Limestone and gypsum effects on calcium nutrition of ‘Florunner’ and ‘NC‐7’ Peanuts

Abstract

Minimum sufficiency levels of hull and seed Ca for maximum yield and grade of runner or Virginia type peanuts (Arachis hypogaea L.) have not been established and there is limited information on single and combined effects of limestone and gypsum on production and quality of peanuts. Field experiments were conducted on runner and Virginia type peanuts to study single and combined effects of limestone and gypsum on yield and grade, and to attempt to establish minimum sufficiency levels of hull and seed Ca for maximum yield and grade of each type. Gypsum treatments, O, low, medium, and high rates, were superimposed on residual limestone rates on three sites with ‘Florunner’ (runner type) and on one site with ‘NC‐7’ (Virginia type) peanuts. Yield and grade of Florunner peanuts were not increased by limestone or gypsum treatments on any site even though soil Ca concentrations (Mehlich 1) ranged from 152 to 200 mg/kg among the sites. These levels were lower than the Georgia recommended minimum sufficiency value of 250 mg/kg. However, yield and grade of ‘NC‐7’ peanuts were increased by limestone or gypsum, but maximum yield occurred only where gypsum was applied even with soil Ca levels of 682 mg/kg. The minimum hull Ca level of 1.2 g/kg and seed Ca of 0.42 g/kg were sufficient for Florunner peanuts since yields and quality were not increased by limestone or gypsum application. Maximim yield and grade were achieved with Florunner at leaf, hull, and seed Ca concentrations of 13.2, 1.2, and 0.42 g/kg as compared with 26.0, 1.9, and 0.58 g/kg for NC‐7, respectively. These data show that NC‐7 has a higher Ca requirement than Florunner.     

Acid soil tolerances of two wheat cultivars related to soil Ph,KCl‐extractable aluminum and degree of aluminum saturation

Aluminum toxicity, associated with soil acidity, is a major growth‐limiting factor for plants in many parts of the world. More precise criteria are needed for the identification of potential Al toxicity in acid soils. The objective of the current study was to relate the acid soil tolerances of two wheat cultivars to three characteristics of an acid Tatum subsoil (clayey, mixed, thermic, typic Hapludult): pH in a 1:1 soil to water suspension; KCl‐extractable Al; and degree of Al saturation. Aluminum‐tolerant ‘BH 1146’ (Brazil) and Al‐sensitive ‘Sonora 63’ (Mexico) wheat cultivars were grown in greenhouse pots of soil treated with CaCO₃ to establish final soil pH levels of 4.1, 4.6, 4.7, 4.9, 5.2 and 7.3. Soil Al, Ca and Mg were extracted with 1 N KCl, and Al saturation was calculated as KCl‐Al/KCl Al + Ca + Mg%.

Within the soil pH range of 4.1 to 4.9, BH 1146 tops and roots produced significantly more dry matter than did those of Sonora 63; however, at pH 5.2 and 7.3, the top and root yields of the two cultivars were not significantly different. Significant cultivar differences in yield occurred over a range of 36 to 82% saturation of the Tatum soil. Graphs of relative top or root yields against soil pH, KCl‐extractable Al and Al saturation indicated that the two cultivars could be separated for tolerance to Tatum soil under the following conditions: pH less than 5.2 (1:1 soil‐water); KCl‐Al levels greater than 2 c mole kg^‐1 and Al saturations greater than 20%. Results demonstrated that any soil test used to predict Al toxicity in acid soils must take into account the Al tolerances of the plant cultivars involved.     

