Field of Science

Showing posts with label Otomorpha. Show all posts
Showing posts with label Otomorpha. Show all posts

Many Kinds of Herring

The original herring: Baltic herrings Clupea harengus membras, copyright Riku Lumiaro.


The subject of today's post is something that I'm sure that you've all encountered at one time or another. It's a group of animals that features highly in the world's food supply. Some of you may be grat fans of these animals and seek them out on a regular basis; others may not be so enthused. They go by many names: herring, sardines, sprats, shad... but all are members of the fish family Clupeidae.

For the most part, clupeids are a prime example of what I think of as 'fishy' fish: that is, fish that look exactly how the majority of people imagine a fish to look (as opposed, say, to some of those deep-sea jobs that are all teeth and poor muscle tone). They are most diverse in marine waters of the continental shelf though many spend part or all of their lives in fresh water. Most form schools, sometimes very large ones; it is this tendency to congregate that makes them such an important part of the food chain for humans and other predators. The clupeids themselves are mostly micro-predators, feeding on minute plankton. Most are medium-sized to small fish with large species getting up to a couple of feet in length*. Conversely, species of the south-east Asian freshwater genus Sundasalanx (on which more below) reach maturity at only 15 mm in length.

*Bond (1996) makes the remarkable statement that "Palonia castelnaudi, a freshwater herring of South America, reaches at least 1.5 m (Dr. Barry Chernoff, personal communication)". Not only have I been unable to find another reference to a clupeid of this size, I have been unable to confirm the existence of a species of this name. The same reference gives a maximum length for the Chirocentridae as 3.5 m; a quick search online suggests the correct figure is less than a third of that.

Another commercially significant species: sardines Sardina pilchardus, photographed by Alessandro Duci.


The exact circumscription of the Clupeidae has varied over time. It is the largest family in a clade called the Clupeoidei which is well defined by characters such as a reduction in the lateral line and the presence of the recessus lateralis, a channel running through the pterotic bone between the swim bladder and the inner ear. Other families within the Clupeoidei are the Engraulidae (anchovies), Pristigasteridae (ilishas) and Chirocentridae (wolf herrings). While each of the other families is fairly distinctive, the Clupeidae lack clear uniting features of their own and have tended to be defined as 'the rest'. Historically, some authors have united some or all of the other families within the Clupeidae, or recognised clupeid subgroups as their own additional families.

It therefore would not have come as too much of a surprise when a molecular phylogenetic analysis of the Clupeoidei by Lavoué et al. (2013) did not identify the Clupeidae as a monophyletic group. Instead, both the Pristigasteridae and Chirocentridae were nested within the Clupeidae. What is more, not one of the five subfamilies currently recognised within the clupeids was monophyletic either. Instead, Lavoué et al. found six distinct sublineages within the clupeids; each of these was individually well supported but the broader relationships between them were not. Four of these potentially formed a clade that may correspond to a restricted Clupeidae. However, members of the 'Dussumieriinae' (which differ from other clupeids in the shape of their pelvic scutes) formed two external lineages: one was potentially the sister group to all other clupeoids except the Engraulidae whereas the round herring genus Etrumeus was weakly placed as sister to the Chirocentridae. To the best of my knowledge, no-one has yet suggested a formal reclassification of the clupeoids as a result of such studies, but it seems likely that we will either see the Clupeidae expanded to include the chirocentrids and pristigasterids, or restricted to exclude the dussumieriines. Again, either one of these options would align with alternative classifications used in the past.

The paedomorphic Sundasalanx microps, copyright Michael Lo.


Also of note in recent studies on clupeid phylogeny is the position of the south-east Asian freshwater genus Sundasalanx. When first described in 1981, this genus was not recognised as a clupeid or even as a clupeoid. Instead, it was originally placed in the fish order Osmeriformes, the smelts, together with another fish genus Salanx. Members of these two genera are indeed similar in appearance: they are tiny and transparent, looking overall like whitebait but never growing into a larger adult. However, a study of the morphology of Sundasalanx in 1997 lead to the conclusion that the shared features of Salanx and Sundasalanx were actually convergences resulting from both exhibiting paedomorphy, becoming reproductively mature while still effectively in the larval stage. A relationship of Sundasalanx to the clupeoids was suggested instead and this was later corroborated by molecular analyses (Ishiguro et al. 2005). In fact, Sundasalanx is nested well within the Clupeidae, even in the family's restricted sense. Recent years have seen something of a surge in descriptions of paedomorphic fish (many of which were previously mistaken for juveniles of related taxa). Lavoué et al. (2008) recorded another paedomorphic clupeoid from marine waters of south-east Asia that the identified by molecular analysis as related to the dussumieriines, but to the best of my knowledge this species remains unnamed.

REFERENCES

Bond, C. E. 1996. Biology of Fishes 2nd ed. Saunders College Publishing.

Ishiguro, N. B., M. Miya, J. G. Inoue & M. Nishida. 2005. Sundasalanx (Sundasalangidae) is a progenetic clupeiform, not a closely-related group of salangids (Osmeriformes): mitogenomic evidence. Journal of Fish Biology 67: 561–569.

Lavoué, S., M. Miya, A. Kawaguchi, T. Yoshino & M. Nishida. 2008. The phylogenetic position of an undescribed paedomorphic clupeiform taxon: mitogenomic evidence. Ichthyol. Res. 55: 328–334.

