Effects of Water Deficit Induced by PEG and NaCl onChickpea (Cicer arietinum L.) Cultivars and Lines at Early Seedling Stages
G.U. Journal of Science
22(1): 5-14 (2009)
www.gujs.org
Effects of Water Deficit Induced by PEG and NaCl on
Chickpea (Cicer arietinum L.) Cultivars and Lines at
Early Seedling Stages
Tuğçe KALEFETOĞLU MACAR1, Özlem TURAN 1, Yasemin EKMEKÇĐ 1♠
1
Hacettepe University, Faculty of Science, Department of Biology, Ankara, Turkey
Received: 23.07.2007 Revised:23.10.2008 Accepted: 02.12.2008
ABSTRACT
The effects of water deficit induced by different osmotic potential levels [0 (control), -0.4, -0.6 and -0.8 MPa]
of PEG 6000 and NaCl treatments on chickpea (Cicer arietinum L.) cultivars and lines at germination and early
growth stages by sampling on 4th and 8th days of incubation consisting of 4 days each of dark and subsequent 16
hours illumination. All of these treatments affected germination percentages of all genotypes but PEG was more
effective in inhibition than NaCl at the MPa levels tested. The experimental studies showed that all of the
genotypes tested could be classified as tolerant, moderately tolerant and sensitive ones. But the tolerance levels
were not found to be correlated directly with MPa levels applied, as Canıtez and ILC-3279 were tolerant to
PEG, but ILC-3279 was sensitive to NaCl treatment. Within this context the classification can be summarized
as below: PEG tolerant (Canıtez and ILC-3279), moderately tolerant (AkN 87, FLIP 87-59C, Gökçe and
Uzunlu), sensitive (AkN 290 and ER 99). NaCl tolerant (Uzunlu and FLIP 87-59C), moderately tolerant
(Gökçe, Canıtez, AkN 290 and AkN 87) and sensitive (ER 99 and ILC-3279).
Key Words: Drought, early seedling stage, germination, NaCl, PEG, salinity, water deficit
1. INTRODUCTION
Chickpea (Cicer arietinum L.) is an ancient legume
crop believed to be originated in South East Turkey,
and the adjoining part of Syria [1, 2]. It is the fourth
most important food legume with a total annual global
production of 9.1 million M tones from 11.2 million ha
[3]. Besides being an important source of human and
animal food, chickpea also plays an important role in
the maintenance of soil fertility, particularly in the dry,
rainfed areas [4, 5]. One of the most important abiotic
factors limiting plant germination and early seedling
stages is water stress brought about by drought and
salinity [6, 7], which are widespread problems around
the world [8]. Salinity and drought affect the plants in a
similar way [9]. Reduced water potential is a common
consequence of both salinity and drought [10]. Water
stress acts by decreasing the percentage and rate of
germination [11] and seedling growth [8, 12, 13]. Since
chickpea is grown mostly as a rainfed and post-rainy
season crop, water stress during vegetative and/or
reproductive growth stages is one of the most limiting
factors for the chickpea growth [14].
Germination of seeds, one of the most critical phases of
plant life, is greatly influenced by salinity [15]. Salinity
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is reported to decrease as well as delay germination of
most of the crops. Chickpea is a salt-sensitive crop
especially during germination [16]. Lower levels of
salinity delayed germination whereas higher levels
reduced the final percentage of seed germination [17]
and vegetative plant growth is suppressed under saline
conditions [18]. In addition, salinity imposes on plants
other stresses such as ion toxicity, as a result of ion
entry in excess of appropriate compartmentation, and
nutrient imbalances, as commonly seen in the
displacement of potassium by sodium. In fact, salinity
damage is mainly due to altered water relations caused
by high salt accumulation in the intercellular spaces
[19].
Drought, like salinity, plays an important role not only
in determining germination rates, but also influences
seedling development [20]. Establishment of seedlings
is the most critical life stage in dry environments and a
lack of soil moisture is often a major reason for seedling
mortality [21]. With increasing drought stress, water
availability decreases, changing the percentage and
velocity of germination and growth of seedlings
adversely. Osmotic solutions are used to impose water
stress reproducibly under in vitro conditions [7]. PEG
6
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G.U. J. Sci., 22(1): 5-14 (2009)/ Tuğçe KALEFETOĞLU MACAR, Özlem TURAN, Yasemin EKMEKÇĐ
widely used to induce water stress, is a non-ionic water
polymer, which is not expected to penetrate into plant
tissue rapidly [22]. PEG molecules with a Mr ≥ 6000
cannot penetrate the cell wall pores [23]. Because PEG
does not enter the apoplast, water is withdrawn not only
from the cell but also from the cell wall. Therefore,
PEG solutions mimic dry soil more closely than
solutions of low–Mr osmotica, which infiltrate the cell
wall with solute [24].
The present investigation has been performed to
evaluate chickpea (Cicer arietinum L.) tolerance to
osmotic stress induced by polyethylene glycol (PEG) or
NaCl during germination and the early seedling stages
of plant development. Eight chickpea genotypes [four
cultivars (Gökçe, Canıtez, ER 99 and Uzunlu) and four
lines (AkN 87, AkN 290, ILC-3279 and FLIP 87-59C)]
were tested.
This is the first work aimed at selecting drought and
salinity tolerant chickpea genotypes in the germination
and early seedling stages by using PEG or NaCl in in
vitro conditions.
2. MATERIALS AND METHODS
The seeds of chickpea cultivars and lines were obtained
from Ankara Central Research Institute for Field Crops
for this research. The effects of drought and salt stresses
induced by different osmotic potential levels [0
(control), -0.4, -0.6 and -0.8 MPa] of polyethylene
glycol 6000 (PEG 6000) and NaCl treatments on
germination and early seedling development of
chickpea (Cicer arietinum L.) cultivars and lines were
investigated for two sampling dates (4 and 8 days). The
seeds of the cultivars (Canıtez, ER 99, Gökçe and
Uzunlu) and the lines (AkN 87, AkN 290, FLIP 8759C, ILC-3279) which were imbibed in deionized water
were incubated under dark conditions for 4 days and
subsequently 16 h photoperiod with 250 µmol.m-2s-1
light intensity for four days at 23±2 °C on humidified
filter paper with an aliquot of solution of different
osmotic potentials of PEG 6000 or NaCl. The wet filter
papers were changed when germination of seeds was
measured for the first sample day after sowing. The
osmotic potentials of PEG 6000 were calculated as
described by Michael and Kaufman [25] . At end of the
each sampling dates, the percentage of germination (%)
was determined and, the length of roots and epicotyls of
genotypes were also measured (mm seedling-1) for PEG
and NaCl treatments. Determination of the tolerance of
the genotypes used based on the inhibition percentage
of root elongation as compared with the control groups
for both of the treatments. Then genotypes were
classified according to their tolerance index values.
The experiment was arranged in a completely
randomized design with three replicates of eight
seedlings per replications (n=24) in each sampling da (...truncated)