Remobilisation of carbon and nitrogen supports seed filling in chickpea subjected to water deficit

2000 ◽  
Vol 51 (7) ◽  
pp. 855 ◽  
Author(s):  
S. L. Davies ◽  
N. C. Turner ◽  
J. A. Palta ◽  
K. H. M. Siddique ◽  
J. A. Plummer
Keyword(s):  
Water Deficit ◽  
Genotypic Variation ◽  
Net Photosynthesis ◽  
Sink Strength ◽  
Alternative Source ◽  
Seed Filling ◽  
Vegetative Tissues ◽  
Terminal Drought ◽  
Developing Seed ◽  
C And N

In the Mediterranean-type environment of south-western Australia, pod filling of chickpea occurs when net photosynthesis and nitrogen fixation is low as a result of the onset of terminal drought. Remobilisation of carbon (C) and nitrogen (N) from vegetative parts to developing seed may be an important alternative source of C and N for seed filling. The contribution of stored pre-podding C and N to seed filling was studied by labelling the vegetative tissues with the stable isotopes, 13C and 15N, prior to podding and following their subsequent movement to the seed. In ICCV88201, an advanced desi breeding line, 9% of the C and 67% of the N in the seed were derived from pre-podding C and N in well-watered plants compared with 13% of the seed C and 88% of the seed N in water-stressed plants. Furthermore, the contribution of pre-podding C and N was higher for earlier set compared with later set seeds. Pre-podding C and N were derived predominantly from the leaves with relatively little from the stems, roots, and pod walls. Genotypic variation in remobilisation ability was identified in contrasting desi (Tyson) and kabuli (Kaniva) cultivars. In well-watered Tyson, 9% of the seed C and 85% of the seed N were remobilised from vegetative tissues compared with 7% of the seed C and 62% of seed N in well-watered Kaniva. Water deficit decreased the amount of C remobilised by 3% in Tyson compared with 66% in Kaniva, whereas the total amount of N remobilised was decreased by 11% in Tyson and 48% in Kaniva. This was related to the maintenance of greater sink strength in Tyson, in which the number of filled pods was reduced by 66% in stressed plants compared with a 91% decrease in Kaniva. This indicates that better drought tolerance in desi genotypes is partly a consequence of better remobilisation and higher pod number. These studies show that C and N assimilated prior to podding can supplement the supply of current assimilates to the filling seed in both well-watered and water-stressed chickpea. Remobilisation of pre-podding N is an essential source of N for seed filling irrespective of environmental stress.

scholarly journals Changes in timing of water uptake and phenology favours yield gain in terminal water stressed chickpea AtDREB1A transgenics

2015 ◽  
Vol 42 (1) ◽  
pp. 84 ◽  
Author(s):  
Krithika Anbazhagan ◽  
Pooja Bhatnagar-Mathur ◽  
Kiran K. Sharma ◽  
Rekha Baddam ◽  
P. B. Kavi Kishor ◽  
...  
Keyword(s):  
Water Uptake ◽  
Seed Yield ◽  
Water Conservation ◽  
Temporal Pattern ◽  
Genotypic Variation ◽  
Lower Percentage ◽  
Seed Filling ◽  
Terminal Drought ◽  
Yield Gain ◽  
Crop Cycle

Terminal drought causes major yield loss in chickpea, so it is imperative to identify genotypes with best suited adaptive traits to secure yield in terminal drought-prone environments. Here, we evaluated chickpea (At) rd29A:: (At) DREB1A transgenic events (RD2, RD7, RD9 and RD10) and their untransformed C235 genotype for growth, water use and yield under terminal water-stress (WS) and well-watered (WW) conditions. The assessment was made across three lysimetric trials conducted in contained environments in the greenhouse (2009GH and 2010GH) and the field (2010F). Results from the greenhouse trials showed genotypic variation for harvest index (HI), yield, temporal pattern of flowering and seed filling, temporal pattern of water uptake across crop cycle, and transpiration efficiency (TE) under terminal WS conditions. The mechanisms underlying the yield gain in the WS transgenic events under 2009GH trial was related to conserving water for the reproductive stage in RD7, and setting seeds early in RD10. Water conservation also led to a lower percentage of flower and pod abortion in both RD7 and RD10. Similarly, in the 2010GH trial, reduced water extraction during vegetative stage in events RD2, RD7 and RD9 was critical for better seed filling in the pods produced from late flowers in RD2, and reduced percentage of flower and pod abortion in RD2 and RD9. However, in the 2010F trial, the increased seed yield and HI in RD9 compared with C235 came along only with small changes in water uptake and podding pattern, probably not causal. Events RD2 (2010GH), RD7 (2010GH) and RD10 (2009GH) with higher seed yield also had higher TE than C235. The results suggest that DREB1A, a transcription factor involved in the regulation of several genes of abiotic stress response cascade, influenced the pattern of water uptake and flowering across the crop cycle, leading to reduction in the percentage of flower and pod abortion in the glasshouse trials.

Effect of different physiological traits on grain yield in barley grown under irrigated and terminal water deficit conditions

2010 ◽  
Vol 148 (3) ◽  
pp. 319-328 ◽  
Author(s):  
A. GONZÁLEZ ◽  
V. BERMEJO ◽  
B. S. GIMENO
Keyword(s):  
Water Deficit ◽  
Chlorophyll Concentration ◽  
Net Photosynthesis ◽  
Physiological Traits ◽  
Breeding Lines ◽  
Terminal Drought ◽  
Leaf Chlorophyll ◽  
Drought Tolerant ◽  
Relationship Of ◽  
The Relationship

SUMMARYDrought is the main factor limiting the productivity of crops in Mediterranean areas. The introduction of physiological traits into crops that improve their tolerance to drought is necessary if yields under these conditions are to be efficiently improved. The effect of drought on different gas exchange variables, i.e. net photosynthesis (A), stomatal conductance (gs) and leaf chlorophyll concentration (Chl), and the relationship of these variables with yield were studied in 12 barley genotypes grown under irrigated and terminal drought conditions. The variable most sensitive to water deficit was gs (mean reduction 43% with respect to control conditions), followed by A (mean reduction 34%). The mean reduction of yield by terminal drought was 27%. A significant correlation was seen between these physiological traits and yield. The effect of water deficit on A, gs and Chl was smaller in the breeding lines than in the traditional varieties assayed, in agreement with the results found for yield. These results suggest a potential indirect selection of physiological characteristics in these breeding lines that allow greater tolerance to drought. The response of the different genotypes examined was not homogeneous across all the variables analysed. This variability is important in programmes aiming to obtain drought-tolerant genotypes via the optimization of traits such as those above.

scholarly journals Sink Strength Maintenance Underlies Drought Tolerance in Common Bean

Plants ◽  
2021 ◽  
Vol 10 (3) ◽  
pp. 489
Author(s):  
Amber Hageman ◽  
Elizabeth Van Volkenburgh
Keyword(s):  
Common Bean ◽  
Sink Strength ◽  
Total Biomass ◽  
Seed Filling ◽  
Uptake Rates ◽  
Determinate Growth ◽  
Determinate Growth Habit ◽  
Water Limitations ◽  
Uptake And Metabolism ◽  
Do So

Drought is a major limiter of yield in common bean, decreasing food security for those who rely on it as an important source of protein. While drought can have large impacts on yield by reducing photosynthesis and therefore resources availability, source strength is not a reliable indicator of yield. One reason resource availability does not always translate to yield in common bean is because of a trait inherited from wild ancestors. Wild common bean halts growth and seed filling under drought and awaits better conditions to resume its developmental program. This trait has been carried into domesticated lines, where it can result in strong losses of yield in plants already producing pods and seeds, especially since many domesticated lines were bred to have a determinate growth habit. This limits the plants ability to produce another flush of flowers, even if the first set is aborted. However, some bred lines are able to maintain higher yields under drought through maintaining growth and seed filling rates even under water limitations, unlike their wild predecessors. We believe that maintenance of sink strength underlies this ability, since plants which fill seeds under drought maintain growth of sinks generally, and growth of sinks correlates strongly with yield. Sink strength is determined by a tissue’s ability to acquire resources, which in turn relies on resource uptake and metabolism in that tissue. Lines which achieve higher yields maintain higher resource uptake rates into seeds and overall higher partitioning efficiencies of total biomass to yield. Drought limits metabolism and resource uptake through the signaling molecule abscisic acid (ABA) and its downstream affects. Perhaps lines which maintain higher sink strength and therefore higher yields do so through decreased sensitivity to or production of ABA.

