Matches in SemOpenAlex for { <https://semopenalex.org/work/W2330169892> ?p ?o ?g. }
- W2330169892 endingPage "1202" @default.
- W2330169892 startingPage "1191" @default.
- W2330169892 abstract "The native land‐snail fauna of the Hawaiian islands was investigated from a combined perspective of ecological and historical, vicariant, and dispersalist biogeography. There were more than 750 described, valid species; almost all were endemic to the archipelago, many to single islands. Path analysis showed that island area, per se, had the strongest influence on numbers of species. Island altitude and number of plant communities, both strongly related to area and both dimensions of habitat diversity, also had major influences. The influence of island age was complex. A direct effect, older islands having more species, was more than counterbalanced by the strong indirect effects of age on area and altitude: older islands are smaller and lower, and smaller, lower islands had fewer species. Distance of an island from a source of colonization was of minor importance. Species richness thus appears to be related almost exclusively to evolutionary radiation in situ and not to an equilibrium between immigration and extinction. Islands need not be extremely isolated for evolutionary radiation to be more important than immigration/extinction dynamics in determining species richness, but isolation is a relative term dependent on the dispersal abilities of the organisms in question. Numbers of recorded species were also strongly correlated with collecting effort on each island, a result that stands as a warning to others involved in such studies. Numbers of species in different families were not evenly distributed across islands. Notably, Kauai had more amastrids and helicinids and fewer achatinellids than predicted; Oahu had more amastrids but fewer pupillids and succineids than predicted; Hawaii exhibited the opposite pattern from Oahu. These patterns may partly reflect the vagaries of collecting/describing effort, but some may be due to the combined effects of historical factors and competitive exclusion. The distribution of shell height/diameter was bimodal with a distinct absence of more or less equidimensional species, a general pattern seen in other faunas. Among the pulmonates, tall species predominated, suggesting a relative lack of opportunity for globular/flat species. Notably, amastrids occurred in both modes, evidence that, at least in part, ecological not taxonomic factors underlie the bimodality. The proportions of tall and globular/flat species did not vary among islands. Prosobranchs were mostly low‐spired but generally less flat than the pulmonates in the low‐spired mode. The islands were probably colonized originally by small taxa. Large, tall shells are found only on Kauai and Niihau, the oldest of the main islands, suggesting that opportunities for such species are probably available on other islands." @default.
- W2330169892 created "2016-06-24" @default.
- W2330169892 creator A5024079655 @default.
- W2330169892 date "1995-12-01" @default.
- W2330169892 modified "2023-10-16" @default.
- W2330169892 title "VARIATION IN SPECIES DIVERSITY AND SHELL SHAPE IN HAWAIIAN LAND SNAILS: IN SITU SPECIATION AND ECOLOGICAL RELATIONSHIPS" @default.
- W2330169892 cites W1562869184 @default.
- W2330169892 cites W1963601641 @default.
- W2330169892 cites W1972382451 @default.
- W2330169892 cites W1975003732 @default.
- W2330169892 cites W1989395314 @default.
- W2330169892 cites W1996503254 @default.
- W2330169892 cites W2006511029 @default.
- W2330169892 cites W2010964876 @default.
- W2330169892 cites W2013508576 @default.
- W2330169892 cites W2016269030 @default.
- W2330169892 cites W2016368267 @default.
- W2330169892 cites W2019024359 @default.
- W2330169892 cites W2019508278 @default.
- W2330169892 cites W2042846488 @default.
- W2330169892 cites W2050154431 @default.
- W2330169892 cites W2065745399 @default.
- W2330169892 cites W2081358230 @default.
- W2330169892 cites W2084441001 @default.
- W2330169892 cites W2085950272 @default.
- W2330169892 cites W2091411094 @default.
- W2330169892 cites W2104459716 @default.
- W2330169892 cites W2145913928 @default.
- W2330169892 cites W2149885376 @default.
- W2330169892 cites W2323309853 @default.
