On the public citation graph
Inferences of evolutionary history of a widely distributed mangrove species, Bruguiera gymnorrhiza, in the Indo‐West Pacific region
0 signed · 92 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf02101694openalex-snapshot
Dating of the human-ape splitting by a molecular clock of mitochondrial DNA
inferredcites →https://doi.org/10.1007/s10592-006-9151-8openalex-snapshot
Phylogeography of Ceriops tagal (Rhizophoraceae) in Southeast Asia: the land barrier of the Malay Peninsula has caused population differentiation between the Indian Ocean and South China Sea
inferredcites →https://doi.org/10.1007/s10592-009-9806-3openalex-snapshot
Highly differentiated population structure of a Mangrove species, Bruguiera gymnorhiza (Rhizophoraceae) revealed by one nuclear GapCp and one chloroplast intergenic spacer trnF–trnL
inferredcites →https://doi.org/10.1007/s10709-007-9182-1openalex-snapshot
Population genetic structure of three tree species in the mangrove genus Ceriops (Rhizophoraceae) from the Indo West Pacific
inferredcites →https://doi.org/10.1016/0304-3770(89)90105-8openalex-snapshot
Techniques for the electrophoresis of mangrove tissue
inferredcites →https://doi.org/10.1016/b978-1-4832-3211-9.50009-7openalex-snapshot
Evolution of Protein Molecules
inferredcites →https://doi.org/10.1016/j.aquabot.2009.09.003openalex-snapshot
Low genetic variation detected within the widespread mangrove species Nypa fruticans (Palmae) from Southeast Asia
inferredcites →https://doi.org/10.1016/j.plantsci.2006.03.015openalex-snapshot
Sequencing and analysis of 14,842 expressed sequence tags of burma mangrove, Bruguiera gymnorrhiza
inferredcites →https://doi.org/10.1046/j.1365-2699.2000.00489.xopenalex-snapshot
Maps of Pleistocene sea levels in Southeast Asia: shorelines, river systems and time durations
inferredcites →https://doi.org/10.1046/j.1365-294x.2000.01020.xopenalex-snapshot
TCS: a computer program to estimate gene genealogies
inferredcites →https://doi.org/10.1046/j.1365-294x.2000.01089.xopenalex-snapshot
Microsatellite analysis of genetic structure in the mangrove species Avicennia marina (Forsk.) Vierh. (Avicenniaceae)
inferredcites →https://doi.org/10.1073/pnas.0611164104openalex-snapshot
Integration within the Felsenstein equation for improved Markov chain Monte Carlo methods in population genetics
inferredcites →https://doi.org/10.1073/pnas.93.19.10274openalex-snapshot
Substitution rate comparisons between grasses and palms: synonymous rate differences at the nuclear gene Adh parallel rate differences at the plastid gene rbcL.
inferredcites →https://doi.org/10.1086/499611openalex-snapshot
Genetic Variation of Two Mangrove Species inKandelia(Rhizophoraceae) in Vietnam and Surrounding Area Revealed by Microsatellite Markers
inferredcites →https://doi.org/10.1093/bioinformatics/btm404openalex-snapshot
Clustal W and Clustal X version 2.0
inferredcites →https://doi.org/10.1093/bioinformatics/btp187openalex-snapshot
DnaSP v5: a software for comprehensive analysis of DNA polymorphism data
inferredcites →https://doi.org/10.1093/genetics/111.1.147openalex-snapshot
STATISTICAL PROPERTIES OF THE NUMBER OF RECOMBINATION EVENTS IN THE HISTORY OF A SAMPLE OF DNA SEQUENCES
inferredcites →https://doi.org/10.1093/genetics/155.2.945openalex-snapshot
Inference of Population Structure Using Multilocus Genotype Data
inferredcites →https://doi.org/10.1093/genetics/164.4.1547openalex-snapshot
DNA Variation in a Conifer, Cryptomeria japonica (Cupressaceae sensu lato)
inferredcites →https://doi.org/10.1093/genetics/164.4.1567openalex-snapshot
Inference of Population Structure Using Multilocus Genotype Data: Linked Loci and Correlated Allele Frequencies
inferredcites →https://doi.org/10.1093/genetics/61.4.893openalex-snapshot
THE NUMBER OF HETEROZYGOUS NUCLEOTIDE SITES MAINTAINED IN A FINITE POPULATION DUE TO STEADY FLUX OF MUTATIONS
inferredcites →https://doi.org/10.1093/molbev/msj100openalex-snapshot
Genetic Structure and Evolutionary History of a Diploid Hybrid Pine Pinus densata Inferred from the Nucleotide Variation at Seven Gene Loci
inferredcites →https://doi.org/10.1093/molbev/msl131openalex-snapshot
Fossil Calibration of Molecular Divergence Infers a Moderate Mutation Rate and Recent Radiations for Pinus
inferredcites →https://doi.org/10.1093/molbev/msm209openalex-snapshot
