11 results on '"Abrantes K"'
Search Results
2. Whale sharks as oceanic nurseries for Golden Trevally.
- Author
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Sheaves, M., Mattone, C., Barnett, A., Abrantes, K., Bradley, M., Sheaves, A., Sheaves, J., and Waltham, N. J.
- Subjects
MEGAFAUNA ,WHALE shark - Abstract
The Golden Trevally, Gnathanodon speciosus , is a large predatory fish with an extremely broad tropical Indo-Pacific distribution that crosses many biogeographical boundaries. Both published information and freely available imagery suggest that small juvenile G. speciosus are often associated with whale sharks, Rhincodon typus ; an association that could explain the unusually widespread distribution of G. speciosus , and suggests a novel nursery relationship. The possibility of such an association has the potential to reshape our understanding of the ecological roles played by long-range migrants such as R. typus and other megafauna, our understanding of the full extent of their conservation value, and how we manage both members of the relationship. The Golden Trevally, Gnathanodon speciosus , is a large predatory fish with an extremely broad tropical Indo-Pacific distribution crossing many biogeographical boundaries. Published information and freely available imagery suggest that small juvenile G. speciosus are often associated with whale sharks, Rhincodon typus ; an association that could explain their unusually wide-spread distribution, and suggests a novel nursery relationship. The occurrence of such an association reshapes our understanding of the ecological roles played by long-range migrants such as R. typus and other megafauna. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF
3. Whale sharks as oceanic nurseries for Golden Trevally
- Author
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Sheaves, M., primary, Mattone, C., additional, Barnett, A., additional, Abrantes, K., additional, Bradley, M., additional, Sheaves, A., additional, Sheaves, J., additional, and Waltham, N. J., additional
- Published
- 2023
- Full Text
- View/download PDF
4. Intraspecific variability in flatback turtle habitat use - δ15N as indicator of foraging locations
- Author
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Abrantes, K, primary, Wildermann, N, additional, Miller, IB, additional, Hamann, M, additional, Limpus, CJ, additional, Madden Hof, CA, additional, Bell, I, additional, Sheaves, M, additional, and Barnett, A, additional
- Published
- 2023
- Full Text
- View/download PDF
5. Diving into the vertical dimension of elasmobranch movement ecology
- Author
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Andrzejaczek, S., Lucas, T.C.D., Goodman, M.C., Hussey, N.E., Armstrong, A.J., Carlisle, A., Coffey, D.M., Gleiss, A.C., Huveneers, C., Jacoby, D.M.P., Meekan, M.G., Mourier, J., Peel, L.R., Abrantes, K., Afonso, A.S., Ajemian, M.J., Anderson, B.N., Anderson, S.D., Araujo, G., Armstrong, A.O., Bach, P., Barnett, A., Bennett, M.B., Bezerra, N.A., Bonfil, R., Boustany, A.M., Bowlby, H.D., Branco, I., Braun, C.D., Brooks, E.J., Brown, J., Burke, P.J., Butcher, P., Castleton, M., Chapple, T.K., Chateau, O., Clarke, M., Coelho, R., Cortés, E., Couturier, L.I.E., Cowley, P.D., Croll, D.A., Cuevas, J.M., Curtis, T.H., Dagorn, L., Dale, J.J., Daly, R., Dewar, H., Doherty, P.D., Domingo, A., Dove, A.D.M., Drew, M., Dudgeon, C.L., Duffy, C.A.J., Elliott, R.G., Ellis, J.R., Erdmann, M.V., Farrugia, T.J., Ferreira, L.C., Ferretti, F., Filmalter, J.D., Finucci, B., Fischer, C., Fitzpatrick, R., Forget, F., Forsberg, K., Francis, M.P., Franks, B.R., Gallagher, A.J., Galván-Magaña, F., García, M.L., Gaston, T.F., Gillanders, B.M., Gollock, M.J., Green, J.R., Green, S., Griffiths, C.A., Hammerschlag, N., Hasan, A., Hawkes, L.A., Hazin, F., Heard, M., Hearn, A., Hedges, K.J., Henderson, S.M., Holdsworth, J., Holland, K.N., Howey, L.A., Hueter, R.E., Humphries, N.E., Hutchinson, M., Jaine, F.R.A., Jorgensen, S.J., Kanive, P.E., Labaja, J., Lana, F.O., Lassauce, H., Lipscombe, R.S., Llewellyn, F., Macena, B.C.L., Mambrasar, R., McAllister, J.D., McCully