Marie Hildreth Meiere

Understanding the drivers of species richness patterns is a major goal of ecology and evolutionary biology, and the drivers vary across regions and taxa. Here, we assessed the influence of environmental factors and evolutionary history on the pattern of species richness in the genus Sorbus (110 species). We mapped the global species richness pattern of Sorbus at a spatial resolution of 200 × 200 km, using 10,652 specimen records. We used stepwise regression to assess the relationship between 23 environmental predictors and species richness and estimated the diversification rate of Sorbus based on chloroplast genome data. The effects of environmental factors were explained by adjusted R2, and evolutionary factors were inferred based on differences in diversification rates. We found that the species richness of Sorbus was highest in the Hengduan Mountains (HDM), which is probably the center of diversity. Among the selected environmental predictors, the integrated model including all environmental predictors had the largest explanatory power for species richness. The determinants of species richness show regional differences. On the global and continental scale, energy and water availability become the main driving factors. In contrast, climate seasonality is the primary factor in the HDM. The diversification rate results showed no significant differences between HDM and non-HDM, suggesting that evolutionary history may have limited impact on the pattern of Sorbus species richness. We conclude that environmental factors play an important role in shaping the global pattern of Sorbus species richness, while diversification rates have a lesser impact.

Some plant lineages remain within the same biome over time (biome conservatism), whereas others seem to adapt more easily to new biomes. The c. 398 species (14 genera) of subfamily Cercidoideae (Leguminosae or Fabaceae) are found in many biomes around the world, particularly in the tropical regions of South America, Asia and Africa, and display a variety of growth forms (small trees, shrubs, lianas and herbaceous perennials). Species distribution maps derived from cleaned occurrence records were compiled and compared with existing biome maps and with the literature to assign species to biomes. Rainforest (144 species), succulent (44 species), savanna (36 species), and temperate (10 species) biomes were found to be important in describing the global distribution of Cercidoideae, with many species occurring in more than one biome. Two phylogenetically isolated species-poor temperate ( Cercis ) and succulent ( Adenolobus ) biome lineages are sister to two broadly distributed species-rich tropical clades. Ancestral state reconstructions on a time-calibrated phylogeny suggest biome shifts occurred throughout the evolutionary history of the subfamily, with shifts between the succulent and rainforest biomes, from the rainforest to savanna, from the succulent to savanna biome, and one early occurring shift into (or from) the temperate biome. Of the 26 inferred shifts in biome, three are closely associated with a shift from the ancestral tree/shrub growth form to a liana or herbaceous perennial habit. Only three of the 13 inferred transcontinental dispersal events are associated with biome shifts. Overall, we find that biome shifts tend to occur within the same continent and that dispersals to new continents tend to occur within the same biome, but that nonetheless the biome-conserved and biogeographically structured Cercidoideae have been able to adapt to different environments through time.

Drylands cover ca. 40% of the land global surface and deliver significant ecosystem services. These regions are the most sensitive, prone to suffer the effects of climate and distribution changes, so estimates on projected range shifts are crucial to complement traditional approaches to biodiversity conservation and sustainability. Shrubs of the Monte Desert dominate the largest temperate dryland in South America. Our goal is to assess the spatial distribution and niche overlap of three native shrubs (Larrea cuneifolia (LC), L. divaricata (LD), and L. nitida (LN)), under present climate conditions, to retrodict their potential past distribution, and anticipate their predicted range under future climate scenarios. We used ecological niche modeling that were projected to the past (LGM and Mid Holocene) and future (2050 and 2070) under two scenarios of greenhouse gas emissions and two model of global circulation. All species have high niche overlap (67–89%), but showed species-specific responses, highlighting the need to develop mitigation measures particularly for LD and LN in the face of climate change and land use pressures. Global South deserts are being highly degraded and information on future potential ranges of endemic species can support the development of sustainable conservation and management plans.

