Good alpha taxonomy is central to biology. On the basis of a survey of arthropod studies that used multiple disciplines for species delimitation, we evaluated the performance of single disciplines. All included disciplines had a considerable failure rate. Rigor in species delimitation can thus be increased when several disciplines chosen for complementarity are used. We present a flexible procedure and stopping rule for integrative taxonomy that uses the information from different disciplines separately. Disagreement among disciplines over the number and demarcation of species is resolved by elucidating and invoking evolutionary explanations for disagreement. With the identification of further promising study organisms and of new questions for in-depth analysis, evolutionary biology should profit from integrative taxonomy. An important rationale is clarity in researcher bias in the decision-making process. The success of integrative taxonomy will further increase through methodological progress, taxonomic training of evolutionary biologists, and balanced resource allocation.

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Spatial modelling of species distributions has become an important tool in the study of biological invasions. Here, we examine the utility of combining distribution and ecological niche modelling for retrieving information on invasion processes, based on species occurrence data from native and introduced ranges. Specifically, we discuss questions, concerning (1) the global potential to spread to other ranges, (2) the potential to spread within established invasions, (3) the detectability of niche differences across ranges, and (4) the ability to infer invasion history through data from the introduced range. We apply this approach to two congeneric pavement ants, Tetramorium sp.E (formerly T. caespitum (Linnaeus 1758)) and T. tsushimae Emery 1925, both introduced to North America. We identify (1) the potential of both species to inhabit ranges worldwide, and (2) the potential of T. sp.E and T. tsushimae, to spread to 23 additional US states and to five provinces of Canada, and to 24 additional US states and to one province of Canada, respectively. We confirm that (3) niche modelling can be an effective tool to detect niche shifts, identifying an increased width of T. sp.E and a decreased width of T. tsushimae following introduction, with potential changes in niche position for both species. We make feasible that (4) combined modelling could become an auxiliary tool to reconstruct invasion history, hypothesizing admixture following multiple introductions in North America for T. sp.E, and a single introduction to North America from central Japan, for T. tsushimae. Combined modelling represents a rapid means to formulate testable explanatory hypotheses on invasion patterns and helps approach a standard in predictive invasion research.

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Mutualism, whereby species interact to their mutual benefit, is extraordinary in a competitive world. To recognize general patterns of origin and maintenance from the plethora of mutualistic associations proves a persisting challenge. The simplest situation is believed to be that of a single mutualist specific to a single host, vertically transmitted from one host generation to the next. We characterized ascomycete fungal associates cultured for nest architecture by the ant subgenera Dendrolasius and Chthonolasius. The ants probably manage their fungal mutualists by protecting them against fungal competitors. The ant subgenera display different ant-to-fungus specificity patterns, one-to-two and manyto-one, and we infer vertical transmission, in the latter case overlaid by horizontal transmission. Possible evolutionary trajectories include a reversal from fungiculture by other Lasius subgenera and inheritance of fungi through life cycle interactions of the ant subgenera. The mosaic indicates how specificity patterns can be shaped by an interplay between host life-cycles and transmission adaptations.insect fungiculture ͉ Lasius ants ͉ mutualism ͉ social insects C ooperation is improbable (1, 2) and it is only through evolution that these interactions become reliable for the players. Cooperation is needed to forge new levels of organization, from genomes to human society (2). Mutualism, species interactions beneficial for all players, offers some of the most arresting cases of evolution (3). These cases stimulated the development of theoretical frameworks on the why and how of mutualism (e.g., refs. 3-7), but true life examples are needed to test any hypothesis (8). Finding suitable model systems is not a trivial task (9). Only a fraction of the extant associations have been studied (10), with the number and identities of the players often unknown.Insect fungiculture provides prime systems for studying mutualism (11). The New World attine ants (Myrmicinae: Attini) that cultivate fungi for food have especially served as models for investigating host-use specificity and transmission patterns (12-15). Another ant-fungus association has been less investigated: Old World Lasius ants (Formicinae) of the subgenera Dendrolasius and Chthonolasius nourish fungi with honeydew to bind shredded wood or soil into a composite building material (16,17). The fungi are used for reinforcement of the nest walls, which allows building stable nests in tree and soil cavities. Little has been known about the associations' phylogenetic and ecological specificities, and the transmission mode, but it has been generally accepted (18) that the Lasius-fungi associations are simple with each of the two subgenera culturing a single fungus (19)(20)(21)(22). Chthonolasius and Dendrolasius are both obligate temporary social parasites, i.e., young queens enter an established colony of another Lasius subgenus and replace the queen. Dendrolasius is confined to the Palearctic and hyperparasitizes Chthonolasius (16). Chthonolasius exhibits complexity wit...

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An ant supercolony is a very large entity with very many queens. Although normal colonies of small extent and few queens remain distinct, a supercolony is integrated harmoniously over a large area [1, 2]. The lack of aggression is advantageous: Aggression is costly, involving direct and indirect losses and recognition errors [3, 4]. Indeed, supercolonial ants are among the ecologically most successful organisms [5-7]. But how supercolonies arise remains mysterious [1, 2, 8]. Suggestions include that reduced within-colony relatedness or reduced self-nonself discrimination would foster supercolony formation [1, 2, 5, 7, 9-12]. However, one risks confusing correlation and causality in deducing the evolution from distinct colonies to supercolonies when observing established supercolonies. It might help to follow up observations of another lack of aggression, that between single-queened colonies in some ant species. We show that the single-queened Lasius austriacus lacks aggression between colonies and occasionally integrates workers across colonies but maintains high within-colony relatedness and self-nonself discrimination. Provided that the ecological framework permits, reduced aggression might prove adaptive for any ant colony irrespective of within-colony relatedness. Abandoning aggression while maintaining discrimination might be a first stage in supercolony formation. This adds to the emphasis of ecology as central to the evolution of cooperation in general [13].

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.