Phytosiderophore release as a criterion for genotypic evaluation of iron efficiency in oat

Iron (Fe) deficiency in small grains grown on calcareous soils results in reduced yields, is difficult and expensive to treat with fertilizer, and is complicated to overcome by genetic field screening due to heterogeneous soil and environmental conditions. Recently, phytosiderophore release has been linked to ability of species and genotypes to resist Fe‐deficiency chlorosis. We propose a laboratory technique to measure phytosiderophore release by Fe‐deficient oat (Avena sativa L.) genotypes as a selection method for Fe‐deficiency chlorosis resistance in oat. Plants were grown in Fe‐limiting nutrient solution and phytosiderophore release was measured on 11 days. Summations of daily phytosiderophore release by 17 oat genotypes correlate well with Fe‐deficiency chlorosis scores in the field (r = ‐0.70, p = 0.01). The proposed method consistently identified the genotypes most susceptible to Fe deficiency but did not clearly separate the moderately susceptible genotypes. In these latter genotypes, other factors such as active uptake sites, root growth rate, utilization of acquired Fe, or soil interactions may be modifying factors to phytosiderophore in Fe efficiency. Quantification of phytosiderophore provides a useful selection criterion for oat by eliminating the most inefficient types and with refinement, may become a powerful tool for identifying Fe efficiency in grass crops.     

Activities of Iron‐Containing Enzymes in Leaves of Two Tomato Genotypes Differing in Their Resistance to Fe Chlorosis

Abstract

Two tomato (Lycopersicon esculentum Mill., cvs. Pakmor and Target) genotypes differing in resistance to iron (Fe) deficiency were grown in nutrient solution under controlled environmental conditions over 50 days to study the relationships between severity of leaf chlorosis, total concentration of Fe, and activities of Fe‐containing enzymes in leaves. The activities of Fe‐containing enzymes ascorbate peroxidase, catalase, and guaiacol peroxidase, and additionaly the activity of glutathione reductase, an enzyme that does not contain Fe, were measured. Plants were supplied with 2 × 10^?7 M (Fe deficient) and 10^?4 M (Fe sufficient) FeEDTA, respectively. Leaf chlorosis appeared more rapidly and severely in Target (Fe deficiency senstive genotype) than Pakmor (Fe deficiency resistant genotype). On day 50, Pakmor had 2‐fold more chlorophyll than Target under Fe deficiency, while at adequate supply of Fe the two genotypes were very similar in chlorophyll concentration. Despite distinct differences in development of leaf chlorosis and chlorophyll concentrations, Pakmor and Target were very similar in concentrations of total Fe under Fe deficiency. In contrast to Fe concentration, activities of Fe‐containing enzymes were closely related to the severity of leaf chlorosis. The Fe‐containing enzymes studied, especially catalase, showed a close relationship with the concentration of chlorophyll and thus differential sensitivity of tomato genotypes to Fe deficiency. Glutathione reductase did not show relationship between Fe deficiency chlorosis and enzyme activity. The results confirm that measurement of Fe‐containing enzymes in leaves is more reliable than the total concentration of Fe for characterization of Fe nutritional status of plants and for assessing genotypical differences in resistance to Fe deficiency. It appears that Fe deficiency‐resistant genotype contains more physiologically available Fe in tissues than the genotype with high sensitivity to Fe deficiency.     

Screening for resistance to iron deficiency chlorosis in dry bean using iron reduction capacity

