Use este identificador para citar ou linkar para este item: http://rima.ufrrj.br/jspui/handle/20.500.14407/26229
Registro completo de metadados
Campo DCValorIdioma
dc.contributor.authorGuedes, Gustavo Henrique Soares-
dc.date.accessioned2026-08-27T15:50:33Z-
dc.date.available2026-08-27T15:50:33Z-
dc.date.issued2026-07-30-
dc.identifier.citationGUEDES, Gustavo Henrique Soares. Peixes anuais (Cyprinodontiformes: Rivulidae): diversidade, endemismo, ameaças e conservação. 2026. 185 f. Tese (Doutorado em Biologia Animal) - Instituto de Ciências Biológicas e da Saúde, Universidade Federal Rural do Rio de Janeiro, Seropédica, 2026.pt_BR
dc.identifier.urihttp://rima.ufrrj.br/jspui/handle/20.500.14407/26229-
dc.description.abstractPeixes-anuais (Cyprinodontiformes: Rivulidae) representam um dos componentes mais singulares e ameaçados da biodiversidade brasileira, associados a áreas úmidas temporárias e marcados por forte sazonalidade, elevado endemismo e diapausa embrionária. A vulnerabilidade desse grupo é sem paralelo: os peixes-anuais reúnem mais espécies ameaçadas de extinção, do que o número total de mamíferos, répteis ou anfíbios ameaçados no Brasil. Isso torna o avanço do conhecimento sobre essas espécies não apenas necessário, mas urgente. Esta tese integra ecologia, biogeografia e biologia da conservação para compreender padrões e processos que estruturam a diversidade de peixes-anuais e, simultaneamente, avaliar ameaças emergentes e instrumentos aplicados de conservação. Organizada em seis capítulos (cinco já publicados), a tese segue um gradiente do macro ao micro: da região Neotropical (do México até a Argentina), a estudos em escala nacional (Brasil) e regional (Estado do Rio de Janeiro), combinando teoria e prática. Em escala Neotropical (Capítulo 1: publicado no Journal of Biogeography em 2025), avalia como escolhas de unidade espacial e regionalizações influenciam padrões de endemismo e composição de espécies. Em escala nacional (Capítulo 2: publicado em Biological Conservation em 2026), quantifica a exposição de habitats e espécies ao fogo em diferentes biomas, e testa a efetividade da proteção territorial no Brasil. Em escala regional (Capítulo 3: under review no Journal of Nature Conservation em 2026), examina como o licenciamento ambiental incorpora (ou falha em incorporar) diagnósticos robustos para táxons raros e sazonalmente “invisíveis”, sistematizando evidências e recomendações para reduzir falsas ausências e qualificar decisões no Estado do Rio de Janeiro. A tese também avalia a contaminação por microplásticos em rivulídeos de ambientes temporários e manguezais (Capítulo 4: publicado em Wetlands: Ecology and Management em 2026), demonstrando exposição disseminada e refutando a hipótese de que poças temporárias funcionariam como refúgios frente à poluição plástica. Por fim, aprofunda mecanismos de história de vida e resiliência em zonas úmidas temporárias ao descrever traços reprodutivos e trade-offs (Capítulo 5: publicado em Wetlands em 2023); e sintetiza dados de distribuição, biologia populacional e perda de habitat para uma espécie focal, evidenciando o papel de áreas protegidas na mitigação de impactos nos habitats (Capítulo 6: publicado em Neotropical Ichthyology em 2023). Ao estabelecer uma ponte entre disciplinas transversais (ecologia, biogeografia e biologia da conservação), diferentes atores (pesquisa, órgãos ambientais, consultores), abordagens multi-escalas (Região Neotropical, Brasil, Estado do Rio de Janeiro), longos períodos (1985-2024), espécies ameaçadas (até 159 spp), teoria e aplicação, esta tese avança no sentido de tornar a conservação mais “executável”, ao traduzir evidências ecológicas e biogeográficas em critérios operacionais para planejamento territorial, monitoramento e tomada de decisão. Ela reforça um ponto crítico: conservar habitats efêmeros e espécies sazonalmente “invisíveis” depende de diagnósticos robustos e decisões antecipatórias, construídas de forma multidisciplinar e coordenada entre múltiplos atores, para que o conhecimento científico se converta em prática antes que perdas silenciosas se tornem irreversíveispt_BR
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESpt_BR
dc.languageporpt_BR
dc.publisherUniversidade Federal Rural do Rio de Janeiropt_BR
dc.subjectRivulidaept_BR
dc.subjectPeixes-anuaispt_BR
dc.subjectConservaçãopt_BR
dc.subjectEcologiapt_BR
dc.subjectBiogeografiapt_BR
dc.subjectannual fishpt_BR
dc.subjectconservationpt_BR
dc.subjectecologypt_BR
dc.subjectbiogeographypt_BR
dc.titlePeixes anuais (Cyprinodontiformes: Rivulidae): diversidade, endemismo, ameaças e conservaçãopt_BR
dc.title.alternativeAnnual fish (Cyprinodontiformes: Rivulidae): diversity, endemism, threats, and conservationen
dc.typeTesept_BR
dc.description.abstractOtherAnnual fish (Cyprinodontiformes: Rivulidae) represent one of the most singular and threatened components of Brazilian biodiversity, associated with temporary wetlands and characterized by strong seasonality, high endemism, and embryonic diapause. The vulnerability of this group is unparalleled: annual fish account for more endangered species than the total number of threatened mammals, reptiles, or amphibians in Brazil combined. This makes advancing knowledge about these species not only necessary but urgent. This thesis integrates ecology, biogeography, and conservation biology to understand the patterns and processes that structure annual fish diversity while simultaneously assessing emerging threats and applied conservation instruments. Organized into six chapters (five published), the thesis follows a gradient from macro to micro scales: from the Neotropical region (Mexico to Argentina) to national (Brazil) and regional (Rio de Janeiro State) studies, bridging theory and practice. At the Neotropical scale (Chapter 1: published in Journal of Biogeography in 2025), it evaluates how choices of spatial units and regionalization influence patterns of endemism and species composition. At the national scale (Chapter 2: published in Biological Conservation in 2026), it quantifies the exposure of habitats and species to fire across different biomes and tests the effectiveness of territorial protection in Brazil. At the regional scale (Chapter 3: under review in Journal for Nature Conservation in 2026), it examines how environmental licensing incorporates (or fails to incorporate) robust assessments for rare and seasonally “invisible” taxa, systematizing evidence and recommendations to reduce false absences and improve decision-making in the State of Rio de Janeiro. The thesis also evaluates microplastic contamination in rivulids from temporary environments and mangroves (Chapter 4: published in Wetlands Ecology and Management in 2026), demonstrating widespread exposure and refuting the hypothesis that temporary ponds serve as refuges from plastic pollution. Furthermore, it delves into life-history mechanisms and resilience in temporary wetlands by describing reproductive traits and trade-offs (Chapter 5: published in Wetlands in 2023). Finally, it synthesizes distribution