Morphology of the urogenital papilla of the male marine teleost Black Rockfish, Sebastes schlegelii (Hilgendorf, 1880), and its role in internal fertilization.
androgens
external genitalia
fishes
viviparous
Journal
Journal of morphology
ISSN: 1097-4687
Titre abrégé: J Morphol
Pays: United States
ID NLM: 0406125
Informations de publication
Date de publication:
01 2023
01 2023
Historique:
revised:
20
09
2022
received:
11
07
2022
accepted:
09
10
2022
pubmed:
15
11
2022
medline:
21
12
2022
entrez:
14
11
2022
Statut:
ppublish
Résumé
There are few detailed descriptions of the morphology of the male external genitalia, the urogenital papilla (UGP), of the Black Rockfish (Sebastes schlegelii Hilgendorf, 1880). The purpose of this study was to evaluate this organ histologically and to determine the time of development of the UGP in Black Rockfish. Twelve adult males, three adult females and around 500 juveniles were used in the experiment. The juveniles were divided into normal developmental and androgen groups. The androgen group was exposed to methyltestosterone (100 μg/L) for 2 h daily for 38 days. Samples (N = 10 per sampling) were randomly selected for analysis every 5 days from 30 to 116 days after birth. Parameters assessed included the type of epithelium, composition of connective tissue, muscular tissue, and the timing of UGP development. Differences in these parameters between normal developmental and androgen groups were evaluated. The results indicated that the UGP of the adult fish contains the sperm duct and ureter, which have the function of transporting sperm and urine, respectively. The androgen-treated juvenile fish developed the UGP earlier than the normal development group. This study provides a reference for understanding the external genitalia of other viviparous fishes by studying the UGP of the male Black Rockfish.
Substances chimiques
Androgens
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e21534Informations de copyright
© 2022 Wiley Periodicals LLC.
Références
Bhatia, H. & Kumar, A. (2016). Does anti-androgen, flutamide cancel out the in vivo effects of the androgen, dihydrotestosterone on sexual development in juvenile Murray rainbowfish (Melanotaenia fluviatilis)? Aquatic Toxicology, 170, 72-80. https://doi.org/10.1016/j.aquatox.2015.11.010
Bisazza, A., J. Rogers, L., & Vallortigara, G. (1998). The origins of cerebral asymmetry: A review of evidence of behavioural and brain lateralization in fishes, reptiles and amphibians. Neuroscience & Biobehavioral Reviews, 22, 411-426. https://doi.org/10.1016/s0149-7634(97)00050-x
Blaschko, S. D., Cunha, G. R., & Baskin, L. S. (2012). Molecular mechanisms of external genitalia development. Differentiation, 84, 261-268. https://doi.org/10.1016/j.diff.2012.06.003
Bond, E. R. & Forsgren, K. L. (2022). External reproductive structures of Male surfperches (Embiotocidae): Urogenital papilla. The Anatomical Record, 305, 1712-1723. https://doi.org/10.1002/ar.24836
Carisle, S. L., Marxer-Miller, S. K., Canario, A. V. M., Oliveira, R. F., Carneiro, L., & Grober, M. S. (2000). Effects of 11-ketotestosterone on genital papilla morphology in the sex changing fish Lythrypnus dalli. Journal of Fish Biology, 57, 445-456. https://doi.org/10.1006/jfbi.2000.1320
Eversolef, W. J. (1938). ≪The effects of androgens upon the fish (lebistes reticu- latus).pdf>. Endocrinology, 25, 328-330. https://doi.org/10.1210/endo-25-2-328
Fishelson, L., Gon, O., Holdengreber, V., & Delarea, Y. (2006). Comparative morphology and cytology of the Male sperm-transmission organs in viviparous species of clinid fishes (Clinidae: Teleostei, perciformes. Journal of Morphology, 267, 1406-1414. https://doi.org/10.1002/jmor.10485
Galindo-Villegas, J. & Sosa-Lima, F. (2002). Gonopodial system review and a new fish record of Poeciliopsis infans (Cyprinodontiformes: Poeciliidae) for lake patzcuaro, michoacan, central Mexico. Revista de Biologia Tropical, 50, 1151-1157.
