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Is the seasonal change of sexual differences in shell use by the hermit crab Pagurus minutus considered to be driven by growth or reproduction?

Published online by Cambridge University Press:  15 November 2018

Chiaki I. Yasuda*
Affiliation:
Graduate School of Fisheries Sciences, Hokkaido University, Minato-cho, Hakodate, Hokkaido, 041-8611, Japan Faculty of Education, Wakayama University, Sakaedani, Wakayama, 640-8510, Japan
Yuki Takiya
Affiliation:
Faculty of Education, Wakayama University, Sakaedani, Wakayama, 640-8510, Japan
Masaya Otoda
Affiliation:
Faculty of Education, Wakayama University, Sakaedani, Wakayama, 640-8510, Japan
Reiko Nakano
Affiliation:
Faculty of Education, Wakayama University, Sakaedani, Wakayama, 640-8510, Japan
Tsunenori Koga
Affiliation:
Faculty of Education, Wakayama University, Sakaedani, Wakayama, 640-8510, Japan
*
Author for correspondence: Chiaki I. Yasuda, E-mail: [email protected]

Abstract

Sexual differences in behaviours are often affected by the difference in individual interests between the sexes: growth in males and egg production in females. Some hermit crabs show sexual differences in shell use patterns during the reproductive season. In the non-reproductive season, however, when both sexes are focused on increasing growth, this sexual difference is expected to be reduced. In this study, we compared the pattern of shell use in the hermit crab Pagurus minutus between seasons, while focusing on the effects of shell shape on growth or egg production. As we predicted, sexual differences in shell use in P. minutus showed seasonal change. In the non-reproductive season, both sexes appeared to use shells well suited for growth. In the reproductive season, sexual differences became more evident, especially in larger solitary crabs and guarding pairs; males monopolized round-type shells such as those of Umbonium moniliferum, whereas more than 80% of females relied on high-spired Batillaria-type shells such as those of Batillaria zonalis. A lack of advantage for egg number in females using Batillaria-type shells suggests that female shell use is explained by factors other than maximizing clutch size. Both sexes can moult during the reproductive season, and larger body size is advantageous for reproduction. Given that Batillaria-type shells resulted in a lower growth increment and males have an advantage in shell fights in congeneric crabs, our findings suggest the importance of intersexual competition for shells and female compromise in determining the seasonal change of shell use patterns in P. minutus.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2018 

