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From Descriptive to Accurate Horseshoe Crab Size Variations in Wild Populations

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Horseshoe crabs have survived until Holocene, but their persistence beyond the Anthropocene is challenged by drastic environment changes that entail impoverishments and the resultant unusual growth sizes. Previously, allometry via morphometric ratio was introduced to classify horseshoe crabs into normal-abnormal growth. However, the descriptive size and weight analysis indicated a considerable portion of Tachypleus gigas with normal allometry. This error was caused by the median sorting of values. Therefore, the same data was treated with correlation before generating a linear equation. By being sexual dimorphs, these arthropods actually have gender-specific morphology indicators which could generate a functional allometry. Since the assessed arthropods were mature, the 19 % yield of smaller female T. gigas was possibly due to degradation effects from poor diets or stress. Yet, for this population, an added risk was female-only harvest. Perhaps, close sizing to male counterparts could be perceived a survival strategy by the female T. gigas. More evidence is needed to strengthen this opinion but for now, this assessment method is novel for accurate allometry assessments in the species with sexual dimorphism. Overall, capture fisheries could have negative impacts and when made severe by sex-specific harvest, the unaccounted practices could collapse sustaining populations.
Słowa kluczowe
Rocznik
Strony
273--284
Opis fizyczny
Bibliogr. 21 poz., rys., tab.
Twórcy
autor
  • Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu, Malaysia
autor
  • Institute of Oceanography and Maritime Studies, Kulliyyah of Science, International Islamic University Malaysia, Kuantan, Malaysia
  • IIUM molecular and cellular biology research cluster (iMoleC), International Islamic University Malaysia, Jalan hospital campus 25100, Kuantan, Malaysia
  • Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu, Malaysia
  • College of Environment and Ecology, Xiamen University, 361102 Xiamen, Fujian, China
  • Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu, Malaysia
autor
  • School of Business and Management, RMIT University, Vietnam, Handi Resco Building, 521 Kim Ma, Ba Dinh District, Hanoi, Vietnam
autor
  • Center of Fundamental and Continuing Education, Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu, Malaysia
  • Faculty of Earth Science, Universiti Malaysia Kelantan, 17600, Jeli, Kelantan, Malaysia
  • Skills Innovation and Academic Network Institute, Association for Biodiversity Conservation and Research, 756001, Odisha, India
  • Institute of Tropical Biodiversity and Sustainable Development, Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu, Malaysia
Bibliografia
  • 1. Ariffin M.S.A., Ramlee M.N.A., Pati S., Edinur H.A. Nelson B.R. 2022. Fish Distribution in Tropical Bidong Island, South China Sea Under Influence from Nearshore Sea Acidification. Springer Cham, Switzerland.
  • 2. Chatterji A., Pati S. 2014. Allometric relationship in the adult population of the Malaysian horseshoe crab (Tachypleus tridentatus; Leach). International Journal of Research, 1, 1378–1385.
  • 3. Fairuz-Fozi N., Satyanarayana B., Zauki N.A.M., Muslim A.M., Husain M.L., Ibrahim S., Nelson B.R. 2018. Carcinoscorpius rotundicauda (Latreille, 1802) population status and spawning behaviour at Pendas coast, Peninsular Malaysia. Global Ecology and Conservation, 15, e00422.
  • 4. Jaffar M., Yunus N.M., Nelson B.R. 2019. Regional tinfoil barb imports can alter its native species genetic makeup. Journal of Sustainability Science and Management, 14, 51–65.
  • 5. 5. Jisr N., Younes G., Sukhn C., El-Dakdouki M.H. 2018. Length-weight relationships and relative condition factor of fish inhabiting the marine area of the Eastern Mediterranean city, Tripoli-Lebanon. Egyptian Journal of Aquatic Research, 44, 299–305.
  • 6. 6. John B.A., Nelson B.R., Sheikh H.I., Cheung S.G., Wardiatno Y., Dash B.P., Tsuchiya K., Iwasaki Y., Pati S. 2018. A review on fisheries and conservation status of Asian horseshoe crabs. Biodiversity and Conservation, 27, 3573–3598.
