human | Q5 |
P856 | official website | https://www.biology.pitt.edu/person/tia-lynn-ashman |
P496 | ORCID iD | 0000-0002-9884-5954 |
P108 | employer | University of Pittsburgh | Q235034 |
P106 | occupation | researcher | Q1650915 |
Q46657295 | A first test of elemental allelopathy via heterospecific pollen receipt |
Q33822618 | A phylogenetically controlled analysis of the roles of reproductive traits in plant invasions |
Q33352358 | A piece of the puzzle: a method for comparing pollination quality and quantity across multiple species and reproductive events |
Q37885571 | A quantitative synthesis of pollen supplementation experiments highlights the contribution of resource reallocation to estimates of pollen limitation |
Q37941231 | About PAR: the distinct evolutionary dynamics of the pseudoautosomal region |
Q51305024 | An altitudinal cline in UV floral pattern corresponds with a behavioral change of a generalist pollinator assemblage. |
Q51743075 | An experimental test of the effects of resources and sex ratio on maternal fitness and phenotypic selection in gynodioecious Fragaria virginiana. |
Q46708397 | Apparent vs. effective mating in an experimental population of Raphanus sativus |
Q52722076 | Are flower-visiting ants mutualists or antagonists? A study in a gynodioecious wild strawberry. |
Q91265556 | Autopolyploidy alters nodule-level interactions in the legume-rhizobium mutualism |
Q48039889 | Bioclimatic, ecological, and phenotypic intermediacy and high genetic admixture in a natural hybrid of octoploid strawberries |
Q56552659 | CONSTRAINTS ON THE EVOLUTION OF MALES AND SEXUAL DIMORPHISM: FIELD ESTIMATES OF GENETIC ARCHITECTURE OF REPRODUCTIVE TRAITS IN THREE POPULATIONS OF GYNODIOECIOUS FRAGARIA VIRGINIANA |
Q114092767 | Chromosome-scale assembly with a phased sex-determining region resolves features of early Z and W chromosome differentiation in a wild octoploid strawberry |
Q46941209 | Coflowering community context influences female fitness and alters the adaptive value of flower longevity in Mimulus guttatus |
Q37106167 | Community-wide assessment of pollen limitation in hummingbird-pollinated plants of a tropical montane rain forest |
Q34387004 | Comparative genetic mapping points to different sex chromosomes in sibling species of wild strawberry (Fragaria) |
Q51567572 | Comparative mapping reveals autosomal origin of sex chromosome in octoploid Fragaria virginiana. |
Q41067198 | Comparison of nuclear, plastid, and mitochondrial phylogenies and the origin of wild octoploid strawberry species |
Q56654701 | Consequences of invasion for pollen transfer and pollination revealed in a tropical island ecosystem |
Q50794393 | Consequences of vegetative herbivory for maintenance of intermediate outcrossing in an annual plant. |
Q36408720 | Considering the unintentional consequences of pollinator gardens for urban native plants: is the road to extinction paved with good intentions? |
Q115059399 | Damage and recovery from drift of synthetic-auxin herbicide dicamba depends on concentration and varies among floral, vegetative, and lifetime traits in rapid cycling Brassica rapa |
Q60178623 | Delimiting plant diversity that is functionally related via interactions with diurnal pollinators: An expanded use of rarefaction curves |
Q34497994 | Dioecy does not consistently accelerate or slow lineage diversification across multiple genera of angiosperms |
Q51757295 | Direct and indirect effects of a sex-biased antagonist on male and female fertility: consequences for reproductive trait evolution in a gender-dimorphic plant. |
Q112834750 | Diversity and composition of pollen loads carried by pollinators are primarily driven by insect traits, not floral community characteristics |
Q44645566 | Edaphic factors and plant-insect interactions: direct and indirect effects of serpentine soil on florivores and pollinators |
Q41200196 | Effects of floral metal accumulation on floral visitor communities: introducing the elemental filter hypothesis |
Q88811828 | Effects of heterospecific pollen from a wind-pollinated and pesticide-treated plant on reproductive success of an insect-pollinated species |
Q125407462 | Evaluating the influences of floral traits and pollinator generalism on α and β diversity of heterospecific pollen on stigmas |