Identifying cultivars resistant to iron (Fe) deficiency chlorosis so prevalent in calcareous soils is a more economical solution than fertilizer application in field crops. The current method of screening for resistance using chlorosis ratings in field trials is time consuming and highly variable. Root Fe reduction successfully separated cultivars or rootstocks, varying widely in resistance, of soybean (Glycine max L.), peach (Prunus persica L.), and grape (Vitis spp.), but was unsuccessful in sub‐clover (Trifolium subterraneum L.). Dry bean (Phaseolus vulgaris L.) exhibits Fe deficiency chlorosis in calcareous soils and initiates Fe reduction by the roots in response to such stress. The resistance of 24 dry bean cultivars to Fe deficiency chlorosis was assessed by measuring and summing daily Fe reduction by the roots. The cultivars were grown both hydroponically in an environmental chamber in low Fe solutions (0.05 mg‐L^‐1) and at three field sites in both 1995 and 1996. A significant relationship (P<0.01) between field chlorosis scores made 36 days after planting and root Fe reduction summations was observed for all sites in 1995 and 1996 (r = ‐0.42 to ‐0.71). The variability of chlorosis scores among sites, especially in 1996, points out the difficulty of using field chlorosis scores for screening. These results indicate that measurements of root Fe reduction can be used to predict resistance to Fe deficiency chlorosis in dry bean. Successful implementation of this technique should reduce if not eliminate field trials for screening resistance to Fe deficiency chlorosis.     

Evaluation of world collection of kabuli chickpea for resistance to iron-deficiency chlorosis

Summary Iron-deficiency chlorosis is often seen in chickpea (Cicer arietinum L.) fields in the Mediterranean region and is particularly severe in fields where iron-deficiency susceptible cultivars are sown. Therefore, ICARDA's breeding programme field evaluated 6224 kabuli chickpea germplasm accessions for iron-deficiency chlorosis on a high pH Calcic Rhodoxeralf soil (pH 8.5, 20–25% calcium carbonate) at Tel Hadya, Syria during the winter and spring of 1987/88. Two resistant and 17 susceptible lines were grown during autumn, winter and spring of 1988/89 to examine the effect of sowing time on the appearance of the deficiency. About 99% of accessions showed no iron-deficiency symptoms. Evaluation of susceptible accessions during autumn, winter, and spring sowing revealed that iron-deficiency chlorosis was more pronounced during winter sowing. There were also significant genotype x season interactions, indicating differential responses of genotypes to time of sowing. Since the iron-deficiency chlorosis character is controlled by recessive genes, a negative selection to discard the susceptible lines from breeding material is recommended as an effective breeding strategy.Joint contribution from ICARDA and ICRISAT (International Crops Research Institute for Semi-Arid Tropics), Patancheru P.O., A. P. 502 324, India.     

Genetic Differences in Resistance to Iron Deficiency Chlorosis in Peanut

Iron (Fe) deficiency has been a widespread problem in peanut (Arachis hypogaea L.) grown on calcareous soils of northern China and has resulted in significant yield losses. Field observations showed considerable variability in visual chlorosis symptoms among peanut cultivars in the same soil. The objective of this study was to confirm the genetic differences in resistance to Fe-deficiency chlorosis in peanut and to identify feasible indicators for screening Fe-efficient genotypes. Resistance to Fe chlorosis of sixteen peanut cultivars grown on calcareous soil was evaluated in the field and physiological responses to Fe-deficiency stress were studied in nutrient solution. There were significant differences in resistance to Fe-deficiency chlorosis among the sixteen peanut cultivars tested, which was identified with SPAD readings, active Fe concentrations in young leaves in the early growth stages, and the pod yield. For Fe-resistant peanut cultivars, Fe-reduction capacity and quality of releasing hydrogen ions from roots increased under Fe-deficiency stress. Highly correlated relationships were observed between the summation of root Fe reduction and field chlorosis scores for sixteen cultivars (r² = 0.79). It was concluded that Fe-reduction capacity was a better physiological indicator for screening Fe-efficient peanut genotypes of the mechanisms measured.     

Modified procedures for commercial adaptation of root iron‐reducing capacity as a screening technique

Abstract

Genotypic evaluation is critical to development of soybean [Glycine max (L.) Merr.] cultivars with genetic resistance to Fe‐deficiency chlorosis. Root Fe³⁺ reducing activity is correlated with genotypic resistance to Fe chlorosis measured in field nurseries, and thus may be a reliable method for identifying chlorosis‐resistat genotypes. However, to develop methods useful for large‐scale screening, several modifications of the previously published procedure for measuring root Fe³⁺ reducing activity were investigated. Several hydroponic experiments were conducted to test proposed modifications. It was determined that: (a) different genotypes may be grown together in the same nutrient solution without affecting Fe³⁺ reduction, (b) genotype separation is maximized by growth in CaCO₃ buffered solution (37.5 mg L^?1), (c) a labor‐intensive elongation step can be eliminated, and (d) denotype evaluation can be accomplished without introducing Fe into the hydroponic solutions. These refinements to the procedure should allow its adaptation and use in soybean breeding programs.     

