| P50 | author | W. John Kress | Q6166224 |
| | Aleena Xavier | Q127779251 |
| | Vinita Gowda | Q21812824 |
| | Marlina Ardiyani | Q36619715 |
| | Ajith Ashokan | Q88806388 |
| P2093 | author name string | Piyakaset Suksathan | |
| | Jana Leong-Škorničková | |
| | Mark Newman | |
| P2860 | cites work | The Anolis Lizards of Bimini: Resource Partitioning in a Complex Fauna | Q101634667 |
| | Progress on Southeast Asia’s Flora projects | Q104120562 |
| | Tempo and mode in evolution: phylogenetic inertia, adaptation and comparative methods | Q104206903 |
| | Diversity hotspots: Coldspots of speciation? | Q104281806 |
| | Plants will cross the lines: climate and available land mass are the major determinants of phytogeographical patterns in the Sunda–Sahul Convergence Zone | Q105882011 |
| | PHYLOGENY OF HEDYCHIUM AND RELATED GENERA (ZINGIBERACEAE) BASED ON ITS SEQUENCE DATA | Q109828720 |
| | Biodiversity hotspots for conservation priorities | Q22122401 |
| | Bayesian phylogenetics with BEAUti and the BEAST 1.7 | Q24286945 |
| | SIMMAP: stochastic character mapping of discrete traits on phylogenies | Q25255632 |
| | Maximum likelihood inference of geographic range evolution by dispersal, local extinction, and cladogenesis | Q28267497 |
| | Automatic detection of key innovations, rate shifts, and diversity-dependence on phylogenetic trees | Q28540154 |
| | The abiotic and biotic drivers of rapid diversification in Andean bellflowers (Campanulaceae) | Q28596111 |
| | Biotic interchange between the Indian subcontinent and mainland Asia through time | Q28596822 |
| | Evolutionary dynamics and biogeography of Musaceae reveal a correlation between the diversification of the banana family and the geological and climatic history of Southeast Asia | Q28597383 |
| | Evolution of Epiphytism and Fruit Traits Act Unevenly on the Diversification of the Species-Rich Genus Peperomia (Piperaceae) | Q28598125 |
| | Origin and diversification of living cycads: a cautionary tale on the impact of the branching process prior in Bayesian molecular dating | Q28646401 |
| | Refugial isolation and range expansions drive the genetic structure of Oxyria sinensis (Polygonaceae) in the Himalaya-Hengduan Mountains | Q28647010 |
| | Evolutionary diversifications of plants on the Qinghai-Tibetan Plateau | Q28659210 |
| | BEAST 2: a software platform for Bayesian evolutionary analysis | Q28660145 |
| | Undersampling taxa will underestimate molecular divergence dates: an example from the South american lizard clade liolaemini | Q28662094 |
| | The role of glacial cycles in promoting genetic diversity in the Neotropics: the case of cloud forests during the Last Glacial Maximum | Q28709613 |
| | Effects of Pleistocene glaciations and rivers on the population structure of Bornean orangutans (Pongo pygmaeus) | Q28744138 |
| | The current refugial rainforests of Sundaland are unrepresentative of their biogeographic past and highly vulnerable to disturbance | Q28752292 |
| | Atmosphere, ecology and evolution: what drove the Miocene expansion of C(4) grasslands? | Q28757382 |
| | PHYLOGENY AND DISJUNCTION IN ROSCOEA (ZINGIBERACEAE) | Q29038303 |
| | Southeast Asian biodiversity: an impending disaster | Q29303487 |
| | Terrestrial Ecoregions of the World: A New Map of Life on Earth | Q29543325 |
| | APE: Analyses of Phylogenetics and Evolution in R language | Q29546513 |
| | Inferring the historical patterns of biological evolution | Q29547170 |
| | Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data | Q29547401 |
| | Universal primers for amplification of three non-coding regions of chloroplast DNA | Q29547617 |
| | Environmental niche equivalency versus conservatism: quantitative approaches to niche evolution | Q29616175 |
| | The Impacts of Oil Palm on Recent Deforestation and Biodiversity Loss. | Q30382384 |
| | Borneo and Indochina are major evolutionary hotspots for Southeast Asian biodiversity. | Q30839239 |
