Root distribution patterns of peanut genotypes with different drought resistance levels under early‐season drought stress

Drought severely limits crop yield of peanut. Yet cultivars with enhanced root development enable the exploration of a greater volume of soil for water and nutrients, helping the plant survive. Root distribution patterns of three genotypes (ICGV 98305, ICGV 98324 and Tifton‐8) were compared when grown in well‐watered rhizoboxes and when grown in rhizoboxes where an early‐season drought was imposed using rain‐exclusion shelters. The treatments were arranged in a completely randomized design with three replications, and the experiment was conducted during two seasons at the Field Crop Research Station of Khon Kaen University, in Khon Kaen, Thailand. The root system of ICGV 98305, when grown under drought, had a significantly higher root length in the 30–110 cm deep soil layers and less roots in the 0–30 cm soil layers when under drought than when grown under well‐watered conditions. Roots of Tifton‐8 had the largest reductions in root length in upper soil layer and reduced in most soil layers. Tifton‐8 grown under drought was smaller than under well‐watered control for all root traits, showing negative response to drought. The peanut genotypes with high root traits in deeper soil layer under early‐season drought might contribute to drought avoidance mechanism.     

Chlorophyll Stability is an Indicator of Drought Tolerance in Peanut

Chlorophyll stability during drought might be a promising criterion for selection for drought resistance in peanut. The study describes two field trials conducted at Khon Kaen University, Thailand which investigate genotype × drought interactions in a wide range of peanut germplasm in general and assess the relationship between chlorophyll stability and genotypic performance in particular, under drought. Two field experiments (during 2003/2004 and 2004/2005 dry seasons) were conducted in a split plot design with three water regimes [field capacity, 2/3 available water (AW) and 1/3 AW] as main, and 12 peanut genotypes as subtreatments, replicated four times. Observations on total dry matter (TDM), chlorophyll density (ChlD) (chlorophyll content per unit leaf area), chlorophyll content (chlorophyll content per plant) and SPAD chlorophyll meter readings (SCMR) were recorded at 30, 60 and 90 days after emergence. Transpiration (T) and transpiration efficiency (TE) were computed using the data on amount of water input and TDM. Drought stress significantly reduced TDM, T and chlorophyll content across genotypes but significantly increased TE and ChlD in peanut. However, there were significant differences among genotypes for TE and chlorophyll parameters. The genotype × drought interaction effects for chlorophyll characters (content and density) were not significant suggesting a strong genetic effect. The correlation coefficients between TDM and chlorophyll content (r = 0.51, P = 0.01 to r = 0.91, P = 0.01) and between TE and ChlD (r = 0.46, P = 0.05 to r = 0.77, P = 0.01) were positive and significant. These findings suggest that chlorophyll parameters are strongly linked with drought tolerance in peanut. There were highly significant and positive relationships between ChlD and SCMR (r = 0.67, P = 0.01 to r = 0.93, P = 0.01), between SCMR and TE (r = 0.41, P = 0.05 to r = 0.80, P = 0.01) suggesting that SCMR could be used as a tool for rapid assessment of relative chlorophyll status in peanut genotypes as well as for the indirect selection of drought tolerance in peanut.     

Association of root dry weight and transpiration efficiency of peanut genotypes under early season drought

Root characters have been well established as drought resistance traits in peanut. However, the relationships of root characters with transpiration efficiency (TE) have not been well understood. The objective of this study was to investigate the relationships between root traits and TE under early season drought. Two greenhouse experiments were conducted during February-May 2004 and November 2004-March 2005 at the Field Crop Research Station of Khon Kaen University, in Khon Kaen province of Thailand. A randomized complete block design (RCBD) was used with 2 factorial set-up with four replications. Factor A consisted of two water regimes, i.e. irrigated control (FC) and 1/3 available soil water (1/3 AW) from emergence to 40 days after emergence followed by adequate water supply, and factor B comprised of 11 peanut genotypes. Data were recorded for specific leaf area (SLA) and SPAD chlorophyll meter reading (SCMR) at 40 and 60 days after emergence (DAE) and TE and root dry weight (RDW) at harvest. Early season drought increased SCMR, TE and RDW but it reduced SLA. Strong and more consistent variation for TE were observed among 11 peanut genotypes across seasons. Across both seasons, ICGV 98300, KK 60-3 and Tifton-8 had high TE and also had large root systems under drought conditions. KK 60-3 and Tifton-8 had low SLA and high SCMR under early season drought conditions. Root dry weight had a contribution to TE under well-watered and drought conditions, especially under drought condition. SCMR and SLA had smaller contributions to TE under well-watered and ESD conditions. From this study it was apparent that root dry weight was an important trait for TE under early season drought.     