Phillips, S.R., McGregor, F., McMillan, M.N., McNaughton, L.M., Mendonça, S.A., Meyer, C.G., Meyers, M., Mohan, J.A., Montgomery, J.C., Mucientes, G., Musyl, M.K., Nasby-Lucas, N., Natanson, L.J., O’Sullivan, J.B., Oliveira, P., Papastamtiou, Y.P., Patterson, T.A., Pierce, S.J., Queiroz, N., Radford, C.A., Richardson, A.J., Righton, D., Rohner, C.A., Royer, M.A., Saunders, R.A., Schaber, M., Schallert, R.J., Scholl, M.C., Seitz, A.C., Semmens, J.M., Setyawan, E., Shea, B.D., Shidqi, R.A., Shillinger, G.L., Shipley, O.N., Shivji, M.S., Sianipar, A.B., Silva, J.F., Sims, D.W., Skomal, G.B., Sousa, L.L., Southall, E.J., Spaet, J.L.Y., Stehfest, K.M., Stevens, G., Stewart, J.D., Sulikowski, J.A., Syakurachman, I., Thorrold, S.R., Thums, M., Tickler, D., Tolloti, M.T., Townsend, K.A., Travassos, P., Tyminski, J.P., Vaudo, J.J., Veras, D., Wantiez, L., Weber, S.B., Wells, R.J.D., Weng, K.C., Wetherbee, B.M., Williamson, J.E., Witt, M.J., Wright, S., Zilliacus, K., Block, B.A., Curnick, D.J., Andrzejaczek, S., Lucas, T.C.D., Goodman, M.C., Hussey, N.E., Armstrong, A.J., Carlisle, A., Coffey, D.M., Gleiss, A.C., Huveneers, C., Jacoby, D.M.P., Meekan, M.G., Mourier, J., Peel, L.R., Abrantes, K., Afonso, A.S., Ajemian, M.J., Anderson, B.N., Anderson, S.D., Araujo, G., Armstrong, A.O., Bach, P., Barnett, A., Bennett, M.B., Bezerra, N.A., Bonfil, R., Boustany, A.M., Bowlby, H.D., Branco, I., Braun, C.D., Brooks, E.J., Brown, J., Burke, P.J., Butcher, P., Castleton, M., Chapple, T.K., Chateau, O., Clarke, M., Coelho, R., Cortés, E., Couturier, L.I.E., Cowley, P.D., Croll, D.A., Cuevas, J.M., Curtis, T.H., Dagorn, L., Dale, J.J., Daly, R., Dewar, H., Doherty, P.D., Domingo, A., Dove, A.D.M., Drew, M., Dudgeon, C.L., Duffy, C.A.J., Elliott, R.G., Ellis, J.R., Erdmann, M.V., Farrugia, T.J., Ferreira, L.C., Ferretti, F., Filmalter, J.D., Finucci, B., Fischer, C., Fitzpatrick, R., Forget, F., Forsberg, K., Francis, M.P., Franks, B.R., Gallagher, A.J., Galván-Magaña, F., García, M.L., Gaston, T.F., Gillanders, B.M., Gollock, M.J., Green, J.R., Green, S., Griffiths, C.A., Hammerschlag, N., Hasan, A., Hawkes, L.A., Hazin, F., Heard, M., Hearn, A., Hedges, K.J., Henderson, S.M., Holdsworth, J., Holland, K.N., Howey, L.A., Hueter, R.E., Humphries, N.E., Hutchinson, M., Jaine, F.R.A., Jorgensen, S.J., Kanive, P.E., Labaja, J., Lana, F.O., Lassauce, H., Lipscombe, R.S., Llewellyn, F., Macena, B.C.L., Mambrasar, R., McAllister, J.D., McCully Phillips, S.R., McGregor, F., McMillan, M.N., McNaughton, L.M., Mendonça, S.A., Meyer, C.G., Meyers, M., Mohan, J.A., Montgomery, J.C., Mucientes, G., Musyl, M.K., Nasby-Lucas, N., Natanson, L.J., O’Sullivan, J.B., Oliveira, P., Papastamtiou, Y.P., Patterson, T.A., Pierce, S.J., Queiroz, N., Radford, C.A., Richardson, A.J., Righton, D., Rohner, C.A., Royer, M.A., Saunders, R.A., Schaber, M., Schallert, R.J., Scholl, M.C., Seitz, A.C., Semmens, J.M., Setyawan, E., Shea, B.D., Shidqi, R.A., Shillinger, G.L., Shipley, O.N., Shivji, M.S., Sianipar, A.B., Silva, J.F., Sims, D.W., Skomal, G.B., Sousa, L.L., Southall, E.J., Spaet, J.L.Y., Stehfest, K.M., Stevens, G., Stewart, J.D., Sulikowski, J.A., Syakurachman, I., Thorrold, S.R., Thums, M., Tickler, D., Tolloti, M.T., Townsend, K.A., Travassos, P., Tyminski, J.P., Vaudo, J.J., Veras, D., Wantiez, L., Weber, S.B., Wells, R.J.D., Weng, K.C., Wetherbee, B.M., Williamson, J.E., Witt, M.J., Wright, S., Zilliacus, K., Block, B.A., and Curnick, D.J.
