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Volume: 01, Issue: 01, Page: 21-25

First report of hard shell female mating in the crenate swimming crab, Thalamita crenata Ruppell, 1830 (Crustacea: Decapoda: Portunidae)

1 Curtin Aquaculture Research Laboratory, Faculty of Engineering and Science, Curtin University Malaysia, CDT 250, 98000, Miri, Sarawak, Malaysia

2 Institute of Biodiversity and Environmental Conservation, Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia

3 Department of Animal Science and Fishery, Faculty of Agriculture Science and Technology, Universiti Putra Malaysia Bintulu Campus, 97008, Bintulu, Sarawak, Malaysia

*Corresponding authors

Email address: lirongyuabit@curtin.edu.my (Lirong Yu Abit)

                      kamill@upm.edu.my (Kamil Latif)

doi: https://doi.org/10.69517/aier.2024.01.01.0004 

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Received:
25 April 2024

Revised:
26 November 2024

Accepted:
20 December 2024

Published:
29 December 2024

Highlights

  • First report of hard shell female mating in Thalamita crenata, a rare adaptation in Thalamitinae.
  • Observed mating involved forceful gripping, flipping, and brief copulation lasting 8 minutes.
  • Study used a controlled aquarium setup to monitor crenata reproductive behaviour in captivity.
  • Highlights unique reproductive strategy with no pre- or post-copulatory guarding in crenata.
  • Findings support potential captive breeding and broader understanding of portunid crab reproduction.

Abstract

The mating behaviour of crustaceans, particularly brachyuran crabs, is commonly associated with the female molting cycle, with soft shell mating prevalent among sexually reproducing species, while hard shell mating is a rarely observed adaptation within the subfamily Thalamitinae. This study marks the initial documentation of hard shell female mating in Thalamita crenata, a portunid crab. The study aims to elucidate the reproductive dynamics of T. crenata by capturing and observing mating behaviours in captivity. Mature T. crenata individuals of both sexes were captured and housed in controlled conditions. Observations were conducted to document hard shell mating behaviours, employing digital video and photography for detailed analysis. After 50 days, a notable instance of hard shell mating was observed, characterized by forceful gripping and flipping manoeuvres by the male, culminating in copulation lasting approximately 8 minutes. This discovery enriches our understanding of T. crenata‘s reproductive ecology, providing insights into unique mating strategies within the subfamily Thalamitinae. This discovery encourages further exploration of captive breeding possibilities and contributes to a holistic comprehension of crustacean mating strategies.

Graphical abstract

Keywords

Reproductive behaviour, Portunid crab, Mating adaptation, Crustacean ecology, Captive breeding

