Population structure and fecundity of Upogebia omissa (Decapoda: Gebiidea: Upogebiidae) in an estuarine region in Sergipe, northeastern Brazil

Detalhes bibliográficos
Autor(a) principal: Santos, Rafael de Carvalho
Data de Publicação: 2018
Outros Autores: Santos Silva, Luiz Filipe, dos Santos, Bruna, Motta, Juliana Menezes, Rodrigues Alves, Douglas Fernandes
Tipo de documento: Artigo
Idioma: por
Título da fonte: Pesquisa e Ensino em Ciências Exatas e da Natureza
Texto Completo: https://cfp.revistas.ufcg.edu.br/cfp/index.php/RPECEN/article/view/1064
Resumo: Camarões de lama da família Upogebiidae são organismos importantes de comunidades de substrato não consolidado, onde eles cavam tocas agindo como engenheiros ecossistêmicos. O presente estudo descreve alguns parâmetros da estrutura populacional e biologia reprodutiva do camarão de lama Upogebia omissa. A coleta dos indivíduos foi realizada no estuário do rio Vaza-Barris, estado de Sergipe, nordeste do Brasil. Em laboratório, os espécimes foram sexados e mensurados quanto ao comprimento da carapaça (CL). Fêmeas ovígeras tiveram o total de ovos contados. O tamanho do corpo variou entre 3,0 e 12,9 mm CL, sendo os machos significativamente menores que as fêmeas. A razão sexual média foi de 0,34, voltado para as fêmeas (teste binomial, P = 0,001). A fecundidade variou de 240 a 2339 ovos por fêmea, e foi significativamente afetada pelo tamanho do corpo. Dimorfismo sexual evidenciado pelo tamanho médio de cada sexo é um padrão comum em decápodes que incubam ovos, e nesse caso, a fecundidade normalmente varia em função do tamanho do corpo. Por fim, sugerimos que estudos adicionais são necessários, devido à importância ecológica desses camarões de lama e da escassez de estudos sobre eles.Palavras chave: Fecundidade, dimorfismo sexual, camarão de lama, estuário.
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spelling Population structure and fecundity of Upogebia omissa (Decapoda: Gebiidea: Upogebiidae) in an estuarine region in Sergipe, northeastern BrazilCamarões de lama da família Upogebiidae são organismos importantes de comunidades de substrato não consolidado, onde eles cavam tocas agindo como engenheiros ecossistêmicos. O presente estudo descreve alguns parâmetros da estrutura populacional e biologia reprodutiva do camarão de lama Upogebia omissa. A coleta dos indivíduos foi realizada no estuário do rio Vaza-Barris, estado de Sergipe, nordeste do Brasil. Em laboratório, os espécimes foram sexados e mensurados quanto ao comprimento da carapaça (CL). Fêmeas ovígeras tiveram o total de ovos contados. O tamanho do corpo variou entre 3,0 e 12,9 mm CL, sendo os machos significativamente menores que as fêmeas. A razão sexual média foi de 0,34, voltado para as fêmeas (teste binomial, P = 0,001). A fecundidade variou de 240 a 2339 ovos por fêmea, e foi significativamente afetada pelo tamanho do corpo. Dimorfismo sexual evidenciado pelo tamanho médio de cada sexo é um padrão comum em decápodes que incubam ovos, e nesse caso, a fecundidade normalmente varia em função do tamanho do corpo. Por fim, sugerimos que estudos adicionais são necessários, devido à importância ecológica desses camarões de lama e da escassez de estudos sobre eles.Palavras chave: Fecundidade, dimorfismo sexual, camarão de lama, estuário.Unidade Acadêmica de Ciências Exatas e da Natureza/CFP/UFCGSantos, Rafael de CarvalhoSantos Silva, Luiz Filipedos Santos, BrunaMotta, Juliana MenezesRodrigues Alves, Douglas