The relationships among 53 genera of Tanganyikan cichlid fishes were analyzed based on internal and external morphological features. Comparison of the morphological cladistic tree with a previously proposed classification showed 5 of 12 tribes to be nonmonophyletic. Sixteen tribes were recognized, the changes in classification being that Trematocarini was treated as a junior synonym of Bathybatini; 5 new tribes were established for each of the following genera, Benthochromis, Boulengerochromis, "Ctenochromis" benthicola, Cyphotilapia, and Greenwoodochromis; "Ctenochromis" horei was transferred from Haplochromini to Tropheini; and "Gnathochromis" pfefferi was transferred from Limnochromini to Tropheini. The revised classification was supported by previously proposed molecular trees.

Divergent natural selection is thought to play a vital role in speciation, but clear, measurable examples from nature are still few. Among the many possible sources of divergent natural selection, predation pressure may be important because predators are ubiquitous in food webs. Here, we show evidence for divergent natural selection in a Lake Tanganyika cichlid, Telmatochromis temporalis, which uses burrows under stones or empty snail shells as shelters. This species contains normal and dwarf morphs at several localities. The normal morph inhabits rocky shorelines, whereas the dwarf morph invariably inhabits shell beds, where empty snail shells densely cover the lake bottom. Genetic evidence suggested that the dwarf morph evolved independently from the normal morph at two areas, and morphological analysis and evaluation of habitat structure revealed that the body sizes of morphs closely matched the available shelter sizes in their habitats. These findings suggest that the two morphs repeatedly evolved through divergent natural selection associated with the strategy for sheltering from predators.

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Theoretically, competition can initiate divergence in habitat use between individuals of a species, leading to restricted gene flow and eventual speciation. Evidence that sister species differ in habitat use is commonplace and consistent with this mechanism, but empirical experimental support is surprisingly scarce. Here we provide evidence that competition has taken a key role in the evolution of genetically distinct ecomorphs of the Lake Tanganyika cichlid fish Telmatochromis temporalis. Experiments show that differences in substrate use between a large-bodied rock-living ecomorph and a neighbouring small-bodied shell-living ecomorph are mediated by size-dependent competition that drives assortative mate-pair formation. Specifically, adults of the larger ecomorph outcompete adults of the smaller ecomorph on favoured rock substrate, compelling the smaller adults to use shell habitat. These results support a role for competition in maintaining reproductive isolation, and highlight the need to identify ecological processes that impose selection to improve our understanding of speciation and adaptive radiation.

Morphological dimorphism in the mouth-opening direction (‘lefty’ versus ‘righty’) has been documented in several fish species. It has been suggested that this deflection is heritable in a Mendelian one-locus, two-allele fashion. Several population models have demonstrated that lateral dimorphism is maintained by negative frequency-dependent selection, resulting from interactions between predator and prey species. However, other mechanisms for the maintenance of lateral dimorphism have not yet been tested. Here, we found that the scale-eating cichlid fish Perissodus microlepis exhibited disassortative mating, in which reproductive pairings between lefties and righties occurred at higher than expected frequency ( p <0.001). A previous study reported that a lefty–righty pairing produces a 1 : 1 ratio of lefty : righty young, suggesting that disassortative mating contributes to the maintenance of lateral dimorphism. A combination of disassortative mating and negative frequency-dependent selection may stabilize lateral dimorphism more than would a single mechanism.