1. Introduction

Crustacean mating cycles are intricately linked to the female moulting cycle, with most sexually reproducing species engaging in mating exclusively during the "soft shell" phase, immediately post-ecdysis when the female carapace is pliable (Abdullah‐Zawawi et al., 2021; Bublitz et al., 2008; Chang and Mykles, 2011). This phenomenon, known as "softshell mating," is predominant among brachyuran crabs (Ali et al., 2020; Brink and McLay, 2010; Comeau et al., 1998). Those that exhibit soft-shell-female mating generally adhere to a rigorous courtship and guarding behavioral pattern, ensuring protection for the mated female and the inheritance of male genetic information in the offspring (Forstmeier et al., 2011; McLay and Becker, 2015). Hard shell mating, a less common adaptation, is primarily observed in semi-terrestrial species, particularly in the families Grapsidae and Ocypodidae (Hartnoll, 1975; João et al., 2021). Within portunid crabs, a rarely observed strategy, hard shell mating, has been documented in only four species all belonging to the subfamily Thalamitinae—Thalamita sima, T. picta, T. prymna, and Charybdis longicollis (Baker et al., 2018; Faria et al., 2021; Kobayashi and Vazquez-Archdale, 2018). In hard shell mating, intermoult female crabs form mating pairs with intermoult male crabs, and in species employing this strategy, both pre and post-copulatory guarding behaviors are typically absent (Herborg et al., 2006; João et al., 2021; Kobayashi and Vazquez Archdale, 2020). Thalamita crenata, commonly known as the crenate or mangrove swimming crab, is a widely distributed portunid crab in marine and brackish waters of the Indo-West Pacific Regions (Mustaquim et al., 2022). The multifaceted nature of T. crenata, the mangrove swimming crab, unfolds through an array of scientific investigations spanning diverse ecological and physiological dimensions. Research endeavors illuminate the influence of dissolved oxygen on metabolic rates and thermal sensitivity, unravelling the intricate dance between this tropical aquatic crab and its heterogeneous environments (Fusi et al., 2021). From Thailand's coastal habitats, a comprehensive case study showcases how increasing habitat complexity intricately shapes crab density, offering insights into the interplay of environmental factors on population dynamics (Tuntiprapas et al., 2021). Notably, studies delve into the critical thermal maxima of T. crenata, alongside the intertidal crab species Scylla olivacea, revealing thermal acclimation nuances vital for understanding these crustaceans' physiological adaptations (Azra et al., 2020). As we journey across Southeast Asian waters, from Setiu Wetlands in Malaysia to Lasongko Bay in Indonesia, investigations unfold the biological aspects and size at maturity of male T. crenata, shedding light on the species' life history (Amin-Safwan et al., 2019; Hamid et al., 2019). Genomic explorations extend our understanding, unravelling the complete mitochondrial genome of the spiny rock crab and tracing its phylogenetic relationships (Tan et al., 2016; Xie et al., 2018). Meanwhile, ecological surveys in various regions, from Terengganu Coastal Waters to Kung Krabaen Bay, Thailand, assess species diversity, abundance, and the impact of collapsible crab trap fisheries on marine crab populations (Kunsook and Dumrongrojwatthana, 2017; Muhd-Farouk et al., 2017). Further studies delve into T.  crenata role as a bio indicator, evaluating its ability to accumulate and biodegrade butyltin compounds in Taiwan's Kaohsiung Harbor (Chen et al., 2016). From gender-specific metal bioaccumulation effects to homing mechanisms based on underwater landmark memory, and the intricate feeding behaviour of this cannibalistic scavenger, a mosaic of knowledge emerges (Cannicci et al., 1995, 1996, 2000; Chen et al., 2005; Mckillup and Mckillup, 1996). These collective efforts contribute to a holistic understanding of T. crenata, encapsulating its ecology, behaviour, and physiological adaptations in response to a myriad of environmental stimuli (Kannupandi et al., 1997; Lin et al., 2015; Tullis and Kamemoto, 1974; Vezzosi et al., 1994a; Vezzosi et al., 1994b). The mating behaviour of crustaceans, particularly in the context of brachyuran crabs, has been extensively studied, with a predominant focus on soft shell mating (Asakura, 2009; Hayden et al., 2007). However, the phenomenon of hard shell mating, characterized by mating events occurring between intermoult female and male crabs, is a scarcely documented adaptation within portunid crabs (Orensanz et al., 1995; Sayekti et al., 2020; Watanabe et al., 2008). This study addresses the significant gap in our understanding by presenting the first report of hard shell female mating in T. crenata, a widely distributed portunid crab. The rarity of hard shell mating in portunids, coupled with the absence of pre and post-copulatory guarding behaviour in species employing this strategy, raises intriguing questions about the reproductive dynamics and adaptations in T. crenata. Moreover, the feasibility and challenges of breeding this species in captivity remain largely unexplored. This investigation aims to contribute to the broader knowledge of crustacean mating strategies, specifically shedding light on the unique reproductive behaviour observed in the crenate swimming crab, and further exploring the potential for breeding T. crenata in captivity, which could have implications for conservation and aquaculture practices.

2. Materials and Methods

2.1 Ethical approval

No ethical approval is required for this study.