Fernandes2018-12-28info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://cfp.revistas.ufcg.edu.br/cfp/index.php/RPECEN/article/view/106410.29215/pecen.v2i2.1064Pesquisa e Ensino em Ciências Exatas e da Natureza; v. 2, n. 2 (2018): Pesquisa e Ensino em Ciências Exatas e da Natureza2526-823610.29215/pecen.v2i2reponame:Pesquisa e Ensino em Ciências Exatas e da Naturezainstname:Universidade Federal de Campina Grande (UFCG)instacron:UFCGporhttps://cfp.revistas.ufcg.edu.br/cfp/index.php/RPECEN/article/view/1064/436/*ref*/Anderson F.O. & Kristensen E. (1991) Effects of burrowing macrofauna on organic matter decomposition in coastal marine sediments. Symposia of the Zoological Society of London, 63: 69–88./*ref*/Atkinson R.J.A. & Taylor A.C. (1988) Physiological ecology of burrowing decapods. Symposia of the Zoological Society of London, 59: 201–226./*ref*/Bauer R.T. & Martin J.W. (1991) Crustacean sexual biology. New York: Columbia University Press. 355 p./*ref*/Botter-Carvalho M.L., Costa L.B., Gomes L.L., Clemente C.C.C. & Carvalho P.V.V. da C. (2015) Reproductive biology and population structure of Axianassa australis (Crustacea, Axianassidae) on a sand-mud flat in north-east Brazil. Journal of the Marine Biological Association of the United Kingdom, 95: 735–745. DOI: 10.1017/S002531541400174X/*ref*/Byers J.E. & Grabowski J.H. (2014) Soft-sediment communities (p. 227–249). In: Bertness M.D., Bruno J.F., Silliman B.R. & Stachowicz J.J. (Eds). Marine Community Ecology and Conservation. Sunderland, Massachusetts: Sinauer Associates. 560 p. Carvalho M.E. & Fontes A.L. (2007) A carcinocultura no espaço litorâneo Sergipano. Revista da Fapese, 3: 87–112./*ref*/Coelho V.R., Cooper R.A. & Rodrigues S.A. (2000) Burrow morphology and behavior of the mud shrimp Upogebia omissa (Decapoda: Thalassinidea: Upogebiidae). Marine Ecology Progress Series, 200: 229–240. DOI: 10.3354/meps200229/*ref*/Coelho P.A., Almeida A.O., Bezerra, L.E.A. & Souza-Filho J.F. (2007) An updated checklist of decapod crustaceans (infraorders Astacidea, Thalassinidea, Polychelida, Palinura, and Anomura) from the northern and northeastern Brazilian coast. Zootaxa, 1519: 1–16. DOI: 10.11646/zootaxa.1519.1.1/*ref*/D’Andrea A.F.D. & DeWitt T.H. (2009) Geochemical ecosystem engineering by the mud shrimp Upogebia pugettensis (Crustacea: Thalassinidea) in Yaquina Bay, Oregon: Density-dependent effects on organic matter remineralization and nutrient cycling. Limnology and Oceanography, 54: 1911–1932. DOI: 10.4319/lo.2009.54.6.1911/*ref*/Das S., Tseng L., Wang L. & Hwang J. (2017) Burrow characteristics of the mud shrimp Austinogebia edulis, an ecological engineer causing sediment modification of a tidal flat. Plos One, 12: 1–17. DOI: 10.1371/journal.pone.0187647/*ref*/Dumbauld B.R., Armstrong D.A. & Feldman K.L. (1996) Life-history characteristics of two sympatric Thallassinidean shrimps, Neotropica californiensis and Upogebia pugettensis, with implications for oyster culture. Journal of Crustacean Biology, 16: 689–708./*ref*/Dumbauld B.R., Chapman J.W., Torchin M.E. & Kuris A.M. (2010) Is the collapse of mud shrimp (Upogebia pugettensis) populations along the Pacific Coast of North America caused by outbreaks of a previously unknown bopyrid isopod parasite (Orthione griffenis)? Estuaries and Coasts, 34: 336–350. DOI: 10.1007/s12237-010-9316-z/*ref*/Dworschak P.C. (1987) The biology of Upogebia pusilla (PETAGNA) (Decapoda, Thalassinidea) - II Environments and zonation. P.S.Z.N.I.: Marine Ecology, 8: 337–358./*ref*/Dworschak P.C. (1988) The biology of Upogebia pusilla (PETAGNA) (Decapoda, Thalassinidea) - III Growth and