Population Genetics of Speciation in Nonmodel Organisms: I. Ancestral Polymorphism in Mangroves
inferredcites →https://doi.org/10.1093/molbev/msp296openalex-snapshot
Isolation with Migration Models for More Than Two Populations
inferredcites →https://doi.org/10.1093/molbev/msq079openalex-snapshot
Genome Wide Analyses Reveal Little Evidence for Adaptive Evolution in Many Plant Species
inferredcites →https://doi.org/10.1093/molbev/msr102openalex-snapshot
Population Genetics in Nonmodel Organisms: II. Natural Selection in Marginal Habitats Revealed by Deep Sequencing on Dual Platforms
inferredcites →https://doi.org/10.1093/nar/8.19.4321openalex-snapshot
Rapid isolation of high molecular weight plant DNA
inferredcites →https://doi.org/10.1111/j.1365-294x.2004.02396.xopenalex-snapshot
FAST‐TRACK: Integrating QTL mapping and genome scans towards the characterization of candidate loci under parallel selection in the lake whitefish (Coregonus clupeaformis)
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02553.xopenalex-snapshot
Detecting the number of clusters of individuals using the software structure : a simulation study
inferredcites →https://doi.org/10.1111/j.1365-294x.2006.02908.xopenalex-snapshot
Refugia, differentiation and postglacial migration in arctic‐alpine Eurasia, exemplified by the mountain avens ( Dryas octopetala L.)
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.03948.xopenalex-snapshot
Mating system, pollen and propagule dispersal, and spatial genetic structure in a high‐density population of the mangrove tree Kandelia candel
inferredcites →https://doi.org/10.1111/j.1558-5646.1984.tb05657.xopenalex-snapshot
ESTIMATING F -STATISTICS FOR THE ANALYSIS OF POPULATION STRUCTURE
inferredcites →https://doi.org/10.1111/j.1755-0998.2009.02591.xopenalex-snapshot
Inferring weak population structure with the assistance of sample group information
inferredcites →https://doi.org/10.1111/j.1755-0998.2010.02847.xopenalex-snapshot
Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows
inferredcites →https://doi.org/10.1186/1471-2148-8-149openalex-snapshot
Testing a hypothesis of unidirectional hybridization in plants: Observations on Sonneratia, Bruguiera and Ligularia
inferredcites →https://doi.org/10.1266/ggs.84.277openalex-snapshot
Levels and patterns of DNA variation in two sympatric mangrove species, Rhizophora apiculata and R. mucronata from Thailand
inferredcites →https://doi.org/10.1353/psc.2001.0004openalex-snapshot
Maximum Longevities of Rhizophora apiculata and R. mucronata Propagules
inferredcites →https://doi.org/10.1371/journal.pone.0019671openalex-snapshot
Genomic Markers Reveal Introgressive Hybridization in the Indo-West Pacific Mangroves: A Case Study
inferredcites →https://doi.org/10.1534/genetics.104.033795openalex-snapshot
A Multilocus Sequence Survey in Arabidopsis thaliana Reveals a Genome-Wide Departure From a Neutral Model of DNA Sequence Polymorphism
inferredcites →https://doi.org/10.2307/2997695openalex-snapshot
Factors Influencing Biodiversity and Distributional Gradients in Mangroves
inferredcites →https://doi.org/10.3732/ajb.1000392openalex-snapshot
Postglacial north–south expansion of populations of Rhizophora mangle (Rhizophoraceae) along the Brazilian coast revealed by microsatellite analysis
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.4885613openalex-extracted
Global Warming Exacerbates the Risk of Habitat Loss for Regional Mangrove Species
inferred← citeshttps://doi.org/10.1002/ece3.5099openalex-snapshot
The presence of a cryptic barrier in the West Pacific Ocean suggests the effect of glacial climate changes on a widespread sea‐dispersed plant, Vigna marina (Fabaceae)
inferred← citeshttps://doi.org/10.1002/ece3.6460openalex-snapshot
Land masses and oceanic currents drive population structure of Heritiera littoralis, a widespread mangrove in the Indo‐West Pacific
inferred← citeshttps://doi.org/10.1007/978-981-13-5832-6_8openalex-snapshot
Current Understanding of the Mangrove Forests of India
inferred← citeshttps://doi.org/10.1007/978-981-16-2494-0_2openalex-snapshot
Biogeography of the Mangrove Ecosystem: Floristics, Population Structure, and Conservation Strategies
inferred← citeshttps://doi.org/10.1007/s10592-014-0647-3openalex-snapshot