2.2 Study area and period

The mature individuals of T. crenata encompassing both sexes (male and female) were procured through the utilization of baited box traps deployed in Telok Melano, Sematan, Sarawak (2.0070° N, 109.6461° E) during the period from 1st June to 21st June 2022 (Figure 1).


aier.11.0004.fig1 Figure 1. The area from where the crabs were captured Telok Melano, Sematan, Sarawak, Malaysia.
2.3 Laboratory observation

Subsequent to capture, the specimens were transported to the Aquatic Research and Teaching Laboratory at Universiti Putra Malaysia Bintulu, Sarawak (UPMKB), Malaysia. Under laboratory settings, the crabs were collectively housed in a glass aquarium measuring 2 m in width, 1 m in length, and 0.2 m in height, filled with filtered seawater (25 PSU). The aquarium was equipped with essential amenities including an overhead filter, protein skimmer, aerator, and ultraviolet sterilizer (Figure 2). The water conditions were maintained at ambient temperatures. A cohort of 22 inter-moult crabs, comprising 10 females and 12 males, with carapace widths ranging from 53 to 89 mm, were introduced into the tank on 23rd June 2022. Rectangular plastic baskets were provided as shelters within the tank. The rearing facility, situated indoors, allowed for natural light penetration through lightly tinted glass windows. The crabs were subjected to a daily feeding regimen consisting of squid and marine fish. Tank maintenance involved the siphoning of uneaten food and waste every two days, with water replenishment conducted accordingly. The absence of substrate facilitated unhindered observations and simplified cleaning procedures. Throughout the experimental trial, the crabs were afforded unrestricted mobility within the confines of their enclosure. Daily observations were conducted to detect any instances of pre or post-copulatory guarding behaviours.


aier.11.0004.fig2 Figure 2. Experimental tank for observing the mating crabs.

3. Results and Discussion

After a 50-day period following the initial stocking on August 13, 2022, a noteworthy occurrence of mating was observed within the T. crenata population. Remarkably, a mating pair consisting of both male and female crabs in the intermoult stage engaged in copulation, an event meticulously documented through the use of digital video and photographic records. The observed mating behaviour exhibited distinctive characteristics, with the male employing a forceful grip to grasp the female and utilizing one cheliped to position her beneath him, facilitating copulation (Figure 3). Subsequent to this intricate manoeuvre, the male promptly extended his abdomen, effecting copulation by inserting it inside the female’s abdomen. The entire copulatory process transpired within a relatively brief timeframe, lasting approximately 8 minutes. Following copulation, the male disengaged his abdominal flap from the female and released her. The significance of this observation lies in its representation of the first report documenting T. crenata engaging in hard shell female mating. This particular mating strategy, characterized by its rarity, has previously been documented in various crab species within the subfamily Thalamitinae (Asakura, 2009; João et al., 2021). The violent gripping and positioning observed in T. crenata aligns with the broader patterns observed in hard shell mating behaviours within the subfamily, further contributing to our understanding of the diverse reproductive strategies exhibited by crustaceans in the family Portunidae. The brevity of the copulation period, lasting approximately 8 minutes, is noteworthy and warrants consideration in the context of the species' reproductive biology and evolutionary adaptations.


aier.11.0004.fig3a aier.11.0004.fig3b Figure 3. Mating hard shell pair of Thalamita crenata.

4. Conclusions

In conclusion, this discovery enriches our understanding of T. crenata's reproductive ecology, opening avenues for further investigations into the underlying mechanisms and implications of hard shell mating in this species and others within the genus Thalamita.

Acknowledgements

The first author gratefully acknowledges the logistical support provided by Universiti Putra Malaysia Bintulu, Sarawak (UPMKB), Malaysia.

Data availability statement

All data are presented inside the manuscript.

Informed consent statement

Not applicable.

Conflict of interest

The authors declare no conflict of interest.

Author contributions

Lirong Yu Abit: conceptualization, technique, research, formal analysis, original draft writing, review, and editing; Julia Moh: reviews, editing, and formal analysis; Jongkar Grinang: formal analysis, writing, review, and editing; Wan Zabidi Wan Morni: writing, editing, and reviewing; Abdulla-Al-Asif: writing, editing, and reviewing; Kamil Latif: conceptualization, writing, editing, and reviewing. All authors critically reviewed the manuscript and agreed to submit final version of the article.

