Unraveling the mating system of the burrowing shrimp Lepidophthalmus siriboia (Decapoda Callichiridae) based on life history traits

REFERENCES

• Alcock J. 2001. Animal behavior: an evolutionary approach. Sunderland (MA): Sinauer Associates, Inc.
   Google Scholar
• Alves DFR, de Paiva Barros-Alves S, de Almeida AC, Cobo VJ, Bauer RT. 2021. Mating system of the snapping shrimp Synalpheus brevicarpus (Caridea, Alpheidae) inhabiting sponges Dysidea sp. (Demospongiae). Biol Bull. 240:132–143. doi:10.1086/713005
   PubMed Web of Science ®Google Scholar
• Andersson MB. 1994. Sexual selection. Princeton (NJ): Princeton University Press.
   Google Scholar
• Baeza JA. 1999. Indicators of monogamy in the commensal crab Pinnixa transversalis (Milne Edwards and Lucas) (Decapoda: Brachyura: Pinnotheridae): population distribution, male-female association and sexual dimorphism. Rev Biol Mar Oceanogr. 34:303–313.
   Google Scholar
• Baeza JA, Asorey CM. 2012. Testing the role of male-male competition in the evolution of sexual dimorphism: a comparison between two species of porcelain crabs. Biol J Linn Soc. 105(3):548–558. doi:10.1111/j.1095-8312.2011.01803.x
   Web of Science ®Google Scholar
• Baeza JA, Simpson L, Ambrosio LJ, Guéron R, Mora N, Schausberger P. 2016. Monogamy in a hyper-symbiotic shrimp. PLoS ONE. 11(3):e0149797. doi:10.1371/journal.pone.0149797
   PubMed Web of Science ®Google Scholar
• Bauer RT. 2000. Simultaneous hermaphroditism in caridean shrimps: a unique and puzzling sexual system in the Decapoda. J Crustac Biol. 20(5):116–128. doi:10.1163/1937240X-90000014
   Google Scholar
• Bauer RT. 2004. Remarkable shrimps. Norman (OK): Oklahoma University Press.
   Google Scholar
• Bertics VJ, Sohm JA, Treude T, Chow Ch-ET, Capone DG, Fuhrman JA, Ziebis W. 2010. Burrowing deeper into benthic nitrogen cycling: the impact of bioturbation on nitrogen fixation coupled to sulfate reduction. Mar Ecol Prog Ser. 409:1–15. doi:10.3354/meps08639
   Web of Science ®Google Scholar
• Bilodeau AL, Felder DL, Neigel JE. 2005. Multiple paternity in the thalassinidean ghost shrimp, Callichirus islagrande (Crustacea: Decapoda: Callianassidae). Mar Biol. 146(2):381–385. doi:10.1007/s00227-004-1444-1
   Web of Science ®Google Scholar
• Bonduriansky R. 2007. Sexual selection and allometry: a critical reappraisal of the evidence and ideas. Evolution. 61(4):838–849. doi:10.1111/j.1558-5646.2007.00081.x
   PubMed Web of Science ®Google Scholar
• Botter-Carvalho ML, Santos PJP, Carvalho PVVC. 2007. Population dynamics of Callichirus major (Say, 1818) (Crustacea, Thalassinidea) on a beach in northeastern Brazil. Estuar Coast Shelf Sci. 71(3–4):508–516. doi:10.1016/j.ecss.2006.09.001
   Web of Science ®Google Scholar
• Bueno SLS, Shimizu RM. 2009. Allometric growth, sexual maturity, and adult male chelae dimorphism in Aegla franca (Decapoda: Anomura: Aeglidae). J Crustac Biol. 29(3):317–328. doi:10.1651/07-2973.1
   Web of Science ®Google Scholar
• Butler SN, Manieka R, Bird FL. 2009. Population biology of the ghost shrimps, Trypaea australiensis and Biffarius arenosus (Decapoda: Thalassinidea), in Western Port, Victoria. Mem Mus Vic. 66(1):43–59. doi:10.24199/j.mmv.2009.66.6
   Google Scholar
• Cheverud JM. 1982. Relationships among ontogenetic, static, and evolutionary allometry. Am J Phys Anthropol. 59(2):139–149. doi:10.1002/ajpa.1330590204
   PubMed Web of Science ®Google Scholar
• Corey S, Reid DM. 1991. Comparative fecundity of decapod crustaceans I. The fecundity of thirty-three species of nine families of caridean shrimp. Crustaceana. 60(3):270–294. doi:10.1163/156854091X00056
   Web of Science ®Google Scholar
• Corgos A, Freire J. 2006. Morphometric and gonad maturity in the spider crab Maja brachydactyla: a comparison of methods for estimating size at maturity in species with determinate growth. Ices J Mar Sci. 63(5):851–859. doi:10.1016/j.icesjms.2006.03.003
   Web of Science ®Google Scholar
• Correa C, Thiel M. 2003. Mating systems in caridean shrimp (Decapoda: Caridea) and their evolutionary consequences for sexual dimorphism and reproductive biology. Rev Chil Hist Nat. 76(2):187–203. doi:10.4067/S0716-078X2003000200006
   Web of Science ®Google Scholar
• Darwin C. 1871. The descent of man, and selection in relation to sex. London (UK): John Murray.
