On the public citation graph

Pollen movement within a continuous forest of wind-pollinated Araucaria angustifolia, inferred from paternity and TwoGener analysis

https://doi.org/10.1007/s10592-007-9411-2

0 signed · 131 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1537-2197.1995.tb12679.xopenalex-snapshot

Spatial genetic structure of a tropical understory shrub, PSYCHOTRIA OFFICINALIS (RuBIACEAE)

inferredcites →https://doi.org/10.1007/978-94-011-1749-4_20openalex-snapshot

The influence of seed dispersal mechanisms on the genetic structure of tropical tree populations

inferredcites →https://doi.org/10.1007/bf00052230openalex-snapshot

The influence of seed dispersal mechanisms on the genetic structure of tropical tree populations

inferredcites →https://doi.org/10.1007/bf00251112openalex-snapshot

Estimation of gene flow into two seed orchards of loblolly pine (Pinus taeda L.)

inferredcites →https://doi.org/10.1007/s10980-005-5415-9openalex-snapshot

Genetic analysis of landscape connectivity in tree populations

inferredcites →https://doi.org/10.1007/s11295-006-0035-3openalex-snapshot

Spatial structure and genetic diversity of three tropical tree species with different habitat preferences within a natural forest

inferredcites →https://doi.org/10.1016/0040-5809(86)90006-7openalex-snapshot

The relationship between single parent and parent pair genetic likelihoods in genealogy reconstruction

inferredcites →https://doi.org/10.1016/0169-5347(93)90197-wopenalex-snapshot

Assessing minimum viable population size: Demography meets population genetics

inferredcites →https://doi.org/10.1016/j.foreco.2004.05.016openalex-snapshot

Pollen movement under alternative silvicultural practices in native populations of Scots pine (Pinus sylvestris L.) in central Spain

inferredcites →https://doi.org/10.1016/j.foreco.2004.05.049openalex-snapshot

Measuring pollen flow in forest trees: an exposition of alternative approaches

inferredcites →https://doi.org/10.1017/s0016672301005341openalex-snapshot

Two-generation analysis of pollen flow across a landscape. III. Impact of adult population structure

inferredcites →https://doi.org/10.1038/hdy.1994.35openalex-snapshot

Estimating the relative rates of pollen and seed migration among plant populations

inferredcites →https://doi.org/10.1038/hdy.1996.139openalex-snapshot

Mating patterns and pollen dispersal in a natural knobcone pine (Pinus attenuate Lemmon.) stand

inferredcites →https://doi.org/10.1038/sj.hdy.6800542openalex-snapshot

Patterns of pollen dispersal in a small population of Pinus sylvestris L. revealed by total-exclusion paternity analysis

inferredcites →https://doi.org/10.1038/sj.hdy.6800709openalex-snapshot

Optimal sampling strategy for estimation of spatial genetic structure in tree populations

inferredcites →https://doi.org/10.1038/sj.hdy.6800712openalex-snapshot

To self, or not to self… A review of outcrossing and pollen-mediated gene flow in neotropical trees

inferredcites →https://doi.org/10.1038/sj.hdy.6800748openalex-snapshot

Effect of gene flow on spatial genetic structure in the riparian canopy tree Cercidiphyllum japonicum revealed by microsatellite analysis

inferredcites →https://doi.org/10.1038/sj.hdy.6801019openalex-snapshot

Patterns of pollen and seed dispersal in a small, fragmented population of the wind-pollinated tree Araucaria angustifolia in southern Brazil

inferredcites →https://doi.org/10.1038/sj.hdy.6884040openalex-snapshot

Multiple paternity in Eucalyptus rameliana (Myrtaceae)

inferredcites →https://doi.org/10.1038/sj.hdy.6886220openalex-snapshot

Comparative study of genetic variation and differentiation of two pedunculate oak (Quercus robur) stands using microsatellite and allozyme loci

