Abstract:In a greenhouse experiment the mycorrhizal fungus, Glomus fasciculatus, significantly increased growth of Troyer citrange (Poncirus trifoliata L.) (TC) seedlings in 20 of 26 methylbromide‐fumigated citrus soils from southern California. Of the six soils in which G. fasciculatus provided no growth increase, two were greenhouse soils, three were nursery soils, and only one was a field soil. Glomus fasciculatus increased foliar P, K, and Cu concentrations and decreased foliar Mg and Na concentrations of TC grown … Show more
“…Menge et al (1982) found that the mycorrhizal dependency of Troyer citrange on G. fasciculatus isolate 0-1 in 26 citrus soils from California was inversely correlated with soil P, Zn, Mn, Cu, percentage organic matter and cation exchange capacity, and was positively correlated with soil pH. In general, arid soils are alkaline in pH, as was the California soil we used (pH 7-3), whereas soils from humid regions, such as Florida, have a pH below 7 (Brady, 1974).…”
Section: Discussionmentioning
confidence: 99%
“…For citrus the magnitude of growth response produced by VAM is referred to as mycorrhizal dependency which is determined in part by the efficiency of the fungus. Mycorrhizal dependency may vary with cultivar, soil factors and mycorrhizal fungus (Menge et al, 1978(Menge et al, , 1982Nemec, 1978). In a test of six citrus cultivars, Nemec (1978) found that differences in efficiency of three Glomus species varied with both rootstock and phosphorus fertilization.…”
SUMMARYThe hypothesis was tested that the amount of external hyphae of a vesicular-arbuscular mycorrhizal (VAM) fungus extending from roots out into soil is not always proportional to the extent of colonization of the root cortex. Growth enhancement and amount of external hyphae were compared for eight isolates of five Glomus spp. that differed in their geographic origin and capacity to enhance growth of Troyer citrange, but were similar in their capacity to extensively colonize Troyer citrange roots. In general, isolates from California increased growth in a P-deficient (9-8 mg kg"^) California soil more than did non-native isolates from Florida soils. The difference between the capacity of California and Florida isolates to enhance growth was not a function of the degree to which they colonized the roots since all had colonized over 95 % of the root length by the time of harvest. Differences in growth enhancement did appear, however, to be a function of the amount of external hyphae that had developed as estimated by the weight of soil they had bound into aggregates. This study suggests that isolates of VA mycorrhizal fungi may differ in their capacity to develop an external hyphal system independent of their capacity to colonize the root cortex, and that we cannot assume that high levels of colonization will necessarily nnean the fungus has also developed the mycelium in the soil necessary to transport nutrients responsible for plant growth enhancement.
“…Menge et al (1982) found that the mycorrhizal dependency of Troyer citrange on G. fasciculatus isolate 0-1 in 26 citrus soils from California was inversely correlated with soil P, Zn, Mn, Cu, percentage organic matter and cation exchange capacity, and was positively correlated with soil pH. In general, arid soils are alkaline in pH, as was the California soil we used (pH 7-3), whereas soils from humid regions, such as Florida, have a pH below 7 (Brady, 1974).…”
Section: Discussionmentioning
confidence: 99%
“…For citrus the magnitude of growth response produced by VAM is referred to as mycorrhizal dependency which is determined in part by the efficiency of the fungus. Mycorrhizal dependency may vary with cultivar, soil factors and mycorrhizal fungus (Menge et al, 1978(Menge et al, , 1982Nemec, 1978). In a test of six citrus cultivars, Nemec (1978) found that differences in efficiency of three Glomus species varied with both rootstock and phosphorus fertilization.…”
SUMMARYThe hypothesis was tested that the amount of external hyphae of a vesicular-arbuscular mycorrhizal (VAM) fungus extending from roots out into soil is not always proportional to the extent of colonization of the root cortex. Growth enhancement and amount of external hyphae were compared for eight isolates of five Glomus spp. that differed in their geographic origin and capacity to enhance growth of Troyer citrange, but were similar in their capacity to extensively colonize Troyer citrange roots. In general, isolates from California increased growth in a P-deficient (9-8 mg kg"^) California soil more than did non-native isolates from Florida soils. The difference between the capacity of California and Florida isolates to enhance growth was not a function of the degree to which they colonized the roots since all had colonized over 95 % of the root length by the time of harvest. Differences in growth enhancement did appear, however, to be a function of the amount of external hyphae that had developed as estimated by the weight of soil they had bound into aggregates. This study suggests that isolates of VA mycorrhizal fungi may differ in their capacity to develop an external hyphal system independent of their capacity to colonize the root cortex, and that we cannot assume that high levels of colonization will necessarily nnean the fungus has also developed the mycelium in the soil necessary to transport nutrients responsible for plant growth enhancement.
