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Meseguer, A. S.

Publications and source records attributed to Meseguer, A. S..

8 recordsLinked to original sources

No evidence that polyploids arise during periods of environmental upheaval. A reply to Chen et al. (2026)

Ancient whole-genome duplications (WGDs) are thought to have played a major role in plant evolution, but robust inference of the patterns and drivers of polyploid establishment through deep time remains challenging. We re-evaluate the recent large-scale study by Chen et al. (2026), which linked polyploid establishment throughout angiosperm evolution to periods of climatic instability and low species richness. We identify five conceptual and methodological issues that substantially affect these conclusions and collectively undermine the proposed temporal and ecological associations. We hope that clarifying these issues will support future efforts to understand the evolutionary role of polyploidy in plant evolution.

evolutionary biology↗

Enrichment Probe Sets Combining Universal and Lineage-Specific Targets Help Resolve Recalcitrant Lineages

The combination of target capture sequencing (TCS) with low-coverage whole genome sequencing (lcWGS), an approach known as Hyb-Seq, has allowed the integration of natural history collections into the genomics revolution, transforming biodiversity research. To implement Hyb-Seq, a collection of genomic targets, often nuclear orthologs, is needed to design probes for TCS. In flowering plants, the universal Angiosperms353 probe set has been proven resolutive at multiple evolutionary scales, with caveats. Malpighiales is known to be one of the most challenging flowering plant orders to resolve. Within this order, the clusioid clade ([~]2.2K species, 94 genera, five families) is no exception. To resolve phylogenetic relationships in this recalcitrant clade, we design a custom probe set, the Clusioids626 kit, composed of 39,936 120-mer probes targeting 626 nuclear orthologs ([~]6.6M nucleotides). This probe set includes all Angiosperms353 targets and 273 clusioid-specific ones, carefully chosen taking copy-number, length evenness, and phylo-informativeness into account. We test our probe set on 70 accessions representing all families and tribes in the clusioid clade. On average, 50.4% of TCS reads mapped to our targets, recovering a median of [~]600 orthologs. Relationships for all clusioid families are fully resolved for our nuclear targets. Additionally, 105 plastid coding DNA sequences were retrieved from the lcWGS fraction. A strong cyto-nuclear conflict was detected. The Clusioids626 kit performs better than the universal Angiosperms353 enrichment panel alone. Our kit design workflow can be extended into other lineages for which a universal probe set exists but more resolution is needed.

evolutionary biology↗

The conquest and diversification of leafy spurges across the Holarctic and beyond: biogeography and evolution of life-history of Euphorbia subgenus Esula

Euphorbia subgenus Esula is one of four main lineages within the megadiverse angiosperm genus Euphorbia. It comprises 490 species, including herbs, shrubs, dendroid shrubs, and succulents. The subgenus is a northern temperate lineage, most diverse in the Irano-Turanian and Mediterranean regions. We assembled the largest taxon sampling of subg. Esula to date (321 spp.), using DNA sequences from nuclear ITS and plastid ndhF regions, and updated previous phylogenetic analyses and sectional classification of the group. We used Bayesian methods to estimate divergence times and reconstruct ancestral ranges, characterising the tempo and mode of lineage diversification that shaped the present distribution and extant diversity of the subgenus. We tested whether changes in life-history (annual vs. perennial) played a role in the diversification and current elevational distribution of subg. Esula. Our results show that subg. Esula diverged from its sister clade in the Mid-Eocene and started to diversify in the Late Eocene. The Western Palearctic was inferred to be the ancestral area of the subgenus, where the first diversification events began 41 Mya. Expansion to other continents was dated as occurring in the last 10 million years. This coincided with an increase in the diversification rate and with clade-specific rate shifts coupled with changes from annual to perennial life-histories. We found a positive correlation between perenniality and high elevations. These results support that the recent rapid diversification of subg. Esula could be associated with an evolutionary shift to perenniality, allowing colonisation of montane habitats and global range expansion beyond the Western Palearctic.

evolutionary biology↗

On the utility of Deep Learning for model classification and parameter estimation on complex diversification scenarios.

