38 results on '"Windsor E. Aguirre"'
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2. Freshwater Colonization, Adaptation, and Genomic Divergence in Threespine Stickleback
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Windsor E Aguirre, Kerry Reid, Jessica Rivera, David C Heins, Krishna R Veeramah, and Michael A Bell
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Lakes ,Animals ,Animal Science and Zoology ,Genomics ,Plant Science ,Selection, Genetic ,Adaptation, Physiological ,Alleles ,Smegmamorpha - Abstract
The Threespine Stickleback is ancestrally a marine fish, but many marine populations breed in fresh water (i.e., are anadromous), facilitating their colonization of isolated freshwater habitats a few years after they form. Repeated adaptation to fresh water during at least 10 My and continuing today has led to Threespine Stickleback becoming a premier system to study rapid adaptation. Anadromous and freshwater stickleback breed in sympatry and may hybridize, resulting in introgression of freshwater-adaptive alleles into anadromous populations, where they are maintained at low frequencies as ancient standing genetic variation. Anadromous stickleback have accumulated hundreds of freshwater-adaptive alleles that are disbursed as few loci per marine individual and provide the basis for adaptation when they colonize fresh water. Recent whole-lake experiments in lakes around Cook Inlet, Alaska have revealed how astonishingly rapid and repeatable this process is, with the frequency of 40% of the identified freshwater-adaptive alleles increasing from negligible (∼1%) in the marine founder to ≥50% within ten generations in fresh water, and freshwater phenotypes evolving accordingly. These high rates of genomic and phenotypic evolution imply very intense directional selection on phenotypes of heterozygotes. Sexual recombination rapidly assembles freshwater-adaptive alleles that originated in different founders into multilocus freshwater haplotypes, and regions important for adaptation to freshwater have suppressed recombination that keeps advantageous alleles linked within large haploblocks. These large haploblocks are also older and appear to have accumulated linked advantageous mutations. The contemporary evolution of Threespine Stickleback has provided broadly applicable insights into the mechanisms that facilitate rapid adaptation.
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- 2022
3. Effects of temperature and water turbulence on vertebral number and body shape in Astyanax mexicanus (Teleostei: Characidae).
- Author
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Winer Daniel Reyes Corral and Windsor E Aguirre
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Medicine ,Science - Abstract
Environmental changes can modify the phenotypic characteristics of populations, which in turn can influence their evolutionary trajectories. In ectotherms like fishes, temperature is a particularly important environmental variable that is known to have significant impacts on the phenotype. Here, we raised specimens of the surface ecomorph of Astyanax mexicanus at temperatures of 20°C, 23°C, 25°C, and 28°C to examine how temperature influenced vertebral number and body shape. To increase biological realism, specimens were also subjected to two water turbulence regimes. Vertebral number was counted from x-rays and body shape variation was analysed using geometric morphometric methods. Temperature significantly impacted mean total vertebral number, which increased at the lowest and highest temperatures. Fish reared at lower temperatures had relatively more precaudal vertebrae while fish reared at higher temperatures had relatively more caudal vertebrae. Vertebral anomalies, especially vertebral fusions, were most frequent at the extreme temperature treatments. Temperature significantly impacted body shape as well, with fish reared at 20°C being particularly divergent. Water turbulence also impacted body shape in a generally predictable manner, with specimens reared in high turbulence environments being more streamlined and having extended dorsal and anal fin bases. Variation in environmental variables thus resulted in significant changes in morphological traits known to impact fish fitness, indicating that A. mexicanus has the capacity to exhibit a range of phenotypic plasticity when challenged by environmental change. Understanding the biochemical mechanisms underlying this plasticity and whether adaptive plasticity has influenced the evolutionary radiation of the Characidae, are major directions for future research.
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- 2019
- Full Text
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4. Global urban environmental change drives adaptation in white clover
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James S. Santangelo, Rob W. Ness, Beata Cohan, Connor R. Fitzpatrick, Simon G. Innes, Sophie Koch, Lindsay S. Miles, Samreen Munim, Pedro R. Peres-Neto, Cindy Prashad, Alex T. Tong, Windsor E. Aguirre, Philips O. Akinwole, Marina Alberti, Jackie Álvarez, Jill T. Anderson, Joseph J. Anderson, Yoshino Ando, Nigel R. Andrew, Fabio Angeoletto, Daniel N. Anstett, Julia Anstett, Felipe Aoki-Gonçalves, A. Z. Andis Arietta, Mary T. K. Arroyo, Emily J. Austen, Fernanda Baena-Díaz, Cory A. Barker, Howard A. Baylis, Julia M. Beliz, Alfonso Benitez-Mora, David Bickford, Gabriela Biedebach, Gwylim S. Blackburn, Mannfred M. A. Boehm, Stephen P. Bonser, Dries Bonte, Jesse R. Bragger, Cristina Branquinho, Kristien I. Brans, Jorge C. Bresciano, Peta D. Brom, Anna Bucharova, Briana Burt, James F. Cahill, Katelyn D. Campbell, Elizabeth J. Carlen, Diego Carmona, Maria Clara Castellanos, Giada Centenaro, Izan Chalen, Jaime A. Chaves, Mariana Chávez-Pesqueira, Xiao-Yong Chen, Angela M. Chilton, Kristina M. Chomiak, Diego F. Cisneros-Heredia, Ibrahim K. Cisse, Aimée T. Classen, Mattheau S. Comerford, Camila Cordoba Fradinger, Hannah Corney, Andrew J. Crawford, Kerri M. Crawford, Maxime Dahirel, Santiago David, Robert De Haan, Nicholas J. Deacon, Clare Dean, Ek del-Val, Eleftherios K. Deligiannis, Derek Denney, Margarete A. Dettlaff, Michelle F. DiLeo, Yuan-Yuan Ding, Moisés E. Domínguez-López, Davide M. Dominoni, Savannah L. Draud, Karen Dyson, Jacintha Ellers, Carlos I. Espinosa, Liliana Essi, Mohsen Falahati-Anbaran, Jéssica C. F. Falcão, Hayden T. Fargo, Mark D. E. Fellowes, Raina M. Fitzpatrick, Leah E. Flaherty, Pádraic J. Flood, María F. Flores, Juan Fornoni, Amy G. Foster, Christopher J. Frost, Tracy L. Fuentes, Justin R. Fulkerson, Edeline Gagnon, Frauke Garbsch, Colin J. Garroway, Aleeza C. Gerstein, Mischa M. Giasson, E. Binney Girdler, Spyros Gkelis, William Godsoe, Anneke M. Golemiec, Mireille Golemiec, César González-Lagos, Amanda J. Gorton, Kiyoko M. Gotanda, Gustaf Granath, Stephan Greiner, Joanna S. Griffiths, Filipa Grilo, Pedro E. Gundel, Benjamin Hamilton, Joyce M. Hardin, Tianhua He, Stephen B. Heard, André F. Henriques, Melissa Hernández-Poveda, Molly C. Hetherington-Rauth, Sarah J. Hill, Dieter F. Hochuli, Kathryn A. Hodgins, Glen R. Hood, Gareth R. Hopkins, Katherine A. Hovanes, Ava R. Howard, Sierra C. Hubbard, Carlos N. Ibarra-Cerdeña, Carlos Iñiguez-Armijos, Paola Jara-Arancio, Benjamin J. M. Jarrett, Manon Jeannot, Vania Jiménez-Lobato, Mae Johnson, Oscar Johnson, Philip P. Johnson, Reagan Johnson, Matthew P. Josephson, Meen Chel Jung, Michael G. Just, Aapo Kahilainen, Otto S. Kailing, Eunice Kariñho-Betancourt, Regina Karousou, Lauren A. Kirn, Anna Kirschbaum, Anna-Liisa Laine, Jalene M. LaMontagne, Christian Lampei, Carlos Lara, Erica L. Larson, Adrián Lázaro-Lobo, Jennifer H. Le, Deleon S. Leandro, Christopher Lee, Yunting Lei, Carolina A. León, Manuel E. Lequerica Tamara, Danica C. Levesque, Wan-Jin Liao, Megan Ljubotina, Hannah Locke, Martin T. Lockett, Tiffany C. Longo, Jeremy T. Lundholm, Thomas MacGillavry, Christopher R. Mackin, Alex R. Mahmoud, Isaac A. Manju, Janine Mariën, D. Nayeli Martínez, Marina Martínez-Bartolomé, Emily K. Meineke, Wendy Mendoza-Arroyo, Thomas J. S. Merritt, Lila Elizabeth L. Merritt, Giuditta Migiani, Emily S. Minor, Nora Mitchell, Mitra Mohammadi Bazargani, Angela T. Moles, Julia D. Monk, Christopher M. Moore, Paula A. Morales-Morales, Brook T. Moyers, Miriam Muñoz-Rojas, Jason Munshi-South, Shannon M. Murphy, Maureen M. Murúa, Melisa Neila, Ourania Nikolaidis, Iva Njunjić, Peter Nosko, Juan Núñez-Farfán, Takayuki Ohgushi, Kenneth M. Olsen, Øystein H. Opedal, Cristina Ornelas, Amy L. Parachnowitsch, Aaron S. Paratore, Angela M. Parody-Merino, Juraj Paule, Octávio S. Paulo, João Carlos Pena, Vera W. Pfeiffer, Pedro Pinho, Anthony Piot, Ilga M. Porth, Nicholas Poulos, Adriana Puentes, Jiao Qu, Estela Quintero-Vallejo, Steve M. Raciti, Joost A. M. Raeymaekers, Krista M. Raveala, Diana J. Rennison, Milton C. Ribeiro, Jonathan L. Richardson, Gonzalo Rivas-Torres, Benjamin J. Rivera, Adam B. Roddy, Erika Rodriguez-Muñoz, José Raúl Román, Laura S. Rossi, Jennifer K. Rowntree, Travis J. Ryan, Santiago Salinas, Nathan J. Sanders, Luis Y. Santiago-Rosario, Amy M. Savage, J.F. Scheepens, Menno Schilthuizen, Adam C. Schneider, Tiffany Scholier, Jared L. Scott, Summer A. Shaheed, Richard P. Shefferson, Caralee A. Shepard, Jacqui A. Shykoff, Georgianna Silveira, Alexis D. Smith, Lizet Solis-Gabriel, Antonella Soro, Katie V. Spellman, Kaitlin Stack Whitney, Indra Starke-Ottich, Jörg G. Stephan, Jessica D. Stephens, Justyna Szulc, Marta Szulkin, Ayco J. M. Tack, Ítalo Tamburrino, Tayler D. Tate, Emmanuel Tergemina, Panagiotis Theodorou, Ken A. Thompson, Caragh G. Threlfall, Robin M. Tinghitella, Lilibeth Toledo-Chelala, Xin Tong, Léa Uroy, Shunsuke Utsumi, Martijn L. Vandegehuchte, Acer VanWallendael, Paula M. Vidal, Susana M. Wadgymar, Ai-Ying Wang, Nian Wang, Montana L. Warbrick, Kenneth D. Whitney, Miriam Wiesmeier, J. Tristian Wiles, Jianqiang Wu, Zoe A. Xirocostas, Zhaogui Yan, Jiahe Yao, Jeremy B. Yoder, Owen Yoshida, Jingxiong Zhang, Zhigang Zhao, Carly D. Ziter, Matthew P. Zuellig, Rebecca A. Zufall, Juan E. Zurita, Sharon E. Zytynska, Marc T. J. Johnson, Ecological Science, Animal Ecology, Biology, Faculty of Economic and Social Sciences and Solvay Business School, Faculty of Medicine and Pharmacy, ON, University of North Carolina, LA, QC, DePaul University, IN, Universidad San Francisco de Quito USFQ, University of Georgia, Uppsala University, Hokkaido University, NSW, Programa de Pós-Graduação em Geografia da UFMT, University of British Columbia, A. C., CT, Universidad