Plant genotypes of Trifolium subterraneum L. (subterranean clover) were evaluated for differences in symbiotic N 2 fixation with soil rhizobia, with the long-term aim of using plant selection to overcome sub-optimal N 2 fixation associated with poorly effective soil rhizobia. Symbiotic performance (SP) was assessed for 49 genotypes of subterranean clover with each of four pure Rhizobium strains isolated from soil. Plants were grown in N free media in the greenhouse and their shoot dry weights measured and expressed as a percentage of dry weight with R. leguminosarm bv. trifolii WSM1325, the recommended commercial inoculant. Average SP with two Rhizobium strains (H and J) ranged from completely ineffective to 80% of potential for the subterranean clover genotypes. Two clover cultivars with high (cv. Campeda) and low (cv. Clare) SP values were investigated in more detail. Campeda typically fixed more N 2 than Clare when inoculated with 30 soil extracts (4.2 vs 2.4 mg N 2 fixed/shoot) and with 14 pure strains isolated from those soils (4.2 vs 2.2 mg N 2 fixed/shoot). The poor performance of Clare could be attributed to interruptions at multiple stages of the symbiotic association, from nodule initiation (less nodules), nodule development (small, white nodules), through to reduced nodule function (N 2 fixed/mg nodule) depending on the inoculation treatment. Through the careful use of subterranean clover genotypes by plant breeders it should be possible to make significant gains in the SP of future subterranean clover cultivars.
Three major responses to N(2)-fixation incompatibility between Trifolium spp. and R. l. trifolii strains were found: failed bacterial endocytosis from infection threads into plant cortical cells, bacteroid differentiation aborted prematurely, and a reduced pool of functional bacteroids which underwent premature senescence. We discuss possible underlying genetic causes of these developmental abnormalities and consider impacts on N(2)-fixation of clovers.
Naturalised soil rhizobia that nodulate clover occur in high number and are known to vary in their symbiotic performance (SP) with subterranean clover (Trifolium subterraneum L.). However, the extent of suboptimal fixation across a range of other clover species is not well understood. T. subterraneum and nine other annual clover species of Mediterranean origin were evaluated for their SP in combination with the naturalised clover rhizobia in 71 Australian soils and five strains of Rhizobium leguminosarum bv. trifolii that have been used in the inoculants produced for clovers. The most probable number method, using subterranean clover as the trap plant was used to estimate the number of clover rhizobia in the soils. Ninety-two percent of soils tested contained more than 1000 rhizobia/g. An extract of each soil, or strain of rhizobia was used to inoculate plants growing in N-deficient media in the greenhouse. Plants were grown for 4 weeks after inoculation and shoot dry matter determined and expressed as a percentage of the ‘best’ soil rhizobia treatment, to provide a proportional measure of SP for each clover species. SP (mean of clover species) ranged from 96% with the current inoculant strain for annual clovers (WSM1325) down to 48% with former inoculant strain WU95. When inoculated with soils predominantly from mainland Australia, SP (mean of soil treatments) of the different Trifolium spp. was 55% (resupinatum), 53–47% (subterraneum), 50% (nigrescens), 49% (michelianum), 48% (isthmocarpum), 38% (hirtum), 35% (purpureum), 32% (vesiculosum), 25% (spumosum) and 21% (glanduliferum). Within each of the clover species, SP resulting from individual soil treatments ranged from 100% (by definition for the best soil treatment) down to close to zero. Trifolium glanduliferum formed nodules readily with the inoculant strains but nodulation was erratic with the rhizobia in many soils. It is therefore proposed that the naturalised rhizobia in many soils are unlikely to be inoculant strains. This research demonstrates symbiotic efficiency across annual clover species is compromised where diverse populations of clover rhizobia have naturalised in soils.
The population size and symbiotic performance (ability to fix N2) of rhizobia (Rhizobium leguminosarum bv. viciae) capable of nodulating field pea (Pisum sativum) were assessed in 114 soils from Mediterranean-type environments of southern Australia. All soils were collected in autumn, before the growing season, and had a history of crop legumes including field pea, faba bean, lentil, or vetch. The most probable number (MPN) technique, with vetch as a trap plant, was used to estimate the numbers of pea rhizobia in soils. Of the soils tested, 29% had low numbers of pea rhizobia (<100 rhizobia/g), 38% had moderate numbers (100–1000/g), and the remaining 33% had >1000/g. Soil pH, the frequency of a host crop in the rotation, and the number of summer days with a maximum temperature >35°C were strongly correlated with the pea rhizobia population size. Symbiotic performance (SP) of pea rhizobia in soils was assessed for soils with a MPN >100 rhizobia/g. An extract of the soils was used to inoculate two field pea cultivars growing in a nitrogen-deficient potting media in the greenhouse. Plants were grown for 5 weeks after inoculation and shoot dry matter was expressed as a percentage of the dry matter of plants grown with a commercial strain R. leguminosarum bv. viciae, SU303. Symbiotic performance ranged from 25 to 125%. One-quarter of the soils assessed had suboptimal SP (i.e. <70%). Soil and climatic variables were weakly associated with SP, with pH and average annual rainfall accounting for 17% of the variance. This research highlights the complexity of factors influencing population size and symbiotic performance of pea rhizobia in soils. Options for the improved management of populations of pea rhizobia in Mediterranean environments are discussed. Specifically, our data indicate that inoculation of pea crops is likely to be beneficial where pH(H2O) <6.6, particularly when summers have been hot and dry and when a host has been absent for ≥5 years, as numbers of rhizobia are likely to be below the thresholds needed to optimise nodulation and crop growth. New inoculation technologies and plant breeding will be required to overcome large populations of pea rhizobia with suboptimal SP.
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