWC), 8.8 ng/g ± 5.1 ng/g (LA), and 22.6 ng/g ± 6.3 ng/g (LW). No relationship was observed between THg in alligator nest material and corresponding yolk samples, nor between THg in maternal alligator blood and estimated age and number of nesting years of these animals. However, significant positive relationships were observed between THg in blood of nesting female alligators and THg in their corresponding egg yolk. We observed that 12.8% of the maternal blood THg is found in the corresponding egg yolk, and a highly significant correlation was observed between the two sample types (r = 0.66; p < 0.0001). The egg dosing experiment revealed that Hg did not transfer through the eggshell at developmental stage 19. Overall, this study provides new information regarding Hg transfer in American alligators which can improve biomonitoring efforts and may inform ecotoxicological investigations and population management programs in areas of high Hg contamination.
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Affiliation(s)
- Frances M Nilsen
- National Institute of Standards and Technology, Chemical Sciences Division, Hollings Marine Laboratory, Charleston, SC, USA; Medical University of South Carolina, Marine Bio-Medicine and Environmental Science Program, Charleston, SC, USA.
| | - Thomas R Rainwater
- Baruch Institute of Coastal Ecology and Forest Science, Clemson University, P.O. Box 596, Georgetown, SC, USA; Tom Yawkey Wildlife Center, South Carolina Department of Natural Resources, 1 Yawkey Way South, Georgetown, SC, USA.
| | - Phil M Wilkinson
- Tom Yawkey Wildlife Center, South Carolina Department of Natural Resources, 1 Yawkey Way South, Georgetown, SC, USA
| | - Arnold M Brunell
- Florida Fish & Wildlife Conservation Commission, 601 W. Woodward Ave., Eustis, FL, USA.
| | | | - John A Bowden
- National Institute of Standards and Technology, Chemical Sciences Division, Hollings Marine Laboratory, Charleston, SC, USA; Current Address- Center for Environmental and Human Toxicology, Department of Physiological Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL, USA.
| | - Louis J Guillette
- Medical University of South Carolina, Marine Bio-Medicine and Environmental Science Program, Charleston, SC, USA
| | - Stephen E Long
- National Institute of Standards and Technology, Chemical Sciences Division, Hollings Marine Laboratory, Charleston, SC, USA.
| | - Tracey B Schock
- National Institute of Standards and Technology, Chemical Sciences Division, Hollings Marine Laboratory, Charleston, SC, USA.
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32
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Sorais M, Mazerolle MJ, Giroux JF, Verreault J. Landfills represent significant atmospheric sources of exposure to halogenated flame retardants for urban-adapted gulls. ENVIRONMENT INTERNATIONAL 2020; 135:105387. [PMID: 31841804 DOI: 10.1016/j.envint.2019.105387] [Citation(s) in RCA: 27] [Impact Index Per Article: 5.4] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 08/20/2019] [Revised: 10/28/2019] [Accepted: 12/02/2019] [Indexed: 06/10/2023]
Abstract
Halogenated flame retardants (HFRs) are contaminants that are abundantly emitted from waste management facilities (WMFs) and that became ubiquitous in air of urbanized regions. Urban birds including gulls have adapted to exploiting human food resources (refuse) in WMFs, and have thus experienced population explosions worldwide. However, foraging in WMFs for birds may result in exposure to HFRs that have been shown to be toxic for animals. The objective of this study was to determine the influence of foraging near or in various WMFs on the atmospheric exposure of birds to HFRs, and to localize other sources of HFRs at the regional scale in a highly urbanized environment. We measured the atmospheric exposure to HFRs in one of the most abundant gull species in North America, the ring-billed gull (Larus delawarensis), breeding in the densely-populated Montreal area (Canada) using a novel approach combining bird-borne GPS dataloggers and miniature passive air samplers (PASs). We determined concentrations of 11 polybrominated diphenyl ethers (PBDEs) and three emerging HFRs of high environmental concern in PASs carried by gulls. We show that the daily sampling rates (pg/day) of PBDEs in PASs were highest in gulls foraging in or around landfills, but were not influenced by meteorological variables. In contrast, the daily sampling rates of emerging HFRs were lower compared to PBDEs and were not influenced by the presence of gulls in or near WMFs. This study demonstrates that atmospheric exposure to HFRs and perhaps other semi-volatile contaminants is underestimated, yet important for birds foraging in landfills.
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Affiliation(s)
- Manon Sorais
- Centre de recherche en toxicologie de l'environnement (TOXEN), Département des sciences biologiques, Université du Québec à Montréal, P.O. Box 8888, Succursale Centre-ville, Montreal, QC H3C 3P8, Canada
| | - Marc J Mazerolle
- Centre d'étude de la forêt (CEF), Département des sciences du bois et de la forêt, Université Laval, 2405 rue de la Terrasse, Quebec, QC G1V 0A6, Canada
| | - Jean-François Giroux
- Groupe de recherche en écologie comportementale et animale (GRECA), Département des sciences biologiques, Université du Québec à Montréal, P.O. Box 8888, Succursale Centre-Ville, Montreal, QC H3C 3P8, Canada
| | - Jonathan Verreault
- Centre de recherche en toxicologie de l'environnement (TOXEN), Département des sciences biologiques, Université du Québec à Montréal, P.O. Box 8888, Succursale Centre-ville, Montreal, QC H3C 3P8, Canada.
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33
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Currier HA, Fremlin KM, Elliott JE, Drouillard KG, Williams TD. Bioaccumulation and biomagnification of PBDEs in a terrestrial food chain at an urban landfill. CHEMOSPHERE 2020; 238:124577. [PMID: 31450111 DOI: 10.1016/j.chemosphere.2019.124577] [Citation(s) in RCA: 35] [Impact Index Per Article: 7.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 04/26/2019] [Revised: 08/08/2019] [Accepted: 08/10/2019] [Indexed: 06/10/2023]
Abstract
Biota samples from the Vancouver municipal landfill located in Delta, BC, Canada, have some of the highest polybrominated diphenyl ether (PBDE) levels reported from North America. We followed a population of European starlings (Sturnus vulgaris) breeding in a remediated area in the landfill to identify exposure routes and bioaccumulation of PBDEs in a simple terrestrial food chain. This population was compared to a reference farm site located 40 km east in Glen Valley. We analyzed samples of European starling eggs and nestling livers as well as invertebrate prey species consumed by starlings for PBDE concentrations. We also collected soil samples from starling foraging areas. All samples from the Delta landfill had higher PBDE congener concentrations compared to the Glen Valley reference site and were dominated by BDE-99 and BDE-47. Stable nitrogen (δ N15) and carbon (δ C13) isotope analysis of starling blood samples and provisioned invertebrates revealed that stable δC13 signatures differed between the sites indicating that the diet of starlings in the Delta landfill included a component of human refuse. Biota-soil accumulation factors (BSAFs) > 1 demonstrated that PBDEs were bioaccumulating in soil invertebrates, particularly earthworms, which were readily accessible to foraging starlings in the landfill. Biomagnification factors (BMFs) calculated from foraged food items and starling egg and liver samples were >1, indicating that a diet of soil invertebrates and refuse contributed substantially to the PBDE exposure of local starlings.