de Chile, Mount Allison University, Instituto de Ecología A. C., University of Cambridge, FL, Universidad Bernardo O'Higgins, Ghent University, West Long Branch, Lisboa, KU Leuven, Massey University, University of Cape Town, University of Münster, AB, University of Sussex, Stockholm University, Universidad San Francisco de Quito, East China Normal University, Shanghai Engineering Research Center of Sustainable Plant Innovation, MI, TX, Facultad de Agronomía, NS, Université de Rennes, IA, MN, Manchester Metropolitan University, UNAM, Aristotle University of Thessaloniki, University of Helsinki, University of Glasgow, Hendrix College, Vrije Universiteit Amsterdam, Universidad Técnica Particular de Loja, Universidade Federal de Sergipe (UFS), University of Tehran, Norwegian University of Science and Technology, AZ, Max Planck Institute for Plant Breeding Research, Universidad Nacional Autónoma de México, Potsdam-Golm, University of Alaska Anchorage, Tropical Diversity, Université de Moncton, MB, University of New Brunswick, Lincoln University, Universidad Adolfo Ibáñez, Brock University, ICB - University of Talca, Curtin University, Murdoch University, Western Oregon University, Facultad de Ciencias de la Vida, Institute of Ecology and Biodiversity (IEB), Lund University, Universidad Autónoma de Guerrero -CONACYT, University of Illinois at Chicago, Dufferin-Peel Catholic District School Board, U.S. Army ERDC-CERL, Tübingen, University of Zurich, Urban Wildlife Institute, Universidad Católica de la Santísima Concepción, CO, MS, Rutgers University-Camden, Chinese Academy of Sciences, Beijing Normal University, NM, University of Wisconsin - Eau Claire, Iranian Research Organization for Science and Technology (IROST), ME, Universidad de Antioquia, MA, Universidad de Sevilla, Universidad Mayor, Naturalis Biodiversity Center, Kyoto University, University of Alaska Fairbanks, Senckenberg Research Institute and Natural History Museum Frankfurt, Universidade Estadual Paulista (UNESP), WI, Swedish University of Agricultural Sciences, Universidad CES, Hofstra University, Nord University, VA, University of Almería, Faculty of Biological Sciences, Leiden University, Jyväskylä, KY, University of Tokyo, Ecologie Systématique et Evolution, Martin Luther University Halle-Wittenberg, University of Warsaw, Davidson College, Huazhong Agricultural University, Technical University of Munich, Lanzhou University, University of Bern, University of Liverpool, Repositório da Universidade de Lisboa, University of Toronto at Mississauga, University of North Carolina [Chapel Hill] (UNC), University of North Carolina System (UNC), University of Louisiana, Ecosystèmes, biodiversité, évolution [Rennes] (ECOBIO), Université de Rennes (UR)-Institut Ecologie et Environnement (INEE), Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Observatoire des Sciences de l'Univers de Rennes (OSUR), Université de Rennes (UR)-Institut national des sciences de l'Univers (INSU - CNRS)-Université de Rennes 2 (UR2)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Institut national des sciences de l'Univers (INSU - CNRS)-Université de Rennes 2 (UR2)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Centre National de la Recherche Scientifique (CNRS), Ecologie Systématique et Evolution (ESE), AgroParisTech-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Biodiversité agroécologie et aménagement du paysage (UMR BAGAP), Ecole supérieure d'Agricultures d'Angers (ESA)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Institut Agro Rennes Angers, Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro), Huazhong Agricultural University [Wuhan] (HZAU), California State University [Northridge] (CSUN), Saint Mary's University [Halifax], Kunming Institute of Botany [CAS] (KIB), Chinese Academy of Sciences [Beijing] (CAS), Concordia University [Montreal], University of Houston, Universidad San Francisco de Quito (USFQ), Technische Universität München = Technical University of Munich (TUM), and The Global Urban Evolution project was primarily funded by an NSERC DiscoveryGrant, Canada Research Chair and NSERC Steacie Fellowship to M.T.J.J.. J.S.S. receivedfunding from an NSERC CGS and C.R.F. is funded by an NSERC PDF. P.R.P.-N., R.W.N. andJ.C.C. were supported by NSERC Discovery grants. M.A. was funded by NSF RCN DEB-1840663. F.A. received funding from CAPES. MTKA was funded by CONICYT PIA APOYOCCTE AFB170008. J.R.B, T.C.L., and S.A.S were supported by Monmouth University Sch. ofSci. SRP. E.G. was funded by D. Biologie, Université de Moncton. C.G.-L. received fundingfrom the Center of Applied Ecology and Sustainability (CAPES), and ANID PIA/BASALFB0002. S.G. was funded by the Max Planck Society. P.J.-A. was funded by ANID PIA/BASALFB210006. I.N. and M.S. were supported by Leiden Municipality. K.M.O. was funded by USNSF awards IOS-1557770 and DEB-1601641. J.C.P. thanks FAPESP process 2018/00107-3, andM.C.R. thanks CNPq and FAPESP.
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sopeutuminen ,Rural Population ,valkoapila ,Multidisciplinary ,Urbanization ,evoluutio ,kasvillisuus ,Genes, Plant ,Adaptation, Physiological ,Biological Evolution ,SDG 11 - Sustainable Cities and Communities ,evoluutioekologia ,Hydrogen Cyanide ,570 Life sciences ,biology ,Trifolium ,kaupungistuminen ,[SDE.BE]Environmental Sciences/Biodiversity and Ecology ,Cities ,ympäristönmuutokset ,Ecosystem ,Genome, Plant - Abstract
Made available in DSpace on 2022-04-28T19:52:06Z (GMT). No. of bitstreams: 0 Previous issue date: 2022-03-18 Urbanization transforms environments in ways that alter biological evolution. We examined whether urban environmental change drives parallel evolution by sampling 110,019 white clover plants from 6169 populations in 160 cities globally. Plants were assayed for a Mendelian antiherbivore defense that also affects tolerance to abiotic stressors. Urban-rural gradients were associated with the evolution of clines in defense in 47% of cities throughout the world. Variation in the strength of clines was explained by environmental changes in drought stress and vegetation cover that varied among cities. Sequencing 2074 genomes from 26 cities revealed that the evolution of urban-rural clines was best explained by adaptive evolution, but the degree of parallel adaptation varied among cities. Our results demonstrate that urbanization leads to adaptation at a global scale. Department of Biology University of Toronto Mississauga ON Centre for Urban Environments University of Toronto Mississauga ON Department of Biology University of North Carolina, Chapel Hill Department of Biology University of Louisiana LA Department of Biology Queen's University ON Department of Biology Concordia University QC Department of Biological Sciences DePaul University Department of Biology DePauw University IN Department of Urban Design and Planning, University of Washington, Seattle, WA, USA Colegio de Ciencias Biológicas y Ambientales Universidad San Francisco de Quito USFQ Department of Genetics University of Georgia Department of Ecology and Genetics Evolutionary Biology Centre Uppsala University Field Science Center for Northern Biosphere Hokkaido University Natural History Museum Zoology University of New England NSW Programa de Pós-Graduação em Geografia da UFMT campus de Rondonópolis Department of Botany and Biodiversity Research Centre University of British Columbia Graduate Program in Genome Sciences and Technology Genome Sciences Centre University of British Columbia Department of Microbiology and Immunology University of British Columbia Red de Biología Evolutiva Instituto de Ecología A. C. School of the Environment Yale University CT Departamento de Ciencias Ecológicas Universidad de Chile, Facultad de Ciencias Instituto de Ecología y Biodiversidad Universidad de Chile Department of Biology Mount Allison University Red de Ecoetología Instituto de Ecología A. C. Department of Biology University of Ottawa ON Department of Zoology University of Cambridge Department of Biology, Washington University in St. Louis, St. Louis, MO, USA Department of Biology University of Miami FL Centro de Investigación en Recursos Naturales y Sustentabilidad (CIRENYS) Universidad Bernardo O'Higgins Department of Biology, University of La Verne, La Verne, CA, USA Département des sciences du bois et de la forêt Université Laval QC Evolution & Ecology Research Centre School of Biological Earth and Environmental Sciences UNSW Sydney NSW Department of Biology Ghent University Department of Biology Monmouth University West Long Branch Centre for Ecology Evolution and Environmental Changes Faculdade de Ciências Universidade de Lisboa Lisboa Department of Biology KU Leuven School of Agriculture and Environment Wildlife and Ecology group Massey University, Palmerston North Department of Biological Sciences University of Cape Town Institute of Landscape Ecology University of Münster Gosnell School of Life Sciences, Rochester Institute of Technology, Rochester, NY, USA Department of Biological Sciences University of Alberta AB Louis Calder Center and Department of Biological Sciences, Fordham University, Armonk, NY, USA Departamento de Ecología Tropical, Universidad Autónoma de Yucatán, Mérida, Yucatán, México School of Life Sciences University of Sussex Department of Ecology Environment and Plant Sciences Stockholm University iBIOTROP Instituto de Biodiversidad Tropical Universidad San Francisco de Quito Department of Biology, San Francisco State University, San Francisco, CA, USA Unidad de Recursos Naturales, Centro de Investigación Científica de Yucatán AC, Mérida, Yucatán, México School of Ecological and Environmental Sciences East China Normal University Shanghai Engineering Research Center of Sustainable Plant Innovation Centre for Ecosystem Science School of Biological Earth and Environmental Sciences UNSW Sydney NSW Department of Ecology and Evolutionary Biology University of Michigan MI Department of Biosciences Rice University TX IFEVA Universidad de Buenos Aires Facultad de Agronomía, CONICET Biology Department Saint Mary's University NS Department of Biological Sciences, Universidad de los Andes Department of Biology and Biochemistry University of Houston TX Université de Rennes Department of Zoology and Biodiversity Research Centre University of British Columbia Department of Environmental Studies Dordt University Sioux Center IA Department of Biology Minneapolis Community and Technical College MN Department of Natural Sciences Ecology and Environment Research Centre