| | Getting the measure of biodiversity. | Q30872577 |
| | Selectivity in mammalian extinction risk and threat types: a new measure of phylogenetic signal strength in binary traits | Q33534424 |
| | Ecological opportunity and the origin of adaptive radiations | Q33609183 |
| | Uplift-driven diversification in the Hengduan Mountains, a temperate biodiversity hotspot | Q33620073 |
| | Improving marginal likelihood estimation for Bayesian phylogenetic model selection | Q34571311 |
| | Bayesian evolutionary model testing in the phylogenomics era: matching model complexity with computational efficiency | Q34772835 |
| | Adaptive radiation, correlated and contingent evolution, and net species diversification in Bromeliaceae | Q35090108 |
| | The role of the uplift of the Qinghai-Tibetan Plateau for the evolution of Tibetan biotas. | Q35160591 |
| | The ubiquity of alpine plant radiations: from the Andes to the Hengduan Mountains | Q35545622 |
| | Adaptive radiation versus 'radiation' and 'explosive diversification': why conceptual distinctions are fundamental to understanding evolution | Q35649102 |
| | Plastid primers for angiosperm phylogenetics and phylogeography | Q35665658 |
| | Is BAMM flawed? Theoretical and practical concerns in the analysis of multi-rate diversification models | Q36320328 |
| | Plio-Pleistocene phylogeography of the Southeast Asian Blue Panchax killifish, Aplocheilus panchax | Q38368955 |
| | The phylogeny, evolution, and classification of the genus Globba and tribe Globbeae (Zingiberaceae): appendages do matter | Q39595487 |
| | Detecting Hidden Diversification Shifts in Models of Trait-Dependent Speciation and Extinction | Q39887706 |
| | Eco-evolutionary dynamics. | Q43118522 |
| | Model selection in historical biogeography reveals that founder-event speciation is a crucial process in Island Clades | Q43506643 |
| | Phylogeographic evidence for the existence of an ancient biogeographic barrier: the Isthmus of Kra Seaway | Q45331154 |
| | Out of the Qinghai-Tibet Plateau: evidence for the origin and dispersal of Eurasian temperate plants from a phylogeographic study of Hippophaë rhamnoides (Elaeagnaceae). | Q47851584 |
| | Parallelization of MAFFT for large-scale multiple sequence alignments. | Q51557070 |
| | Using an integrated approach to identify cryptic species, divergence patterns and hybrid species in Asian ladies' tresses orchids (Spiranthes, Orchidaceae). | Q52368418 |
| | A biologist's guide to Bayesian phylogenetic analysis. | Q54339947 |
| | Maps of Pleistocene sea levels in Southeast Asia: shorelines, river systems and time durations | Q55882640 |
| | Evolutionary diversification of alpine ginger reflects the early uplift of the Himalayan–Tibetan Plateau and rapid extrusion of Indochina | Q56030926 |
| | Ecological Opportunity and Adaptive Radiation | Q56038385 |
| | The biogeographic regions reconsidered | Q56048007 |
| | WorldClim 2: new 1-km spatial resolution climate surfaces for global land areas | Q56210311 |
| | ecospat: an R package to support spatial analyses and modeling of species niches and distributions | Q56331633 |
| | Phylogenetics of Utricularia (Lentibulariaceae) and molecular evolution of the trnK intron in a lineage with high substitutional rates | Q56480682 |
| | The biogeographic and tectonic history of India | Q56503461 |
| | Measuring ecological niche overlap from occurrence and spatial environmental data | Q56567714 |
| | Chloroplast rps16 intron phylogeny of the tribe Sileneae (Caryophyllaceae) | Q56639854 |
| | phytools: an R package for phylogenetic comparative biology (and other things) | Q56659873 |
| | Frugivory by introduced black rats (Rattus rattus) promotes dispersal of invasive plant seeds | Q56764009 |
| | Building the monocot tree of death: Progress and challenges emerging from the macrofossil-rich Zingiberales | Q56803987 |