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Affiliation(s)
- Heidi A Currier
- Simon Fraser University, Dept. of Biological Sciences, 8888 University Drive, Burnaby, British Columbia, V5A 1S6, Canada.
| | - Kate M Fremlin
- Simon Fraser University, Dept. of Biological Sciences, 8888 University Drive, Burnaby, British Columbia, V5A 1S6, Canada.
| | - John E Elliott
- Environment Canada, Pacific Wildlife Research Center, 5421 Robertson Road, Delta, British Columbia, V4K 3N2, Canada; Simon Fraser University, Dept. of Biological Sciences, 8888 University Drive, Burnaby, British Columbia, V5A 1S6, Canada.
| | - Ken G Drouillard
- Great Lakes Institute for Environmental Research, University of Windsor, 2990 Riverside Drive West, Windsor, Ontario, N9B 3P4, Canada.
| | - Tony D Williams
- Simon Fraser University, Dept. of Biological Sciences, 8888 University Drive, Burnaby, British Columbia, V5A 1S6, Canada.
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Hitchcock DJ, Andersen T, Varpe Ø, Borgå K. Effects of Maternal Reproductive Investment on Sex-Specific Pollutant Accumulation in Seabirds: A Meta-Analysis. ENVIRONMENTAL SCIENCE & TECHNOLOGY 2019; 53:7821-7829. [PMID: 31136156 DOI: 10.1021/acs.est.9b01296] [Citation(s) in RCA: 22] [Impact Index Per Article: 3.7] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 06/09/2023]
Abstract
Avian egg production demands resources such as lipids and proteins. Relative egg size and mass varies across species, reflecting differences in maternal investment. This variability may affect the maternal transfer of anthropogenic pollutants including lipophilic polychlorinated biphenyls (PCBs) and protein-associated per- and polyfluoroalkyl substances (PFASs) and mercury (Hg). We conducted a meta-analysis on seabirds and investigated whether interspecies variation in maternal investment contributes toward skewed pollutant concentration ratios between males and females, as Cmale/Cfemale (80 studies). Overall concentrations of PCBs and perfluorooctanesulfonic acid (PFOS) were 1.6 and 1.3 times higher, respectively, in males than females, whereas mercury was similar between sexes. Few studies compared females and eggs ( n = 6), highlighting a knowledge gap. We found that an increasing maternal investment as a clutch-to-female mass ratio resulted in lower PCB concentrations in females than in males during the incubation period, but no sex-specific differences were observed for mercury and PFOS. Egg production is both a lipid dominated and protein-limited process. Females transfer lipophilic pollutants more easily to eggs, and to a higher degree with increasing maternal investment, but feeding ecology may be more important. Interspecies variation in maternal pollutant transfer may lead to negative effects scaling from an offspring to population level.
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Affiliation(s)
| | - Tom Andersen
- Department of Biosciences , University of Oslo , 0316 Oslo , Norway
| | - Øystein Varpe
- Department of Arctic Biology , University Centre in Svalbard , 9171 Longyearbyen , Norway
- Norwegian Institute for Nature Research , 5006 Bergen , Norway
| | - Katrine Borgå
- Department of Biosciences , University of Oslo , 0316 Oslo , Norway
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Warner NA, Sagerup K, Kristoffersen S, Herzke D, Gabrielsen GW, Jenssen BM. Snow buntings (Plectrophenax nivealis) as bio-indicators for exposure differences to legacy and emerging persistent organic pollutants from the Arctic terrestrial environment on Svalbard. THE SCIENCE OF THE TOTAL ENVIRONMENT 2019; 667:638-647. [PMID: 30833262 DOI: 10.1016/j.scitotenv.2019.02.351] [Citation(s) in RCA: 19] [Impact Index Per Article: 3.2] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 11/13/2018] [Revised: 02/22/2019] [Accepted: 02/22/2019] [Indexed: 06/09/2023]
Abstract
Eggs of snow buntings (Plectrophenax nivealis) were applied as a bio-indicator to examine differences in exposure to legacy persistent organic pollutants (POPs) and perflouroalkyl subtances (PFAS) from the terrestrial environment surrounding the settlements of Longyearbyen, Barentsburg and Pyramiden on Svalbard, Norway. Significantly higher concentrations of summed polychlorinated biphenyls (sumPCB7) in eggs collected from Barentsburg (2980 ng/g lipid weight (lw)) and Pyramiden (3860 ng/g lw) compared to Longyearbyen (96 ng/g lw) are attributed to local sources of PCBs within these settlements. Similar findings were observed for p,p'-dichlorodiphenyldichloroethylene (p,p'-DDE) where higher median concentrations observed in Pyramiden (173 ng/g lw) and Barentsburg (75 ng/g lw) compared to Longyearbyen (48 ng/g lw) may be influenced by guano inputs from breeding seabird populations, although other point sources cannot be ruled out. Concentrations of perfluorooctane sulphonate (PFOS) and several perfluorinated carboxylic acids (PFCAs) in snow bunting eggs were found to be statistically higher in the populated settlements of Longyearbyen and Barentsburg compared to the abandoned Pyramiden. Narrow foraging ranges of snow buntings during breeding season was useful in assessing point sources of exposure for PCBs and PFAS at particular sites with extreme differences observed between nest locations. SumPCB7 concentrations ranged from 2 μg/g ww to below detection limits between nest sites located less than a kilometer from each other in Pyramiden. Similar findings were observed in Longyearbyen, where several PFCAs ranged from 2 to 55 times higher between nest sites with similar spatial distances. These findings indicate that snow buntings can be a useful bio-indicator offering high spatial resolution for contaminant source apportionment in terrestrial environments on Svalbard.
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Affiliation(s)
- Nicholas A Warner
- NILU-Norwegian Institute for Air Research, Fram Centre, NO-9296 Tromsø, Norway.
| | | | - Siv Kristoffersen
- Department of Biology, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway; Norwegian Polar Institute, Fram Centre, NO-9296 Tromsø, Norway
| | - Dorte Herzke
- NILU-Norwegian Institute for Air Research, Fram Centre, NO-9296 Tromsø, Norway
| | - Geir W Gabrielsen
- Norwegian Polar Institute, Fram Centre, NO-9296 Tromsø, Norway; Department of Arctic Technology, University Center in Svalbard, NO-9171 Longyearbyen, Norway
| | - Bjørn M Jenssen
- Department of Biology, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway; Department of Arctic Technology, University Center in Svalbard, NO-9171 Longyearbyen, Norway
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36
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Hitchcock DJ, Andersen T, Varpe Ø, Loonen MJJE, Warner NA, Herzke D, Tombre IM, Griffin LR, Shimmings P, Borgå K. Potential Effect of Migration Strategy on Pollutant Occurrence in Eggs of Arctic Breeding Barnacle Geese ( Branta leucopsis). ENVIRONMENTAL SCIENCE & TECHNOLOGY 2019; 53:5427-5435. [PMID: 30938990 DOI: 10.1021/acs.est.9b00014] [Citation(s) in RCA: 4] [Impact Index Per Article: 0.7] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 06/09/2023]
Abstract
Arctic-breeding geese acquire resources for egg production from overwintering grounds, spring stopover sites and breeding grounds, where pollutant exposure may differ. We investigated the effect of migration strategy on pollutant occurrence of lipophilic polychlorinated biphenyls (PCBs) and protein-associated poly- and perfluoroalkyl substances (PFASs) and mercury (Hg) in eggs of herbivorous barnacle geese ( Branta leucopsis) from an island colony on Svalbard. Stable isotopes (δ13C and δ15N) in eggs and vegetation collected along the migration route were similar. Pollutant concentrations in eggs were low, reflecting their terrestrial diet (∑PCB = 1.23 ± 0.80 ng/g ww; ∑PFAS = 1.21 ± 2.97 ng/g ww; Hg = 20.17 ± 7.52 ng/g dw). PCB concentrations in eggs increased with later hatch date, independent of lipid content which also increased over time. Some females may remobilize and transfer more PCBs to their eggs, by delaying migration several weeks, relying on more polluted and stored resources, or being in poor body condition when arriving at the breeding grounds. PFAS and Hg occurrence in eggs did not change throughout the breeding season, suggesting migration has a greater effect on lipophilic pollutants. Pollutant exposure during offspring production in arctic-breeding migrants may result in different profiles, with effects becoming more apparent with increasing trophic levels.