Screening Kentucky bluegrass for aluminum tolerance

Aluminum (Al) toxicity is a growth‐limiting factor in acid soils for many turfgrasses. The genetic diversity among turfgrass cultivars for Al tolerance is not well known. One hundred‐fifty Kentucky bluegrass (Poa pratensis L.) genotypes (cultivars, selections, and breeding lines) belonging to seven ecotypes were selected to screen for Al tolerance under greenhouse conditions using solution culture, sand culture, and an acid Tatum subsoil (Clayey, mixed, thermic, typic, Hapludult). This soil had 69% exchangeable Al and a pH of 4.4. An Al concentration of 320 μM and a pH of 4.0 in a modified 1/4 strength Hoagland nutrient solution was used in solution screening and sand screening. The grasses were seeded and grown four to five weeks before harvesting. Differences were identified among cultivars and the seven ecotypes by measuring relative growth. ‘Battan’, ‘Viva’, and ‘Nassau’ were the most Al‐tolerant cultivars based on the rank average of the three screening methods. Among the seven ecotypes, BVMG, which refers to cultivars such as ‘Baron’, ‘Victa’, ‘Merit’, and ‘Gnome’, were most Al tolerant while Midwest ecotypes, which are frequently referred to as common Kentucky bluegrasses, consistently exhibited the least Al tolerance. The results indicate that the Kentucky bluegrass cultivars vary genetically in Al tolerance and that there is potential to improve such tolerance with breeding and to refine cultivar‐specific management recommendations regarding soil pH.     

Role of water stress in differential aluminum tolerance of six sunflower cultivars grown in an acid soil

Six cultivars of sunflower (Helianthus annuus L.), were screened under controlled environmental conditions for tolerance to Al stress and water stress imposed separately and in combination with one another. Plants were grown for 4 weeks in waxed cartons containing 1 kg of acid, Al‐toxic Tatum, subsoil (clayey, mixed, thermic, Typic Hapludult) at high (pH 4.3) or low (pH 6.3) Al stress. During the final 2 weeks they were also subjected to low (‐20 to ‐40 kPa) or high (‐60 to ‐80 kPa) water stress. Plant growth responses and symptoms of Al toxicity suggested that a wide range of cultivar sensitivity existed. ‘Manchurian’, ‘S‐212’, ‘S‐254’, and ‘S‐265’ were relatively tolerant to Al toxicity while cultlvars ‘Romania HS‐52’ and ‘RM‐52’ were extremely sensitive. Under high Al stress and high water stress, chloroplasts in cells from the Al‐sensitive cultivar ‘Romania HS‐52’ were smaller and contained less starch than chloroplasts from the Al‐tolerant cultivar ‘Manchurian’. Furthermore, the smaller chloroplasts tended to have fewer grana stacks per unit area than did the chloroplasts from tolerant plants. These differences were not apparent when the Al‐sensitive cultivar was grown either in the absence of Al or water stress. In general, Al‐sensitive cultivars of sunflower were more tolerant to water stress than were Al‐tolerant cultivars. Increasing the soil moisture level reduced Al toxicity in Al‐sensitive cultivars. Similarly, decreasing Al stress partially overcame the detrimental effects of high water stress. Hence, Al stress and water stress are interrelated factors which must be considered in the characterization and breeding of plants for better adaptation to acid soils.     

Differential tolerances of oat cultivars to aluminum in nutrient solutions and in acid soils of Poland

Aluminum tolerant oat cultivars are needed for use on acid soil sites where neutralization of soil acidity by liming is not economically feasible. Oat germplasm in Poland has not been examined for range of Al tolerance. Eleven Polish oat cultivars were screened for Al tolerance in nutrient solutions containing 0, 5 and 15 mg L^‐1 Al. Three of these cultivars showing high to moderate tolerance to Al in nutrient solutions were also grown in greenhouse pots of soil and in field plots of soil over a pH range of 3.8 to 5.5 as determined in 1 N KC1.

The eleven oat cultivars differed significantly in tolerance to Al in nutrient solutions. Based on relative root yield (15 mg L^‐1 Al/no A1%), the cultivars ‘Solidor’ and ‘Diadem’ were most tolerant and ‘Pegaz’ and ‘B‐20’ were least tolerant. For these three cultivars, the order of tolerance to acid soil agreed with the order of tolerance to Al in nutrient solution ‐ namely, Solidor > Diadem > Leanda. Hence, for these cultivars, the nutrient solution methods used appear adequate for selecting plants that are more tolerant to Al in strongly acid soils. Additional study is needed to assess the value of this method for screening a broad range of germplasm.

Superior tolerance of the Solidor cultivar to acid soil was associated with significantly higher concentrations of N in the grain. Hence, results suggest that selecting for acid soil or Al tolerance may increase N efficiency in oats.     

