Age and rate of diversification of the Hawaiian silversword alliance (Compositae) - Wikidata - wikimedia - TriplyDB

Age and rate of diversification of the Hawaiian silversword alliance (Compositae)

Age and rate of diversification of the Hawaiian silversword alliance (Compositae)

http://www.wikidata.org/entity/Q28776525

about

Moorean tree snail survival revisited: a multi-island genealogical perspective Going to Extremes: Contrasting Rates of Diversification in a Recent Radiation of New World Passerine Birds Whole-mtDNA Genome Sequence Analysis of Ancient African Lineages Using plastid genome-scale data to resolve enigmatic relationships among basal angiosperms Timing the origin and expansion of the Mexican tropical dry forest.Density-dependent diversification in North American wood warblers Origin, adaptive radiation and diversification of the Hawaiian lobeliads (Asterales: Campanulaceae)Rosid radiation and the rapid rise of angiosperm-dominated forests Explosive Pleistocene diversification and hemispheric expansion of a "great speciator"How old is the Hawaiian biota? Geology and phylogeny suggest recent divergence Biogeographic calibrations for the molecular clock Confluence, synnovation, and depauperons in plant diversification Páramo is the world's fastest evolving and coolest biodiversity hotspot The origins of reproductive isolation in plants Unequal evolutionary rates between annual and perennial lineages of checker mallows (Sidalcea, Malvaceae): evidence from 18S-26S rDNA internal and external transcribed spacers Molecular phylogeny, recent radiation and evolution of gross morphology of the rhubarb genus Rheum (Polygonaceae) inferred from chloroplast DNA trnL-F sequences Multiple intercontinental dispersals shaped the distribution area of Hordeum (Poaceae)The abiotic and biotic drivers of rapid diversification in Andean bellflowers (Campanulaceae)Species diversity driven by morphological and ecological disparity: a case study of comparative seed morphology and anatomy across a large monocot order Evolution in an extreme environment: developmental biases and phenotypic integration in the adaptive radiation of antarctic notothenioids Equilibrium and non-equilibrium dynamics simultaneously operate in the Galápagos islands Spintharus flavidus in the Caribbean-a 30 million year biogeographical history and radiation of a 'widespread species'Evolution of Asian Interior Arid-Zone Biota: Evidence from the Diversification of Asian Zygophyllum (Zygophyllaceae)Multiple independent origins of auto-pollination in tropical orchids (Bulbophyllum) in light of the hypothesis of selfing as an evolutionary dead end Oligocene niche shift, Miocene diversification - cold tolerance and accelerated speciation rates in the St. John's Worts (Hypericum, Hypericaceae)The establishment of Central American migratory corridors and the biogeographic origins of seasonally dry tropical forests in Mexico Impact of the terrestrial-aquatic transition on disparity and rates of evolution in the carnivoran skull Global phylogenetic structure of the hyperdiverse ant genus Pheidole reveals the repeated evolution of macroecological patterns Molecular systematics and biogeography of Crawfurdia, Metagentiana and Tripterospermum (Gentianaceae) based on nuclear ribosomal and plastid DNA sequences Phylogenetics of the antopocerus-modified tarsus clade of Hawaiian Drosophila: diversification across the Hawaiian Islands Ecological opportunity and the adaptive diversification of lineages Eocene diversification of crown group rails (Aves: Gruiformes: Rallidae)Building megaphylogenies for macroecology: taking up the challenge Multiple ITS copies reveal extensive hybridization within Rheum (Polygonaceae), a genus that has undergone rapid radiation The explosive radiation of Cheirolophus (Asteraceae, Cardueae) in Macaronesia On the biogeography of Centipeda: a species-tree diffusion approach Molecular phylogenetics of New Caledonian Diospyros (Ebenaceae) using plastid and nuclear markers Evidence of constant diversification punctuated by a mass extinction in the African cycads The timetable for allopolyploidy in flowering plants Diversification and dispersal of the Hawaiian Drosophilidae: the evolution of Scaptomyza