inferredcites →https://doi.org/10.1046/j.0962-1083.2001.01342.xopenalex-snapshot

Seed dispersal by animals: exact identification of source trees with endocarp DNA microsatellites

inferredcites →https://doi.org/10.1046/j.1365-2540.2000.00684.xopenalex-snapshot

Paternity and gene dispersal in limber pine (Pinus flexilis James)

inferredcites →https://doi.org/10.1046/j.1365-2540.2001.00913.xopenalex-snapshot

Outcrossing and paternity analysis of Pinus densiflora (Japanese red pine) by microsatellite polymorphism

inferredcites →https://doi.org/10.1046/j.1365-294x.1998.00374.xopenalex-snapshot

Statistical confidence for likelihood‐based paternity inference in natural populations

inferredcites →https://doi.org/10.1046/j.1365-294x.1998.00397.xopenalex-snapshot

Understanding the population genetic structure of Gleditsia triacanthos L.: seed dispersal and variation in female reproductive success

inferredcites →https://doi.org/10.1046/j.1365-294x.1999.00637.xopenalex-snapshot

Pollen dispersal inferred from paternity analysis in a mixed oak stand of Quercus robur L. and Q. petraea (Matt.) Liebl.

inferredcites →https://doi.org/10.1046/j.1365-294x.2001.01251.xopenalex-snapshot

Pollen pool heterogeneity in shortleaf pine, Pinus echinata Mill.

inferredcites →https://doi.org/10.1046/j.1365-294x.2002.01574.xopenalex-snapshot

Pollen movement in declining populations of California Valley oak, Quercus lobata: where have all the fathers gone?

inferredcites →https://doi.org/10.1046/j.1365-294x.2004.02076.xopenalex-snapshot

New insights from fine‐scale spatial genetic structure analyses in plant populations

inferredcites →https://doi.org/10.1046/j.1471-8286.2002.00305.xopenalex-snapshot

spag e d i: a versatile computer program to analyse spatial genetic structure at the individual or population levels

inferredcites →https://doi.org/10.1046/j.1523-1739.2002.00317.xopenalex-snapshot

Effects of Dry Tropical Forest Fragmentation on the Reproductive Success and Genetic Structure of the Tree Samanea saman

inferredcites →https://doi.org/10.1046/j.1523-1739.2003.01140.xopenalex-snapshot

Effects of Forest Fragmentation and Flowering Phenology on the Reproductive Success and Mating Patterns of the Tropical Dry Forest Tree Pachira quinata

inferredcites →https://doi.org/10.1071/bt02037openalex-snapshot

Pollen dispersal and gene flow by pollen in Araucaria angustifolia

inferredcites →https://doi.org/10.1086/491661openalex-snapshot

A Genetic Evaluation of Seed Dispersal in the Neotropical TreeJacaranda copaia(Bignoniaceae)

inferredcites →https://doi.org/10.1093/genetics/127.3.619openalex-snapshot

Hierarchical patterns of correlated mating in Acacia melanoxylon.

inferredcites →https://doi.org/10.1093/genetics/157.2.851openalex-snapshot

Two-generation analysis of pollen flow across a landscape. II. Relation between phi(ft), pollen dispersal and interfemale distance.

inferredcites →https://doi.org/10.1093/genetics/161.1.355openalex-snapshot

Two-Generation Analysis of Pollen Flow Across a Landscape. IV. Estimating the Dispersal Parameter

inferredcites →https://doi.org/10.1093/jhered/89.1.62openalex-snapshot

High levels of gene flow in bur oak revealed by paternity analysis using microsatellites

inferredcites →https://doi.org/10.1093/jhered/esl022openalex-snapshot

Mating Patterns of Black Oak Quercus velutina (Fagaceae) in a Missouri Oak-Hickory Forest

inferredcites →https://doi.org/10.1093/jhered/esl031openalex-snapshot

Internal Genetic Structure and Outcrossing Rate in a Natural Population of Araucaria angustifolia (Bert.) O. Kuntze

inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a023034openalex-snapshot

Population Density and Mating Pattern in Western Larch

inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb01291.xopenalex-snapshot

TWO-GENERATION ANALYSIS OF POLLEN FLOW ACROSS A LANDSCAPE. I. MALE GAMETE HETEROGENEITY AMONG FEMALES

inferredcites →https://doi.org/10.1111/j.0014-3820.2005.tb01037.xopenalex-snapshot