Sink strength of citrus rootstocks under water deficit

2021 ◽  
Author(s):  
Simone F da Silva ◽  
Marcela T Miranda ◽  
Vladimir E Costa ◽  
Eduardo C Machado ◽  
Rafael V Ribeiro
Keyword(s):  
Plant Growth ◽  
Root Growth ◽  
Water Deficit ◽  
Carbon Allocation ◽  
Sink Strength ◽  
Rangpur Lime ◽  
Carbon Supply ◽  
Valencia Orange ◽  
Source Sink ◽  
Orange Trees

Abstract Carbon allocation between source and sink organs determines plant growth and is influenced by environmental conditions. Under water deficit, plant growth is inhibited before photosynthesis and shoot growth tends to be more sensitive than root growth. However, the modulation of source-sink relationship by rootstocks remain unsolved in citrus trees under water deficit. Citrus plants grafted on Rangpur lime are drought tolerant, which may be related to a fine coordination of the source-sink relationship for maintaining root growth. Here, we followed 13C allocation and evaluated physiological responses and growth of Valencia orange trees grafted on three citrus rootstocks (Rangpur lime, Swingle citrumelo and Sunki mandarin) under water deficit. As compared to plants on Swingle and Sunki rootstocks, ones grafted on Rangpur lime showed higher stomatal sensitivity to the initial variation of water availability and less accumulation of non-structural carbohydrates in roots under water deficit. High 13C allocation found in Rangpur lime roots indicates this rootstock has high sink demand associated with high root growth under water deficit. Our data suggest that Rangpur lime rootstock used photoassimilates as sources of energy and carbon skeletons for growing under drought, which is likely related to increases in root respiration. Taken together, our data revealed that carbon supply by leaves and delivery to roots are critical for maintaining root growth and improving drought tolerance, with citrus rootstocks showing differential sink strength under water deficit.

Red spruce seedling gas exchange in response to elevated CO2, water stress, and soil fertility treatments

1994 ◽  
Vol 24 (5) ◽  
pp. 954-959 ◽  
Author(s):  
L.J. Samuelson ◽  
J.R. Seiler
Keyword(s):  
Water Stress ◽  
Gas Exchange ◽  
Soil Fertility ◽  
Net Photosynthesis ◽  
Growing Season ◽  
Red Spruce ◽  
Fertility Treatment ◽  
Sink Strength ◽  
Growth Enhancement ◽  
Growing Seasons

The interactive influences of ambient (374 μL•L−1) or elevated (713 μL•L−1) CO2, low or high soil fertility, well-watered or water-stressed treatment, and rooting volume on gas exchange and growth were examined in red spruce (Picearubens Sarg.) grown from seed through two growing seasons. Leaf gas exchange throughout two growing seasons and growth after two growing seasons in response to elevated CO2 were independent of soil fertility and water-stress treatments, and rooting volume. During the first growing season, no reduction in leaf photosynthesis of seedlings grown in elevated CO2 compared with seedlings grown in ambient CO2 was observed when measured at the same CO2 concentration. During the second growing season, net photosynthesis was up to 21% lower for elevated CO2-grown seedlings than for ambient CO2-grown seedlings when measured at 358 μL•L−1. Thus, photosynthetic acclimation to growth in elevated CO2 occurred gradually and was not a function of root-sink strength or soil-fertility treatment. However, net photosynthesis of seedlings grown and measured at an elevated CO2 concentration was still over 2 times greater than the photosynthesis of seedlings grown and measured at an ambient CO2 concentration. Growth enhancement by CO2 was maintained, since seedlings grown in elevated CO2 were 40% larger in both size and weight after two growing seasons.

An early transient water deficit reduces flower number and pod production but increases seed size in chickpea (Cicer arietinum L.)

