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Sex‐specific differences in reproductive life‐history traits of the moss Weissia jamaicensis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ajb2.1128openalex-snapshot
Rapid population sex‐ratio changes in the moss Ceratodon purpureus
inferredcites →https://doi.org/10.1002/ajb2.1619openalex-snapshot
Stomata: the holey grail of plant evolution
inferredcites →https://doi.org/10.1002/j.1537-2197.1993.tb13844.xopenalex-snapshot
CONTROL OF SEX RATIOS IN HAPLOID POPULATIONS OF THE MOSS, CERATODON PURPUREUS
inferredcites →https://doi.org/10.1007/978-3-662-03908-3_6openalex-snapshot
Sexual Dimorphism in Life History
inferredcites →https://doi.org/10.1007/bf00317375openalex-snapshot
Sex ratio from germination through maturity and its reproductive consequences in the liverwort Sphaerocarpos texanus
inferredcites →https://doi.org/10.1007/bf02857918openalex-snapshot
Sexual specialization and inbreeding avoidance in the evolution of dioecy
inferredcites →https://doi.org/10.1007/s001140050763openalex-snapshot
Life history evolution: successes, limitations, and prospects
inferredcites →https://doi.org/10.1007/s11258-021-01127-3openalex-snapshot
Male-biased effective sex ratio across populations of the threatened Zamia boliviana (Zamiaceae)
inferredcites →https://doi.org/10.1007/s11284-013-1125-yopenalex-snapshot
Effect of sex ratio, habitat factors and neighborhood competition on stem growth in the dioecious tree Fraxinus mandshurica
inferredcites →https://doi.org/10.1016/0006-3207(92)90566-6openalex-snapshot
Reproduction and rarity in British mosses
inferredcites →https://doi.org/10.1016/b978-0-12-800049-6.00083-4openalex-snapshot
Life History, What is?
inferredcites →https://doi.org/10.1016/j.cub.2020.03.048openalex-snapshot
Phylogenomic Evidence for the Monophyly of Bryophytes and the Reductive Evolution of Stomata
inferredcites →https://doi.org/10.1023/a:1013968421254openalex-snapshot
Sex expression and sex dimorphism in sporophytic populations of the desert moss Syntrichia caninervis
inferredcites →https://doi.org/10.1023/a:1026531122302openalex-snapshot
Costs of sporophyte production in the moss, Dicranum polysetum
inferredcites →https://doi.org/10.1046/j.1469-8137.2002.00477.xopenalex-snapshot
The costs of reproduction in plants
inferredcites →https://doi.org/10.1080/03736687.2016.1264662openalex-snapshot
Can the meiotic sex ratio explain the sex ratio bias in adult populations in the dioicous moss Drepanocladus lycopodioides?
inferredcites →https://doi.org/10.1086/409052openalex-snapshot
Life-History Tactics: A Review of the Ideas
inferredcites →https://doi.org/10.1086/425671openalex-snapshot
Do the Sexes of the Desert Moss Syntrichia caninervis Differ in Desiccation Tolerance? A Leaf Regeneration Assay
inferredcites →https://doi.org/10.1086/670154openalex-snapshot
Males Are Not Shy in the Wetland Moss Drepanocladus lycopodioides
inferredcites →https://doi.org/10.1093/aob/mcl238openalex-snapshot
Generational Differences in Response to Desiccation Stress in the Desert Moss Tortula inermis
inferredcites →https://doi.org/10.1093/aob/mcr027openalex-snapshot
Does the silver moss Bryum argenteum exhibit sex-specific patterns in vegetative growth rate, asexual fitness or prezygotic reproductive investment?