- Abstract
Knowledge of the three-dimensional movement patterns of elasmobranchs is vital to understand their ecological roles and exposure to anthropogenic pressures. To date, comparative studies among species at global scales have mostly focused on horizontal movements. Our study addresses the knowledge gap of vertical movements by compiling the first global synthesis of vertical habitat use by elasmobranchs from data obtained by deployment of 989 biotelemetry tags on 38 elasmobranch species. Elasmobranchs displayed high intra- and interspecific variability in vertical movement patterns. Substantial vertical overlap was observed for many epipelagic elasmobranchs, indicating an increased likelihood to display spatial overlap, biologically interact, and share similar risk to anthropogenic threats that vary on a vertical gradient. We highlight the critical next steps toward incorporating vertical movement into global management and monitoring strategies for elasmobranchs, emphasizing the need to address geographic and taxonomic biases in deployments and to concurrently consider both horizontal and vertical movements.
- Published
- 2022
6. Global collision-risk hotspots of marine traffic and the world’s largest fish, the whale shark
- Author
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Womersley, F.C., Humphries, N.E., Queiroz, N., Vedor, M., da Costa, I., Furtado, M., Tyminski, J.P., Abrantes, K., Araujo, G., Bach, S.S., Barnett, A., Berumen, M.L., Bessudo Lion, S., Braun, C.D., Clingham, E., Cochran, J.E.M., de la Parra, R., Diamant, S., Dove, A.D.M., Dudgeon, C.L., Erdmann, M.V., Espinoza, E., Fitzpatrick, R., Cano, J.G., Green, J.R., Guzman, H.M., Hardenstine, R., Hasan, A., Hazin, F.H.V., Hearn, A.R., Hueter, R.E., Jaidah, M.Y., Labaja, J., Ladino, F., Macena, B.C.L., Morris, J.J., Norman, B.M., Peñaherrera-Palma, C., Pierce, S.J., Quintero, L.M., Ramirez-Macias, D., Reynolds, S.D., Richardson, A.J., Robinson, D.P., Rohner, C.A., Rowat, D.R.L., Sheaves, M., Shivji, M.S., Sianipar, A.B., Skomal, G.B., Soler, G., Syakurachman, I., Thorrold, S.R., Webb, D.H., Wetherbee, B.M., White, T.D., Clavelle, T., Kroodsma, D.A., Thums, M., Ferreira, L.C., Meekan, M.G., Arrowsmith, L.M., Lester, E.K., Meyers, M.M., Peel, L.R., Sequeira, A.M.M., Eguíluz, V.M., Duarte, C.M., Sims, D.W., Womersley, F.C., Humphries, N.E., Queiroz, N., Vedor, M., da Costa, I., Furtado, M., Tyminski, J.P., Abrantes, K., Araujo, G., Bach, S.S., Barnett, A., Berumen, M.L., Bessudo Lion, S., Braun, C.D., Clingham, E., Cochran, J.E.M., de la Parra, R., Diamant, S., Dove, A.D.M., Dudgeon, C.L., Erdmann, M.V., Espinoza, E., Fitzpatrick, R., Cano, J.G., Green, J.R., Guzman, H.M., Hardenstine, R., Hasan, A., Hazin, F.H.V., Hearn, A.R., Hueter, R.E., Jaidah, M.Y., Labaja, J., Ladino, F., Macena, B.C.L., Morris, J.J., Norman, B.M., Peñaherrera-Palma, C., Pierce, S.J., Quintero, L.M., Ramirez-Macias, D., Reynolds, S.D., Richardson, A.J., Robinson, D.P., Rohner, C.A., Rowat, D.R.L., Sheaves, M., Shivji, M.S., Sianipar, A.B., Skomal, G.B., Soler, G., Syakurachman, I., Thorrold, S.R., Webb, D.H., Wetherbee, B.M., White, T.D., Clavelle, T., Kroodsma, D.A., Thums, M., Ferreira, L.C., Meekan, M.G., Arrowsmith, L.M., Lester, E.K., Meyers, M.M., Peel, L.R., Sequeira, A.M.M., Eguíluz, V.M., Duarte, C.M., and Sims, D.W.