data, population biology, and habitat loss for a focal species, highlighting the role of protected areas in mitigating habitat impacts (Chapter 6: published in Neotropical Ichthyology in 2023). By bridging cross-cutting disciplines (ecology, biogeography, and conservation biology), different actors (researchers, environmental agencies, and consultants), multi-scale approaches (the Neotropical Region, Brazil, and the state of Rio de Janeiro), long time periods (1985–2024), threatened species (up to 159 spp.), and theory and application, this thesis advances the goal of making conservation more “actionable” by translating ecological and biogeographic evidence into operational criteria for spatial planning, monitoring, and decision-making. It reinforces a critical point: conserving ephemeral habitats and seasonally “invisible” species depends on robust diagnoses and anticipatory decisions, built through multidisciplinary approaches and coordinated among multiple actors, so that scientific knowledge is converted into practice before silent losses become irreversibleen
dc.contributor.advisor1Araújo, Francisco Gerson-
dc.contributor.advisor1IDhttps://orcid.org/0000-0003-4551-1974pt_BR
dc.contributor.advisor1Latteshttp://lattes.cnpq.br/7898069293489622pt_BR
dc.contributor.referee1Araújo, Francisco Gerson-
dc.contributor.referee1IDhttps://orcid.org/0000-0003-4551-1974pt_BR
dc.contributor.referee1Latteshttp://lattes.cnpq.br/7898069293489622pt_BR
dc.contributor.referee2Santangelo, Jayme Magalhães-
dc.contributor.referee2Latteshttp://lattes.cnpq.br/8292200467538527pt_BR
dc.contributor.referee3Santos, Igor Cavalcanti de Araújo Souto-
dc.contributor.referee3IDhttps://orcid.org/0000-0001-8443-7039pt_BR
dc.contributor.referee3Latteshttp://lattes.cnpq.br/7935498665042507pt_BR
dc.contributor.referee4Lanés, Luis Esteban Krause-
dc.contributor.referee4Latteshttp://lattes.cnpq.br/4969483972915961pt_BR
dc.contributor.referee5Berbel Filho, Waldir Miron-
dc.contributor.referee5IDhttps://orcid.org/0000-0001-6991-4685pt_BR
dc.contributor.referee5Latteshttp://lattes.cnpq.br/5643358622376992pt_BR
dc.creator.IDhttps://orcid.org/0000-0001-8155-8337pt_BR
dc.creator.Latteshttp://lattes.cnpq.br/5066100936347376pt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.departmentInstituto de Ciências Biológicas e Da Saúdept_BR
dc.publisher.initialsUFRRJpt_BR
dc.publisher.programPrograma de Pós-Graduação em Biologia Animalpt_BR
dc.relation.referencesArenzon A, Carvalho Peret A, Camino Bohrer MB (1999) Reproduction of the annual fish Cynopoecilus melanotaenia (Regan, 1912) in a temporary water body in Rio Grande do sul, Brazil (Cyprinodontiformes, Rivulidae). Hydrobiologia (incorporating JAQU) 411:65–70. https://doi.org/10.1023/A:1003868711295 Arezo MJ, D’Alessandro S, Papa N, de Sá R, Berois N (2007) Sex differentiation pattern in the annual fish Austrolebias charrua (Cyprinodontiformes: Rivulidae). Tissue and Cell 39:89–98. https://doi.org/10.1016/j.tice.2007.01.004 Barneche DR, Robertson DR, White CR, Marshall DJ (2018a) Fish reproductive-energy output increases disproportionately with body size. Science 360(6389):642– 645. https://doi.org/10.1126/science.aao6868 Barneche DR, Burgess SC, Marshall DJ (2018b) Global environmental drivers of marine fish egg size. Global Ecology and Biogeography 27:890– 898. https://doi.org/10.1111/geb.12748 Berois N, Arezo MJ, Papa NG, Chalar C (2016) Cycle, Reproduction, and Development in Annual Fishes: Cellular and Molecular Aspects. In: Berois N, García G, de Sá RO (eds) Annual Fishes: life history strategy, diversity, and evolution. CRC Press, Boca Ratón, pp 33–46 156 Bonisławska M, Formicki K, Korzelecka-Orkisz A, Winnicki A (2001) Fish egg size variability: biological significance. Electronic Journal of Polish Agricultural Universities–Fisheries 4:1–15 Brown-Peterson NJ, Wyanski DM, Saborido-Rey F, Macewicz BJ, Lowerre-Barbieri SK (2011) A standardized terminology for describing reproductive development in fishes. Marine and Coastal Fisheries 3:52– 70. https://doi.org/10.1080/19425120.2011.555724 Calhoun AJK, Mushet DM, Bell KP, Boix D, Fitzsimons JA, Isselin-Nondedeu F (2017) Temporary wetlands: challenges and solutions to conserving a ‘disappearing’ ecosystem. Biological Conservation 211:3– 11. https://doi.org/10.1016/j.biocon.2016.11.024 Cassel M, Mehanna M, Mateus L, Ferreira A (2013) Gametogenesis and reproductive cycle of Melanorivulus aff. Punctatus (Boulenger, 1895) (Cyprinodontiformes, Rivulidae) in Chapada dos Guimarães, Mato Grosso, Brazil. Neotropical Ichthyology 11(1):179–192. https://doi.org/10.1590/S1679-62252013000100021 Castro RMC, Polaz CNM (2020) Small-sized fish: the largest and most threatened portion of the megadiverse neotropical freshwater fish fauna. Biota Neotropica 20:e20180683. https://doi.org/10.1590/1676-0611-bn-2018-0683 Cavalheiro LW, Fialho CB (2015) Reproductive strategy of a non-annual rivulid in a perennial wetland. Iheringia 105:288–296. https://doi.org/10.1590/1678- 476620151053288296 Costa WJEM (2008) Monophyly and taxonomy of the neotropical seasonal killifish genus Leptolebias (Teleostei: Aplocheiloidei: Rivulidae), with the description of a new genus. Zoological Journal of the Linnean Society 153:147– 160. https://doi.org/10.1111/j.1096-3642.2008.00380.x Costa WJEM, Leal F (2009) Egg surface morphology in the neotropical seasonal killifish genus Leptolebias (Teleostei: Aplocheiloidei: Rivulidae). Vertebrate Zoology 59:25– 29 Costa WJEM (2016) Comparative morphology and classification of south american cynopoeciline killifishes (Cyprinodontiformes: Aplocheilidae), with notes on family- group names used for aplocheiloids. Vertebrate Zoology 66:125–140 Costa WJEM, Amorim PF, Mattos JLO (2016) Molecular phylogeny and evolution of internal fertilization in south american seasonal cynopoeciline killifishes. Molecular Phylogenetics and Evolution 95:94– 99. https://doi.org/10.1016/j.ympev.2015.11.011 Costa WJEM (2019) Description of a new species of cynopoeciline killifish (Cyprinodontiformes, Aplocheilidae), possibly extinct, from the Atlantic Forest of south-eastern Brazil. ZooKeys 867:73– 85. https://doi.org/10.3897/zookeys.867.34034 157 Domínguez-Castanedo O, Uribe MC (2019) Reproductive biology in males of the annual killifish Millerichthys robustus (Cyprinodontiformes: Cynolebiidae). Environmental Biology of Fishes 102:1365–1375. https://doi.org/10.1007/s10641-019-00912-4 Domínguez-Castanedo O, Uribe MC, Rosales-Torres AM (2017) Life history strategies of annual killifish Millerichthys robustus (Cyprinodontiformes:Cynolebiidae) in a seasonally ephemeral water body in Veracruz, México. Environmental Biology of Fishes 100(8):995–1006. https://doi.org/10.1007/s10641-017-0617-y Domínguez-Castanedo O, Valdez-Carbajal S, Muñoz-Campos TM, Huber JH, Reichard M (2022) Protogynous functional hermaphroditism in the north american annual killifish, Millerichthys robustus. Scientific Reports 12:9230. https://doi.org/10.1038/s41598-022-12947-2 Duarte CM, Alcaraz M (1989) To produce many small or few large eggs: a size- independent