Phylogenetic analysis of viviparity, matrotrophy, and other reproductive patterns in chondrichthyan fishes
- PMID: 38562006
- DOI: 10.1111/brv.13070
Phylogenetic analysis of viviparity, matrotrophy, and other reproductive patterns in chondrichthyan fishes
Abstract
The reproductive diversity of extant cartilaginous fishes (class Chondrichthyes) is extraordinarily broad, reflecting more than 400 million years of evolutionary history. Among their many notable reproductive specialisations are viviparity (live-bearing reproduction) and matrotrophy (maternal provision of nutrients during gestation). However, attempts to understand the evolution of these traits have yielded highly discrepant conclusions. Here, we compile and analyse the current knowledge on the evolution of reproductive diversity in Chondrichthyes with particular foci on the frequency, phylogenetic distribution, and directionality of evolutionary changes in their modes of reproduction. To characterise the evolutionary transformations, we amassed the largest empirical data set of reproductive parameters to date covering nearly 800 extant species and analysed it via a comprehensive molecular-based phylogeny. Our phylogenetic reconstructions indicated that the ancestral pattern for Chondrichthyes is 'short single oviparity' (as found in extant holocephalans) in which females lay successive clutches (broods) of one or two eggs. Viviparity has originated at least 12 times, with 10 origins among sharks, one in batoids, and (based on published evidence) another potential origin in a fossil holocephalan. Substantial matrotrophy has evolved at least six times, including one origin of placentotrophy, three separate origins of oophagy (egg ingestion), and two origins of histotrophy (uptake of uterine secretions). In two clades, placentation was replaced by histotrophy. Unlike past reconstructions, our analysis reveals no evidence that viviparity has ever reverted to oviparity in this group. Both viviparity and matrotrophy have arisen by a variety of evolutionary sequences. In addition, the ancestral pattern of oviparity has given rise to three distinct egg-laying patterns that increased clutch (brood) size and/or involved deposition of eggs at advanced stages of development. Geologically, the ancestral oviparous pattern arose in the Paleozoic. Most origins of viviparity and matrotrophy date to the Mesozoic, while a few that are represented at low taxonomic levels are of Cenozoic origin. Coupled with other recent work, this review points the way towards an emerging consensus on reproductive evolution in chondrichthyans while offering a basis for future functional and evolutionary analyses. This review also contributes to conservation efforts by highlighting taxa whose reproductive specialisations reflect distinctive evolutionary trajectories and that deserve special protection and further investigation.
Keywords: Chondrichthyes; embryo nutrition; fish reproduction; matrotrophy; oviparity; placentation; reproductive patterns; reproductive‐mode evolution; viviparity.
© 2024 Cambridge Philosophical Society.
Similar articles
-
Evolution of vertebrate viviparity and specializations for fetal nutrition: A quantitative and qualitative analysis.J Morphol. 2015 Aug;276(8):961-90. doi: 10.1002/jmor.20272. Epub 2014 Mar 21. J Morphol. 2015. PMID: 24652663
-
Matrotrophy and placentation in invertebrates: a new paradigm.Biol Rev Camb Philos Soc. 2016 Aug;91(3):673-711. doi: 10.1111/brv.12189. Epub 2015 Apr 29. Biol Rev Camb Philos Soc. 2016. PMID: 25925633 Free PMC article. Review.
-
Maternal investment evolves with larger body size and higher diversification rate in sharks and rays.Curr Biol. 2024 Jun 17;34(12):2773-2781.e3. doi: 10.1016/j.cub.2024.05.019. Epub 2024 Jun 5. Curr Biol. 2024. PMID: 38843829
-
Which came first: The lizard or the egg? Robustness in phylogenetic reconstruction of ancestral states.J Exp Zool B Mol Dev Evol. 2015 Sep;324(6):504-16. doi: 10.1002/jez.b.22642. Epub 2015 Jul 30. J Exp Zool B Mol Dev Evol. 2015. PMID: 26227660
-
Evolution of viviparous reproduction in Paleozoic and Mesozoic reptiles.Int J Dev Biol. 2014;58(10-12):935-48. doi: 10.1387/ijdb.150087db. Int J Dev Biol. 2014. PMID: 26154334 Review.
References
REFERENCES
-
- *Abdel‐Aziz, S. H. (1994). Observations on the biology of the common torpedo (Torpedo torpedo, Linnaeus, 1758) and marbled electric ray (Torpedo marmorata, Risso, 1810) from Egyptian Mediterranean waters. Marine and Freshwater Research 45(4), 693–704.
-
- *Abdel‐Aziz, S. H., Khalil, A. N. & Abdel‐Maguid, S. A. (1993). Reproductive cycle of the common guitarfish, Rhinobatos rhinobatos (Linnaeus, 1758), in Alexandria waters, Mediterranean Sea. Marine and Freshwater Research 44(3), 507–517.
-
- *Abilhoa, V., Bornatowski, H. & Oliveira Freitas, M. (2007). Some information on reproduction and embryonic development of the lesser guitarfish Zapteryx brevirostris in Southern Brazil. Acta Adriatica: International Journal of Marine Sciences 48(2), 185–190.
-
- *Acevedo, K., Bohórquez Herrera, J., Moreno, F., Moreno, C., Molina, E., Marcela, G. B. & Gómez Canchong, P. (2005). Aspectos reproductivos de tres Rajiformes capturados incidentalmente en la pesquería camaronera de arrastre en el mar Caribe de Colombia. Proceedings of the Gulf and Caribbean Fisheries Institute 58, 219–225.
-
- *Acevedo, K., Moreno, F., Grijalba‐Bendeck, M. & Acero, A. (2015). Reproductive biology of the Venezuela round stingray Urotrygon venezuelae Schultz from the Colombian Caribbean. Caldasia 37(1), 197–209.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous