PACT: an efficient and powerful algorithm for generating area cladograms

Aim To introduce and describe the functioning of a new algorithm, phylogenetic analysis for comparing trees (PACT), for generating area cladograms that provide accurate representation of information contained in taxon–area cladograms. Methods PACT operates in the following steps. Convert all phylogenies to taxon–area cladograms. Convert all taxon–area cladograms to Venn diagrams. Choose any taxon–area cladogram from the set of taxon–area cladograms to be analysed and determine its elements. This will be the template area cladogram. Select a second taxon–area cladogram. Determine its elements. Document which elements in the second tree occur in the template tree (denoted by ‘Y’) and which do not (denoted by ‘N’). Each ‘Y’ indicates a match with previous pattern and these are combined. Each ‘N’ is a new element and is attached to the template area cladogram at the node where it is linked with a Y. This requires two rules: (1) ‘Y + Y = Y’ (combine common elements) as long as they are connected at the same node; and (2) ‘Y + N = YN’ (add novel elements to the template area cladogram at the node where they first appear). Once the novel elements in the second taxon–area cladogram have been added to the template area cladogram, see if any of them can be further combined. This requires three additional rules: (1) ‘Y(Y? = Y(Y?’ (do not combine Y's if they are attached at different nodes on the template area cladogram); (2) ‘Y + YN = YN’ (Y is part of group YN); and (3) ‘YN + YN = YNN’ (Y is the same for each, but each N is different). Repeat for all available taxon–area cladograms. Results Three exemplars demonstrate that PACT provides the most accurate area cladograms for vicariance‐driven biotic diversification, dispersal‐driven biotic diversification and taxon pulse‐driven biotic diversification. PACT can also be used as an a priori method of biogeographical analysis. Main conclusions PACT embodies all the strong points and none of the weaknesses of previously proposed methods of historical biogeography. It is most useful as an a posteriori method, but it is also superior to all previous a priori methods because it does not specify costs, or weights or probabilities, or likelihoods of particular biogeographical processes a priori and is thus sensitive to clade‐specific historical contingencies.     

Evidence for reticulate palaeogeography: beetle diversity linked to connection-disjunction cycles of the Gibraltar strait

Aim Dispersal barriers between areas within some regions have appeared and disappeared throughout evolutionary time. Here we describe the distributional patterns displayed by three taxa living in such kind of regions. These patterns can be better explained considering a reticulated rather than a hierarchically branched palaeogeography. Location Western Mediterranean. Methods The taxa studied are Misolampus (Coleoptera, Tenebrionidae), Tentyria (Coleoptera, Tenebrionidae) and Thorectes (Coleoptera, Geotrupidae). All them are flightless and show a high degree of endemicity. The individual pattern of area relationships was determined separately for each genus by Brooks Parsimony Analysis (BPA). A theoretical general area cladogram was constructed based on the palaeogeographical history of the region. Finally, the general area cladogram is reconciled with the individual ones. Results The ancestor of Misolampus probably was North African. Land dispersal toward the Iberian Peninsula is proposed. Speciation within Iberia is related to specific vicariance events, and the presence of insular (Balearic Islands) populations is explained by sea‐surface or, more probably, human‐mediated dispersal. The ancestor of Tentyria was Iberic. The proposed hypothesis to explain the current species distribution mainly relies on the occurrence of specific vicariance events. However, the occurrence of some sea‐surface dispersal event is not discarded. Almost all possible vicariance events can be recognized in the first clade of the Thorectes genus. There is evidence for dispersal between Africa and Europe at different dates and in both directions. In spite of some uncertainties, the appearance of the second Thorectes clade can also be explained by the occurrence of specific historical events. An ancient dispersal toward the eastern Mediterranean and several dispersal events during the Messinian seem likely. Main conclusions The same historical events have specific outcomes in every tree (even in every branch within a tree) depending on the ability for dispersal and speciation of each taxon. Connection‐disjunction cycles of dispersal barriers have acted as diversity producers.     

Evolutionary and biogeographic relationships of related Ranunculus taxa: dispersal,vicariance and pseudovicariance as mechanisms of change

Background: The disjunct distribution patterns of a taxon may arise when previously continuous distribution ranges are fragmented. The phenomena of vicariance and dispersal, together with hybridisation as an important source of genetic variation in natural populations, can play an important role for structuring the distribution of taxa.

Aims: We investigated the biogeographical relationships of the Iberian endemic plant Ranunculus angustifolius s.l. by reconstructing ancestral geographical distributions, using a combination of phylogenetic and distributional information.

Methods: Phylogenetic and network analyses of nuclear internal transcribed spacers and plastid sequence data (rpl32-trnL, rps16-trnQ, trnK-matK and ycf6-psbM) were used to infer vicariance and dispersal events.