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Affiliation(s)
| | - Tom Andersen
- Department of Biosciences , University of Oslo , 0316 Oslo , Norway
| | - Øystein Varpe
- Department of Arctic Biology , University Centre in Svalbard , 9171 Longyearbyen , Norway
- Akvaplan-niva , Fram Centre, 9296 Tromsø , Norway
| | | | - Nicholas A Warner
- Norwegian Institute for Air Research , Fram Centre, 9296 Tromsø , Norway
| | - Dorte Herzke
- Norwegian Institute for Air Research , Fram Centre, 9296 Tromsø , Norway
| | - Ingunn M Tombre
- Department of Arctic Ecology , Norwegian Institute for Nature Research , Fram Centre, 9296 Tromsø , Norway
| | - Larry R Griffin
- Wildfowl & Wetlands Trust , Caerlaverock Wetland Centre , Dumfriesshire DG1 4RS , United Kingdom
| | | | - Katrine Borgå
- Department of Biosciences , University of Oslo , 0316 Oslo , Norway
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Anderson CM, Gilchrist HG, Ronconi RA, Shlepr KR, Clark DE, Weseloh DVC, Roberston GJ, Mallory ML. Winter home range and habitat selection differs among breeding populations of herring gulls in eastern North America. MOVEMENT ECOLOGY 2019; 7:8. [PMID: 30891245 PMCID: PMC6404351 DOI: 10.1186/s40462-019-0152-x] [Citation(s) in RCA: 6] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Subscribe] [Scholar Register] [Received: 08/21/2018] [Accepted: 02/07/2019] [Indexed: 06/02/2023]
Abstract
BACKGROUND Recognizing the factors influencing migratory individuals throughout their annual cycle is important for understanding the drivers of population dynamics. Previous studies have found that Herring Gulls (Larus argentatus) in the Atlantic region have lower survival rates than those in the Great Lakes and the Arctic. One possible explanation for divergent survival rates among these populations is differences in their non-breeding habitats. METHODS We tracked Herring Gulls from five populations, breeding in the eastern Arctic, the Great Lakes, Newfoundland, Sable Island, and the Bay of Fundy. We assessed the extent of migratory connectivity between breeding and wintering sites, and tested if there were differences in home range size or habitat selection among these populations during the winter. RESULTS The tracked Herring Gulls had strong migratory connectivity between their breeding and wintering areas. We found that Herring Gulls from the Arctic spent most of the winter in marine habitats, while the other populations used a wider variety of habitats. However, the Newfoundland and Sable Island populations selected for urban habitats, and almost all individuals the specialized in urban habitats came from one of the three Atlantic populations. CONCLUSIONS Our results suggest that there could potentially be a link between urban habitat use during the winter and reduced adult survival in Atlantic Canada Herring Gulls.
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Affiliation(s)
- Christine M. Anderson
- Department of Biology, Acadia University, 33 Westwood Ave, Wolfville, NS B4P 2R6 Canada
| | - H. Grant Gilchrist
- Wildlife Research Division, Environment and Climate Change Canada, National Wildlife Research Centre, Ottawa, ON K1S 5B6 Canada
| | - Robert A. Ronconi
- Canadian Wildlife Service, Environment and Climate Change Canada, 45 Alderney Dr, Dartmouth, NS B2Y 2N6 Canada
| | - Katherine R. Shlepr
- Atlantic Lab for Avian Research, Department of Biology, University of New Brunswick, P.O. Box 4400, 10 Bailey Drive, Fredericton, NB E3B 5A3 Canada
| | - Daniel E. Clark
- Massachusetts Department of Conservation and Recreation, Division of Water Supply Protection, 485 Ware Road, Belchertown, MA 01007 USA
| | - D. V. Chip Weseloh
- Canadian Wildlife Service, Environment and Climate Change Canada, 4905 Dufferin Ave, Toronto, ON M3H 5T4 Canada
| | - Gregory J. Roberston
- Wildlife Research Division, Environment and Climate Change Canada, 6 Bruce Street, Mount Pearl, NL A1N 4T3 Canada
| | - Mark L. Mallory
- Department of Biology, Acadia University, 33 Westwood Ave, Wolfville, NS B4P 2R6 Canada
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Leat EHK, Bourgeon S, Hanssen SA, Petersen A, Strøm H, Bjørn TH, Gabrielsen GW, Bustnes JO, Furness RW, Haarr A, Borgå K. The effect of long-range transport, trophic position and diet specialization on legacy contaminant occurrence in great skuas, Stercorarius skua, breeding across the Northeast Atlantic. ENVIRONMENTAL POLLUTION (BARKING, ESSEX : 1987) 2019; 244:55-65. [PMID: 30321712 DOI: 10.1016/j.envpol.2018.10.005] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.3] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 06/01/2018] [Revised: 09/04/2018] [Accepted: 10/01/2018] [Indexed: 06/08/2023]
Abstract
High levels of halogenated organic contaminants (HOCs) have been found in the marine predatory seabird great skua (Stercorarius skua) from breeding colonies in the Northeastern Atlantic, with large unexplained inter-colony variation. The present study aimed at analyzing if the HOCs occurrence in breeding great skuas in remote colonies was explained by local baseline food web exposure determined by long-range transport, or by ecological factors such as diet specialization and relative trophic position in the breeding area. The occurrence of organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), and polybrominated diphenyl ethers (PBDEs) was analyzed in plasma of 204 adult great skuas collected over two years (2008 and 2009) and 5 colonies across the North-Atlantic from Shetland to Svalbard. The ΣHOCs levels in plasma ranged across two orders of magnitude, from 40 to 7600 ng/g (wet weight) and differed significantly across the great skua colonies. The variation in contaminant occurrence among colonies did not reflect long-range transport through a latitudinal or remoteness gradient, as the second northernmost colony (Bjørnøya), had the highest contaminant concentrations. No latitudinal or remoteness gradient was evident in the contaminant pattern among the colonies. The contaminant levels increased significantly with increasing δ15N values, and regurgitated pellets of undigested prey suggested that great skuas with higher δ15N values had a higher proportion of bird prey in their diet, mostly seabirds. In contrast, great skuas from colonies with lower δ15N and lower contaminant level fed mostly on fish. The enrichment of δ13C increased with decreasing δ15N and lower contaminant levels. Therefore, individual behavior of great skuas, such as migration strategies and diet specialization, rather than long-range transport and thus baseline food web exposure, explain among and within colony variance in contaminant occurrence.
