| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Spencer Charles Hilton Barrett | Q2426542 |
| Jannice Friedman | Q57718576 | ||
| P2860 | cites work | Why be an hermaphrodite? | Q59065574 |
| OVULE PACKAGING IN STOCHASTIC POLLINATION AND FERTILIZATION ENVIRONMENTS | Q60504260 | ||
| SEXUAL ALLOCATION STRATEGY IN WIND-POLLINATED PLANTS | Q60504267 | ||
| When looks can kill: the evolution of sexually dimorphic floral display and the extinction of dioecious plants | Q63379845 | ||
| Effects of distance and pollen competition on gene flow in the wind-pollinated grass Festuca pratensis Huds | Q73590991 | ||
| Pollination systems as isolating mechanisms in angiosperms | Q80306243 | ||
| Functional associations of floret and inflorescence traits among grass species | Q84286634 | ||
| VARIATION IN MALE REPRODUCTIVE INVESTMENT AND MALE REPRODUCTIVE SUCCESS IN WHITE SPRUCE | Q88197016 | ||
| THE EVOLUTION OF SELF-FERTILIZATION AND INBREEDING DEPRESSION IN PLANTS. II. EMPIRICAL OBSERVATIONS | Q88197405 | ||
| THE AERODYNAMICS OF POLLEN CAPTURE IN TWO SYMPATRIC EPHEDRA SPECIES | Q88197651 | ||
| SEX ALLOCATION AND OUTCROSSING RATE: A TEST OF THEORETICAL PREDICTIONS USING BROMEGRASSES (BROMUS) | Q88197770 | ||
| MODE OF POLLINATION AND FLORAL SEXUALITY IN THALICTRUM | Q88199797 | ||
| POLLEN-OVULE RATIOS: A CONSERVATIVE INDICATOR OF BREEDING SYSTEMS IN FLOWERING PLANTS | Q88205781 | ||
| INCIDENCE OF MONOECY AND DICHOGAMY IN RELATION TO SELF-FERTILIZATION IN ANGIOSPERMS | Q91110156 | ||
| The distribution of plant mating systems: study bias against obligately outcrossing species | Q22065121 | ||
| The consequences of monoecy and protogyny for mating in wind-pollinated Carex | Q28305671 | ||
| Generalization in Pollination Systems, and Why it Matters | Q29010939 | ||
| Abiotic pollen and pollination: Ecological, functional, and evolutionary perspectives | Q30048054 | ||
| Contrasting flowering phenology and species richness in abiotically and biotically pollinated angiosperms | Q31016367 | ||
| Pollen limitation causes an Allee effect in a wind-pollinated invasive grass (Spartina alterniflora). | Q34342042 | ||
| Environmental influence on primary sex ratio in a dioecious plant | Q36825394 | ||
| Intrapopulation gender variation in common ragweed (Asteraceae: Ambrosia artemisiifolia L.), a monoecious, annual herb | Q39238000 | ||
| Phylogenetic analysis of the ecological correlates of dioecy in angiosperms | Q39546911 | ||
| Wind pollination and reproductive assurance in Linanthus parviflorus (Polemoniaceae), a self-incompatible annual | Q42605685 | ||
| Pollen movement in declining populations of California Valley oak, Quercus lobata: where have all the fathers gone? | Q45975708 | ||
| Pollen-limited reproduction in blue oak: implications for wind pollination in fragmented populations. | Q46037533 | ||
| Predicting the pathway to wind pollination: heritabilities and genetic correlations of inflorescence traits associated with wind pollination in Schiedea salicaria (Caryophyllaceae). | Q46155821 | ||
| Dioecy and the evolution of pollination systems inSchiedea and Alsinidendron (Caryophyllaceae:Alsinoideae) in the Hawaiian Islands | Q46242969 | ||
| Anemophilous plants select pollen from their own species from the air. | Q46452176 | ||
| Regional variation in sex ratios and sex allocation in androdioecious Mercurialis annua. | Q46662482 | ||
| Size-dependent variation of gender in high density stands of the monoecious annual, Ambrosia artemisiifolia (Asteraceae). | Q47447865 | ||
| Allometric gender allocation in Ambrosia Artemisiifolia (Asteraceae) has adaptive plasticity. | Q51165311 | ||
| Floral sex ratio strategy in wind-pollinated monoecious species subject to wind-pollination efficiency and competitive sharing among male flowers as a game. | Q51836046 | ||
| Pollen limitation of reproductive success in two sympatric alpine willows (Salicaceae) with contrasting pollination strategies. | Q52588982 | ||
| Pollen limitation of reproductive effort in willows. | Q52866009 | ||
