about
Species-specific traits plus stabilizing processes best explain coexistence in biodiverse fire-prone plant communities.The anatomy and chemistry of the colour bands of grasstree stems (Xanthorrhoea preissii) used for plant age and fire history determinationPre-Gondwanan-breakup origin of Beauprea (Proteaceae) explains its historical presence in New Caledonia and New ZealandA Cretaceous origin for fire adaptations in the Cape floraSeed size, fecundity and postfire regeneration strategy are interdependent in HakeaFire-adapted Gondwanan Angiosperm floras evolved in the CretaceousHerbivory, serotiny and seedling defence in Western Australian Proteaceae.Banksia born to burnThe worldwide leaf economics spectrumLong-distance seed dispersal in a metapopulation of Banksia hookeriana inferred from a population allocation analysis of amplified fragment length polymorphism data.Soil vs. canopy seed storage and plant species coexistence in species-rich Australian shrublands.Relative effects of mammal herbivory and plant spacing on seedling recruitment following fire and mining.Temporal patterns of genetic variation across a 9-year-old aerial seed bank of the shrub Banksia hookeriana (Proteaceae).Simulating the effects of different spatio-temporal fire regimes on plant metapopulation persistence in a Mediterranean-type region.The fire ephemeral Tersonia cyathiflora (Gyrostemonaceae) germinates in response to smoke but not the butenolide 3-methyl-2H-furo[2,3-c]pyran-2-oneFire-adapted traits of Pinus arose in the fiery Cretaceous.Low rate of between-population seed dispersal restricts genetic connectivity and metapopulation dynamics in a clonal shrub.Fire-Proneness as a Prerequisite for the Evolution of Fire-Adapted Traits.Genetic connectivity and inter-population seed dispersal of Banksia hookeriana at the landscape scale.A test for lottery recruitment among four Banksia species based on their demography and biological attributes.Assessing the generality of global leaf trait relationships.Small-seeded Hakea species tolerate cotyledon loss better than large-seeded congenersSeed dormancy, after-ripening and light requirements of four annual Asteraceae in south-western Australia.Ants cannot account for interpopulation dispersal of the arillate pea Daviesia triflora.Response to water deficit and high temperature of transgenic peas (Pisum sativum L.) containing a seed-specific alpha-amylase inhibitor and the subsequent effects on pea weevil (Bruchus pisorum L.) survival.Leaf specific mass confounds leaf density and thickness.LMA, density and thickness: recognizing different leaf shapes and correcting for their nonlaminarity.Soil bacteria hold the key to root cluster formation.Unearthing belowground bud banks in fire-prone ecosystems.Contrasting impacts of pollen and seed dispersal on spatial genetic structure in the bird-pollinated Banksia hookeriana.Polymorphic microsatellite DNA markers for Banksia hookeriana (Proteaceae).Population fragmentation may reduce fertility to zero in Banksia goodii - a demonstration of the Allee effect.Fire enhances weed invasion of roadside vegetation in southwestern AustraliaEvolutionary history of fire-stimulated resprouting, flowering, seed release and germinationKangaroos Avoid Eating Seedlings with or Near Others with Volatile Essential OilsQ60325057
P50
Q27317358-F49AD578-82C5-4498-8C81-FA3235B2398BQ28315810-1F0062CD-2623-45F1-A85C-A2E0F5264901Q28596984-1E077D30-0FC2-4AD1-BAC3-280ECB81B367Q28597972-E9615815-204D-4D26-8226-AED7CC0867B8Q28645964-D43F3387-3266-45B6-9FD3-ABED218DE4CEQ28710135-B7089473-2F60-4825-B6C0-729204A1FCD1Q29392584-61FBAE18-95EE-4805-B060-4F0E544FF39FQ29544096-C6F21744-C70A-4773-8E3C-D2E1B463B37DQ29616838-8978CAC3-BD1B-4C59-B72B-1AF9E62AD098Q30920789-FFAFA8B0-5BFE-4CD6-9271-801761C8AE52Q33301682-621FFC7A-6FF6-4C4E-9111-0D3C79F15DB9Q33304243-FBDA5C22-A885-4C8C-B173-C56114DAFC82Q33449158-2B822A86-2281-4649-9FEB-81E5076CD562Q33450541-D8E58B2B-6AD3-464C-B7C8-9D09C1795835Q34012207-2AEACF84-E9F3-41D1-A91C-1C82390E7D57Q34255630-F39AC640-DAFA-472B-8191-ADA44FA24198Q34500785-500FEB62-DD80-4E38-A0DE-D0B1D092FCA8Q39029818-AA011BD8-8BB4-4713-AD3B-F8EA71A24C50Q39061467-0B56AEF1-1F4A-4670-8CA6-14EB0DEA625DQ39158737-C430A4DD-DAA7-47D2-9C17-AADDF27E8D9CQ40431916-FFA17F5C-3EF1-4C19-9097-2B00D39CDD12Q41881687-E4E00ABE-A03E-485A-9738-55A5648E4B4DQ42084006-BDC7EEF9-590F-4424-B2C5-3752908788D9Q44063829-FF68A6A6-02B4-43D2-8002-13FBF9E318EFQ44491966-5C32974E-FF46-46C7-9BE5-40F05901BD32Q46315132-E7912910-6B84-4ACD-AC78-6177E8EC7494Q46729694-C1F8400A-288A-4C3A-B492-E72D7261338CQ46795397-32764235-BCA1-4566-B2EA-741A49416B25Q47674506-A53250E2-5355-4B4F-90E3-67DF8F33D0F4Q52695170-1FEA8F63-02CD-48F5-9211-EEF6447D9F51Q53525462-940CD789-BCCA-45B3-8D9C-94608D6E3AA7Q54405119-CC4E952F-F458-4565-B47A-B2CFCFB3F96EQ55839039-D94772E6-5895-4A90-BDD2-135F9F33DAFDQ60324962-4B7C44A3-5C07-4E42-8786-4F46337B2B94Q60325042-53D890E4-EBB0-445A-ADCE-F521EC42E86CQ60325057-734F70E9-A0BF-4965-9B0B-55F5B9ADB63F
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Byron B Lamont
@nl
Byron B Lamont
@sl
Byron B. Lamont
@en
Byron B. Lamont
@es
type
label
Byron B Lamont
@nl
Byron B Lamont
@sl
Byron B. Lamont
@en
Byron B. Lamont
@es
prefLabel
Byron B Lamont
@nl
Byron B Lamont
@sl
Byron B. Lamont
@en
Byron B. Lamont
@es
P106
P1153
24556291700
P214
739149719102511130006
P31
P496
0000-0001-9279-7149