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Affiliation(s)
- Eliza H K Leat
- College of Medical Veterinary and Life Sciences, Graham Kerr Building, University of Glasgow, Glasgow, G12 8QQ, UK
| | - Sophie Bourgeon
- The Arctic University of Norway (UiT), Department of Arctic and Marine Biology, Tromsø, Norway; Norwegian Institute for Nature Research (NINA), Fram Centre, N-9296 Tromsø, Norway
| | - Sveinn A Hanssen
- Norwegian Institute for Nature Research (NINA), Fram Centre, N-9296 Tromsø, Norway
| | | | - Hallvard Strøm
- Norwegian Polar Institute FRAM Centre, Postbox 6606, Langnes, NO- 9296, Tromsø, Norway
| | | | - Geir W Gabrielsen
- Norwegian Polar Institute FRAM Centre, Postbox 6606, Langnes, NO- 9296, Tromsø, Norway
| | - Jan Ove Bustnes
- Norwegian Institute for Nature Research (NINA), Fram Centre, N-9296 Tromsø, Norway
| | - Robert W Furness
- College of Medical Veterinary and Life Sciences, Graham Kerr Building, University of Glasgow, Glasgow, G12 8QQ, UK
| | - Ane Haarr
- Department of Biosciences, University of Oslo, Pb 1066, Blindern, 0316, Oslo, Norway
| | - Katrine Borgå
- Department of Biosciences, University of Oslo, Pb 1066, Blindern, 0316, Oslo, Norway; Norwegian Institute for Water Research Gaustadalleén, 21 0349, Oslo, Norway.
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Braune BM, Gaston AJ, Mallory ML. Temporal trends of legacy organochlorines in eggs of Canadian Arctic seabirds monitored over four decades. THE SCIENCE OF THE TOTAL ENVIRONMENT 2019; 646:551-563. [PMID: 30059916 DOI: 10.1016/j.scitotenv.2018.07.291] [Citation(s) in RCA: 5] [Impact Index Per Article: 0.8] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 06/18/2018] [Revised: 07/19/2018] [Accepted: 07/20/2018] [Indexed: 06/08/2023]
Abstract
We compared temporal trends of legacy organochlorine pesticides and PCBs in eggs of five seabird species breeding at Prince Leopold Island in the Canadian high Arctic. Concentrations of most of the major organochlorine groups/compounds have either declined (e.g. Σ35PCB, ΣDDT, ΣCBz, ΣCHL, octachlorostyrene) or shown no consistent directional change (e.g. heptachlor epoxide) since 1975 in eggs of thick-billed murres (Uria lomvia), northern fulmars (Fulmarus glacialis) and black-legged kittiwakes (Rissa tridactyla). Aside from β-HCH, which increased in most species, the major organochlorine compounds either declined or showed no trend between 1993 and 2013 in eggs of five seabird species (thick-billed murre, northern fulmar, black-legged kittiwake, black guillemot Cepphus grylle, glaucous gull Larus hyperboreus). Most of the declines occurred during the 1970s to 1990s followed by little change during the 2000s. Glaucous gull eggs had the highest concentrations of almost all organochlorines in the five years compared (1993, 1998, 2003/04, 2008, 2013), and murre eggs generally had among the lowest concentrations. The primary organochlorines found in eggs of all five species were Σ35PCB, ΣDDT (mainly p,p'-DDE), ΣCBz (mainly hexachlorobenzene) and ΣCHL (mainly oxychlordane) although proportions varied by species and year. The major PCB congeners found in eggs of all five species were CB-153, -138, -118 and -180. The penta-, hexa- and heptachlorobiphenyl homologs comprised the largest proportion of Σ35PCB in all five species. Although levels of most legacy organochlorines have declined since 1975, the potential for climate change to alter chemical transport pathways as well as exposure pathways in the biotic environment could affect temporal trends. Therefore, it is important to continue to monitor these legacy contaminants in order to determine how these changes will affect the temporal trends observed to date.
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Affiliation(s)
- Birgit M Braune
- Environment and Climate Change Canada, National Wildlife Research Centre, Carleton University, Raven Road, Ottawa, Ontario, Canada K1A 0H3.
| | - Anthony J Gaston
- Environment and Climate Change Canada, National Wildlife Research Centre, Carleton University, Raven Road, Ottawa, Ontario, Canada K1A 0H3
| | - Mark L Mallory
- Biology Department, Acadia University, Wolfville, Nova Scotia, Canada B4P 2R6; Canada Fulbright Chair in Arctic Studies, University of Washington, Box 353650, Seattle, WA, USA, 98195-3650
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Desjardins CF, Mazerolle MJ, Verreault J. Is the urban-adapted ring-billed gull a biovector for flame retardants? ENVIRONMENTAL POLLUTION (BARKING, ESSEX : 1987) 2019; 244:109-117. [PMID: 30321706 DOI: 10.1016/j.envpol.2018.10.003] [Citation(s) in RCA: 4] [Impact Index Per Article: 0.7] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 07/19/2018] [Revised: 09/08/2018] [Accepted: 10/01/2018] [Indexed: 06/08/2023]
Abstract
Birds may act as biovectors of nutrients and contaminants at the regional scale and potentially increase the exposure to such substances in ecosystems frequented by these birds. However, no study has estimated biotransport of contaminants by individual birds through their feces (guano). Elevated concentrations of halogenated flame retardants (HFRs) have been reported in ring-billed gulls (Larus delawarensis) breeding near Montreal (QC, Canada)- a known hotspot for HFRs. The objective of the present study was to investigate the concentrations of polybrominated diphenyl ethers (PBDEs) and selected emerging HFRs (e.g., Dechlorane-related compounds) in guano of individual ring-billed gulls, and to assess the relative accumulation of these HFRs by comparing concentrations in plasma (absorbed) versus guano (excreted). A second objective was to determine the importance of one of the largest ring-billed gull colony (Deslauriers Island) in North America located near Montreal as a vector of HFR biotransport at the regional scale. Elevated concentrations of PBDEs and Dechlorane plus were determined in guano and plasma of ring-billed gulls, although in general no difference was found between males and females. However, plasma to guano concentration ratios were significantly greater in females for the highly hydrophobic BDE-209 and Dechlorane plus compared to males. Overall, for both sexes combined, the total amount of HFRs (sum of the 16 major PBDEs and five emerging HFRs) deposited by this entire colony (64,980 gulls) in the Montreal area through guano during the 28-days incubation period was estimated to 1 g. This study showed that urban-adapted ring-billed gulls from this large colony represent an underestimated biovector of HFRs, which may contribute to augment exposure to these toxic compounds in nearby ecosystems.