- Abstract
Marine traffic is increasing globally yet collisions with endangered megafauna such as whales, sea turtles, and planktivorous sharks go largely undetected or unreported. Collisions leading to mortality can have population-level consequences for endangered species. Hence, identifying simultaneous space use of megafauna and shipping throughout ranges may reveal as-yet-unknown spatial targets requiring conservation. However, global studies tracking megafauna and shipping occurrences are lacking. Here we combine satellite-tracked movements of the whale shark, Rhincodon typus, and vessel activity to show that 92% of sharks’ horizontal space use and nearly 50% of vertical space use overlap with persistent large vessel (>300 gross tons) traffic. Collision-risk estimates correlated with reported whale shark mortality from ship strikes, indicating higher mortality in areas with greatest overlap. Hotspots of potential collision risk were evident in all major oceans, predominantly from overlap with cargo and tanker vessels, and were concentrated in gulf regions, where dense traffic co-occurred with seasonal shark movements. Nearly a third of whale shark hotspots overlapped with the highest collision-risk areas, with the last known locations of tracked sharks coinciding with busier shipping routes more often than expected. Depth-recording tags provided evidence for sinking, likely dead, whale sharks, suggesting substantial “cryptic” lethal ship strikes are possible, which could explain why whale shark population declines continue despite international protection and low fishing-induced mortality. Mitigation measures to reduce ship-strike risk should be considered to conserve this species and other ocean giants that are likely experiencing similar impacts from growing global vessel traffic.
- Published
- 2022
7. Identifying priority sites for whale shark ship collision management globally.
- Author
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Womersley FC, Rohner CA, Abrantes K, Afonso P, Arunrugstichai S, Bach SS, Bar S, Barash A, Barnes P, Barnett A, Boldrocchi G, Buffat N, Canon T, Perez CC, Chuangcharoendee M, Cochran JEM, de la Parra R, Diamant S, Driggers W, Dudgeon CL, Erdmann MV, Fitzpatrick R, Flam A, Fontes J, Francis G, Galvan BE, Graham RT, Green SM, Green JR, Grosmark Y, Guzman HM, Hardenstine RS, Harvey M, Harvey-Carroll J, Hasan AW, Hearn AR, Hendon JM, Putra MIH, Himawan MR, Hoffmayer E, Holmberg J, Hsu HH, Jaidah MY, Jansen A, Judd C, Kuguru B, Lester E, Macena BCL, Magson K, Maguiño R, Manjaji-Matsumoto M, Marcoux SD, Marcoux T, McKinney J, Meekan M, Mendoza A, Moazzam M, Monacella E, Norman B, Perry C, Pierce S, Prebble C, Macías DR, Raudino H, Reynolds S, Robinson D, Rowat D, Santos MD, Schmidt J, Scott C, See ST, Sianipar A, Speed CW, Syakurachman I, Tyne JA, Waples K, Winn C, Yuneni RR, Zareer I, and Araujo G
- Subjects
- Animals, Endangered Species, Environmental Monitoring, Sharks physiology, Ships, Conservation of Natural Resources
- Abstract
The expansion of the world's merchant fleet poses a great threat to the ocean's biodiversity. Collisions between ships and marine megafauna can have population-level consequences for vulnerable species. The Endangered whale shark (Rhincodon typus) shares a circumglobal distribution with this expanding fleet and tracking of movement pathways has shown that large vessel collisions pose a major threat to the species. However, it is not yet known whether they are also at risk within aggregation sites, where up to 400 individuals can gather to feed on seasonal bursts of planktonic productivity. These "constellation" sites are of significant ecological, socio-economic and cultural value. Here, through expert elicitation, we gathered information from most known constellation sites for this species across the world (>50 constellations and >13,000 individual whale sharks). We defined the spatial boundaries of these sites and their overlap with shipping traffic. Sites were then ranked based on relative levels of potential collision danger posed to whale sharks in the area. Our results showed that researchers and resource managers may underestimate the threat posed by large ship collisions due to a lack of direct evidence, such as injuries or witness accounts, which are available for other, sub-lethal threat categories. We found that constellations in the Arabian Sea and adjacent waters, the Gulf of Mexico, the Gulf of California, and Southeast and East Asia, had the greatest level of collision threat. We also identified 39 sites where peaks in shipping activity coincided with peak seasonal occurrences of whale sharks, sometimes across several months. Simulated collision mitigation options estimated potentially minimal impact to industry, as most whale shark core habitat areas were small. Given the threat posed by vessel collisions, a coordinated, multi-national approach to mitigation is needed within priority whale shark habitats to ensure collision protection for the species., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)
- Published
- 2024
- Full Text
- View/download PDF
8. From little things big things grow: enhancement of an acoustic telemetry network to monitor broad-scale movements of marine species along Australia's east coast.
