No sympatric speciation here: multiple data sources show that the ant Myrmica microrubra is not a separate species but an alternate reproductive morph of Myrmica rubra.

No aspect of speciation is as controversial as the view that new species can evolve sympatrically, among populations in close physical contact. Social parasitism has been suggested to yield necessary disruptive selection for sympatric speciation. Recently, mitochondrial DNA phylogeography has shown that the ant Myrmica microrubra is closely related to its host, Myrmica rubra, leading to the suggestion that sympatric speciation has occurred. We investigated the relationships between the two ant forms using mitochondrial and nuclear DNA sequences, microsatellite genotyping and morphometrics. Molecular phylogenetic and population structure analyses showed that M. microrubra does not evolve separately to its host but rather shares a gene pool with it. Probability analysis showed that mitochondrial DNA data previously adduced in favour of sympatric speciation do not in fact do so. Morphometrically, M. microrubra is most readily interpreted as a miniature queen form of M. rubra, not a separate species. Myrmica microrubra is not an example of speciation. The large (typical M. rubra) and small (M. microrubra) queen forms are alternative reproductive strategies of the same species. Myrmica microrubraSeifert 1993 is consequently synonymized here with M. rubra Linnaeus, 1758.

A unique strategy of host colony exploitation in a parasitic ant: workers of Polyrhachis lama rear their brood in neighbouring host nests.

The formicine ant Polyrhachis lama is a social parasite, exploiting its ponerine host ant species Diacamma sp. In most social parasitic associations, the parasitic species are closely related to their host species group, evolving directly from independent ancestors of the host species. However, in the Polyrhachis lama- Diacamma sp. association, the associated species belong to different ant subfamilies. Based on preliminary field surveys, we had presumed that P. lama might have given up its reproductive division of labour, i.e. workers would be able to produce males as well as workers and females parthenogenetically. In this study, this hypothesis was disproved: Polyrhachis lama workers cannot be fertilized and are only able to produce males. In the host-parasite association originating from nests possessing a P. lama queen, workers penetrate surrounding Diacamma sp. nests, carrying brood for rearing within these satellite nests. In this peculiar way, a single P. lama colony is able to exploit several Diacamma sp. colonies simultaneously.

Morphology and ultrastructure of a specialized bacterial pouch in the digestive tract of Tetraponera ants (Formicidae, Pseudomyrmecinae).

The digestive tract in workers of some species of the pseudomyrmecine ant genus Tetraponera is characterized by a conspicuous pear-shaped diverticulum at the transition between the midgut and the intestine, that so far has not been found in any other ant species. As this organ is filled with a mass of bacteria, we propose to designate it as a bacterial pouch. Its distal wall is formed by a thin ectodermal epithelium, through which tens of tracheal branches penetrate into the bacterial mass that fills the pouch lumen. The proximal wall, in contrast, is formed by a cylindrical epithelium with a conspicuous microvillar differentiation of the apical cell membrane, but without a cuticular lining. The contact region between both epithelia occurs as a complex fold surrounding the pouch like a belt. The Malpighian tubules open into the pouch through the cylindrical epithelium adjacent to the belt fold. The functional significance of the bacterial pouch remains unknown, although the abundant presence of bacteria may indicate a symbiotic function. The conspicuous tracheolar supply illustrates the metabolic activity in the pouch, while the microvillar differentiation of the cylindrical epithelium may be interpreted in the uptake of metabolites from the pouch lumen.

Mitochondrial DNA sequences reveal close relationships between social parasitic ants and their host species.

In the tribe Leptothoracini, the phylogenetic relationship of socially parasitic ants (Doronomyrmex kutteri, D. goesswaldi and Harpagoxenus sublaevis) and their host species Leptothorax acervorum has been controversial. Even more controversial is the relationship between the socially parasitic ant Chalepoxenus muellerianus and its host species Leptothorax unifasciatus, L. nigriceps, L. interruptus and L. recedens. On the basis of morphological, ecological and ethological criteria it has been argued that socially parasitic ants and their respective hosts always evolved from common ancestors, and hence it has been postulated that these species should be included in common taxonomical groups. This would require the division of the tribe Leptothoracini into two subgroups, one comprising the subgenus Leptothorax (s. str.) and the other the subgenus Myrafant, together with their respective parasitic genera. We have used the polymerase chain reaction (PCR) to compare a 360-bp sequence of the mitochondrial cytochrome b gene of 14 species belonging to the tribe Leptothoracini and an outgroup species Tetramorium impurum (Tetramoriini). The results generally agree with the morphological studies which suggest that a common ancestral species differentiated into host and parasite species. This relationship is very obvious within the Leptothorax (s. str.) group but less pronounced in the species belonging to the Myrafant group. Leptothorax (Temnothorax) recedens shows a greater sequence divergence than the outgroup species T. impurum.

Evolution of social parasitism in ants.

Slave raids of Amazon ants, the beheading of the host colony's queen by a parasitic Bothriomyrmex female, or the protracted throttling of the host queen by an Epimyrma female which has penetrated a Leptothorax nest, are among the most intriguing behaviors to be observed in social parasitic ants. The evolutionary origin of these behaviors, however, is quite obscure, and further work is needed to elucidate how parasitic life cycles could have arisen from the ordinary social organization of ants.