  • 7. Hamasaki K., Ishii M., Dan S. 2020. Reproductive traits and population structure of the porcellanid crab Petrolisthes japonicus (Decapoda: Anomura: Porcellanidae). Crustacean Research, 49, 121–132.
  • 8. Hare R.M., Simmons L.W. 2019. Sexual selection and its evolutionary consequences in female animals. Biological Reviews, 94(3), 929–956.
  • 9. Mashar A., Butet N.A., Juliandi B., Qonita Y., Hakim A.A., Wardiatno Y. 2017. Biodiversity and distribution of horseshoe crabs in northern coast of Java and southern coast of Madura. Environmental Earth Sciences, 54, 012076.
  • 10. Mohamad F., Manca A., Ahmad A., Fawwaz M. 2016. Width-weight and length-weight relationships of the tri-spine horseshoe crab, Tachypleus tridentatus (Leach 1819) from two populations in Sabah, Malaysia: implications for population management. Journal of Sustainability Science and Management, 11, 1–13.
  • 11. Mohamed R., Paul N.A., Isa N.S., Damanhuri J.H., Shahimi S., Pati S., John A., Nelson B.R. 2021. Using applied statistics for accurate size classification of the endangered Tachypleus tridentatus horseshoe crab. Journal of Ecological Engineering, 22, 273–282.
  • 12. Nelson B.R., John A., Zhong J.H., Jalal K.C.A. 2020. Membrane retention potential of Tachypleus gigas during early embryogenesis. Desalination and Water Treatment, 187, 17–23.
  • 13. Post J.R., Parkinson E.A. 2001. Energy allocation strategy in young fish: allometry and survival. Ecology, 82, 1040–1051.
  • 14. Pramanik A., Rajesh A.S., Tudu S., Beata M.M., Shahimi S., Nelson B.R., Sarkar T., Satyanarayana B., Pati S., Dash B.P. 2021. Review on biology, distribution and conservation challenges for horseshoe crabs in India. Journal of Sustainability Science and Management, 16, 332–346.
  • 15. Razak M.R., Kassim Z. 2018. Comparison of horseshoe crabs (Tachypleus gigas) morphometry between different populations using allometric analysis. Aquaculture, Aquarium, Conservation & Legislation, 11, 143–157.
  • 16. Sahu A.C., Dey L. 2013. Spawning density and morphometric characteristics of the horseshoe crab Tachypleus gigas (Müller) on the Balasore coast of Bay of Bengal, India. Science Vision, 13, 76–84.
  • 17. Sastraprawira S.M., Razak I.H.A., Shahimi S., Pati S., Edinur H.A., John A.B., Ahmad A., Kumaran J.V., Martin M.B., Chong J.L., Nelson B.R. 2020. A review on introduced Cichla spp. and emerging concerns. Heliyon, 6, e05370.
  • 18. Smith M.D., Brockmann H.J. 2014. The evolution and maintenance of sexual size dimorphism in horseshoe crabs: an evaluation of six functional hypotheses. Animal Behaviour, 96, 127–139.
  • 19. 19. Tan A.N., Christianus A., Shakibazadeh S., Hajeb P. 2012. Horseshoe crab, Tachypleus gigas (Müller, 1785) spawning population at Balok Beach, Kuantan, Pahang, Malaysia. Pakistan Journal of Biological Sciences, 15, 610–620.
  • 20. Vijayakumar R., Das S., Chatterji A., Parulekar A.H. 2000. Morphometric characteristics in the horseshoe crab Tachypleus gigas (Arthropoda: Merostomata). Indian Journal of Marine Sciences, 29, 333–335.
  • 21. Zauki N.A.M., Satyanarayana B., Fairuz-Fozi N., Nelson B.R., Martin M.B., Akbar-John B., Chowdhury A.J.K. 2019. Citizen science frontiers horseshoe crab population regain at their spawning beach in East Peninsular Malaysia. Journal of Environmental Science and Management, 232, 1012–1020.
Uwagi
Opracowanie rekordu ze środków MEiN, umowa nr SONP/SP/546092/2022 w ramach programu "Społeczna odpowiedzialność nauki" - moduł: Popularyzacja nauki i promocja sportu (2022-2023).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-624e40ea-0165-4174-8a88-f9bc8bdc72af
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