| Size-dependent ESS sex allocation in wind-pollinated cosexual plants: fecundity vs. stature effects | Q52951037 | ||
| Reproductive biology of two dominant prairie grasses (Andropogon gerardii and Sorghastrum nutans, Poaceae): male-biased sex allocation in wind-pollinated plants? | Q53085635 | ||
| Evolution of Dioecy in Flowering Plants | Q54226155 | ||
| INFLUENCE OF ENVIRONMENT ON THE FLORAL SEX RATIO OF MONOECIOUS PLANTS. | Q54520961 | ||
| THE INFLUENCE OF WIND AND ANIMAL POLLINATION ON VARIATION IN OUTCROSSING RATES. | Q54753709 | ||
| Dioecy and Its Correlates in the Flowering Plants | Q55872070 | ||
| Pollination Syndromes and Floral Specialization | Q55890323 | ||
| Wind Pollination in the Angiosperms: Evolutionary and Environmental Considerations | Q55891989 | ||
| Inflorescence architecture and wind pollination in six grass species | Q56047515 | ||
| The Evolutionary Enigma of Mixed Mating Systems in Plants: Occurrence, Theoretical Explanations, and Empirical Evidence | Q56082823 | ||
| The evolution of wind pollination in angiosperms | Q56171569 | ||
| THE DISTRIBUTION OF PLANT MATING SYSTEMS: STUDY BIAS AGAINST OBLIGATELY OUTCROSSING SPECIES | Q56454471 | ||
| SEX AMONG THE FLOWERS: THE DISTRIBUTION OF PLANT MATING SYSTEMS | Q56601077 | ||
| Pollinators of Tropical Dioecious Angiosperms: A Reassessment? No, not yet | Q56913505 | ||
| Pollinators of Tropical Dioecious Angiosperms | Q56913515 | ||
| POLLEN LIMITATION OF PLANT REPRODUCTION: ECOLOGICAL AND EVOLUTIONARY CAUSES AND CONSEQUENCES | Q57045405 | ||
| Is pollen limited? The answer is blowin' in the wind | Q57233989 | ||
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | pollination | Q134624 |
| P1104 | number of pages | 13 | |
| P304 | page(s) | 1515-1527 | |
| P577 | publication date | 2009-02-14 | |
| P1433 | published in | Annals of Botany | Q1821243 |
| P1476 | title | Wind of change: new insights on the ecology and evolution of pollination and mating in wind-pollinated plants | |
| P478 | volume | 103 |
| Q34308210 | A DNA barcoding approach to characterize pollen collected by honeybees |
| Q111629568 | Airborne conifer pollen grains are rarely deposited on stigmas of coflowering insect‐pollinated angiosperms |
| Q56451949 | Alien grass disrupts reproduction and post-settlement recruitment of co-occurring native vegetation: a mechanism for diversity decline in invaded forest? |
| Q116816780 | An insect‐pollinated species in a wind‐pollinated genus: case study of the endemic plant, Laramie chickensage Artemisia simplex |
| Q92430000 | An overview on pollination of the Neotropical Poales |
| Q57001813 | Combined effects of climate and management on plant diversity and pollination type in alpine grasslands |
| Q111629643 | Combined genotype and phenotype analyses reveal patterns of genomic adaptation to local environments in the subtropical oak Quercus acutissima |
| Q27021370 | Constraints imposed by pollinator behaviour on the ecology and evolution of plant mating systems |
| Q46746964 | Convergent and correlated evolution of major life-history traits in the angiosperm genus Leucadendron (Proteaceae). |
| Q33726254 | Darwin's legacy: the forms, function and sexual diversity of flowers |
| Q56530265 | Detecting the provenance of Galápagos non-native pollen: The role of humans and air currents as transport mechanisms |
| Q35163063 | Dioecy is associated with higher diversification rates in flowering plants |
| Q36828714 | Directional genetic differentiation and relative migration. |
| Q46902046 | Distinct male reproductive strategies in two closely related oak species |
| Q92963764 | Divergent selection on the biomechanical properties of stamens under wind and insect pollination |
| Q39266660 | Drivers of tree fecundity in pedunculate oak (Quercus robur) refugial populations at the species' southwestern range margin. |
| Q28709610 | Ecological importance of sedges: a survey of the Australasian Cyperaceae genus Lepidosperma |