Iron‐manganese interactions among clones of Nilegrass

Tetraploid clones of Nilegrass (Acroceras macrum, Stapf.) develop a chlorosis resembling iron (Fe) deficiency on acid (pH 5.0) soils in the Midlands of KwaZulu, Natal, South Africa. Hexaploid and pentaploid clones appear more resistant to the disorder. Iron deficiency would not be expected in such acid soils, but foliar sprays of Fe sulfate reduce the symptoms within 24 hours. Aluminum (Al) toxiciry has been ruled out as a cause of this chlorosis on the basis of soil tests. Manganese (Mn)‐induced Fe deficiency has been postulated. Six Nilegrass clones, differing in ploidy levels, were grown under low Fe or high Mn levels in nutrient solutions, in Mn‐toxic soil, in calcareous soil and in a standard potting soil at pH 7.0. Differential chlorosis symptoms, similar to those observed in the field, were reproduced in plants grown in low Fe or high Mn solutions, in neutral potting soil and in calcareous soil at pH 7.8. Based on plant symptoms and dry weights, the tetraploids were generally more sensitive to these conditions than hexaploid or pentaploid clones. However, in Mn‐toxic soil, plants had leaf tip necrosis rather than the chlorosis typical of Fe deficiency. When grown in a standard potting soil at pH 7.0, plants showing chlorosis accumulated higher concentrations of phosphorus (P), Al, copper (Cu), Mn, Fe, and zinc (Zn) than non‐chlorotic plants. Differential susceptibility to chlorosis is apparently associated with interference of such elements in Fe metabolism, and not with differential Fe concentrations in plant shoots. Additional studies are needed to determine the chemical states of Fe and Mn in root zones and within plant shoots of these clones. Resolution of the differential chlorosis phenomenon would contribute to fundamental knowledge in mineral nutrition and could be helpful in tailoring plant genotypes to fit problem soils.     

Factors related to iron uptake by dicotyledonous and monocotyledonous plants. I. pH and reductant

Some plants respond to Fe‐deficiency stress by inducing Fe‐solubilizing reactions at or near the root surface. In their ability to solubilize Fe, dicotyledonous plants are more effective than monocotyledonous plants. In this study we determined how representative plants differ in their response when subjected to Fe‐deficiency stress in a calcareous soil and in nutrient solutions. Iron‐inefficient genotypes of tomato, soybean, oats, and corn all developed Fe chlorosis when grown in soil, whereas Fe‐efficient genotypes of these same species remained green. The same genotypes were grown in complete nutrient solutions and then transferred to nutrient solutions containing N (as NO₃ ^‐) and no Fe.

The T3238 FER tomato (Lycopersican esculentum Mill.) Fe‐efficient) was the only genotype that released significant amounts of H from the roots (the pH was lowered to 3.9) and concomitantly released reductants. Under similar conditions, Hawkeye soyhean [Glycine max (L.) Merr.] released reductants but the solution pH was not lowered. Both Fe‐inefficient and Fe‐efficient genotypes of oats (Avena sativa L.) and corn (Zea mays L.) released insufficient H or reductant from their roots to solubilize Fe; as a result, each of these genotypes developed Fe‐deficiency (chlorosis).

The marked differences observed among these genotypes illustrate the genetic variability inherent within many plant species. A given species or genotype may accordingly not be adapted to a particular soil. Conversely, a given species or genotype may be found (or developed) that is precisely suited for a particular soil. In this event, the need for soil amendments may be reduced or eliminated.     