Ozone tolerance related to flavonol glycoside genes in soybean

Ozone toxicity can reduce soybean yields by an estimated 5 to 20%. The most economical and practical solution to the problem would be to use ozone‐tolerant cultivars. Because ozone toxicity is an oxidative stress, one would expect that plants having higher concentrations and proper kinds of antioxidants would be more tolerant. To test this hypothesis, 20 soybean lines or cultivars varying in contents of flavonol glycosides (naturally occurring antioxidants) were tested for ozone tolerance in a fumigation chamber and in phyto‐toxic concentrations of ozone in ambient, unfiltered, air in a greenhouse. In general, ozone tolerance was associated with the presence of kaempferol glycosides, particularly K3 through K6 and K9. Lines containing no kaempferol glycosides (OX942 & OX281) were among the most sensitive to ozone stress. The K9 compound has been associated with reduced numbers of stomata, drought tolerance, and slower growth rates, and this could reduce ozone absorption and toxicity, or K9 may be more effective in detoxifying ozone than other glycosides. Lee soybean was more tolerant to ozone and to manganese (Mn) toxicity (also an oxidative stress) than Forrest. Cross tolerances of plant genotypes to these two stresses deserve additional study. Among cultivars compared, Mukden was ozone tolerant, Columbia and Harosoy were sensitive, and Blackhawk was moderately sensitive.     

Responses of Kentucky bluegrass cultivars to excess aluminum in nutrient solutions

Kentucky bluegrass, Poa pratensis L., is generally regarded as an acid‐soil‐sensitive species. However, previous studies in our laboratory showed that cultivars within the species differed widely in tolerance to acid Tatum subsoil (pH 4.6) which is used routinely to screen plants for aluminum (Al) tolerance. In the early studies, specific differential Al tolerance was not demonstrated. The objective of the current study was to test the hypothesis of differential Al tolerance more precisely in nutrient solutions. In one experiment, acid‐soil‐tolerant Victa and Fylking and acid‐soil‐sensitive Windsor and Kenblue cultivars were grown for 35 days in nutrient solutions containing 0, 2, 4, 6, 12, and 24 mg Al L^‐1, at initial pH 4.5, with no subsequent adjustment. In a second experiment, Victa and Windsor were grown for 30 days in solutions containing 0, 4, and 6 mg Al L^‐1, at initial pH 4.5, with no further adjustment. For Victa and Windsor, tolerance to Al in nutrient solution corresponded with tolerance to acid Tatum subsoil, however, the cultivar difference in tolerance, based on relative root dry weight, was only about 2‐fold, compared with 20‐fold in acid Tatum subsoil. Fylking and Kenblue cultivars, which showed a wide difference in tolerance to acid Tatum subsoil, did not show distinct differences in tolerance to Al in nutrient solutions. Possible reasons for this discrepancy are discussed. Superior Al tolerance of Victa (compared with Windsor) was associated with a greater plant‐induced increase in the pH of its nutrient solutions and a corresponding decrease in concentrations of soluble Al in the filtered solutions at the end of the experiments. Greater Al sensitivity in Windsor (compared with Victa) was not related to reduced uptake of phosphorus (P) or excessive uptake of Al; neither cultivar accumulated appreciable Al concentrations in its shoots. The observed differential acid soil and Al tolerance among bluegrass cultivars appears worthy of further study. Improved understanding of Al tolerance mechanisms would contribute to fundamental knowledge of plant mineral nutrition and could aid plant breeders in tailoring plants for greater tolerance to acid subsoils.     

Tolerance of barley cultivars to an acid,aluminum‐toxic subsoil related to mineral element concentrations in their shoots

