Korjent van Dijk

Dr. Korjent van Dijk

Adelaide University
orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 April 2024 in Nature
Verified
Journal Article
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AZAlexandre R. Zuntini
Alexandre R. Zuntini
TCTom Carruthers
Tom Carruthers
OMOlivier Maurin
Olivier Maurin
PBPaul C. Bailey
Paul C. Bailey
KLKevin Leempoel
Kevin Leempoel
WBWilliam J. Baker
William J. Baker
Angiosperms are the cornerstone of most terrestrial ecosystems and human livelihoods1,2. A robust understanding of angiosperm evolution is required to explain their rise to ecological dominance. So far, the angiosperm tree of life has been determined primarily by means of analyses of the plastid genome3,4. Many studies have drawn on this foundational work, such as classification and first insights into angiosperm diversification since their Mesozoic origins5–7. However, the limited and biased sampling of both taxa and genomes undermines confidence in the tree and its implications. Here, we build the tree of life for almost 8,000 (about 60%) angiosperm genera using a standardized set of 353 nuclear genes8. This 15-fold increase in genus-level sampling relative to comparable nuclear studies9 provides a critical test of earlier results and brings notable change to key groups, especially in rosids, while substantiating many previously predicted relationships. Scaling this tree to time using 200 fossils, we discovered that early angiosperm evolution was characterized by high gene tree conflict and explosive diversification, giving rise to more than 80% of extant angiosperm orders. Steady diversification ensued through the remaining Mesozoic Era until rates resurged in the Cenozoic Era, concurrent with decreasing global temperatures and tightly linked with gene tree conflict. Taken together, our extensive sampling combined with advanced phylogenomic methods shows the deep history and full complexity in the evolution of a megadiverse clade.

28 January 2021 in Ecological Management & Restoration
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Journal Article
Closed access
ESElizabeth A. Sinclair
Elizabeth A. Sinclair
CSCraig Sherman
Craig Sherman
JSJohn Statton
John Statton
CCCraig Copeland
Craig Copeland
AMAndrew Matthews
Andrew Matthews
GKGary Kendrick
Gary Kendrick

7 September 2021 in bioRxiv
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Preprint
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MWMichelle Waycott
Michelle Waycott
Korjent van DijkKorjent van Dijk
Korjent van Dijk
EBEd Biffin
Ed Biffin
Novel multi-gene targeted capture probes have been developed with the objective of obtaining multi-locus high quality sequence reads across any angiosperm lineage. Using existing genomic and transcriptomic data, two independent single assay probe/bait sets have been developed, the first targeting conserved exons from 20 low copy nuclear genes (OzBaits_NR V1.0) and the second, 19 plastid gene regions (OZBaits_CP V1.0). These ‘universal’ bait sets can efficiently generate DNA sequence data that are suitable for systematics and evolutionary studies of flowering plants. The bait sets can be ordered as Daicel-Arbor Sciences custom myBaits. We demonstrate the utility of the bait set in consistently recovering the targeted genomic regions across an evolutionarily broad range of angiosperm taxa.

1 May 2020 in Forensic Science International: Genetics
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Journal Article
Closed access
EDE.E. Dormontt
E.E. Dormontt
DJD.I. Jardine
D.I. Jardine
Korjent van DijkKorjent van Dijk
Korjent van Dijk
BDB.F. Dunker
B.F. Dunker
RDR.R.M. Dixon
R.R.M. Dixon
ALAndrew Lowe
Andrew Lowe

1 September 2021 in Regional Studies in Marine Science
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Journal Article
Closed access
UHUdhi Eko Hernawan
Udhi Eko Hernawan
PLPaul S. Lavery
Paul S. Lavery
GKGary A. Kendrick
Gary A. Kendrick
Korjent van DijkKorjent van Dijk
Korjent van Dijk
YUYaya Ihya Ulumuddin
Yaya Ihya Ulumuddin
KMKathryn M. McMahon
Kathryn M. McMahon

29 August 2018 in Ecology and Evolution
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Journal Article
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Korjent van DijkKorjent van Dijk
Korjent van Dijk
EBEric Bricker
Eric Bricker
BTBrigitta Ine Van Tussenbroek
Brigitta Ine Van Tussenbroek
MWMichelle Waycott
Michelle Waycott
Many marine species have widespread geographic ranges derived from their evolutionary and ecological history particularly their modes of dispersal. Seagrass (marine angiosperm) species have ranges that are unusually widespread, which is not unexpected following recent reviews of reproductive strategies demonstrating the potential for long‐distance dispersal combined with longevity through clonality. An exemplar of these dual biological features is turtle grass (Thalassia testudinum) which is an ecologically important species throughout the tropical Atlantic region. Turtle grass has been documented to have long‐distance dispersal via floating fruits and also extreme clonality and longevity. We hypothesize that across its range, Thalassia testudinum will have very limited regional population structure due to these characteristics and under typical models of population structure would expect to detect high levels of genetic connectivity. There are very few studies of range‐wide genetic connectivity documented for seagrasses or other sessile marine species. This study presents a population genetic dataset that represents a geographic area exceeding 14,000 km2. Population genetic diversity was evaluated from 32 Thalassia testudinum populations sampled across the Caribbean and Gulf of Mexico. Genotypes were based on nine microsatellites, and haplotypes were based on chloroplast DNA sequences. Very limited phylogeographic signal from cpDNA reduced the potential comparative analyses possible. Multiple analytical clustering approaches on population genetic data revealed two significant genetic partitions: (a) the Caribbean and (b) the Gulf of Mexico. Genetic diversity was high (HE = 0.641), and isolation by distance was significant; gene flow and migration estimates across the entire range were however modest, we suggest that the frequency of successful recruitment across the range is uncommon. Thalassia testudinum maintains genetic diversity across its entire distribution range. The genetic split may be explained by genetic drift during recolonization from refugia following relatively recent reduction in available habitat such as the last glacial maxima.