Perp. punya vol. X. Flowering plant, eudicots : sapindales, cucurbitales, myrtaceae. Perp.punya: 1eks.

The Families And Genera Of Vascular Plants

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

Bateman’s principle states that male fitness is usually limited by the number of matings achieved, while female fitness is usually limited by the resources available for reproduction. When applied to flowering plants this principle leads to the expectation that pollen limitation of fruit and seed set will be uncommon. However, if male searching for mates (including pollen dissemination via external agents) is not sufficiently successful, then the reproductive success of both sexes (or both sex functions in hermaphroditic plants) will be limited by number of matings rather than by resources, and Bateman’s principle cannot be expected to apply. Limitation of female success due to inadequate pollen receipt appears to be a common phenomenon in plants. Using published data on 258 species in which fecundity was reported for natural pollination and hand pollination with outcross pollen, I found significant pollen limitation at some times or in some sites in 159 of the 258 species (62%). When experiments were performed multiple times within a growing season, or in multiple sites or years, the statistical significance of pollen limitation commonly varied among times, sites or years, indicating that the pollination environment is not constant. There is some indication that, across species, supplemental pollen leads to increased fruit set more often than increased seed set within fruits, pointing to the importance of gamete packaging strategies in plant reproduction. Species that are highly self-incompatible obtain a greater benefit relative to natural pollination from artificial application of excess outcross pollen than do self-compatible species. This suggests that inadequate pollen receipt is a primary cause of low fecundity rates in perennial plants, which are often self-incompatible. Because flowering plants often allocate considerable resources to pollinator attraction, both export and receipt of pollen could be limited primarily by resource investment in floral advertisement and rewards. But whatever investment is made is attraction, pollinator behavioral stochasticity usually produces wide variation among flowers in reproductive success through both male and female functions. In such circumstances the optimal deployment of resources among megaspores, microspores, and pollinator attraction may often require more flowers or more ovules per flower than will usually be fertilized, in order to benefit from chance fluctuations that bring in large number of pollen grains. Maximizing seed set for the entire plant in a stochastic pollination environment might thus entail a packaging strategy for flower number or ovule number per flower that makes pollen limitation of fruit or seed set likely. Pollen availability may limit female success in individual flowers, entire plants (in a season or over a lifetime), or populations. The appropriate level must be distinguished depending on the nature of the question being addressed.

Bateman's principle and plant reproduction: The role of pollen limitation in fruit and seed set

https://www.agroparistech.fr/IMG/pdf/wilcocket_al.pdf

Pollination failure in plants: why it happens and when it matters.

Introduction. Ecologically Meaningful Germination Studies. Types of Seed Dormancy. Germination Ecology of Seeds with Nondeep Physiological Dormancy. Germination Ecology of Seeds with Morphophysiological Dormancy. Germination Ecology of Seeds with Physical Dormancy. Germination Ecology of Seeds in the Persistent Seed Bank. Causes of Within-Species Variations in Seed Dormancy and Germination Characteristics. A Geographical Perspective on Germination Ecology: Tropical and Subtropical Zones. A Geographical Perspective on Germination Ecology: Temperate and Arctic Zones. Germination Ecology of Plants with Specialized Life Cycles and/or Habitats. Biogeographical and Evolutionary Aspects of Seed Dormancy. Subject Index.

A Definitive Book on Seed Ecology@@@Seeds: Ecology, Biogeography, and Evolution of Dormancy and Germination

Sex Ratio and Reproductive Effort in the Dioecious Juniperus communis subsp. alpina (Suter) Čelak. (Cupressaceae) Along an Altitudinal Gradient

https://www.uibk.ac.at/botany/staff/publikationen/schoenswetter_peter/24.pdf

Range-wide phylogeography of Juniperus thurifera L., a presumptive keystone species of western Mediterranean vegetation during cold stages of the Pleistocene.

Temporal and spatial patterns of seed dispersal in two Cistus species (Cistaceae).

The ant-pollination system of Cytinus hypocistis (Cytinaceae), a Mediterranean root holoparasite.

• Chromosomal duplications and increases in DNA amount have the potential to alter quantitative plant traits like flower number, plant stature or stomata size. This has been documented often across species, but information on whether such effects also occur within species (i.e. at the microevolutionary or population scale) is scarce. • We studied trait covariation associated with polyploidy and genome size (both monoploid and total) in 22 populations of Dianthus broteri s.l., a perennial herb with several cytotypes (2x, 4x, 6x and 12x) that do not coexist spatially. Principal component scores of organ size/number variations were assessed as correlates of polyploidy, and phylogenetic relatedness among populations was controlled using phylogenetic generalized least squares. • Polyploidy covaried with organ dimensions, causing multivariate characters to increase, remain unchanged, or decrease with DNA amount. Variations in monoploid DNA amount had detectable consequences on some phenotypic traits. According to the analyses, some traits would experience phenotypic selection, while others would not. • We show that polyploidy contributes to decouple variation among traits in D. broteri, and hypothesize that polyploids may experience an evolutionary advantage in this plant lineage, for example, if it helps to overcome the constraints imposed by trait integration.

https://nph.onlinelibrary.wiley.com/doi/pdf/10.1111/j.1469-8137.2011.03787.x

Salvador Talavera

Papers

Sex Ratio and Reproductive Effort in the Dioecious Juniperus communis subsp. alpina (Suter) Čelak. (Cupressaceae) Along an Altitudinal Gradient

Range-wide phylogeography of Juniperus thurifera L., a presumptive keystone species of western Mediterranean vegetation during cold stages of the Pleistocene.

Temporal and spatial patterns of seed dispersal in two Cistus species (Cistaceae).

The ant-pollination system of Cytinus hypocistis (Cytinaceae), a Mediterranean root holoparasite.

Phenotypic consequences of polyploidy and genome size at the microevolutionary scale: a multivariate morphological approach