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1.
Turnover of southern cypresses in the post-Gondwanan world: extinction, transoceanic dispersal, adaptation and rediversification.
New Phytol
; 221(4): 2308-2319, 2019 03.
Article
in English
| MEDLINE | ID: mdl-30367483
2.
Three explanations for biodiversity hotspots: small range size, geographical overlap and time for species accumulation. An Australian case study.
New Phytol
; 207(2): 390-400, 2015 Jul.
Article
in English
| MEDLINE | ID: mdl-25442328
3.
Interpreting the modern distribution of Myrtaceae using a dated molecular phylogeny.
Mol Phylogenet Evol
; 93: 29-43, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-26211451
4.
Ploidy and domestication are associated with genome size variation in Palms.
Am J Bot
; 102(10): 1625-33, 2015 Oct.
Article
in English
| MEDLINE | ID: mdl-26437888
5.
Biogeographic calibrations for the molecular clock.
Biol Lett
; 11(9): 20150194, 2015 Sep.
Article
in English
| MEDLINE | ID: mdl-26333662
6.
Phylogenetic biome conservatism on a global scale.
Nature
; 458(7239): 754-6, 2009 Apr 09.
Article
in English
| MEDLINE | ID: mdl-19219025
7.
Evolutionary consequences of shifts to bird-pollination in the Australian pea-flowered legumes (Mirbelieae and Bossiaeeae).
BMC Evol Biol
; 14(1): 43, 2014 Mar 07.
Article
in English
| MEDLINE | ID: mdl-24602227
8.
Clock model makes a large difference to age estimates of long-stemmed clades with no internal calibration: a test using Australian grasstrees.
BMC Evol Biol
; 14: 263, 2014 Dec 19.
Article
in English
| MEDLINE | ID: mdl-25523814
9.
Climate, not Aboriginal landscape burning, controlled the historical demography and distribution of fire-sensitive conifer populations across Australia.
Proc Biol Sci
; 280(1773): 20132182, 2013 Dec 22.
Article
in English
| MEDLINE | ID: mdl-24174110
10.
Not an ancient relic: the endemic Livistona palms of arid central Australia could have been introduced by humans.
Proc Biol Sci
; 279(1738): 2652-61, 2012 Jul 07.
Article
in English
| MEDLINE | ID: mdl-22398168
11.
Phylogenetic niche conservatism: what are the underlying evolutionary and ecological causes?
New Phytol
; 196(3): 681-694, 2012 Nov.
Article
in English
| MEDLINE | ID: mdl-22943495
12.
Are pollen fossils useful for calibrating relaxed molecular clock dating of phylogenies? A comparative study using Myrtaceae.
Mol Phylogenet Evol
; 63(1): 15-27, 2012 Apr.
Article
in English
| MEDLINE | ID: mdl-22197806
13.
The impact of multiple biogeographic barriers and hybridization on species-level differentiation.
Am J Bot
; 99(12): 2045-57, 2012 Dec.
Article
in English
| MEDLINE | ID: mdl-23221499
14.
Cenozoic extinctions account for the low diversity of extant gymnosperms compared with angiosperms.
New Phytol
; 192(4): 997-1009, 2011 Dec.
Article
in English
| MEDLINE | ID: mdl-21895664
15.
Isolation and characterization of 52 polymorphic EST-SSR markers for Callitris columellaris (Cupressaceae).
Am J Bot
; 98(12): e363-8, 2011 Dec.
Article
in English
| MEDLINE | ID: mdl-22106440
16.
AusTraits, a curated plant trait database for the Australian flora.
Sci Data
; 8(1): 254, 2021 09 30.
Article
in English
| MEDLINE | ID: mdl-34593819
17.
Livistona palms in Australia: ancient relics or opportunistic immigrants?
Mol Phylogenet Evol
; 54(2): 512-23, 2010 Feb.
Article
in English
| MEDLINE | ID: mdl-19766198
18.
Evolution of exceptional species richness among lineages of fleshy-fruited Myrtaceae.
Ann Bot
; 106(1): 79-93, 2010 Jul.
Article
in English
| MEDLINE | ID: mdl-20462850
19.
Tree thinking for all biology: the problem with reading phylogenies as ladders of progress.
Bioessays
; 30(9): 854-67, 2008 Sep.
Article
in English
| MEDLINE | ID: mdl-18693264
20.
Congruent species delineation of Tulasnella using multiple loci and methods.
New Phytol
; 201(1): 6-12, 2014 Jan.
Article
in English
| MEDLINE | ID: mdl-24028679