Closely related and sympatric but not all the same: genetic variation of Indo-West Pacific Rhizophora mangroves across the Malay Peninsula
inferred← citeshttps://doi.org/10.1007/s10592-016-0849-yopenalex-snapshot
Bruguiera hainesii, a critically endangered mangrove species, is a hybrid between B. cylindrica and B. gymnorhiza (Rhizophoraceae)
inferred← citeshttps://doi.org/10.1007/s10750-017-3409-7openalex-snapshot
Chloroplast phylogeography of a widely distributed mangrove species, Excoecaria agallocha, in the Indo-West Pacific region
inferred← citeshttps://doi.org/10.1007/s10750-020-04372-1openalex-snapshot
Chloroplast DNA phylogeography of the Holly mangrove Acanthus ilicifolius in the Indo-West Pacific
inferred← citeshttps://doi.org/10.1016/j.ecss.2026.110228openalex-snapshot
Southeast African mangroves: an exceptionally young paleobotanical record
inferred← citeshttps://doi.org/10.1016/j.egg.2020.100078openalex-snapshot
A review on the genetic structure of ecologically and economically important mangrove species in the Indo-West Pacific
inferred← citeshttps://doi.org/10.1016/j.foreco.2017.10.026openalex-snapshot
Historical seed use and transfer affects geographic specificity in genetic diversity and structure of old planted Pinus thunbergii populations
inferred← citeshttps://doi.org/10.1016/j.rsma.2021.101861openalex-snapshot
Moving past barriers — Sea-drifted seeds shape regional distribution of genetic diversity of a coastal legume in the Indo-West Pacific
inferred← citeshttps://doi.org/10.1038/s41598-021-84304-8openalex-snapshot
Expansion of the mangrove species Rhizophora mucronata in the Western Indian Ocean launched contrasting genetic patterns
inferred← citeshttps://doi.org/10.1038/s41598-025-04364-yopenalex-snapshot
Global warming exacerbates the risk of habitat loss for regional mangrove species
inferred← citeshttps://doi.org/10.1038/srep29486openalex-snapshot
Pronounced genetic differentiation and recent secondary contact in the mangrove tree Lumnitzera racemosa revealed by population genomic analyses
inferred← citeshttps://doi.org/10.1093/g3journal/jkaa025openalex-snapshot
A high-quality genome assembly and annotation of the gray mangrove, Avicennia marina
inferred← citeshttps://doi.org/10.1093/treephys/tpag072openalex-snapshot
Response of two mangrove species to elevated temperatures: a comparative study on photosynthetic physiological sensitivity and acclimation to simulated climate warming
inferred← citeshttps://doi.org/10.1111/ddi.70147openalex-snapshot
Population Genetic Structure and Colonisation History of the Widely Distributed Mangrove Avicennia marina Across the Western Indian Ocean
inferred← citeshttps://doi.org/10.1111/gcb.13968openalex-snapshot
Extremely low genetic diversity across mangrove taxa reflects past sea level changes and hints at poor future responses
inferred← citeshttps://doi.org/10.1111/jbi.12770openalex-snapshot
Genetic discontinuities in a dominant mangrove Rhizophora apiculata (Rhizophoraceae) in the Indo‐Malesian region
inferred← citeshttps://doi.org/10.1111/jbi.13151openalex-snapshot
Differing phylogeographic patterns within the Indo‐West Pacific mangrove genus Xylocarpus (Meliaceae)
inferred← citeshttps://doi.org/10.1111/jse.12746openalex-snapshot
Deciphering the global phylogeography of a coastal shrub (Scaevola taccada) reveals the influence of multiple forces on contemporary population structure
inferred← citeshttps://doi.org/10.1111/jse.12923openalex-snapshot
Deep phylogeographic splits and limited mixing by sea surface currents govern genetic population structure in the mangrove genus Lumnitzera (Combretaceae) across the Indonesian Archipelago
inferred← citeshttps://doi.org/10.1111/mec.16290openalex-snapshot
Population subdivision promoted by a sea‐level‐change‐driven bottleneck: A glimpse from the evolutionary history of the mangrove plant Aegiceras corniculatum
inferred← citeshttps://doi.org/10.1111/mec.17260openalex-snapshot
Rapid diversification of grey mangroves (Avicennia marina) driven by geographic isolation and extreme environmental conditions in the Arabian Peninsula
inferred← citeshttps://doi.org/10.1186/s12862-016-0849-zopenalex-snapshot
Effects of Pleistocene sea-level fluctuations on mangrove population dynamics: a lesson from Sonneratia alba
inferred← citeshttps://doi.org/10.1186/s12870-015-0560-zopenalex-snapshot
