INFLUENCE OF TEMPERATURE ON SPONTANEOUS LOCOMOTOR ACTIVITY OF THE SADDLER BICHIR POLYPTERUS ENDLICHERII (POLYPTERIDAE)
- Авторлар: Kasumyan A.O1, Zdanovic V.V1, Sataeva V.V1
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Мекемелер:
- Lomonosov Moscow State University
- Шығарылым: Том 65, № 5 (2025)
- Беттер: 618-624
- Бөлім: Articles
- URL: https://bakhtiniada.ru/0042-8752/article/view/362404
- DOI: https://doi.org/10.7868/S3034514625050081
- ID: 362404
Дәйексөз келтіру
Аннотация
Негізгі сөздер
Авторлар туралы
A. Kasumyan
Lomonosov Moscow State UniversityMoscow, Russia
V. Zdanovic
Lomonosov Moscow State University
Email: zdanovich@mail.ru
Moscow, Russia
V. Sataeva
Lomonosov Moscow State UniversityMoscow, Russia
Әдебиет тізімі
- Зданович В.В., Сатаева В.В., Касумян А.О. 2024. Термоизбирание у симпатрических многопёров: сенегальского Polypterus senegalus и Эндлихера P. endlicherii (Polypteridae) // Вопр. ихтиологии. Т. 64. № 6. С. 763–772. https://doi.org/10.31857/S0042875224060108
- Касумян А.О., Зданович В.В., Сатаева В.В. 2024. Двигательная активность интактного и зрительно депривированного сенегальского многопёра Polypterus senegalus (Cladistia) при разной температуре воды // Вопр. ихтиологии. Т. 64. № 3. С. 354–362. https://doi.org/10.31857/S0042875224030097
- Касумян А.О., Зданович В.В., Сатаева В.В. 2025. Термоидеферендное поведение сенегальского многопёра Polypterus senegalus (Polypteridae) при хронической зрительной депривации // Вопр. ихтиологии. Т. 65. № 1. С. 114–123. https://doi.org/10.31857/S0042875225010086
- Смирнов А.К., Смирнова Е.С. 2020. Влияние температуры на двигательную активность и плавательную способность молодых плотвы Rutilus rutilus (Cyprinidae) // Вопр. ихтиологии. Т. 60. № 2. С. 219–228. https://doi.org/10.31857/S0042875220020228
- Coates M. 2017. Plenty of fish in the tree // Nature. V. 549. № 7671. P. 167–169. https://doi.org/10.1038/s49167a
- Foster K.L., Dhuper M., Standen E.M. 2018. Fin and body neuromuscular coordination changes during walking and swimming in Polypterus senegalus // J. Exp. Biol. V. 221. № 17. Article jeb168716. https://doi.org/10.1242/jeb.168716
- Froese R., Pauly D. (eds.). 2024. FishBase. World Wide Web electronic publication (www.fishbase.org. Version 10/2024).
- Gardin A., Otero O., Reveillac E. et al. 2023. Seasonality and growth in tropical freshwater ectotherm vertebrates: results from one-year experimentation in the African grey bichir, girafie catfish, and the West African mud turtle // Ecol. Evol. V. 13. № 3. Article e9936. https://doi.org/10.1002/ece3.9936
- Gardiner B.G., Schaeffer B., Masserie J.A. 2005. A review of the lower actinopterygian phylogeny // Zool. J. Linn. Soc. V. 144. № 4. P. 511–525. https://doi.org/10.1111/j.1096-3642.2005.00181.x
- Giles S., Xu G.-H., Near T.J., Friedman M. 2017. Early members of "living fossil" lineage imply later origin of modern ray-finned fishes // Nature. V. 549. № 7671. P. 265–268. https://doi.org/10.1038/nature23654
- Hurley I.A., Mueller R.L., Dunn K.A. et al. 2007. A new time-scale for ray-finned fish evolution // Proc. R. Soc. B. V. 274. № 1609. P. 489–498. https://doi.org/10.1098/rspb.2006.3749
- Lachance S., Magnan P., FitzGerald G.J. 1987. Temperature preferences of three sympatric sticklebacks (Gasterosteidae) // Can. J. Zool. V. 65. № 6. P. 1573–1576. https://doi.org/10.1139/z87-245
- Lauder G.V. Jr. 1980. Evolution of the feeding mechanism in primitive actinopterygian fishes: a functional anatomical analysis of Polypterus, Lepisosteus, and Amia // J. Morphol. V. 163. № 3. P. 283–317. https://doi.org/10.1002/jmor.1051630305
- Lévêque C. 1997. Biodiversity dynamics and conservation: the freshwater fish of tropical Africa. Cambridge: Cambridge Univ. Press, 452 p.