inferredcites →https://doi.org/10.1098/rstb.2010.0002openalex-snapshot
Ecological genetics of sex ratios in plant populations
inferredcites →https://doi.org/10.1098/rstb.2015.0535openalex-snapshot
Living together and living apart: the sexual lives of bryophytes
inferredcites →https://doi.org/10.1111/boj.12159openalex-snapshot
Sex ratio, sex-specific pattern in vegetative growth and gemma production in an aquatic liverwort,Scapania undulata(Marchantiophyta: Scapaniaceae)
inferredcites →https://doi.org/10.1111/evo.12001openalex-snapshot
COMPARATIVE ANALYSES OF SEX-RATIO VARIATION IN DIOECIOUS FLOWERING PLANTS
inferredcites →https://doi.org/10.1111/j.1399-3054.2006.00590.xopenalex-snapshot
Gender‐specific heat‐shock tolerance of hydrated leaves in the desert moss Syntrichia caninervis
inferredcites →https://doi.org/10.1111/mec.14020openalex-snapshot
On the rarity of dioecy in flowering plants
inferredcites →https://doi.org/10.1111/plb.13122openalex-snapshot
How do sexual expression, reproductive phenology and reproductive success relate to sexual systems in Fissidens Hedw. (Fissidentaceae)? A case study comparing two different sexual systems in mosses
inferredcites →https://doi.org/10.1127/0941-2948/2013/0507openalex-snapshot
Köppen's climate classification map for Brazil
inferredcites →https://doi.org/10.1179/037366802125002113openalex-snapshot
Reproductive phenology ofOctoblepharum albidum(Bryopsida, Leucobryaceae) in a tropical lowland forest of north-eastern Brazil
inferredcites →https://doi.org/10.1179/1743282014y.0000000104openalex-snapshot
The male gender as a key for understanding the reproductive biology ofAnomobryum concinnatum(Spruce) Lindb.
inferredcites →https://doi.org/10.1179/174328205x69959openalex-snapshot
Sex ratio patterns in dioicous bryophytes re-visited
inferredcites →https://doi.org/10.1179/174328213x13662092820316openalex-snapshot
Sex ratio, spatial segregation, and fertilization rates of the epiphyllous mossCrossomitrium patrisiae(Brid.) Müll.Hal. in the Brazilian Atlantic rainforest
inferredcites →https://doi.org/10.1179/jbr.2001.23.1.3openalex-snapshot
Biomass allocation to sexual and asexual reproduction in a leafy hepaticLophozia silvicolaBuch
inferredcites →https://doi.org/10.1590/0102-33062015abb0012openalex-snapshot
Diversity and conservation of Pottiaceae (Pottiales) in the Atlantic Rainforest
inferredcites →https://doi.org/10.1590/s0102-33061998000400007openalex-snapshot
Reprodução sexuada em musgos acrocárpicos do Estado de Pernambuco, Brasil
inferredcites →https://doi.org/10.1639/0007-2745(2002)105[0384:reacos]2.0.co;2openalex-snapshot
Reproductive Effort and Cost of Sexual Reproduction in Female Dicranum polysetum
inferredcites →https://doi.org/10.1639/0007-2745-113.4.788openalex-snapshot
Sex ratios and the shy male hypothesis in the moss Bryum argenteum (Bryaceae)
inferredcites →https://doi.org/10.1639/0007-2745-116.1.043openalex-snapshot
An experimental demonstration of rhizautoicy, self-incompatibility, and reproductive investment inAloina bifrons(Pottiaceae)
inferredcites →https://doi.org/10.2307/2656595openalex-snapshot
Sex expression, skewed sex ratios, and microhabitat distribution in the dioecious desert moss Syntrichia caninervis (Pottiaceae)
inferredcites →https://doi.org/10.2307/2656736openalex-snapshot
The cost of realized sexual reproduction: assessing patterns of reproductive allocation and sporophyte abortion in a desert moss
inferredcites →https://doi.org/10.2307/2656812openalex-snapshot
Life history variation in gametophyte populations of the moss Ceratodon purpureus (Ditrichaceae)
inferredcites →https://doi.org/10.2307/3242472openalex-snapshot
Spatial Pattern and Gamete Dispersal Distances in Atrichum angustatum, a Dioicous Moss
inferredcites →https://doi.org/10.2307/3243344openalex-snapshot
Ecological Consequences of Sexual versus Asexual Reproduction in Dicranum flagellare and Tetraphis pellucida
inferredcites →https://doi.org/10.2478/pfs-2018-0001openalex-snapshot
A new synonym of Weissia jamaicensis (Pottiaceae, Bryophyta), and extension of its range from the Neotropics to the Palaeotropics
