The geography of demography: long-term demographic studies and species distribution models reveal a species border limited by adaptation.

Potential causes of species' geographic distribution limits fall into two broad classes: (1) limited adaptation across spatially variable environments and (2) limited opportunities to colonize unoccupied areas. Combining demographic studies, analyses of demographic responses to environmental variation, and species distribution models, we investigated the causes of range limits in a model system, the eastern border of the California annual plant Clarkia xantiana ssp. xantiana. Vital rates of 20 populations varied with growing season temperature and precipitation: fruit number and overwinter survival of 1-year-old seeds declined steeply, while current-year seed germination increased modestly along west-to-east gradients in decreasing temperature, decreasing mean precipitation, and increasing variation in precipitation. Long-term stochastic finite rate of increase, λ(s), exhibited a fourfold range and varied among geologic surface materials as well as with temperature and precipitation. Growth rate declined significantly toward the eastern border, falling below 1 in three of the five easternmost populations. Distribution models employing demographically important environmental variables predicted low habitat favorability beyond the eastern border. Models that filtered or weighted population presences by λ(s) predicted steeper eastward declines in favorability and assigned greater roles in setting the distribution to among-year variation in precipitation and to geologic surface material. These analyses reveal a species border likely set by limited adaptation to declining environmental quality.

Growth form evolution and shifting habitat specialization in annual plants.

Optimal plant growth form should vary across environments. We examined the potential for mutations causing large changes in growth form to produce new optimal phenotypes across light environments. We predicted that the upright growth form would be favoured in a light limiting environment as leaves were in a position to maximize light interception, while a rosette (leaves in a basal position) growth form would be favoured in a high light environment. Growth form genotypes of Brassica rapa (upright wild-type and rosette mutants) and Arabidopsis thaliana (large rosette wild-type and increasingly upright growth form mutants) were grown in a greenhouse in control (ambient) and filtered (low) light treatments. Compared to upright genotypes, rosette genotypes had relatively high fitness in control light but had a relatively large fitness reduction in filtered light. Our results demonstrate the potential importance of rapid growth form evolution in plant adaptation to new or changing environments.

Reproductive assurance and the evolutionary ecology of self-pollination in Clarkia xantiana (Onagraceae).

The reproductive assurance hypothesis posits that selection favors self-pollination in flowering plants where mates and/or pollinators are scarce. A corollary is that self-pollinating populations are expected to be superior colonizers of mate- and pollinator-scarce environments. The California annual Clarkia xantiana includes outcrossing populations (ssp. xantiana) and autogamously self-pollinating populations (ssp. parviflora). Outcrossing is ancestral, and the subspecies have parapatric distributions with a narrow contact zone. We tested aspects of the reproductive assurance hypothesis by examining geographic and subspecies variation in the densities of mates and pollinators (native bees) and the density dependence of pollinator visitation and pollen receipt. Plant and flower densities, pollinator density, and pollinator visitation rates were lowest in the region of exclusively self-pollinating populations. Pollinator assemblages there lacked Clarkia-associated pollinator taxa that were common elsewhere. Self-pollinating populations in the contact zone generally had densities and visitation rates intermediate between allopatric self-pollinating populations and outcrossing populations. Visitation rate and pollen receipt increased significantly with plant density. These findings suggest that selection for reproductive assurance influenced the origin of self-pollination and/or that reproductive assurance influenced the geographic distribution of self-pollination. Geographic variation in pollinator assemblages may have generated variation in the value of reproductive assurance.

Evolution of the self-pollinating flower in Clarkia xantiana (Onagraceae). I. Size and development of floral organs.

Clarkia xantiana has two subspecies that differ in breeding system: ssp. xantiana, which is outcrossing, and ssp. parviflora, which is self-fertilizing. Outcrossing is the ancestral breeding system for the genus Clarkia. Flowers of ssp. parviflora have characteristics commonly associated with selfing taxa: they are smaller and have little temporal and spatial separation between mature anthers and stigma (dichogamy and herkogamy, respectively). Flower morphology and development were studied in four populations of each subspecies to establish the developmental changes that occurred in the evolution of selfing. In particular, we sought to evaluate the hypothesis that the selfing flower may have arisen as a byproduct of selection for rapid maturation in the arid environment occupied by ssp. parviflora. This hypothesis predicts that development time should be reduced in spp. parviflora relative to ssp. xantiana. We also sought to compare the pattern of covariation of flower morphology and development between subspecies to that within subspecies. Similar within vs. between patterns of covariation could be indicative of developmental or functional constraints on the independent evolution of floral parts. In spite of significant variation among populations within subspecies, the subspecies clearly differ in flower morphology and development. All floral organs, except ovaries, are smaller in ssp. parviflora than in ssp. xantiana. The flower plastochron, the duration of flower development from bud initiation to anthesis, and the duration of protandry are all shorter in ssp. parviflora than in ssp. xantiana. Maximum relative growth rates are higher for all organs in ssp. parviflora than in ssp. xantiana. Thus, progenesis (i.e., via a reduction in development time) is combined with growth acceleration in the evolution of the selfing flower. Since reduced development time and growth acceleration both allow selfing flowers to mature earlier than outcrossing ones, selection for early maturation may have contributed to the evolution of the selfing flower form. The pattern of trait covariation differs within spp. parviflora relative to the patterns within spp. xantiana and between the two subspecies, suggesting that floral parts can and have evolved independently of one another.