Rooting patterns of four crop legumes in response to seed-placement depths in the dry season

Abstract

On sandy paddy fields, key factors for successful crops in the dry season without irrigation are a shallow water table and practices such as deep seed-placement but only some legume species are adapted to such conditions. To understand the adaptation of legume species to deep seed-placement over shallow water tables, we studied their rooting patterns on two sandy soils. Cowpea (Vigna unguiculata), mungbean (Vigna radiata), peanut (Arachis hypogaea) and soybean (Glycine max) seeds were sown shallow (～5 cm) or deep (～15 cm) in deep sandy soils after harvesting rice in two shallow water table locations in north-east Thailand. The legumes depended mainly on capillary water rising from the water table and none experienced water deficit throughout the growing season. Generally, deeper seed-placement decreased overall root dry weight, but it increased the root surface area to weight ratio. Deep seed-placement promoted a greater fraction of root growth into the subsoil for cowpea (86–99% of total root length), mungbean (61–93% of total root length) and peanut (78–98% of total root length) where the soil contained more water throughout the growing season. Moreover, deep seed-placement at the site with the lower water table promoted deeper penetration of roots of cowpea (～20 cm deeper), mungbean (～20–40 cm deeper) and peanut (～20–40 cm deeper) which improved water access, especially late during the growing season when topsoils dried to close to wilting point. Unlike other species, the soybean rooting pattern did not respond much to seed-placement depths, or soil moisture.     

Association between aflatoxin contamination and drought tolerance traits in peanut

The current study investigates the association between drought tolerance traits and aflatoxin contamination in peanut grown under long-term drought. Two field experiments were conducted at Khon Kaen University, Thailand using a split–split plot design with three drought stress levels as main plots, 11 genotypes as sub-plots, and two soil inoculations of Aspergillus flavus treatments as sub-sub-plots. The effects of temperature, soil moisture and A. flavus population on kernel colonization and aflatoxin contamination, and drought tolerance traits viz. specific leaf area (SLA) and root length density (RLD) were measured. The results demonstrated that elevated soil temperatures and reduced soil moisture, favored aflatoxin production. Drought in combination with higher levels of A. flavus inoculum load in the soil resulted in an increase in the fungal populations in the soil which in turn resulted in increased kernel colonization and subsequent aflatoxin contamination. A combination of SLA and RLD, and kernel colonization had a significant influence on aflatoxin contamination under drought conditions in both seasons (r = 0.73** and 0.76**). The results revealed that drought tolerance traits (SLA and RLD) could be contributing to resistance to aflatoxin contamination suggesting that a combination of SLA, RLD and kernel colonization could be used as selection criteria in selecting parents for aflatoxin resistance.     

Root Distribution of Drought-Resistant Peanut Genotypes in Response to Drought

The ability of a plant to modify its root distribution to exploit deeper stored soil water may be an important mechanism to avoid drought. This study aimed at assessing root distributions, variations in root length density (RLD) and percentage of root distribution, and the relevance of root traits for yield of drought‐resistant peanut genotypes under different available soil water levels. The experiment was conducted in the dry season during the years 2003/04 and 2004/05. Eleven peanut genotypes (ICGV 98300, ICGV 98303, ICGV 98305, ICGV 98308, ICGV 98324, ICGV 98330, ICGV 98348, ICGV 98353, Tainan 9, KK 60‐3 and Tifton‐8) and three soil moisture levels [field capacity (FC), 2/3 available soil water (AW) and 1/3 AW] were laid out in a split‐plot design with four replications. Roots were sampled by a core sampler at 37, 67 and 97 days after sowing (DAS). Root length was determined by a scanner and the WINRHIZO Pro 2004a software. RLD was calculated as the ratio of root length (cm) and soil volume (cm³). Graphical illustration of root distribution was constructed by merging RLD in the first and second soil layers (0–40 cm) as upper roots and pooling RLD at the third, fourth and fifth layers (40–100 cm) as lower roots. Pod yield, biomass and harvest index (HI) were recorded at harvest. A drought tolerance index (DTI) was calculated for each parameter as the ratio of the parameter under stress treatment to that under well‐watered conditions. Variations in RLD in 40 to 100 cm layer (RLD_{40 to 100 cm}) were found under well‐watered conditions, and the peanut genotypes could be readily identified as high, intermediate and low for this trait. Changes in RLD in the 40 to 100 cm soil layer were found at 2/3 AW and were more evident at 1/3 AW. ICGV 98300, ICGV 98303, ICGV 98305, ICGV 98308 and KK 60‐3 were classified as drought responsive as they increased RLD in the deeper subsoil level in response to drought. In general, RLD under drought conditions was not related to biomass production. The ability to maintain the percentage of RLD (DTI for %RLD) was related to pod yield, DTI for pod yield and DTI for HI. ICGV 98300, ICGV 98303, ICGV 98305 exhibited high DTI (RLD_{40 to 100 cm}) which may explain their high pod yield, DTI (PY) and DTI (HI). Based on these observations we classified them as drought‐avoiding genotypes.     