References

Abdullah‐Zawawi M, Afiqah‐Aleng N, Ikhwanuddin M, Sung YY, Tola S, Fazhan H and Waiho K, 2021. Recent development in ecdysone receptor of crustaceans: current knowledge and future applications in crustacean aquaculture. Reviews in Aquaculture, 13(4): 1938–1957. https://doi.org/10.1111/raq.12552

Ali MY, Hossain MB, Sana S, Rouf MA, Yasmin S and Sarower MG, 2020. Identifying peak breeding season and estimating size at first maturity of mud crab (Scylla olivacea) from a coastal region of Bangladesh. Heliyon, 6(6): e04318. https://doi.org/10.1016/j.heliyon.2020.e04318

Amin-Safwan A, Nurazira A, Syafiqah-Nurain KS, Mardhiyyah MP, Muhd-Farouk H, Mahsol HH, Syahnon M and Ikhwanuddin M, 2019. Comparison on natural diets dietary composition and foregut fullness between sexes of crenate swimming crab, Thalamita crenata (Rüppell, 1830) from Setiu wetlands, Terengganu coastal waters, Malaysia. Journal of Sustainability Science and Management, 14(4): 25–37.

Asakura Ak, 2009. The evolution of mating systems in decapod crustaceans. In: Decapod Crustacean Phylogenetics (pp. 121–182). https://doi.org/10.1201/9781420092592-c8

Azra MN, Mohamad A, Hidir A, Taufik M, Abol-Munafi AB and Ikhwanuddin M, 2020. Critical thermal maxima of two species of intertidal crabs, Scylla olivacea and Thalamita crenata at different acclimation temperatures. Aquaculture Reports, 17: 100301. https://doi.org/10.1016/j.aqrep.2020.100301

Baker CF, Gublin Y and Reeve KA, 2018. Observations of hard-shell mating in the portunid crab Charybdis japonica (A. Milne-Edwards, 1861) (Decapoda: Brachyura). Journal of Crustacean Biology, 38(4): 504–508. https://doi.org/10.1093/jcbiol/ruy029

Brink AMV and McLay CL, 2010. Competing for last place: Mating behaviour in a pill-box crab, Halicarcinus cookii (Brachyura: Hymenosomatidae). Zoologischer Anzeiger – A Journal of Comparative Zoology, 249: 21–32. https://doi.org/10.1016/j.jcz.2010.01.002

Bublitz R, Sainte-Marie B, Hardege J, Fletcher N, Newcomb-Hodgetts C and Smith M, 2008. Interspecific activity of the sex pheromone of the European shore crab (Carcinus maenas). Behaviour, 145(10): 1465–1478. https://doi.org/10.1163/156853908785765872

Cannicci S, Barelli C and Vannini M, 2000. Homing in the swimming crab Thalamita crenata: a mechanism based on underwater landmark memory. Animal Behaviour, 60(2): 203–210. https://doi.org/10.1006/anbe.2000.1458

Cannicci S, Dahdouh-Guebas F, Dyane A and Vannini M, 1996. Natural diet and feeding habits of Thalamita Crenata (Decapoda: Portunidae). Journal of Crustacean Biology, 16(4): 678–683. https://doi.org/10.1163/193724096X00766

Cannicci S, Dahdouh‐Guebas F, Anyona D and Vannini M, 1995. Homing in the mangrove swimming crab Thalamita crenata (Decapoda: Portunidae). Ethology, 100(3): 242–252. https://doi.org/10.1111/j.1439-0310.1995.tb00328.x

Chang ES and Mykles DL, 2011. Regulation of crustacean molting: A review and our perspectives. General and Comparative Endocrinology, 172(3): 323–330. https://doi.org/10.1016/j.ygcen.2011.04.003

Chen CW, Chen CF, Ju YR and Dong CD, 2016. Assessment of the bioaccumulation and biodegradation of butyltin compounds by Thalamita crenata in Kaohsiung Harbor, Taiwan. International Biodeterioration and Biodegradation, 113: 97–104. https://doi.org/10.1016/j.ibiod.2016.02.018

Chen MH, Chen CY, Chou HY and Wen TC, 2005. Gender and size effects of metal bioaccumulation on the rock crab, Thalamita crenata, in Dapeng Bay, southwestern Taiwan. Marine Pollution Bulletin, 50(4): 463–469. https://doi.org/10.1016/j.marpolbul.2005.01.012