2011 ◽  
Vol 62 (6) ◽  
pp. 481 ◽  
Author(s):  
X.-W. Fang ◽  
N. C. Turner ◽  
F.-M. Li ◽  
K. H. M. Siddique
Keyword(s):  
Water Content ◽  
Water Deficit ◽  
Cicer Arietinum ◽  
Seed Size ◽  
Seed Yield ◽  
Flower Number ◽  
Cicer Arietinum L ◽  
Flower Production ◽  
Terminal Drought ◽  
Seed Growth

Terminal drought is known to decrease flower production, increase flower and pod abortion, and decrease yield of chickpea (Cicer arietinum L.), but the effects of early-season drought have not been evaluated. The influence of an early transient water deficit on flower and pod production and abortion, and seed yield and its components was evaluated in two chickpea cultivars, Rupali, a desi type, and Almaz, a kabuli type. Thirty-six-day-old plants were subjected to: (i) a transient water deficit by withholding water for 35 days, and then rewatered (WS), and (ii) kept well watered (WW) throughout. In the WS treatment the soil water content, leaf relative water content and leaf photosynthetic rate decreased after water was withheld and, following rewatering, recovered to the WW level. Despite the WS treatment being imposed at different phenological stages in the two cultivars, WS reduced flower number per plant by ~50% in Rupali and Almaz, respectively, compared with the WW plants. In WW plants, ~15% of flowers aborted in both cultivars, and 42 and 67% of the pods aborted in Rupali and Almaz, respectively, whereas in WS plants, 18 and 23% of flowers aborted and 27 and 67% of pods aborted in Rupali and Almaz, respectively. While seed growth in WS plants of Rupali and Almaz occurred primarily after the plants were rewatered, the duration of seed growth decreased by 17 and 36 days, the maximum rate of seed filling increased by 3 times and 5 times, and seed size increased by 26 and 16%, respectively, compared with the WW plants. Seed yield per plant in WS plants decreased by 31% in Rupali and 38% in Almaz compared with the WW controls. The early transient water deficit decreased flower production, but improved flower and pod development; increased the rate of seed growth and increased final seed size; and had a smaller effect on seed yield compared with chickpea subjected to terminal drought.

Transpiration Response to Vapor Pressure Deficit in Field Grown Peanut

2012 ◽  
Vol 39 (1) ◽  
pp. 53-61 ◽  
Author(s):  
Maria Balota ◽  
Steve McGrath ◽  
Thomas G. Isleib ◽  
Shyam Tallury
Keyword(s):  
Vapor Pressure ◽  
Soil Water ◽  
Water Deficit ◽  
Water Conservation ◽  
Vapor Pressure Deficit ◽  
Stomatal Closure ◽  
Genotypic Variation ◽  
Moisture Stress ◽  
Breeding Lines ◽  
Wide Range

Abstract Water deficit, i.e., rainfall amounts and distribution, is the most common abiotic stress that limits peanut production worldwide. Even though extensive research efforts have been made to improve drought tolerance in peanut, performance of genotypes largely depends upon the environment in which they grow. Based on greenhouse experiments, it has been hypothesized that stomata closure under high vapor pressure deficit (VPD) is a mechanism of soil water conservation and it has been shown that genotypic variation for the response of transpiration rate to VPD in peanut exists. The objective of this study was to determine the relationship between stomatal conductance (gs) and VPD for field grown peanut in Virginia-Carolina (VC) rainfed environments. In 2009, thirty virginia-type peanut cultivars and advanced breeding lines were evaluated for gs at several times before and after rain events, including a moisture stress episode. In 2010, eighteen genotypes were evaluated for gs under soil water deficit. In 2009, VPD ranged from 1.3 to 4.2 kPa and in 2010 from 1.78 to 3.57 kPa. Under water deficit, genotype and year showed a significant effect on gs (P  =  0.0001), but the genotype × year interaction did not. During the water deficit episodes while recorded gs values were relatively high, gs was negatively related to VPD (R2  =  0.57, n  =  180 in 2009; R2  =  0.47, n  =  108 in 2010), suggesting that stomata closure is indeed a water conservation mechanism for field grown peanut. However, a wide range of slopes among genotype were observed in both years. Genotypes with significant negative relationships of gs and VPD under water deficit in both years were Florida Fancy, Gregory, N04074FCT, NC-V11, and VA-98R. While Florida Fancy, Gregory, and NC-V11 are known to be high yielding cultivars, VA-98R and line N04074FCT are not. The benefit of stomatal closure during drought episodes in the VC environments is further discussed in this paper.

scholarly journals The nitrogen, carbon and greenhouse gas budget of a grazed, cut and fertilised temperate grassland

2016 ◽  
Author(s):  
Stephanie K. Jones ◽  
Carole Helfter ◽  
Margaret Anderson ◽  
Mhairi Coyle ◽  
Claire Campbell ◽  
...  
Keyword(s):  
Greenhouse Gas ◽  
Soil Layer ◽  
The Body ◽  
Sink Strength ◽  
N2o Emissions ◽  
N Budget ◽  
N Losses ◽  
Enteric Fermentation ◽  
C And N ◽  
Ch4 And N2o

Abstract. Intensively managed grazed grasslands in temperate climates are globally important environments for the exchange of the greenhouse gases (GHGs) carbon dioxide (CO2), nitrous oxide (N2O) and methane (CH4). We assessed the N and C budget of a mostly grazed, occasionally cut, and fertilized grassland in SE Scotland by measuring or modelling all relevant imports and exports to the field as well as changes in soil C and N pools over time. The N budget was dominated by import from inorganic and organic fertilisers (21.9 g N m2 yr−1) and losses from leaching (5.3 g N m2 yr−1), N2 emissions and NOx and NH3 volatilisation (6.4 g N m2 yr−1). The efficiency of N use by animal products (meat and wool) averaged 11 %. On average over nine years (2002–2010) the balance of N fluxes suggested that 7.2 ± 4.6 g N m−2 y−1 (mean ± confidence interval at p > 0.95) were stored in the soil. The largest component of the C budget was the net ecosystem exchange of CO2 (NEE), at an average uptake rate of 218 ± 155 g C m−2 y−1 over the nine years. This sink strength was offset by carbon export from the field mainly as harvest (48.9 g C m2 yr−1) and leaching (16.4 g C m2 yr−1). The other export terms, CH4 emissions from the soil, manure applications and enteric fermentation were negligible and only contributed to 0.02–4.2 % of the total C losses. Only a small fraction of C was incorporated into the body of the grazing animals. Inclusion of these C losses in the budget resulted in a C sink strength of 163 ± 140 g C m−2 y−1. On the contrary, soil stock measurements taken in May 2004 and May 2011 indicated that the grassland sequestered N in the 0–60 cm soil layer at 4.51 ± 2.64 g N m−2 y−1 and lost C at a rate of 29.08 ± 38.19 g C m−2 y-1, respectively. Potential reasons for the discrepancy between these estimates are probably an underestimation of C and N losses, especially from leaching fluxes as well as from animal respiration. The average greenhouse gas (GHG) balance of the grassland was −366 ± 601 g CO2 eq m−2 y−1 and strongly affected by CH4 and N2O emissions. The GHG sink strength of the NEE was reduced by 54 % by CH4 and N2O emissions. Enteric fermentation from the ruminating sheep proved to be an important CH4 source, exceeding the contribution of N2O to the GHG budget in some years.

Antioxidant defences in olive trees during drought stress: changes in activity of some antioxidant enzymes

2005 ◽  
Vol 32 (1) ◽  
pp. 45 ◽  
Author(s):  
Adriano Sofo ◽  
Bartolomeo Dichio ◽  
Cristos Xiloyannis ◽  
Andrea Masia
Keyword(s):  
Drought Stress ◽  
Water Deficit ◽  
Active Oxygen Species ◽  
Net Photosynthesis ◽  
Cellular Damage ◽  
Guaiacol Peroxidase ◽  
Severe Drought ◽  
Antioxidant Defences ◽  
Stress Changes ◽  
Olive Trees

The effects of drought on the activities of superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX), guaiacol peroxidase (POD), indoleacetate oxidase (IAAox) and polyphenol oxidase (PPO) were studied in 2-year old Olea europaea L. (cv. ‘Coratina’) plants grown under high temperatures and irradiance levels and gradually subjected to a controlled water deficit. After 20 d without irrigation, mean predawn leaf water potential fell from –0.37 to –5.37 MPa, and decreases in net photosynthesis and transpiration occurred. The activities of SOD, APX, CAT and POD increased in relation to the severity of drought stress in both leaves and roots. In particular, a marked increase in APX activity was found in leaves of plants at severe drought stress. CAT activity increased during severe water deficit conditions in leaves and fine roots. The patterns of POD and IAA oxidase activity ran in parallel and showed increases in relation to the degree of drought. In contrast, PPO activity decreased during the progression of stress in all the tissues studied. The results show that the ability of olive trees to up-regulate the enzymatic antioxidant system might be an important attribute linked to drought tolerance. This could limit cellular damage caused by active oxygen species during water deficit.

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