Birth-Death models applied to dated phylogenies are a useful tool to study past diversification dynamics. Parameters in these stochastic models are typically inferred using likelihood-based methods such as Maximum Likelihood Estimation (MLE) or Bayesian Inference. However, these approaches exhibit computational tractability issues in the case of models of moderate to high complexity. One approach to increase model complexity while remaining computationally tractable in the context of birth-death modelling is machine learning. So far, these techniques have been explored in the context of serially-sampled phylogenies (phylodynamics) and trait-dependent birth-death models. Here, we explored the power of Convolutional Neural Networks (CNNs), a type of Deep Learning (DL) method, to solve classification and regression (parameter estimation) tasks under constant-rate and time-homogeneous, rate-variable birth-death models. In particular, we compared six diversification scenarios: Constant Birth-Death, High-Extinction, Mass-Extinction, Diversity-Dependent, Stasis-and-Radiate, and Waxing-and-Waning. We simulated 10, 000 phylogenetic trees under each diversification scenario, which were encoded using a vectorization procedure that captures the topology and branch length information. The encoded trees were used to train or test a set of CNNs models that were designed to tailor three empirical case studies differing in the number of tips. We compared CNNs performance with MLE inference. Our results show that CNNs exhibited classification accuracy levels of 93-78%, whereas maximum likelihood estimation achieved levels of 74-70%. The most difficult scenarios to predict for the CNNs were the high-extinction and mass-extinction scenarios, which were often misidentified as one another. For the regression tasks, mean average errors were comparable between CNNs models and MLE inference, and they also coincided in their difficulty estimating ratio parameters such as mass extinction survival and turnover. Finally, we applied our CNNs to three empirical studies (eucalypts, conifers and cetaceans) and discussed potential shortcomings and future avenues for improvement in the application of deep-learning birth-death modelling approaches.

evolutionary biology↗

The origin and drivers of Neotropical plant and tetrapod diversification

The origins and evolution of the outstanding Neotropical biodiversity are still debated. A comprehensive understanding is hindered by the lack of deep-time comparative data across wide phylogenetic and ecological contexts. Here, we evaluate four evolutionary scenarios assuming different diversification trajectories and drivers of Neotropical diversification, and assess their variation across Neotropical regions and taxa. Our analysis of 150 phylogenies (12,512 species) of seed plants and tetrapods reveals that Neotropical diversity has mostly expanded through time (70% of the clades), while scenarios of saturated and declining diversity also account for 21% and 9% of Neotropical diversity, respectively. We identify five biogeographic areas that represent distinctive units of long-term Neotropical evolution (Pan-Amazonia, Dry Diagonal, Bahama-Antilles, Galapagos, and an elsewhere region) and find that diversity dynamics do not differ across these areas, suggesting no geographic structure in long-term Neotropical diversification. In contrast, diversification dynamics differ substantially across taxa: plant diversity mostly expanded through time (88%), while a substantial fraction (43%) of tetrapod diversity accumulated at a slower pace or declined toward the present. These opposite evolutionary patterns may reflect different capacities for plants and tetrapods to cope with climate change, with potential implications for future adaptation and ecosystem resilience.

evolutionary biology↗

The grass subfamily Pooideae: late Cretaceous origin and climate-driven Cenozoic diversification

* AimFrost is among the most dramatic stresses a plant can experience and complex physiological adaptations are needed to endure long periods of sub-zero temperatures. Due to the need for evolving these complex adaptations, transitioning from tropical to temperate climates is regarded difficult and only half of the worlds seed plant families have temperate representatives. Here, we study the transition from tropical to temperate climates in the grass subfamily Pooideae, which dominates the northern temperate grass floras. Specifically, we investigate the role of climate cooling in diversification.\n\n* LocationGlobal, temperate regions\n\n* Time periodLate Cretaceous-Cenozoic\n\n* Major taxaThe grass subfamily Pooideae\n\n* MethodsWe date a comprehensive Pooideae phylogeny and test for the impact of paleoclimates on diversification rates. Using ancestral state reconstruction, we investigate if Pooideae ancestors experienced frost and winter. To locate the area of origin of Pooideae we perform biogeographical analyses.\n\n* ResultsWe estimated a late Cretaceous origin of the Pooideae (66 million years ago (Mya)), and all major clades had already diversified at the Eocene-Oligocene transition climate cooling (34 Mya). Climate cooling was a probable driving force of Pooideae diversification. Pooideae likely evolved in mountainous regions of southwestern Eurasia in a temperate niche experiencing frost, but not long winters.\n\n* Main conclusionPooideae originated in a temperate niche and experienced cold temperatures and frost long before the expansion of temperate biomes after the Eocene-Oligocene transition. This suggests that the Pooideae ancestor had adaptations to temperate climate and that extant Pooideae grasses share responses to low temperature stress in Pooideae. Throughout the Cenozoic falling temperatures triggered diversification. However, complex mechanisms for enduring strongly seasonal climate with long, cold winters most likely evolved independently in lower taxonomic lineages. Our findings provide insight into how adaptations to historic changes in chill and frost exposure influence distribution of plant diversity today.