Comeau M, Robichaud G, Starr M, Therriault JC and Conan GY, 1998. Mating of snow crab Chionoecetes opilio (Ο. Fabricius, 1788) (Decapoda, Majidae) in the Fjord of Bonne Bay, Newfoundland. Crustaceana, 71(8): 925–941. https://doi.org/10.1163/156854098X00932

Faria FA, Repenning Má, Tavares NG, Senner NR and Bugoni L, 2021. Breeding habitats, phenology and size of a resident population of Two‐banded Plover (Charadrius falklandicus) at the northern edge of its distribution. Austral Ecology, 46(8): 1311–1321. https://doi.org/10.1111/aec.13074

Forstmeier W, Martin K, Bolund E, Schielzeth H and Kempenaers B, 2011. Female extrapair mating behavior can evolve via indirect selection on males. Proceedings of the National Academy of Sciences, 108(26): 10608–10613. https://doi.org/10.1073/pnas.1103195108

Fusi M, Daffonchio D, Booth J and Giomi F, 2021. Dissolved oxygen in heterogeneous environments dictates the metabolic rate and thermal sensitivity of a tropical aquatic crab. Frontiers in Marine Science, 8: 767471. https://doi.org/10.3389/fmars.2021.767471

Hamid A, Wardiatno Y and Irawati N, 2019. Biological aspects of genus Thalamita Latreille, 1829 (Decapoda: Portunidae) in Lasongko Bay, Southeast Sulawesi, Indonesia. AACL Bioflux, 12(4): 1335–1348.

Hartnoll RG, 1975. The Grapsidae and Ocypodidae (Decapoda: Brachyura) of Tanzania. Journal of Zoology, 177(3): 305–328. https://doi.org/10.1111/j.1469-7998.1975.tb02235.x

Hayden D, Jennings A, Müller C, Pascoe D, Bublitz R, Webb H, Breithaupt T, Watkins L, and Hardege J, 2007. Sex-specific mediation of foraging in the shore crab, Carcinus maenas. Hormones and Behavior, 52(2): 162–168. https://doi.org/10.1016/j.yhbeh.2007.03.004

Herborg LM, Bentley MG, Clare AS and Last KS, 2006. Mating behaviour and chemical communication in the invasive Chinese mitten crab Eriocheir sinensis. Journal of Experimental Marine Biology and Ecology, 329: 1–10. https://doi.org/10.1016/j.jembe.2005.08.001

João MCA, Kriegler N, Freire AS and Pinheiro AMA, 2021. Mating strategies of the endangered insular land crab Johngarthia lagostoma (H. Milne Edwards, 1837). Invertebrate Reproduction and Development, 65(4): 256–267. https://doi.org/10.1080/07924259.2021.1961885

Kannupandi T, Krishnan T and Shanmugam A, 1997. Effect on salinity on the larva of an edible estuarine crab, Thalamita crenata (Crustacea: Decapoda: Portunidae). Indian Journal of Marine Science, 26: 315–318.

Kobayashi S and Vazquez-Archdale M, 2020. Mating behaviour of the leucosiid crab Pyrhila pisum (De Haan, 1841). Journal of the Marine Biological Association of the United Kingdom, 100: 103–113. https://doi.org/10.1017/S0025315419001140

Kobayashi S and Vazquez-Archdale M, 2018. Growth and reproductive ecology of the portunid crab Charybdis japonica in an open seacoast and an inland bay in Fukuoka, Japan. Journal of Sea Research, 142: 52–65. https://doi.org/10.1016/j.seares.2018.09.006

Kunsook C and Dumrongrojwatthana P, 2017. Species diversity and abundance of marine crabs (Portunidae: Decapoda) from a collapsible crab trap fishery at Kung Krabaen Bay, Chanthaburi Province, Thailand. Tropical Life Sciences Research, 28: 45–67. https://doi.org/10.21315/tlsr2017.28.1.4

Lin H, Zhang C, Liao J, Yang F, Zhong S, Jiang P, Chen X and Nagashima Y, 2015. Neutralizing effect of hemolymph from the shore crab, Thalamita crenata, on paralytic shellfish toxins. Toxicon, 99: 51–57. https://doi.org/10.1016/j.toxicon.2015.03.010

