The Amazon River prawn Macrobrachium amazonicum shows populations with four well-defined morphotypes in males. Dominant males of morphotypes green claw 1 (GC1) and green claw 2 (GC2) have large bodies and chelipeds and a higher reproductive success in comparison with the submissive morphotypes - translucent claw (TC) and cinnamon claw (CC). However, recently, some populations of the species do not have dominant morphotypes. Here, we compared the patterns of spermatic production and concentration among morphotypes and populations with three different phenotypes: (i) large-size amphidromous prawns, and (ii) large-size ("i" and "ii" with dominant morphotypes) and (iii) small-size hololimnetic prawns (without morphotypes). We described the spermatogenesis and the histochemical features of vasa deferentia (VD) and evaluated the relationship between the investment in spermatic production and sexual weapons acquisition in males of different phenotypes. The spermatic production and concentration in populations with four morphotypes were similar between morphotypes. The exception was the CC morphotype in which males had the seminiferous tubules filled with spermatocytes and low spermatic concentration. The spermatogenesis, spermiogenesis, and VD structure were not different among the studied phenotypes and populations. The seminal fluid of M. amazonicum is comprised by glycoproteins and by concentric layers of secretions of types I, II (basophilic), and III (eosinophilic). We could infer that males of dominant morphotypes allocate a higher amount of energy to the development of strong sexual weapons at the expense of the energy allocated to the reproductive system during the sequential growth. Inversely, small-size males direct more energy toward the spermatic production and transference at the expense of sexual weapons. Therefore, there is a clear trade-off between the investment in the gonadal and sexual weapons development in males of M. amazonicum.
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http://dx.doi.org/10.1016/j.zool.2022.126029 | DOI Listing |
Bull Entomol Res
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Laboratório de Entomologia Aplicada, Departamento de Zoologia, Centro de Biociências, Universidade Federal de Pernambuco, Recife, PE, Brasil.
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View Article and Find Full Text PDFPathogens
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Department of Infectious Agents and Hygiene, University Hospital of Saint-Etienne, 42023 Saint-Etienne, France.
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Laboratorio de Reproducción Animal, Unidad de Investigación Multidisciplinaria, Facultad de Estudios Superiores Cuautitlán, Universidad Nacional Autónoma de Mexico, Cuautitlán Izcalli 54714, Mexico.
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Laboratory of Animal Physiology, School of Veterinary Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, GR-54124 Thessaloniki, Greece.
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Specialized Surgical Hospital "Doctor Malinov", 46, Gotse Delchev blvd., 1860 Sofia, Bulgaria.
The cryopreservation of human spermatozoa is an integral part of cryobiology, aiming to support the in-vitro fertilization. The latter relies on the availability of as much as possible reproductively active spermatozoa, whose number after thawing decreases due to the accompanied freezing injury and the cytotoxicity of cryoprotectants. An innovative option to circumvent these obstacles is to make the freezing interface non-wettable, by coating it with rapeseed oil soot possessing intrinsic cryoprotective properties, delaying the ice formation and possibly providing identical rates of intracellular dehydration and extracellular crystallization.
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