1995
DOI: 10.2307/1938144
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Changes in Soil Phosphorus Fractions and Ecosystem Dynamics across a Long Chronosequence in Hawaii

Abstract: We tested the Walker and Syers (1976) conceptual model of soil development and its ecological implications by analyzing changes in soil P, vegetation, and other ecosystem properties on a soil chronosequence with six sites ranging in age from 300 yr to 4.1 x 106 yr. Climate, dominant vegetation, slope, and parent material of all of the sites were similar. As fractions of total P, the various pools of soil phosphorus behaved very much as predicted by Walker and Syers. HCI—extractable P (presumably primary minera… Show more

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Cited by 869 publications
(828 citation statements)
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“…Soil chronosequences, by contrast, enable comparisons between ecosystems within much smaller regions, where factors such as climate and parent material are controlled [50,51]. The available data reveal that total plant species richness usually increases with soil age across soil chronosequences spanning boreal, temperate, subtropical, and Mediterranean climates [4,5,24] (Figure II). Together, these global and smallerscale patterns motivate the search for underlying mechanisms that can explain the greater plant diversity on older soils.…”
Section: Box 1 Long-term Pedogenesis and Local Plant Species Diversitymentioning
confidence: 99%
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“…Soil chronosequences, by contrast, enable comparisons between ecosystems within much smaller regions, where factors such as climate and parent material are controlled [50,51]. The available data reveal that total plant species richness usually increases with soil age across soil chronosequences spanning boreal, temperate, subtropical, and Mediterranean climates [4,5,24] (Figure II). Together, these global and smallerscale patterns motivate the search for underlying mechanisms that can explain the greater plant diversity on older soils.…”
Section: Box 1 Long-term Pedogenesis and Local Plant Species Diversitymentioning
confidence: 99%
“…Soil chronosequences provide some support for the productivity-diversity hypothesis, in that total plant species richness generally increases as ecosystem retrogression proceeds (and productivity declines) [4,5]. By contrast, according to the resource-ratio theory [12], higher plant diversity is maintained under equilibrium conditions if multiple resources limit productivity [14], such that a positive relation is expected between the number of colimiting resources and plant diversity [14].…”
Section: Potential Factors Controlling Plant Diversity Nutrient Availmentioning
confidence: 99%
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“…Previous studies of vars. incana and glaberrima on Hawaiʻi Island documented different leaf nitrogen contents , and the differential adaptation of their seedlings to light and nitrogen (Morrison and Stacy, 2014), both of which vary significantly between new and old substrates on east Hawaiʻi Island (Crews et al, 1995). Other studies of glabrous and pubescent seedlings or trees from lower elevations (indicative of these two varieties) grown in a common garden revealed differences in water retention (Stemmermann, 1983), cuticle thickness and possibly osmotic potentials and photosynthesis rates (Kitayama et al, 1997).…”
Section: Introductionmentioning
confidence: 96%
“…Analyses of these patterns have contributed to the formulation of ecological theories and to a greater understanding of biogeochemical controls of ecosystem dynamics (Hooper and Vitousek, 1997;Vitousek and Farrington, 1997;Chadwick et al, 1999). For instance, the roles of phosphorus, nitrogen and eolian nutrient inputs have been clearly documented through long-term observations of Hawaiian chronosequences (Crews et al, 1995;Chadwick et al, 1999;Neff et al, 2000).…”
Section: Introductionmentioning
confidence: 99%