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This paper presents numeric morphology-based evidence on the broadly overlapping distribution of two thief ant species Solenopsis fugax (Latreille, 1798) and S. juliae (Arakelian, 1991) in the East European Pontic-Caspian region. The paper integrates two autonomous data collections and independent analyses performed by different researchers, using different equipment, considering different character combinations, and evaluating partially different samples. Five type series, the neotype series of Solenopsis fugax (Latreille 1798) and the type series of S. flavidula (Nylander, 1849), S. (Diplorhoptrum) fugax var. furtiva Santschi, 1934, S. (Diplorhoptrum) fugax var. pontica Santschi, 1934, S. (Diplorhoptrum) fugax var. scytica Santschi, 1934 were nested in one cluster and we propose the junior synonymy of the latter four taxa names with S. fugax. The other cluster contained only one type specimen of Solenopsis nitida (Dlussky & Radchenko, 1994) measured from AntWeb images. The naming of this cluster was based on both verbal statements and measurements of gynes given in the original description of Solenopsis juliae (Arakelian, 1991), which represents the oldest available name for this cluster. Hence, S. nitida is proposed as junior synonym of S. juliae. Solenopsis cypridis Santschi, 1934 is raised to species rank based on investigation of worker and gyne type specimens.

In this paper, we provide numeric morphology-based evidence that the dark-colored Ponera coarctata var. lucida Emery, 1898, formerly considered a synonym of P. coarctata (Latreille, 1802), is conspecific with the lighter-colored Ponera testacea Emery, 1895. Species hypotheses are developed via NC-PART clustering, combined with Partitioning Algorithm based on Recursive Thresholding (PART), and via PCA combined with gap statistics. We obtained our results from an extensive dataset from the 10 continuous morphometric traits measured on 165 workers belonging to 73 nest samples. Linear discriminant analysis (LDA) confirmed the grouping of hypotheses generated by exploratory analyses with 100% classification success when all ten morphometric traits were involved. The Anatolian Turkish black and the predominantly European yellow samples, did not separate based on their morphometric characteristics. These two color variations broadly overlap in their geographic range in Anatolian Turkey. The investigated type series of Ponera coarctata var. lucida Emery, 1898 (collected from Kazakhstan) fell within the P. testacea cluster instead of P. coarctata and is also classified with high certainty as P. testacea by confirmatory LDA. Therefore, we propose the synonymy of Ponera coarctata var. lucida Emery, 1898 with Ponera testacea Emery, 1895. As no other morphological differences than color patterns were detected between the “black” and “pale” P. testacea samples, we hold that these populations constitute geographically occurring color variations of the same species. Finally, our quantitative morphology-based results show that relying on color patterns is not a robust approach in identifying European Ponera samples, particularly in the east, but using multivariate analyses of morphometric traits is advised instead.

The ant genus Camponotus (Mayr, 1861) is one of the most abundant and species rich ant genera in the Malagasy zoogeographical region. Although this group is commonly encountered, its taxonomy is far from complete. Here, we clarify the taxonomy of the Malagasy-endemic Camponotus subgenus Myrmopytia (Emery, 1920). Species delimitation was based on traditional morphological characters and multivariate morphometric analyses, including exploratory Nest Centroid clustering and confirmatory cross-validated Linear Discriminant Analysis. Four species are recognized: Camponotus imitator (Forel, 1891), Camponotus jodina sp. n., Camponotus karaha sp. n., and Camponotus longicollis sp. n. All four species appear to mimic co-occurring Aphaenogaster species. A diagnosis of the subgenus Myrmopytia, species descriptions, an identification key based on minor and major subcastes of workers, and the known geographical distribution of each species are provided.

Here we describe the diversity of the Malagasy Nesomyrmex brevicornis-group as the final installment of series describing the complete Malagasy Nesomyrmex fauna. In the current paper introduce the N. brevicornis-group, a newly outlined species group. We split this group from one of the four former groups, N. madecassus-group (sensu Csősz and Fisher 2015). The relatively small number of individuals available within the N. brevicornis-group relative to the large number of OTUs hampers the use of sophisticated statistical techniques to evaluate the morphological data. Instead, we assess the diversity of the N. brevicornis-group via a conventional morphology-based approach relying upon non-numeric characters (shape, sculpture, color etc.) recorded by simple eye inspection. Morphometric data are used as secondary data to confirm the most probable boundaries between species, but without employing statistical analyses. We rejected prior species hypotheses imposed by the primary approach if a non-overlapping range of a single index calculated from continuous numeric traits was found between two hypothesized species. Our methods render every species in this revisionary work separable via both salient features and morphometric traits. Our approach reveals the existence of nine morphologically distinct species, Nesomyrmex brevicornis sp. n., N. brunneus sp. n., N. cingulatus sp. n., N. edentates sp. n., N. flavigaster sp. n., N. longiceps sp. n., N. minutus sp. n., N. punctaticeps sp. n., and N. sellaris sp. n.. Geographic maps showing the distribution of each species are provided, along with an updated key to workers of Malagasy Nesomyrmex species groups that includes the newly outlined N. brevicornis-group.

The paper integrates two independent studies of numeric morphology-based alpha-taxonomy of the cryptic ant species Temnothorax crassispinus (Karavajev, 1926) and T. crasecundus sp. n. conducted by different investigators, using different equipment, considering different character combinations and evaluating different samples. Samples investigated included 603 individual workers from 203 nests – thereof 104 nest samples measured by Seifert and 99 by Csösz. The material originated from Europe, Asia Minor and Caucasia. There was a very strong interspecific overlap in any of the 29 shape characters recorded and subjective expert determination failed in many cases. Primary classification hypotheses were formed by the exploratory data analysis Nest Centroid (NC) clustering and corrected to final species hypotheses by an iterative linear discriminant analysis algorithm. The evaluation of Seifert’s and Csösz’s data sets arrived at fully congruent conclusions. NC-Ward and NC-K-means clustering disagreed from the final species hypothesis in only 1.9 and 1.9% of the samples in Seifert’s data set and by 1.1 and 2.1% in Csösz’s data set which is a strong argument for heterospecificity. The type series of T. crassispinus and T. crasecundus sp. n. were allocated to different clusters with p = 0.9851 and p = 0.9912 respectively. The type series of the junior synonym T. slavonicus (Seifert, 1995) was allocated to the T. crassispinus cluster with p = 0.9927. T. crasecundus sp. n. and T. crassispinus are parapatric species with a long contact zone stretching from the Peloponnisos peninsula across Bulgaria northeast to the southern Ukraine. There is no indication for occurrence of interspecifically mixed nests or intraspecific polymorphism. However, a significant reduction of interspecific morphological distance at sites with syntopic occurrence of both species indicates local hybridization. The results are discussed within the context of the Pragmatic Species Concept of Seifert (2014). The taxonomic description and a differential diagnosis of T. crasecundus sp. n. are given.