HISTORICAL AND CONTEMPORARY MATING PATTERNS IN REMNANT POPULATIONS OF THE FOREST TREE FRAXINUS EXCELSIOR L

inferredcites →https://doi.org/10.1111/j.1365-294x.2004.02127.xopenalex-snapshot

Long‐distance pollen flow and tolerance to selfing in a neotropical tree species

inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02593.xopenalex-snapshot

Parentage versus two‐generation analyses for estimating pollen‐mediated gene flow in plant populations

inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02736.xopenalex-snapshot

Interannual genetic heterogeneity of pollen pools accepted by Quercus salicina individuals

inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02830.xopenalex-snapshot

Inferring colonization history from analyses of spatial genetic structure within populations of Pinus strobus and Quercus rubra

inferredcites →https://doi.org/10.1111/j.1365-294x.2006.03126.xopenalex-snapshot

Contemporary pollen and seed dispersal in a Prunus mahaleb population: patterns in distance and direction

inferredcites →https://doi.org/10.1111/j.1365-294x.2007.03089.xopenalex-snapshot

Revising how the computer program cervus accommodates genotyping error increases success in paternity assignment

inferredcites →https://doi.org/10.1111/j.1461-0248.2006.00897.xopenalex-snapshot

Genetic evidence of frequent long‐distance recruitment in a vertebrate‐dispersed tree

inferredcites →https://doi.org/10.1111/j.1471-8286.2005.00899.xopenalex-snapshot

Characterization of nuclear microsatellite loci in South American Araucariaceae species

inferredcites →https://doi.org/10.1111/j.1558-5646.1969.tb03496.xopenalex-snapshot

VARIANCE OF GENE FREQUENCIES

inferredcites →https://doi.org/10.1111/j.1558-5646.1989.tb05182.xopenalex-snapshot

CORRELATED MATINGS IN THE PARTIAL SELFER MIMULUS GUTTATUS

inferredcites →https://doi.org/10.1111/j.1558-5646.1990.tb05195.xopenalex-snapshot

THE DEVELOPMENT AND APPLICATION OF A REFINED METHOD FOR ESTIMATING GENE FLOW FROM ANGIOSPERM PATERNITY ANALYSIS

inferredcites →https://doi.org/10.1126/science.1105034openalex-snapshot

Genetic Consequences of Tropical Second-Growth Forest Regeneration

inferredcites →https://doi.org/10.1515/sg-2004-0003openalex-snapshot

Variation and Population Structure at Enzyme Gene Loci in Araucaria angustifolia (Bert.) O. Ktze

inferredcites →https://doi.org/10.1534/genetics.104.027714openalex-snapshot

Fine-Scale Genetic Structure and Gene Dispersal in Centaurea corymbosa (Asteraceae). II. Correlated Paternity Within and Among Sibships

inferredcites →https://doi.org/10.1590/s0100-84042004000400017openalex-snapshot

Fenologia reprodutiva e produção de sementes em Araucaria angustifolia (Bert.) O. Kuntze

inferredcites →https://doi.org/10.2307/2657086openalex-snapshot

Cross‐fertility in two tropical tree species: evidence of inbreeding depression within populations and genetic divergence among populations

inferredcites →https://doi.org/10.2307/3491214openalex-snapshot

A Genetic Evaluation of Seed Dispersal in the Neotropical Tree Jacaranda copaia (Bignoniaceae)

inferredcites →https://doi.org/10.2307/3558436openalex-snapshot

Pollen load size, reproductive success, and progeny kinship of naturally pollinated flowers of the tropical dry forest tree Pachira quinata (Bombacaceae)