   Google Scholar
• de Rodrigues SA. 1966. Estudos sobre Callianassa: Sistemática, biologia e anatomia [Studies on Callianassa: Systematics, biology and anatomy]. [PhD Thesis]. São Paulo (Brazil): Universidade de São Paulo. Portuguese.
   Google Scholar
• Devine CE. 1966. Ecology of Callianassa filholi Milne-Edwards, 1878 (Crustacea, Thalassinidea). Trans R Soc NZ. 8:93–110.
   Web of Science ®Google Scholar
• Dworschak PC. 2015. Methods collecting Axiidea and Gebiidea (Decapoda): a review. Ann Naturhist Mus Wien B Bot Zool. 117:5–21.
   Google Scholar
• Dworschak PC, Felder DL, Tudge CC. 2012. Infraorders Axiidea de Saint Laurent, 1979 and Gebiidea de Saint Laurent, 1979 (formerly known collectively as Thalassinidea). In: Schram FR, et al., editors. Treatise on zoology – anatomy, taxonomy, biology. The Crustacea. Complementary to the volumes translated from the French of the Traité de Zoologie [founded by P.-P. Grassé]. Vol. 9, part B. Eucarida: Decapoda: Astacidea p.p. (Enoplometopoidea, Nephropoidea), Glypheidea, Axiidea, Gebiidea, and Anomura. Leiden (Netherland): Brill; p. 109–219.
   Google Scholar
• Dworschak PC, Koller H, Abed-Navandi D. 2006. Burrow structure, burrowing and feeding behaviour of Corallianassa longiventris and Pestarella tyrrhena (Crustacea, Thalassinidea, Callianassidae). Mar Biol. 148(6):1369–1382. doi:10.1007/s00227-005-0161-8
   Web of Science ®Google Scholar
• Eberhard WG, Huber BA, Rodriguez RL, Briceño RD, Salas I, Rodriguez V. 1998. One size fits all? Relationships between the size and degree of variation in genitalia and other body parts in twenty species of insects and spiders. Evolution. 52(2):415–431. doi:10.2307/2411078
   PubMed Web of Science ®Google Scholar
• Eberhard WG, Rodriguez RL, Huber BA, Speck B, Miller H, Buzatto BA, Machado G. 2018. Sexual selection and static allometry: the importance of function. Q Rev Biol. 93(3):207–250. doi:10.1086/699410
   Web of Science ®Google Scholar
• Elliott JM. 1983. Some methods for the statistical analysis of samples of benthic invertebrates. Far Sawrey (UK): Freshwater Biological Association.
