Moricandia arvensis cytoplasm based system of cytoplasmic male sterility in Brassica juncea: Reappraisal of fertility restoration and agronomic potential

Cytoplasmic male sterility (CMS) system based on the cytoplasm from Moricandia arvensis (mori) was investigated for fertility restoration and agronomic potential. Fertility restorer gene for mori CMS was introgressed from cytoplasm donor species as all the evaluated Brassica juncea genotypes (155) acted as sterility maintainers. The allosyndetic pairing between M^a and the A/B genome chromosomes in the monosomic addition plants (2n= 18II + 1M^a) facilitated the gene introgression. Partial fertility restoration (43–52% pollen grain stainability) in F₁ hybrids and absence of segregation for male sterility in F₂ progenies suggested gametophytic control of fertility restoration. The pollen fertility in the F₁ hybrids was, however, sufficient to ensure complete seed set upon bag selfing. Introgression from M. arvensis also helped in correction of chlorosis associated with mori cytoplasm in CMS and fertile alloplasmic B. juncea plants. Yield evaluation of thirty F₁ hybrids having the same nuclear genotype but varied male sterilizing cytoplasms (mori, oxy, lyr, refined ogu), in comparison to respective euplasmic hand bred control hybrids, allowed an estimate of yield penalty associated with different CMS systems. It ranged from 1.8% to 61.6%. Hybrids based on cytoplasmically refined ogu were most productive followed by those based on cytoplasmically refined mori CMS. The male sterility systems emanating from somatic hybridization were found superior than those developed from sexual hybridization.     

Inheritance and molecular mapping of restorer‐of‐fertility (Rf) gene in A2 hybrid system in pigeonpea (Cajanus cajan)

Inheritance of fertility restorer gene in pigeonpea was studied using F₂ and BC₁F₁ populations derived from cross AL103A × IC245273. It was found to be controlled by single dominant gene. Out of 228 SSR primer pairs, 33 primer pairs showed parental polymorphism, while four primers were found polymorphic in bulk segregant analysis (BSA). These four primers viz., CcM 1615, CcM 0710, CcM 0765 and CcM 1522 were used for genotyping of F₂ population and were found to be placed at 3.1, 5.1, 28.1 and 45.8 cM, respectively. Two of them, CcM 1615 and CcM 0710, evinced clear and unambiguous bands for fertility restoration in F₂ population. The Rf gene was mapped on linkage group 6 between the SSR markers CcM 1615 and CcM 0710 with the distances of 3.1 and 5.1 cM, respectively. The accuracy of the CcM 1615 was validated in 18 restorers and six maintainer lines. The marker CcM 1615 amplified in majority of male restorer lines with a selection accuracy of 91.66%.     

Inheritance of alloplasmic fertility restoration in eggplant (Solanum melongena L.)

Cytoplasmic male sterility (CMS) system has been exploited worldwide in field and vegetable crops. In eggplant, alloplasmic CMS lines were developed through interspecific hybridization between Solanum aethiopicum L.?×?S. melongena L., while the restorer (R) lines were isolated from the reciprocal cross. The knowledge about inheritance of Rf gene is must for its further use in breeding and molecular studies. Therefore, four sets of CMS (D-CMS 291A, D-CMS 99A, D-CMS 5A and D-CMS 72A) and restorer (R 2-1, R 3-4, R 6-2 and R 2596-2) lines were used to develop F₁, F₂ and backcross progenies, to understand the inheritance mechanism. Phenotyping of all the populations and test of goodness of fit revealed involvement of a single dominant gene (Rf) for fertility restoration. The visual scoring of flowers for male sterility and fertility was further validated with the tests on pollen stainability, germination and index. Among others, media containing 0.5% agar?+?300 ppm calcium nitrate?+?5% sucrose?+?50 mg/l boric acid?+?400 mg/l PEG 4000 furnished the best results for in vitro pollen germination. Differences between and within male sterile and restorer lines were observed for pistil and stamen length and girth, pollen stainability and germination. Stable expression of CGMS and restorer lines in all the generation progenies confirmed their utility in future eggplant breeding programs.