Biogeography of the Phalaenopsis amabilis species complex inferred from nuclear and plastid DNAs
inferred← citeshttps://doi.org/10.13057/biodiv/d230962openalex-snapshot
Mangrove zonation, community structure and healthiness in Kei Islands, Maluku, Indonesia
inferred← citeshttps://doi.org/10.1360/ssv-2024-0144openalex-snapshot
Phylogenetic origin, population evolution, and ecological adaptation of Mangroves
inferred← citeshttps://doi.org/10.1515/bot-2026-0058openalex-snapshot
Phylogenetics of Bruguiera spp. from the west coast of Peninsular Malaysia with emphasis on the population genetic structure of Bruguiera gymnorrhiza
inferred← citeshttps://doi.org/10.22541/au.165451878.80994363/v4openalex-snapshot
Rapid diversification of gray mangroves ( Avicennia marina ) driven by geographic isolation and extreme environmental conditions in the Arabian Peninsula
inferred← citeshttps://doi.org/10.3354/ab00761openalex-snapshot
Genetic diversity and population structure of the upriver orange mangrove Bruguiera sexangula along the coastlines of Thailand
inferred← citeshttps://doi.org/10.3389/fcosc.2021.726676openalex-snapshot
Complete Chloroplast Genome Variants Reveal Discrete Long-Distance Dispersal Routes of Rhizophora in the Western Indian Ocean
inferred← citeshttps://doi.org/10.3389/fmars.2025.1565908openalex-snapshot
Migration history of Avicennia marina populations: a legacy of mangrove expansion on the Sunda Shelf
inferred← citeshttps://doi.org/10.3389/fpls.2016.01434openalex-snapshot
Comparative Analysis of the Pattern of Population Genetic Diversity in Three Indo-West Pacific Rhizophora Mangrove Species
inferred← citeshttps://doi.org/10.3389/fpls.2016.01618openalex-snapshot
Ancient Geographical Barriers Drive Differentiation among Sonneratia caseolaris Populations and Recent Divergence from S. lanceolata
inferred← citeshttps://doi.org/10.3389/fpls.2021.637009openalex-snapshot
Contrasting Phylogeographic Patterns in Lumnitzera Mangroves Across the Indo-West Pacific
inferred← citeshttps://doi.org/10.3390/f14040693openalex-snapshot
Elucidating SNP-Based Population Structure and Genetic Diversity of Bruguiera gymnorhiza (L.) Savigny in Thailand
inferred← citeshttps://doi.org/10.3390/f8120480openalex-snapshot
Genetic Structure and Population Demographic History of a Widespread Mangrove Plant Xylocarpus granatum J. Koenig across the Indo-West Pacific Region
inferred← citeshttps://doi.org/10.3390/pharmaceutics14112406openalex-snapshot
Halophyte Plants as Potential Sources of Anticancer Agents: A Comprehensive Review
inferred← citeshttps://doi.org/10.7287/peerj.4315v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Strong genetic differentiation in tropical seagrass Enhalus acoroides (Hydrocharitaceae) at the Indo-Malay Archipelago revealed by microsatellite DNA (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.4315v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Strong genetic differentiation in tropical seagrass Enhalus acoroides (Hydrocharitaceae) at the Indo-Malay Archipelago revealed by microsatellite DNA (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.4315v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Strong genetic differentiation in tropical seagrass Enhalus acoroides (Hydrocharitaceae) at the Indo-Malay Archipelago revealed by microsatellite DNA (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.4315v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Strong genetic differentiation in tropical seagrass Enhalus acoroides (Hydrocharitaceae) at the Indo-Malay Archipelago revealed by microsatellite DNA (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.4315v0.3/reviews/2openalex-snapshot
Peer Review #2 of "Strong genetic differentiation in tropical seagrass Enhalus acoroides (Hydrocharitaceae) at the Indo-Malay Archipelago revealed by microsatellite DNA (v0.3)"
inferred← citeshttps://doi.org/10.7717/peerj.12268openalex-snapshot
Complete chloroplast genome sequences of five Bruguiera species (Rhizophoraceae): comparative analysis and phylogenetic relationships
inferred← citeshttps://doi.org/10.7717/peerj.4315openalex-snapshot
Strong genetic differentiation in tropical seagrass Enhalus acoroides (Hydrocharitaceae) at the Indo-Malay Archipelago revealed by microsatellite DNA
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.