Question: A set of easily-measured ('soft') plant traits has been identified as potentially useful predictors of ecosystem functioning in previous studies. Here we aimed to discover whether the screening techniques remain operational in widely contrasted circumstances, to test for the existence of axes of variation in the particular sets of traits, and to test for their links with 'harder' traits of proven importance to ecosystem functioning. Location: central-western Argentina, central England, northern upland Iran, and northeastern Spain. Recurrent patterns of ecological specialization: Through ordination of a matrix of 640 vascular plant taxa by 12 standardized traits, we detected similar patterns of specialization in the four floras. The first PCA axis was identified as an axis of resource capture, usage and release. PCA axis 2 appeared to be a size-related axis. Individual PCA for each country showed that the same traits remained valuable as predictors of resource capture and utilization in all of them, despite their major differences in climate, biogeography and land-use. The results were not significantly driven by particular taxa: the main traits determining PCA axis 1 were very similar in eudicotyledons and monocotyledons and Asteraceae, Fabaceae and Poaceae. Links between recurrent suites of 'soft' traits and 'hard' traits: The validity of PCA axis 1 as a key predictor of resource capture and utilization was tested by comparisons between this axis and values of more rigorously established predictors ('hard' traits) for the floras of Argentina and England. PCA axis 1 was correlated with variation in relative growth rate, leaf nitrogen content, and litter decomposition rate. It also coincided with palatability to model generalist herbivores. Therefore, location on PCA axis 1 can be linked to major ecosystem processes in those habitats where the plants are dominant. Conclusion: We confirm the existence at the global scale of a major axis of evolutionary specialization, previously recog-nised in several local floras. This axis reflects a fundamental trade-off between rapid acquisition of resources and conservation of resources within well-protected tissues. These major trends of specialization were maintained across different environmental situations (including differences in the proximate causes of low productivity, i.e. drought or mineral nutrient deficiency). The trends were also consistent across floras and major phylogenetic groups, and were linked with traits directly relevant to ecosystem processes.
Question: A set of easily-measured ('soft') plant traits has been identified as potentially useful predictors of ecosystem functioning in previous studies. Here we aimed to discover whether the screening techniques remain operational in widely contrasted circumstances, to test for the existence of axes of variation in the particular sets of traits, and to test for their links with 'harder' traits of proven importance to ecosystem functioning. Location: central-western Argentina, central England, northern upland Iran, and northeastern Spain. Recurrent patterns of ecological specialization: Through ordination of a matrix of 640 vascular plant taxa by 12 standardized traits, we detected similar patterns of specialization in the four floras. The first PCA axis was identified as an axis of resource capture, usage and release. PCA axis 2 appeared to be a size-related axis. Individual PCA for each country showed that the same traits remained valuable as predictors of resource capture and utilization in all of them, despite their major differences in climate, biogeography and land-use. The results were not significantly driven by particular taxa: the main traits determining PCA axis 1 were very similar in eudicotyledons and monocotyledons and Asteraceae, Fabaceae and Poaceae. Links between recurrent suites of 'soft' traits and 'hard' traits: The validity of PCA axis 1 as a key predictor of resource capture and utilization was tested by comparisons between this axis and values of more rigorously established predictors ('hard' traits) for the floras of Argentina and England. PCA axis 1 was correlated with variation in relative growth rate, leaf nitrogen content, and litter decomposition rate. It also coincided with palatability to model generalist herbivores. Therefore, location on PCA axis 1 can be linked to major ecosystem processes in those habitats where the plants are dominant. Conclusion: We confirm the existence at the global scale of a major axis of evolutionary specialization, previously recog-nised in several local floras. This axis reflects a fundamental trade-off between rapid acquisition of resources and conservation of resources within well-protected tissues. These major trends of specialization were maintained across different environmental situations (including differences in the proximate causes of low productivity, i.e. drought or mineral nutrient deficiency). The trends were also consistent across floras and major phylogenetic groups, and were linked with traits directly relevant to ecosystem processes.
There is some evidence that traits of fresh leaves that provide structural or chemical protection (' defence ') remain operational in the leaf litter and control interspecific variation in decomposition rate in or on the soil. We tested experimentally whether the negative relationship between foliar defence and litter decomposition rate is fundamental, i.e. whether it is seen consistently across higher plant species and life forms, and whether it is repeated in the floras of geographically and climatically distinct areas separated by an ocean. We employed the published results of two outdoor litter bag experiments, in which we simultaneously compared the relative mass losses (' decomposibility ') of leaf litters of a wide range of plant species. One experiment was in Co! rdoba, Argentina, and included 48 Argentine species typical of the dry, subtropical landscapes along a steep altitudinal gradient. The other was in Sheffield, UK, and hosted 72 British species typical of the temperate-Atlantic landscape there. We linked the two experiments through a similar experiment in Sheffield that hosted litters of subsets of both the Argentine and British species. We also tested fresh leaves of all species from the same areas for tensile strength (' toughness ') and relative palatability to generalist herbivorous snails in multi-species ' cafeteria ' experiments. Both in Argentina and in Great Britain there were highly significant correlations between leaf palatability (r l 0.61 ; 0.73) or leaf tensile strength (r l k0.60 ; k0.60) and litter mass loss across all species. These relationships could be explained by variation both between and within broad life-form groups. Specific leaf area (area : dry mass) of fresh leaves was consistently correlated only with litter mass loss within British life form groups. We illustrated the possible ecosystem consequences of these relationships by comparing functional traits of British species differing in leaf habit. In comparison with deciduous species, evergreens generally had innately slow growth, which corresponded to their longer-lived leaves of lower specific leaf area, higher tensile strength and lower palatability to generalist invertebrate herbivores. Correspondingly, evergreens produced more resistant leaf litter. Thus, slow-growing evergreens might maintain their position in infertile ecosystems through leaf traits that help them to conserve their nutrients efficiently and to keep nutrient mineralization low, thereby not allowing potentially fast-growing deciduous species to outcompete them.
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