Production. P.S.Z.N.I.: Marine Ecology, 9: 51–77./*ref*/Dworschak P.C. (2000) Global diversity in the Thalassinidea (Decapoda). Journal of Crustacean Biology, 20: 238–245. DOI: 10.1163/1937240X-90000025/*ref*/Felder D.L. & Lovett D.L. (1989) Relative growth and sexual maturation in the estuarine ghost shrimp Callianassa louisianensis Schmitt, 1935. Journal of Crustacean Biology, 9: 540–553. DOI: 10.2307/1548586/*ref*/Griffis R.B. & Suchanek T.H. (1991) A model of burrow architecture and trophic modes in thalassinidean shrimp (Decapoda: Thalassinidea). Marine Ecology Progress Series, 79: 171–183. DOI: 10.3354/meps079171/*ref*/Hanekon N. & Erasmus T. (1989) Determinations of the reproductive output of populations of thalassinid prawn Upogebia africana (Ortmann) in the Swartkops estuary. South African Journal of Zoology, 24: 244–250. DOI: 10.1080/02541858.1989.11448160 Hanekon N. & Baird D. (1992) Growth, production and consumption of the thallasinid prawn Upogebia afriana (Ortmann) in the Swartkops estuary. South African Journal of Zoology, 27: 130–139. DOI: 10.1080/02541858.1992.11448273/*ref*/Hill B.J. (1977) The effect of heated effluent on egg production in the estuarine prawn Upogebia africana (Ortmann). Journal of Experimental Marine Biology and Ecology, 29: 291–302. DOI: 10.1016/0022-0981(77)90072-7/*ref*/Hirose L.H., Souza L.S., Silva S.L.R., Alves D.F.R. & Negreiros-Fransozo M.L. (2015) Population structure of the red mangrove crab, Goniopsis cruentata (Decapoda: Grapsidae) under different fishery impacts: Implications for resource management. Revista de Biologia Tropical, 63: 443–457. DOI: 10.15517/rbt.v63i2.15432/*ref*/Jones C.G., Lawton J.H. & Shachak M. (1994) Organism as ecosystem engineers. Oikos, 69: 373–386. DOI: 10.1007/978-1-4612-4018-1_14/*ref*/Jugovic J., Horvat E. & Lipej L. (2017) Seasonal abundance, vertical distribution and life history traits of Mediterranean mud shrimp Upogebia pusilla (Decapoda: Gebiidea) on the Slovenian coast. Acta Adriatica, 58: 297–312./*ref*/Kevrekidis T., Gouvis N. & Koukouras A. (1997) Population dynamics, reproduction and growth of Upogebia pusilla (Decapoda, Thalassinidea) in the Evros Delta (North Egean Sea). Crustaceana, 70: 799–812. DOI: 10.1163/156854097X00249/*ref*/Kinoshita K. & Itani G. (2005) Interspecific differences in the burrow morphology between the sympatric mud shrimp, Austinogebia narutensis and Upogebia issaeffi (Crustacea: Thalassinidea: Upogebiidae). Journal of the Marine Biological Association of the United Kingdom, 85: 943–947. DOI: 10.1017/S0025315405011926/*ref*/Kinoshita K., Itani G. & Uchino T. (2010) Burrow morphology and associated animals of the mud shrimp Upogebia yokoyai (Crustacea: Thalassinidea: Upogebiidae). Journal of the Marine Biological Association of the United Kingdom, 90: 947–952. DOI: 10.1017/S002531541 0000214/*ref*/Meadows P.S. & Meadows A. (1991) The environmental impact of burrowing animals and animal burrows. Oxford: Clarendon Press for the Zoological Society of London. 349 p./*ref*/Melo G.A.S. (1999) Manual de identificação dos Crustacea Decapoda do litoral brasileiro: Anomura, Thalassinidea, Palinuridea e Astacidea. São Paulo: Ed.Plêiade/FAPESP. 551 p./*ref*/Moraes I.R.R., Wolf M.R., Gonçalves G.R.L. & Castilho A.L. (2017) Fecundity and reproductive output of the caridean shrimp Periclimenes paiva associated with scyphozoan jellyfish. Invertebrate Reproduction & Development, 61: 71–77. DOI: 10.1080/07924259.2017.1282890/*ref*/Nickell L.A. & Atkinson R.J.A. (1995) Functional morphology of burrows and trophic modes of three thalassinidean shrimp species, and a new approach to the classification of thalassinidean burrow morphology. Marine Ecology Progress Series, 128: 181–197. DOI: 10.3354/meps128181/*ref*/Pandian T.J. (2016) Reproduction and development in Crustacea. New York: CRC Press, Taylor & Francis Group. 