Abstract

Barley, Hordeum vulgare L., is extremely sensitive to excess soluble or exchangeable aluminum (Al) in acid soils having pH values below about 5.5. Aluminum tolerant cultivars are needed for use in rotations with potatoes which require a soil pH below 5.5 for control of scab disease. They are also potentially useful in the currently popular “low input, sustainable agriculture (LISA)”; in which liming even the plow layer of soil is not always possible or cost effective, or in situations where surface soils are limed but subsoils are acidic and Al toxic to roots. Ten barley cultivars were screened for Al tolerance by growing them for 25 days in greenhouse pots of acid, Al‐toxic Tatum subsoil (clayey, mixed, thermic, typic Hapludult) treated with either 750 or 4000 μg?g^‐1 CaCO₃ to produce final soil pH values of 4.4 and 5.7, respectively. Based on relative shoot dry weight (weight at pH 4.4/weight at pH 5.7 X 100), Tennessee Winter 52, Volla (England), Dayton and Herta (Denmark) were significantly more tolerant to the acid soil than Herta (Hungary), Kearney, Nebar, Dicktoo, Kenbar and Dundy cultivars. Relative shoot dry weights averaged 28.6% for tolerant and 14.1% for sensitive cultivar groups. Comparable relative root dry weights were 41.7% and 13.7% for tolerant and sensitive cultivars, respectively. At pH 4.4, Al concentrations were nearly three times as high in shoots of sensitive cultivars as in those of the tolerant group (646 vs. 175 μg?g^‐1), but these differences were reduced or absent at pH 5.7. At pH 4.4, acid soil sensitive cultivars also accumulated phosphorus concentrations that were twice as high as those in tolerant cultivars (1.2% vs. 0.64%). At pH 5.7, these P differences were equalized at about 0.7% for both tolerant and sensitive groups. At pH 4.4, shoots of the Al‐sensitive cultivar Nebar contained 1067 μg?g^‐1 Al and 1.5% P. Concentrations of Al and P in the shoots of acid soil sensitive cultivars grown at pH 4.4 exceeded levels reported to produce toxicity in barley. The observed accumulation of such concentrations of Al and P in the shoots of plants grown under Al stress is unusual and deserves further study.     

Soil zinc and pH effects on leaf zinc and the interaction of leaf calcium and zinc on zinc toxicity of peanuts

Abstract

Zinc toxicity of peanuts (Arachis hypogaea L.), resulting from excessive amounts of Zn applied to previous crops, has been observed for many years in a limited number of peanut fields in Georgia. A tentative critical value of 12 mg/kg of Mehlich No.1 extractable soil Zn has been reported, but soil pH should be considered in establishing a more precise critical value since availability of soil Zn is affected greatly by soil acidity. A 3‐year study was conducted on a Tifton loamy sand (thermic, Plinthic Paleudults) to evaluate the relationship between soil pH and soil Zn on concentration of Zn in peanut leaves. Factorial treatments were 0, residual, medium, and high rates of Zn and soil pH levels near 5.5, 5.9, 6.2, and 6.8. Pod yields were not affected by treatments and Zn toxicity was not observed. Leaf Zn was affected more by soil pH than by soil Zn, but correlation coefficients were highest where both soil pH and soil Zn were included in the determination. A regression equation, based on soil pH and soil Zn, showed that an increase in soil Zn from 1.0 to 10.0 mg/kg increased leaf Zn 202 mg/kg at soil pH 4.6 and only 9 mg/kg at pH 6.6. Data from growers’ fields, in which samples were collected from eight healthy and toxic areas, indicated that a leaf Ca:Zn ratio of 50 or less was required for Zn toxicity of peanuts rather than high concentrations of leaf Zn per se.     

Ozone tolerances of soybean cultivars and near‐isogenic lines in a fumigation chamber

Ozone (O₃) toxicity is a potential yield‐limiting factor for soybean (Glycine max L. Merr.) in the United States and worldwide. The most economical solution to the problem is to use O₃‐tolerant cultivars. Thirty‐four cultivars and 87 near‐isogenic lines (NILS) of soybean were screened for O₃ tolerance in a fumigation chamber (250 ppb for three hrs). Most tolerant cultivars tested were ‘Cloud’, ‘T‐276’, ‘T263’, and ‘Kindu’. Moderately tolerant cultivars included ‘Davis’, ‘T‐210’, and ‘Elton’. Most sensitive cultivars were ‘Corsoy 79’, ‘Noir’, and ‘Midwest’. The original ‘Clark’ cultivar was not tested, but ‘Clark 63’ tended to be more tolerant than ‘Harosoy’. The aluminum (Al)‐tolerant ‘Perry’ cultivar also tended toward greater O₃ tolerance than the Al‐sensitive ‘Chief’, as observed earlier. Our rankings of ‘Hark’ as moderately sensitive and ‘Davis’ as moderately tolerant are also in agreement with earlier reports. Among NILS, the order of O₃ tolerance was generally Williams>Clark>Harosoy, but differences were also observed within these parental groups. For example, L68–560 was more tolerant than some other NILS of ‘Harosoy’. ‘L76–1988’ appeared more tolerant to O₃ than other NILS of ‘Williams’, but all ‘Williams’ NILS were more tolerant than most NILS of ‘Harosoy’ and ‘Clark’. Ozone‐tolerant and ‐sensitive soybean cultivars or NILS identified in our study may be useful tools in studies on mechanisms of 03 tolerance and differential 03 tolerances in plants and in the development of ameliorative measures.     