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References

Abrams, PA (1988) Sexual difference in resource use in hermit crabs: consequences and causes. In Chelazzi, G and Vannini, M (eds), Behavioral Adaptations to Intertidal Life. New York, NY: Plenum Press, pp. 283296.Google Scholar
Akaike, H (1983) Information measures and model selection. Bulletin of the International Statistical Institute 44, 277291.Google Scholar
Andersson, M (1994) Sexual Selection. Princeton, NJ: Princeton University Press.Google Scholar
Asakura, A (1995) Sexual differences in life history and resource utilization by the hermit crab. Ecology 76, 22952313.Google Scholar
Basolo, AL (1990) Female preference for male sword length in the green swordtail, Xiphophorus helleri (Pisces: Poeciliidae). Animal Behaviour 40, 332338.Google Scholar
Beck, CA, Iverson, SJ, Bowen, WD and Blanchard, W (2007) Sex differences in grey seal diet reflect seasonal variation in foraging behaviour and reproductive expenditure: evidence from quantitative fatty acid signature analysis. Journal of Animal Ecology 76, 490502.Google Scholar
Bertness, MD (1981) The influence of shell-type on hermit crab growth rate and clutch size (Decapoda, Anomura). Crustaceana 40, 197205.Google Scholar
Blackstone, NW (1985) The effects of shell size and shape on growth and form in the hermit crab Pagurus longicarpus. Biological Bulletin 168, 7590.Google Scholar
Briffa, M and Dallaway, D (2007) Inter-sexual contests in the hermit crab Pagurus bernhardus: females fight harder but males win more encounters. Behavioral Ecology and Sociobiology 61, 17811787.Google Scholar
Crane, J (1975) Fiddler Crabs of the World. Princeton, NJ: Princeton University Press.Google Scholar
Davies, NB, Krebs, JR and West, SA (2012) Sexual selection, sperm competition and sexual conflict. In Davies, NB, Krebs, JR and West, SA (eds), An Introduction to Behavioral Ecology, 4th Edn. Hoboken, NJ: Wiley Blackwell, pp. 179221.Google Scholar
Elwood, RW and Neil, SJ (1992) Assessments and Decisions: A Study of Information Gathering by Hermit Crabs. London: Chapman & Hall.Google Scholar
Elwood, RW, Marks, N and Dick, JTA (1995) Consequences of shell-species preferences for female reproductive success in the hermit crab Pagurus bernhardus. Marine Biology 123, 431434.Google Scholar
Elwood, RW, Pothanikat, RME and Briffa, M (2006) Honest and dishonest displays, motivational state and subsequent decisions in hermit crab shell fights. Animal Behaviour 72, 853859.Google Scholar
Figler, MH, Blank, GS and Peeke, HVS (2005) Shelter competition between resident male red swamp crayfish Procambarus clarkii (Girard) and conspecific intruders varying by sex and reproductive status. Marine and Freshwater Behaviour and Physiology 38, 237248.Google Scholar
Fotheringham, N (1976) Effects of shell stress on the growth of hermit crabs. Journal of Experimental Marine Biology and Ecology 23, 299305.Google Scholar
Fotheringham, N (1980) Effects of shell utilization on reproductive patterns in tropical hermit crabs. Marine Biology 55, 287293.Google Scholar
Garcia, RB and Mantelatto, FL (2001) Shell selection by the tropical hermit crab Calcinus tibicen (Herbst, 1791) (Anomura, Diogenidae) from Southern Brazil. Journal of Experimental Marine Biology and Ecology 265, 114.Google Scholar
Goshima, S, Kawashima, T and Wada, S (1998) Mate choice by males of the hermit crab Pagurus filholi: do males assess ripeness and/or fecundity of females? Ecological Research 13, 151161.Google Scholar
Hazlett, BA (1981) The behavioral ecology of hermit crabs. Annual Review of Ecology and Systematics 12, 122.Google Scholar
Imafuku, M (1986) Sexual discrimination in the hermit crab Pagurus geminus. Journal of Ethology 4, 3947.Google Scholar
Imazu, M and Asakura, A (1994) Distribution, reproduction and shell utilization patterns in three species of intertidal hermit crabs on a rocky shore on the Pacific coast of Japan. Journal of Experimental Marine Biology and Ecology 184, 4165.Google Scholar
Jormalainen, V, Honkanen, T, Mäkinen, A, Hemmi, A and Vesakoski, O (2001) Why does herbivore sex matter? Sexual differences in utilization of Fucus vesiculosus by the isopod Idotea baltica. Oikos 93, 7786.Google Scholar
Koga, T and Fukuda, Y (2008) Distribution, sex ratio and body size of three hermit crab species in summer in the Waka-River Estuary. Japanese Journal of Benthology 63, 2329.Google Scholar
Lewis, S, Benvenuti, S, Dall-Antonia, L, Griffiths, R, Money, L, Sherratt, TN, Wanless, S and Hamer, KC (2002) Sex-specific foraging behaviour in a monomorphic seabird. Proceedings of the Royal Society of London B 269, 16871693.Google Scholar