   Google Scholar
• Emlen ST, Oring LW. 1977. Ecology, sexual selection, and the evolution of mating systems. Sci. 197(4300):215–223. doi:10.1126/science.327542
   PubMed Web of Science ®Google Scholar
• Felder DL, Lovett DL. 1989. Relative growth and sexual maturation in the estuarine ghost shrimp Callianassa louisianensis Schmitt, 1935. J Crustac Biol. 9(4):540–553. doi:10.2307/1548586
   Web of Science ®Google Scholar
• Forbes AT. 1978. Maintenance of non-breeding populations of the estuarine prawn Callianassa kraussi (Crustacea, Anomura, Thalassinidea). Zool Afr. 13(1):33–40. doi:10.1080/00445096.1978.11447603
   Web of Science ®Google Scholar
• Gould SJ. 1966. Allometry and size in ontogeny and phylogeny. Biol Rev. 41(4):587–638. doi:10.1111/j.1469-185X.1966.tb01624.x
   PubMed Web of Science ®Google Scholar
• Gould SJ. 1974. The origin and function of “bizarre” structures: antler size and skull size in the “Irish elk,” Megaloceros giganteus. Evolution. 28(2):191–220. doi:10.1111/j.1558-5646.1974.tb00740.x
   PubMed Web of Science ®Google Scholar
• Graham ZA, Garde E, Heide-Jørgensen MP, Palaoro AV. 2020. The longer the better: evidence that narwhal tusks are sexually selected. Biol Lett. 16(3):20190950. doi:10.1098/rsbl.2019.0950
   PubMed Web of Science ®Google Scholar
• Hartnoll R. 1978. The determination of relative growth in Crustacea. Crustaceana. 34(3):281–293. doi:10.1163/156854078X00844
   Web of Science ®Google Scholar
• Hartnoll R. 1982. Growth. In: Abele L, editor. The biology of Crustacea. Embryology, morphology and genetics. New York (NY): Academic Press; p. 111–196.
   Google Scholar
• Hernáez P. 2018a. Diversidade e distribuição geográfica de camarões corruptos (Infraordens Axiidea e Gebiidea), ao longo do litoral brasileiro: uma aproximação ecológica aos padrões biogeográficos de distribuição. Relatório Final, Projeto de Pós-Doutorado FAPESP proc. no. 2015/09020-0 [Diversity and geographic distribution of corrupt shrimp (Infraorders Axiidea and Gebiidea) along the Brazilian coast: an ecological approach to biogeographic distribution patterns. Final Report, FAPESP Postdoctoral Project proc. at the. 2015/09020-0]. Available from: https://bv.fapesp.br/pt/bolsas/160590/diversidade-e-distribuicao-geografica-de-camaroes-corruptos-infraordens-axiidea-e-gebiidea-ao-lon/ [Accessed 2022 Mar 28]. Portuguese.
   Google Scholar
• Hernáez P. 2018b. An update on reproduction in ghost shrimps (Decapoda: Axiidea) and mud lobsters (Decapoda: Gebiidea). In: Türkoğlu M, et al., editors. Marine ecology: biotic and abiotic interactions. London (UK): IntechOpen; p. 231–253. doi:10.5772/intechopen.75067
   Google Scholar
• Hernáez P, Buchmann FS, Santana W. 2020. A new species of Callichirus (Axiidea, Callianassidae) from the Pleistocene bioclastic sediment of southeast Brazil. J S Am Earth Sci. 101:102602. doi:10.1016/j.jsames.2020.102602
   Web of Science ®Google Scholar
• Hernáez P, Gamboa-González A, de Grave S. 2015. Callichirus garthi is a valid species, distinct from C. seilacheri (Decapoda: Axiidea: Callianassidae). Mar Biol Res. 11(9):990–997. doi:10.1080/17451000.2015.1044999
   Web of Science ®Google Scholar
• Hernáez P, João MCA. 2018. Social structure, sexual dimorphism and relative growth in the ghost shrimp Callichirus seilacheri (Bott, 1955) (Decapoda, Axiidea, Callianassidae) from the tropical eastern Pacific. Mar Biol Res. 14(8):856–867. doi:10.1080/17451000.2018.1529415
   Web of Science ®Google Scholar
• Hernáez P, Miranda MS, Rio JPP, Pinheiro MAA. 2022a. A new Callichirus ghost shrimp species from the south-western Atlantic, long confounded with C. major (Say, 1818) (Decapoda: Axiidea: Callichiridae). J Nat Hist. 56(9–12):533–563. doi:10.1080/00222933.2022.2067016
   Web of Science ®Google Scholar