315 p. Pinn E.H., James R., Atkinson A. & Rogerson A. (2001) Sexual dimorphism and intersexuality in Upogebia stellate (Crustacea: Decapoda: Thalassinidea). Journal of the Marine Biological Association of the United Kingdom, 81: 1061–1062./*ref*/Poore G.C.B. (2016) The names of the higher taxa of Crustacea Decapoda. Journal of Crustacean Biology, 36: 248–255. DOI: 10.1163/1937240X-00002415/*ref*/Robles R., Tudge C.C., Dworschak P.C., Poore G.C.B. & Felder D.L. (2009) Molecular phylogeny of the Thalassinidea based on nuclear and mithocondrial genes (p. 309–326). In: Martin J.W., Crandal K.A. & Felder D.L. (Eds). Decapod Crustacean phylogenetics. Volume 18. Boca Raton: CRC Press. 633 p./*ref*/Rotherham D. & West R.J. (2009) Patterns in reproductive dynamics of burrowing ghost shrimp Trypaea australiensis from small to intermediate scales. Marine Biology, 156: 1277–1287. DOI: 10.1007/s00227-009-1169-2/*ref*/Selin N.I. (2014) Some features of the biology of the mud shrimp Upogebia issaeffi (Balls, 1913) (Decapoda: Upogebiidae) from the subtidal zone of Vostok Bay, Sea of Japan. Russian Journal of Marine Biology, 40: 24–29. DOI: 10.1134/S1063074014010088/*ref*/Tunberg B. (1986) Studies on the population ecology of Upogebia deltaura (Leach) (Crustacea, Thalassinidea). Estuarine, Coastal and Shelf Science, 22: 753–765./*ref*/Wehrtmann I.S. & Lardies M.A. (1999) Egg production of Austropandalus grayi (Decapoda, Caridea, Pandalidae) from the Magellan region, South America. Scientia Marina, 63: 325–331./*ref*/Wenner A.M. (1972) Sex ratio as a function of size in marine Crustacea. American Naturalist, 106: 321–350./*ref*/Wilde P.A.W.J. (1991) Interactions in burrowing communities and their effects on the structure of marine benthic ecosystems (p. 107–117). In: Meadows P.S. & Meadows A. (Eds) The environmental impact of burrowing animals and animal burrows. London: Claredon Press. 349 p./*ref*/Wilson K. & Hardy I.C.W. (2002) Statistical analysis of sex ratios: an introduction (p. 48–92). In: Hardy I.C.W. (Eds). Sex Ratios: Concepts and Research Methods. Volume 1. Cambridge: Cambridge University Press. 424 p./*ref*/Yamasaki M., Nanri T., Taguchi S., Takada Y. & Saigusa M. (2010) Latitudinal and local variations of the life history characteristics of the thalassinidean decapod, Upogebia yokayai: A hypothesis based on trophic conditions. Estuarine, Coastal and Shelf Science, 87: 346–356./*ref*/Zar J.H. (2010) Biostatistical Analysis. 5º edição. Upper Saddle River: Prentice-Hall. 944 p.Direitos autorais 2018 Autor e Revista mantêm os direitos da publicaçãoinfo:eu-repo/semantics/openAccess2022-08-31T14:44:59Zoai:ojs.cfp.revistas.ufcg.edu.br:article/1064Revistahttps://cfp.revistas.ufcg.edu.br/cfp/index.php/RPECENPUBhttps://cfp.revistas.ufcg.edu.br/cfp/index.php/RPECEN/oai||cienciasexatasenatureza@gmail.com2526-82362526-8236opendoar:2022-08-31T14:44:59Pesquisa e Ensino em Ciências Exatas e da Natureza - Universidade Federal de Campina Grande (UFCG)false
dc.title.none.fl_str_mv Population structure and fecundity of Upogebia omissa (Decapoda: Gebiidea: Upogebiidae) in an estuarine region in Sergipe, northeastern Brazil
title Population structure and fecundity of Upogebia omissa (Decapoda: Gebiidea: Upogebiidae) in an estuarine region in Sergipe, northeastern Brazil
