<mods:mods version="3.3" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><mods:titleInfo><mods:title>Physiological and genetic deciphering of water,&#13;
salinity and relative humidity stress in chickpea&#13;
(Cicer arietinum L.)</mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given">R</mods:namePart><mods:namePart type="family">Pushpavalli</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:abstract>Chickpea (Cicer arietinum L.), an important cool-season, food legume&#13;
crop, is known to be sensitive to several abiotic stresses: drought, salinity&#13;
and heat. The yield losses caused by these stresses are accounted to 6.4&#13;
million tonnes (t)/ year on global production. To improve any existing&#13;
cultivar and harness the genetic regions involved in the tolerance it is&#13;
important to understand the genetic and physiological mechanisms that&#13;
underlie any tolerance. The objectives of this study were to (i)&#13;
understanding the effect of either water deficit or salt stress on the&#13;
reproductive biology of genotypes know to contrast for either salt or&#13;
drought stress and (ii) construction of genetic map and identification of&#13;
QTLs and candidate genes for salinity tolerance in 188 RILs derived from&#13;
the ICCV 2 × JG 11 cross.&#13;
In the water deficit study conducted in two consecutive years, ten&#13;
genotypes with contrasting yields under terminal drought stress in the&#13;
field were exposed to a gradual, but similar, water stress in the&#13;
glasshouse. Nine parameters related to yield were recorded in wellwatered&#13;
plants (WW) and in water-stressed plants (WS) when the level of&#13;
deficit was mild (phase I), and when the stress was severe (phase II). The&#13;
WS treatment reduced seed yield, seed and pod number, but not flower +&#13;
pod + seed abortion percentage or 100-seed weight. The controlled&#13;
drought imposition in glass house conditions revealed genotypic&#13;
differences inthe sensitivity of the reproductive process to drought. The&#13;
seed yield differences in chickpea were largely related to the capacity to&#13;
produce a large number of flowers and to set seeds, especially when the&#13;
degree of water deficit was mild.&#13;
In the salinity experiments, fourteen genotypes of chickpea (Cicer&#13;
arietinum L.) were used to study yield parameters, and eight genotypes&#13;
were selected for ion analysis after being grown in soil treated with 0 mM&#13;
and 80 mM NaCl, to assess any possible relationship between salt ion&#13;
accumulation in different plant tissues and yield reduction. Salinity&#13;
delayed flowering and the delay was greater in sensitive than tolerant&#13;
genotypes under salt stress. Filled pod and seed numbers, but not seed&#13;
size, were associated with seed yield in saline conditions, suggesting that&#13;
salinity impaired reproductive success more in sensitive than tolerant&#13;
lines. The delay in flowering was associated with higher concentrations of&#13;
Na+ in the laminae of fully expanded young leaves (R2=0.61) and old&#13;
green leaves (R2=0.51). Na+ accumulation in leaves was associated with&#13;
delayed flowering that in turn could have played a role of the lower&#13;
reproductive success in the sensitive lines.&#13;
In QTL mapping for salinity tolerance, yield and components were&#13;
assessed in 188 recombinant inbred lines (RILs) derived from cross ICCV&#13;
2 × JG 11, in soil treated with either 0 mM NaCl (control) or 80 mM NaCl&#13;
(salinity) over two consecutive years. Salinity significantly (P&lt;0.05)&#13;
affected almost all traits across years. The mean yield reduction under&#13;
salinity compared to control was around 40% across years. A genetic&#13;
map was constructed using 56 (SSR, SNP) polymorphic markers. The&#13;
QTL analysis revealed two key genomic regions on CaLG05 (28.6 cM) and&#13;
on CaLG07 (19.4 cM) that harboured QTLs for salinity tolerance&#13;
associated traits. Two major QTLs for higher yield in the salinity&#13;
treatment (explaining 12 and 17% of the phenotyping variation) wereidentified within the two key genomic regions. Comparison with already&#13;
published chickpea genetic maps showed that these regions conferred&#13;
salinity tolerance across two other populations and the markers can be&#13;
deployed for enhancing salinity tolerance in chickpea. Based on gene&#13;
ontology annotation 48 putative candidate genes responsive to salinity&#13;
stress were found. Most of them were believed to be involved in achieving&#13;
osmoregulation under stress conditions.&#13;
In the relative humidity stress study, five genotypes that contrasting for&#13;
yield under heat stress were studied. The plants were grown in three&#13;
different vapor pressure deficit conditions (2.5, 3.0, 3.4 kPa) where the&#13;
temperature was maintained constant (30°C) and the RH varied as 40,&#13;
30, 20% respectively. Genotypic variation found for almost all traits&#13;
across treatments. The traits seed number and seed weight differentiated&#13;
tolerant and sensitive group significantly at VPD conditions 2.5 and 3.0&#13;
but not in 3.4 kPa. Seed size was unaffected under 2.5 and 3.0 kPa VPD&#13;
regimes but did get reduced upto 45% under 3.4 kPa treatment&#13;
compared to 2.5 kPa treatment. The lowest RH treatment, even under&#13;
fully well-watered condition, as any other abiotic stress reduced yield.&#13;
Thus, it is important to consider the effect of low RH and the&#13;
mechanisms behindits tolerance and sensitivity in future heat tolerance&#13;
studies. The pollen viability or pollen in vivo germination was unaffected&#13;
in this study.&#13;
All the four studies have revealed that certain parameters can be used for&#13;
achieving water deficit, salinity and relative humidity stress tolerance in&#13;
future chickpea improvement programs.</mods:abstract><mods:classification authority="lcc">Chickpea</mods:classification><mods:originInfo><mods:dateIssued encoding="iso8061">2015</mods:dateIssued></mods:originInfo><mods:originInfo><mods:publisher>Bharathidasan University,Tiruchirappalli, Tamil Nadu;Department of Plant Science Center of Excellence in Life Sciences</mods:publisher></mods:originInfo><mods:genre>Thesis</mods:genre></mods:mods>