Q28597795 | Evolutionary origins and dynamics of octoploid strawberry subgenomes revealed by dense targeted capture linkage maps |
Q51194022 | Explaining phenotypic selection on plant attractive characters: male function, gender balance or ecological context? |
Q90831546 | Floral organs act as environmental filters and interact with pollinators to structure the yellow monkeyflower (Mimulus guttatus) floral microbiome |
Q36035433 | Floral pigmentation patterns provide an example of Gloger's rule in plants |
Q115409052 | Flower colour and flowering phenology mediate plant–pollinator interaction assembly in a diverse co‐flowering community |
Q59082895 | Flower lifespan and disease risk |
Q51691113 | Flower morphology and pollinator dynamics in Solanum carolinense (Solanaceae): implications for the evolution of andromonoecy. |
Q34444084 | Fragaria: a genus with deep historical roots and ripe for evolutionary and ecological insights |
Q35753316 | Functional characterization of gynodioecy in Fragaria vesca ssp. bracteata (Rosaceae). |
Q57040210 | Functional trait divergence and trait plasticity confer polyploid advantage in heterogeneous environments |
Q92816579 | Gazing into the anthosphere: considering how microbes influence floral evolution |
Q45070200 | Genetic Mapping and Phylogenetic Analysis Reveal Intraspecific Variation in Sex Chromosomes of the Virginian Strawberry |
Q47344958 | Genetic architecture of sexual dimorphism in a subdioecious plant with a proto-sex chromosome |
Q91303884 | Genome duplication effects on functional traits and fitness are genetic context and species dependent: studies of synthetic polyploid Fragaria |
Q35753281 | Gynodioecy to dioecy: are we there yet? |
Q111629914 | Herbicides and their potential to disrupt plant‐insect chemical communication |
Q96434027 | Herbicides as anthropogenic drivers of eco-evo feedbacks in plant communities at the agro-ecological interface |
Q57137948 | Herbivory and competition interact to affect reproductive traits and mating system expression in Impatiens capensis |
Q33967240 | Heterospecific pollen deposition: does diversity alter the consequences? |
Q56379726 | Higher ploidy is associated with reduced range breadth in the Potentilleae tribe |
Q37357474 | Homomorphic ZW chromosomes in a wild strawberry show distinctive recombination heterogeneity but a small sex-determining region |
Q59085398 | How long should flowers live? |
Q51310500 | Insights into phylogeny, sex function and age of Fragaria based on whole chloroplast genome sequencing. |
Q125554878 | Integration of historic collections can shed light on patterns of change in plant–pollinator interactions and pollination service |
Q92405593 | Interactive effects between donor and recipient species mediate fitness costs of heterospecific pollen receipt in a co-flowering community |
Q125555041 | Interspecific variation in resistance and tolerance to herbicide drift reveals potential consequences for plant community co-flowering interactions and structure at the agro-eco interface |
Q56390925 | Invasion status and phylogenetic relatedness predict cost of heterospecific pollen receipt: implications for native biodiversity decline |
Q95642757 | Is heterospecific pollen receipt the missing link in understanding pollen limitation of plant reproduction? |
Q60178629 | Is reproduction of endemic plant species particularly pollen limited in biodiversity hotspots? |
Q98302840 | Land use and pollinator dependency drives global patterns of pollen limitation in the Anthropocene |
Q46578296 | Macroevolutionary patterns of ultraviolet floral pigmentation explained by geography and associated bioclimatic factors. |
Q38770777 | Macroevolutionary synthesis of flowering plant sexual systems |
Q37032003 | Maternal sex effects and inbreeding depression under varied environmental conditions in gynodioecious Fragaria vesca subsp. bracteata |
Q35107477 | Meta-analysis of pollen limitation reveals the relevance of pollination generalization in the Atlantic forest of Brazil |
Q36383157 | Multilocus Sex Determination Revealed in Two Populations of Gynodioecious Wild Strawberry, Fragaria vesca subsp. bracteata |
Q51473231 | Nickel accumulation by Streptanthus polygaloides (Brassicaceae) reduces floral visitation rate. |
