Frontiers of Biogeography
Parent: UC Merced
eScholarship stats: Breakdown by Item for October, 2024 through January, 2025
| Item | Title | Total requests | Download | View-only | %Dnld |
|---|---|---|---|---|---|
| 15d2b65t | perspective: The keystone species concept: a critical appraisal | 771 | 323 | 448 | 41.9% |
| 7tp2k884 | 12,500+ and counting: biodiversity of the Brazilian Pampa | 698 | 124 | 574 | 17.8% |
| 9m64g001 | Globally important plant functional traits for coping with climate change | 535 | 125 | 410 | 23.4% |
| 5gc3c3pj | A tale of two niches: methods, concepts, and evolution | 416 | 115 | 301 | 27.6% |
| 44j7n141 | Probabilistic historical biogeography: new models for founder-event speciation, imperfect detection, and fossils allow improved accuracy and model-testing | 405 | 81 | 324 | 20.0% |
| 8hq04438 | A simulation-based method for selecting calibration areas for ecological niche models and species distribution models | 329 | 97 | 232 | 29.5% |
| 5cj2r993 | Macroecological links between the Linnean, Wallacean, and Darwinian shortfalls | 290 | 58 | 232 | 20.0% |
| 9gv7n6d3 | From dinosaurs to dodos: who could and should we de-extinct? | 282 | 56 | 226 | 19.9% |
| 3vc5s2t3 | Where on Earth are the “tropics”? | 262 | 68 | 194 | 26.0% |
| 00k1v9rs | perspective: The responses of tropical forest species to global climate change: acclimate, adapt, migrate, or go extinct? | 258 | 47 | 211 | 18.2% |
| 5zh8n8r7 | The unifying, fundamental principles of biogeography: understanding <em>Island Life</em> | 256 | 49 | 207 | 19.1% |
| 8ds858zq | Biogeographic history of the pantropical family Gesneriaceae with a focus on the Indian plate and diversification through the Old World | 230 | 97 | 133 | 42.2% |
| 4m84b50k | The distribution and abiotic drivers of subtropical plant taxa in the southwestern U.S. sky island region: identifying hotspots of conservation significance with an aggregation of peripheral species | 229 | 45 | 184 | 19.7% |
| 5wf311d1 | Volcanoes, evolving landscapes, and biodiversity in Neotropical mountains | 229 | 39 | 190 | 17.0% |
| 71h17705 | Long-distance dispersal in amphibians | 228 | 33 | 195 | 14.5% |
| 90z6w9kk | The two South American dry diagonals | 228 | 49 | 179 | 21.5% |
| 69s884m3 | Fungi species description rates confirm high global diversity and suggest half remain unnamed | 222 | 77 | 145 | 34.7% |
| 86b9971p | A framework for disentangling ecological mechanisms underlying the island species–area relationship | 209 | 53 | 156 | 25.4% |
| 0x4387f3 | Advances in the biogeography of littoral environments: a multidisciplinary perspective | 203 | 7 | 196 | 3.4% |
| 5051b6dm | Biogeography of the world’s worst invasive species has spatially biased knowledge gaps but is predictable | 187 | 65 | 122 | 34.8% |
| 5bm866sw | The global ecology of bird migration: patterns and processes | 187 | 49 | 138 | 26.2% |
| 5kk8703h | Conference program and abstracts. International Biogeography Society 7th Biennial Meeting. 8–12 January 2015, Bayreuth, Germany. Frontiers of Biogeography Vol. 6, suppl. 1. International Biogeography Society, 246 pp. | 185 | 136 | 49 | 73.5% |
| 30m4r519 | research letter: Species richness, habitable volume, and species densities in freshwater, the sea, and on land | 173 | 24 | 149 | 13.9% |
| 3mr1d0z4 | The universal evolutionary and ecological significance of 20 oC | 173 | 47 | 126 | 27.2% |
| 5wb5p6dt | Dispersal vs. vicariance: the origin of India’s extant tetrapod fauna | 170 | 36 | 134 | 21.2% |
| 2k00787j | Steps towards decolonising biogeography | 165 | 28 | 137 | 17.0% |
