<mets:mets OBJID="eprint_5747" LABEL="Eprints Item" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd" xmlns:mets="http://www.loc.gov/METS/" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><mets:metsHdr CREATEDATE="2023-07-05T15:33:53Z"><mets:agent ROLE="CUSTODIAN" TYPE="ORGANIZATION"><mets:name>OAR@ICRISAT</mets:name></mets:agent></mets:metsHdr><mets:dmdSec ID="DMD_eprint_5747_mods"><mets:mdWrap MDTYPE="MODS"><mets:xmlData><mods:titleInfo><mods:title>Genetic analysis of adaptation differences between highland and lowland tropical maize using molecular markers </mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given">C</mods:namePart><mods:namePart type="family">Jiang</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">G O</mods:namePart><mods:namePart type="family">Edmeades</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">I</mods:namePart><mods:namePart type="family">Armstead</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">H R</mods:namePart><mods:namePart type="family">Lafitte</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">M D</mods:namePart><mods:namePart type="family">Hayward</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">D A</mods:namePart><mods:namePart type="family">Hoisington</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:abstract>Molecular-marker loci were used to investigate&#13;
the adaptation differences between highland and&#13;
lowland tropical maize. An F2 population from the cross&#13;
of two inbred lines independently derived from highland&#13;
and lowland maize germplasm was developed, and extracted&#13;
F3:4 lines were phenotype in replicated field trials&#13;
at four thermally diverse tropical testing sites, ranging&#13;
from lowland to extreme highland (mean growing season&#13;
temperature range 13.2–24.6°C). Traits closely related&#13;
with adaptation, such as biomass and grain yield, yield&#13;
components, days from sowing to male and female flowering,&#13;
total leaf number, plant height and number of primary&#13;
tassel branches (TBN), were analyzed. A large line&#13;
´ environment interaction was observed for most traits.&#13;
The genetic basis of this interaction was reflected by significant,&#13;
but systematic, changes from lowland to highland&#13;
sites in the correlation between the trait value and&#13;
genomic composition (designated by the proportion of&#13;
marker alleles with the same origin). Joint analysis of&#13;
quantitative trait loci (QTLs) over sites detected 5–8&#13;
QTLs for each trait (except disease scores, with data only&#13;
from one site). With the exception of one QTL for&#13;
TBN, none of these accounted for more than 15% of the&#13;
total phenotypic variation. In total, detected QTLs accounted&#13;
for 24–61% of the variation at each site on average.&#13;
For yield, yield components and disease scores, alleles&#13;
generally favored the site of origin. Highland-derived&#13;
alleles had little effect at lowland sites, while lowland-&#13;
derived alleles showed relatively broader adaptation.&#13;
Gradual changes in the estimated QTL effects with&#13;
increasing mean site temperature were observed, and&#13;
paralleled the observed patterns of adaptation in high land and lowland germplasm. Several clusters of QTLs&#13;
for different traits reflected the relative importance in the&#13;
adaptation differences between the two germplasm types,&#13;
and pleiotropy is suggested as the main cause for the&#13;
clustering. Breeding for broad thermal adaptation should&#13;
be possible by pooling genes showing adaptation to specific&#13;
thermal regimes, though perhaps at the expense of&#13;
reduced progress for adaptation to a specific site. Molecular&#13;
marker-assisted selection would be an ideal tool for&#13;
this task, since it could greatly reduce the linkage drag&#13;
caused by the unintentional transfer of undesirable traits</mods:abstract><mods:classification authority="lcc">Genetics and Genomics</mods:classification><mods:classification authority="lcc">Maize</mods:classification><mods:originInfo><mods:dateIssued encoding="iso8061">1990</mods:dateIssued></mods:originInfo><mods:originInfo><mods:publisher>Springer Verlag</mods:publisher></mods:originInfo><mods:genre>Article</mods:genre></mets:xmlData></mets:mdWrap></mets:dmdSec><mets:amdSec ID="TMD_eprint_5747"><mets:rightsMD ID="rights_eprint_5747_mods"><mets:mdWrap MDTYPE="MODS"><mets:xmlData><mods:useAndReproduction>
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