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Affiliation(s)
- Chloé F Desjardins
- Centre de recherche en toxicologie de l'environnement (TOXEN), Département des sciences biologiques, Université du Québec à Montréal, P.O. Box 8888, Station Centre-ville, Montréal, QC, H3C 3P8, Canada
| | - Marc J Mazerolle
- Centre d'étude de la forêt, Département des sciences du bois et de la forêt, Université Laval, 2405 rue de la Terrasse, Québec, QC, G1V 0A6, Canada
| | - Jonathan Verreault
- Centre de recherche en toxicologie de l'environnement (TOXEN), Département des sciences biologiques, Université du Québec à Montréal, P.O. Box 8888, Station Centre-ville, Montréal, QC, H3C 3P8, Canada.
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Steyn L, Hoffman J, Bouwman H, Maina AW, Maina JN. Bone density and asymmetry are not related to DDT in House Sparrows: Insights from micro-focus X-ray computed tomography. CHEMOSPHERE 2018; 212:734-743. [PMID: 30179838 DOI: 10.1016/j.chemosphere.2018.08.119] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 05/17/2018] [Revised: 08/09/2018] [Accepted: 08/23/2018] [Indexed: 06/08/2023]
Abstract
In organisms, DDT (Dichlorodiphenyltrichloroethane) and its metabolites, DDE (Dichlorodiphenyldichloroethylene) and DDD (Dichlorobischlorophenylethane) are endocrine mimics. They can influence bone density and other bone structural features. This study was conducted on House Sparrows (Passer domesticus) caught from the Free State - and the Limpopo Provinces of South Africa (SA). The sites were chosen based on spraying patterns of DDT for malaria control or non-spraying. The bone mineral densities of the femurs as well as the lengths of the left- and right leg bones were determined using micro-focus X-ray computed tomography (μ-XCT). The concentrations of DDT and its metabolites in the liver were determined with gas-chromatography mass-spectrometry to provide baseline concentrations of DDT in the body, allowing comparison of the various groups of birds. There was no asymmetry between the lengths of the bones of the left- and the right legs. DDT concentrations in the liver did not correlate with bone lengths. In addition, there were no significant differences between the relative densities of the left- and right leg bones with increase of concentrations of DDT. The concentrations of DDT and its metabolites did not have a significant effect on the measured bone parameters of House Sparrows. It is possible that the concentrations of DDT and its metabolites in the environments were too low to be injurious to the birds and/or tolerance to the insecticide has developed in the birds over more than six decades of almost continuous application of DDT.
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Affiliation(s)
- L Steyn
- Department of Zoology, University of Johannesburg, Auckland Park, 2006, South Africa.
| | - J Hoffman
- Department of Radiation Science, South African Nuclear Energy Corporation, (Necsa), Pelindaba, Pretoria, South Africa
| | - H Bouwman
- Research Unit, Environmental Sciences and Management, North-West University, Potchefstroom, 2520, South Africa
| | - A W Maina
- Department of Orthopaedic Surgery, Department of Surgery, University of the Witwatersrand, Parktown, Johannesburg, South Africa; Consultant Orthopaedic Surgeon, Department of Orthopaedic Surgery, Department of Surgery, Charlotte Maxeke Johannesburg Academic Hospital Parktown, Johannesburg, South Africa
| | - J N Maina
- Department of Zoology, University of Johannesburg, Auckland Park, 2006, South Africa
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Blévin P, Shaffer SA, Bustamante P, Angelier F, Picard B, Herzke D, Moe B, Gabrielsen GW, Bustnes JO, Chastel O. Organochlorines, perfluoroalkyl substances, mercury, and egg incubation temperature in an Arctic seabird: Insights from data loggers. ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY 2018; 37:2881-2894. [PMID: 30094864 DOI: 10.1002/etc.4250] [Citation(s) in RCA: 3] [Impact Index Per Article: 0.4] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 04/01/2018] [Revised: 05/08/2018] [Accepted: 08/08/2018] [Indexed: 06/08/2023]
Abstract
In birds, incubation-related behaviors and brood patch formation are influenced by hormonal regulation such as prolactin secretion. Brood patch provides efficient heat transfer between the incubating parent and the developing embryo in the egg. Importantly, several environmental contaminants are already known to have adverse effects on avian reproduction. However, relatively little is known about the effect of contaminants on incubation temperature (Tinc ) in wild birds. By using temperature thermistors placed into artificial eggs, we investigated whether the most contaminated parent birds are less able to provide appropriate egg warming and thus less committed to incubating their clutch. Specifically, we investigated the relationships among 3 groups of contaminants (organochlorines, perfluoroalkyl substances [PFASs], and mercury [Hg]) with Tinc and also with prolactin concentrations and brood patch size in incubating Arctic black-legged kittiwakes (Rissa tridactyla). Our results reveal that among the organochlorines considered, only blood levels of oxychlordane, the main metabolite of chlordane, a banned pesticide, were negatively related to the minimum incubation temperature in male kittiwakes. Levels of PFASs and Hg were unrelated to Tinc in kittiwakes. Moreover, our study suggests a possible underlying mechanism: since we reported a significant and negative association between blood oxychlordane concentrations and the size of the brood patch in males. Finally, this reduced Tinc in the most oxychlordane-contaminated kittiwakes was associated with a lower egg hatching probability. Environ Toxicol Chem 2018;37:2881-2894. © 2018 SETAC.
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Affiliation(s)
- Pierre Blévin
- Centre d'Etudes Biologiques de Chizé, UMR 7372-Centre National de la Recherche Scientifique, Université de La Rochelle, Villiers-en-Bois, France
- Littoral Environnement et Sociétés, UMR 7266-Centre National de la Recherche Scientifique, Université de La Rochelle, La Rochelle, France
| | - Scott A Shaffer
- Department of Biological Sciences, San Jose State University, San Jose, California, USA
| | - Paco Bustamante
- Littoral Environnement et Sociétés, UMR 7266-Centre National de la Recherche Scientifique, Université de La Rochelle, La Rochelle, France
| | - Frédéric Angelier
- Centre d'Etudes Biologiques de Chizé, UMR 7372-Centre National de la Recherche Scientifique, Université de La Rochelle, Villiers-en-Bois, France
| | - Baptiste Picard
- Centre d'Etudes Biologiques de Chizé, UMR 7372-Centre National de la Recherche Scientifique, Université de La Rochelle, Villiers-en-Bois, France
| | - Dorte Herzke
- Norwegian Institute for Air Research, Tromsø, Norway
| | - Børge Moe
- Norwegian Institute for Nature Research, Trondheim, Norway
| | | | | | - Olivier Chastel
- Centre d'Etudes Biologiques de Chizé, UMR 7372-Centre National de la Recherche Scientifique, Université de La Rochelle, Villiers-en-Bois, France
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Técher R, Houde M, Verreault J. Changes in thyroid axis responses in two ring-billed gull sub-populations differentially exposed to halogenated flame retardants. CHEMOSPHERE 2018; 211:844-854. [PMID: 30103139 DOI: 10.1016/j.chemosphere.2018.07.155] [Citation(s) in RCA: 6] [Impact Index Per Article: 0.9] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 05/04/2018] [Revised: 07/24/2018] [Accepted: 07/25/2018] [Indexed: 06/08/2023]
Abstract
Developing bird embryos may be affected by a number of thyroid disrupting chemicals through maternal transfer. However, thyroid disruption in developing embryos of wild birds remains largely unstudied, especially with respect to exposure to ubiquitous environmental contaminant classes including halogenated flame retardants (HFRs). The objective of the present study was to investigate responses of the hypothalamic-pituitary-thyroid (HPT) axis of developing birds that are exposed to elevated concentrations of HFRs in their environment. Ring-billed gulls (Larus delawarensis) were collected at the external pipping stage (i.e., just prior to hatching) from two sub-populations that are differentially exposed to HFRs in the St. Lawrence River (QC, Canada). Plasma levels of thyroid hormones (THs) and transcription levels of thyroid-related genes in three tissues (i.e., liver, thyroid gland and brain) were related to liver concentrations of HFRs in pipping gulls from these two colonies. Liver polybrominated diphenyl ether (PBDE) concentrations were negatively correlated with plasma total T4 and total T4/T3 in pipping ring-billed gulls. Moreover, plasma TH levels and hepatic PBDE concentrations were correlated with the transcription of genes involved in metabolism (deiodinases type 1, 2 and 3) and synthesis (sodium iodide symporter and thyroglobulin) in the thyroid gland, negative feedback loop (thyrotropin and corticotropin releasing hormones) in the brain and the pituitary and targeted action (TH receptors) in the three tissues of gulls. The present study suggested that the alteration of TH homeostasis in developing wild birds through changes in the transcription of several thyroid-related genes may be related to potential PBDE-mediated effects.
