Frontiers of Biogeography
Parent: UC Merced
eScholarship stats: History by Item for June through September, 2026
| Item | Title | Total requests | 2026-09 | 2026-08 | 2026-07 | 2026-06 |
|---|---|---|---|---|---|---|
| 3kb4c5jr | Conference program and abstracts. International Biogeography Society 6th Biennial Meeting – 9-13 January 2013, Miami, Florida, USA | 1,216 | 660 | 146 | 269 | 141 |
| 44j7n141 | Probabilistic historical biogeography: new models for founder-event speciation, imperfect detection, and fossils allow improved accuracy and model-testing | 919 | 184 | 296 | 161 | 278 |
| 7tp2k884 | 12,500+ and counting: biodiversity of the Brazilian Pampa | 901 | 271 | 267 | 140 | 223 |
| 8hq04438 | A simulation-based method for selecting calibration areas for ecological niche models and species distribution models | 879 | 468 | 179 | 115 | 117 |
| 69s884m3 | Fungi species description rates confirm high global diversity and suggest half remain unnamed | 775 | 229 | 246 | 144 | 156 |
| 2cc00316 | <em>Bos primigenius</em> in Ancient Egyptian art – historical evidence for the continuity of occurrence and ecology of an extinct key species | 698 | 174 | 240 | 122 | 162 |
| 3vc5s2t3 | Where on Earth are the “tropics”? | 600 | 177 | 151 | 125 | 147 |
| 30m4r519 | research letter: Species richness, habitable volume, and species densities in freshwater, the sea, and on land | 588 | 186 | 213 | 88 | 101 |
| 15d2b65t | perspective: The keystone species concept: a critical appraisal | 581 | 137 | 178 | 105 | 161 |
| 8ds858zq | Biogeographic history of the pantropical family Gesneriaceae with a focus on the Indian plate and diversification through the Old World | 580 | 73 | 99 | 170 | 238 |
| 90z6w9kk | The two South American dry diagonals | 569 | 123 | 168 | 93 | 185 |
| 5gc3c3pj | A tale of two niches: methods, concepts, and evolution | 568 | 159 | 141 | 114 | 154 |
| 5wb5p6dt | Dispersal vs. vicariance: the origin of India’s extant tetrapod fauna | 536 | 148 | 178 | 63 | 147 |
| 9m64g001 | Globally important plant functional traits for coping with climate change | 505 | 116 | 164 | 93 | 132 |
| 5cj2r993 | Macroecological links between the Linnean, Wallacean, and Darwinian shortfalls | 471 | 92 | 117 | 90 | 172 |
| 5zh8n8r7 | The unifying, fundamental principles of biogeography: understanding <em>Island Life</em> | 459 | 120 | 109 | 86 | 144 |
| 61q4k1sp | Land snails on islands: building a global inventory | 449 | 119 | 132 | 82 | 116 |
| 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. | 445 | 87 | 92 | 103 | 163 |
| 8vv2g57c | With what precision can the population size of Tyrannosaurus rex be estimated? A reply to Meiri | 439 | 82 | 140 | 79 | 138 |
| 12v5v73v | High-elevation limits and the ecology of high-elevation vascular plants: legacies from Alexander von Humboldt | 430 | 139 | 137 | 80 | 74 |
| 4jg256x0 | Does habitat stability structure intraspecific genetic diversity? It’s complicated... | 424 | 288 | 45 | 47 | 44 |
| 3mr1d0z4 | The universal evolutionary and ecological significance of 20 oC | 420 | 99 | 136 | 96 | 89 |
| 7n80854n | Dale & Fortin – the revised guide to spatial analysis | 416 | 126 | 88 | 85 | 117 |
| 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 | 412 | 68 | 108 | 100 | 136 |
| 5bm866sw | The global ecology of bird migration: patterns and processes | 402 | 144 | 103 | 66 | 89 |
| 5qm701p2 | Doubling diversity: a cautionary tale of previously unsuspected mammalian diversity on a tropical oceanic island | 402 | 105 | 158 | 73 | 66 |
