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1.
Glob Chang Biol ; 21(10): 3827-35, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26033529

RESUMO

Plants are often genetically specialized as ecotypes attuned to local environmental conditions. When conditions change, the optimal environment may be physically displaced from the local population, unless dispersal or in situ evolution keep pace, resulting in a phenomenon called adaptational lag. Using a 30-year-old reciprocal transplant study across a 475 km latitudinal gradient, we tested the adaptational lag hypothesis by measuring both short-term (tiller population growth rates) and long-term (17-year survival) fitness components of Eriophorum vaginatum ecotypes in Alaska, where climate change may have already displaced the optimum. Analyzing the transplant study as a climate transfer experiment, we showed that the climate optimum for plant performance was displaced ca. 140 km north of home sites, although plants were not generally declining in size at home sites. Adaptational lag is expected to be widespread globally for long-lived, ecotypically specialized plants, with disruptive consequences for communities and ecosystems.


Assuntos
Mudança Climática , Cyperaceae/fisiologia , Dispersão Vegetal , Adaptação Fisiológica , Alaska , Cyperaceae/crescimento & desenvolvimento , Raízes de Plantas , Crescimento Demográfico
2.
Am J Bot ; 99(9): 1562-71, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22922398

RESUMO

PREMISE OF THE STUDY: In a large reciprocal transplant experiment, Eriophorum vaginatum tussocks transplanted along a latitudinal gradient in Alaska's interior exhibited genetic differentiation and phenotypic plasticity for vegetative traits. Using the same tussocks 30 yr later, we used estimates of growing season temperature at each site to ask whether there was a climatic cline for stomatal density, size, and conductance. METHODS: We created impressions of the abaxial leaf surfaces of the transplanted individuals for viewing under a microscope and measured stomatal density (SD) and length (SL) for 224 individuals. We used SD and SL to estimate stomatal conductance (C). Separate one-way analyses of variance were performed to quantify the effect of population genetic differences and latitudinal environmental variation on stomatal characteristics. KEY RESULTS: Our data suggest that stomatal size was influenced by both genetics and environment and that plasticity for stomatal density produced highest densities at the coolest sites. Stomatal conductance increased with decreasing temperature of site from which the populations originated. CONCLUSIONS: Our results demonstrate a cline in stomatal conductance in E. vaginatum, with some ability of populations to plastically produce an appropriate phenotypic response in a new environment. Because the species is a dominant species in many arctic plant communities, its ability to produce an appropriate stomatal phenotype and to optimize water use efficiency by decreasing stomatal conductance in warmer environments could affect both community composition and total primary productivity in future, warmer climates.


Assuntos
Clima , Cyperaceae/fisiologia , Estômatos de Plantas/fisiologia , Alaska , Regiões Árticas , Cyperaceae/citologia , Geografia , Estômatos de Plantas/citologia , Porosidade , Análise de Regressão , Estações do Ano , Temperatura
3.
Evolution ; 52(3): 678-691, 1998 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28565238

RESUMO

Because interactions among plants are spatially local, the scale of environmental heterogeneity can have large effects on evolutionary dynamics. However, very little is known about the spatial patterns of variation in fitness and the relative magnitude of spatial and temporal variation in selection. Replicates of 12 genotypes of Erigeron annuus (Asteraceae) were planted in 288 locations within a field, separated by distances of 0.1 to 30.0 m, and replicated in two years. In a given year, most spatial variation in relative fitness (genotype-environment [G × E] interactions for fitness) occurred over distances of only 50 cm. Year effects were as large or larger than the spatial variation in fitness; in particular there was a large, three-way, genotype-year-environment interaction at the smallest spatial scale. The genetic correlation of fitness across years at a given location was near zero, 0.03. Thus, the relative fitness of genotypes is spatially unpredictable and a map of the selective environment has constantly shifting locations of peaks and valleys. Including measurements of soil nutrients as covariates in the analysis removed most of the spatial G × E interaction. Vegetation and microtopography had no effect on the G × E terms, suggesting that differential response to soil nutrients is the cause of spatial variation in fitness. However, the slope of response to NH4 and P04 was negative; therefore the soil nutrients are probably just indicators of other, unknown, environmental factors. We explored via simulation the evolutionary consequences of spatial and temporal variation in fitness and showed that, for this system, the spatial scale of variation was too fine grained (by a factor of 3 to 5) to be a powerful force maintaining genetic variation in the population. The inclusion of both spatial and temporal variation in fitness actually reduced the coexistence of genotypes compared to pure spatial models. Thus the presence of spatial or temporal variation in selection does not guarantee that it is an effective evolutionary force maintaining diversity. Instead the pattern of selection favors generalist genotypes.

4.
Evolution ; 50(3): 1083-1097, 1996 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28565302

RESUMO

Population response to selection depends on the presence of additive genetic variance for traits under selection. When a population enters an alien environment, environment-induced changes in the expression of genetic variance may occur. These could have large effects on the response to selection. To investigate the environment-dependence of genetic variance, we conducted a reciprocal transplant experiment between two ecotypically differentiated populations of Impatiens pallida using the progeny of a standard mating design. The floodplain site was characterized by high water availability, moderate temperatures, and continuous dense stands of Impatiens. The hillside site was drier, with larger temperature extremes and supported only scattered patches of Impatiens with significantly lower seed production and earlier mortality. Estimates of heritability were low for each of the 13 traits measured in each population and site (range from 0-28%). Additive genetic variance for life-history traits tended to be larger than for morphological traits, but genetic variance in fitness was estimated to be not significantly different from zero in all cases. Significant heritability was detected in both populations for one trait (date of first cleistogamous flower) known to be closely related to fitness on the hillside. In general, heritability was reduced for populations when grown in the hillside site relative to the floodplain site, suggesting that stress acts to reduce the expression of genetic variance and the potential to respond to selection there. Consistent reductions in heritability associated with more stressful environments suggest that populations invading such sites may undergo little adaptive differentiation and be more prone to local extinction.

5.
Evolution ; 49(2): 317-324, 1995 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-28564999

RESUMO

Multiple-regression techniques for measuring phenotypic selection have been used in a large number of recent field studies. One benefit of this technique is its ability to discern the direct action of selection on traits by removing effects of correlated traits. However, covariation among traits expressed at different stages in an organism's life history is often poorly estimated because individuals that die before reaching adulthood cannot be measured as adults. Accurate estimates of trait covariances are necessary for the correct interpretation of the direct action of selection on a trait. If phenotypic characters expressed at different life-history stages are of interest, and mortality occurs between stages, the components of the selection model will be biased by not including those individuals that died (the "invisible fraction").

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