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Affiliation(s)
- Romy Técher
- Centre de recherche en toxicologie de l'environnement (TOXEN), Département des sciences biologiques, Université du Québec à Montréal, C.P. 8888, Succursale Centre-ville, Montreal, QC H3C 3P8, Canada
| | - Magali Houde
- Environment and Climate Change Canada, 105 McGill Street, Montreal, QC H2Y 2E7, Canada
| | - Jonathan Verreault
- Centre de recherche en toxicologie de l'environnement (TOXEN), Département des sciences biologiques, Université du Québec à Montréal, C.P. 8888, Succursale Centre-ville, Montreal, QC H3C 3P8, Canada.
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Won EJ, Choi B, Hong S, Khim JS, Shin KH. Importance of accurate trophic level determination by nitrogen isotope of amino acids for trophic magnification studies: A review. ENVIRONMENTAL POLLUTION (BARKING, ESSEX : 1987) 2018; 238:677-690. [PMID: 29621727 DOI: 10.1016/j.envpol.2018.03.045] [Citation(s) in RCA: 37] [Impact Index Per Article: 5.3] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 12/13/2017] [Revised: 03/13/2018] [Accepted: 03/14/2018] [Indexed: 06/08/2023]
Abstract
During the last several decades, persistent organic pollutants and metals cause great concern for their toxicity in organisms as well as for their bioaccumulation and/or trophic transfer through the food chains in ecosystems. A large number of studies therefore have focused on the trophic levels of organisms to illustrate food web structure, as a critical component in the study of pollutant dynamics and biomagnification. The trends in biomagnification of pollutants in food webs indeed provide fundamental information about the properties and fates of pollutants in ecosystems. The trophic magnification supports the establishment of a reliable trophic structure, which can further aid the understanding of the transport and exposure routes of contaminants in accumulation and risk assessments. Recently, efforts to interpret the food web structure using carbon and nitrogen stable isotope ratios have contributed to better understanding of the fate of pollutants in the ecosystem. However, it is known that this isotope analysis of bulk ones has many weaknesses, particularly for uncertainties on the estimate of trophic levels and therefore of magnification factors for studied organisms, enough to support a regulatory interpretation. In this review, we collate studies that investigated biomagnification characteristics of pollutants in aquatic ecosystems, along with calculated trophic magnification factors. Moreover, we introduce a novel approach, compound-specific stable isotope analysis of nitrogen in amino acids, to establish reliable food web structures and accurate trophic levels for biomagnification studies. This method promises to provide sound results for interpreting the influence of the pollutant in organisms, along with their bioaccumulation and magnification characteristics, as well as that in ecosystem.
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Affiliation(s)
- Eun-Ji Won
- Department of Marine Science and Convergent Technology, Hanyang University, Ansan, 15588, Republic of Korea; Department of Marine Chemistry & Geochemistry Research Center, Korea Institute of Ocean Science and Technology, Busan, 49111, Republic of Korea
| | - Bohyung Choi
- Department of Marine Science and Convergent Technology, Hanyang University, Ansan, 15588, Republic of Korea
| | - Seongjin Hong
- Department of Ocean Environmental Sciences, Chungnam National University, Daejeon, 34134, Republic of Korea
| | - Jong Seong Khim
- School of Earth and Environmental Sciences & Research Institute of Oceanography, Seoul National University, Seoul, 08826, Republic of Korea
| | - Kyung-Hoon Shin
- Department of Marine Science and Convergent Technology, Hanyang University, Ansan, 15588, Republic of Korea.
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The Risk of Polychlorinated Biphenyls Facilitating Tumors in Hawaiian Green Sea Turtles ( Chelonia mydas). INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH 2018; 15:ijerph15061243. [PMID: 29895772 PMCID: PMC6025165 DOI: 10.3390/ijerph15061243] [Citation(s) in RCA: 1] [Impact Index Per Article: 0.1] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Received: 05/16/2018] [Revised: 05/31/2018] [Accepted: 06/10/2018] [Indexed: 11/24/2022]
Abstract
The Hawaiian green turtle (Chelonia mydas) is on the list of threatened species protected under the U.S. Endangered Species Act in 1978 in large part due to a severe tumor-forming disease named fibropapillomatosis. Chemical pollution is a prime suspect threatening the survival of C. mydas. In this study, PCBs concentrations were determined in 43 C. mydas plasma samples archived on Tern Island. The total PCBs concentration in male C. mydas (mean 1.10 ng/mL) was two times more than that of females (mean 0.43 ng/mL). The relationship between straight carapace length and PCBs concentration in females has also been studied, which was negatively related. To figure out the possible existence of correlations between PCBs and tumor status, we measured the PCBs concentration in turtles with no tumor, moderate or severe tumor affliction. PCBs concentration of two afflicted groups was much higher than the healthy group, suggesting that PCBs may play a role in fibropapillomatosis in Hawaiian green turtle.