     

Morpho-physio and anatomical characterization of the indigenous Himalayan crabapple: Malus baccata (L.) Borkh. (Rohru) and exotic Malus pumila Mill. for dwarfing traits

Genetic Resources and Crop Evolution - The wild Malus germplasm is considered as a gene reservoir for various biotic and abiotic stresses tolerance/resistance genes, including important novel...     

Soil respiration rate and its sensitivity to temperature in pasture systems of dry-tropics

Abstract

Tree clearing is a topical issue the world over. In Queensland, the high rates of clearing in the past were mainly to increase pasture production. The present research evaluates the impact of clearing on some soil biological properties, i.e. total soil respiration, root respiration, microbial respiration, and microbial biomass (C and N), and the response of soil respiration to change in temperature.

In-field and laboratory (polyhouse) experiments were undertaken. For in-field studies, paired cleared and uncleared pasture plots were selected to represent three major tree communities of the region, i.e. Eucalyptus populnea, E. melanophloia, and Acacia harpophylla. The cleared sites were chosen to represent three different time-since-clearing durations (5, 11–13, and 33 years; n=18 for cleared and uncleared plots) to determine the temporal impact of clearing on soil biological properties. Experiments were conducted in the polyhouse to study in detail the response of soil respiration to changes in soil temperature and soil moisture, and to complement in-field studies for estimating root respiration.

The average rate of CO₂ emission was 964 g CO₂/m²/yr, with no significant difference (P<0.05) among cleared and uncleared sites. Microbial respiration and microbial biomass were greater at uncleared compared with those at cleared sites. The Q ₁₀-value of 1.42 (measured for different seasons in a year) for in-field measurements suggested a small response of soil respiration to soil temperature, possibly due to the limited availability of soil moisture and/or organic matter. However, results from the polyhouse experiment suggested greater sensitivity of root respiration to temperature change than for total soil respiration. Since root biomass (herbaceous roots) was greater at the cleared than at uncleared sites, and root respiration increased with an increase in temperature, we speculate that with rising ambient temperature and consequently soil temperature, total soil respiration in cleared pastures will increase at a faster rate than that in uncleared pastures.     

Effect of different levels of nitrogen and farmyard manure on yield and quality of spinach (Spinacea oleracea L.)

The effect of different levels of nitrogen N₀(0kg/ha), N₁(30 kg/ha), N₂ (60 kg/ha), and N₃ (90 kg/ha) and farmyard manure F₀ (0 tonnes/ha), F₁ (10 tonnes/ha), and F₂ (20 tonnes/ha) on the yield and nutrient composition of spinach and its uptake was investigated on a sandy loam soil. Yield; phosphorus, iron, manganese, zinc, and copper uptakes; and ascorbic acid content increased with the application of both the inorganic nitrogen fertilizer and the farmyard manure, with a maximum at the N₃F₂ level, i.e. at 90 kg N/ha with 20 tonnes FYM/ha. However, the contents of protein, -carotene, and reducing sugars were maximum at the highest dose of nitrogen without the application of farmyard manure.     

Growth and carcass composition of giant freshwater prawn, Macrobrachium rosenbergii (De Man), fed different isonitrogenous and isocaloric diets