Results: Phylogenetic and biogeographical analyses suggested that both dispersal and vicariance were important in creating the current disjunct distribution pattern. Some other factors, such as hybridisation, introgression and vicariance (or pseudovicariance), were important in the evolutionary history of the taxa R. angustifolius s.l.

Conclusions: Our results demonstrate the importance for analysing biogeographical patterns with the use of both nuclear and chloroplast DNA to infer the evolutionary history of plant species with a disjunct distribution. Our results show that phenomena such as dispersal, vicariance and pseudovicariance are not mutually exclusive.     

Macroevolutionary patterns in the diversification of parrots: effects of climate change,geological events and key innovations

Aim Parrots are thought to have originated on Gondwana during the Cretaceous. The initial split within crown group parrots separated the New Zealand taxa from the remaining extant species and was considered to coincide with the separation of New Zealand from Gondwana 82–85 Ma, assuming that the diversification of parrots was mainly shaped by vicariance. However, the distribution patterns of several extant parrot groups cannot be explained without invoking transoceanic dispersal, challenging this assumption. Here, we present a temporal and spatial framework for the diversification of parrots using external avian fossils as calibration points in order to evaluate the relative importance of the influences of past climate change, plate tectonics and ecological opportunity. Location Australasian, African, Indo‐Malayan and Neotropical regions. Methods Phylogenetic relationships were investigated using partial sequences of the nuclear genes c‐mos, RAG‐1 and Zenk of 75 parrot and 21 other avian taxa. Divergence dates and confidence intervals were estimated using a Bayesian relaxed molecular clock approach. Biogeographic patterns were evaluated taking temporal connectivity between areas into account. We tested whether diversification remained constant over time and if some parrot groups were more species‐rich than expected given their age. Results Crown group diversification of parrots started only about 58 Ma, in the Palaeogene, significantly later than previously thought. The Australasian lories and possibly also the Neotropical Arini were found to be unexpectedly species‐rich. Diversification rates probably increased around the Eocene/Oligocene boundary and in the middle Miocene, during two periods of major global climatic aberrations characterized by global cooling. Main conclusions The diversification of parrots was shaped by climatic and geological events as well as by key innovations. Initial vicariance events caused by continental break‐up were followed by transoceanic dispersal and local radiations. Habitat shifts caused by climate change and mountain orogenesis may have acted as a catalyst to the diversification by providing new ecological opportunities and challenges as well as by causing isolation as a result of habitat fragmentation. The lories constitute the only highly nectarivorous parrot clade, and their diet shift, associated with morphological innovation, may have acted as an evolutionary key innovation, allowing them to explore underutilized niches and promoting their diversification.     

Diversification of subgenus Calathus (Coleoptera: Carabidae) in the Mediterranean region – glacial refugia and taxon pulses

Aim To investigate the effects of Pleistocene climatic variations on the diversification rate of the subgenus Calathus (Coleoptera: Carabidae), and to estimate the role of vicariance and dispersal for explaining current distributional patterns. Location Western Palaearctic Region, particularly the Mediterranean Basin. Methods Fragments of the mitochondrial cox1–cox2 and the nuclear 28S and EF1α genes were analysed by Bayesian inference. Lineage divergence times were estimated using a Bayesian relaxed molecular clock. Three diversification rate analyses were conducted, namely gamma (γ)‐statistic, birth–death likelihood (BDL) test and survival analyses, in order to test departures from a constant rate model of diversification. A Bayesian approach to dispersal–vicariance analysis was developed to reconstruct the most probable ancestral area of subgenus Calathus and subsequent events of dispersal and colonization. Results A constant rate of speciation events from the late Miocene onwards was found for the subgenus Calathus, whereas recent Pleistocene climatic oscillations played an important role only in shaping intraspecific diversity. Overall diversification patterns for the subgenus are best explained by at least four westward dispersal events from the eastern Mediterranean Basin. Three distinct phylogroups were found for the widely distributed Calathus fuscipes. Incongruence between mitochondrial and nuclear loci was found for a number of species. Main conclusions Diversification analyses suggest either a constant rate of diversification (BDL analysis) or a decrease in diversification rates for the subgenus (survival or γ‐statistics analyses), but not an increase related to the effects of glaciation cycles. Diversification patterns in the subgenus Calathus agree with predictions of the taxon pulse model. From the middle Miocene onwards the Anatolian Peninsula was possibly the main centre of diversification, with successive dispersal events towards the western Mediterranean Basin. Range expansion and secondary contact zones are postulated between members of different phylogroups in C. fuscipes.