inferredcites →https://doi.org/10.24278/2178-5031.2002142412openalex-snapshot

NÚMERO DE ÁRVORES MATRIZES E CONCEITOS GENÉTICOS NA COLETA DE SEMENTES PARA REFLORESTAMENTOS COM ESPÉCIES NATIVAS

inferredcites →https://doi.org/10.3732/ajb.92.2.262openalex-snapshot

A two‐generation analysis of pollen pool genetic structure in flowering dogwood, Cornus florida (Cornaceae), in the Missouri Ozarks

inferredcites →https://doi.org/10.3732/ajb.92.2.370openalex-snapshot

Effects of pollination by bats on the mating system of Ceiba pentandra (Bombacaceae) populations in two tropical life zones in Costa Rica

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.4687897openalex-extracted

inferred← citeshttps://doi.org/10.1002/ecs2.4454openalex-snapshot

Heritability of plastic trait changes in drought‐exposed ponderosa pine seedlings

inferred← citeshttps://doi.org/10.1007/978-3-642-41554-8_75-1openalex-snapshot

Genetics and Tropical Forests

inferred← citeshttps://doi.org/10.1007/978-3-642-54601-3_75openalex-snapshot

Genetics and Tropical Forests

inferred← citeshttps://doi.org/10.1007/978-4-431-53901-8_3openalex-snapshot

Pollination Efficiencies of Insects Visiting Magnolia obovata, as Determined by Single-Pollen Genotyping

inferred← citeshttps://doi.org/10.1007/s00606-013-0759-0openalex-snapshot

Comparison of mating system parameters and genetic structure in three natural scenarios of Acacia visco (Leguminosae, Mimosoideae)

inferred← citeshttps://doi.org/10.1007/s00606-013-0775-0openalex-snapshot

Impact of monoecy in the genetic structure of a predominately dioecious conifer species, Araucaria angustifolia (Bert.) O. Kuntze

inferred← citeshttps://doi.org/10.1007/s10453-019-09594-yopenalex-snapshot

Pollen dispersion in Myrica esculenta (Myricaceae): a dioecious anemophilous tree species of Himalaya

inferred← citeshttps://doi.org/10.1007/s10453-020-09626-yopenalex-snapshot

Daily, seasonal, and interannual variability of airborne pollen of Araucaria angustifolia growing in the subtropical area of Argentina

inferred← citeshttps://doi.org/10.1007/s10530-015-0867-6openalex-snapshot

Among-population pollen movement and skewed male fitness in a dioecious weed

inferred← citeshttps://doi.org/10.1007/s10531-009-9600-zopenalex-snapshot

Integrating approaches towards the conservation of forest genetic resources: a case study of Araucaria angustifolia

inferred← citeshttps://doi.org/10.1007/s10592-009-9961-6openalex-snapshot

Short-distance gene flow in Populus nigra L. accounts for small-scale spatial genetic structures: implications for in situ conservation measures

inferred← citeshttps://doi.org/10.1007/s10592-010-0046-3openalex-snapshot

Understanding the effects of isolation on seed and pollen flow, spatial genetic structure and effective population size of the dioecious tropical tree species Myracrodruon urundeuva

inferred← citeshttps://doi.org/10.1007/s10592-011-0183-3openalex-snapshot

Genetic diversity, genetic drift and mixed mating system in small subpopulations of Dyckia ibiramensis, a rare endemic bromeliad from Southern Brazil

inferred← citeshttps://doi.org/10.1007/s10592-011-0292-zopenalex-snapshot

Mating system parameters at hierarchical levels of fruits, individuals and populations in the Brazilian insect-pollinated tropical tree, Tabebuia roseo-alba (Bignoniaceae)

inferred← citeshttps://doi.org/10.1007/s10592-011-0296-8openalex-snapshot

Genetic analysis of 50-year old Brazilian pine (Araucaria angustifolia) plantations: implications for conservation planning