Q34004250 | Nickel accumulation in leaves, floral organs and rewards varies by serpentine soil affinity |
Q50743891 | Ovule number per flower in a world of unpredictable pollination. |
Q57045405 | POLLEN LIMITATION OF PLANT REPRODUCTION: ECOLOGICAL AND EVOLUTIONARY CAUSES AND CONSEQUENCES |
Q35823399 | Patterns of among- and within-species variation in heterospecific pollen receipt: The importance of ecological generalization |
Q92214378 | Plant traits moderate pollen limitation of introduced and native plants: a phylogenetic meta-analysis of global scale |
Q57045392 | Pollen Limitation of Plant Reproduction: Pattern and Process |
Q111171250 | Pollen transfer networks reveal alien species as main heterospecific pollen donors with fitness consequences for natives |
Q28768621 | Pollination decays in biodiversity hotspots |
Q112811884 | Pollinators contribute to the maintenance of flowering plant diversity |
Q115389533 | Pollinators mediate floral microbial diversity and microbial network under agrochemical disturbance |
Q91573773 | Polyploid plants obtain greater fitness benefits from a nutrient acquisition mutualism |
Q39648451 | Polyploidy and sexual system in angiosperms: Is there an association? |
Q42587513 | Present-day sympatry belies the evolutionary origin of a high-order polyploid |
Q56431773 | Quantitative Variation, Heritability, and Trait Correlations for Ultraviolet Floral Traits in Argentina anserina (Rosaceae): Implications for Floral Evolution |
Q58700493 | Repeated translocation of a gene cassette drives sex-chromosome turnover in strawberries |
Q30275567 | Reproductive character displacement and environmental filtering shape floral variation between sympatric sister taxa |
Q21092698 | Sex determination: why so many ways of doing it? |
Q51499954 | Sex ratio and subdioecy in Fragaria virginiana: the roles of plasticity and gene flow examined. |
Q43185612 | Sources of floral scent variation: can environment define floral scent phenotype? |
Q112840273 | Spatially explicit depiction of a floral epiphytic bacterial community reveals role for environmental filtering within petals |
Q46245385 | THE RELATIVE IMPORTANCE OF INBREEDING AND MATERNAL SEX IN DETERMINING PROGENY FITNESS IN SIDALCEA OREGANA SSP. SPICATA, A GYNODIOECIOUS PLANT. |
Q92348862 | TRY plant trait database - enhanced coverage and open access |
Q37079532 | Targeted sequence capture provides insight into genome structure and genetics of male sterility in a gynodioecious diploid strawberry, Fragaria vesca ssp. bracteata (Rosaceae). |
Q128235099 | The Plant Science Blogging Project: A curriculum to develop student science communication skills |
Q47813721 | The direct effects of plant polyploidy on the legume-rhizobia mutualism |
Q46313615 | The effects of aluminum and nickel in nectar on the foraging behavior of bumblebees |
Q52629485 | The effects of host species and sexual dimorphism differ among root, leaf and flower microbiomes of wild strawberries in situ. |
Q22122058 | The genome of woodland strawberry (Fragaria vesca) |
Q37266206 | The impact of biochemistry vs. population membership on floral scent profiles in colour polymorphic Hesperis matronalis |
Q52684077 | The interactive effects of herbivory and mixed mating for the population dynamics of Impatiens capensis. |
Q51836863 | The limits on sexual dimorphism in vegetative traits in a gynodioecious plant. |
Q111321324 | The pollen virome of wild plants and its association with variation in floral traits and land use |
Q125404104 | The pollen virome: A review of pollen‐associated viruses and consequences for plants and their interactions with pollinators |
Q36927661 | The role of natural enemies in the expression and evolution of mixed mating in hermaphroditic plants and animals |
Q46215547 | Toward a predictive understanding of the fitness costs of heterospecific pollen receipt and its importance in co-flowering communities |
Q51793379 | Trait selection in flowering plants: how does sexual selection contribute? |
Q57162193 | Variation in sampling effort affects the observed richness of plant-plant interactions via heterospecific pollen transfer: implications for interpretation of pollen transfer networks |
Q111324954 | Widespread vulnerability of flowering plant seed production to pollinator declines |
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