Beginning with Emlen (1966) and MacArthur and Pianka (1966) and extending through the last ten years, several authors have sought to predict the foraging behavior of animals by means of mathematical models. These models are very similar,in that they all assume that the fitness of a foraging animal is a function of the efficiency of foraging measured in terms of some "currency" (Schoener, 1971) -usually energy- and that natural selection has resulted in animals that forage so as to maximize this fitness. As a result of these similarities, the models have become known as "optimal foraging models"; and the theory that embodies them, "optimal foraging theory." The situations to which optimal foraging theory has been applied, with the exception of a few recent studies, can be divided into the following four categories: (1) choice by an animal of which food types to eat (i.e., optimal diet); (2) choice of which patch type to feed in (i.e., optimal patch choice); (3) optimal allocation of time to different patches; and (4) optimal patterns and speed of movements. In this review we discuss each of these categories separately, dealing with both the theoretical developments and the data that permit tests of the predictions. The review is selective in the sense that we emphasize studies that either develop testable predictions or that attempt to test predictions in a precise quantitative manner. We also discuss what we see to be some of the future developments in the area of optimal foraging theory and how this theory can be related to other areas of biology. Our general conclusion is that the simple models so far formulated are supported are supported reasonably well by available data and that we are optimistic about the value both now and in the future of optimal foraging theory. We argue, however, that these simple models will requre much modification, espicially to deal with situations that either cannot easily be put into one or another of the above four categories or entail currencies more complicated that just energy.

Citation classic - optimal foraging - a selective review of theory and tests

Reactive oxygen species

1. Introductory remarks 2. Convolvulacaea 2. Scrophulariaceae, Gesneriaceae, Labiatae, etc. 4. Cruciferae, Papaveraceae, Resedaceae, etc. 5. Geraniaceae, Leguminosae, Onagraceae, etc. 6. Solanaceae, Primulaceae, Polygoneae, etc. 7. Summary of the heights and weights of the crossed and self-fertilised plants 8. Difference between crossed and self-fertilised plants in constitutional vigour and in other respects 9. The effects of cross-fertilisation and self-fertilisation on the production of seeds 10. Means of fertilisation 11. The habits of insects in relation to the fertilisation of flowers 12. General results Index.

The Effects of Cross and Self Fertilisation in the Vegetable Kingdom: CONVOLVULACEÆ

Developmental Plasticity and Evolution. In: Mary Jane West-Eberhard, Editor, Oxford University Press (2003) Pp. xi+794. Price $50.00 paper.

Structural equation modeling , Structural equation modeling , کتابخانه دیجیتال جندی شاپور اهواز

Structural Equation Modeling

Intraspecific variation in stomatal traits, leaf traits and physiology reflects adaptation along aridity gradients in a South African shrub

 Premise of the study: The processes maintaining fl ower color polymorphisms have long been of evolutionary interest. Mechanistic explanations include selection through pollinators, antagonists, local environments, drift, and pleiotropic effects. We examined the maintenance of infl orescence color polymorphisms in the genus Protea (Proteaceae) of South Africa, in which ~40% of species contain different color morphs.  Methods: We studied 10 populations of four bird-pollinated Protea species and compared adult performance, fl oral and leaf morphology, vegetative pigmentation, germination, and seedling survival between co-occurring pink and white morphs. We also tested for differences in pollination success and pre-dispersal seed predation.  Key results: White morphs produced seeds 10% heavier and 3.5 times more likely to germinate, which all else being equal, should fuel positive selection on white. In one studied population per species, however, white morphs were more susceptible to seed predation by endophagous larvae. Pollinators had no morph-specifi c effects on female fecundity, as measured by amount or probability of seed set. Differences in stem color indicated that white morphs produced smaller quantities of pigment and associated compounds throughout, possibly explaining their higher seed palatability.  Conclusions: Our fi ndings suggest a mechanism for some white protea polymorphisms: deleterious pleiotropic effects on pink morphs are occasionally offset by reduced losses to seed-eating larvae. Because trends were repeated across species, we suggest that similar processes may also occur in other proteas, placing a new emphasis on seed predators for infl uencing some of South Africa ’ s amazing fl oral diversity.