Manchester Metropolitan University Instituto de Investigaciones en Ecosistemas y Sustentabilidad UNAM Department of Botany School of Biology Aristotle University of Thessaloniki Faculty of Biological and Environmental Science Organismal & Evolutionary Biology Research Programme University of Helsinki Institute of Biodiversity Animal Health and Comparative Medicine University of Glasgow Department of Biology Hendrix College Department of Ecological Science Vrije Universiteit Amsterdam Departamento de Ciencias Biológicas y Agropecuarias Universidad Técnica Particular de Loja Departamento de Biologia Universidade Federal de Santa Maria (UFSM) Department of Plant Sciences School of Biology College of Science University of Tehran NTNU University Museum Norwegian University of Science and Technology Red de Estudios Moleculares Avanzados Instituto de Ecología A. C. School of Biological Sciences, University of Reading, Whiteknights Park, Reading, Berkshire, UK Department of Biology Northern Arizona University AZ Department of Biological Sciences MacEwan University AB Max Planck Institute for Plant Breeding Research Departamento de Ecología Evolutiva Instituto de Ecología Universidad Nacional Autónoma de México Max Planck Institute of Molecular Plant Physiology Potsdam-Golm BIO5 Institute University of Arizona AZ Alaska Center for Conservation Science University of Alaska Anchorage Tropical Diversity, Royal Botanical Garden of Edinburgh Département de biologie Université de Moncton Department of Biological Sciences University of Manitoba MB Departments of Microbiology & Statistics University of Manitoba MB Department of Biology University of New Brunswick Department of Biology Kalamazoo College MI BioProtection Research Centre Lincoln University Departamento de Ciencias Facultad de Artes Liberales Universidad Adolfo Ibáñez Department of Ecology Evolution Behaviour University of Minnesota MN Department of Biological Sciences Brock University Department of Environmental Toxicology, University of California, Davis, CA, USA ICB - University of Talca School of Molecular and Life Science Curtin University College of Science Health Engineering and Education Murdoch University, Murdoch School of Life and Environmental Sciences University of Sydney NSW School of Biological Sciences, Monash University, Melbourne, VIC, Australia Department of Biological Sciences Wayne State University MI Department of Biology Western Oregon University, OR School of Natural Resources and the Environment University of Arizona AZ Departamento de Ecología Humana, Cinvestav Mérida Departamento de Ciencias Biológicas y Departamento de Ecología y Biodiversidad Facultad de Ciencias de la Vida, Universidad Andrés Bello Institute of Ecology and Biodiversity (IEB) Department of Biology Lund University Department of Biology Norwegian University of Science and Technology Escuela Superiro de Desarrollo Sustentable Universidad Autónoma de Guerrero -CONACYT Clarkson Secondary School Peel District School Board ON Homelands Sr. Public School Peel District School Board ON Department of Biological Sciences University of Illinois at Chicago Dufferin-Peel Catholic District School Board, St. James Catholic Global Learning Centre Department of Biosciences University of Calgary AB Ecological Processes Branch U.S. Army ERDC-CERL Department of Biology, Oberlin College, Oberlin, OH, USA Escuela Nacional de Estudios Superiores Unidad Morelia UNAM Institute of Evolution and Ecology University of Tübingen Tübingen Department of Evolutionary Biology and Environmental Studies University of Zurich, Winterthurerstrasse Urban Wildlife Institute Department of Conservation and Science, Lincoln Park Zoo Departamento de Ecología Universidad Católica de la Santísima Concepción Department of Biological Sciences University of Denver CO Department of Biological Sciences Mississippi State University MS Department of Biology Center for Computational & Integrative Biology Rutgers University-Camden Kunming Institute of Botany Chinese Academy of Sciences Department of Chemistry & Biochemistry Laurentian University ON Ministry of Education Key Laboratory for Biodiversity Science and Ecological Engineering College of Life Sciences Beijing Normal University School of BioSciences, University of Melbourne, Melbourne, VIC, Australia Posgrado en Ciencias Biológicas Universidad Nacional Autónoma de México Department of Biological Sciences, Auburn University, Auburn, AL, USA Department of Entomology and Nematology, University of California, Davis, CA, USA Department of Biology University of New Mexico NM Department of Biology University of Wisconsin - Eau Claire Agriculture Institute Iranian Research Organization for Science and Technology (IROST) Department of Biology Colby College ME Instituto de Biología Universidad de Antioquia Department of Biology University of Massachusetts Boston MA Agricultural Biology Colorado State University CO Departamento de Biología Vegetal y Ecología Facultad de Biología Universidad de Sevilla, Av. Reina Mercedes s/n Facultad de Estudios Interdisciplinarios Centro GEMA- Genómica Universidad Mayor Evolutionary Ecology Group Naturalis Biodiversity Center Department of Biology and Chemistry Nipissing University ON, North Bay Center for Ecological Research Kyoto University Bonanza Creek Long Term Ecological Research Program University of Alaska Fairbanks Department of Botany and Molecular Evolution Senckenberg Research Institute and Natural History Museum Frankfurt Departamento de Biodiversidade Instituto de Biociências Univ Estadual Paulista - UNESP Nelson Institute for Environmental Studies University of Wisconsin-Madison WI Department of Biology, California State University, Northridge, Los Angeles, CA, USA Department of Ecology Swedish University of Agricultural Sciences Facultad de Ciencias y Biotecnologia Universidad CES Department of Biology Hofstra University Faculty of Biosciences and Aquaculture Nord University, Bodø Division of Biological Sciences, University of California San Diego, San Diego, CA, USA Department of Biology University of Richmond VA Estación de Biodiversidad Tiputini Colegio de Ciencias Biológicas y Ambientales Universidad San Francisco de Quito USFQ Department of Biological Sciences Institute of Environment Florida International University FL Agronomy Department University of Almería Department of Biological Sciences and Center for Urban Ecology and Sustainability Butler University IN Department of Biological Sciences Louisiana State University LA Faculty of Biological Sciences, Goethe University Frankfurt Institute of Biology Leiden Leiden University Department of Biological and Environmental Science University of Jyväskylä Jyväskylä Department of Biology University of Louisville KY Organization for Programs on Environmental Science University of Tokyo CNRS AgroParisTech Ecologie Systématique et Evolution, Université Paris-Saclay Department of Biology, Providence College, Providence, RI, USA General Zoology Institute for Biology Martin Luther University Halle-Wittenberg International Arctic Research Center University of Alaska Fairbanks Science, Technology and Society Department, Rochester Institute of Technology, Rochester, NY, USA SLU Swedish Species Information Centre Swedish University of Agricultural Sciences Department of Biology Westfield State University MA Centre of New Technologies University of Warsaw Department of Biology, Stanford University, Stanford, CA, USA Plant Biology Department Michigan State University MI Biology Department Davidson College College of Horticulture and Forestry Sciences/ Hubei Engineering Technology Research Center for Forestry Information Huazhong Agricultural University School of Life Sciences Technical University of Munich School of Life Sciences Lanzhou University Institute of Ecology and Evolution University of Bern Department of Evolution Ecology and Behaviour University of Liverpool Departamento de Biodiversidade Instituto de Biociências Univ Estadual Paulista - UNESP
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- 2022
5. Parallel body shape divergence in the Neotropical fish genus Rhoadsia (Teleostei: Characidae) along elevational gradients of the western slopes of the Ecuadorian Andes.
- Author
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Grace Malato, Virginia R Shervette, Ronald Navarrete Amaya, Jonathan Valdiviezo Rivera, Fredy Nugra Salazar, Paola Calle Delgado, Kirby C Karpan, and Windsor E Aguirre
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Medicine ,Science - Abstract
Neotropical mountain streams are important contributors of biological diversity. Two species of the characid genus Rhoadsia differing for an ecologically important morphological trait, body depth, have been described from mountain streams of the western slopes of the Andes in Ecuador. Rhoadsia altipinna is a deeper-bodied species reported from low elevations in southwestern Ecuador and northern Peru, and Rhoadsia minor is a more streamlined species that was described from high elevations (>1200 m) in the Esmeraldas drainage in northwestern Ecuador. Little is known about these species and their validity as distinct species has been questioned. In this study, we examine how their body shape varies along replicated elevational gradients in different drainages of western Ecuador using geometric morphometrics and the fineness ratio. We also use sequences of the mitochondrial cytochrome oxidase c I gene and the second intron of the S7 nuclear gene to examine whether genetic data are consistent with the existence of two species. We found that body depth varies continuously among populations within drainages as a function of elevation, and that body shape overlaps among drainages, such that low elevation populations of R. minor in the Esmeraldas drainage have similar body depths to higher elevation R. altipinna in southern drainages. Although a common general trend of declining body depth with elevation is clear, the pattern and magnitude of body shape divergence differed among drainages. Sequencing of mitochondrial and nuclear genes failed to meet strict criteria for the recognition of two species (e.g., reciprocal monophyly and deep genetic structure). However, there was a large component of genetic variation for the COI gene that segregated among drainages, indicating significant genetic divergence associated with geographic isolation. Continued research on Rhoadsia in western Ecuador may yield significant insight into adaptation and speciation in Neotropical mountain streams.
