Previous research revealed complex diversification patterns in the parthenogenetic weevil Naupactus cervinus. To understand the origin of clonal diversity and successful spreading of this weevil, we investigated its geographic origin and possible dispersal routes and whether parthenogens can persist in habitats under unsuitable environmental conditions. This study is based on samples taken throughout a broad area of the species’ range. We used both mitochondrial and nuclear markers and applied phylogenetic and network analyses to infer possible relationships between haplotypes. Bayesian phylogeographic analyses and ecological niche modeling were used to investigate the processes that shaped genetic diversity and enabled the colonization of new geographic areas. Southeastern Brazil emerges as the original distribution area of N. cervinus. We detected two range expansions, one along natural corridors during the Pleistocene and the other in countries outside South America during recent times. Isolation due to climate shifts during the early Pleistocene led to diversification in two divergent clades, which probably survived in different refugia of the Paranaense Forest and the Paraná River delta. The origin of the clonal diversity was probably a complex process including mutational diversification, hybridization, and secondary colonization. The establishment of N. cervinus in areas outside its native range may indicate adaptation to drier and cooler conditions. Parthenogenesis would be advantageous for the colonization of new environments by preventing the breakup of successful gene combinations. As in other insect pests, the present distribution of N. cervinus results from both its evolutionary history and its recent history related to human activities.

We investigated the taxonomic status of two sympatric morphospecies of squat lobsters from southern South America (Beagle Channel, Strait of Magellan, and Burdwood Bank), Munida gregaria and Munida subrugosa, by DNA sequence analysis of three mitochondrial (mt)DNA gene fragments [416 bp of 16S rDNA(165), 566 bp of cytochrome c oxidase subunit I(COI) and 418 bp of NADH dehydrogenase subunit 1 (ND1)]; and the nuclear rDNA internal transcribed spacer (ITS) 1 (883-952 bp). We obtained a total of 79 sequences from 32 individuals. The 16S sequences of all M. gregaria and M. subrugosa were invariant and identical, whereas COI and ND1 showed 12 and 15 variable sites, respectively. These polymorphisms were shared between morphospecies. Interspecific TamuraNei distances for COI and ND1 sequences were 0.0024 and 0.0032, respectively, and were not significantly different from intraspecific distances (Kruskal-Wallis tests: P = 0.58 and P = 0.69, for COI and ND1, respectively). Similar to the results obtained from the mtDNA sequences, no relationship was found between the ITS1 maximum parsimony tree topology and the morphologic classification of specimens in M. gregaria and M. subrugosa. We conclude that M. gregaria and M. subrugosa from southern South America may either represent a case of a dimorphic species, or a case of incomplete lineage sorting. The fact that these two morphospecies did not show fixed differences over a total of 1947 bp analysed reinforces the hypothesis of a single dimorphic species.

Aim Trimerotropis pallidipennis represents a species complex of band-winged grasshopper distributed over North and South America. Previous studies indicated a North American origin of the species and suggested that colonization of South America occurred during the Pleistocene after the closure of the Isthmus of Panama. Here we use a phylogeographical approach in order to test different biogeographical scenarios and determine how many distinct units exist within the species complex.Location North and South America with specific emphasis on the Andes mountains of South America.Methods We sequenced two mitochondrial and two nuclear genes for multiple specimens belonging to each taxonomic unit. Using the concatenated dataset and a coalescent-based approach we estimated the phylogeny of the complex. In order to distinguish the different biogeographical and species delimitation hypotheses we constrained our dataset to different taxon sets and ran Bayesian analyses in *beast. Posterior probabilities and DensiTree plots allowed us to determine the best hypotheses. We used a molecular clock approach to correlate geological events with observed phylogenetic splits. ResultsAll analyses indicate the existence of at least three distinct genetic lineages: Trimerotropis pallidipennis from North America, Trimerotropis ochraceipennis from Chile and an undescribed Trimerotropis species from Argentina. The split between North and South American forms took place about 1.3 Ma, long after the Isthmus of Panama had been completed. Biogeographical analyses suggest a first dispersal event from North to South America. Subsequent dispersion and vicariance probably led to the differentiation of the endemics now found in Chile and Argentina. Main conclusionsWe demonstrate the existence of three distinct genetic lineages in the Trimerotropis pallidipennis species complex. These lineages are also chromosomally differentiated as previous studies have indicated. Dispersion of T. pallidipennis from North to South America probably occurred during the early Pleistocene, when climatic conditions were more suitable. Subsequent diversification in South America was the result of range expansion and vicariance, possibly in response to later Pleistocene glaciations of the Andes.