- Author
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Barnett A, Jaine FRA, Bierwagen SL, Lubitz N, Abrantes K, Heupel MR, Harcourt R, Huveneers C, Dwyer RG, Udyawer V, Simpfendorfer CA, Miller IB, Scott-Holland T, Kilpatrick CS, Williams SM, Smith D, Dudgeon CL, Hoey AS, Fitzpatrick R, Osborne FE, Smoothey AF, Butcher PA, Sheaves M, Fisher EE, Svaikauskas M, Ellis M, Kanno S, Cresswell BJ, Flint N, Armstrong AO, Townsend KA, Mitchell JD, Campbell M, Peddemors VM, Gustafson JA, and Currey-Randall LM
- Abstract
Background: Acoustic telemetry has become a fundamental tool to monitor the movement of aquatic species. Advances in technology, in particular the development of batteries with lives of > 10 years, have increased our ability to track the long-term movement patterns of many species. However, logistics and financial constraints often dictate the locations and deployment duration of acoustic receivers. Consequently, there is often a compromise between optimal array design and affordability. Such constraints can hinder the ability to track marine animals over large spatial and temporal scales. Continental-scale receiver networks have increased the ability to study large-scale movements, but significant gaps in coverage often remain., Methods: Since 2007, the Integrated Marine Observing System's Animal Tracking Facility (IMOS ATF) has maintained permanent receiver installations on the eastern Australian seaboard. In this study, we present the recent enhancement of the IMOS ATF acoustic tracking infrastructure in Queensland to collect data on large-scale movements of marine species in the northeast extent of the national array. Securing a relatively small initial investment for expanding receiver deployment and tagging activities in Queensland served as a catalyst, bringing together a diverse group of stakeholders (research institutes, universities, government departments, port corporations, industries, Indigenous ranger groups and tourism operators) to create an extensive collaborative network that could sustain the extended receiver coverage into the future. To fill gaps between existing installations and maximise the monitoring footprint, the new initiative has an atypical design, deploying many single receivers spread across 2,100 km of Queensland waters., Results: The approach revealed previously unknown broad-scale movements for some species and highlights that clusters of receivers are not always required to enhance data collection. However, array designs using predominantly single receiver deployments are more vulnerable to data gaps when receivers are lost or fail, and therefore "redundancy" is a critical consideration when designing this type of array., Conclusion: Initial results suggest that our array enhancement, if sustained over many years, will uncover a range of previously unknown movements that will assist in addressing ecological, fisheries, and conservation questions for multiple species., (© 2024. The Author(s).)