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- 2017
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6. Vertebral number covaries with body form and elevation along the western slopes of the Ecuadorian Andes in the Neotropical fish genusRhoadsia(Teleostei: Characidae)
- Author
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Pedro J. Jiménez‐Prado, Fredy Nugra-Salazar, Paola Calle-Delgado, Windsor E. Aguirre, Ashley Young, Virginia R. Shervette, Thomas L Borders, Roberto V. Cucalón, Ronald Navarrete-Amaya, and Jonathan Valdiviezo-Rivera
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Characidae ,Rhoadsia ,Teleostei ,biology ,Genus ,Neotropical fish ,Elevation ,Zoology ,biology.organism_classification ,Ecology, Evolution, Behavior and Systematics - Published
- 2019
7. Freshwater Biodiversity: Status, Threats and Conservation. Ecology, Biodiversity and Conservation. By David Dudgeon. Cambridge and New York: Cambridge University Press. $89.99 (hardcover); $44.99 (paper). xvi + 499 p. + 28 pl.; ill.; species and general indexes. ISBN: 978-0-521-76803-0 (hc); 978-0-521-74519-2 (pb). 2020
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Windsor E. Aguirre
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Geography ,Ecology ,Biodiversity ,Conservation ecology ,General Agricultural and Biological Sciences - Published
- 2021
8. Conservation threats and future prospects for the freshwater fishes of Ecuador: A hotspot of Neotropical fish diversity
- Author
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Pedro Jorge Jiménez Prado, Ivan Vinicio Jacome-Negrete, Gabriela Alvarez‐Mieles, Windsor E. Aguirre, Enrique Laaz, Juan Francisco Rivadeneira, Daniel Escobar-Camacho, Ronald Navarrete-Amaya, Edwin Zárate Hugo, Fernando Anaguano-Yancha, Ricardo Burgos Morán, Fredy Nugra Salazar, Willan Revelo, Jonathan Valdiviezo Rivera, Roberto V. Cucalón, and Katherin Miranda‐Troya
- Subjects
Conservation of Natural Resources ,Neotropics ,Fisheries ,Biodiversity ,Fresh Water ,Aquatic Science ,Freshwater ecosystem ,Deforestation ,Animals ,Ecosystem ,Ecology, Evolution, Behavior and Systematics ,Review Paper ,Overfishing ,biology ,Aquatic ecosystem ,Fishes ,conservation ,biology.organism_classification ,freshwater fishes ,Fishery ,endemism ,Neotropical fish ,Freshwater fish ,Conservation status ,Ecuador - Abstract
Freshwater fish communities in Ecuador exhibit some of the highest levels of diversity and endemism in the Neotropics. Unfortunately, aquatic ecosystems in the country are under serious threat and conditions are deteriorating. In 2018–19, the government of Ecuador sponsored a series of workshops to examine the conservation status of Ecuador''s freshwater fishes. Concerns were identified for 35 species, most of which are native to the Amazon region, and overfishing of Amazonian pimelodid catfishes emerged as a major issue. However, much of the information needed to make decisions across fish groups and regions was not available, hindering the process and highlighting the need for a review of the conservation threats to Ecuador''s freshwater fishes. Here, we review how the physical alteration of rivers, deforestation, wetland and floodplain degradation, agricultural and urban water pollution, mining, oil extraction, dams, overfishing, introduced species and climate change are affecting freshwater fishes in Ecuador. Although many of these factors affect fishes throughout the Neotropics, the lack of data on Ecuadorian fish communities is staggering and highlights the urgent need for more research. We also make recommendations, including the need for proper enforcement of existing environmental laws, restoration of degraded aquatic ecosystems, establishment of a national monitoring system for freshwater ecosystems, investment in research to fill gaps in knowledge, and encouragement of public engagement in citizen science and conservation efforts. Freshwater fishes are an important component of the cultural and biological legacy of the Ecuadorian people. Conserving them for future generations is critical. © 2021 The Authors. Journal of Fish Biology published by John Wiley & Sons Ltd on behalf of Fisheries Society of the British Isles.
- Published
- 2021
9. Variación corporal paralela en peces de dos ríos costeros del Chocó ecuatoriano
- Author
-
Pedro Jiménez-Prado and Windsor E. Aguirre
- Subjects
Morphometrics ,Phenotypic plasticity ,Altitude ,Geography ,Genetic drift ,Ecology ,Fauna ,Allometry ,General Agricultural and Biological Sciences ,Genetic adaptation ,Local adaptation - Abstract
Introducción: Las diferencias morfológicas son el producto de la plasticidad fenotípica, la adaptación genética o la deriva genética, pero no siempre se requiere de poblaciones muy antiguas para conseguir adaptaciones locales si se presentan factores selectivos. Objetivo: Este trabajo examina la variación en la forma del cuerpo de peces en ríos costeros de baja altitud para determinar si existen patrones de variación morfológica entre especies y entre zonas a lo largo de estos cauces. Métodos: Desde julio 2016 a junio 2017 se realizaron una serie de muestreos ictiológicos que permitieron analizar la forma del cuerpo de tres especies, a lo largo de todo el cauce en dos ríos costeros del noroccidente ecuatoriano, con el uso de la morfometría geométrica y técnicas de análisis multivariante. Resultados: Se encontró un paralelismo en el cambio de la forma del cuerpo de las tres especies, desde la zona baja hacia la zona alta, caracterizado por una reducción en la profundidad del cuerpo. También encontramos diferentes niveles de variación alométrica en la forma del cuerpo de las tres especies. Conclusiones: Peces en estas cuencas presentan variación fenotípica influenciada por procesos ecológicos y evolutivos que se expresan en cambios paralelos en la forma del cuerpo en diferentes especies incluso en ríos que tienen rangos de altitud muy pequeños, resaltando la importancia que tienen estas cuencas como reservorios del legado evolutivo de la fauna y flora neotropical.
- Published
- 2020
10. Effects of temperature and water turbulence on vertebral number and body shape in Astyanax mexicanus (Teleostei: Characidae)
- Author
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Windsor E. Aguirre and Winer Daniel Reyes Corral
- Subjects
0106 biological sciences ,0301 basic medicine ,Vertebrae ,Physiology ,Organogenesis ,01 natural sciences ,Vertebral fusion ,Medicine and Health Sciences ,Musculoskeletal System ,Teleostei ,Multidisciplinary ,Physics ,Temperature ,Classical Mechanics ,Eukaryota ,Freshwater Fish ,Somites ,Ectotherm ,Physical Sciences ,Vertebrates ,Freshwater fish ,Medicine ,Anatomy ,Anatomic Landmarks ,Research Article ,Fish Biology ,Science ,Zoology ,Fluid Mechanics ,Biology ,Research and Analysis Methods ,010603 evolutionary biology ,Continuum Mechanics ,03 medical and health sciences ,Fish physiology ,Fish Physiology ,Water Movements ,Animals ,Animal Physiology ,Swimming ,Phenotypic plasticity ,Biological Locomotion ,Characidae ,Fish fin ,Organisms ,Biology and Life Sciences ,Fluid Dynamics ,biology.organism_classification ,Spine ,Vertebrate Physiology ,Turbulence ,030104 developmental biology ,Fish ,Specimen Preparation and Treatment ,Organism Development ,Developmental Biology - Abstract
Environmental changes can modify the phenotypic characteristics of populations, which in turn can influence their evolutionary trajectories. In ectotherms like fishes, temperature is a particularly important environmental variable that is known to have significant impacts on the phenotype. Here, we raised specimens of the surface ecomorph of Astyanax mexicanus at temperatures of 20°C, 23°C, 25°C, and 28°C to examine how temperature influenced vertebral number and body shape. To increase biological realism, specimens were also subjected to two water turbulence regimes. Vertebral number was counted from x-rays and body shape variation was analysed using geometric morphometric methods. Temperature significantly impacted mean total vertebral number, which increased at the lowest and highest temperatures. Fish reared at lower temperatures had relatively more precaudal vertebrae while fish reared at higher temperatures had relatively more caudal vertebrae. Vertebral anomalies, especially vertebral fusions, were most frequent at the extreme temperature treatments. Temperature significantly impacted body shape as well, with fish reared at 20°C being particularly divergent. Water turbulence also impacted body shape in a generally predictable manner, with specimens reared in high turbulence environments being more streamlined and having extended dorsal and anal fin bases. Variation in environmental variables thus resulted in significant changes in morphological traits known to impact fish fitness, indicating that A. mexicanus has the capacity to exhibit a range of phenotypic plasticity when challenged by environmental change. Understanding the biochemical mechanisms underlying this plasticity and whether adaptive plasticity has influenced the evolutionary radiation of the Characidae, are major directions for future research.
