| Conceptual and statistical problems with the DEC plus J model of founder-event speciation and its comparison with DEC via model selection |
75 |
| Without quality presence-absence data, discrimination metrics such as TSS can be misleading measures of model performance |
33 |
| The International Tree-Ring Data Bank (ITRDB) revisited: Data availability and global ecological representativity |
28 |
| The flickering connectivity system of the north Andean paramos |
24 |
| Local environment and space drive multiple facets of stream macroinvertebrate beta diversity |
19 |
| Beyond climate control on species range: The importance of soil data to predict distribution of Amazonian plant species |
18 |
| Beyond trees: Biogeographical regionalization of tropical Africa |
18 |
| Resist, recover or both? Growth plasticity in response to drought is geographically structured and linked to intraspecific variability in Pinus pinaster |
17 |
| Range shifts in response to past and future climate change: Can climate velocities and species' dispersal capabilities explain variation in mammalian range shifts? |
16 |
| Outstanding plant endemism levels strongly support the recognition of campo rupestre provinces in mountaintops of eastern South America |
16 |
| Discovering floristic and geoecological gradients across Amazonia |
15 |
| Improving species distribution models for invasive non-native species with biologically informed pseudo-absence selection |
14 |
| Spatial patterns and climate relationships of major plant traits in the New World differ between woody and herbaceous species |
14 |
| Shifts in plant distributions in response to climate warming in a biodiversity hotspot, the Hengduan Mountains |
13 |
| Predicting beta diversity of terrestrial and aquatic beetles using ecogeographical variables: insights from the replacement and richness difference components |
12 |
| What makes the Sino-Himalayan mountains the major diversity hotspots for pheasants? |
12 |
| Assessing similarity of n-dimensional hypervolumes: Which metric to use? |
12 |
| High beta diversity among small islands is due to environmental heterogeneity rather than ecological drift |
12 |
| Past climate changes and strong oceanographic barriers structured low-latitude genetic relics for the golden kelp Laminaria ochroleuca |
11 |
| From Gondwana to GAARlandia: Evolutionary history and biogeography of ogre-faced spiders (Deinopis) |
11 |
| Historical hybrid zone movement: More pervasive than appreciated |
11 |
| Elevational and microclimatic drivers of thermal tolerance in Andean Pristimantis frogs |
11 |
| Origins of global mountain plant biodiversity: Testing the 'mountain-geobiodiversity hypothesis' |
11 |
| Pre-Pleistocene origin of phylogeographical breaks in African rain forest trees: New insights from Greenwayodendron (Annonaceae) phylogenomics |
11 |
| Functional and phylogenetic diversity of bird assemblages are filtered by different biotic factors on tropical mountains |
10 |
| Contrasting phylogeography of two Western Palaearctic fish parasites despite similar life cycles |
10 |
| Patch-scale biodiversity retention in fragmented landscapes: Reconciling the habitat amount hypothesis with the island biogeography theory |
10 |
| Phylogeography, evolutionary history and effects of glaciations in a species (Zootoca vivipara) inhabiting multiple biogeographic regions |
10 |
| Principal factors controlling biodiversity along an elevation gradient: Water, energy and their interaction |
10 |
| Oceanic islands of Wallacea as a source for dispersal and diversification of murine rodents |
10 |
| The spectre of biogeographical regionalization |
10 |
| Patterns and drivers of species diversity in the Indo-Pacific red seaweed Portieria |
10 |
| Global priority areas for amphibian research |
9 |
| Copepod diapause and the biogeography of the marine lipidscape |
9 |
| Phylogeography and historical demography of the arboreal pit viper Bothrops bilineatus (Serpentes, Crotalinae) reveal multiple connections between Amazonian and Atlantic rain forests |
9 |
| Small mammal species richness is directly linked to regional productivity, but decoupled from food resources, abundance, or habitat complexity |
9 |
| Nonlinear higher order abiotic interactions explain riverine biodiversity |
9 |
| Rapid diversification of alpine bamboos associated with the uplift of the Hengduan Mountains |
9 |
| Winter matters: Sensitivity to winter climate and cold events increases towards the cold distribution margin of European beech (Fagus sylvatica L.) |
9 |
| Subtropical streams harbour higher genus richness and lower abundance of insects compared to boreal streams, but scale matters |
8 |
| Species richness of birds along a complete rain forest elevational gradient in the tropics: Habitat complexity and food resources matter |
8 |
| Incomplete species lists derived from global and regional specimen-record databases affect macroecological analyses: A case study on the vascular plants of China |
8 |
| East Asian origins of European holly oaks (Quercus section Ilex Loudon) via the Tibet-Himalaya |
8 |
| The impact of early Quaternary climate change on the diversification and population dynamics of a South American cactus species |
8 |
| Using biotic interactions in broad-scale estimates of species' distributions |
8 |
| Similar compositional turnover but distinct insular environmental and geographical drivers of native and exotic ants in two oceans |
8 |
| Global biogeographical regions of freshwater fish species |
8 |
| Sky, sea, and forest islands: Diversification in the African leaf-folding frog Afrixalus paradorsalis (Anura: Hyperoliidae) of the Lower Guineo-Congolian rain forest |
8 |
| Challenges and opportunities for biogeography-What can we still learn from von Humboldt? |
8 |
| Do functional groups of planktonic copepods differ in their ecological niches? |
8 |
