TY - JOUR
T1 - Plant DNA-barcode library and community phylogeny for a semi-arid East African savanna
AU - Gill, Brian A.
AU - Musili, Paul M.
AU - Kurukura, Samson
AU - Hassan, Abidikadir A.
AU - Goheen, Jacob R.
AU - Kress, W. John
AU - Kuzmina, Maria
AU - Pringle, Robert M.
AU - Kartzinel, Tyler R.
N1 - Publisher Copyright:
© 2019 John Wiley & Sons Ltd
PY - 2019/7
Y1 - 2019/7
N2 - Applications of DNA barcoding include identifying species, inferring ecological and evolutionary relationships between species, and DNA metabarcoding. These applications require reference libraries that are not yet available for many taxa and geographic regions. We collected, identified, and vouchered plant specimens from Mpala Research Center in Laikipia, Kenya, to develop an extensive DNA-barcode library for a savanna ecosystem in equatorial East Africa. We amassed up to five DNA barcode markers (rbcL, matK, trnL-F, trnH–psbA, and ITS) for 1,781 specimens representing up to 460 species (~92% of the known flora), increasing the number of plant DNA barcode records for Africa by ~9%. We evaluated the ability of these markers, singly and in combination, to delimit species by calculating intra- and interspecific genetic distances. We further estimated a plant community phylogeny and demonstrated its utility by testing if evolutionary relatedness could predict the tendency of members of the Mpala plant community to have or lack “barcode gaps”, defined as disparities between the maximum intra- and minimum interspecific genetic distances. We found barcode gaps for 72%–89% of taxa depending on the marker or markers used. With the exception of the markers rbcL and ITS, we found that evolutionary relatedness was an important predictor of barcode-gap presence or absence for all of the markers in combination and for matK, trnL-F, and trnH–psbA individually. This plant DNA barcode library and community phylogeny will be a valuable resource for future investigations.
AB - Applications of DNA barcoding include identifying species, inferring ecological and evolutionary relationships between species, and DNA metabarcoding. These applications require reference libraries that are not yet available for many taxa and geographic regions. We collected, identified, and vouchered plant specimens from Mpala Research Center in Laikipia, Kenya, to develop an extensive DNA-barcode library for a savanna ecosystem in equatorial East Africa. We amassed up to five DNA barcode markers (rbcL, matK, trnL-F, trnH–psbA, and ITS) for 1,781 specimens representing up to 460 species (~92% of the known flora), increasing the number of plant DNA barcode records for Africa by ~9%. We evaluated the ability of these markers, singly and in combination, to delimit species by calculating intra- and interspecific genetic distances. We further estimated a plant community phylogeny and demonstrated its utility by testing if evolutionary relatedness could predict the tendency of members of the Mpala plant community to have or lack “barcode gaps”, defined as disparities between the maximum intra- and minimum interspecific genetic distances. We found barcode gaps for 72%–89% of taxa depending on the marker or markers used. With the exception of the markers rbcL and ITS, we found that evolutionary relatedness was an important predictor of barcode-gap presence or absence for all of the markers in combination and for matK, trnL-F, and trnH–psbA individually. This plant DNA barcode library and community phylogeny will be a valuable resource for future investigations.
KW - East Africa
KW - Forest Global Earth Observatory
KW - Mpala Research Centre
KW - barcode gap
KW - biodiversity
KW - comparative phylogenetics
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U2 - 10.1111/1755-0998.13001
DO - 10.1111/1755-0998.13001
M3 - Article
C2 - 30703281
AN - SCOPUS:85065441591
SN - 1755-098X
VL - 19
SP - 838
EP - 846
JO - Molecular Ecology Resources
JF - Molecular Ecology Resources
IS - 4
ER -