“…Research has shown that considerable variation exists between mycorrhizal species in their effect on citrus nutrition and growth and between citrus species in their dependence on mycorrhiza (Camprubi & Calvet 1996). of the few published studies on the effect of mycorrhiza on Mg nutrition of citrus, three showed that inoculation with mycorrhiza reduced Mg uptake (Menge 1982;Rocha et al 1995;Souza 2000) and one found an increase (Gendiah & Zaghloul 1997). Melloni & Cordoso (1999) found that the relationship between Mg uptake and the amount of mycorrhizal mycelium on the roots varied depending on the species of citrus grown.…”
Magnesium (Mg) deficiency is widespread in citrus on the Gisborne plains. Soil-applied and foliar Mg fertilisers have done little to raise leaf Mg concentrations. Data analysis indicates that this deficiency is a result of high ratios of exchangeable potassium (K) and calcium (Ca) relative to Mg in Gisborne soils (0.5:1 and 7.4:1, respectively). Data from the literature suggests that K:Mg and Ca:Mg ratios greater than 0.4:1 and 7:1, respectively, can cause Mg deficiency. Significant responses to Mg by citrus, in terms of yield or fruit quality, are only likely in instances of severe Mg deficiency. Reductions in yield or fruit quality under conditions of mild Mg deficiency, such as are found in Gisborne, are only likely in some years. To increase our understanding of Mg deficiency in Gisborne citrus, future research should quantify the effect of mild Mg deficiency on fruit quality and yield and investigate the use of Mg:K and Mg:Ca ratios in soil samples deeper than the standard 0.15 cm for diagnosing Mg deficiency. further, the effects of soil moisture and rooting depth on the seasonal patterns of Mg, K, and Ca uptake and the effect of manipulating the shoot:root ratio on leaf Mg concentrations need to be understood. Nutrient management strategies for Mg must be developed following an evaluation of the effects of foliar sprays as well as long-term use of different forms of Mg besides kieserite, irrigation, mulching, and groundcover manipulation. Another option for addressing Mg deficiency is to select or breed citrus rootstocks for improved ability to obtain Mg from Gisborne soils.
“…In short, some mycorrhizal fungi may not readily adapt to soils with a pH unlike that of the soil of their origin, thus pH may constrain establishment of arbuscular mycorrhizas. Studies suggesting that this relationship may exist involved the direct liming of soils (Kucey and Diab, 1984;Newbould and Rangeley, 1984), analyses of arbuscular mycorrhizas across diverse soil types (Sylvia et al, 1993b;Menge et al, 1982;Skipper and Smith, 1979), and various management treatments that included fertilizing or physically modifying the soil (e.g. organic amendments, Soedarjo and Habte, 1993).…”
The majority of plants have mycorrhizal fungi associated with them. Mycorrhizal fungi are ecologically significant because they form relationships in and on the roots of a host plant in a symbiotic association. The host plant provides the fungus with soluble carbon sources, and the fungus provides the host plant with an increased capacity to absorb water and nutrients from the soil. Adverse conditions are a pervasive feature in both natural and agronomic soils. The soil environment is constantly changing with regard to moisture, temperature and nutrient availability. In addition, soil properties are often manipulated to improve crop yields. In many cases, soils may be contaminated through disposal of chemicals that are toxic to plants and microorganisms. The formation and function of mycorrhizal relationships are affected by edaphic conditions such as soil composition, moisture, temperature, pH, cation exchange capacity, and also by anthropogenic stressors including soil compaction, metals and pesticides. Arbuscular mycorrhizal fungi are of interest for their reported roles in alleviation of diverse soil-associated plant stressors, including those induced by metals and polychlorinated aliphatic and phenolic pollutants. Much mycorrhizal research has investigated the impact of extremes in water, temperature, pH and inorganic nutrient availability on mycorrhizal formation and nutrient acquisition. Evaluation of the efficacy of plant-mycorrhizal associations to remediate soils contaminated with toxic materials deserves increased attention. Before the full potential benefits of arbuscular mycorrhizal fungi to reclaim contaminated soils can be realized, research advances are needed to improve our understanding of the physiology of mycorrhizae subjected to adverse physical and chemical conditions. This paper will review literature and discuss the implications of soil contamination on formation and function of arbuscular mycorrhizal associations. C
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