spellingShingle Population structure and fecundity of Upogebia omissa (Decapoda: Gebiidea: Upogebiidae) in an estuarine region in Sergipe, northeastern Brazil
Santos, Rafael de Carvalho
title_short Population structure and fecundity of Upogebia omissa (Decapoda: Gebiidea: Upogebiidae) in an estuarine region in Sergipe, northeastern Brazil
title_full Population structure and fecundity of Upogebia omissa (Decapoda: Gebiidea: Upogebiidae) in an estuarine region in Sergipe, northeastern Brazil
title_fullStr Population structure and fecundity of Upogebia omissa (Decapoda: Gebiidea: Upogebiidae) in an estuarine region in Sergipe, northeastern Brazil
title_full_unstemmed Population structure and fecundity of Upogebia omissa (Decapoda: Gebiidea: Upogebiidae) in an estuarine region in Sergipe, northeastern Brazil
title_sort Population structure and fecundity of Upogebia omissa (Decapoda: Gebiidea: Upogebiidae) in an estuarine region in Sergipe, northeastern Brazil
author Santos, Rafael de Carvalho
author_facet Santos, Rafael de Carvalho
Santos Silva, Luiz Filipe
dos Santos, Bruna
Motta, Juliana Menezes
Rodrigues Alves, Douglas Fernandes
author_role author
author2 Santos Silva, Luiz Filipe
dos Santos, Bruna
Motta, Juliana Menezes
Rodrigues Alves, Douglas Fernandes
author2_role author
author
author
author
dc.contributor.none.fl_str_mv
dc.contributor.author.fl_str_mv Santos, Rafael de Carvalho
Santos Silva, Luiz Filipe
dos Santos, Bruna
Motta, Juliana Menezes
Rodrigues Alves, Douglas Fernandes
description Camarões de lama da família Upogebiidae são organismos importantes de comunidades de substrato não consolidado, onde eles cavam tocas agindo como engenheiros ecossistêmicos. O presente estudo descreve alguns parâmetros da estrutura populacional e biologia reprodutiva do camarão de lama Upogebia omissa. A coleta dos indivíduos foi realizada no estuário do rio Vaza-Barris, estado de Sergipe, nordeste do Brasil. Em laboratório, os espécimes foram sexados e mensurados quanto ao comprimento da carapaça (CL). Fêmeas ovígeras tiveram o total de ovos contados. O tamanho do corpo variou entre 3,0 e 12,9 mm CL, sendo os machos significativamente menores que as fêmeas. A razão sexual média foi de 0,34, voltado para as fêmeas (teste binomial, P = 0,001). A fecundidade variou de 240 a 2339 ovos por fêmea, e foi significativamente afetada pelo tamanho do corpo. Dimorfismo sexual evidenciado pelo tamanho médio de cada sexo é um padrão comum em decápodes que incubam ovos, e nesse caso, a fecundidade normalmente varia em função do tamanho do corpo. Por fim, sugerimos que estudos adicionais são necessários, devido à importância ecológica desses camarões de lama e da escassez de estudos sobre eles.Palavras chave: Fecundidade, dimorfismo sexual, camarão de lama, estuário.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-28
dc.type.none.fl_str_mv
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://cfp.revistas.ufcg.edu.br/cfp/index.php/RPECEN/article/view/1064
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url https://cfp.revistas.ufcg.edu.br/cfp/index.php/RPECEN/article/view/1064
identifier_str_mv 10.29215/pecen.v2i2.1064
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dc.relation.none.fl_str_mv https://cfp.revistas.ufcg.edu.br/cfp/index.php/RPECEN/article/view/1064/436
/*ref*/Anderson F.O. & Kristensen E. (1991) Effects of burrowing macrofauna on organic matter decomposition in coastal marine sediments. Symposia of the Zoological Society of London, 63: 69–88.
