Frontiers of Biogeography
Parent: UC Merced
eScholarship stats: Breakdown by Item for May through August, 2026
| Item | Title | Total requests | Download | View-only | %Dnld |
|---|---|---|---|---|---|
| 44j7n141 | Probabilistic historical biogeography: new models for founder-event speciation, imperfect detection, and fossils allow improved accuracy and model-testing | 992 | 188 | 804 | 19.0% |
| 7tp2k884 | 12,500+ and counting: biodiversity of the Brazilian Pampa | 915 | 189 | 726 | 20.7% |
| 3kb4c5jr | Conference program and abstracts. International Biogeography Society 6th Biennial Meeting – 9-13 January 2013, Miami, Florida, USA | 782 | 611 | 171 | 78.1% |
| 8ds858zq | Biogeographic history of the pantropical family Gesneriaceae with a focus on the Indian plate and diversification through the Old World | 768 | 531 | 237 | 69.1% |
| 2cc00316 | <em>Bos primigenius</em> in Ancient Egyptian art – historical evidence for the continuity of occurrence and ecology of an extinct key species | 742 | 322 | 420 | 43.4% |
| 69s884m3 | Fungi species description rates confirm high global diversity and suggest half remain unnamed | 735 | 250 | 485 | 34.0% |
| 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. | 634 | 429 | 205 | 67.7% |
| 15d2b65t | perspective: The keystone species concept: a critical appraisal | 632 | 132 | 500 | 20.9% |
| 5gc3c3pj | A tale of two niches: methods, concepts, and evolution | 611 | 265 | 346 | 43.4% |
| 8hq04438 | A simulation-based method for selecting calibration areas for ecological niche models and species distribution models | 599 | 167 | 432 | 27.9% |
| 3vc5s2t3 | Where on Earth are the “tropics”? | 597 | 154 | 443 | 25.8% |
| 7bx9x5wn | Origin, diversification, and biogeography of forest birds across temperate forest regions in the Northern Hemisphere | 595 | 105 | 490 | 17.6% |
| 90z6w9kk | The two South American dry diagonals | 593 | 146 | 447 | 24.6% |
| 5cj2r993 | Macroecological links between the Linnean, Wallacean, and Darwinian shortfalls | 589 | 158 | 431 | 26.8% |
| 5wb5p6dt | Dispersal vs. vicariance: the origin of India’s extant tetrapod fauna | 578 | 90 | 488 | 15.6% |
| 8vv2g57c | With what precision can the population size of Tyrannosaurus rex be estimated? A reply to Meiri | 560 | 187 | 373 | 33.4% |
| 9m64g001 | Globally important plant functional traits for coping with climate change | 537 | 151 | 386 | 28.1% |
| 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 | 525 | 385 | 140 | 73.3% |
| 30m4r519 | research letter: Species richness, habitable volume, and species densities in freshwater, the sea, and on land | 502 | 187 | 315 | 37.3% |
| 61q4k1sp | Land snails on islands: building a global inventory | 468 | 120 | 348 | 25.6% |
| 09k4j03g | Ecological characterisation of urban ponds in the Netherlands: a study based on data collected by volunteers | 454 | 82 | 372 | 18.1% |
| 5zh8n8r7 | The unifying, fundamental principles of biogeography: understanding <em>Island Life</em> | 451 | 122 | 329 | 27.1% |
| 5qm701p2 | Doubling diversity: a cautionary tale of previously unsuspected mammalian diversity on a tropical oceanic island | 447 | 125 | 322 | 28.0% |
| 3mr1d0z4 | The universal evolutionary and ecological significance of 20 oC | 435 | 118 | 317 | 27.1% |
| 00k1v9rs | perspective: The responses of tropical forest species to global climate change: acclimate, adapt, migrate, or go extinct? | 430 | 115 | 315 | 26.7% |
| 5wf311d1 | Volcanoes, evolving landscapes, and biodiversity in Neotropical mountains | 430 | 114 | 316 | 26.5% |
| 89m124fr | Cover | 426 | 324 | 102 | 76.1% |
| 12v5v73v | High-elevation limits and the ecology of high-elevation vascular plants: legacies from Alexander von Humboldt | 425 | 139 | 286 | 32.7% |
| 5qn1x4tk | Cover | 420 | 322 | 98 | 76.7% |
| 7n80854n | Dale & Fortin – the revised guide to spatial analysis | 420 | 70 | 350 | 16.7% |
| 8mj4015f | Population sizes of T. rex cannot be precisely estimated | 416 | 125 | 291 | 30.0% |
| 34v0x2mv | Cover | 409 | 356 | 53 | 87.0% |
| 3m7719vv | Operationalizing expert knowledge in species' range estimates using diverse data types | 408 | 84 | 324 | 20.6% |
| 86b9971p | A framework for disentangling ecological mechanisms underlying the island species–area relationship | 402 | 107 | 295 | 26.6% |
| 83d7x15m | Cover | 395 | 328 | 67 | 83.0% |
| 5051b6dm | Biogeography of the world’s worst invasive species has spatially biased knowledge gaps but is predictable | 384 | 122 | 262 | 31.8% |
| 9hx8h1tk | How to assess the absence of a species? A revision of the geographical range of the horned sea star, Protoreaster nodosus (Echinodermata; Asteroidea) | 384 | 116 | 268 | 30.2% |
| 1nc7f8kp | Cover | 383 | 329 | 54 | 85.9% |
| 3835r78s | Gondwanan origin of the Dipterocarpaceae-Cistaceae-Bixaceae is supported by fossils, areocladograms, ecomorphological traits and tectonic-plate dynamics | 379 | 85 | 294 | 22.4% |
| 71h17705 | Long-distance dispersal in amphibians | 369 | 97 | 272 | 26.3% |
| 33t709x4 | Tramps in transition: genetic differentiation between populations of an iconic "supertramp" taxon in the Central Indo-Pacific | 368 | 91 | 277 | 24.7% |
| 5bm866sw | The global ecology of bird migration: patterns and processes | 366 | 103 | 263 | 28.1% |
| 77k5k5nc | Which is the richest of them all? Comparing area-adjusted plant diversities of Mediterranean- and tropical-climate regions | 352 | 89 | 263 | 25.3% |
| 2c2888g8 | Flying snails: immigrant selection and the taxon cycle in Pacific Island land snails | 349 | 131 | 218 | 37.5% |
| 1fz6z5mm | Macroecological correlates of richness, body size, and species range size in terrestrial vertebrates across the world | 348 | 91 | 257 | 26.1% |
| 6601q78t | The interface between Macroecology and Conservation: existing links and untapped opportunities | 346 | 138 | 208 | 39.9% |
| 09t665nx | Optimizing biodiversity informatics to improve information flow, data quality, and utility for science and society | 342 | 152 | 190 | 44.4% |
| 2sk0g052 | Phylogenetic diversity of ferns reveals different patterns of niche conservatism and habitat filtering between epiphytic and terrestrial assemblages | 341 | 102 | 239 | 29.9% |
| 1n12z17n | The Cerrado and restinga pathways: two ancient biotic corridors in the Neotropics | 340 | 77 | 263 | 22.6% |
| 5596q2g4 | Geologically recent rearrangements in central Amazonian river network and their importance for the riverine barrier hypothesis | 332 | 103 | 229 | 31.0% |
Note: Due to the evolving nature of web traffic, the data presented here should be considered approximate and subject to revision. Learn more.