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Haarr A, Hylland K, Eckbo N, Gabrielsen GW, Herzke D, Bustnes JO, Blévin P, Chastel O, Moe B, Hanssen SA, Sagerup K, Borgå K. DNA damage in Arctic seabirds: Baseline, sensitivity to a genotoxic stressor, and association with organohalogen contaminants. ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY 2018; 37:1084-1091. [PMID: 29120089 DOI: 10.1002/etc.4035] [Citation(s) in RCA: 3] [Impact Index Per Article: 0.4] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 06/30/2017] [Revised: 09/06/2017] [Accepted: 11/08/2017] [Indexed: 06/07/2023]
Abstract
Environmental contaminants are found throughout Arctic marine ecosystems, and their presence in seabirds has been associated with toxicological responses. However, there are few studies of genotoxicity in Arctic avian wildlife. The purpose of the present study was to quantify deoxyribonucleic acid (DNA) damage in lymphocytes of selected seabird species and to examine whether accumulation of organohalogen contaminants (ΣOHCs) affects DNA damage. Blood was sampled from common eider (Somateria mollissima), black guillemot (Cepphus grylle), black-legged kittiwake (Rissa tridactyla), glaucous gull (Larus hyperboreus), arctic skua (Stercorarius parasiticus), and great skua (Stercorarius skua) in Kongsfjorden, Svalbard (Norway). Contaminant concentrations found in the 6 species differed, presumably because of foraging ecology and biomagnification. Despite large differences in contaminant concentrations, ranging from ΣOHCs 3.3 ng/g wet weight in the common eider to ΣOHCs 895 ng/g wet weight in the great skua, there was no strong difference among the species in baseline DNA damage or sensitivity to a genotoxic stressor (hydrogen peroxide). Baseline levels of DNA damage were low, with median values ranging from 1.7% in the common eider to 8.6% in the great skua. There were no associations between DNA damage and contaminants in the investigated species, suggesting that contaminant concentrations in Kongsfjorden are too low to evoke genotoxic effects, or possibly that lymphocytes are resistant to strand breakage. Clearly, genotoxicity is a topic for future studies of Arctic seabirds. Environ Toxicol Chem 2018;37:1084-1091. © 2017 SETAC.
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Affiliation(s)
- Ane Haarr
- Department of Biosciences, University of Oslo, Oslo, Norway
| | - Ketil Hylland
- Department of Biosciences, University of Oslo, Oslo, Norway
| | - Norith Eckbo
- Department of Biosciences, University of Oslo, Oslo, Norway
| | | | - Dorte Herzke
- Norwegian Institute of Air Research (NILU), Fram Centre, Tromsø, Norway
| | - Jan Ove Bustnes
- Norwegian Institute of Nature Research (NINA), Fram Centre, Tromsø, Norway
| | - Pierre Blévin
- Centre d'Etudes Biologiques de Chizé (CEBC), Conseil National de la Recherche Scientifique (CNRS) and Université de la, Rochelle, France
| | - Olivier Chastel
- Centre d'Etudes Biologiques de Chizé (CEBC), Conseil National de la Recherche Scientifique (CNRS) and Université de la, Rochelle, France
| | - Børge Moe
- Norwegian Institute of Nature Research (NINA), Fram Centre, Tromsø, Norway
| | - Sveinn Are Hanssen
- Norwegian Institute of Nature Research (NINA), Fram Centre, Tromsø, Norway
| | | | - Katrine Borgå
- Department of Biosciences, University of Oslo, Oslo, Norway
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Zheng S, Wang P, Sun H, Matsiko J, Hao Y, Meng D, Li Y, Zhang G, Zhang Q, Jiang G. Tissue distribution and maternal transfer of persistent organic pollutants in Kentish Plovers (Charadrius alexandrines) from Cangzhou Wetland, Bohai Bay, China. THE SCIENCE OF THE TOTAL ENVIRONMENT 2018; 612:1105-1113. [PMID: 28892854 DOI: 10.1016/j.scitotenv.2017.08.323] [Citation(s) in RCA: 5] [Impact Index Per Article: 0.7] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 07/04/2017] [Revised: 08/24/2017] [Accepted: 08/31/2017] [Indexed: 05/28/2023]
Abstract
Several persistent organic pollutants, including polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs) and organochlorine pesticides (OCPs), were comprehensively investigated in the egg, muscle and liver samples of Kentish Plover (Charadrius alexandrines) collected from Cangzhou Wetland in western Bohai Bay, China. DDTs were the most abundant contaminants (35.4-9853ngg-1 lipid weight, lw), followed by HCHs, PCBs, PBDEs and HCB. PCDD/Fs exhibited the lowest concentrations in all tissues (8.74-4763pgg-1 lw). PCBs and PCDD/Fs were dominated by penta- and hexa-homologs, and PBDEs mostly consisted of the signature congeners of BDE formulations, such as BDE-209, -47, -153 and -99. Significant correlations were found between the lipid-normalized concentrations in muscle and liver (r: 0.37-0.90, p<0.05) and no significant differences (p<0.05), indicating the homogenous distribution of POPs in tissue lipids at steady state. The ratios of concentrations in muscle and liver (M/L) ranged from 0.20 to 1.51, and higher ratios of M/L were found for those compounds with log Kow in the range of 6.5-7.0, suggesting the preferential accumulation of mid-halogenated compounds in muscle. Significant correlations were generally observed between the concentrations in egg and the maternal tissue (p<0.05). The concentration ratios of egg to liver (E/L) were in the range of 0.10-1.24 except for p,p'-DDT (12.7), and compounds with log Kow of 6.5-7.0 exhibited higher E/L ratios, suggesting the selective maternal transfer of mid-halogenated compounds.
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Affiliation(s)
- Shucheng Zheng
- State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China
| | - Pu Wang
- State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China
| | - Huizhong Sun
- State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China
| | - Julius Matsiko
- State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China
| | - Yanfen Hao
- State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China
| | - Derong Meng
- Cangzhou Normal University, Cangzhou 061000, China
| | - Yingming Li
- State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China
| | - Guogang Zhang
- Research Institute of Forest Ecology, Environment and Protection, Chinese Academy of Forestry, Beijing 100091, China
| | - Qinghua Zhang
- State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China; Institute of Environment and Health, Jianghan University, Wuhan 430056, China.
| | - Guibin Jiang
- State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China
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48
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Braune BM, Jacobs SR, Gaston AJ. Variation in organochlorine and mercury levels in first and replacement eggs of a single-egg clutch breeder, the thick-billed murre, at a breeding colony in the Canadian Arctic. THE SCIENCE OF THE TOTAL ENVIRONMENT 2018; 610-611:462-468. [PMID: 28818661 DOI: 10.1016/j.scitotenv.2017.08.076] [Citation(s) in RCA: 1] [Impact Index Per Article: 0.1] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 05/11/2017] [Revised: 08/08/2017] [Accepted: 08/09/2017] [Indexed: 06/07/2023]
Abstract
Contaminant concentrations may vary among sequentially-laid eggs in multi-egg clutches, and this variation has implications for the interpretation of contaminant concentrations in monitoring programs. The thick-billed murre (Uria lomvia) is a key species for monitoring contaminants in the Canadian Arctic and lays only a single egg per year. Therefore, the potential issue of intra-clutch variation in contaminant concentrations is avoided. However, if the egg is removed or lost early in the incubation stage, the adult female murre will relay. In this study, we examined contaminant concentrations and patterns in first-laid and replacement eggs of thick-billed murres breeding in northern Hudson Bay in order to determine whether or not these eggs could be sampled interchangeably. Concentrations of the major legacy organochlorines (e.g. PCBs, DDT, chlordanes) were generally higher, and total mercury concentrations lower, in the replacement eggs compared with the first-laid eggs. The organochlorine profile was comprised primarily of ΣDDT and Σ70PCB, and Σ70PCB was comprised primarily of hexa-hepta PCBs in both first-laid and replacement eggs. As both concentrations and organochlorine patterns showed differences between first-laid and replacement eggs, we recommend that randomly selected first-laid eggs of thick-billed murres be consistently sampled for contaminant monitoring in the Canadian Arctic.