- Published
- 2024
- Full Text
- View/download PDF
9. Diving into the vertical dimension of elasmobranch movement ecology.
- Author
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Andrzejaczek S, Lucas TCD, Goodman MC, Hussey NE, Armstrong AJ, Carlisle A, Coffey DM, Gleiss AC, Huveneers C, Jacoby DMP, Meekan MG, Mourier J, Peel LR, Abrantes K, Afonso AS, Ajemian MJ, Anderson BN, Anderson SD, Araujo G, Armstrong AO, Bach P, Barnett A, Bennett MB, Bezerra NA, Bonfil R, Boustany AM, Bowlby HD, Branco I, Braun CD, Brooks EJ, Brown J, Burke PJ, Butcher P, Castleton M, Chapple TK, Chateau O, Clarke M, Coelho R, Cortes E, Couturier LIE, Cowley PD, Croll DA, Cuevas JM, Curtis TH, Dagorn L, Dale JJ, Daly R, Dewar H, Doherty PD, Domingo A, Dove ADM, Drew M, Dudgeon CL, Duffy CAJ, Elliott RG, Ellis JR, Erdmann MV, Farrugia TJ, Ferreira LC, Ferretti F, Filmalter JD, Finucci B, Fischer C, Fitzpatrick R, Forget F, Forsberg K, Francis MP, Franks BR, Gallagher AJ, Galvan-Magana F, García ML, Gaston TF, Gillanders BM, Gollock MJ, Green JR, Green S, Griffiths CA, Hammerschlag N, Hasan A, Hawkes LA, Hazin F, Heard M, Hearn A, Hedges KJ, Henderson SM, Holdsworth J, Holland KN, Howey LA, Hueter RE, Humphries NE, Hutchinson M, Jaine FRA, Jorgensen SJ, Kanive PE, Labaja J, Lana FO, Lassauce H, Lipscombe RS, Llewellyn F, Macena BCL, Mambrasar R, McAllister JD, McCully Phillips SR, McGregor F, McMillan MN, McNaughton LM, Mendonça SA, Meyer CG, Meyers M, Mohan JA, Montgomery JC, Mucientes G, Musyl MK, Nasby-Lucas N, Natanson LJ, O'Sullivan JB, Oliveira P, Papastamtiou YP, Patterson TA, Pierce SJ, Queiroz N, Radford CA, Richardson AJ, Richardson AJ, Righton D, Rohner CA, Royer MA, Saunders RA, Schaber M, Schallert RJ, Scholl MC, Seitz AC, Semmens JM, Setyawan E, Shea BD, Shidqi RA, Shillinger GL, Shipley ON, Shivji MS, Sianipar AB, Silva JF, Sims DW, Skomal GB, Sousa LL, Southall EJ, Spaet JLY, Stehfest KM, Stevens G, Stewart JD, Sulikowski JA, Syakurachman I, Thorrold SR, Thums M, Tickler D, Tolloti MT, Townsend KA, Travassos P, Tyminski JP, Vaudo JJ, Veras D, Wantiez L, Weber SB, Wells RJD, Weng KC, Wetherbee BM, Williamson JE, Witt MJ, Wright S, Zilliacus K, Block BA, and Curnick DJ
- Abstract
Knowledge of the three-dimensional movement patterns of elasmobranchs is vital to understand their ecological roles and exposure to anthropogenic pressures. To date, comparative studies among species at global scales have mostly focused on horizontal movements. Our study addresses the knowledge gap of vertical movements by compiling the first global synthesis of vertical habitat use by elasmobranchs from data obtained by deployment of 989 biotelemetry tags on 38 elasmobranch species. Elasmobranchs displayed high intra- and interspecific variability in vertical movement patterns. Substantial vertical overlap was observed for many epipelagic elasmobranchs, indicating an increased likelihood to display spatial overlap, biologically interact, and share similar risk to anthropogenic threats that vary on a vertical gradient. We highlight the critical next steps toward incorporating vertical movement into global management and monitoring strategies for elasmobranchs, emphasizing the need to address geographic and taxonomic biases in deployments and to concurrently consider both horizontal and vertical movements.
- Published
- 2022
- Full Text
- View/download PDF
10. Restricting α-synuclein transport into mitochondria by inhibition of α-synuclein-VDAC complexation as a potential therapeutic target for Parkinson's disease treatment.