DROUGHT STRESS: Physiological Basis for Genotypic Variation in Tolerance to and Recovery from Pre‐flowering Drought in Peanut

Drought during the pre‐flowering stage can increase yield of peanut. There is limited information on genotypic variation for tolerance to and recovery from pre‐flowering drought (PFD) and more importantly the physiological traits underlying genotypic variation. The objectives of this study were to determine the effects of moisture stress during the pre‐flowering phase on pod yield and to understand some of the physiological responses underlying genotypic variation in response to and recovery from PFD. A glasshouse and field experiments were conducted at Khon Kaen University, Thailand. The glasshouse experiment was a randomized complete block design consisting of two watering regimes, i.e. fully‐irrigated control and 1/3 available soil water from emergence to 40 days after emergence followed by adequate water supply, and 12 peanut genotypes. The field experiment was a split‐plot design with two watering regimes as main‐plots, and 12 peanut genotypes as sub‐plots. Measurements of N₂ fixation, leaf area (LA) were made in both experiments. In addition, root growth was measured in the glasshouse experiment. Imposition of PFD followed by recovery resulted in an average increase in yield of 24 % (range from 10 % to 57 %) and 12 % (range from 2 % to 51 %) in the field and glasshouse experiments, respectively. Significant genotypic variation for N₂ fixation, LA and root growth was also observed after recovery. The study revealed that recovery growth following release of PFD had a stronger influence on final yield than tolerance to water deficits during the PFD. A combination of N₂ fixation, LA and root growth accounted for a major portion of the genotypic variation in yield (r = 0.68–0.93) suggesting that these traits could be used as selection criteria for identifying genotypes with rapid recovery from PFD. A combined analysis of glasshouse and field experiments showed that LA and N₂ fixation during the recovery had low genotype × environment interaction indicating potential for using these traits for selecting genotypes in peanut improvement programs.     

Relationship between Biomass Production and Nitrogen Fixation under Drought-Stress Conditions in Peanut Genotypes with Different Levels of Drought Resistance

The relationship between biomass production and N₂ fixation under drought‐stress conditions in peanut genotypes with different levels of drought resistance is not well understood. The objective of this study was to determine the effect of drought on biomass production and N₂ fixation by evaluating the relative values of these two traits under well watered and water‐stress conditions. Twelve peanut genotypes were tested under field conditions in the dry seasons of 2003/2004 and 2004/2005 in north‐east Thailand. A split‐plot design with four replications was used. Main‐plot treatments were three water regimes [field capacity (FC), 2/3 available soil water (AW) and 1/3 AW], and sub‐plot treatments were 12 peanut lines. Data were recorded on biomass production and N₂ fixation under well watered and water‐stress conditions. Genotypic variations in biomass production and N₂ fixation were found at all water regimes. Biomass production and N₂ fixation decreased with increasing levels of drought stress. Genotypes did not significantly differ in reductions for biomass production, but did differ for reductions in N₂ fixation. High biomass production under both mild and severe drought‐stress conditions was due largely to high potential biomass production under well‐watered conditions and, to a lesser extent, the ability to maintain high biomass production under drought‐stress conditions. High N₂ fixation under drought stress also was due largely to high N₂ fixation under well‐watered conditions with significant but lower contributions from the ability to maintain high nitrogen fixation under drought stress. N₂ fixation at FC was not correlated with the reduction in N₂ fixation at 2/3 AW and 1/3 AW. Positive relationships between N₂ fixed and biomass production of the tested peanut genotypes were found at both levels of drought stress, and the relationship was stronger the more severe the drought stress. These results suggested that the ability to maintain high N₂ fixation under drought stress could aid peanut genotypes in maintaining high yield under water‐limited conditions.     

Rooting traits of peanut genotypes with different yield responses to pre-flowering drought stress

Water stress during the vegetative development normally is not detrimental and sometimes actually increases yield of peanut (Arachis hypogaea L.). Root growth might play an important role in response to early season drought in peanut and might result in an increase in yield. Information on the response of root characters of diverse peanut genotypes to these conditions will provide useful information for explaining mechanisms and improving peanut genotypes for exploiting positive interaction for pod yield under pre-flowering drought. The aim of this study, therefore, was to investigate the root dry weight and root length density of peanut genotypes with different yield responses to pre-flowering drought stress and their relationships with pod yield. Field experiments were conducted at the Field Crop Research Station of Khon Kaen University, Khon Kaen, Thailand during February to July 2007 and during February to July 2009. A split-plot experiment in a randomized complete block design was used. Two water management treatments were assigned as the main plots, i.e. field capacity and pre-flowering stress, and six peanut genotypes as the sub-plots. Total crop dry matter, root dry weight and root length density were recorded at 25 DAE, R5 and R7. Top dry weight and pod yield were measured at harvest and pod harvest index (PHI) was computed using the data on pod yield and biomass. Peanut genotypes were categorized into three groups based on their responses to drought for pod yield, e.g. increasing, decreasing and non-responsive groups. The genotypes of each group showed a differential response for root quantity and distribution. The increasing pod yield group had more root dry weight and root length density in the deeper soil layers during pre-flowering stress compared to the non-stress treatment. The non-responsive group showed no root response under pre-flowering drought conditions compared to the non-stress treatment. A larger root system alone without considering distribution may not contribute much to pod yield but a higher RLD at deeper layers may allow plants to mine more available water in the sub-soil. However, as yield is a complex trait, several mechanisms may be involved. The increasing pod yield group also had the ability to maintain a high PHI.