P2860

Q21093405-CC087B84-954E-4FC4-8064-044F05C84F76 Q21994772-585EA273-4569-4D33-9773-CAE10BC4D3DF Q22066015-88BD8EB8-85B7-46A9-8677-595D7F6081EC Q22066318-87A8D79A-39B5-4DA6-BD5E-00B7550B1BE5 Q24534318-205A80AD-30C8-4370-B515-E436C913FEE0 Q24644802-D639116B-CD6B-482A-845D-572ABD4CCCF6 Q24648292-AA423BAF-3F91-4520-9808-8894C1D2031A Q24651414-FA542351-5151-4AD7-B70D-D849EC49A0BC Q24651677-4EAAEDC9-CEB7-4A81-9E2F-3DD44F9C3D3C Q24669838-CB57A4C1-E1F8-4E4B-BDA4-1462926633FD Q26786387-CC1992B0-26FE-4F7F-93A0-3AFB0D8463DD Q26828042-CA1798BA-D827-4C8B-94A9-1E1EEBACFD8D Q27021176-85C864DB-78BC-4D65-BD81-F33758C3EB33 Q27022437-6F2750A5-2754-4177-8EDB-124EDB6197E3 Q28190408-31B367D5-1B40-4E06-A0B9-8D8101ECE1B3 Q28259760-AD98E606-7A05-4CDD-83C0-DE255845FA76 Q28291769-FD98F21C-6265-4126-AE05-52E0DE966DF2 Q28596111-33DBA576-BBCC-40E8-A631-EC28F0F8356B Q28596616-2643F45B-FE2E-4D3A-80F8-9D613741FD98 Q28597017-55BD6648-D679-4D93-85B5-14E5179C7FB7 Q28601189-BC8C9968-CE72-423B-98AC-94A9A7C8F358 Q28607148-EB4BE334-55F3-4137-B7E3-75516E3AB6D6 Q28607379-BB38ECC7-0049-4F0C-A017-CF4A1261A9D3 Q28607542-B2BD6624-0A6C-4A1C-91B9-9A97D9534098 Q28647944-315D1F72-E41F-4742-92E1-A9C28FB0B72B Q28649494-F045DCC0-B56A-4CED-9849-505DCA74D41B Q28649932-198680EB-696A-4FDA-8C1A-E7D1E0191C7B Q28650031-C20F4F68-AFBB-4404-BEC0-2893F31C6345 Q28651117-7406F728-5326-4161-9089-16198F1A6DD5 Q28651516-0533191F-E700-41E0-AB0D-85B39FA3606C Q28652099-322B95FF-A152-4B15-861C-863D4A3ADF3F Q28654929-A992B839-605D-456A-AC21-B7E123AD1E71 Q28658248-3A0A6AE2-4C73-4BAC-9D59-60E81917A170 Q28658460-146D99D2-CE25-4228-9E4E-2EC26585CB6D Q28658702-74A269C8-3B28-415F-8AF2-C1DCE43F1E01 Q28659007-1A72511A-62FE-444F-9D5F-7B1DE89DFED0 Q28659564-35B8BA7F-4D4C-44BE-816E-08C12B6EF51D Q28660553-2194CB6E-68E2-461C-B381-9929956BCCFE Q28662194-CFFDB220-FFBA-4022-8F6C-BB160B83195C Q28681071-F0C28F3F-6949-42C5-95E5-731E97833BC5

P2860

Age and rate of diversification of the Hawaiian silversword alliance (Compositae)

http://www.wikidata.org/entity/Q28776525

description

1998 nî lūn-bûn

@nan

1998 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

1998年の論文

@ja

1998年論文

@yue

1998年論文

@zh-hant

1998年論文

@zh-hk

1998年論文

@zh-mo

1998年論文

@zh-tw

1998年论文

@wuu

name

Age and rate of diversification of the Hawaiian silversword alliance (Compositae)

@ast

Age and rate of diversification of the Hawaiian silversword alliance (Compositae)

@en

type

label

Age and rate of diversification of the Hawaiian silversword alliance (Compositae)

@ast

Age and rate of diversification of the Hawaiian silversword alliance (Compositae)