- Author
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Rajendran M, Queralt-Martín M, Gurnev PA, Rosencrans WM, Rovini A, Jacobs D, Abrantes K, Hoogerheide DP, Bezrukov SM, and Rostovtseva TK
- Subjects
- HeLa Cells, Humans, Lipids, Mitochondria metabolism, Voltage-Dependent Anion Channels metabolism, Parkinson Disease drug therapy, Parkinson Disease metabolism, alpha-Synuclein metabolism
- Abstract
Involvement of alpha-synuclein (αSyn) in Parkinson's disease (PD) is complicated and difficult to trace on cellular and molecular levels. Recently, we established that αSyn can regulate mitochondrial function by voltage-activated complexation with the voltage-dependent anion channel (VDAC) on the mitochondrial outer membrane. When complexed with αSyn, the VDAC pore is partially blocked, reducing the transport of ATP/ADP and other metabolites. Further, αSyn can translocate into the mitochondria through VDAC, where it interferes with mitochondrial respiration. Recruitment of αSyn to the VDAC-containing lipid membrane appears to be a crucial prerequisite for both the blockage and translocation processes. Here we report an inhibitory effect of HK2p, a small membrane-binding peptide from the mitochondria-targeting N-terminus of hexokinase 2, on αSyn membrane binding, and hence on αSyn complex formation with VDAC and translocation through it. In electrophysiology experiments, the addition of HK2p at micromolar concentrations to the same side of the membrane as αSyn results in a dramatic reduction of the frequency of blockage events in a concentration-dependent manner, reporting on complexation inhibition. Using two complementary methods of measuring protein-membrane binding, bilayer overtone analysis and fluorescence correlation spectroscopy, we found that HK2p induces detachment of αSyn from lipid membranes. Experiments with HeLa cells using proximity ligation assay confirmed that HK2p impedes αSyn entry into mitochondria. Our results demonstrate that it is possible to regulate αSyn-VDAC complexation by a rationally designed peptide, thus suggesting new avenues in the search for peptide therapeutics to alleviate αSyn mitochondrial toxicity in PD and other synucleinopathies., (© 2022. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.)
- Published
- 2022
- Full Text
- View/download PDF
11. Global collision-risk hotspots of marine traffic and the world's largest fish, the whale shark.
- Author
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Womersley FC, Humphries NE, Queiroz N, Vedor M, da Costa I, Furtado M, Tyminski JP, Abrantes K, Araujo G, Bach SS, Barnett A, Berumen ML, Bessudo Lion S, Braun CD, Clingham E, Cochran JEM, de la Parra R, Diamant S, Dove ADM, Dudgeon CL, Erdmann MV, Espinoza E, Fitzpatrick R, Cano JG, Green JR, Guzman HM, Hardenstine R, Hasan A, Hazin FHV, Hearn AR, Hueter RE, Jaidah MY, Labaja J, Ladino F, Macena BCL, Morris JJ Jr, Norman BM, Peñaherrera-Palma C, Pierce SJ, Quintero LM, Ramírez-Macías D, Reynolds SD, Richardson AJ, Robinson DP, Rohner CA, Rowat DRL, Sheaves M, Shivji MS, Sianipar AB, Skomal GB, Soler G, Syakurachman I, Thorrold SR, Webb DH, Wetherbee BM, White TD, Clavelle T, Kroodsma DA, Thums M, Ferreira LC, Meekan MG, Arrowsmith LM, Lester EK, Meyers MM, Peel LR, Sequeira AMM, Eguíluz VM, Duarte CM, and Sims DW
- Subjects
- Animals, Endangered Species, Plankton, Ships, Sharks
- Abstract
Marine traffic is increasing globally yet collisions with endangered megafauna such as whales, sea turtles, and planktivorous sharks go largely undetected or unreported. Collisions leading to mortality can have population-level consequences for endangered species. Hence, identifying simultaneous space use of megafauna and shipping throughout ranges may reveal as-yet-unknown spatial targets requiring conservation. However, global studies tracking megafauna and shipping occurrences are lacking. Here we combine satellite-tracked movements of the whale shark, Rhincodon typus, and vessel activity to show that 92% of sharks’ horizontal space use and nearly 50% of vertical space use overlap with persistent large vessel (>300 gross tons) traffic. Collision-risk estimates correlated with reported whale shark mortality from ship strikes, indicating higher mortality in areas with greatest overlap. Hotspots of potential collision risk were evident in all major oceans, predominantly from overlap with cargo and tanker vessels, and were concentrated in gulf regions, where dense traffic co-occurred with seasonal shark movements. Nearly a third of whale shark hotspots overlapped with the highest collision-risk areas, with the last known locations of tracked sharks coinciding with busier shipping routes more often than expected. Depth-recording tags provided evidence for sinking, likely dead, whale sharks, suggesting substantial “cryptic” lethal ship strikes are possible, which could explain why whale shark population declines continue despite international protection and low fishing-induced mortality. Mitigation measures to reduce ship-strike risk should be considered to conserve this species and other ocean giants that are likely experiencing similar impacts from growing global vessel traffic.
- Published
- 2022
- Full Text
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