| 7bx9x5wn | Origin, diversification, and biogeography of forest birds across temperate forest regions in the Northern Hemisphere | 401 | 100 | 146 | 49 | 106 |
| 8mj4015f | Population sizes of T. rex cannot be precisely estimated | 386 | 119 | 113 | 59 | 95 |
| 86b9971p | A framework for disentangling ecological mechanisms underlying the island species–area relationship | 356 | 95 | 77 | 71 | 113 |
| 3835r78s | Gondwanan origin of the Dipterocarpaceae-Cistaceae-Bixaceae is supported by fossils, areocladograms, ecomorphological traits and tectonic-plate dynamics | 355 | 120 | 106 | 42 | 87 |
| 9hx8h1tk | How to assess the absence of a species? A revision of the geographical range of the horned sea star, Protoreaster nodosus (Echinodermata; Asteroidea) | 350 | 103 | 93 | 49 | 105 |
| 00k1v9rs | perspective: The responses of tropical forest species to global climate change: acclimate, adapt, migrate, or go extinct? | 348 | 91 | 78 | 59 | 120 |
| 77k5k5nc | Which is the richest of them all? Comparing area-adjusted plant diversities of Mediterranean- and tropical-climate regions | 334 | 92 | 90 | 68 | 84 |
| 5wf311d1 | Volcanoes, evolving landscapes, and biodiversity in Neotropical mountains | 311 | 56 | 65 | 77 | 113 |
| 09t665nx | Optimizing biodiversity informatics to improve information flow, data quality, and utility for science and society | 308 | 76 | 78 | 83 | 71 |
| 1m8441pb | Climatic niche overlap models reveal niche partitioning among black widow spiders and potential ecological impacts of invasive brown widows in North America | 302 | 110 | 90 | 47 | 55 |
| 33t709x4 | Tramps in transition: genetic differentiation between populations of an iconic "supertramp" taxon in the Central Indo-Pacific | 300 | 75 | 61 | 101 | 63 |
| 89m124fr | Cover | 299 | 32 | 60 | 82 | 125 |
| 3qx2m92s | Evaluating records of trans-Atlantic dispersal of drifting disseminules to European shores. | 297 | 91 | 88 | 67 | 51 |
| 1kq0f5vd | Birds and barriers: present and past seas are dominant correlates of avian turnover in the Indo-Australian Archipelago | 296 | 77 | 110 | 38 | 71 |
| 3m7719vv | Operationalizing expert knowledge in species' range estimates using diverse data types | 296 | 66 | 75 | 74 | 81 |
| 34v0x2mv | Cover | 295 | 38 | 65 | 72 | 120 |
| 744009b2 | Oceanic archipelagos: a perspective on the geodynamics and biogeography of the World’s smallest biotic provinces | 293 | 72 | 104 | 59 | 58 |
| 5qn1x4tk | Cover | 290 | 32 | 57 | 79 | 122 |
| 1wt383wf | Phylogeography and Conservation Biogeography of the Humphead Wrasse, Cheilinus undulatus | 288 | 106 | 72 | 50 | 60 |
| 5596q2g4 | Geologically recent rearrangements in central Amazonian river network and their importance for the riverine barrier hypothesis | 288 | 62 | 83 | 77 | 66 |
| 71h17705 | Long-distance dispersal in amphibians | 287 | 55 | 69 | 77 | 86 |
| 5051b6dm | Biogeography of the world’s worst invasive species has spatially biased knowledge gaps but is predictable | 285 | 51 | 90 | 58 | 86 |
| 3s37q6mg | Potential decline in the distribution and food provisioning services of the mopane worm (Gonimbrasia belina) in southern Africa | 284 | 79 | 74 | 46 | 85 |
| 6w55v67b | Archipelagos and meta-archipelagos | 283 | 103 | 76 | 36 | 68 |
Note: Due to the evolving nature of web traffic, the data presented here should be considered approximate and subject to revision. Learn more.