| | Phylogenetic Analyses of Polemoniaceae Using Nucleotide Sequences of the Plastid Gene matK | Q57141869 |
| | Bayesian estimation of the global biogeographical history of the Solanaceae | Q57217968 |
| | Evaluating the influence of connectivity and distance on biogeographical patterns in the south-western deserts of North America | Q57217988 |
| | Posterior Summarization in Bayesian Phylogenetics Using Tracer 1.7 | Q57272965 |
| | The Evolutionary and Biogeographic Origin and Diversification of the Tropical Monocot Order Zingiberales | Q57568718 |
| | The Brahmaputra tale of tectonics and erosion: Early Miocene river capture in the Eastern Himalaya | Q57685811 |
| | Quantifying the rise of the Himalaya orogen and implications for the South Asian monsoon | Q57978570 |
| | Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi-gene analyses, and a functional model for the origin of monocots | Q58117888 |
| | Nuclear and chloroplast DNA phylogeography suggests an Early Miocene southward expansion of Lithocarpus (Fagaceae) on the Asian continent and islands | Q58576866 |
| | Geophysical upheavals and evolutionary diversification of plant species in the Himalaya | Q58695782 |
| | SequenceMatrix: concatenation software for the fast assembly of multi-gene datasets with character set and codon information | Q59359180 |
| | Large rivers and orogens: The evolution of the Yarlung Tsangpo–Irrawaddy system and the eastern Himalayan syntaxis | Q59837615 |
| | Volcanic Phenomena in Borneo | Q60274789 |
| | Evolutionary significance of seed structure in Alpinioideae (Zingiberaceae) | Q60560945 |
| | (Zingiberaceae), a new species of ginger lily from Northeast India | Q61798952 |
| | Mid-Pleistocene transition in glacial cycles explained by declining CO and regolith removal | Q63071776 |
| | Intensification of the Asian monsoon and a chemical weathering event in the late Miocene–early Pliocene: Implications for late Neogene climate change | Q63259125 |
| | Mountains as Evolutionary Arenas: Patterns, Emerging Approaches, Paradigm Shifts, and Their Implications for Plant Phylogeographic Research in the Tibeto-Himalayan Region | Q64079855 |
| | Resolving the rapid plant radiation of early diverging lineages in the tropical Zingiberales: Pushing the limits of genomic data | Q90665157 |
| | Autopolyploid lineage shows climatic niche expansion but not divergence in Arabidopsis arenosa | Q90880302 |
| | Tibet, the Himalaya, Asian monsoons and biodiversity - In what ways are they related? | Q91215281 |
| | Hidden state models improve state-dependent diversification approaches, including biogeographical models | Q91503463 |
| | Origin and evolution of the genus Piper in Peninsular India | Q92317603 |
| | The ecology and significance of below-ground bud banks in plants | Q92541713 |
| | Plants obey (and disobey) the island rule | Q92709103 |
| | Geophytism in monocots leads to higher rates of diversification | Q93009574 |
| | Extant timetrees are consistent with a myriad of diversification histories | Q93164031 |
| | Southeast Asia's changing palaeogeography | Q96025136 |
| | The convergence history of India-Eurasia records multiple subduction dynamics processes | Q96137168 |
| | Ancient orogenic and monsoon-driven assembly of the world's richest temperate alpine flora | Q98176053 |
| | Species complex delimitations in the genus Hedychium: A machine learning approach for cluster discovery | Q98240831 |
| P921 | main subject | Zingiberaceae | Q37021 |
| P304 | page(s) | 107440 | |
| P577 | publication date | 2022-05-01 | |
| P1433 | published in | Molecular Phylogenetics and Evolution | Q4248868 |
| P1545 | series ordinal | 107440 | |
| P1476 | title | Himalayan orogeny and monsoon intensification explain species diversification in an endemic ginger (Hedychium: Zingiberaceae) from the Indo-Malayan Realm | |
| P478 | volume | 170 | |