Mckillup SC and Mckillup RV, 1996. The feeding behaviour of Thalamita crenata (Portunidae, Decapoda), a cannibalistic marine scavenger. Marine and Freshwater Behaviour and Physiology, 28(4): 255–267. https://doi.org/10.1080/10236249609378995

McLay CL and Becker C, 2015. Reproduction in Brachyura. In: Treatise on Zoology – Anatomy, Taxonomy, Biology. The Crustacea, Volume 9 Part C (2 vols) (pp. 185–243). Brill. https://doi.org/10.1163/9789004190832_006

Muhd-Farouk H, Amin-Safwan A, Arif MS and Ikhwanuddin M, 2017. Biological information and size at maturity of male crenate swimming crab, Thalamita crenata from Setiu Wetlands, Terengganu Coastal Waters. Journal of Sustainability Science and Management, 12(2): 119–127.

Mustaquim J, Khatoon S and Rashid S, 2022. A note on sex ratio, size at maturity, fecundity and breeding season of the portunid crab, Thranita crenata (Rüppell, 1830) from the Pakistani coast. Crustaceana, 95(2): 127–136. https://doi.org/10.1163/15685403-bja10179

Orensanz JM, Parma AM, Armstrong DA, Armstrong J and Wardrup P, 1995. The breeding ecology of Cancer gracilis (Crustacea: Decapoda: Cancridae) and the mating systems of cancrid crabs. Journal of Zoology, 235(3): 411–437. https://doi.org/10.1111/j.1469-7998.1995.tb01760.x

Sayekti PR, Fahrunnida F, Cerniauskas G, Robert C, Retnoaji B and Alam P, 2020. The impact behaviour of crab carapaces in relation to morphology. Materials, 13(18): 3994. https://doi.org/10.3390/ma13183994

Tan MH, Gan HM, Lee YP and Austin CM, 2016. The complete mitogenome of the swimming crab Thalamita crenata (Rüppell, 1830) (Crustacea; Decapoda; Portunidae). Mitochondrial DNA, 27(2): 1275–1276. https://doi.org/10.3109/19401736.2014.945553

Tullis RE and Kamemoto FI, 1974. Separation and biological effects of CNS factors affecting water balance in the decapod crustacean Thalamita crenata. General and Comparative Endocrinology, 23: 19–28. https://doi.org/10.1016/0016-6480(74)90049-5

Tuntiprapas P, Rattanachot E and Prathep A, 2021. Increasing habitat complexity enhances crab density: A case study from Thailand. Ecological Research, 36(2): 293–302. https://doi.org/10.1111/1440-1703.12196

Vezzosi R, Barbaresi S, Anyona D and Vannini M, 1994a. Activity patterns in Thalamita crenata Portunidae, decapoda): A shaping by the tidal cycles. Marine Behaviour and Physiology, 24(4): 207–214. https://doi.org/10.1080/10236249509378895

Vezzosi R, Cannicci S and Anyona D, 1994b. Swimming rhythms and hydrostatic pressure responses of Thalamita crenata (Latreille). Bolletino Di Zoologia, 61: 26–26. https://doi.org/10.1080/11250009409355949

Watanabe S, Doi W, Yokota M and Strüssmann CA, 2008. Growth and reproduction of the Portunid crab Charybdis bimaculata (Decapoda: Brachyura) in Tokyo Bay. Journal of Crustacean Biology, 28(4): 641–651. https://doi.org/10.1651/07-2964.1

Xie Z, Lai T, Waiho K, Tan H and Ma H, 2018. Complete mitochondrial genome of the spiny rock crab Thalamita crenata (rüppell, 1830) (Crustacea: Decapoda: Portunidae) from China coast and its phylogeny. Mitochondrial DNA Part B, 3(2): 1019–1020. https://doi.org/10.1080/23802359.2018.1508384

How to cite

Abit LY, Moh JHZ, Grinang J, Morni WZW, Asif AA and Latif K 2024.First report of hard shell female mating in the crenate swimming crab, Thalamita crenata Ruppell, 1830 (Crustacea: Decapoda: Portunidae) Aquatic Invertebrates and Ecosystem Research, 1(1): 21-25. https://doi.org/10.69517/aier.2024.01.01.0004

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