| 5kd801km | From Korean to northeast Asian endemicity: on the occurrence of Pelophylax chosenicus along the Eastern Coastal Yellow Sea | 157 | 56 | 101 | 35.7% |
| 6601q78t | The interface between Macroecology and Conservation: existing links and untapped opportunities | 157 | 35 | 122 | 22.3% |
| 5fs9s640 | Mountain biodiversity and elevational gradients | 156 | 41 | 115 | 26.3% |
| 8nz474j9 | Quantifying local-scale changes in Amazonian forest cover using phytoliths | 154 | 48 | 106 | 31.2% |
| 4f00x5r6 | Non-overlapping climatic niches and biogeographic barriers explain disjunct distributions of continental Urania moths | 153 | 37 | 116 | 24.2% |
| 2m2539gp | A present and future assessment of the effectiveness of existing reserves in preserving three critically endangered freshwater turtles in Southeast Asia and South Asia | 151 | 57 | 94 | 37.7% |
| 6hx3r9fb | Energy use of modern terrestrial large mammal communities mirrors Late Pleistocene megafaunal extinctions | 151 | 51 | 100 | 33.8% |
| 6vk3z94m | Writing the future of biogeography | 150 | 16 | 134 | 10.7% |
| 8cg266sb | Impacts of climate change on marine species invasions in northern hemisphere high-latitude ecosystems | 150 | 16 | 134 | 10.7% |
| 83z3b1nw | An argument supporting de-extinction and a call for field research | 149 | 22 | 127 | 14.8% |
| 5qm701p2 | Doubling diversity: a cautionary tale of previously unsuspected mammalian diversity on a tropical oceanic island | 145 | 40 | 105 | 27.6% |
| 99s5x80m | Evolutionary diversification in the marine realm: a global case study with marine mammals | 144 | 24 | 120 | 16.7% |
| 3gz504j3 | Fitting and comparing competing models of the species abundance distribution: assessment and prospect | 143 | 35 | 108 | 24.5% |
| 1f70180p | Climatic drivers of Sphagnum species distributions | 142 | 48 | 94 | 33.8% |
| 7bd3p8q2 | Paleo-climates and past introgression explain the spatio-temporal distribution of genetic structure in Triodanis perfoliata | 141 | 22 | 119 | 15.6% |
| 5n41f6cc | perspective: Why biogeography matters: historical biogeography vs. phylogeography and community phylogenetics for inferring ecological and evolutionary processes | 137 | 16 | 121 | 11.7% |
| 9hx8h1tk | How to assess the absence of a species? A revision of the geographical range of the horned sea star, Protoreaster nodosus (Echinodermata; Asteroidea) | 136 | 49 | 87 | 36.0% |
| 2cc00316 | <em>Bos primigenius</em> in Ancient Egyptian art – historical evidence for the continuity of occurrence and ecology of an extinct key species | 135 | 50 | 85 | 37.0% |
| 5cv3v9d1 | Uncovering the distribution and limiting factors of Ericaceae-dominated shrublands in the French Alps | 135 | 66 | 69 | 48.9% |
| 2c2888g8 | Flying snails: immigrant selection and the taxon cycle in Pacific Island land snails | 133 | 40 | 93 | 30.1% |
| 61q4k1sp | Land snails on islands: building a global inventory | 128 | 36 | 92 | 28.1% |
| 7ts9g1qz | Analysis of tropical and temperate elevational gradients in arthropod abundance | 126 | 24 | 102 | 19.0% |
| 6rp0v802 | Species distribution modeling to inform transboundary species conservation and management under climate change: promise and pitfalls | 124 | 23 | 101 | 18.5% |
| 6mq7s158 | Climate change threatens the conservation of one of the world’s most endangered transboundary tree species: Magnolia grandis | 118 | 28 | 90 | 23.7% |
Note: Due to the evolving nature of web traffic, the data presented here should be considered approximate and subject to revision. Learn more.