Variation among populations of Clarkia Unguiculata (Onagraceae) along altitudinal and latitudinal gradients.

We investigated phenotypic variation in 15 traits in greenhouse-grown plants from 16 populations of Clarkia unguiculata from three elevational habitats and six latitudinal transects. Populations from the lowest and highest elevations were geographically and ecologically marginal within the species' range. We (1) describe patterns of trait variation with elevation and latitude; (2) compare latitutidinal variation between marginal and central areas of the species' range; and (3) compare patterns of variation within C. unguiculata to interspecific patterns within the genus. Although there was some evidence that traits varied clinally (i.e., increased/decreased monotonically) along environmental gradients, interaction effects between altitude and latitude dominated patterns of variation. For most traits, latitudinal trends at the low-elevation margin of the species' range differed from trends at mid- and high-elevation areas. Based on interspecific comparisons, populations at the hotter, more arid ends of both environmental gradients were expected to have rapid development, small flowers and vegetative size, low levels of herkogamy and protandry, and high rates of gas exchange. Instead, we found that while some traits were correlated with one gradient in the expected way (e.g., development time with elevation, gas-exchange physiology with latitude), all traits were not consistently associated with each other along both gradients, and intraspecific patterns of variation differed from interspecific patterns.

Genetic variation in stomatal and biochemical limitations to photosynthesis in the annual plant, Polygonum arenastrum.

Terrestrial plant photosynthesis may be limited both by stomatal behavior and leaf biochemical capacity. While inferences have been made about the importance of stomatal and biochemical limitations to photosynthesis in a variety of species in a range of environments, genetic variation in these limitations has never been documented in wild plant populations. Genetic variation provides the raw material for adaptive evolution in rates of carbon assimilation. We examined genetic variation in gas exchange physiology and in stomatal and biochemical traits in 16 genetic lines of the annual plant, Polygonum arenastrum. The photosynthesis against leaf internal CO2 (A-ci) response curve was measured on three greenhouse-grown individuals per line. We measured the photosynthetic rate (A) and stomatal conductance (g), and calculated the internal CO2 concentration (ci) at ambient CO2 levels. In addition, the following stomatal and biochemical characteristics were obtained from the A-ci curve on each individual: the degree of stomatal limitation to photosynthesis (Ls), the maximum ribulose 1,5-biphosphate carboxylase-oxygenase (Rubisco) activity (Vcmax) and electron transport capacity (Jmax). All physiological traits were genetically variable, with broad sense heritabilities ranging from 0.66 for Ls to 0.94 for Jmax. Strong positive genetic correlations were found between Vcmax and Jmax, and between g and biochemical capacity. Path analyses revealed strong causal influences of stomatal conductance and leaf biochemistry on A and ci. Path analysis also indicated that Ls confounds both stomatal and biochemical effects, and is an appropriate measure of stomatal influences on photosynthesis, only when biochemical variation is accounted for. In total, our results indicate that differences among lines in photosynthesis and ci result from simultaneous changes in biochemical and stomatal characteristics and are consistent with theoretical predictions that there should be co-limitation of photosynthesis by ribulose-1,5-biphosphate (RuBP) utilization and regeneration, and by stomatal conductance and leaf biochemistry. Gas exchange characteristics of genetic lines in the present study were generally consistent with measurements of the same lines in a previous field study. Our new results indicate that the mechanisms underlying variation in gas exchange include variation in both stomatal conductance and biochemical capacity. In addition, A, g, and ci in the present study tended also to be positively correlated with carbon isotope discrimination (Δ), and negatively correlated with time to flowering, life span, and leaf size based on earlier work. The pattern of correlation between physiology and life span among genetic lines of P. arenastrum parallels interspecific patterns of character correlations. We suggest that the range of trait constellations among lines in P. arenastrum represents a continuum between stress avoidance (rapid development, high gas exchange metabolism) and stress tolerance (slow development, low gas exchange metabolism), and that genetic variation in these character combinations may be maintained by environmental variation in stress levels in the species' ruderal habitat.