• Hernáez P, Mugnai R, Souza-Filho JF, Pinheiro MAA. 2022b. Monogamy in the burrowing shrimp Axianassa australis Rodrigues & Shimizu, 1992 (Decapoda, Gebiidea, Axianassidae). Biol Bull. 242(2):87–96. doi:10.1086/719408
   PubMedGoogle Scholar
• Hernáez P, Palma S. 2003. Fecundidad, volumen del huevo y rendimiento reproductivo de cinco especies de porcelánidos intermareales del norte de Chile (Decapoda, Porcellanidae) [Fertility, egg volume, and reproductive yield of five species of intertidal porcelanids from northern Chile (Decapoda, Porcellanidae)]. Investig Mar. 31(2):35–46. Portuguese. doi:10.4067/S0717-71782003000200004
   Google Scholar
• Hernáez P, Palma S, Wehrtmann IS. 2008. Egg production of the burrowing shrimp Callichirus seilacheri (Bott 1955) (Decapoda, Callianassidae) in northern Chile. Helgol Mar Res. 62(4):351–356. doi:10.1007/s10152-008-0122-y
   Web of Science ®Google Scholar
• Hernáez P, Pinheiro MAA, Alves-Junior FA, Santana W. 2022c. Intertidal burrowing shrimps (Axiidea: Callianassidae, Callichiridae; Gebiidea: Axiannassidae, Upogebiidae) collected along the Brazilian coast. Mar Biol Res. 18(5–6):380–408. doi:10.1080/17451000.2022.2105893
   Web of Science ®Google Scholar
• Hernáez P, Villegas-Castro E, João MCA, Duarte RC, Rivadeneira MM. 2021. Inferring the mating system in the burrowing shrimp Lepidophthalmus bocourti (Decapoda, Axiidea, Callichiridae) from the social structure and sexual dimorphism. Behav Ecol Sociobiol. 75(6):99. doi:10.1007/s00265-021-03031-2
   Web of Science ®Google Scholar
• Hernáez P, Villegas-Jiménez E, Villalobos-Rojas F, Wehrtmann IS. 2012. Reproductive biology of the ghost shrimp Lepidophthalmus bocourti (A. Milne-Edwards, 1870) (Decapoda: Axiidea: Callianassidae): a tropical species with a seasonal reproduction. Mar Biol Res. 8(7):635–643. doi:10.1080/17451000.2011.653369
   Web of Science ®Google Scholar
• Hernáez P, Wehrtmann IS. 2007. Population biology of the burrowing shrimp Callichirus seilacheri (Decapoda: Callianassidae) in northern Chile. Rev Biol Trop. 55:141–152.
   Web of Science ®Google Scholar
• Heuring WL, Hughes M. 2020. Continuously choosy males and seasonally faithful females: sex and season differences underlie size-assortative pairing. Anim Behav. 160:91–98. doi:10.1016/j.anbehav.2019.12.003
   Web of Science ®Google Scholar
• Hines AH. 1991. Fecundity and reproductive output in nine species of Cancer crabs (Crustacea, Brachyura, Cancridae). Can J Fish Aquat Sci. 48(2):267–275. doi:10.1139/f91-037
   Web of Science ®Google Scholar
• Huber BA. 2005. Sexual selection research on spiders: progress and biases. Biol Rev. 80(3):363–385. doi:10.1017/S1464793104006700
   PubMed Web of Science ®Google Scholar
• Hughes M. 2000. Deception with honest signals: signal residuals and signal function in snapping shrimp. Behav Ecol. 11:614–623. doi:10.1007/s00265-016-2221-0
   Web of Science ®Google Scholar
• Huxley JS, Tessier G. 1936. Terminology of relative growth. Nature. 137(3471):780–781. doi:10.1038/137780b0
   Google Scholar
• Jormalainen V. 1998. Precopulatory mate guarding in crustaceans: male competitive strategy and intersexual conflict. Q Rev Biol. 73(3):275–304. doi:10.1086/420306
   Web of Science ®Google Scholar
• Kensley B. 1981. Notes on Axiopsis (Axiopsis) serratifrons (A. Milne Edwards) (Crustacea: Decapoda: Thalassinidea). Proc Biol Soc Wash. 93:1253–1263.
   Google Scholar
• Klingenberg CP, Zimmermann M. 1992. Static, ontogenetic, and evolutionary allometry: a multivariate comparison in nine species of water striders. Am Nat. 140(4):601–620. doi:10.1086/285430
   Web of Science ®Google Scholar
• Kneer D. 2006. The role of Neaxius acanthus (Thalassinidea: Strahlaxiidae) and its burrows in a tropical seagrass meadow, with some remarks on Corallianassa coutierei (Thalassinidea: Callianassidae). [Thesis]. Berlin (Germany): Freie Universität Berlin.