A feeding experiment was conducted for 135 days to observe the effect of different isonitrogenous (35% crude protein) and isocaloric (385 kcal) diets on the growth and carcass composition of giant freshwater prawn, Macrobrachium rosenbergii ( De Man 1879 ). Three experimental diets (ED1, ED2 and ED3) were prepared using locally available ingredients. These diets differed mainly in terms of percent contribution of major protein sources such as fish meal, soybean meal, groundnut oil cake and mustard oil cake. Experimental diets were evaluated against a commercial diet, which served as the control (CD). Juveniles 1.87–2.44 g in size were stocked at a population density of 40 000 ha⁻¹ and fed thrice daily at 10% in the beginning and reducing gradually to 7% and 5% of the body weight during the experimental period. No significant differences (P>0.05) in the growth performance were observed; however, a significantly (P<0.05) higher yield (721.9 kg ha⁻¹ 135 days⁻¹) was recorded for prawn fed with control diet, followed by experimental diet 2 (676.5 kg ha⁻¹ 135 days⁻¹, having soybean meal as a major protein source). The survival ranged between 63.8% and 77.7%, with different diets showing significantly higher survival. The apparent feed conversion ratio values of diets ranged between 3.15 and 3.49, with experimental and control diets showing non‐significantly lower AFCR values. At the end of the experiment, representative specimens from each treatment were collected and their carcass composition was measured. Analysis of variance showed that carcass protein and total carbohydrate contents were significantly (P<0.05) higher in prawns fed on a fish–soybean meal‐based diet (ED3) and a control diet. The total lipid contents of prawns, however, did not differ significantly among the various dietary treatments. The results of our study suggest that the experimental diets could be used effectively for M. rosenbergii without compromising growth and flesh quality.     

Molecular Variability in Different Indian Isolates of Equine Herpesvirus-1

Three abortigenic Indian isolates of equine herpesvirus-1 (EHV-1) (Tohana, Hisar and Bikaner), along with two exotic abortigenic isolates (AB4 and V592) and another EHV-1 isolate (Jind) obtained from a case of perinatal foal mortality, were studied for variability. For this purpose, PCR and restriction endonuclease (RE) digestion techniques were used simultaneously as a DNA fingerprinting system. Nine different regions of EHV-1 virus were amplified by PCR using primer pairs specific for the regions and the products obtained from these regions were subsequently subjected to various restriction endonucleases to further assess the variability in the number of RE sites as well as in their positions. No difference was observed in all the four abortigenic isolates in terms of the size of different PCR products amplified by all the nine primer pairs, except for primer pairs ‘E’ and ‘C’. PCR products obtained with primer pair E revealed that Tohana and Bikaner isolates were most similar while Hisar isolate was like V592 isolate. However, the PCR product obtained from Jind isolate had a size between the PCR products of Hisar and Tohan/Bikaner isolates. The primer pair ‘C’ used to amplify the region between 1151 to 3679 in ‘Gene 1,2,3’ clearly differentiated the EHV-1 isolate obtained from a case of perinatal foal mortality from isolates obtained from abortion cases. This primer pair needs to be exploited more extensively for use as a potential marker for differentiating the EHV-1 isolates, mainly the abortion cases from perinatal foal mortality ones. Restriction endonuclease studies done with PCR product of all the isolates with various primer pairs did not reveal any changes in the position or number of RE sites present in the products amplified, indicating no variation in different RE sites within the amplified PCR products. However, this study clarified that all the Indian isolates belonged to the IP group of EHV-1.     

Breeding for boron tolerance in lentil (Lens culinaris Medik.) using a high‐throughput phenotypic assay and molecular markers

This study describes the identification of a quantitative trait locus (QTL) in the recombinant inbred line population of ILL2024 × ILL6788 and subsequent validation of associated molecular markers. A high‐quality genetic linkage map was constructed with 758 markers that cover 1,057 cM, with an average intermarker distance of 2 cM. QTL analysis revealed a single genomic region on Lc2 to be associated with B tolerance and accounted for up to 76% of phenotypic variation (Vp). The best markers for B tolerance were assessed for their utility in routine breeding applications using validation panels of diverse lentil germplasm and breeding material derived from ILL2024. A marker generated from the dense genetic map of this study was found to be the most accurate of all markers available for B tolerance in lentil, with a success rate of 93% within a large breeding pool derived from ILL2024. However, given the number of the unrelated lines for which the marker–trait association was not conserved, B tolerance screening is still required at later stages to confirm predicted phenotypes.