Zinc toxicity symptom development and partitioning of biomass and zinc in peanut plants 1

High soil zinc (Zn) concentrations can cause Zn toxicity in peanuts (Arachis hypogaea L.), which decreases productivity and can be fatal to the plants. The objectives of this study were 1) to determine the optimal sampling time and plant part for diagnosis of Zn toxicity in peanuts, 2) to relate toxicity symptoms to plant Zn concentrations and calcium:zinc (Ca:Zn) ratios, and 3) to model the distribution of Zn and biomass into plant parts in relation to Zn concentration in the whole plant. A greenhouse study utilized four soils (Lakeland sand, Tifton loamy sand, Greenville sandy clay loam, and Greenville sandy clay) with Zn applications of 0, 10, 20, and 40 mg Zn/kg soil. Plants were sampled for analysis of nutrient concentrations, and Zn toxicity ratings were recorded biweekly. Toxicity symptoms became visible 4–8 weeks after planting, with stunting appearing at four weeks, horizontal leaf growth and leaflet folding at six weeks, and stem splitting at eight weeks. Optimal sampling time for diagnosis of Zn toxicity using plant Zn concentrations in peanuts was 6–10 weeks after planting. Zinc toxicity ratings were more highly correlated with plant Zn concentration in stems (r = 0.84) than leaves (r = 0.79). However, the Zn concentration in the total aboveground plant had a correlation coefficient (r = 0.83) almost as high as for the stems alone and is more convenient to measure. Zinc toxicity symptoms occurred with Zn concentration in plant shoots >240 mg/kg, and Ca:Zn ratios <35. Increases in total plant Zn concentration were partitioned into peanut stems more than into leaves. Zinc toxicity also reduced stem biomass accumulation to a greater degree than leaf biomass.     

Aluminum toxicity and high bulk density: Role in limiting shoot and root growth of selected aluminum indicator plants and eastern gamagrass in an acid soil

Abstract

Shallow rooting and susceptibility to drought are believed to be caused, at least in part, by strongly acidic (pH <5.5, 1:1 soil‐water), aluminum (Al)‐toxic subsoils. However, this hypothesis has not been clearly confirmed under field conditions. The Al toxicity hypothesis was tested on a map unit of Matawan‐Hammonton loam (0–2% slope) on unlimed and limed field plots (pH range 5.1 to 5.8) at Beltsville, MD, during 1994 to 1998. Aluminum‐tolerant and sensitive pairs of barley (Hordeum vulgare L.), wheat [Triticum aestivum (L.)], snap bean (Phaseolus vulgaris L.), and soybean [Glycine max (L.) Merr.] cultivars were used as indicator plants. Eastern gamagrass [Tripsacum dactyloides (L.) L.], cultivar ‘Pete’, reported to tolerate both chemical and physical stress factors in soils, was grown for comparison. Shoots of Al‐sensitive ‘Romano’ snap beans showed a significant response to liming of the 0–15 cm surface layer, but those of Al‐tolerant ‘Dade’ did not, indicating that Al toxicity was a growth limiting factor in this acid soil at pH 5.1. Lime response of the Al‐tolerant and sensitive cultivars of barley, wheat, and soybean were in the same direction but not significant at the 5% level. Aluminum‐tolerant and sensitive cultivars did not differ in abilities to root in the 15–30 cm soil depth. Only 9 to 25% of total roots were in this layer, and 75 to 91% were in the 0–15 cm zone. No roots were found in the 30–45 cm zone which had a pH of 4.9. Soil bulk density values of 1.44 and 1.50 g cm^?3 in the 15–30 and 30–45 cm zones, respectively, indicated that mechanical impedance was a primary root barrier. Results indicated that restricted shoot growth and shallow rooting of the Al‐indicator plants studied in this acid soil were due to a combination of Al toxicity and high soil bulk density. Confounding of the two factors may have masked the expected response of indicator plants to Al. These two growth restricting factors likely occur in many, if not most acid, problem subsoils. Studies are needed to separate these factors and to develop plant genotypes that have tolerance to multiple abiotic stresses. Unlike the Al indicator cultivars, eastern gamagrass showed high tolerance to acid, compact soils in the field and did not respond to lime applications (pH 5.1–5.8).     