reproductive tactic of fish. Oecologia 80:401– 404. https://doi.org/10.1007/BF00379043 Earley RL, Hanninen AF, Fuller A, Garcia MJ, Lee EA (2012) Phenotypic plasticity and integration in the mangrove rivulus (Kryptolebias marmoratus): a prospectus. Integrative and Comparative Biology 52:814– 827. https://doi.org/10.1093/icb/ics118 Edgar RC (2004) MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Research 32:1792– 1797. https://doi.org/10.1093/nar/gkh340 Einum S, Hendry AP, Fleming IA (2002) Egg-size evolution in aquatic environments: does oxygen availability constrain size? Proceedings of the Royal Society of London. Series B 269:2325–2330. https://doi.org/10.1098/rspb.2002.2150 Evangelista M, Romagosa E, Siqueira-Silva D, Yasui G, Fujimoto T, Senhorini J (2021) Reproductive strategies and chromosomal aberrations affect survival in the Rivuliid fish Hypsolebias sertanejo. Zygote 29:20– 26. https://doi.org/10.1017/S0967199420000362 Eckerström-Liedholm S, Sowersby W, Gonzalez-Voyer A, Rogell B (2017) Time-limited environments affect the evolution of egg–body size allometry. Evolution 71:1900– 1910. https://doi.org/10.1111/evo.13286 Feiner ZS, Wang HY, Einhouse D et al (2016) Thermal environment and maternal effects shape egg size in a freshwater fish. Ecosphere 7(5):e01304. https://doi.org/10.1002/ecs2.1304 Froese R, Pauly D (2022) Fish Base. Electronic version accessed in October 2022. www.fishbase.org Fricke R, Eschmeyer WN, Van der Laan R (2022) Eschmeyer’s catalog of fishes: genera, species, references. California Academy of Science, San Francisco. Electronic version accessed in October 2022. http://researcharchive.calacademy.org/research/ichthyology/catalog/fishcat main.asp 158 Furness AI (2016) The evolution of an annual life cycle in killifish: adaptation to ephemeral aquatic environments through embryonic diapause. Biological Reviews 91:796– 812. https://doi.org/10.1111/brv.12194 Gonçalves CS, Souza UP, Volcan MV (2011) The opportunistic feeding and reproduction strategies of the annual fish Cynopoecilus melanotaenia (Cyprinodontiformes: Rivulidae) inhabiting ephemeral habitats on southern Brazil. Neotropical Ichthyology 9:191–200. https://doi.org/10.1590/S1679-62252011000100019 Grasel D, Mormul RP, Bozelli RL, Thomaz SM, Jarenkow JA (2018) Brazil’s native vegetation protection law threatens to collapse pond functions. Perspectives in Ecology and Conservation 16:234– 237. https://doi.org/10.1016/j.pecon.2018.08.003 Guedes GHS, Salgado FLK, Uehara W, Ferreira DLP, Araújo FG (2020) The recapture of Leptopanchax opalescens (Aplocheiloidei: Rivulidae), a critically endangered seasonal killifish: habitat and aspects of population structure. Zoologia 37:1– 8. https://doi.org/10.3897/zoologia.37.e54982 Handy SM, Deeds JR, Ivanova NV, Hebert PDN, Hanner RH, Moore MM, Yancy HF (2011) A single laboratory validated method for the generation of dna barcodes for the identification of fish for regulatory compliance. Journal of AOAC International 94:201–210. https://doi.org/10.1093/jaoac/94.1.201 Hartig F (2022) Package ‘DHARMa’. http://florianhartig.github.io/DHARMa/, https://cran.r- project.org/web/packages/DHARMa/DHARMa.pdf. Accessed 19 June 2022 Hebert PDN, Cywinska A, Ball SL, de Waard JR (2003a) Biological identifications through DNA barcodes. Proceedings of the Royal Society B 270:313– 321. https://doi.org/10.1098/rspb.2002.2218 Hebert PDN, Ratnasingham S, de Waard JR (2003b) Barcoding animal life: cytochrome c oxidase subunit 1 divergences among closely related species. Proceedings of the