- W2330169892 cites W2328721474 @default.
- W2330169892 cites W2335429847 @default.
- W2330169892 cites W35528628 @default.
- W2330169892 cites W4205913003 @default.
- W2330169892 cites W4234362179 @default.
- W2330169892 cites W4240320831 @default.
- W2330169892 cites W4240472040 @default.
- W2330169892 cites W4255677521 @default.
- W2330169892 cites W4302781015 @default.
- W2330169892 doi "https://doi.org/10.1111/j.1558-5646.1995.tb04446.x" @default.
- W2330169892 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28568515" @default.
- W2330169892 hasPublicationYear "1995" @default.
- W2330169892 type Work @default.
- W2330169892 sameAs 2330169892 @default.
- W2330169892 citedByCount "75" @default.
- W2330169892 countsByYear W23301698922012 @default.
- W2330169892 countsByYear W23301698922013 @default.
- W2330169892 countsByYear W23301698922014 @default.
- W2330169892 countsByYear W23301698922015 @default.
- W2330169892 countsByYear W23301698922017 @default.
- W2330169892 countsByYear W23301698922018 @default.
- W2330169892 countsByYear W23301698922019 @default.
- W2330169892 countsByYear W23301698922020 @default.
- W2330169892 countsByYear W23301698922021 @default.
- W2330169892 countsByYear W23301698922022 @default.
- W2330169892 crossrefType "journal-article" @default.
- W2330169892 hasAuthorship W2330169892A5024079655 @default.
- W2330169892 hasBestOaLocation W23301698921 @default.
- W2330169892 hasConcept C101991246 @default.
- W2330169892 hasConcept C104317684 @default.
- W2330169892 hasConcept C123575903 @default.
- W2330169892 hasConcept C125471540 @default.
- W2330169892 hasConcept C144024400 @default.
- W2330169892 hasConcept C149923435 @default.
- W2330169892 hasConcept C151730666 @default.
- W2330169892 hasConcept C159985019 @default.
- W2330169892 hasConcept C161894630 @default.
- W2330169892 hasConcept C185933670 @default.
- W2330169892 hasConcept C18903297 @default.
- W2330169892 hasConcept C192562407 @default.
- W2330169892 hasConcept C202682190 @default.
- W2330169892 hasConcept C204207459 @default.
- W2330169892 hasConcept C204323151 @default.
- W2330169892 hasConcept C2777182579 @default.
- W2330169892 hasConcept C2780252984 @default.
- W2330169892 hasConcept C2908647359 @default.
- W2330169892 hasConcept C47559259 @default.
- W2330169892 hasConcept C53565203 @default.
- W2330169892 hasConcept C55493867 @default.
- W2330169892 hasConcept C86803240 @default.
- W2330169892 hasConcept C90132467 @default.
- W2330169892 hasConcept C94043034 @default.
- W2330169892 hasConceptScore W2330169892C101991246 @default.
- W2330169892 hasConceptScore W2330169892C104317684 @default.
- W2330169892 hasConceptScore W2330169892C123575903 @default.
- W2330169892 hasConceptScore W2330169892C125471540 @default.
- W2330169892 hasConceptScore W2330169892C144024400 @default.
- W2330169892 hasConceptScore W2330169892C149923435 @default.
- W2330169892 hasConceptScore W2330169892C151730666 @default.
- W2330169892 hasConceptScore W2330169892C159985019 @default.
- W2330169892 hasConceptScore W2330169892C161894630 @default.
- W2330169892 hasConceptScore W2330169892C185933670 @default.
- W2330169892 hasConceptScore W2330169892C18903297 @default.
- W2330169892 hasConceptScore W2330169892C192562407 @default.
- W2330169892 hasConceptScore W2330169892C202682190 @default.
- W2330169892 hasConceptScore W2330169892C204207459 @default.
- W2330169892 hasConceptScore W2330169892C204323151 @default.
- W2330169892 hasConceptScore W2330169892C2777182579 @default.