- Published
- 2019
11. Body Shape Variation and Population Genetic Structure ofRhoadsia altipinna(Characidae: Rhoadsiinae) in Southwestern Ecuador
- Author
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Juan C. Granda, Ronald Navarrete, Windsor E. Aguirre, Grecia Valadez, Grace Malato, Webster F. Vital, Virginia R. Shervette, Paola Calle, Vinh H. Vu, and Maxine K. Loh
- Subjects
0106 biological sciences ,0301 basic medicine ,education.field_of_study ,Riffle ,biology ,Ecology ,Fauna ,Population ,Aquatic Science ,biology.organism_classification ,010603 evolutionary biology ,01 natural sciences ,Characidae ,03 medical and health sciences ,030104 developmental biology ,Geography ,Genus ,Genetic structure ,Genetic variation ,Animal Science and Zoology ,education ,Ecology, Evolution, Behavior and Systematics ,Global biodiversity - Abstract
The genus Rhoadsia is endemic to western Ecuador and northern Peru and includes two described species that differ in body form, size, and the elevations at which they occur. Unfortunately, there is uncertainty about the number of species that should be recognized in the genus and the causes of the morphological variation documented within and between species. We take advantage of a survey of the fish fauna of the Santa Rosa River in southwestern Ecuador that yielded large numbers of Rhoadsia altipinna, to expand knowledge of the ecological, morphological, and genetic variation of this species. Specimens were collected at five sites at elevations between 31 and 613 m above sea level, and each site was sampled in December 2012 and July 2013. Rhoadsia altipinna was the second most abundant species in the Santa Rosa River, was one of only three species collected at all elevations, and was more common in pool mesohabitats than riffle mesohabitats. Geometric morphometric analysis of body shape variation indicat...
- Published
- 2016
12. Range expansion of the genus Sicydium (Teleostei: Gobiidae) to coastal mountain streams of southwestern Ecuador and possibly northwestern Peru
- Author
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Windsor E. Aguirre, Ronald Navarrete Amaya, Gian Carlo Sánchez-Garcés, Fredy Nugra Salazar, and Jonathan Valdiviezo Rivera
- Subjects
Teleostei ,Neotropics ,Pacific Ocean ,Ecology ,biology ,Range (biology) ,QH301-705.5 ,Biodiversity ,STREAMS ,South America ,biology.organism_classification ,Pacific ocean ,Geography ,Genus ,Type description ,Sicydium rosenbergii ,Biology (General) ,Ecology, Evolution, Behavior and Systematics ,Sicydium ,biodiversity - Abstract
We report collections of several specimens of Sicydium in 2013 and 2014 from the Jubones and Santa Rosa Rivers in southwestern Ecuador. These collections substantially expand the known range of the genus southward. The specimens are tentatively identified as Sicydium cf. rosenbergii based on their morphology. Small differences in morphology among specimens from the two rivers are noted, as are discrepancies with the type description. A museum database search uncovered two additional records of the genus south of their previously recognized range including one record from northwestern Peru.
- Published
- 2017
13. Parallel body shape divergence in the Neotropical fish genus Rhoadsia (Teleostei: Characidae) along elevational gradients of the western slopes of the Ecuadorian Andes
- Author
-
Kirby C. Karpan, Fredy Nugra Salazar, Windsor E. Aguirre, Grace Malato, Ronald Navarrete Amaya, Jonathan Valdiviezo Rivera, Virginia R. Shervette, and Paola Calle Delgado
- Subjects
0106 biological sciences ,0301 basic medicine ,Evolutionary Genetics ,Heredity ,Species Delimitation ,Speciation ,Biodiversity ,Population genetics ,Marine and Aquatic Sciences ,lcsh:Medicine ,01 natural sciences ,Geographical locations ,Gene flow ,Monophyly ,Body Size ,lcsh:Science ,Multidisciplinary ,Ecology ,Altitude ,Fishes ,Freshwater Fish ,Genetic Mapping ,Genetic structure ,Vertebrates ,Ecuador ,Research Article ,Freshwater Environments ,Gene Flow ,Evolutionary Processes ,Biology ,010603 evolutionary biology ,Electron Transport Complex IV ,03 medical and health sciences ,Rivers ,Genetics ,Animals ,Morphometrics ,Evolutionary Biology ,Population Biology ,Characidae ,Ecology and Environmental Sciences ,Genetic Drift ,lcsh:R ,Organisms ,Aquatic Environments ,Biology and Life Sciences ,Genetic Variation ,Bodies of Water ,South America ,Genetic divergence ,030104 developmental biology ,Haplotypes ,Neotropical fish ,Earth Sciences ,Genetic Polymorphism ,lcsh:Q ,People and places ,Population Genetics - Abstract
Neotropical mountain streams are important contributors of biological diversity. Two species of the characid genus Rhoadsia differing for an ecologically important morphological trait, body depth, have been described from mountain streams of the western slopes of the Andes in Ecuador. Rhoadsia altipinna is a deeper-bodied species reported from low elevations in southwestern Ecuador and northern Peru, and Rhoadsia minor is a more streamlined species that was described from high elevations (>1200 m) in the Esmeraldas drainage in northwestern Ecuador. Little is known about these species and their validity as distinct species has been questioned. In this study, we examine how their body shape varies along replicated elevational gradients in different drainages of western Ecuador using geometric morphometrics and the fineness ratio. We also use sequences of the mitochondrial cytochrome oxidase c I gene and the second intron of the S7 nuclear gene to examine whether genetic data are consistent with the existence of two species. We found that body depth varies continuously among populations within drainages as a function of elevation, and that body shape overlaps among drainages, such that low elevation populations of R. minor in the Esmeraldas drainage have similar body depths to higher elevation R. altipinna in southern drainages. Although a common general trend of declining body depth with elevation is clear, the pattern and magnitude of body shape divergence differed among drainages. Sequencing of mitochondrial and nuclear genes failed to meet strict criteria for the recognition of two species (e.g., reciprocal monophyly and deep genetic structure). However, there was a large component of genetic variation for the COI gene that segregated among drainages, indicating significant genetic divergence associated with geographic isolation. Continued research on Rhoadsia in western Ecuador may yield significant insight into adaptation and speciation in Neotropical mountain streams.
- Published
- 2017
14. Tinkering with the axial skeleton: vertebral number variation in ecologically divergent threespine stickleback populations
- Author
-
Kendal Walker, Windsor E. Aguirre, and Shawn Gideon
- Subjects
Morphometrics ,Axial skeleton ,Vertebrate ,Stickleback ,Anatomy ,Gasterosteus ,Biology ,biology.organism_classification ,Sexual dimorphism ,medicine.anatomical_structure ,Evolutionary biology ,Adaptive radiation ,biology.animal ,medicine ,Ecology, Evolution, Behavior and Systematics ,Vertebral column - Abstract
Understanding how the vertebral column is impacted as populations adapt to different habitats favouring distinct body forms can provide insight into the origin of evolutionary diversity in the axial skeleton. We examined variation of vertebral number and body shape in morphologically and ecologically divergent anadromous, benthic, and limnetic threespine stickleback populations from Alaska. Variation in vertebral number was substantial and was associated with body shape variation. Both vertebral homeosis and region-specific changes in vertebral number were present. Sexual dimorphism in vertebral number was significant and resulted from vertebral homeosis; females had more abdominal vertebrae and males more caudal vertebrae, although total vertebrae did not differ. Body elongation was associated with an increase in vertebral number, especially in the caudal region, although this varied among populations. Benthics tended to have less caudal vertebrae than limnetics and anadromous stickleback generally had more abdominal vertebrae than either, although this also varied among populations. Variation among individuals indicated that external similarity in body form masks significant vertebral variation in stickleback. Although more research on the underlying mechanisms and functional significance is needed, our findings highlight the potential of the threespine stickleback as a model for studying the evolution of the vertebrate axial skeleton. © 2014 The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 113, 204‐219. ADDITIONAL KEYWORDS: adaptive radiation ‐ evolution ‐ Gasterosteus aculeatus ‐ geometric morphometrics ‐ vertebrae.
- Published
- 2014
15. First record of Iotabrycon praecox Roberts 1973 (Characidae: Stevardiinae) in the Santa Rosa drainage, southwestern Ecuador
- Author
-
Ronald Navarrete, Gian Carlo Sánchez-Garcés, Paola Calle, and Windsor E. Aguirre
- Subjects
Ecology ,biology ,QH301-705.5 ,Iotabrycon praecox ,biology.organism_classification ,Archaeology ,Geographic distribution ,Characidae ,River drainage ,Geography ,new record ,Ecuador ,Drainage ,Biology (General) ,Stevardiinae ,Ecology, Evolution, Behavior and Systematics - Abstract
Iotabrycon praecox (Characidae: Stevardiinae) has been reported as endemic to the Guayas River drainage in Western Ecuador since its description in 1973. We collected one specimen of I. praecox in the Santa Rosa River, Santa Rosa drainage, El Oro Province, approximately 144 km south of the Guayas drainage, significantly expanding the known geographic distribution of the species. Given the severe anthropomorphic pressures impacting fishes in Southwestern Ecuador, there is an urgent need to evaluate the present status of I. praecox in the region.
- Published
- 2014
16. Morphological and Genetic Divergence of Hoplias microlepis (Characiformes: Erythrinidae) in Rivers and Artificial Impoundments of Western Ecuador
- Author
-
Ronald Navarrete, Stergiani Agorastos, Virginia R. Shervette, Paola Calle, and Windsor E. Aguirre
- Subjects
biology ,Ecology ,Aquatic Science ,Characiformes ,biology.organism_classification ,Erythrinidae ,Divergence ,Genetic divergence ,Hoplias microlepis ,Predatory fish ,Congener ,Habitat ,Animal Science and Zoology ,Ecology, Evolution, Behavior and Systematics - Abstract
Little is known about the freshwater fishes of western Ecuador despite serious environmental threats, including the creation of large artificial impoundments. Phenotypic and genetic divergence of populations of a large predatory fish, Hoplias microlepis, is examined in rivers and artificial impoundments of the Guayas River drainage in western Ecuador. Despite the recent formation of the impoundments (∼20 years prior to the sampling), H. microlepis in these habitats diverged morphologically from river populations. Impoundment fish tended to have larger eyes, longer dorsal and caudal fins, and thinner bodies than river fish. Classification rates for habitat of origin based on morphometric measures were relatively high (71.7–83.3%), and the magnitude of morphological divergence was substantial when contrasted with divergence from H. malabaricus, a congener from eastern Ecuador. Frequencies of mtDNA d-loop haplotypes differed significantly among samples. Genetic divergence between river samples implies that t...