   Google Scholar
• Kokko H, Jennions MD. 2008. Parental investment, sexual selection and sex ratios. J Evol Biol. 21(4):919–948. doi:10.1111/j.1420-9101.2008.01540.x
   PubMed Web of Science ®Google Scholar
• Laitano MV, Farias NE, Cledón M. 2013. Prey preference of the stone crab Platyxanthus crenulatus (Decapoda: Platyxanthidae) in laboratory conditions. Nauplius. 21(1):17–23. doi:10.1590/S0104-64972013000100003
   Google Scholar
• Mathews LM. 2002. Tests of the mate-guarding hypothesis for social monogamy: Does population density, sex ratio, or female synchrony affect behavior of male snapping shrimp (Alpheus angulatus)? Behav Ecol Sociobiol. 51(5):426–432. doi:10.1007/s00265-002-0465-3
   Web of Science ®Google Scholar
• McDermott JJ. 2005. Biology of the brachyuran crab Pinnixa chaetopterana Stimpson (Decapoda: Pinnotheridae) symbiotic with tubicolous polychaetes along the Atlantic coast of the United States, with additional notes on other polychaete associations. Proc Biol Soc Wash. 118(4):742–764. doi:10.2988/0006-324X(2005)118[742:BOTBCP]2.0.CO;2
   Web of Science ®Google Scholar
• Nates SF, Felder DL. 1999. Growth and maturation of the ghost shrimp Lepidophthalmus sinuensis Lemaitre and Rodrigues, 1991 (Crustacea, Decapoda, Callianassidae), a burrowing pest in penaeid shrimp culture ponds. Fish Bull. 97:526–541.
   Google Scholar
• Ng PKL, Kang N. 1988. The mud lobster Thalassina. Nat Malaysiana. 13:28–31.
   Google Scholar
• O’Brien DM, Allen CE, Van Kleeck MJ, Hone D, Knell R, Knapp A, Christiansen S, Emlen DJ. 2018. On the evolution of extreme structures: static scaling and the function of sexually selected signals. Anim Behav. 144:95e108. doi:10.1016/j.anbehav.2018.08.005
   Web of Science ®Google Scholar
• Pelabon C, Firmat C, Bolstad GH, Voje KL, Houle D, Cassara J, Le Rouzic A, Hansen TF. 2014. Evolution of morphological allometry. Ann NY Acad Sci. 1320(1):58–75. doi:10.1111/nyas.12470
   PubMedGoogle Scholar
• Pescinelli RA, Almeida AO, Costa RC. 2018. Population structure, relative growth and morphological sexual maturity of the snapping shrimp Alpheus brasileiro Anker, 2012 (Caridea: Alpheidae) from the south-eastern coast of Brazil. Mar Biol Res. 14(6):610–620. doi:10.1080/17451000.2018.1472383
   Web of Science ®Google Scholar
• Pezzuto PR. 1998. Population dynamics of Sergio mirim Rodrigues 1971 Decapoda: Thalassinidea: Callianassidae in Cassino Beach, Southern Brazil. Mar Ecol. 19(2):89–109. doi:10.1111/j.1439-0485.1998.tb00456.x
   Google Scholar
• Pillay D. 2019. Ecosystem engineering by thalassinidean crustaceans: response variability, contextual dependencies and perspectives on future research. Diversity. 11(4):1–20. doi:10.3390/d11040064
   PubMedGoogle Scholar
• R Core Team. 2022. R: A language and environment for statistical computing. Vienna (Austria): R Fundation for Statistical Computing.
   Google Scholar
• Reid DM, Corey S. 1991. Comparative fecundity of decapod crustaceans. II. The fecundity of fifteen species of anomuran and brachyuran crabs. Crustaceana. 61(2):175–189. doi:10.1163/156854091X00669
   Google Scholar
• Rodrigues SdeA. 1985. Sobre o crescimento relativo de Callichirus major (Say, 1818) (Crustacea, Decapoda, Thalassinidea) [On the relative growth of Callichirus major (Say, 1818) (Crustacea, Decapoda, Thalassinidea)]. Bol Zool USP. 9(9):195–211. Portuguese. doi:10.11606/issn.2526-3358.bolzoo.1985.122297
   Google Scholar
• Rodrigues SdeA, Höld W. 1990. Burrowing behaviour of Callichirus major and C. mirim. Wissenschaftlichen Film. 41:48–58.
   Google Scholar
• Rosa Filho JS, Girard TC, Frédou FL. 2013. Population dynamics of the burrowing shrimp Lepidophthalmus siriboia Felder and Rodrigues, 1993 (Reptantia: Axiidea: Callianassidae) on the Amazonian coast. J Crustac Biol. 33(4):503–511. doi:10.1163/1937240X-00002157
   Web of Science ®Google Scholar
• Schenk SC, Wainwright PC. 2001. Dimorphism and the functional basis of claw strength in six brachyuran crabs. J Zool Lond. 255(1):105–119. doi:10.1017/S0952836901001157
   Google Scholar
• Schmitt WL. 1935. Mud shrimps of the Atlantic coast of North America. Smithsonian Misc Collect. 93:1–21.