Royal Society B 270(Supplement 1):596– 599. https://doi.org/10.1098/rsbl.2003.0025 Hill MJ, Greaves HM et al (2021) Pond ecology and conservation: research priorities and knowledge gaps. Ecosphere 12:e03853. https://doi.org/10.1002/ecs2.3853 Hirshfield MF, Tinkle DW (1975) Natural selection and the evolution of reproductive effort. Proceedings of the National Academy of Sciences of the United States of America 72:2227–2231. https://doi.org/10.1073/pnas.72.6.2227 ICMBio (2018) Livro Vermelho da Fauna Brasileira Ameaçada de Extinção. Instituto Chico Mendes de Conservação da Biodiversidade, Brasília Iglesias-Rios R, Lobón-Cervià J, Amaral CRL, Garber R, Mazzoni R (2022) Egg size is a good predictor of parental care behaviour among bony fishes. Ecology of Freshwater Fish 31:492–498. https://doi.org/10.1111/eff.12645 Jennings WB (2017) Phylogenomic data acquisition: principles and practice. CRC Press/Taylor and Francis, Boca Raton. https://doi.org/10.1201/9781315181431 159 Jennings WB, Ruschi PA, Ferraro G, Quijada CC, SilvaMalanski ACG, Prosdocimi F, Buckup PA (2019) Barcoding the neotropical freshwater fish fauna using a new pair of universal COI primers with a discussion of primer dimers and M13 primer tails. Genome 62:77–83. https://doi.org/10.1139/gen-2018-0145 Junk WJ, Piedade MTF, Lourival R, Wittmann F, Kandus P, Lacerda LD, Bozelli RL, Esteves FA, Nunes da Cunha C, Maltchik L, Schöngart J, Schaeffer-Novelli Y, Agostinho AA (2014) Brazilian wetlands: their definition, delineation, and classification for research, sustainable management, and protection. Aquatic Conservation: Marine and Freshwater Ecosystems 24(1):5–22. https://doi.org/10.1002/aqc.2386 Kimura M (1980) A simple method for estimating evolutionary rate of base substitutions through comparative studies of nucleotide sequences. Journal of Molecular Evolution 16:111–120. https://doi.org/10.1007/BF01731581 Kumar S, Stecher G, Li K, Knyaz C, Tamura K (2018) MEGA X: Molecular Evolutionary Genetics Analysis across computing platforms. Molecular Biology and Evolution 35:1547–1549. https://doi.org/10.1093/molbev/msy096 Lis JT (1980) Fractionation of DNA fragments by polyethylene glycol induced precipitation. Methods in Enzymology 65:347–353. https://doi.org/10.1016/s0076- 6879(80)65044-7 Loureiro M, Sá RO, Serra SW, Alonso F, Lanés LEK, Volcan MV, Calviño PA, Nielsen D, Duarte A, García G (2018) Review of the family Rivulidae (Cyprinodontiformes, Aplocheiloidei) and a molecular and morphological phylogeny of the annual fish genus Austrolebias Costa 1998. Neotropical Ichthyology 16:1– 20. https://doi.org/10.1590/1982-0224-20180007 Lowe-McConnell RH (1987) Ecological Studies in Tropical Fish Communities. Cambridge University Press, Cambridge. https://doi.org/10.1017/CBO9780511721892 McBride RS, Somarakis S, Fitzhugh GR, Albert A, Yaragina NA, Wuenschel MJ, Alonso- Fernández A, Basilone G (2015) Energy acquisition and allocation to egg production in relation to fish reproductive strategies. Fish and Fisheries 16:23– 57. https://doi.org/10.1111/faf.12043 Marshall DJ, Pettersen AK, Cameron H (2018) A global synthesis of offspring size variation, its eco-evolutionary causes and consequences. Functional Ecology 32:1436– 1446. https://doi.org/10.1111/1365-2435.13099 Malabarba LR, Malabarba MC (2020) Phylogeny and classification of Neotropical fish. In: Baldisserotto B, Urbinati EC, Cyrino JEP (Eds) Biology and Physiology of Freshwater Neotropical Fish, Academic. https://doi.org/10.1016/B978-0-12-815872-2.00001-4 Miller SA, Dykes DD, Polesky