evolutionary biology↗

Ancient tropical extinctions contributed to the latitudinal diversity gradient

Biodiversity currently peaks at the equator, decreasing toward the poles. Growing fossil evidence suggest that this hump-shaped latitudinal diversity gradient (LDG) has not been persistent through time, with similar species diversity across latitudes flattening out the LDG during past greenhouse periods. This provides a new starting point for LDG research. Most studies assume the processes shaping the LDG have acted constantly through time and seek to understand why diversity accumulated in the Holarctic at lower levels than at the equator, e.g. as the result of limited dispersal, or higher turnover in Holarctic regions. However, fossil investigations suggest that we need to explain when and why diversity was lost at high latitudes to generate the LDG. Unfortunately, diversity lost scenarios in the Holarctic have been repeatedly proposed but not yet clearly demonstrated. Here, we use diversification approaches for both phylogenies and fossils to study the LDG of Testudines, Crocodilia and Lepidosauria. We show the LDG of these groups has varied over time, with high latitudes serving as a source of tropical diversity but suffering disproportionate extinction during transitional periods to cold climate. We outline the asymmetric gradient of extinction and dispersal (AGED) framework, which contextualizes previous ideas behind the LDG under a time-variable scenario. We suggest the current steep LDG may be explained by the extinction of clades adapted to warmer conditions from the new temperate regions formed in the Neogene, together with the equator-ward dispersal of organisms tracking their own climatic preferences, when tropical biomes became restricted to the equator. Conversely, high rates of speciation and pole-ward dispersals can account for the formation of an ancient flat LDG during the Cretaceous-Paleogene greenhouse period. Our results demonstrate that the inclusion of fossils in macroevolutionary studies allows detecting extinction events less detectable in analyses restricted to present-day data only.

evolutionary biology↗

Buchnera has changed flatmate but the repeated replacement of co-obligate symbionts is not associated with the ecological expansions of their aphid hosts

Symbiotic associations with bacteria have facilitated important evolutionary transitions in insects and resulted in long-term obligate interactions. Recent evidence suggests that these associations are not always evolutionarily stable and that symbiont replacement and/or supplementation of an obligate symbiosis by an additional bacterium has occurred during the history of many insect groups. Yet, the factors favoring one symbiont over another in this evolutionary dynamic are not well understood; progress has been hindered by our incomplete understanding of the distribution of symbionts across phylogenetic and ecological contexts. While many aphids are engaged into an obligate symbiosis with a single Gammaproteobacterium, Buchnera aphidicola, in species of the Lachninae subfamily, this relationship has evolved into a \"menage a trois\", in which Buchnera is complemented by a cosymbiont, usually Serratia symbiotica. Using deep sequencing of 16S rRNA bacterial genes from 128 species of Cinara (the most diverse Lachninae genus), we reveal a highly dynamic dual symbiotic system in this aphid lineage. Most species host both Serratia and Buchnera but, in several clades, endosymbionts related to Sodalis, Erwinia or an unnamed member of the Enterobacteriaceae have replaced Serratia. Endosymbiont genome sequences from four aphid species+confirm that these coresident symbionts fulfill essential metabolic functions not ensured by Buchnera. We further demonstrate through comparative phylogenetic analyses that co-symbiont replacement is not associated with the adaptation of aphids to new ecological conditions. We propose that symbiont succession was driven by factors intrinsic to the phenomenon of endosymbiosis, such as rapid genome deterioration or competitive interactions between bacteria with similar metabolic capabilities.

evolutionary biology↗