- Published
- 2013
17. Genetic divergence of a sympatric lake-resident-anadromous three-spined sticklebackGasterosteus aculeatusspecies pair
- Author
-
C. J. Drevecky, R. Falco, and Windsor E. Aguirre
- Subjects
Genetic divergence ,Fish migration ,biology ,Sympatric speciation ,Ecology ,Three-spined stickleback ,Allopatric speciation ,Stickleback ,Reproductive isolation ,Gasterosteus ,Aquatic Science ,biology.organism_classification ,Ecology, Evolution, Behavior and Systematics - Abstract
The genetic relationship between sympatric, morphologically divergent populations of anadromous and lake-resident three-spined stickleback Gasterosteus aculeatus in the Jim Creek drainage of Cook Inlet, Alaska, was examined using microsatellite loci and mitochondrial d-loop sequence data. Resident samples differed substantially from sympatric anadromous samples in the Jim Creek drainage with the magnitude of the genetic divergence being similar to that between allopatric resident and anadromous populations in other areas. Resident samples were genetically similar within the Jim Creek drainage, as were the anadromous samples surveyed. Neighbour-joining and Structure cluster analysis grouped the samples into four genetic clusters by ecomorph (anadromous v. all resident) and geographic location of the resident samples (Jim Creek, Mat-Su and Kenai). There was no evidence of hybridization between resident and anadromous G. aculeatus in the Jim Creek drainage, which thus appear to be reproductively isolated.
- Published
- 2013
18. Twenty years of body shape evolution in a threespine stickleback population adapting to a lake environment
- Author
-
Michael A. Bell and Windsor E. Aguirre
- Subjects
education.field_of_study ,Natural selection ,biology ,Ecology ,Population ,Stickleback ,biology.organism_classification ,Spatial heterogeneity ,Habitat ,Evolutionary biology ,Adaptive radiation ,Allometry ,Parallel evolution ,education ,Ecology, Evolution, Behavior and Systematics - Abstract
Analysis of contemporary evolution can provide important insights into the pattern and rate of phenotypic evolution. The threespine stickleback population in Loberg Lake was exterminated in 1982, and a new population was founded between 1983 and 1989 by anadromous stickleback. The body shape of the Loberg Lake population resembled that of anadromous populations in 1990, although it had diverged markedly by 1992. Between 1992 and 2009, the population evolved more slowly to resemble typical lake populations in the region, diverging approximately 68% of the distance separating its putative ancestor and the original native population by 2009. Temporal evolution is the main source of variation, although spatial heterogeneity, armour phenotype, and allometry contribute significant variation. There was no significant effect of ancestral phenotypic shape covariance on the evolutionary trajectory of this population. Temporal variation in the Loberg Lake population provides a rare glimpse into the evolutionary response of a complex trait to natural selection after a major habitat shift. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, 105, 817–831.
- Published
- 2012
19. Frequency of Ectodysplasin alleles and limited introgression between sympatric threespine stickleback populations
- Author
-
Anup K. Gangavalli, Michael A. Bell, Windsor E. Aguirre, and Adam J. Bewick
- Subjects
Sympatry ,biology ,Ecology ,Zoology ,Introgression ,Stickleback ,Locus (genetics) ,Gasterosteus ,Reproductive isolation ,Aquatic Science ,biology.organism_classification ,Gene flow ,Sympatric speciation ,Ecology, Evolution, Behavior and Systematics - Abstract
The threespine stickleback (Gasterosteus aculeatus) is primitively an anadromous or resident marine species but has repeatedly colonized fresh water, where predictable phenotypic divergence usually occurs rapidly. A conspicuous element of this divergence is change of the number and position of lateral armor plates from about 33 that cover the entire flank (complete) to
- Published
- 2010
20. Microgeographical diversification of threespine stickleback: body shape-habitat correlations in a small, ecologically diverse Alaskan drainage
- Author
-
Windsor E. Aguirre
- Subjects
Fish migration ,Natural selection ,Habitat ,Ecology ,Geographical distance ,Adaptive radiation ,Stickleback ,Biology ,Adaptation ,biology.organism_classification ,Ecology, Evolution, Behavior and Systematics ,Limnetic zone - Abstract
Adaptive radiations are a major source of evolutionary diversity in nature, and understanding how they originate and how organisms diversify during the early stages of adaptive radiation is a major problem in evolutionary biology. The relationship between habitat type and body shape variation was investigated in a postglacial radiation of threespine stickleback in the upper Fish Creek drainage of Cook Inlet, Alaska. Although small, the upper Fish Creek drainage includes ecologically diverse lakes and streams in close proximity to one another that harbour abundant stickleback. Specimens from ancestral anadromous and derived resident freshwater populations differed substantially and could be distinguished by body shape alone, suggesting that the initial stages of adaptation contribute disproportionately to evolutionary divergence. Body shape divergence among resident freshwater populations was also considerable, and phenotypic distances among samples from freshwater populations were associated with habitat type but not geographical distance. As expected, stream stickleback from slow-moving, structurally complex environments tended to have the deepest bodies, stickleback from lakes with a mostly benthic habitat were similar but less extreme, and stickleback from lakes with a mostly limnetic habitat were the most shallow-bodied, elongate fish. Beyond adapting rapidly to conditions in freshwater environments, stickleback can diversify rapidly over small geographical scales in freshwater systems despite opportunities for gene flow. This study highlights the importance of ecological heterogeneity over small geographical scales for evolutionary diversification during the early stages of adaptive radiation, and lays the foundation for future research on this ecologically diverse, postglacial system. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 98, 139‐151.
- Published
- 2009
21. Evolutionary diversification of opercle shape in Cook Inlet threespine stickleback
- Author
-
Saad Arif, Michael A. Bell, and Windsor E. Aguirre
- Subjects
education.field_of_study ,Facial bone ,biology ,Population ,Stickleback ,Microevolution ,biology.organism_classification ,Population bottleneck ,Evolutionary biology ,Adaptive radiation ,Parallel evolution ,Adaptation ,education ,Ecology, Evolution, Behavior and Systematics - Abstract
We investigated the evolution of a large facial bone, the opercle (OP), in lake populations of the threespine stickleback that were founded by anadromous ancestors, in Cook Inlet, Alaska. Recent studies characterized OP variation among marine and lake populations and mapped a quantitative trait locus with a large influence on OP shape. Using populations from diverse environments and independent evolutionary histories, we examined divergence of OP shape from that of the anadromous ancestor. We report preliminary evidence for divergence between benthic and generalist lake ecotypes, necessitating further investigation. Furthermore, rapid divergence of OP shape has occurred in a lake population that was founded by anadromous stickleback in the 1980s, which is consistent with divergence of other phenotypic traits and with OP diversification in other lake populations. By contrast, there has been limited evolution of OP shape in a second lake population that may have experienced a genetic bottleneck early in its history and lacks genetic variation for OP divergence. Taken together, the results obtained from these two populations are consistent with studies of other stickleback phenotypic traits that implicate ancestral variation in postglacial adaptive radiation of threespine stickleback in fresh water. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 97, 832–844.
- Published
- 2009
22. Phenotypic variation and sexual dimorphism in anadromous threespine stickleback: implications for postglacial adaptive radiation
- Author
-
Windsor E. Aguirre, Kaitlyn E. Ellis, Mary Kusenda, and Michael A. Bell
- Subjects
Morphometrics ,education.field_of_study ,biology ,Directional selection ,Population ,Zoology ,Stickleback ,Gasterosteus ,biology.organism_classification ,Sexual dimorphism ,Adaptive radiation ,Adaptation ,education ,Ecology, Evolution, Behavior and Systematics - Abstract
Ancestral properties can influence patterns of evolutionary diversification, but ancestors can rarely be observed directly. We examined variation and sexual dimorphism of morphological traits in an anadromous threespine stickleback population representing the ancestral form for resident postglacial stickleback populations in the area. A combination of traditional and geometric morphometric methods were used to study variation over multiple years in an anadromous population that breeds in Rabbit Slough, Cook Inlet, Alaska. Major armor anomalies were extremely rare but their occurrence at measurable frequencies suggests that significant standing variation for armor phenotypes exists in anadromous populations. Sexual dimorphism was a major source of variation, and most traits differed significantly between sexes, particularly head length, length of the pelvic girdle, and body shape. Consequently, some degree of sexual dimorphism appears to be the ancestral condition for many traits in derived resident freshwater stickleback radiations. Morphological variation among years, especially in body shape, was significant in both sexes, but the magnitude of annual variation was always less than variation due to other factors. Phenotypic means were relatively stable over short time scales. Postglacial stickleback radiations are among the most enlightening cases of adaptive radiation, and our detailed study of variation in an anadromous stickleback population provides crucial insight into a key component of adaptive radiation, the variation on which directional selection acts at the onset of the radiation. © 2008 The Linnean Society of London, Biological Journal of the Linnean Society, 2008, 95, 465–478. ADDITIONAL KEYWORDS: Alaska – ancestral variation – evolutionary diversification – Gasterosteus aculeatus – geometric morphometrics.
- Published
- 2008
23. Spondylitis in a humpback whale (Megaptera novaeangliae) from the southeast Pacific
- Author
-
Ben Haase, Windsor E. Aguirre, and Fernando Félix
- Subjects
Male ,Population impact ,Zoology ,Cetacea ,Ectoparasitic Infestations ,Aquatic Science ,Biology ,Pacific ocean ,Humpback whale ,Fatal Outcome ,Spondylarthritis ,medicine ,Animals ,Amphipoda ,Spondylitis ,Ecology, Evolution, Behavior and Systematics ,Humpback Whale ,Arthritis, Infectious ,Pacific Ocean ,Anatomy ,biology.organism_classification ,medicine.disease ,Spine ,Young age ,medicine.anatomical_structure ,Ecuador ,Vertebral column - Abstract
A 7.25 m long male humpback whale (Megaptera novaeangliae) with spondylitis was found beached on August 13, 1994 at Ancon, Ecuador (2 degrees 23' S, 80 degrees 47' W). The condition involved at least 11 vertebrae, 7 lumbar (L4 to L11) and 4 caudal (Ca1 to Ca4). Partial fusion of vertebrae was observed as a result of intervertebral bony proliferation, likely impeding full motion. The relatively young age of this specimen and the severity of the deformities suggest an infectious, rather than degenerative, process. The gross findings are most consistent with some type of spondyloarthritis. Although this condition has previously been identified in a number of cetacean species, the pathogenesis, population impact and ecologic implications have not been fully assessed. This is the third case described for humpback whales and the first for a humpback whale from the SE Pacific.
