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The first evidence of intersexuality in Atka mackerel Pleurogrammus monopterygius (Hexagrammidae)
Published online by Cambridge University Press: 15 January 2021
Summary
Histological examination of Atka mackerel ovotestes reveals the possibility of intersexuality. Individuals with bisexual gonads have been caught in the North Pacific near the south-east coast of the Kamchatka peninsula. While intersex appeared to be normal females with developing ovaries, histological analysis showed the presence of both female and male tissue in the same gonad. Specifically, primary growth, cortical alveolar and primary vitellogenic oocytes were located among spermatogonia cysts. The prevalence of intersexuality in the population was less than 0.1%.
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- © The Author(s), 2021. Published by Cambridge University Press
References
Atz, JW (1964). Intersexuality in fishes. In Armstrong, CN and Marshall, AJ (Eds), Intersexuality in Vertebrates Including Man. London: Academic Press, pp. 145–232.Google Scholar
Antonov, NP, Klovatch, NV, Orlov, AM, Datsky, AV, Lepskaya, VА, Kuznetsov, VV, Yarzhombek, АА, Abramov, АА, Alekseev, DО, Moiseev, SI, Evseeva, NА and Sologub, DО (2016). Fishery in Far Eastern fishery basin in 2013, Trudy VNIRO 160, 133–211.Google Scholar
Bahamonde, PA, Munkittrick, KR and Martyniuk, CJ (2013). Intersex in teleost fish: are we distinguishing endocrine disruption from natural phenomena? Gen Comp Endocrinol 192, 25–35.CrossRefGoogle ScholarPubMed
Blazer, VS (2002). Histopathological assessment of gonadal tissue in wild fishes. Fish Physiol Biochem 26, 85–101.CrossRefGoogle Scholar
Brown-Peterson, NJ, Wyanski, DM, Saborido-Rey, F, Macewicz, BJ and Lowerre-Barbieri, SK (2011). A standardized terminology for describing reproductive development in fishes. Mar Coastal Fish 3, 52–70.CrossRefGoogle Scholar
Cooper, D and McDermott, S (2011). Seasonal, small-scale distribution of Atka mackerel in the Aleutian Islands, Alaska, with respect to reproduction. Mar Coastal Fish 3, 10–20.CrossRefGoogle Scholar
Cooper, DW, McDermott, SF and Ianelli, JN (2010). Spatial and temporal variability in Atka mackerel female maturity at length and age. Mar Coastal Fish 2, 329–38.CrossRefGoogle Scholar
Devlin, RH and Nagahama, Y (2002). Sex determination and sex differentiation in fish: an overview of genetic, physiological, and environmental influences. Aquaculture 208, 191–364.CrossRefGoogle Scholar
Gorbunova, NN (1962). Spawning and development of greenlings (family Hexagrammidae). Trudy Instituta Okeanologii Akademiya Nauk SSSR 59, 118–20. [Translated from Russian 1970: Israel Program for Scientific Translations, Jerusalem; available from National Technical Information Services, Springfield, Virginia as SFCSI-INT TT-69-55097].Google Scholar
Jobling, S, Nolan, M, Tyler, CR, Brighty, G and Sumpter, JP (1998). Widespread sexual disruption in wild fish. Environ Sci Technol 32, 2498–506.CrossRefGoogle Scholar
Lauth, RR, Guthridge, J, Nichol, DG, McEntire, SW and Hillgruber, N (2007). Timing of nesting, spawning, and brooding periods of Atka mackerel, Pleurogrammus monopterygius, in the North Pacific Ocean. Fish Bull 105, 560–70.Google Scholar
Lauth, RR, Guthridge, JL, Cooper, DW and McEntire, SW (2010). Behavioral ecology of color patterns in Atka mackerel. Mar Coast Fish 2, 399–411.CrossRefGoogle Scholar
Lowe, S, Ianelli, J, Wilkins, M, Aydin, K, Lauth, R and Spies, I (2008). Stock assessment of Bering Sea/Aleutian Islands Atka mackerel. In Appendix A, Stock Assessment and Fishery Evaluation Report for the Groundfish Resources of the Bering Sea/Aleutian Islands Regions. North Pacific Fishery Management Council. Anchorage, Alaska, pp. 1119–98.Google Scholar
McBride, RS, Somarakis, S, Fitzhugh, GR, Albert, A, Yaragina, NA, Wuenschel, MJ, Alonso-Fernandez, A and Basilone, G (2015). Energy acquisition and allocation to egg production in relation to fish reproductive strategies. Fish Fish 16, 23–57.CrossRefGoogle Scholar
McDermott, SF and Lowe, SA (1997). The reproductive cycle of Atka mackerel (Pleurogrammus monopterygius) in Alaska waters. Fish Bull 95, 231–333.Google Scholar
Sadovy, Y and Shapiro, DY (1987). Criteria for the diagnosis of hermaphroditism in fishes. Copeia 1, 136–56.CrossRefGoogle Scholar
Sadovy de Mitcheson, Y and Liu, M (2008). Functional hermaphroditism in teleosts. Fish Fish 9, 1–43
CrossRefGoogle Scholar
Tancioni, L, Caprioli, R, Dawood, Al, Khafaji, A, Mancini, L, Boglione, C, Ciccotti, E and Cataudella, S (2016). Anthropogenic threats to fish of interest in aquaculture: gonad intersex in a wild population of thinlip grey mullet Liza ramada (Risso, 1827) from a polluted estuary in central Italy. Aquacult Res 2014, 1–5.Google Scholar
Yamamoto, T (1969). Sex differentiation. In Hoar, W.S. & Randall, D.J. (Eds). Fish Physiology, vol. 3A. New York: Academic Press, pp. 117–175.Google Scholar
Zhukova, K and Privalikhin, AM (2015). First record of intersexuality in walleye pollock Theragra chalcogramma (Pallas, 1814). Mar Biodivers Rec 8, e89.CrossRefGoogle Scholar
Zhukova, KA, Gordeev, II and Kuznetsova, EN (2018). Abnormal gonads in the Antarctic toothfish (Dissostichus mawsoni Norman, 1937 [Perciformes: Nototheniidae]): the first record and histological description. Pol Res 37, 1540244.CrossRefGoogle Scholar
Zolotov, OG (1993). Notes on the reproductive biology of Pleurogrammus monopterygius in Kamchatkan waters. J Ichthyol 33, 25–37.Google Scholar