HFRN (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Research 16:1215. https://doi.org/10.1093/nar/16.3.1215 Murphy WJ, Collier GE (1997) A molecular phylogeny for aplocheiloid fishes (Atherinomorpha, Cyprinodontiformes): the role of vicariance and the origins of 160 annualism. Molecular Biology and Evolution 14(8):790– 799. https://doi.org/10.1093/oxfordjournals.molbev.a025819 Murphy WJ, Thomerson JE, Collier GE (1999) Phylogeny of the neotropical killifish Family Rivulidae (Cyprinodontiformes, Aplocheiloidei) inferred from mitochondrial DNA sequences. Molecular Phylogenetics and Evolution 13:289– 301. https://doi.org/10.1006/mpev.1999.0656 Parenti LR, Grier HJ (2004) Evolution and phylogeny of gonad morphology in bony fishes. Integrative and Comparative Biology 44:333– 348. https://doi.org/10.1093/icb/44.5.333 Patil I (2021) Visualizations with statistical details: the ‘ggstatsplot’ approach. Journal of Open Source Software 6:3167. https://doi.org/10.21105/joss.03167 Pereira LHG, Hanner R, Foresti F, Oliveira C (2013) Can DNA barcoding accurately discriminate megadiverse neotropical freshwater fish fauna. BMC Genetics 14:20. https://doi.org/10.1186/1471-2156-14-20 Pettersen AK, White CR, Bryson-Richardson RJ, Marshall DJ (2018) Does the cost of development scale allometrically with offspring size? Functional Ecology 32:762– 772. https://doi.org/10.1111/1365-2435.13015 Polačik M, Blažek R, Reichard M (2016) Laboratory breeding of the short-lived annual killifish Nothobranchius furzeri Nature Protocols 11:1396– 1413. https://doi.org/10.1038/nprot.2016.080 Polačik M, Vrtílek M, Reichard M, Žák J, Blažek R, Podrabsky J (2021) Embryo ecology: Developmental synchrony and asynchrony in the embryonic development of wild annual fish populations. Ecology and Evolution 11:4945– 4956. https://doi.org/10.1002/ece3.7402 Podrabsky JE, Lopez JP, Fan TWM, Higashi R, Somero GN (2007) Extreme anoxia tolerance in embryos of the annual killifish Austrofundulus limnaeus: insights from a metabolomics analysis. The Journal of Experimental Biology 210:2253– 2266. https://doi.org/10.1242/jeb.005116 Podrabsky JE, Riggs CL, Wagner JT (2016) Tolerance of Environmental Stress. In: Berois N, García G, de Sá RO (Eds) Annual Fishes: life history strategy, diversity, and evolution. CRC Press, Boca Ratón R Core Team (2022) R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna. https://www.R-project.org/ Reichard M (2016) The Evolutionary Ecology of African Annual Fishes. In: Berois N, García G, de Sá RO (eds) Annual Fishes: life history strategy, diversity, and evolution. CRC Press, Boca Ratón, pp 133–158 Rollinson N, Hutchings JA (2013) Environmental quality predicts optimal egg size in the Wild. The American Naturalist 182:76–90. https://doi.org/10.1086/670648 161 Riesch R, Plath M, Schlupp I, Tobler M, Brian LR, Gaillard JM (2014) Colonisation of toxic environments drives predictable life-history evolution in livebearing fishes (Poeciliidae). Ecology Letters 17(1):65–71. https://doi.org/10.1111/ele.12209 Rizzo E, Bazzoli N (2020) Reproduction and embryogenesis. In: Baldisserotto B, Urbinati EC, Cyrino JEP (eds) Biology and Physiology of Freshwater Neotropical Fish. Academic, London, pp 287–313. https://doi.org/10.1016/B978-0-12-815872- 2.00013-0 Santi F, Vella E, Jeffress K, Deacon A, Riesch R (2021) Phenotypic responses to oil pollution in a poeciliid fish. Environmental Pollution 290:118023. https://doi.org/10.1016/j.envpol.2021.118023 Schalk CM, Montaña CG, Libson ME (2014) Reproductive strategies