Natural selection on inflorescence color polymorphisms in wild Protea populations: The role of pollinators, seed predators, and intertrait correlations

The evolution of secondary sexual floral traits may be driven by selection through male or female reproductive success. Even so, the gender-biased function of a floral trait is often unapparent because secondary sexual traits and primary sexual organs of both genders co-occur within most bisexual flowers. Within dichogamous plants, however, secondary sexual traits may be unambiguously expressed in association with the primary sexual organs of one gender, making these species uniquely suited to studies of natural and sexual selection on floral traits. The objectives of this article are to summarize patterns of gender-biased nectar production and to critically explore theories relevant to its evolution. We list 41 species with gender-biased nectar production and provide two sets of adaptive hypotheses for the trait: sexual selection hypotheses and inbreeding avoidance hypotheses. We formulate these hypotheses using sexual selection theory in plants and the literature that relates pollinator foraging to plant inbreeding. We also consider explanations based on resource trade-offs, enemies, and genetic correlations. Support for the sexual selection and inbreeding avoidance hypotheses is provided by only a few well-studied species. We outline a series of experiments that should facilitate sorting among hypotheses. Plants with gender-biased nectar production are likely to provide unique insights into the roles of natural and sexual selection in the evolution of floral traits.

The Evolution of Gender-Biased Nectar Production in Hermaphroditic Plants

Local adaptation along environmental gradients may drive plant species radiation within the Cape Floristic Region (CFR), yet few studies examine the role of ecologically based divergent selection within CFR clades. In this study, we ask whether populations within the monophyletic white protea clade (Protea section Exsertae, Proteaceae) differ in key functional traits along environmental gradients and whether differences are consistent with local adaptation. Using seven taxa, we measured trait–environment associations and selection gradients across 35 populations of wild adults and their offspring grown in two common gardens. Focal traits were leaf size and shape, specific leaf area (SLA), stomatal density, growth, and photosynthetic rate. Analyses on wild and common garden plants revealed heritable trait differences that were associated with gradients in rainfall seasonality, drought stress, cold stress, and less frequently, soil fertility. Divergent selection between gardens generally matched trait–environment correlations and literature-based predictions, yet variation in selection regimes among wild populations generally did not. Thus, selection via seedling survival may promote gradient-wide differences in SLA and leaf area more than does selection via adult fecundity. By focusing on the traits, life stages, and environmental clines that drive divergent selection, our study uniquely demonstrates adaptive differentiation among plant populations in the CFR.

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1558-5646.2010.01131.x

Plant responses to climate in the Cape Floristic Region of South Africa: evidence for adaptive differentiation in the Proteaceae.

The many documented examples of parallel and convergent evolution in similar environments are strong evidence for the role of natural selection in the evolution of trait variation. However, species may respond to selection in different ways; idiosyncrasies of their evolutionary history may affect how different species respond to the same selective pressure. To determine whether evolutionary history affects trait-environment associations in a recently diverged lineage, we investigated within-species trait-environment associations in the white proteas, a closely related monophyletic group. We first used manovas to determine the relative importance of shared response to selection, evolutionary history and unique responses to selection on trait variation. We found that on average, similar associations to the environment across species explained trait variation, but that the species had different mean trait values. We also detected species-specific associations of traits with the environmental gradients. To identify the traits associated uniquely with the environment, we used a structural equation model. Our analysis showed that the species differed in how their traits were associated with each of the environmental variables. Further, in the cases of two root traits (root mass and root length/mass ratio), two species differed in the direction of their associations (e.g. populations in one species had heavier roots in warmer areas, and populations in the other species had lighter roots in warmer areas). Our study shows that even in a closely related group of species, evolutionary history may have an effect on both the size and direction of adaptations to the environment.

/pdf/the-effect-of-historical-legacy-on-adaptation-do-closely-26ivr8hlss.pdf

Jane E. Carlson

Papers

Intraspecific variation in stomatal traits, leaf traits and physiology reflects adaptation along aridity gradients in a South African shrub

Natural selection on inflorescence color polymorphisms in wild Protea populations: The role of pollinators, seed predators, and intertrait correlations

The Evolution of Gender-Biased Nectar Production in Hermaphroditic Plants

Plant responses to climate in the Cape Floristic Region of South Africa: evidence for adaptive differentiation in the Proteaceae.

The effect of historical legacy on adaptation: do closely related species respond to the environment in the same way?