Soybean genotype evaluation for iron deficiency chlorosis using sodium bicarbonate and tissue culture

The evaluation of soybean genotypes for resistance to iron deficiency through field experiments is complicated by variation in symptom expression. The objective of this study was to develop a tissue culture technique that could distinguish between Fe‐efficient and Fe‐inefficient genotypes. Ten soybean genotypes varying in sensitivity to iron deficiency were planted at 5 locations and rated based on chlorosis expression. For the lab evaluation, friable callus of the ten genotypes was placed on a 4MSII medium amended with 10 mM NaHCO₃. Callus growth reduction relative to a control medium without NaHCO₃ was recorded. Callus weight of all cultivars was affected by the addition of NaHCO₃ however, significant differences in growth reduction among genotypes was observed. The high correlation between callus growth reduction and field chlorosis ratings observed (r²=0.92) and the fact that the expiant source plant can be grown to produce seed indicates that this technique would be useful in a soybean breeding program.     

Physiological responses of grapevine callus cultures to iron deficiency

Grapevine is considered a ‘Strategy I’ plant because it performs some peculiar biochemical and physiological responses when grown under iron (Fe) deficiency stress conditions. Callus cultures were started from leaf and internode cuts of micropropagated plantlets of two grapevine genotypes well known for their Fe‐chlorosis characteristic: Vitis riparia a very susceptible genotype and Vitis berlandieri a resistant one. Modification of NADH: ferric (Fe³⁺) reductase activity was spectrophotometrically evaluated by following the formation of the complex ferrous (Fe²⁺)‐(BPDS)₃, while the malic and citric acid production were determined in callus cultures grown both in the presence (+Fe) and absence (‐Fe) of Fe. Moreover, a microsomal fraction was isolated from the calli to evaluate the H⁺‐ATPase and the Fe³⁺‐EDTA reductase activities. As expected, calli of the Fe‐efficient genotype (V. berlandieri) was able to enhance Fe³⁺‐EDTA reductase activity when growing under Fe deficiency while the Fe‐chlorosis susceptible V. riparia could not or did it with lower efficiency. Therefore, the H⁺‐ATPase assay showed a higher enzymatic activity in the microsomal fraction isolated from Vitis berlandieri grown without Fe with respect to its control (+Fe). Organic acid determination gave quite contradictory results, specially regarding malic acid which, under our study conditions, seemed not to be linked with the strategies of response to Fe deficiency.     

On‐farm diagnosis and management of iron chlorosis in groundnut

Abstract

Iron (Fe) chlorosis is a major nutritional constraint to groundnut (Arachis hypogaea L.) productivity in many parts of the world. On‐farm research was conducted at a Fe‐chlorotic site to evaluate the performance of three genotypes (TMV‐2, ICGS‐11, and ICGV‐86031), three fertilizer practices [no fertilizer control, fanners practice (125: 200: 0 kg NPK ha^?1), recommended practice (20: 50: 30 kg NPK ha^?1)], and two Fe treatments (non‐sprayed control and foliar FeSO₄ sprays) for their effect on Fe‐chlorosis and haulm and pod yields. These treatments were tested in a strip‐split plot design with four replicates. Results revealed that TMV‐2 and ICGS‐11 were susceptible to Fe‐chlorosis and produced significantly smaller haulm and pod yield, whereas, ICGV‐8603 1 was tolerant to Fe‐chlorosis. Farmer's fertilizer practice had the highest incidence of Fe‐chlorosis. Extractable Fe and chlorophyll content in the fresh leaves were the best indices of Fe‐status and were significantly (P<0.01) correlated with visual chlorosis ratings. Foliar application of FeSO₄ (0.5 w/ v) was effective in correcting Fe‐chlorosis and increased pod yield by about 30 to 40% in susceptible genotypes. These results suggests that use of tolerant genotypes such as ICGV‐86031 or foliar application of FeSO₄ in susceptible genotypes such as TMV‐2 and ICGS‐11 in combination with recommended fertilizer levels is an effective management package for alleviating Fe‐chlorosis in groundnut.     