Paleoclimate reconstructions can provide a window into the environmental conditions in Earth history when atmospheric carbon dioxide concentrations were higher than today. In the eastern USA, paleoclimate reconstructions are sparse, because terrestrial sedimentary deposits are rare. Despite this, the eastern USA has the largest population and population density in North America, and understanding the effects of current and future climate change is of vital importance. Here, we provide terrestrial paleoclimate reconstructions of the eastern USA from Miocene fossil floras. Additionally, we compare proxy paleoclimate reconstructions from the warmest period in the Miocene, the Miocene Climatic Optimum (MCO), to those of an MCO Earth System Model. Reconstructed Miocene temperatures and precipitation north of 35°N are higher than modern. In contrast, south of 35°N, temperatures and precipitation are similar to today, suggesting a poleward amplification effect in eastern North America. Reconstructed Miocene rainfall seasonality was predominantly higher than modern, regardless of latitude, indicating greater variability in intra-annual moisture transport. Reconstructed climates are almost uniformly in the temperate seasonal forest biome, but heterogeneity of specific forest types is evident. Reconstructed Miocene terrestrial temperatures from the eastern USA are lower than modeled temperatures and coeval Atlantic sea surface temperatures. However, reconstructed rainfall is consistent with modeled rainfall. Our results show that during the Miocene, climate was most different from modern in the northeastern states, and may suggest a drastic reduction in the meridional temperature gradient along the North American east coast compared to today.

We analyzed the geographical distribution of Habromys species based on distributional data from museum specimens, web databases, and literature. We recorded species-presence data of each species in 0.5° × 0.5° grid cells and biogeographic provinces in Mexico and Central America. We analyzed the association between vegetation types and land use. We carried out species distribution models of most species of Habromys and those tree species frequently harboring these mice, finding a high distributional congruence among mice and trees. Species of Habromys occur throughout the montane systems of Mexico and northern Central America, so they can be considered characteristic elements of the Neotropical montane cloud forests. All species of the genus occur in Mexico, whereas Guatemala and El Salvador have only one species. Although all species of Habromys are highly restricted and considered rare species, only one (H. simulatus) is currently protected by Mexican laws. We assigned two species to a high and four to the critical conservation risk. Habromys species contribute to the recognition of Mesoamerica as a biodiversity hotspot.

Digital point‐occurrence records from the Global Biodiversity Information Facility (GBIF) and other data providers enable a wide range of research in macroecology and biogeography. However, data errors may hamper immediate use. Manual data cleaning is time‐consuming and often unfeasible, given that the databases may contain thousands or millions of records. Automated data cleaning pipelines are therefore of high importance. Taking North American Ephedra as a model, we examined how different data cleaning pipelines (using, e.g., the GBIF web application, and four different R packages) affect downstream species distribution models (SDMs). We also assessed how data differed from expert data. From 13,889 North American Ephedra observations in GBIF, the pipelines removed 31.7% to 62.7% false positives, invalid coordinates, and duplicates, leading to datasets between 9484 (GBIF application) and 5196 records (manual‐guided filtering). The expert data consisted of 704 records, comparable to data from field studies. Although differences in the absolute numbers of records were relatively large, species richness models based on stacked SDMs (S‐SDM) from pipeline and expert data were strongly correlated (mean Pearson's r across the pipelines: .9986, vs. the expert data: .9173). Our results suggest that all R package‐based pipelines reliably identified invalid coordinates. In contrast, the GBIF‐filtered data still contained both spatial and taxonomic errors. Major drawbacks emerge from the fact that no pipeline fully discovered misidentified specimens without the assistance of taxonomic expert knowledge. We conclude that application‐filtered GBIF data will still need additional review to achieve higher spatial data quality. Achieving high‐quality taxonomic data will require extra effort, probably by thoroughly analyzing the data for misidentified taxa, supported by experts.

The Qinghai-Tibetan Plateau (QTP) harbors abundant and diverse plant life owing to its high habitat heterogeneity. However, the distribution pattern of biodiversity hotspots and their conservation status remain unclear. Based on 148,283 high-resolution occurrence coordinates of 13,450 seed plants, w…

Understanding the impact of historical and demographic processes on genetic variation is essential for devising conservation strategies and predicting responses to climate change. Recolonization after Pleistocene glaciations is expected to leave distinct genetic signatures, characterised by lower ge…

Concern about the course of the current environmental problems has raised interest in investigating the different scenarios that have taken place in our planet throughout time. To that end, different methodologies have been employed in order to determine the different variables that compose the envi…

The description of a new species is a key step in cataloguing the World’s flora. However, this is only a preliminary stage in a long process of understanding what that species represents. We investigated how long the species discovery process takes by focusing on three key stages: 1, the collection …