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Ten species of parthenogenetic broad-nosed weevils (Coleoptera: Curculionidae: Entiminae) native to Argentina, southern Brazil, and Uruguay were selected for niche modeling analysis based on climatic data and altitude, to evaluate their potential range expansion inside and outside South America. The selected species belong to five genera of the tribe Naupactini affecting economically important crops. Until present, five of the 10 species analyzed here have invaded prairies and steppes of countries outside South America (Australia, New Zealand, Mexico, United States, and South Africa): Aramigus tessellatus (Say), Atrichonotus sordidus (Hustache), Atrichonotus taeniatulus (Berg), Naupactus leucoloma Boheman, and Naupactus peregrinus (Buchanan). Our niche modeling analyses performed with MAXENT demonstrated that these areas would be also suitable for Aramigus conirostris (Hustache), Eurymetopus fallax (Boheman), Pantomorus auripes Hustache, Pantomorus ruizi (Brèthes), and Pantomorus viridisquamosus (Boheman), consequently, they also have the potential to invade areas outside their native ranges, mainly in southeastern United States, some European countries (e.g., Portugal, France, and southern England), South Africa, New Zealand, and southeastern Australia. All the studied species share similar environmental requirements, the most important variables being the Mean Temperature of Driest Quarter, the Annual Mean Temperature and Isothermality. Long distance dispersal through commercial trade, and parthenogenetic reproduction would increase the threat of these weevils to crop production worldwide.

The little fire ant Wasmannia auropunctata, native to the Neotropics, has become a serious pest worldwide over the past 100 years. It was originally distributed from Mexico to northern Argentina and new evidence suggests a recent southern range expansion during the last 60 years reaching central Argentina. This supercolonial ant species has a polymorphic reproductive system. Some populations, mostly found in undisturbed natural environments, are characterised by a classical sexual haplodiploid reproductive system. In other populations, which mainly occur in human-modified habitats, diploid queens and haploid males are produced clonally while workers are produced sexually. Here we studied the association between the recent southern range expansion of W. auropunctata in relation to human activity and clonality. We carried out an extensive survey within the southern limit of the species’ native distribution and characterised the type of habitat where populations were found. Moreover, we genetically determined the type of reproductive system in 35 populations by genotyping at 12 microsatellite loci a total of 191 reproductive individuals (i.e. queens and/or males). Clonality was the most common reproductive system, occurring in 31 out of 35 populations analysed. All the populations found in the recently colonised area in central Argentina were clonal and established in human-modified habitats, suggesting that clonality together with human activity might have facilitated the southwards expansion of W. auropunctata.

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The Andean Mountain range has been recognized as one of the biodiversity hotspots of the world. The proposed mechanisms for such species diversification, among others, are due to the elevation processes occurring during the Miocene and the intensive glacial action during the Pleistocene. In this study we investigated the diversification history of the grasshopper Trimerotropis pallidipennis species complex which shows a particularly wide latitudinal and altitudinal distribution range across the northern, central and southern Andes in South America. Many genetic lineages of this complex have been so far discovered, making it an excellent model to investigate the role of the central Andes Mountains together with climatic fluctuations as drivers of speciation. Phylogenetics, biogeographic and molecular clock analyses using a multi-locus dataset revealed that in Peru there are at least two, and possibly four genetic lineages. Two different stocks originated from a common ancestor from North/Central America—would have dispersed toward southern latitudes favored by the closure of the Panama Isthmus giving rise to two lineages, the coastal and mountain lineages, which still coexist in Peru (i.e., T. pallidipennis and T. andeana). Subsequent vicariant and dispersal events continued the differentiation process, giving rise to three to six genetic lineages (i.e., clades) detected in this study, which were geographically restricted to locations dispersed over the central Andes Mountains in South America. Our results provide another interesting example of “island diversification” motored by the topography plus unstable climatic conditions during the Pleistocene, pointing out the presence of a hotspot of diversification in the Andean region of Peru.