- Published
- 2007
24. Fish communities of a disturbed mangrove wetland and an adjacent tidal river in Palmar, Ecuador
- Author
-
M.A. Gonzalez, Windsor E. Aguirre, Rodrigo Cevallos, E. Blacio, Francisco Pozo, Frances Gelwick, and Virginia R. Shervette
- Subjects
geography ,geography.geographical_feature_category ,Ecology ,Wetland ,Estuary ,Aquatic Science ,Oceanography ,geography.body_of_water ,Habitat destruction ,Habitat ,Tidal river ,Species richness ,Mangrove ,Nursery habitat - Abstract
Coastal Ecuador has lost 20e30% of mangrove wetlands over the past 30 years. Such habitat loss can impair the ecological functions of wetlands. A paucity of information exists concerning mangrove fish communities of Ecuador. In this study we identify the fish community of the remaining mangrove wetland in Palmar, Ecuador. Fish were sampled in the dry season of 2003 and the wet season of 2004 by seining in mangrove creeks and Main channel of Rio Palmar. For comparison, an adjacent tidal river without mangroves, Rio Javita, was also sampled. We collected a total of 12,231 individuals comprising 36 species in 16 families from Rios Palmar and Javita. Gobiidae (7 species) was the most diverse family for mangrove sites followed by Gerreidae (5 species) and Engraulidae (4 species). A total of 34 species were collected in the mangrove wetland, 21 of which were exclusive to the mangroves including three species of juvenile snook (Centropomidae), indicating that the mangrove habitat of Palmar may provide nursery habitat for these economically valued species. In Rio Javita, Carangidae (3 species) was the most diverse family followed by Engraulidae and Gerreidae (2 species each). A total of 14 species were collected in the tidal river, only two of which were exclusive to the river. Multivariate analyses of fish community data indicated significant differences in community composition between the mangrove creeks and the tidal river and between seasons in both. Juvenile white mullet, Mugil curema, were collected in high relative abundance in both Rios Palmar and Javita, as was the tropical silverside Atherinella serrivomer an ecologically important species. Although Rios Palmar and Javita are characterized by relatively low fish species richness compared to other tropical estuarine systems, they appear to provide an important habitat for several economically and ecologically valued species. 2007 Elsevier Ltd. All rights reserved.
- Published
- 2007
25. Morphological diversity of the Cynoscion group (Perciformes: Sciaenidae) in the Gulf of Guayaquil region, Ecuador: A comparative approach
- Author
-
Windsor E. Aguirre and Virginia R. Shervette
- Subjects
Morphometrics ,biology ,Sympatric speciation ,Ecology ,Biodiversity ,Aquatic Science ,Sciaenidae ,biology.organism_classification ,Ecology, Evolution, Behavior and Systematics ,Cynoscion ,Gill raker ,Perciformes ,Cynoscion regalis - Abstract
We assess morphological diversity of species of the Cynoscion group in the Gulf of Guayaquil (GOG) using traditional morphometric methods. Five species from the GOG assemblage (C. albus, C. analis, C. phoxocephalus, C. squamipinnis, and Isopisthus remifer) are compared to four species from a relatively well-studied assemblage in the western Atlantic (C. arenarius, C. nebulosus, C. nothus, and C. regalis). The two regional species assemblages broadly overlap in morphology, but sympatric species segregate relatively well within each assemblage. The GOG species segregate primarily along the major axis of shape variation in the study, which is associated with variation in the anal, second dorsal, and caudal fins. The western Atlantic species segregate primarily along the second major axis of shape variation, which is most strongly associated with variation in gill raker length, and less strongly with pectoral fin length, eye diameter, and length of the third dorsal spine. Patterns of morphological divergence among the western Atlantic species support the hypothesis that morphological divergence is associated with ecological divergence. Comparisons across assemblages indicate that morphological divergence among species in the GOG is substantial. Consequently, Cynoscion species in the GOG may be highly divergent in ecological habits, which would have important management implications, but further ecological research is needed. This study provides a first glimpse into the major patterns of morphological diversification in the Cynoscion group.
- Published
- 2005
26. Isolation of sixteen microsatellite loci for Rhoadsia altipinna (Characiformes: Characidae) from an impacted river basin in western Ecuador
- Author
-
Ronald Navarrete, Antonio Torres, Webster F. Vital, Vinh H. Vu, Maxine Loh, Paola Calle, Virginia R. Shervette, and Windsor E. Aguirre
- Subjects
Linkage disequilibrium ,biology ,Ecology ,Zoology ,Population genetics ,Locus (genetics) ,Characiformes ,biology.organism_classification ,Zygosity ,Loss of heterozygosity ,Characidae ,Genetics ,Microsatellite ,Ecology, Evolution, Behavior and Systematics - Abstract
Sixteen polymorphic, dinucleotide microsatel- lite loci were developed for Rhoadsia altipinna, a small characid fish from impacted rivers in south western Ecua- dor. None of the loci were in linkage disequilibrium or deviated significantly from Hardy-Weinberg equilibrium after sequential Bonferroni correction. Variability was relatively high with allelic richness ranging between 2 and 22 alleles per locus (average = 9.125), observed hetero- zygosity ranging between 0.125 and 0.958 (aver- age = 0.695), and expected heterozygosity ranging between 0.120 and 0.952 (average = 0.736).
- Published
- 2013
27. Genetics of Lateral Plate and Gillraker Phenotypes in a Rapidly Evolving Population of Threespine Stickleback
- Author
-
Patricia K. Doherty, Windsor E. Aguirre, and Michael A. Bell
- Subjects
Genetics ,education.field_of_study ,animal structures ,genetic structures ,biology ,fungi ,Population ,Stickleback ,biology.organism_classification ,Phenotype ,Genetic architecture ,Behavioral Neuroscience ,Evolutionary biology ,Animal Science and Zoology ,education ,psychological phenomena and processes ,reproductive and urinary physiology - Abstract
Twenty-seven crosses were used to study the genetics of rapidly evolving traits in a recently founded population of threespine stickleback in Loberg Lake, Alaska. Lateral plate morph segregation ratios were inconsistent with all published models of lateral plate morph genetics except Avise's (1976) general two-locus model. Incompatibility of the results of our plate morph crosses with those of most previous studies suggests that the genetic architecture underlying lateral plate morphs differs among populations or is more complex than presently recognized. Segregation ratios for lateral plate morphs indicate that consistently low frequencies of partial morphs observed in the Loberg Lake population at least partly reflect genetic architecture. Gillraker number and probably low morph lateral plate number are highly heritable and correlated with each other. Lateral plate asymmetry was high but not significantly heritable. Low and complete morph lateral plate number do not appear to be genetically correlated, indicating a significant element of independent genetic control.
- Published
- 2004
28. Allometric growth of the sulcus in Cynoscion spp. (Sciaenidae)
- Author
-
Windsor E. Aguirre
- Subjects
genetic structures ,biology ,Sense organ ,Anatomy ,Aquatic Science ,Sulcus ,Sciaenidae ,biology.organism_classification ,behavioral disciplines and activities ,body regions ,medicine.anatomical_structure ,medicine ,sense organs ,Allometry ,psychological phenomena and processes ,Ecology, Evolution, Behavior and Systematics ,Medial surface ,Cynoscion ,Otolith - Abstract
The sulcus of Cynoscion spp. exhibited strong positive allometric growth relative to the medial surface of the otolith, and the ratio between the area of the sulcus and the otolith (S:O) increased dramatically with size. The S:O ratios of larger specimens are the highest that have so far been reported.
- Published
- 2003
29. Isolation of microsatellite loci for the predatory fish Hoplias microlepis (Characiformes: Erythrinidae) from a highly impacted river system in western Ecuador
- Author
-
Jane Christman, Windsor E. Aguirre, Vinh H. Vu, and Paola Calle
- Subjects
Hoplias microlepis ,Linkage disequilibrium ,Predatory fish ,biology ,Ecology ,Genetics ,Freshwater fish ,Population genetics ,Microsatellite ,Characiformes ,biology.organism_classification ,Erythrinidae ,Ecology, Evolution, Behavior and Systematics - Abstract
We developed 14 polymorphic, dinucleotide microsatellite loci for Hoplias microlepis, a large predatory fish from a highly impacted river in western Ecuador. These were isolated using a next-generation pyrosequencing approach and tested in a sample of 32 fish. None of the loci were in linkage disequilibrium and all appeared to be in Hardy–Weinberg. Nine of the loci exhibited greater variability, having 3–8 alleles (average = 5.22), observed heterozygosities between 0.22 and 0.81 (average = 0.58), and expected heterozygosities between 0.20 and 0.83 (average = 0.56). The other five loci had 2 alleles and heterozygosity values generally close to 0. This is the first study dedicated to isolating microsatellites for a freshwater fish from the highly impacted aquatic ecosystems of western Ecuador.
- Published
- 2012
30. Occurrence of Schistocephalus solidus in anadromous threespine stickleback
- Author
-
Vinh H. Vu, Windsor E. Aguirre, C. J. Drevecky, and A. Confer
- Subjects
Male ,Range (biology) ,Biology ,Host-Parasite Interactions ,Fish Diseases ,Sex Factors ,medicine ,Prevalence ,Helminths ,Animals ,Seawater ,Cestode infections ,Body cavity ,Ecology, Evolution, Behavior and Systematics ,Fish migration ,Chi-Square Distribution ,Ecology ,Stickleback ,biology.organism_classification ,Cestode Infections ,Smegmamorpha ,Lakes ,medicine.anatomical_structure ,Schistocephalus solidus ,Cestoda ,Parasitology ,Animal Migration ,Female ,Large size ,Alaska - Abstract
Plerocercoids of the cestode Schistocephalus solidus are reported for the first time from the body cavity of anadromous threespine stickleback inhabiting Mud Lake, Alaska. Most infected stickleback harbored a single large plerocerciod (mean weight = 0.447 g, range = 0.228–0.716 g). The overall prevalence of plerocercoids across genders and 2 yr of samples was 1.4%, but prevalence was significantly greater in males than in females. Because of the large size of the plerocercoids, anadromous stickleback were probably infected as juveniles before leaving the lake, suggesting that plerocercoids can live in the body cavity of oceanic stickleback for several years.