inferred← citeshttps://doi.org/10.1007/s10592-013-0451-5openalex-snapshot

Realized pollen and seed dispersal within a continuous population of the dioecious coniferous Brazilian pine [Araucaria angustifolia (Bertol.) Kuntze]

inferred← citeshttps://doi.org/10.1007/s10592-014-0608-xopenalex-snapshot

Long-distance pollen dispersal ensures genetic connectivity of the low-density tree species, Eurycorymbus cavaleriei, in a fragmented karst forest landscape

inferred← citeshttps://doi.org/10.1007/s10592-015-0793-2openalex-snapshot

Using genetic diversity and mating system parameters estimated from genetic markers to determine strategies for the conservation of Araucaria angustifolia (Bert.) O. Kuntze (Araucariaceae)

inferred← citeshttps://doi.org/10.1007/s11295-009-0210-4openalex-snapshot

Genetic effects of forest fragmentation in high-density Araucaria angustifolia populations in Southern Brazil

inferred← citeshttps://doi.org/10.1007/s11295-012-0500-0openalex-snapshot

Short-distance pollen dispersal for an outcrossed, wind-pollinated southern beech (Nothofagus nervosa (Phil.) Dim. et Mil.)

inferred← citeshttps://doi.org/10.1007/s11295-014-0814-1openalex-snapshot

High levels of genetic diversity through pollen flow of the coniferous Araucaria angustifolia: a landscape level study in Southern Brazil

inferred← citeshttps://doi.org/10.1007/s11295-017-1215-zopenalex-snapshot

Mating pattern and pollen dispersal in the wild olive tree (Olea europaea subsp. cuspidata)

inferred← citeshttps://doi.org/10.1007/s11295-018-1250-4openalex-snapshot

Phylogeography of Brazilian pine (Araucaria angustifolia): integrative evidence for pre-Columbian anthropogenic dispersal

inferred← citeshttps://doi.org/10.1007/s11295-021-01509-8openalex-snapshot

Seed and pollen dispersal and fine-scale spatial genetic structure of a threatened tree species: Pericopsis elata (HARMS) Meeuwen (Fabaceae)

inferred← citeshttps://doi.org/10.1007/s11295-022-01550-1openalex-snapshot

Spatial genetic structure and mating system in forest tree populations from seasonally dry tropical forests: a review

inferred← citeshttps://doi.org/10.1016/j.agrformet.2019.05.003openalex-snapshot

Climatic cues for secondary growth and cone production are sex-dependent in the long-lived dioecious conifer Araucaria araucana

inferred← citeshttps://doi.org/10.1016/j.biocon.2010.06.028openalex-snapshot

Fragmented but not isolated: Contribution of single trees, small patches and long-distance pollen flow to genetic connectivity for Gomortega keule, an endangered Chilean tree

inferred← citeshttps://doi.org/10.1016/j.biocon.2024.110606openalex-snapshot

Climate- and scale-dependent sex ratio in threatened Araucaria forests

inferred← citeshttps://doi.org/10.1016/j.foreco.2008.03.017openalex-snapshot

Gene flow pattern and mating system in a small population of Quercus semiserrata Roxb. (Fagaceae)

inferred← citeshttps://doi.org/10.1016/j.foreco.2010.09.016openalex-snapshot

Contemporary pollen flow and mating patterns of a subtropical canopy tree Eurycorymbus cavaleriei in a fragmented agricultural landscape

inferred← citeshttps://doi.org/10.1016/j.foreco.2014.05.044openalex-snapshot

Tree density and population size affect pollen flow and mating patterns in small fragmented forest stands of pedunculate oak ( Quercus robur L.)