inferredcites →https://doi.org/10.3732/ajb.1400156openalex-snapshot
Meiotic sex ratio variation in natural populations of Ceratodon purpureus (Ditrichaceae)
inferredcites →https://doi.org/10.3732/ajb.1400196openalex-snapshot
The relative and absolute frequencies of angiosperm sexual systems: Dioecy, monoecy, gynodioecy, and an updated online database
inferredcites →https://doi.org/10.3732/ajb.1600240openalex-snapshot
Prezygotic resource‐allocation dynamics and reproductive trade‐offs in Calymperaceae (Bryophyta)
inferredcites →https://doi.org/10.3732/ajb.91.1.1openalex-snapshot
Age and sex‐specific rates of leaf regeneration in the Mojave Desert moss Syntrichia caninervis
inferredcites →https://doi.org/10.3732/ajb.93.9.1313openalex-snapshot
Reproductive effort and costs of reproduction do not explain female‐biased sex ratios in the moss Pseudocalliergon trifarium (Amblystegiaceae)
inferredcites →https://doi.org/10.7872/cryb/v39.iss2.2018.271openalex-snapshot
Sexual Dimorphism, Vegetative Growth and Reproductive Investment in the Rhizautoicous MossFissidens flaccidus(Fissidentaceae, Bryopsida)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4774338openalex-extracted
Come Together: Bryophyte Reproduction from a Clonal Integration Perspective
inferred← citeshttps://doi.org/10.1007/s00442-022-05303-8openalex-snapshot
Life-history traits and density dependence in metapopulations of a tropical moss: a monoicous species that is almost dioicous
inferred← citeshttps://doi.org/10.1007/s10531-025-03157-zopenalex-snapshot
Sex-specific responses to climate change in unisexual bryophytes
inferred← citeshttps://doi.org/10.1007/s10682-026-10391-6openalex-snapshot
A model species in focus: the silver-thread moss Bryum argenteum as a model for ecological and evolutionary studies
inferred← citeshttps://doi.org/10.1007/s12229-024-09301-8openalex-snapshot
An Overview of Reproductive Allocation and Reproductive Costs in Bryophytes: Challenges and Prospects
inferred← citeshttps://doi.org/10.1080/03736687.2023.2251776openalex-snapshot
A comparative study of cultured and field plants provides evidence for the shy male hypothesis in tropical genotypes of Bryum argenteum Hedw.
inferred← citeshttps://doi.org/10.1086/734303openalex-snapshot
Come Together: Sexual and Asexual Dynamics in Hyophila involuta Moss Cushion Microenvironments under the Lens of Clonality
inferred← citeshttps://doi.org/10.1093/aob/mcad052openalex-snapshot
The spatial arrangement of sexes is related to reproductive allocation in mosses: a comparative study of reproductive allocation in three different monoicous sexual systems
inferred← citeshttps://doi.org/10.1093/aob/mcae071openalex-snapshot
Understanding desiccation tolerance and sex-specific responses in Bryum argenteum : insights from phenological phases and physiological analyses
inferred← citeshttps://doi.org/10.1111/nph.18691openalex-snapshot
A Physcomitrella PIN protein acts in spermatogenesis and sporophyte retention
inferred← citeshttps://doi.org/10.1111/plb.70200openalex-snapshot
Ecological divergence in the silver moss Bryum argenteum : developmental, ontogenetic and life‐history trait variations across contrasting tropical ecosystems
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1650702/v1openalex-snapshot
Density dependence on male sexual expression in metapopulations of a tropical moss: a monoicous species almost dioicous
inferred← citeshttps://doi.org/10.30970/vlubs.2025.94.05openalex-snapshot
Reproductive strategy, sexual structure and productivity of fertile plants of the epigeic moss Atrichum undulatum (Hedw.) P. Beauv. depending on the microclimatic locality conditions
inferred← citeshttps://doi.org/10.3389/fpls.2025.1456877openalex-snapshot
Factors accounting for limited sexual reproduction in a long-lived unisexual plant species
inferred← citeshttps://doi.org/10.4467/2543702xshs.23.017.17708openalex-snapshot
The Misrepresentation of Petri Dish, as “petri” Dish, in the Scientific Literature
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