   Google Scholar
• Schwartz CR. 2013. Trends and variation in assortative mating: causes and consequences. Annu Rev Sociol. 39(1):451–470. doi:10.1146/annurev-soc-071312-145544
   Google Scholar
• Shimoda K, Wardiatno Y, Kubo K, Tamaki A. 2005. Intraspecific behaviors and major cheliped sexual dimorphism in three congeneric callianassid shrimp. Mar Biol. 146(3):543–557. doi:10.1007/s00227-004-1453-0
   Web of Science ®Google Scholar
• Shine R. 1989. Ecological causes for the evolution of sexual dimorphism: a review of the evidence. Q Rev Biol. 64(4):419–461. doi:10.1086/416458
   PubMed Web of Science ®Google Scholar
• Shuster S. 2007. The evolution of crustacean mating systems. In: Duffy JE, Thiel M, editors. Evolutionary ecology of social and sexual systems: crustaceans as model organisms. New York (NY): Oxford University Press; p. 29–47. doi:10.1093/acprof:oso/9780195179927.003.0002
   Google Scholar
• Sokal RR, Rohlf FJ. 2011. Biometry: the principles and practice of statistics in biological research, 4th ed. New York (NY): WH Freeman.
   Google Scholar
• Somiya R, Tamaki A. 2017. Unraveling mating behavior for Axiidea (Crustacea: Decapoda): burrow-dwelling callianassid shrimp in intertidal sandflat. J Exp Mar Bio Ecol. 486:305–313. doi:10.1016/j.jembe.2016.09.019
   Web of Science ®Google Scholar
• Somjee U. 2021. Positive allometry of sexually selected traits: do metabolic maintenance costs play an important role? BioEssays. 43(6):2000183. doi:10.1002/bies.202000183
   Web of Science ®Google Scholar
• Subramoniam T. 2013. Origin and occurrence of sexual and mating systems in Crustacea: a progression towards communal living and eusociality. J Biosci. 38(5):951–969. doi:10.1007/s12038-013-9392-x
   PubMed Web of Science ®Google Scholar
• Temeles EJ, Pan IL, Brennan JL, Horwitt JN. 2000. Evidence for ecological causation of sexual dimorphism in a hummingbird. Science. 289(5478):441–443. doi:10.1126/science.289.5478.441
   PubMed Web of Science ®Google Scholar
• Tobias JA, Montgomerie R, Lyon BE. 2012. The evolution of female ornaments and weaponry: social selection, sexual selection and ecological competition. Phil Trans R Soc B. 367(1600):2274–2293. doi:10.1098/rstb.2011.0280
   PubMed Web of Science ®Google Scholar
• Torrejon-Magallanes J. 2020. SizeMat: estimate size at sexual maturity. R package, version 1.1.2. Available from: https://CRAN.R-project.org/package=sizeMat
   Google Scholar
• Trivers R. 1972. Parental investment and sexual selection. In: Campbell B, editor. Sexual selection and the descent of man 1871–1971. Chicago (IL): Aldine Press; p. 139–179.
   Google Scholar
• Wang L, Luo Y, Xu N, Lin H, Yu F, Huang C, Li Z. 2022. Signs of claw asymmetry appear in a homochelate crab. Appl Anim Behav Sci. 246:105537. doi:10.1016/j.applanim.2021.105537
   Web of Science ®Google Scholar
• Wilson K, Hardy ICW. 2002. Statistical analysis of sex ratios: an introduction. In: Hardy I, editor. Sex ratios: concepts and research methods. Cambridge (UK): Cambridge University Press; p. 59–85. doi:10.1017/CBO9780511542053
   Google Scholar
• Zar JH. 1996. Biostatistical analysis. Upper Saddle River (NJ): Prentice Hall.
   Google Scholar
• Ziebis W, Forster S, Huettel M, Jørgensen B. 1996. Complex burrows of the mud shrimp Callianassa truncata and their geochemical impact in the sea bed. Nature. 382(6592):619–622. doi:10.1038/382619a0
   Web of Science ®Google Scholar