inferred← citeshttps://doi.org/10.1016/j.foreco.2017.06.007openalex-snapshot

Implications of mating system and pollen dispersal indices for management and conservation of the semi-arid species Prosopis flexuosa (Leguminosae)

inferred← citeshttps://doi.org/10.1016/j.foreco.2019.02.006openalex-snapshot

Guidelines for seed collection of Araucaria angustifolia (Bertol.) Kuntze: A genetic, demographic and geographic approach

inferred← citeshttps://doi.org/10.1016/j.foreco.2020.118716openalex-snapshot

Spatiotemporal variation in mating system and genetic diversity of Araucaria angustifolia: Implications for conservation and seed collection

inferred← citeshttps://doi.org/10.1016/j.revpalbo.2019.03.003openalex-snapshot

A quantitative study of modern pollen–vegetation relationships in southern Brazil's Araucaria forest

inferred← citeshttps://doi.org/10.1017/s0266467416000067openalex-snapshot

Gene flow and fine-scale spatial genetic structure inCabralea canjerana(Meliaceae), a common tree species from the Brazilian Atlantic forest

inferred← citeshttps://doi.org/10.1017/s0266467418000111openalex-snapshot

Pollination of the Australian cycad Cycas ophiolitica (Cycadaceae): the limited role of wind pollination in a cycad with beetle pollinator mutualists, and its ecological significance

inferred← citeshttps://doi.org/10.1038/hdy.2013.8openalex-snapshot

Edge effects enhance selfing and seed harvesting efforts in the insect-pollinated Neotropical tree Copaifera langsdorffii (Fabaceae)

inferred← citeshttps://doi.org/10.1038/s41437-024-00709-xopenalex-snapshot

Inbreeding depression affects the growth of seedlings of an African timber species with a mixed mating reproductive system, Pericopsis elata (Harms) Meeuwen

inferred← citeshttps://doi.org/10.1080/07352689.2010.481167openalex-snapshot

Plant Parentage, Pollination, and Dispersal: How DNA Microsatellites Have Altered the Landscape

inferred← citeshttps://doi.org/10.1093/forsci/fxy026openalex-snapshot

Landscape Genetics and Genetic Conservation of Two Keystone Species from Ombrophilous Dense Forest: Euterpe edulis and Ocotea catharinensis

inferred← citeshttps://doi.org/10.1093/jxb/err154openalex-snapshot

Pollen and seed desiccation tolerance in relation to degree of developmental arrest, dispersal, and survival

inferred← citeshttps://doi.org/10.1111/1365-2664.14807openalex-snapshot

Shedding light on pollination deficits: Cueing into plant spectral reflectance signatures to monitor pollination delivery across landscapes

inferred← citeshttps://doi.org/10.1111/ecog.06756openalex-snapshot

Evaluating the impact of historical climate and early human groups in the Araucaria Forest of eastern South America

inferred← citeshttps://doi.org/10.1111/j.1095-8312.2011.01695.xopenalex-snapshot

Does pollen aerodynamics correlate with pollination vector? Pollen settling velocity as a test for wind versus insect pollination among cycads (Gymnospermae: Cycadaceae: Zamiaceae)

inferred← citeshttps://doi.org/10.1111/j.1365-294x.2009.04365.xopenalex-snapshot

Spatial genetic structure in Milicia excelsa (Moraceae) indicates extensive gene dispersal in a low‐density wind‐pollinated tropical tree

inferred← citeshttps://doi.org/10.1111/j.1523-1739.2009.01357.xopenalex-snapshot

Spontaneous Interspecific Hybridization and Patterns of Pollen Dispersal in Ex Situ Populations of a Tree Species ( Sinojackia xylocarpa ) that is Extinct in the Wild

inferred← citeshttps://doi.org/10.1111/mec.13553openalex-snapshot

Sperm dispersal distances estimated by parentage analysis in a brooding scleractinian coral

inferred← citeshttps://doi.org/10.11606/d.11.2009.tde-05082009-081516openalex-snapshot

Estrutura genética e diversidade clonal de jatobá-do-cerrado (Hymenaea stigonocarpa Mart. ex Hayne) em duas populações no Cerrado do Estado de São Paulo

inferred← citeshttps://doi.org/10.11606/d.11.2011.tde-24052011-102337openalex-snapshot