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Affiliation(s)
- Birgit M Braune
- Environment and Climate Change Canada, National Wildlife Research Centre, Carleton University, Raven Road, Ottawa, Ontario K1A 0H3, Canada.
| | - Shoshanah R Jacobs
- Department of Integrative Biology, University of Guelph, Guelph, Ontario N1G 2W1, Canada
| | - Anthony J Gaston
- Environment and Climate Change Canada, National Wildlife Research Centre, Carleton University, Raven Road, Ottawa, Ontario K1A 0H3, Canada
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49
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Melnes M, Gabrielsen GW, Herzke D, Sagerup K, Jenssen BM. Dissimilar effects of organohalogenated compounds on thyroid hormones in glaucous gulls. ENVIRONMENTAL RESEARCH 2017; 158:350-357. [PMID: 28683408 DOI: 10.1016/j.envres.2017.06.007] [Citation(s) in RCA: 7] [Impact Index Per Article: 0.9] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 02/09/2017] [Revised: 05/09/2017] [Accepted: 06/12/2017] [Indexed: 06/07/2023]
Abstract
The glaucous gull (Larus hyperboreus) is an arctic top predator and scavenger exposed to high levels of mixtures of organohalogenated contaminants (OHCs) of which many interfere with the thyroid hormone (TH) system. In the present study, we applied statistical modeling to investigate the potential combined influence of the mixture of chlorinated, brominated and perfluorinated organic compounds in plasma of glaucous gulls on their plasma TH concentrations. In females, there were significant negative associations between several organochlorinated compounds (OCs) and free thyroxin (FT4) and triiodothyronine (FT3), indicating additive negative effects on FT4 and FT3. However, in these females there was also a significant positive association between perfluorooctane sulfonate (PFOS) and FT3. The inverse associations between several OCs and FT3 and the contrasting positive association between PFOS and FT3, indicate that these two groups of OHCs may have dissimilar and antagonistic effects on FT3 in female glaucous gulls. In males, there were no associations between any of the OHCs and the THs. That OHCs affect THs in a complex manner involving both additive and antagonistic effects add to the challenge of interpreting the overall functional effect of thyroid disruptive chemicals in wildlife. However, experimental studies are needed to confirm or disprove such effects.
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Affiliation(s)
- Marte Melnes
- Department of Biology, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway
| | | | - Dorte Herzke
- Norwegian Institute for Air Research, Fram Centre, NO-9296 Tromsø, Norway
| | | | - Bjørn Munro Jenssen
- Department of Biology, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway; Department of Arctic Technology, University Centre in Svalbard, NO 9171 Longyearbyen, Norway.
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50
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Dehnhard N, Jaspers VLB, Demongin L, Van den Steen E, Covaci A, Pinxten R, Crossin GT, Quillfeldt P, Eens M, Poisbleau M. Organohalogenated contaminants in plasma and eggs of rockhopper penguins: Does vitellogenin affect maternal transfer? ENVIRONMENTAL POLLUTION (BARKING, ESSEX : 1987) 2017; 226:277-287. [PMID: 28392239 DOI: 10.1016/j.envpol.2017.03.071] [Citation(s) in RCA: 3] [Impact Index Per Article: 0.4] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 01/13/2017] [Revised: 03/17/2017] [Accepted: 03/29/2017] [Indexed: 06/07/2023]
Abstract
Although many studies have investigated organohalogenated contaminants (OHCs) in yolk, little is known about the mechanisms and timing of transfer of OHCs from the female to the egg. Vitellogenin, a yolk precursor, has been suggested to play a role in this transport. We here report for the first time the temporal changes in OHC and an index of vitellogenin concentrations in female plasma from the pre-laying period to clutch completion in free-living birds: the southern rockhopper penguin (Eudyptes chrysocome chrysocome) breeding in the Falkland/Malvinas Islands. In addition, OHC concentrations in the corresponding clutches were analysed. OHC concentrations in female plasma and in the yolk of both the first (A-) and the second (B-)eggs followed a similar pattern, with hexachlorobenzene (HCB) > Σpolychlorinated biphenyls (PCBs) > Σdichlorodiphenyltrichloroethanes (DDTs) > Σmethoxylated polybrominated diphenyl ethers (MeO-PBDEs) > Σchlordanes (CHLs) > Σpolybrominated diphenyl ethers (PBDEs) ≈ Σhexachlorocyclohexanes (HCHs). The higher concentrations of MeO-PBDEs compared to PBDEs indicate a diet containing naturally-produced MeO-PBDEs. All OHC compounds except for PBDEs increased from the pre-laying period to A-egg laying and subsequently declined from A-egg laying to B-egg laying, and female plasma vitellogenin showed the same pattern. For ΣPCBs and ΣMeO-PBDEs, we found positive correlations between female plasma during A-egg laying and both eggs, and for HCB between female plasma and A-eggs only. During pre-laying, only ΣMeO-PBDEs correlated between both eggs and female plasma, and no correlations between OHC concentrations in eggs and female plasma were found during B-egg laying, highlighting that maternal transfer of OHCs is time- and compound-specific. Finally, female vitellogenin concentrations did not significantly correlate with any OHC compounds in either female plasma or eggs, and our results therefore did not confirm the suggested role of vitellogenin in the maternal transfer of OHC molecules into their eggs.
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Affiliation(s)
- Nina Dehnhard
- Department of Biology, Behavioural Ecology and Ecophysiology Group, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Antwerp (Wilrijk), Belgium.
| | - Veerle L B Jaspers
- Department of Biology, Norwegian University of Science and Technology, Høgskoleringen 5, 7024 Trondheim, Norway
| | - Laurent Demongin
- Department of Biology, Behavioural Ecology and Ecophysiology Group, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Antwerp (Wilrijk), Belgium
| | - Evi Van den Steen
- Department of Biology, Behavioural Ecology and Ecophysiology Group, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Antwerp (Wilrijk), Belgium
| | - Adrian Covaci
- Toxicological Center, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Antwerp (Wilrijk), Belgium
| | - Rianne Pinxten
- Department of Biology, Behavioural Ecology and Ecophysiology Group, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Antwerp (Wilrijk), Belgium; Faculty of Social Sciences, Antwerp School of Education, University of Antwerp, Venusstraat 35, 2000 Antwerp, Belgium
| | - Glenn T Crossin
- Department of Biology, Dalhousie University, Halifax, Nova Scotia, Canada
| | - Petra Quillfeldt
- Justus-Liebig University Gießen, Heinrich-Buff-Ring 38, 35392 Gießen, Germany
| | - Marcel Eens
- Department of Biology, Behavioural Ecology and Ecophysiology Group, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Antwerp (Wilrijk), Belgium
| | - Maud Poisbleau
- Department of Biology, Behavioural Ecology and Ecophysiology Group, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Antwerp (Wilrijk), Belgium
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