Lavoué, S., M. Miya, P. Musikasinthorn, W.-J. Chen & M. Nishida. 2013. Mitogenomic evidence for an Indo-west Pacific origin of the Clupeoidei (Teleostei: Clupeiformes). PLoS ONE 8(2): e56485. doi:10.1371/journal.pone.0056485.

Cichlids are Not the Only Radiation

The Congo River catfish Chrysichthys brevibarbis, copyright John P. Sullivan.


With their long barbels around the mouth and lack of scales, the catfish of the Siluriformes are one of most instantly recognisable groups of fishes. They are also one of the more diverse, with close to 3000 species and including a third of the world's freshwater fishes (Diogo & Peng 2010). Within the catfish, the Claroteidae are a distinctly African group of thirteen genera divided between two subfamilies, the Claroteinae and Auchenoglanididae. They are characterised by a moderately elongate body with a distinct adipose fin, and strong spines in the dorsal and pectoral fins (Geerinckx et al. 2003). Distinctive features of the Claroteinae include the presence of a toothplate on the palate. The Auchenoglanidinae have a rounded caudal fin and the anterior nostrils moved to the anteroventral side of the upper lip (Geerinckx et al. 2004). For a long time, the claroteids were included in the catfish family Bagridae before being raised to the level of their own family in 1991. A molecular phylogenetic analysis of the Siluriformes by Sullivan et al. (2006) placed the claroteids within a clade of African catfish that they somewhat whimsically labelled as 'Big Africa'. The Bagridae, meanwhile, were placed within 'Big Asia' (though one true bagrid genus, Bagrus, does occur in Africa). Sullivan et al. (2006) questioned claroteid monophyly, finding Auchenoglanidinae to be sister to a clade grouping the Claroteinae with the family Schilbidae, but other morphological studies have found claroteids as a monophyletic unit (Diogo & Peng 2010).

Lake Tanganyika catfish Lophiobagrus brevispinis, from tanganyikacichlide.nl.


The Claroteinae are notable for having undergone something of an adaptive radiation in one of African Great Lakes, Tanganyika. Though not as dramatic as the famous radiation of cichlids in the same lake, the Tanganyikan claroteines comprise over a dozen species divided between four genera (Bailey & Stewart 1984; Hardman 2008). Seven of these are placed in the genus Chrysichthys which has a wide distribution around Africa; the other three genera are unique to the lake. Molecular phylogeny indicates that the majority of Tanganyikan claroteines represent a single colonisation of the lake; only Chrysichthys brachynema has colonised Lake Tanganyika independently (Peart et al 2014). This indicates that the genus Chrysichthys as currently defined is non-monophyletic (something that had previously been suggested on morphological grounds) but any consequent reclassification is yet to occur. The species of Chrysichthys are mostly larger than the endemic Tanganyikan genera, ranging from 19 to 77 cm within Tanganyika (species elsewhere in Africa may reach up to 1.5 m). Of the endemic genera, the monotypic Bathybagrus tetranema is about 15 cm in length but the other two genera Phyllonemus and Lophiobagrus are even smaller, less than 10 cm in length. Bathybagrus and Lophiobagrus also both have reduced subcutaneous eyes. In Bathybagrus, this possibly reflects their occurrence at greater depths than other Tanganyika fish, occurring down to 80 m (nowhere near the depths reached by Lake Baikal sculpins but still impressive enough in the low-oxygen depths of a tropical lake). Lophiobagrus species are specialised to live in the gaps between rocky rubble on the lake bottom. The species of this genus have also been observed secreting a toxic mucus that can be fatal to other fish; this mucus is believed to be secreted from enlarged glands behind the pectoral fins.

Subcutaneous eyes are also found in two claroteines outside Tanganyika: the species Amarginops platus and Rheoglanis dendrophorus, both found in the Upper Congo (Hardman 2008). These two species are specialised for life in river rapids.

REFERENCES

Bailey, R. M., & D. J. Stewart. 1984. Bagrid catfishes from Lake Tanganyika, with a key and descriptions of new taxa. Miscellaneous Publication, Museum of Zoology, University of Michigan 168: 1–41.

Diogo, R., & Z. Peng. 2009. State of the art of siluriform higher-level phylogeny. In: Grande, T., F. Poyato-Ariza & R. Diogo (eds) Gonorynchiformes and Ostariophysan Relationships: A Comprehensive Review pp. 465–515. Science Publishers.

Geerinckx, T., D. Adriaens, G. G. Teugels & W. Verraes. 2003. Taxonomic evaluation and redescription of Anaspidoglanis akiri (Risch, 1987) (Siluriformes: Claroteidae). Cybium 27 (1): 17–25.

Geerinckx, T., D. Adriaens, G. G. Teugels & W. Verraes. 2004. A systematic revision of the African catfish genus Parauchenoglanis (Siluriformes: Claroteidae). Journal of Natural History 38: 775–803.

Hardman, M. 2008. New species of catfish genus Chrysichthys from Lake Tanganyika (Siluriformes: Claroteidae). Copeia 2008 (1): 43–56.

Peart, C. R., R. Bills, M. Wilkinson & J. J. Day. 2014. Nocturnal claroteine catfishes reveal dual colonisation but a single radiation in Lake Tanganyika. Molecular Phylogenetics and Evolution 73: 119–128.

Sullivan, J. P., J. G. Lundberg & M. Hardman. 2006. A phylogenetic analysis of the major groups of catfishes (Teleostei: Siluriformes) using rag1 and rag2 nuclear gene sequences. Molecular Phylogenetics and Evolution 41: 636–662.