Effect of cultivar and cadmium rate upon the nutrient content of soybean plants

An experiment was conducted to evaluate the effect of soybean (Glycine max L.) cultivar, Cd rate, and cultivar x Cd rate interaction upon nutrient concentrations in the plant. Cultivars rated as T (tolerant) or S (susceptible) to Cd were included in the study. A factorial combination of 10 cultivars and 4 levels of Cd were randomized in 4 replications of a completely randomized design. Additions of CdCl₂ dissolved in distilled water were made to weighed quantities of dry soil. The soil was a Flanagan silt loam (Aquic Argiudoll). Four weeks after planting, plants were harvested, air dried and dry ashed. Chemical determinations of Zn, Fe, Mn, Cu, K, Ca, Mg and P in plants were made by emission spectroscopy.

Nutrient concentrations were affected by cultivar and rate of Cd and generally, nutrient concentrations decreased as rate of Cd increased. The Cd linear x cultivar interaction significantly affected plant concentration of each element except P indicating that the linear effect of Cd was not consistent among all cultivars. A comparison of “susceptible”; cultivars with “tolerant”; cultivars showed significant differences in nutrient concentration of each element except K. Plant K concentration was significantly associated with a Cd linear x T (tolerant) vs. S (susceptible) interaction indicating that the linear trend due to Cd rate differed between cultivars rated S or T to Cd.     

Effect of nickel on two common bean cultivars

Two common bean (Phaseolus vulgaris L.) cultivars, Carioca and IAPAR‐14, were grown in a nutrient solution in the presence of 0,1,2, and 4 mg/L of nickel (Ni). Both cultivars developed symptoms of toxicity in the roots and tops., but especially in the leaves. Dry matter was reduced by the higher Ni levels. The IAPAR‐14 cultivar, however, was more tolerant than the Carioca cultivar to Ni. Yield decreased as Ni levels in the solutions were increased. There was no seed production at the 4 mg/L Ni concentration for either of the two cultivars. A 50% reduction in leaf chlorophyll was observed when 4 mg/L Ni was supplied. Mineral analysis of several plant parts showed a build up of Ni concentration in the roots which was accompanied by higher iron (Fe) concentrations. Increasing Ni supply resulted in no significant changes in the concentrations of calcium (Ca), magnesium (Mg), manganese (Mn), and zinc (Zn) in the tissue. The levels of nitrogen (N), phosphorus (P), potasium (K), copper (Cu), and Ni, however, increased, as a consequence either of either the dilution effect, interaction in absorption, or both. No explanation can be given for the observed differential tolerance.     

Changes in total protein profiles of barley cultivars in response to toxic boron concentration

In this study, ten‐day‐old seedlings of barley {Hordeum vulgare L. cultivar Anadolu [boron (B)‐tolerant] and Hamidiye (B‐sensitive)} were used. Boron‐treated plants were grown on H₃BO₃ solution (final concentration of 10 mM) for five days. Control plants received no B treatment during this period. Total protein patterns were obtained by analysis of total protein extract from root and leaf tissues of control and B‐treated plants using two‐dimensional gel electrophoresis followed by silver staining. The protein profile of B‐treated seedlings of each cultivar was compared to the profile of control (no stress treatment) plants of the same cultivar. Silver‐stained gels showed that B stress caused increases or decreases in a number of proteins in root and leaf tissues. Moreover, as a result of B treatment, one newly synthesized protein with relative molecular weight (M_r) of 35.0 kDa was detected in root profile of the tolerant cultivar. This protein failed to show up in root profile of the B‐treated sensitive cultivar. Three proteins were quantitatively increased in B‐treated root profile of both cultivars. Following B treatment, three proteins were increased in root profile of the tolerant cultivar, but were not changed in the sensitive one. In leaf tissues, however, there were remarkable changes in total protein profiles after B treatment, relative to the control. Following B treatment, in leaf tissues, at least seven proteins were increased in amount in tolerant cultivar but were unchanged in the susceptible one. In tolerant and sensitive cultivars, amounts of two proteins were increased in B‐treated plants, relative to control seedlings. In addition, four proteins (M_r:29, 58, 58, and 22 kDa) were unchanged in control and B‐treated seedlings of the tolerant cultivar. In the susceptible cultivar however, among these four proteins, the first one (M_r:29) was very much reduced and the others (M_r: 58, 58, and 22 kDa) were completely lost in B‐treated seedlings. Moreover, following B treatment, a set of high‐molecular‐weight proteins was quantitatively decreased in the susceptible cultivar but was unchanged in the tolerant cultivar. These results indicate that in barley, certain proteins may be involved in tolerance to B toxicity. In this study, changes in polypeptide composition as a result of B toxic concentration in leaf tissues were more abundant than in roots. Therefore, it is suggested that these changes, especially at shoot level may form the basis of the tolerance mechanism to B toxicity.     

