Variation in zinc efficiency among and within Aegilops species

Fifteen accessions of Aegilops tauschii (DD), 10 of Ae. speltoides (SS) and 8 of the tetraploid Aegilops species sharing the U genome were used to study the influence of varied zinc (Zn) supply on development of Zn-deficiency symptoms, and on shoot dry weight and Zn concentration. Plants were grown in a Zn-deficient calcareous soil under greenhouse conditions with (+Zn = 5 mg kg^—1 soil) and without (—Zn) Zn supply. Four accessions of wild tetraploid wheat, Triticum turgidum var. dicoccoides (BBAA), a group known for its high sensitivity to Zn-deficiency, were used in the experiments for comparison. As expected, the accessions of wild T. turgidum var. dicoccoides showed the highest sensitivity to Zn deficiency, and had more severe leaf symptoms of Zn deficiency (whitish-brown necrotic patches). Among the Aegilops species, leaf symptoms of Zn deficiency were, in general, more distinct in Ae. tauschii (DD) and least in Ae. speltoides (SS). Zinc efficiency, expressed as the percentage of shoot dry weight produced under conditions of Zn deficiency compared to Zn supply, averaged, 15% for T. turgidum, 32% for Ae. tauschii, 52% for Ae. speltoides and 61% for the tetraploid Aegilops species carrying the U genome. Differences in Zn efficiency among and within Aegilops species and T. turgidum were significantly correlated with the Zn amount per shoot, but not with the Zn amount per unit dry weight of shoots. The results show that Aegilops species can be exploited as an important genetic source for Zn efficiency genes, particularly Ae. speltoides var. ligustica (SS) and Ae. triuncialis (UUCC). Transfer of these genes to cultivated modern wheat may bring about a greater variation in Zn efficiency in wheat, and facilitate production of Zn-efficient modern wheat cultivars for Zn-deficient soil conditions.     

Profiling soil free-living nematodes in the Namib Desert,Namibia

Functional structure and diversity of soil free-living nematodes in a desert environment depend on plant gender and sampling site.The objective of this study was to compare the composition,abundance and tropic group of soil free-living nematodes in the upper 0–10 cm soil layer under the male and female Acanthosicyos horridus Welw.ex Hook.f.plants and in the inter-shrub open areas(control)in the Namib Desert,Namibia in April 2015.Soil moisture,organic matter(OM)and pH was also analyzed.Free-living nematodes were extracted from 100 g soil using the Baermann funnel procedure,and total number of nematodes was counted under a microscope.Community composition and diversity of soil free-living nematodes were analyzed using 18S rDNA sequences.Results indicated that a total of 67 groups,including 64 species,2 genera and 1 family were identified.Feeding behavior of 58 species were identified as follows:15 bacteria-feeding species,12 fungi-feeding species,10 plant-parasite species,5 omnivorous-predator species,8 animal-parasite species,5 invertebrate-parasite species and 3 non-free-living nematodes,known as marine species.Moreover,soil free-living nematodes were found to be affected by sampling locations and plant gender,and community composition and density of these nematodes were strongly influenced by soil OM content.Result confirmed that spatial location and plant cover were main factors influencing the diversity of soil free-living nematodes.Moreover,molecular tools were found to be very useful in defining the richness of soil non-free-living nematodes.In conclusion,the results elucidated the importance of biotic variables in determining the composition and abundance of soil free-living nematodes in the Namib Desert,Namibia.     

Impact of grafting and rootstock on nutrient-to-water uptake ratios during the first month after planting of hydroponically grown tomato

Tomato plants (cv. Primadonna F₁), non-grafted, self-grafted, or grafted onto the commercial rootstocks ‘He-man’ and ‘Maxifort’, were grown in recirculating nutrient solution. The uptake concentrations (UCs), i.e. mean nutrient-to-water uptake ratios of N, P, K, Ca, Mg, Fe, Mn, Zn, Cu, and B, were estimated based either on depletion from the nutrient solution or on accumulation in the plant biomass. Grafting onto both commercial rootstocks increased the total plant biomass. Hetero-grafting also increased the leaf N, Ca, and Cu concentrations but decreased those of Mg and Fe in comparison with self- and non-grafted plants. The mean UCs of N, Ca, and Cu were higher in plants grafted onto both commercial rootstocks in comparison with self- and non-grafted plants. However, hetero-grafting also raised the UCs of P, Fe, Mn, and B, because of an increased deposition of these nutrients to the roots in comparison with self-rooted plants. The method used to estimate the UCs, i.e. nutrient removal from the recirculating nutrient solution vs. nutrient recovery from plant biomass per volume unit of transpired water, resulted in similar values for N, Ca, Zn, and Cu, but had a significant impact on those of P, K, Mg, Fe, Mn, and B.     

Bacterial and fungal activities in soil: Separation of bacteria and fungi by a rapid fractionated centrifugation technique

With three natural soils from Western and Central Norway it has been shown that by homogenization and fractionated centrifugations, two fractions could be obtained, one containing 50–80% of the bacteria, and the other all the fungi together with soil debris and the rest of the bacteria. When the separation was carried out in the cold and lasting less than 3–4 h, the fractions if used immediately had constant respiratory rates for 1–2 h. The sum of the rates agreed well with that of an unfractionated soil homogenate, making it possible to calculate the ratio between bacterial and fungal respiration. Assuming that the much higher respiration in a homogenate than in intact soil is due to inhibitory conditions in the latter and that these can be analysed by separate experiments, the technique will permit estimates of the ratio between bacterial and fungal respiration in in situ soil under given conditions.The soils used had very great differences between plate and microscopic count values for bacteria. When based on plate counts, the calculated bacterial respiratory intensities became impossibly high, while they were within biologically possible limits when microscopic count values were used. The respiratory intensities for fungi when calculated from hyphal lengths and diameter measurements, were biologically possible.