| Q37241077 | Ecology and evolution of plant-pollinator interactions |
| Q92430507 | Editorial sobre os estudos de Ecologia Funcional da Polinização |
| Q46820132 | Effects of tree architecture on pollen dispersal and mating patterns in Abies pinsapo Boiss. (Pinaceae). |
| Q46332532 | Exploring the potential of gametic reconstruction of parental genotypes by F1 hybrids as a bridge for rapid introgression. |
| Q36109303 | Facultative apomixis and development of fruit in a deciduous shrub with medicinal and nutritional uses |
| Q37069069 | Fertilization Mechanisms in Flowering Plants |
| Q58249925 | First flowering of wind-pollinated species with the greatest phenological advances in Europe |
| Q33726260 | Floral adaptation and diversification under pollen limitation |
| Q58319955 | Floral and environmental gradients on a Late Cretaceous landscape |
| Q46635660 | Floral trait evolution associated with shifts between insect and wind pollination in the dioecious genus Leucadendron (Proteaceae). |
| Q52738323 | Flowering dynamics and pollination system of the sedge Rhynchospora ciliata (Vahl) Kükenth (Cyperaceae): does ambophily enhance its reproductive success? |
| Q48702042 | Functional pleiotropy and mating system evolution in plants: frequency-independent mating |
| Q34344379 | Gender-specific costs of reproduction on vegetative growth and physiological performance in the dioecious shrub Corema album |
| Q35765038 | Genetic architecture of pollination syndrome transition between hummingbird-specialist and generalist species in the genus Rhytidophyllum (Gesneriaceae) |
| Q36371753 | Genetic differentiation for size at first reproduction through male versus female functions in the widespread Mediterranean tree Pinus pinaster |
| Q52725896 | Gone with the wind: understanding evolutionary transitions between wind and animal pollination in the angiosperms. |
| Q60357882 | How do habitat and climate variation affect phenology of the Amazonian palm, Mauritia flexuosa? |
| Q30573812 | How fragmentation and corridors affect wind dynamics and seed dispersal in open habitats |
| Q100711053 | Insects facilitate wind pollination in pollen-limited Crateva adansonii (Capparaceae) |
| Q37592573 | Intensified wind pollination mediated by pollen dimorphism after range expansion in an ambophilous biennial Aconitum gymnandrum |
| Q46919365 | Interspecific variation in pollen-ovule ratio is negatively correlated with pollen transfer efficiency in a natural community |
| Q56435544 | Invasive conifers reduce seed set of a native Andean cedar through heterospecific pollination competition |
| Q28076111 | Kin selection and the evolution of plant reproductive traits |
| Q104581389 | Landscape Genetics of Plants: Challenges and Opportunities |
| Q35428803 | Metapopulation structure and fine-scaled genetic structuring in crop-wild hybrid weed beets |
| Q44625864 | Neither insects nor wind: ambophily in dioecious Chamaedorea palms (Arecaceae). |
| Q58652480 | On the Relationship between Pollen Size and Genome Size |
| Q48276098 | Opportunities for unlocking the potential of genomics for African trees |
| Q57013756 | Past climate-driven range shifts and population genetic diversity in arctic plants |
| Q51434723 | Phylogenetic insights into the correlates of dioecy in meadow-rues (Thalictrum, Ranunculaceae). |
| Q46301220 | Plant reproductive ecology and evolution in the Mediterranean islands: state of the art. |
| Q39888342 | Pollen dispersal and breeding structure in a hawkmoth-pollinated Pampa grasslands species Petunia axillaris (Solanaceae). |
| Q38858045 | Pollen limitation may be a common Allee effect in marine hydrophilous plants: implications for decline and recovery in seagrasses. |
| Q46192841 | Pollen tube development in two species of Trithuria (Hydatellaceae) with contrasting breeding systems. |
| Q111629204 | Production of male flowers does not decrease with plant size in insect-pollinated Sagittaria trifolia, contrary to predictions of size-dependent sex allocation |
| Q46185249 | Rarity and persistence. |