Matsuo, K, Tanikawa, D, Yasuda, CI and Wada, S (2015) Sex-related differences in size, function and regeneration of the major cheliped in the hermit crab Pagurus filholi. Marine Ecology 36, 13911399.Google Scholar
Mima, A, Wada, S and Goshima, S (2003) Antipredator defence of the hermit crab Pagurus filholi induced by predatory crabs. Oikos 102, 104110.Google Scholar
Nakano, R, Yasuda, CI and Koga, T (2016) Temporal changes in egg number and size during a single breeding season in the hermit crab Pagurus minutus. Japanese Journal of Benthology 71, 3236.Google Scholar
Neil, SJ (1985) Size assessment and cues: studies of hermit crab contests. Behaviour 92, 2237.Google Scholar
Okamura, S and Goshima, S (2010) Indirect female choice mediated by sex pheromones in the hermit crab Pagurus filholi. Journal of Ethology 28, 323329.Google Scholar
Okutani, T (ed.) (2017) Marine Mollusks in Japan, 2nd Edn. Kanagawa: Tokai University Press.Google Scholar
Parker, GA (1992) The evolution of sexual size dimorphism in fish. Journal of Fish Biology 41, 120.Google Scholar
R Core Team (2015) R: A Language and Environment for Statistical Computing. Vienna: R Foundation for Statistical Computing.Google Scholar
Shaffer, SA, Weimerskirch, H and Costa, DP (2001) Functional significance of sexual dimorphism in wandering albatrosses, Diomedea exulans. Functional Ecology 15, 203210.Google Scholar
Siu, BFC and Lee, SY (1992) Shell preference and utilization pattern in two hermit crabs, Pagurus trigonocheirus (Stimpson) and Clibanarius bimaculatus (De Haan), on a sheltered rocky shore in Hong Kong. Asian Marine Biology 9, 205216.Google Scholar
Tanikawa, D, Yasuda, C, Suzuki, Y and Wada, S (2012) Effects of male size and mate quality on male–male contest in the hermit crab Pagurus filholi. Japanese Journal of Benthology 67, 1519.Google Scholar
Turra, A and Leite, FPP (2003) The molding hypothesis: linking shell use with hermit crab growth, morphology, and shell-species selection. Marine Ecology Progress Series 265, 155163.Google Scholar
Wada, S (2000) Seasonal growth pattern and the effect of gastropod shells on sexual growth rates in the hermit crab Pagurus middendorffii. Bulletin of the Faculty of Fisheries Hokkaido University 51, 111.Google Scholar
Wada, S, Ito, A and Mima, A (2007) Evolutionary significance of prenuptial molting in female Pagurus hermit crabs. Marine Biology 152, 12631270.Google Scholar
Wada, S, Tanaka, K and Goshima, S (1999) Precopulatory mate guarding in the hermit crab Pagurus middendorffii (Brandt) (Decapoda: Paguridae): effects of population parameters on male guarding duration. Journal of Experimental Marine Biology and Ecology 239, 289298.Google Scholar
Weckerly, FW (1998) Sexual-size dimorphism: influence of mass and mating systems in the most dimorphic mammals. Journal of Mammalogy 79, 3352.Google Scholar
Yasuda, CI and Koga, T (2016) Do weaponless males of the hermit crab Pagurus minutus give up contests without escalation? Behavior of intruders that lack their major cheliped in male–male contests. Journal of Ethology 34, 249254.Google Scholar
Yasuda, CI, Otoda, M, Nakano, R, Takiya, Y and Koga, T (2017) Seasonal change in sexual size dimorphism of the major cheliped in the hermit crab Pagurus minutus. Ecological Research 32, 347357.Google Scholar
Yasuda, C, Suzuki, Y and Wada, S (2011) Function of the major cheliped in male–male competition in the hermit crab Pagurus nigrofascia. Marine Biology 158, 23272334.Google Scholar
Yasuda, CI and Wada, S (2015) Regeneration of major cheliped after the mating season in the hermit crab Pagurus middendorffii. Crustacean Research 44, 2938.Google Scholar
Yoshino, K and Goshima, S (2001) Functional roles of gastropod shells in the hermit crab Pagurus filholi: effects of shell size and species on fitness. Benthos Research 56, 8793.Google Scholar
Yoshino, K and Goshima, S (2002) Sexual dominance in hermit crab shell fights: asymmetries in owner–intruder status, crab size, and resource value between sexes. Journal of Ethology 20, 6369.Google Scholar
Yoshino, K, Goshima, S and Nakao, S (2001) Sexual difference in shell use in the hermit crab Pagurus filholi (de Man) from northern Japan. Crustacean Research 30, 5564.Google Scholar
Yoshino, K, Koga, T, Taniguchi, K and Tasaka, R (2014) Adaptation in a peripheral habitat: intraspecific variation in osmoregulatory traits in an estuarine hermit crab (Pagurus minutus). Journal of Shellfish Research 33, 5359.Google Scholar