Response of five citrus rootstocks to iron deficiency

Citrus established in calcareous soils can be affected by iron (Fe)‐deficiency chlorosis which limits yield and the farmers' income. The degree of deficiency depends on the rootstock, but the resistance to Fe chlorosis still requires further investigation. To study physiological parameters of citrus rootstocks that could be used to evaluate resistance to Fe deficiency, plants of Troyer citrange (Citrus sinensis L. Osb. × Poncitrus trifoliata L. Raf.), Carrizo citrange, Volkamer lemon (Citrus volkameriana Ten. & Pasq.), alemow (Citrus macrophylla Wester), and sour orange (Citrus aurantium L.) were grown in nutrient solutions with 0, 5, 10, 15, or 20 μM Fe. For each rootstock, plant height, root and shoot dry weights, and concentration of Fe in the shoots and roots were measured at the end of the experiment. Chlorophyll (CHL) concentration was estimated throughout the experimental period using a portable CHL meter (SPAD‐502) calibrated for each rootstock. At the end of the experiment, CHL fluorescence parameters were measured in each rootstock with a portable fluorimeter. Maximal and variable fluorescence values indicated that the photochemistry of Troyer was more affected by a low concentration of Fe in the nutrient solution than that of other rootstocks. To compare rootstocks, the absolute CHL concentration was converted into relative yield by employing a scaling divisor based on the maximum value of total CHL in plants without Fe‐deficiency symptoms. Exponential models were developed to determine the minimum Fe concentration in nutrient solution required to maintain leaf CHL at 50% of the maximum CHL concentration (IC50). Models were also developed to assess the period of time the rootstocks were able to grow under Fe‐stress conditions before they reached IC50. Volkamer lemon and sour orange needed the lowest Fe concentration (between 4 and 5 μM Fe) to maintain IC50, and Troyer citrange had the highest Fe requirement (14 μM Fe). Citrus macrophylla and Carrizo citrange required 7 and 9 μM of Fe, respectively. Similarly, Volkamer lemon and sour orange rootstocks withstood more days under total Fe depletion or with a low concentration of Fe (5 μM Fe in nutrient solution) until they reached IC50, compared to the other rootstocks. The approach used led to a classification of the rootstocks into three categories, regarding their internal tolerance to Fe chlorosis: resistance (sour orange and Volkamer lemon), intermediate resistance (C. macrophylla and Carrizo citrange), and reduced resistance (Troyer citrange).     

Associating SSR Markers with Soybean Resistance to Iron Deficiency Chlorosis

Abstract

Iron deficiency chlorosis (IDC) causes soybean yield loss to growers when certain varieties are planted on calcareous soils. Planting IDC‐resistant varieties is the best management practice, although they may still exhibit chlorosis under certain environmental conditions. Environmental variation for chlorosis expression impedes progress in improving IDC resistance. Breeders could use molecular marker‐assisted selection (MAS), an environment‐independent tool, to improve soybeans' resistance to IDC. Our objective was to determine the efficiency of simple sequence repeat (SSR) markers in selecting for IDC resistance in soybean. A breeding population was developed using parents differing in IDC resistance and yield potential. The population was advanced to the F₂ and F_2:4 generations. Foliar chlorosis data were recorded for parents and F_2:4 lines in replicated field tests planted on calcareous soils at two Iowa locations in 2000 and 2001. Chlorosis scores between parents and F_2:4 lines varied according to location and year. Genotypic data were obtained on individual F₂ plants, and association between chlorosis scores and allele segregation was tested by single‐factor analysis of variance using 2001 data. Three SSR markers were associated (P ≤ 0.1) with chlorosis scores at each location; however, the identity of the markers associated with chlorosis scores was different at each location. In addition, two SSR markers associated with IDC resistance were examined for their efficacy in improving breeding efficiency. Preliminary data presented herein demonstrate the importance of environment on expression of this soil‐stress factor and the potential of using SSR markers as an environment‐independent selection tool for breeding IDC resistance in soybean.     