/*ref*/Atkinson R.J.A. & Taylor A.C. (1988) Physiological ecology of burrowing decapods. Symposia of the Zoological Society of London, 59: 201–226.
/*ref*/Bauer R.T. & Martin J.W. (1991) Crustacean sexual biology. New York: Columbia University Press. 355 p.
/*ref*/Botter-Carvalho M.L., Costa L.B., Gomes L.L., Clemente C.C.C. & Carvalho P.V.V. da C. (2015) Reproductive biology and population structure of Axianassa australis (Crustacea, Axianassidae) on a sand-mud flat in north-east Brazil. Journal of the Marine Biological Association of the United Kingdom, 95: 735–745. DOI: 10.1017/S002531541400174X
/*ref*/Byers J.E. & Grabowski J.H. (2014) Soft-sediment communities (p. 227–249). In: Bertness M.D., Bruno J.F., Silliman B.R. & Stachowicz J.J. (Eds). Marine Community Ecology and Conservation. Sunderland, Massachusetts: Sinauer Associates. 560 p. Carvalho M.E. & Fontes A.L. (2007) A carcinocultura no espaço litorâneo Sergipano. Revista da Fapese, 3: 87–112.
/*ref*/Coelho V.R., Cooper R.A. & Rodrigues S.A. (2000) Burrow morphology and behavior of the mud shrimp Upogebia omissa (Decapoda: Thalassinidea: Upogebiidae). Marine Ecology Progress Series, 200: 229–240. DOI: 10.3354/meps200229
/*ref*/Coelho P.A., Almeida A.O., Bezerra, L.E.A. & Souza-Filho J.F. (2007) An updated checklist of decapod crustaceans (infraorders Astacidea, Thalassinidea, Polychelida, Palinura, and Anomura) from the northern and northeastern Brazilian coast. Zootaxa, 1519: 1–16. DOI: 10.11646/zootaxa.1519.1.1
/*ref*/D’Andrea A.F.D. & DeWitt T.H. (2009) Geochemical ecosystem engineering by the mud shrimp Upogebia pugettensis (Crustacea: Thalassinidea) in Yaquina Bay, Oregon: Density-dependent effects on organic matter remineralization and nutrient cycling. Limnology and Oceanography, 54: 1911–1932. DOI: 10.4319/lo.2009.54.6.1911
/*ref*/Das S., Tseng L., Wang L. & Hwang J. (2017) Burrow characteristics of the mud shrimp Austinogebia edulis, an ecological engineer causing sediment modification of a tidal flat. Plos One, 12: 1–17. DOI: 10.1371/journal.pone.0187647
/*ref*/Dumbauld B.R., Armstrong D.A. & Feldman K.L. (1996) Life-history characteristics of two sympatric Thallassinidean shrimps, Neotropica californiensis and Upogebia pugettensis, with implications for oyster culture. Journal of Crustacean Biology, 16: 689–708.
/*ref*/Dumbauld B.R., Chapman J.W., Torchin M.E. & Kuris A.M. (2010) Is the collapse of mud shrimp (Upogebia pugettensis) populations along the Pacific Coast of North America caused by outbreaks of a previously unknown bopyrid isopod parasite (Orthione griffenis)? Estuaries and Coasts, 34: 336–350. DOI: 10.1007/s12237-010-9316-z
/*ref*/Dworschak P.C. (1987) The biology of Upogebia pusilla (PETAGNA) (Decapoda, Thalassinidea) - II Environments and zonation. P.S.Z.N.I.: Marine Ecology, 8: 337–358.
/*ref*/Dworschak P.C. (1988) The biology of Upogebia pusilla (PETAGNA) (Decapoda, Thalassinidea) - III Growth and Production. P.S.Z.N.I.: Marine Ecology, 9: 51–77.