| Q46424912 | Reproductive biology and pollination ecology of Triplaris gardneriana (Polygonaceae): a case of ambophily in the Brazilian Chaco |
| Q56744640 | Reproductive biology of Australian acacias: important mediator of invasiveness? |
| Q28748189 | Reproductive ecology of the basal angiosperm Trithuria submersa (Hydatellaceae) |
| Q38216823 | Resource depletion, pollen coupling, and the ecology of mast seeding. |
| Q90569083 | Scent matters: differential contribution of scent to insect response in flowers with insect vs. wind pollination traits |
| Q58696752 | Selection Signatures Underlying Dramatic Male Inflorescence Transformation During Modern Hybrid Maize Breeding |
| Q39106708 | Self- and intra-morph incompatibility and selection analysis of an inconspicuous distylous herb growing on the Tibetan plateau (Primula tibetica). |
| Q33968266 | Sex-differential herbivory in androdioecious Mercurialis annua |
| Q33789105 | Sex-specific floral morphology, biomass, and phytohormones associated with altitude in dioecious Populus cathayana populations |
| Q34829770 | Sexual dimorphism in a dioecious population of the wind-pollinated herb Mercurialis annua: the interactive effects of resource availability and competition |
| Q111629851 | Sexual dimorphism, temporal niche differentiation, and evidence for the Jack Sprat effect in an annual dioecious plant |
| Q47548589 | Size advantage for male function and size-dependent sex allocation in Ambrosia artemisiifolia, a wind-pollinated plant. |
| Q104486480 | Small-scale alpine topography at low latitudes and high altitudes: refuge areas of the genus Chrysanthemum and its allies |
| Q98735716 | Spatial Patterns and Drivers of Angiosperm Sexual Systems in China Differ Between Woody and Herbaceous Species |
| Q57233939 | Stabilizing selection for within-season flowering phenology confirms pollen limitation in a wind-pollinated tree |
| Q100712415 | Synchronous monoecy in Ecdeiocoleaceae (Poales), in Western Australia |
| Q95277374 | The 'Male Flower' of Ricinus communis (Euphorbiaceae) Interpreted as a Multi-Flowered Unit |
| Q57229370 | The efficacy of wind pollination in a small understory shrub (Coprosma spathulata) in native forest of the Waikato region, New Zealand |
| Q27022414 | The evolution of plant reproductive systems: how often are transitions irreversible? |
| Q58821178 | The geometry of gender: hyper-diversification of sexual systems in Urtica L. (Urticaceae) |
| Q36622138 | The incidence and selection of multiple mating in plants |
| Q34513872 | The interplay between inflorescence development and function as the crucible of architectural diversity |
| Q90166017 | The maintenance of stable yield and high genetic diversity in the agricultural heritage torreya tree system |
| Q38958899 | The role of pollen limitation on the coexistence of two dioecious, wind-pollinated, closely related shrubs in a fluctuating environment |
| Q35598724 | Three new, early diverging Carex (Cariceae, Cyperaceae) lineages from East and Southeast Asia with important evolutionary and biogeographic implications |
| Q35553177 | Trait-based analysis of decline in plant species ranges during the 20th century: a regional comparison between the UK and Estonia |
| Q46614741 | Transition from wind pollination to insect pollination in sedges: experimental evidence and functional traits. |
| Q27346400 | Turbulence-induced resonance vibrations cause pollen release in wind-pollinated Plantago lanceolata L. (Plantaginaceae) |
| Q33743106 | Understanding plant reproductive diversity |
| Q91771673 | Variation in sexual dimorphism in a wind-pollinated plant: the influence of geographical context and life-cycle dynamics |
| Q50419864 | Why are the seed cones of conifers so diverse at pollination? |
| Q46317302 | You'd better walk alone: Changes in forest composition affect pollination efficiency and pre-dispersal cone damage in Iberian Juniperus thurifera forests |
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