- Published
- 2012
31. Sexual dimorphism of head morphology in three-spined stickleback Gasterosteus aculeatus
- Author
-
Windsor E. Aguirre and O. Akinpelu
- Subjects
Male ,education.field_of_study ,Sex Characteristics ,Natural selection ,biology ,Three-spined stickleback ,Ecology ,Population ,Stickleback ,Zoology ,Gasterosteus ,Aquatic Science ,biology.organism_classification ,Smegmamorpha ,Sexual dimorphism ,Sexual selection ,Animals ,Body Size ,Female ,education ,Head ,Ecology, Evolution, Behavior and Systematics ,Sex characteristics - Abstract
This study examined sexual dimorphism of head morphology in the ecologically diverse three-spined stickleback Gasterosteus aculeatus. Male G. aculeatus had longer heads than female G. aculeatus in all 10 anadromous, stream and lake populations examined, and head length growth rates were significantly higher in males in half of the populations sampled, indicating that differences in head size increased with body size in many populations. Despite consistently larger heads in males, there was significant variation in size-adjusted head length among populations, suggesting that the relationship between head length and body length was flexible. Inter-population differences in head length were correlated between sexes, thus population-level factors influenced head length in both sexes despite the sexual dimorphism present. Head shape variation between lake and anadromous populations was greater than that between sexes. The common divergence in head shape between sexes across populations was about twice as important as the sexual dimorphism unique to each population. Finally, much of the sexual dimorphism in head length was due to divergence in the anterior region of the head, where the primary trophic structures were found. It is unclear whether the sexual dimorphism was due to natural selection for niche divergence between sexes or sexual selection. This study improves knowledge of the magnitude, growth rate divergence, inter-population variation and location of sexual dimorphism in G. aculeatus head morphology.
- Published
- 2010
32. A mitochondrial DNA based phylogeny of weakfish species of the Cynoscion group (Pisces: Sciaenidae)
- Author
-
Windsor E. Aguirre, Carlos Vergara-Chen, Eldredge Bermingham, and Mercedes González-Wangüemert
- Subjects
Mitochondrial DNA ,Cytochrome b ,Zoology ,Sciaenidae ,DNA, Mitochondrial ,Isopisthus ,Evolution, Molecular ,Monophyly ,ATPase 8/6 ,Phylogenetics ,Genetics ,Animals ,Geminate species ,Molecular Biology ,Atlantic Ocean ,Ecology, Evolution, Behavior and Systematics ,Phylogeny ,Molecular systematics ,Atractoscion ,Pacific Ocean ,biology ,Plagioscion ,Bayes Theorem ,Sequence Analysis, DNA ,Mitochondrial genes ,biology.organism_classification ,Perciformes ,Genes, Mitochondrial ,Macrodon ,Molecular phylogenetics ,Molecular evolution ,DNA Sequence Analysis ,Cynoscion - Abstract
We infer the phylogeny of fishes in the New World Cynoscion group (Cynoscion, Isopisthus, Macrodon, Atractoscion, Plagioscion) using 1603bp of DNA sequence data from three mitochondrial genes. With the exception of Plagioscion, whose position was ambiguous, the Cynoscion group is monophyletic. However, several genera examined are not monophyletic. Atlantic and Pacific species of Cynoscion are interspersed in the tree and geminate species pairs are identified. Intergeneric relationships in the group are clarified. Our analysis is the first comprehensive phylogeny for the Cynoscion group based on molecular data and provides a baseline for future comparative studies of this important group. info:eu-repo/semantics/publishedVersion
- Published
- 2009
33. Ocurrencia de Sphoeroides rosenblatti Bussing, 1996 (Teleostei: Tetraodontidae) en la costa de la provincia de Guayas, Ecuador, y una comparación con Sphoeroides annulatus (Jenyns, 1842)
- Author
-
Francisco Pozo, M.A. Gonzalez, Windsor E. Aguirre, Rodrigo Cevallos, and Virginia R. Shervette
- Subjects
Teleostei ,biology ,morfometría ,Aquatic Science ,Oceanography ,biology.organism_classification ,Pacífico tropical este ,registro nuevo ,Sphoeroides rosenblatti ,Sphoeroides annulatus ,manglar ,Tetraodontidae ,Humanities ,tamboril - Abstract
Se recolectaron trece ejemplares juveniles de Sphoeroides rosenblatti Bussing, 1996 en un bosque pequeño y fuertemente impactado de mangle situado en Palmar, provincia de Guayas, Ecuador. Esta especie era conocida previamente solo de aguas costeras de Costa Rica y Panamá. Se contrastó la ocurrencia y morfología de S. rosenblatti con ejemplares de Sphoeroides annulatus (Jenyns, 1842) recolectados en la misma área. La presencia de S. rosenblatti no estuvo significativamente asociada con la temperatura del agua, salinidad, o morfología del río, mas hubo evidencia de segregación espacial entre S. rosenblatti y S. annulatus. También encontramos pequeñas pero significativas diferencias entre las características morfométricas de estas especies, que estuvieron en acuerdo con la descripción original basada en especimenes centroamericanos. Utilizando todas las características morfométricas, se realizó un análisis de función discriminante que produjo un vector capaz de clasificar correctamente a todos los ejemplares. Se reporta una ampliación importante de la distribución conocida de S. rosenblatti y se agrega una especie nueva a la ictiofauna de la costa continental del Ecuador
- Published
- 2006
34. Genetic Variation: A Laboratory Manual. Edited by Michael P. Weiner, Stacey B. Gabriel, and, J. Claiborne Stephens. Cold Spring Harbor (New York): Cold Spring Harbor Laboratory Press. $240.00 (hardcover); $165.00 (paper). xxi + 472 p.; ill.; index. 978‐0‐87969‐779‐2 (hc); 978‐0‐87969‐780‐8 (pb). 2007
- Author
-
Windsor E. Aguirre
- Subjects
geography ,Index (economics) ,geography.geographical_feature_category ,media_common.quotation_subject ,Genetic variation ,Spring (hydrology) ,Environmental ethics ,Art ,General Agricultural and Biological Sciences ,Archaeology ,media_common - Published
- 2008
35. Frozen Earth: The Once and Future Story of Ice Ages. By Doug Macdougall. Berkeley (California): University of California Press. $24.95. xi + 256 p; ill.; index. ISBN: 0–520–23922–9. 2004
- Author
-
Windsor E. Aguirre
- Subjects
Index (economics) ,History ,Ice age ,Environmental ethics ,General Agricultural and Biological Sciences ,Archaeology - Published
- 2006
36. Red Snapper Ecology and Fisheries in the U.S. Gulf of Mexico. Based on a symposium held in San Antonio, Texas, 10–12 February 2006. American Fisheries Society Symposium, Volume 60. Edited by William F. PattersonIII, James H. CowanJr., Gary R. Fitzhugh, and, David L. Nieland. Bethesda (Maryland): American Fisheries Society. $69.00 (paper). xi + 396 p.; ill.; no index. 978‐1‐888569‐97‐1. 2007
- Author
-
Windsor E. Aguirre
- Subjects
History ,Index (economics) ,Ecology (disciplines) ,Environmental ethics ,General Agricultural and Biological Sciences ,Archaeology - Published
- 2008
37. Ecology of the Marine Fishes of Cuba.Edited by Rodolfo Claro, Kenyon C Lindeman, and , Lynne R Parenti. Washington (DC): Smithsonian Institution Press. $55.00. xv + 253 p; ill.; index. ISBN: 1–56098–985–8. 2001
- Author
-
Windsor E. Aguirre
- Subjects
Index (economics) ,Smithsonian institution ,Anthropology ,Ecology (disciplines) ,media_common.quotation_subject ,Environmental ethics ,Art ,General Agricultural and Biological Sciences ,media_common - Published
- 2003
38. Twelve years of contemporary armor evolution in a threespine stickleback population
- Author
-
Nathaniel J. Buck, Windsor E. Aguirre, and Michael A. Bell
- Subjects
education.field_of_study ,Time Factors ,biology ,Population ,Adaptation, Biological ,Stickleback ,Animal Structures ,Fresh Water ,Gasterosteus ,biology.organism_classification ,Biological Evolution ,Smegmamorpha ,Habitat ,Species Specificity ,Evolutionary biology ,Adaptive radiation ,Genetics ,Animals ,Body Weights and Measures ,education ,General Agricultural and Biological Sciences ,Alaska ,Ecology, Evolution, Behavior and Systematics - Abstract
Loberg Lake, Alaska was colonized by sea-run Gasterosteus aculeatus between 1983 and 1988, after the original stickleback population was exterminated. Annual samples from 1990 to 2001 reveal substantial evolution of lateral plate (armor) phenotypes. The 1990 sample was nearly monomorphic for the complete plate morph, which is monomorphic in local sea-run populations; the low plate morph, which is usually monomorphic in local freshwater populations, was absent. By 2001, the frequency of completes had declined to 11%, and lows had increased to 75%. The partial plate morph and two unusual intermediate plate phenotypes were generally rare, but occurrence of the intermediates was unexpected. These intermediate phenotypes rarely occur in other, presumably older, polymorphic populations. When low morphs first appeared, they averaged 6.8 plates per side, indicating that the ancestral plate number of low morphs is high, and their mean has subsequently declined. Contemporary evolution in this population indicates that threespine stickleback adapt to freshwater habitats within decades after invasion from the ocean, and thus phenotypes in most populations are adapted to current conditions.
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