Golshan, M., & Alavi, S. M. H. (2019). Androgen signaling in male fishes: Examples of anti-androgenic chemicals that cause reproductive disorders. Theriogenology, 139, 58-71. https://doi.org/10.1016/j.theriogenology.2019.07.020
Guo, H., Zhang, X., & Johnsson, J. I. (2017). Effects of size distribution on social interactions and growth of juvenile black rockfish (Sebastes schlegelii). Applied Animal Behaviour Science, 194, 135-142. https://doi.org/10.1016/j.applanim.2017.05.004
Haishen, W. (2020). Evolutionary mechanism and reproduction physiology in ovoviviparous teleost: A review. Journal of Dalian Ocean University, 35, 469-480. https://xuebao.dlou.edu.cn/EN/10.16535/j.cnki.dlhyxb.2020-084
Iida, A. (2019). Male-specific asymmetric curvature of anal fin in a viviparous teleost, Xenotoca eiseni. Zoology, 134, 1-7. https://doi.org/10.1016/j.zool.2019.03.002
Kobayashi, Y., Usami, T., Sunobe, T., Manabe, H., Nagahama, Y., & Nakamura, M. (2012). Histological observation of the urogenital papillae in the bi-directional sex-changing gobiid fish, Trimma okinawae. Zoological Science, 29, 121-126. https://doi.org/10.2108/zsj.29.121
Lamm, C. G., Hastie, P. M., Evans, N. P., & Robinson, J. E. (2012). Masculinization of the distal tubular and external genitalia in female sheep with prenatal androgen exposure. Veterinary Pathology, 49, 546-551. https://doi.org/10.1177/0300985811419533
Lange, A., Sebire, M., Rostkowski, P., Mizutani, T., Miyagawa, S., Iguchi, T., Hill, E. M., & Tyler, C. R. (2015). Environmental chemicals active as human antiandrogens do not activate a stickleback androgen receptor but enhance a feminising effect of oestrogen in roach. Aquatic Toxicology, 168, 48-59. https://doi.org/10.1016/j.aquatox.2015.09.014
Langerhans, R. B., Layman, C. A., & DeWitt, T. J. (2005). Male genital size reflects a tradeoff between attracting mates and avoiding predators in two live-bearing fish species. Proceedings of the National Academy of Sciences, 102, 7618-7623. https://doi.org/10.1073/pnas.0500935102
Lezama, A. Q. & Malabarba, L. R. (2021). The genital and anal papillae of Compsura heterura (characidae: Cheirodontinae): Morphological structure and possible role in insemination. Neotropical Ichthyology, 19, 13. https://doi.org/10.1590/1982-0224-2020-0079
Løken, O. M., Bjørgen, H., Hordvik, I., & Koppang, E. O. (2020). A teleost structural analogue to the avian bursa of fabricius. Journal of Anatomy, 236, 798-808. https://doi.org/10.1111/joa.13147
Malison, J. A., Held, J. A., & Kaatz, S. E. (2011). Sex determination of yellow perch by external morphology. North American Journal of Aquaculture, 73, 285-287. https://doi.org/10.1080/15222055.2011.601983
Moore, E. C., Roberts, R. B. (2017). Genital morphology and allometry differ by species and sex in Malawi cichlid fishes. Hydrobiologia, 791, 127-143. https://doi.org/10.1007/s10750-016-2912-6
Muñoz, M., Koya, Y., & Casadevall, M. (2002). Histochemical analysis of sperm storage inhelicolenus dactylopterus dactylopterus(teleostei: Scorpaenidae): Histochemical study of sperm storage in rockfish. Journal of Experimental Zoology, 292, 156-164. https://doi.org/10.1002/jez.1151
Nakagawa, M., Okouchi, H., Adachi, J., Hattori, K., & Yamashita, Y. (2007). Effectiveness of stock enhancement of hatchery-released black rockfish sebastes schlegeli in yamada bay-Evaluation by a fish market survey. Aquaculture, 263, 295-302. https://doi.org/10.1016/j.aquaculture.2006.10.023
Parenti, L. R. (2014). A new species of neostethus (teleostei; atherinomorpha; phallostethidae) from Brunei Darussalam, with comments on northwestern borneo as an area of endemism. Raffles Bulletin of Zoology, 62, 175-187.