Zinc alleviates growth inhibition and oxidative stress caused by cadmium in rice

A hydroponic experiment with two rice cultivars differing in cadmium (Cd) tolerance was conducted to investigate the alleviating effect of zinc (Zn) on growth inhibition and oxidative stress caused by Cd. Treatments consisted of all combinations of two Zn concentrations (0.2 and 1 μM), three Cd concentrations (0, 1, and 5 μM), and two rice cultivars (Bing 97252, Cd‐tolerant; Xiushui 63, Cd‐sensitive). Cd toxicity caused a dramatic reduction in plant height and biomass, chlorophyll concentration and photosynthetic rate, and an increase in Cd concentration in both roots and shoots, malondialdehyde (MDA) concentration, and superoxide dismutase (SOD) and peroxidase (POD) activities in shoots. The response of all these parameters was much larger for Xiushui 63 than for Bing 97252. Addition of Zn to the medium solution alleviated Cd toxicity, which was reflected in a significant increase in plant height, biomass, chlorophyll concentration, and photosynthetic rate, and a marked decrease in MDA concentration and activity of anti‐oxidative enzymes. However, it was noted that Zn increased shoot Cd concentration at higher Cd supply, probably due to the enhancement of Cd translocation from roots to shoots. Therefore, further studies are necessary to determine the effect of Zn supply on Cd translocation from vegetative organs to grains or grain Cd accumulation before Zn fertilizer is applied to Cd‐contaminated soils to alleviate Cd toxicity in rice.     

Tolerances of wheat germplasm to acid subsoil

Aluminum toxicity is a major growth limiting factor for plants in many acid soils of the world. Correcting the problem by conventional liming is not always economically feasible, particularly in subsoils. Aluminum tolerant plants provide an alternative and long‐term supplemental solution to the problem. The genetic approach requires the identification of Al tolerance sources that can be transferred to cultivars already having desirable traits. Thirty‐five cultivars and experimental lines of wheat (Triticum aestivum L. em. Thell) were screened for Al tolerance on acid Tatum soil (clayey, mixed thermic, typic Hapludult) receiving either 0 or 3500 mg CaCO₃/kg (pH 4.1 vs. pH 7.1). Entries showed a wide range of tolerance to the acid soil. On unlimed soil at pH 4.3, absolute shoot dry weights differed by 5‐fold, absolute root dry weights by 6.5‐fold, relative shoot weights (wt. at pH 4.3/wt. at pH 7.1 %) by 4.7‐fold and relative root dry weights by 7‐fold. Superior acid soil (Al) tolerance of ‘BH‐1146’ from Brazil and extreme sensitivities of cultivars ‘Redcoat’ (Indiana, USA) and ‘Sonora 63’ (Mexico) were confirmed. Seven experimental (CNT) lines from Brazil showed a range of acid soil tolerance but were generally more tolerant than germplasm from Mexico and the USA. One line, ‘CNT‐1’, was equal to BH‐1146 in tolerance and may be useful in transferring Al tolerance to existing or new cultivars. Five durum cultivars (Triticum, durum, Desf.) were extremely sensitive to the acid Tatum subsoil at pH 4.3 compared with pH 7.1.     