/*ref*/Dworschak P.C. (2000) Global diversity in the Thalassinidea (Decapoda). Journal of Crustacean Biology, 20: 238–245. DOI: 10.1163/1937240X-90000025
/*ref*/Felder D.L. & Lovett D.L. (1989) Relative growth and sexual maturation in the estuarine ghost shrimp Callianassa louisianensis Schmitt, 1935. Journal of Crustacean Biology, 9: 540–553. DOI: 10.2307/1548586
/*ref*/Griffis R.B. & Suchanek T.H. (1991) A model of burrow architecture and trophic modes in thalassinidean shrimp (Decapoda: Thalassinidea). Marine Ecology Progress Series, 79: 171–183. DOI: 10.3354/meps079171
/*ref*/Hanekon N. & Erasmus T. (1989) Determinations of the reproductive output of populations of thalassinid prawn Upogebia africana (Ortmann) in the Swartkops estuary. South African Journal of Zoology, 24: 244–250. DOI: 10.1080/02541858.1989.11448160 Hanekon N. & Baird D. (1992) Growth, production and consumption of the thallasinid prawn Upogebia afriana (Ortmann) in the Swartkops estuary. South African Journal of Zoology, 27: 130–139. DOI: 10.1080/02541858.1992.11448273
/*ref*/Hill B.J. (1977) The effect of heated effluent on egg production in the estuarine prawn Upogebia africana (Ortmann). Journal of Experimental Marine Biology and Ecology, 29: 291–302. DOI: 10.1016/0022-0981(77)90072-7
/*ref*/Hirose L.H., Souza L.S., Silva S.L.R., Alves D.F.R. & Negreiros-Fransozo M.L. (2015) Population structure of the red mangrove crab, Goniopsis cruentata (Decapoda: Grapsidae) under different fishery impacts: Implications for resource management. Revista de Biologia Tropical, 63: 443–457. DOI: 10.15517/rbt.v63i2.15432
/*ref*/Jones C.G., Lawton J.H. & Shachak M. (1994) Organism as ecosystem engineers. Oikos, 69: 373–386. DOI: 10.1007/978-1-4612-4018-1_14
/*ref*/Jugovic J., Horvat E. & Lipej L. (2017) Seasonal abundance, vertical distribution and life history traits of Mediterranean mud shrimp Upogebia pusilla (Decapoda: Gebiidea) on the Slovenian coast. Acta Adriatica, 58: 297–312.
/*ref*/Kevrekidis T., Gouvis N. & Koukouras A. (1997) Population dynamics, reproduction and growth of Upogebia pusilla (Decapoda, Thalassinidea) in the Evros Delta (North Egean Sea). Crustaceana, 70: 799–812. DOI: 10.1163/156854097X00249
/*ref*/Kinoshita K. & Itani G. (2005) Interspecific differences in the burrow morphology between the sympatric mud shrimp, Austinogebia narutensis and Upogebia issaeffi (Crustacea: Thalassinidea: Upogebiidae). Journal of the Marine Biological Association of the United Kingdom, 85: 943–947. DOI: 10.1017/S0025315405011926
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dc.rights.driver.fl_str_mv Direitos autorais 2018 Autor e Revista mantêm os direitos da publicação
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Direitos autorais 2018 Autor e Revista mantêm os direitos da publicação
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Unidade Acadêmica de Ciências Exatas e da Natureza/CFP/UFCG
publisher.none.fl_str_mv Unidade Acadêmica de Ciências Exatas e da Natureza/CFP/UFCG
dc.source.none.fl_str_mv Pesquisa e Ensino em Ciências Exatas e da Natureza; v. 2, n. 2 (2018): Pesquisa e Ensino em Ciências Exatas e da Natureza
2526-8236
10.29215/pecen.v2i2
reponame:Pesquisa e Ensino em Ciências Exatas e da Natureza
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instname_str Universidade Federal de Campina Grande (UFCG)
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reponame_str Pesquisa e Ensino em Ciências Exatas e da Natureza
collection Pesquisa e Ensino em Ciências Exatas e da Natureza
repository.name.fl_str_mv Pesquisa e Ensino em Ciências Exatas e da Natureza - Universidade Federal de Campina Grande (UFCG)
repository.mail.fl_str_mv ||cienciasexatasenatureza@gmail.com
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