of two neotropical killifish, Austrolebias vandenbergi and Neofundulus ornatipinnis (Cyprinodontiformes: Rivulidae) in the bolivian Gran Chaco. Revista de Biologia Tropical 62:09–117 Silva GG, Weber V, Green AJ, Hoffmann P, Silva VS, Volcan M, Lanés LEK, Stenert C, Reichard M, Maltchik L (2019) Killifish eggs can disperse via gut passage through waterfowl. Ecology 100:1–4. https://doi.org/10.1002/ecy.2774 Smith CC, Fretwell SD (1974) The optimal balance between size and number of offspring. The American Naturalist 108:499–506. https://doi.org/10.1086/282929 Souto-Santos ICA, Donadia WGR, Bauer AB, Abreu LAS, Buckup PA (2021) Poça de esperança no meio da cidade grande: Leptopanchax opalescens (Myers, 1942) numa floresta urbana do município do Rio de Janeiro, Brasil (Cyprinodontiformes: Rivulidae). Boletim Sociedade Brasileira de Ictiologia 135:6–10 Thompson AW, Furness AI, StoneC, Rade CM, Ortí G (2017) Microanatomical diversification of the zona pellucida in aplochelioid killifishes. Journal of Fish Biology 91:126–143. https://doi.org/10.1111/jfb.13332 Uribe MC, Grier HJ, Mejía-Roa V (2015) Comparative testicular structure and spermatogenesis in bony fishes. Spermatogenesis 4(3):e983400. https://doi.org/10.4161/21565562.2014.983400 Vazzoler AEAM (1996) Biologia da reprodução de peixes teleósteos: teoria e prática. EDUEM, Brazil Volcan MV, Fonseca AP, Robaldo RB (2011) Reproduction of the threatened annual killifish Austrolebias nigrofasciatus (Cyprinodontiformes: Rivulidae), confined in a natural environment. Journal of Threatened Taxa 3:1864– 1867. https://doi.org/10.11609/JoTT.o2575.1864-7 Volcan MV, Guadagnin DL (2020) Annual and non-annual fish assemblages respond differently to environmental and spatiotemporal variations of temporary wetlands from southern Brazil. Freshwater Biology 65:2023– 2036. https://doi.org/10.1111/fwb.13589 162 Vrtílek M, Reichard M (2015) Highly plastic resource allocation to growth and reproduction in females of an african annual fish. Ecology of Freshwater Fish 24:616–628. https://doi.org/10.1111/eff.12175 Winemiller KO, Rose KA (1992) Patterns of life-history diversification in north american fishes: implications for population regulation. Canadian Journal of Fisheries and Aquatic Sciences 49:2196–2218. https://doi.org/10.1139/f92-242 Wotton RJ, Smith C (2015) Reproductive biology of teleost fishes. Wiley, Chichester. https://doi.org/10.1002/9781118891360 Wourms JP, Sheldon H (1976) Annual fish oogenesis: II. Formation of the secondary egg envelope. Developmental Biology 50:355–366. https://doi.org/10.1016/0012- 1606(76)90157-3 Žák J, Vrtílek M, Polačik M, Blažek R, Reichard M (2021) Short-lived fishes: Annual and multivoltine strategies. Fish and Fisheries 22:546– 561. https://doi.org/10.1111/faf.12535 Zandona E, Kajin M, Buckup PA, Amaral JR, Souto-Santos ICA, Reznick DN (2021) Mode of maternal provisioning in the fish genus Phalloceros: a variation on the theme of matrotrophy. Biological Journal of the Linnean Society 134(4):867– 878. https://doi.org/10.1093/biolinnean/blab121pt_BR
dc.subject.cnpqBiologia Geralpt_BR
dc.subject.cnpqEcologiapt_BR
Aparece nas coleções:Doutorado em Biologia Animal

Se for cadastrado no RIMA, poderá receber informações por email.
Se ainda não tem uma conta, cadastre-se aqui!

Arquivos associados a este item:
Arquivo Descrição TamanhoFormato 
GUSTAVO HENRIQUE SOARES GUEDES.pdf5,63 MBAdobe PDFAbrir


Os itens no repositório estão protegidos por copyright, com todos os direitos reservados, salvo quando é indicado o contrário.