Penning, T. M. (2010). New frontiers in androgen biosynthesis and metabolism. Current Opinion in Endocrinology, Diabetes & Obesity, 17, 233-239. https://doi.org/10.1097/MED.0b013e3283381a31
Rosa-Molinar, E. & Burke, A. C. (2002). Starting from fins: Parallelism in the evolution of limbs and genitalia: The fin-to-genitalia transition. Evolution and Development, 4, 124-126. https://doi.org/10.1046/j.1525-142X.2002.01067.x
Rosen, D. E. & Gordon, M. (1953). Functional anatomy and evolution of male genitalia in poeciliid fishes. Zoologica: Scientific Contributions of the New York Zoological Society. 38, 1-47. https://doi.org/10.5962/p.203441
Rosen, D. E. & Tucker, A. (1961). Evolution of secondary sexual characters and sexual behavior patterns in a family of viviparous fishes (Cyprinodontiformes-poeciliidae). Copeia, 1961, 201. -& https://doi.org/10.2307/1439999
Sanger, T. J., Gredler, M. L., & Cohn, M. J. (2015). Resurrecting embryos of the tuatara, Sphenodon punctatus, to resolve vertebrate phallus evolution. Biology Letters, 11, 20150694. https://doi.org/10.1098/rsbl.2015.0694
Santamaría-Martín, C. J., Plaul, S. E., Campuzano Caballero, J. C., Uribe, M. C., & Barbeito, C. G. (2021). Structure of the gonoduct of the viviparous teleost Cnesterodon decemmaculatus (Jenyns, 1842) (poeciliidae). Journal of Morphology, 282, 533-542. https://doi.org/10.1002/jmor.21326
Spadella, M. A., Oliveira, C., Ortega, H., Quagio-Grassiotto, I., & Burns, J. R. (2012). Male and female reproductive morphology in the inseminating genus astroblepus (ostariophysi: Siluriformes: Astroblepidae). Zoologischer Anzeiger-A Journal of Comparative Zoology, 251, 38-48. https://doi.org/10.1016/j.jcz.2011.05.005
Strange, R. J. & Kibenge, F. S. (2021). Introduction to the anatomy and physiology of the major aquatic animal species in aquaculture. Aquaculture Pharmacology, https://doi.org/10.1016/B978-0-12-821339-1.00001-5
Turner, C. L. (1941). Gonopodial characteristics produced in the anal fins of females of Gambusia affinis affinis by treatment with ethinyl testosterone. The Biological Bulletin, 80, 371-383. https://doi.org/10.2307/1537723
Turner, C. L. (1942). Sexual dimorphism in the pectoral fin of gambusia and the induction of the male character in the female by androgenic hormones. The Biological Bulletin, 83, 389-400. https://doi.org/10.2307/1538237
Wake, M. H. (1985). Oviduct structure and function in non-mammalian vertebrates. Fortschritte der Zoologie, 30, 427-435.
Wourms, J. P., Grove, B. D., & Lombardi, J. (1988). The Maternal-Embryonic relationship in viviparous fishes. In The Physiology of Developing Fish-Viviparity and Posthatching Juveniles, 1-134. http://doi.org/10.1016/S1546-5098(08)60213-7
Xu, X., Sun, X., Bai, Q., Zhang, Y., Qin, J., & Zhang, X. (2021). Molecular identification of an androgen receptor and the influence of long-term aggressive interaction on hypothalamic genes expression in black rockfish (Sebastes schlegelii). Journal of Comparative Physiology A, 207, 401-413. https://doi.org/10.1007/s00359-021-01480-8