Iron deficiency and zinc toxicity in soybean grown in nutrient solution with different levels of sulfur

A typical symptom of iron (Fe) deficiency in plants is yellowing or chlorosis of leaves. Heavy metal toxicity, including that of zinc (Zn), is often also expressed by chlorosis and may be called Fe chlorosis. Iron deficiency and Zn toxicity were evaluated in soybean (Glycine max [L.] Merr.) at two levels each of Zn (0.8 and 40 μM), Fe (0 and 20 μM), and sulfur (S) (0.02 and 20 mM). Reduction in dry matter yield and leaf chlorosis were observed in plants grown under the high level of Zn (toxic level), as well as in the absence of Fe. Zinc toxicity, lack of Fe, and the combination of these conditions reduced dry matter yield to the same extent when compared to the yield of the control plants. The symptoms of Zn toxicity were chlorosis in the trifoliate leaves and a lack of change in the orientation of unifoliate leaves when exposed to light. The main symptoms of Fe deficiency were chlorosis in the whole shoot and brown spots and flaccid areas in the leaves. The latter symptom did not appear in plants grown with Fe but under Zn toxicity. It seems that Fe deficiency is a major factor impairing the growth of plants exposed to high levels of Zn. Under Zn toxicity, Fe and Zn translocation from roots to shoots increased as the S supply to the plants was increased.     

Responses of aerobically grown iron chlorosis tolerant and susceptible rice (Oryza sativa L.) genotypes to soil iron management in an Inceptisol

Iron deficiency is a serious nutritional disorder in aerobic rice, causing chlorosis, poor yields and reduced grain nutritional quality. The problem can be managed by complementing the use of Fe-efficient plant type with a suitable Fe management strategy. In the present paper, we report the effect of eight iron management practices to resolve the problem of iron (Fe) chlorosis through the use of an iron deficiency tolerant (IDTR) and iron deficiency susceptible (IDSR) rice genotype, i.e. Pusa 33 and ADT 39, respectively. Fe deficiency tolerance of these genotypes was related to the root release of PS which enabled a higher uptake of Fe in the IDTR than the IDSR under Fe deficiency. In general, IDTR performed better than the IDSR as evident from a significant increase in total iron, active iron, chlorophyll content and grain and straw yield. IDSR produced the highest grain and straw yield under slow iron release nano clay complex source. Grain Fe content of the IDTR and IDSR increased by 18.9 and 13.4%, respectively, under recommended dose of Fe. The results identified the most effective soil management strategies for the alleviating Fe deficiency chlorosis and improving Fe nutrition of both IDTR and IDSR genotypes.     

A greenhouse technique for screening Trifolium seedlings for iron‐deficiency chlorosis 1

Susceptible Trifolium plants often exhibit symptoms of iron (Fe)‐deficiency chlorosis when grown on high pH, calcareous soils. A greenhouse method was developed to screen seedlings for Fe‐deficiency chlorosis. ‘Yuchi’ arrowleaf (T. vesiculosum Savi.) and ‘Dixie’ crimson (I. incarnatum L.) clover seedlings were grown in “Super Cell”; Cone‐tainers in six calcareous Texas soils differing in Fe and selected other chemical characteristics. At the fourth trifoliolate leaf stage, chlorosis was induced by saturating the soil for a minimum of 2 weeks. The soils differed in their capacity to induce chlorosis in both clovers. Yuchi was more susceptible than Dixie, showing a higher percentage of chlorosis in five of the six soils. The results indicate that this screening method would be a useful tool for studying Fe‐deficiency chlorosis in Trifolium spp.     