- Lutek K., Standen E.M. 2021. Increasing viscosity helps explain locomotor control in swimming Polypterus senegalus // Integr. Org. Biol. V. 3. № 1. Article obab024. https://doi.org/10.1093/iob/obab024
- Lutek K., Foster K.L., Standen E.M. 2022. Behaviour and muscle activity across the aquatic–terrestrial transition in Polypterus senegalus // J. Exp. Biol. V. 225. № 23. Article jeb243902. https://doi.org/10.1242/jeb.243902
- Mandal P., Cai L., Tu Z. et al. 2016. Effects of acute temperature change on the metabolism and swimming ability of juvenile sterlet sturgeon (Acipenser ruthenus, Linnaeus 1758) // J. Appl. Ichthyol. V. 32. № 2. P. 267–271. https://doi.org/10.1111/jai.13033
- Meskendahl L., Fontes R.P., Herrmann J.-P., Temming A. 2019. Metabolic costs of spontaneous swimming in Sprattus sprattus L., at different water temperatures // PLoS One. V. 14. № 11. Article e0225568. https://doi.org/10.1371/journal.pone.0225568
- Morescalchi M.A., Barucca M., Slingo V., Capriglione T. 2010. Polypteridae (Actinopterygii: Cladistia) and DANA-SINES insertions // Mar. Genomics. V. 3. № 2. P. 79–84. https://doi.org/10.1016/j.margen.2010.06.001
- Moritz T. 2017. Fishery impact on bichirs (Polypteridae, Actinopterygii) in the Pendjari River (Benin) // Bull. Fish Biol. V. 16. № 1/2. P. 83–86.
- Moritz T., Britz R. 2019. Revision of the extant Polypteridae (Actinopterygii: Cladistia) // Ichthyol. Explor. Freshw. V. 29. № 2. P. 97–192. https://doi.org/10.23788/IEF-1094
- Moritz T., Lalèyè P. 2018. Fishes of the Pendjari National Park (Benin, West Africa) // Bull. Fish Biol. V. 18. № 1/2. P. 1–57.
- Ohlberger J., Staaks G.B.O., Petzoldt T. et al. 2008. Physiological specialization by thermal adaptation drives ecological divergence in a sympatric fish species pair // Evol. Ecol. Res. V. 10. P. 1173–1185.
- Peck M.A., Buckley L.J., Bengtson D.A. 2006. Effects of temperature and body size on the swimming speed of larval and juvenile Atlantic cod (Gadus morhua): implications for individual-based modelling // Environ. Biol. Fish. V. 75. № 4. P. 419–429. https://doi.org/10.1007/s10641-006-0031-3
- Pfeiffer W. 1969. Der Geruchssinn der Polypteridae (Pisces, Brachiopterygii) // Z. Vergl. Physiol. V. 63. № 2. P. 151–164. https://doi.org/10.1007/BF000298337
- Raji A., Saidu A.K., Maryam A.T. 2004. Preliminary studies on food and feeding habits of Polypterus endlicheri and Polypterus senegalus in Lake Chad // Proc. 18th Ann. conf. Fish. Soc. Nigeria. Owerri: FISON. P. 186–193.
- Reynolds W.W., Casterlin M.E. 1978. Complementarity of thermoregulatory rhythms in Micropterus salmoides and M. dolomieui // Hydrobiologia. V. 60. № 1. P. 89–91. https://doi.org/10.1007/BF00018689
- Sataeva V.V., Kasumyan A.O. 2022. Orosensory preferences and feeding behavior of Cladistia: a comparison of gray bichir Polypterus senegalus and saddle bichir P. endlicherii (Polypteridae) // J. Ichthyol. V. 62. № 7. P. 1501–1520. https://doi.org/10.1134/S003294522204021X
- Schurmann H., Steffensen J.F. 1994. Spontaneous swimming activity of Atlantic cod Gadus morhua exposed to graded hypoxia at three temperatures // J. Exp. Biol. V. 197. № 1. P. 129–142. https://doi.org/10.1242/jeb.197.1.129
- Standen E.M., Du T.Y., Laroche P., Larsson H.C.E. 2016. Locomotor flexibility of Polypterus senegalus across various aquatic and terrestrial substrates // Zoology. V. 119. № 5. P. 447–454. https://doi.org/10.1016/j.zool.2016.05.001
- Sudagar M., Kheirabadi H., Masaeli S. 2023. A review on the morphology, biology, reproduction and breeding of Polypterus fish // J. Ornam. Aquat. V. 10. № 1. P. 35–40. https://dor.isc.ac/dor/20.1001.1.24234575.1402.10.1.4.2
- Van Wassenbergh S., Bonte C., Michel K.B. 2017. Terrestrial capture of prey by the reedfish, a model species for stem tetrapods // Ecol. Evol. V. 7. № 11. P. 3856–3860. https://doi.org/10.1002/ece3.2694
- Vicente P., Almeida J., Ribeiro L. et al. 2024. Effects of water temperature and structural habitat complexity on the routine swimming speed and escape response of post-settlement stage white seabream // Oceans. V. 5. № 1. P. 38–47. https://doi.org/10.3390/oceans5010003
- Whitlow K.R., Rossi C.F., Gidmark N.J. et al. 2022. Suction feeding biomechanics of Polypterus bichir: investigating linkage mechanisms and the contributions of cranial kinesis to oral cavity volume change // J. Exp. Biol. V. 225. № 3. Article jeb243283. https://doi.org/10.1242/jeb.243283
- Wilhelm B.C., Du T.Y., Standen E.M., Larsson H.C.E. 2015. Polypterus and the evolution of fish pectoral musculature // J. Anat. V. 226. № 6. P. 511–522. https://doi.org/10.1111/joa.12302
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