@en

prefLabel

Age and rate of diversification of the Hawaiian silversword alliance (Compositae)

@ast

Age and rate of diversification of the Hawaiian silversword alliance (Compositae)

@en

P1433

Q28776525-C7342AE9-D595-4BFB-85D0-77397F70CC96

P1476

Q28776525-C835A67D-EC82-4058-99E6-A826FA7ED9EB

P2093

Q28776525-40B3DBB1-8C51-4F54-88E6-F49CA58D726D

Q28776525-8F3ED08B-24D6-4D01-B20A-E798C02B49D3

P2860

Q28776525-3134FAE2-AF56-4982-B5CB-A38340B7223D

Q28776525-3753FE3D-76A2-4B43-B2D1-E839F79D70EC

Q28776525-3A4F9DC1-36F6-43E7-97BC-5FBBEC82E6A2

Q28776525-3BE38D14-2E2E-41AF-B92B-30ABABA29107

Q28776525-73FF9680-D0DE-4DC4-804A-CBF47CE6D1A9

Q28776525-7E648078-D8E5-4A31-A2BE-D0C4CC3978AE

Q28776525-83F0864E-F3A4-459D-BB52-FE6F37C71ECC

Q28776525-8CEDCE8B-6534-400C-8F0C-2D1E1773B5FF

Q28776525-8E6E2D22-2419-4311-A670-AE3099653596

Q28776525-A4923091-81A3-44C9-9151-D46166BABA64

P304

Q28776525-89F235E3-C819-4C30-AC66-539FCA8406A4

P31

Q28776525-A88A6496-153E-465D-810A-549D30EF53AE

P3181

Q28776525-B86EA759-1A5E-4A3B-BFCE-1D05DBD47D5F

P356

Q28776525-929618DC-F8D9-4EE3-AC30-B21F9EFEC509

P407

Q28776525-49209DCC-8F53-4AD3-A2D8-24A10A7F7FFA

P433

Q28776525-6DE44477-E119-4A3A-8EFF-EF97E3A987A5

P478

Q28776525-F1559E8E-7AE0-407C-88CB-1840B7C57880

P577

Q28776525-C7635846-B0C7-4AD1-B12E-89F58B642A80

P5875

Q28776525-F38DB5CA-28E4-4530-A0D4-0427D820A776

P698

Q28776525-FD2EA6E1-6C3D-4865-8F69-74E77CA87D39

P932

Q28776525-7135CB0A-ACD3-4B79-BABB-240717D73DF0

P3181

P356

PNAS.95.16.9402

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Age and rate of diversification of the Hawaiian silversword alliance (Compositae)

@en

P2093

B G Baldwin

http://www.w3.org/2001/XMLSchema#string

M J Sanderson

http://www.w3.org/2001/XMLSchema#string

P2860

Origin of the metazoan phyla: molecular clocks confirm paleontological estimates

Phylogenetic utility of the internal transcribed spacers of nuclear ribosomal DNA in plants: an example from the compositae

Phylogenies from molecular sequences: inference and reliability

Phylogenetic methods come of age: testing hypotheses in an evolutionary context

Among-site rate variation and its impact on phylogenetic analyses

The reconstructed evolutionary process

The molecular evolution of the alcohol dehydrogenase locus and the phylogeny of Hawaiian Drosophila.

Chloroplast DNA evidence for a North American origin of the Hawaiian silversword alliance (Asteraceae).

Concerted evolution of repetitive DNA sequences in eukaryotes.

Correlated rates of synonymous site evolution across plant genomes.

P304

9402-6

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

393032

http://www.w3.org/2001/XMLSchema#string

P356

10.1073/PNAS.95.16.9402

http://www.w3.org/2001/XMLSchema#string

P407

P433

16

http://www.w3.org/2001/XMLSchema#string

P478

95

http://www.w3.org/2001/XMLSchema#string

P577

1998-08-04T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

13596314

http://www.w3.org/2001/XMLSchema#string

P698

9689092

http://www.w3.org/2001/XMLSchema#string

P932

21350

http://www.w3.org/2001/XMLSchema#string