Importância da conservação in situ de Copaifera langsdorffii Desf. em remanescentes de cerrado de propriedades particulares rurais

inferred← citeshttps://doi.org/10.11606/d.17.2009.tde-02032010-152105openalex-snapshot

Diversidade genética, sistema reprodutivo e fluxo de pólen em duas populações de Tabebuia roseo-alba (Ridl.) Sand.: implicações para a conservação

inferred← citeshttps://doi.org/10.11606/t.11.2023.tde-05062023-155614openalex-snapshot

Efeitos de diferentes intensidades de corte seletivo sobre a diversidade e estrutura genética de uma população natural de >i /i< (Bertol.) Kuntze (Araucariaceae) acessada por marcadores microssatélites

inferred← citeshttps://doi.org/10.1186/s12870-019-2024-3openalex-snapshot

Mixed mating system and variable mating patterns in tropical woody bamboos

inferred← citeshttps://doi.org/10.1371/journal.pone.0230404openalex-snapshot

A 3K Axiom SNP array from a transcriptome-wide SNP resource sheds new light on the genetic diversity and structure of the iconic subtropical conifer tree Araucaria angustifolia (Bert.) Kuntze

inferred← citeshttps://doi.org/10.1515/sg-2012-0032openalex-snapshot

Estimating coancestry within open-pollinated progenies of a dioecious species: the case study of Myracrodruon urundeuva

inferred← citeshttps://doi.org/10.1515/sg-2013-0003openalex-snapshot

Mendelian segregation in eight microsatellite loci from hand- and open-pollinated progenies of Araucaria angustifolia (Bert.) O. Kuntze (Araucariaceae)

inferred← citeshttps://doi.org/10.1590/s1415-47572009005000052openalex-snapshot

Patterns of genetic diversity in southern and southeastern Araucaria angustifolia (Bert.) O. Kuntze relict populations

inferred← citeshttps://doi.org/10.32929/2446-8355.2017v26n2p203-216openalex-snapshot

DIVERSIDADE GENÉTICA DE POPULAÇÕES NATURAIS DE DIPTERYX ALATA LOCALIZADAS NOS MUNICÍPIOS DE BRASILÂNDIA/MS, INDIARA/GO E ITARUMÃ/GO ESTIMADA POR MARCADORES MICROSSATÉLITES

inferred← citeshttps://doi.org/10.3390/f14051046openalex-snapshot

Logging Affects Genetic Diversity Parameters in an Araucaria angustifolia Population: An Endangered Species in Southern Brazil

inferred← citeshttps://doi.org/10.3732/ajb.1100321openalex-snapshot

AFLP markers provide insights into the evolutionary relationships and diversification of New Caledonian Araucaria species (Araucariaceae)

inferred← citeshttps://doi.org/10.3732/ajb.1300065openalex-snapshot

Mating between Echinacea angustifolia (Asteraceae) individuals increases with their flowering synchrony and spatial proximity

inferred← citeshttps://doi.org/10.3832/ifor0606-009openalex-snapshot

Towards an optimal sampling effort for paternity analysis in forest trees: what do the raw numbers tell us?

inferred← citeshttps://doi.org/10.4238/gmr.15017785openalex-snapshot

Acrocomia emensis (Arecaceae) genetic structure and diversity using SSR molecular markers

inferred← citeshttps://doi.org/10.53846/goediss-8662openalex-snapshot

Vegetation and fire history in Araucaria forest and Grasslands, Southern Brazil

inferred← citeshttps://doi.org/10.70675/76e626ffz9f9cz4babz9169z68571a78dc30openalex-snapshot

Modélisations de la dispersion du pollen et estimation à partir de marqueurs génétiques.

inferred← citeshttps://doi.org/10.7732/kjpr.2015.28.1.101openalex-snapshot

Estimating the Parameters of Pollen Flow and Mating System in Pinus densiflora Population in Buan, South Korea, Using Microsatellite Markers

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.