IRON EFFICIENCY IN KENTUCKY BLUEGRASS NOT RELATED TO PHYTOSIDEROPHORE RELEASE

Some Kentucky bluegrass (KBG; Poa pratensis L.) is susceptible to iron (Fe)-deficiency chlorosis. Under Fe-deficiency stress, phytosiderophore is produced and released by the roots of many grasses to solubilize soil Fe and enhance uptake. In other species, quantifying phytosiderophore screens for Fe-deficiency resistant cultivars. A hydroponic study was conducted at 1 and 10 μM solution Fe to variously stress ‘Baron’, ‘Award’, ‘Limousine’, and ‘Rugby II’ KBG cultivars. One μM Fe solution produced more Fe-deficiency stress in all cultivars compared to 10 μM, resulting in greater chlorosis and phytosiderophore release but reduced shoot and root Fe concentrations and shoot weight. Of the four cultivars, Baron was the most susceptible to Fe deficiency and exhibited severe Fe chlorosis and low shoot Fe but, surprisingly, produced the most phytosiderophore. These results imply that Fe-deficiency susceptibility in KBG may be less related to phytosiderophore release and more related to inefficient uptake or utilization mechanisms.     

Predicting the incidence of iron chlorosis in calcareous soils of southern Spain

Abstract

Iron chlorosis is a serious crop production problem in many calcareous soils of Southern Spain. The objective of this study was to determine which indigenous soil properties (i.e., those which are essentially permanent) were related to Fe chlorosis. Experiments, using two chickpea (Cicer ariethinum L.) cultivars and a sunflower (Helianthus annuuus L.) cultivar, were carried out in a growth chamber with 25 calcareous soils representing widespread Xerofluvents, Xerorthents, Xerochrepts, Haploxeralfs, Rodoxeralfs, Chromoxererts, and Pelloxererts of Southern Spain. The average chlorophyll contents for the three cultivars were significantly correlated with several properties of the carbonate and Fe oxide phases, such as calcium carbonate equivalent (r = 0.69***), “active lime”; (r = 0.58**), acid NH₄‐oxalate extractable Fe (r = 0.68***), Tiron‐extractable Fe (r = 0.61**), and DTPA‐extractable Fe (r = 0.55**). The present and other studies indicate that the soil property most consistently related to Fe chlorosis is acid NH₄‐oxalate extractable Fe (Feo). The Feo critical level separating soils with a high probability from those with a low probability of responding to Fe fertilization was 0.63 g/kg soil, a value similar to those found in other studies. This further supports the use of Feo as a key property to predicting the appearance of Fe chlorosis.     

Differential response of groundnut genotypes to iron‐deficiency stress

Differential response of groundnut genotypes to iron‐deficiency stress was studied in soils containing high calcium carbonate. Genotypes differed significantly for some traits that appeared to be important in determining adaptation to low iron. The genotypes TCGS 273, TCGS 2, TCGS 37, and Kadiri 3 had higher total chlorophyll, total dry matter, and active iron (Fe²⁺) contents under iron‐deficiency stress conditions. Total chlorophyll followed by active iron were found to be sensitive parameters to Fe deficiency. Based on the visual deficiency symptoms (chlorosis score), the genotypes were classified into three groups. Efficient (no genotype was found efficient), moderately efficient (TCGS 273, TCGS 2, TCGS 3, and Kadiri 3), and inefficient (TCGS 1, TCGS 7, TCGS 11, TCGS 26, TCGS 28, TCGS 29, TCGS 30, TCGS 1518, TPT 1, TPT 2, ICGS 11, ICGS 44, Girnar, JL 24, ICGS(E) 21, and TMV 2).     

Effect of the iron supply on the nutrition of different citrus variety/rootstock combinations using dris 1

The Diagnosis and Recommendation Integrated System (DRIS) has been found reliable in diagnosing nutrient requirements, despite changes in the tissue sampling or the time sampling. Relatively few researchers use the results obtained by hydroponic culture to make a DRIS data bank. In this work, results obtained in this way have been utilized as DRIS reference values to evaluate the iron (Fe) supply influence on the nutrition of different citrus combinations under normal and deficient Fe conditions. The DRIS indices have been compared with standard methods to evaluate the effectiveness of this system of interpretation. The Citrus macrophylla rootstock for lemons is more resistant to Fe chlorosis than Sour orange. Based on the diagnosis of visual symptoms, the Citrus volkameriana is more resistant to this nutritional deficiency for oranges than the Cleopatra mandarin.