EFFECTS OF CALCIUM AND SALINITY STRESS ON QUALITY OF LETTUCE IN SOILLESS CULTURE

Abstract

Fine fescues (Festuca spp.) are generally considered acid tolerant compared to other cool‐season turfgrasses. However, there is little information on aluminum (Al) tolerance of fine fescues at both the species and cultivar levels. The objectives of this study were to identy cultivars of fine fescues with superior ability to tolerate Al, and compare the Al tolerance of endophyte infected and endophyte‐free cultivars in Al tolerance. A total of 58 cultrvars of fine fescues belonging to five species or subspecies [14 hard fescue (F. longifolia Thuill), 25 Chewings fescue (F. rubra L. ssp. commutata Gaud), 15 strong creeping red fescue (F. rubra L. ssp. rubra), two slender creeping red fescue (F. rubra L. ssp. trichophylla), and two sheep fescue (F. ovina L.)] were selected from the 1993 National Fineleaf Fescue Test and screened under greenhouse conditions using solution culture, sand culture, and acid Tatum soil (Clayey, mixed, thermic, typic, Hapludult). The acid Tatum soil had 69% exchangeable Al and a pH of 4.4. An Al concentration of 640 μM and a pH of 4.0 were used in solution culture and sand culture screening. The grasses were seeded and grown for three weeks before harvesting. Aluminum tolerance was assessed by measuring relative root length, shoot length, root weight, shoot weight, and total dry matter. Differences in Al tolerance were identified at both the species and cultivar level based on relative growth were as follows: i) hard fescue and Chewings fescue were more Al tolerant than strong creeping red fescue; ii) within species or subspecies, significant differences were found among cultvars of Chewings fescue, strong creeping red fescue, slender creeping red fescue, and sheep fescue; whereas no difference was observed among the hard fescue cultivars; and iii) the cultivars containing endophyte exhibited greater Al tolerance compared the eudophyte‐free cultivars. The results indicate that fine fescues vary in Al tolerance and there is potential to improve Al tolerance with breeding and to refine their management recommendations regarding soil pH.     

Evaluation of switchgrass entries for acid soil tolerance

Abstract

Crop and forage yields are significantly reduced by strong soil acidity throughout much of the northeastern United States. Switchgrass (Panicum virgatum L.) is a valuable perennial warm‐season pasture species generally regarded as tolerant to stress conditions, i.e., infertile, dry, or low pH soils; however, switchgrass has not been studied for variability in acid soil tolerance. The objectives of this study were (a) to compare the responses of different switchgrass entries to soil acidity, and (b) to identify selected agribotanical trait response to unlimed (‐L) and limed (+L) soil. Sixteen entries (cultivars, germplasms, and breeding populations) were studied in short‐ and meso‐term experiments. Unlimed (pH 4.9) and limed (pH 5.9) treatments of a sandy loam soil (Typic Dystrochrept) were used in both experiments. Switchgrass seedlings were exceptionally tolerant of soil acidity in the short‐term experiment. In the meso‐term experiment, acid soil stress significantly reduced all agribotanical traits (plant height, leaf area, top weight, and root weight) determined in the study when compared to +L plants. There were significant, positive correlations among the agribotanical traits; however, the effect of ‐L soil was more obvious on root weight and less so on plant height. Entries 922 GST6, 920 AST6, 921 DST6, and 922 BST6 showed superior general adaptability and promising forage production, while cultivars Carthage and PI 142138 were acid soil tolerant with low productivity. Our data suggests that selection for increased acid soil tolerance in switchgrass may be possible and would result in improved productivity of this grass in acid soil environments.     

不同品种燕麦对镉胁迫响应的差异性研究

利用实验室水培模拟试验,研究了轻度镉胁迫条件下10个燕麦品种生长及吸收积累镉的差异性。结果表明,经5μmol·L-1的镉处理后,供试燕麦品种的株高、根长、地上部与地下部生物量、叶绿素含量、类胡萝卜素含量均出现不同程度的下降,不同品种间存在明显的差异,有的甚至达到极显著水平;不同品种燕麦对镉的吸收与积累也存在明显差异;燕麦镉的吸收转运与耐性没有直接的联系。按照镉胁迫下燕麦耐镉性和镉含量的冠根比进行聚类分析,可将10个品种分为4类：①镉转运少且耐性强;②转运多但耐性强;③转运多且耐性弱;④转运较少但耐性弱。其中品5号地上部生长抑制率最小,并且镉含量、镉转运量较少,表现出较强的耐镉性,在轻度镉污染土壤上种植品5号有利于降低镉污染对人类健康的风险。