Delineating soil nutrient management zones based on optimal sampling interval in medium- and small-scale intensive farming systems

Precision Agriculture - Soil nutrients vary greatly and information regarding their spatial-temporal variability is critical for achieving site-specific nutrient management. However, the problem is...     

Presence of maturation-promoting factor in 17α,20β-dihydroxy-4-pregnen-3-one-induced oocytes of catfish,Clarias batrachus

Full-grown immature Clarias batrachus oocytes respond in vitro to exogenous 17,20-dihydroxy-4-preg-nen-3-one ( 17,20-DP) by undergoing germinal vesicle breakdown (GVBD). Cytosolic extract (CE) prepared from 17,20-DP-induced oocytes has been shown to produce similar effect when microinjected into unstimulated immature oocytes of the same fish. A dose of 50 nl is enough to cause 100% GVBD after 4 h. Maturation-promoting factor was investigated from 17,20-DP-induced, immature and cycloheximide treated oocytes incubated in presence of [³⁵S] methionine. When the proteins were extracted and analyzed on SDS-PAGE, two prominent bands corresponding to molecular weight 34- and 46-kDa were detected in the CE of mature oocytes. However, labelling of [³⁵S] methionine was observed mainly in the region of 46 kDa protein band indicating de novo synthesis of this particular protein during l7,20-DP-induction. Further, immunoblotting study by using rabbit anti-cyclin B₁ antibody has clearly demonstrated that the protein which is newly synthesized is highly homologous to Xenopus cyclin B₁ and goldfish cyclin B.     

Oocyte maturation inClarias batrachus. III. Purification and characterization of maturation-inducing steroid

Maturation-inducing steroid (MIS) in the Indian female catfish,Clarias batrachus, was purified and characterized from the incubation medium in which fully grown but immature folliculated oocytes were incubated with salmon gonadotropin (SG-G100) for 36 h. Maturation-inducing (MI) activity of residues obtained at various steps of extraction and purification was assessed byin vitro germinal vesicle breakdown (GVBD) assay using folliculated oocytes ofC. batrachus. The post incubation medium was extracted with diethyl ether. The ether phase was partitioned using 50% methanol plus n-hexane. The methanol phase which had MI activity was fractionated into 7 fractions using reverse-phase high-performance liquid chromatography. Of these 7 fractions, fraction 3 was found to be active in having MI ability and identified as 17 ,20-dihydroxy-4-pregnen-3-one (17,20-diOHprog). The authenticity of 17,20-diOHprog as the major follicular mediator of gonadotropin-induced oocyte maturation was further confirmed by thin-layer chromatography (TLC) in which fraction 3 was run along with authentic 17,20-diOHprog standard. This investigation gives a direct evidence that 17,20-diOHprog is the major naturally occurring MIS in Indian female catfish,C. batrachus.     

Potassium isotherm partitioning based on modified quantity‐intensity relation and potassium buffering characterization of soils of North India

Background : Potassium (K) availability in soil and plant uptake is restrained by the dynamic interactions among the different pools of K. Aims : To understand these interactions, a study was undertaken to assess the quantity–intensity (Q/I) and buffering characteristics of rainfed maize (Zea mays L.) growing soils. Ten contrasting soils were evaluated for K partitioning changes in exchangeable K (ΔEK) and non‐exchangeable K (ΔNEK) pools in the soil‐solution phase and buffering characteristics using a modified version of Q/I approach. Results : The partitioned Q/I isotherms showed strong adsorption with the increase in K concentration ratio (CR^K) and the changes due to ΔEK were higher than changes due to ΔNEK. Total buffering capacity (PBC^K) significantly correlated (r = 0.92, p <0.01) with clay content with a major share contributed by buffering capacity owing to non‐exchangeable K ( ${\mathrm{PBC}}_{\Delta \mathrm{NEK}}^K$) rather than exchangeable K ( ${\mathrm{PBC}}_{\Delta \mathrm{EK}}^K$). The fixation capacity (β) factor, the magnitude of added K converted into a non‐exchangeable pool, ranged from 41 to 63%, whereas release (α) factor, the magnitude of added K converted to the exchangeable pool, ranged from 19 to 36%. Both threshold solution K (CK_r) and threshold exchangeable K (EK_r) values were found to be high in Satran clay loam (S2) and lower in Doon silty clay loam (S3) soils. The equilibrium exchangeable K (EK_o) was found close to minimum exchangeable K (E_min) in Doon silty clay loam (S3) and Babaweyl sandy clay loam (S1) soils and overall E_min constituted about 8.94 to 0.57% of the EK_o. Conclusion : It may be concluded that K Q/I isotherm partitioning provides a valuable insight to assess the dynamic relations. The ratio of α/β (K recharge index) could be used to evaluate the K enrichment capacity of soil to K additions while EK_r and E_min can be potentially useful in the elucidation of exchangeable K as K fertility index especially in soils with poor K fertilizer management.     

Sorption–desorption of phenolic acids as affected by soil properties

Phenolic acids have been implicated in the process of allelopathy and are, therefore, of interest in plant management as a basis for new herbicide structures. The potential bioavailability of phenolic acids is controlled by sorption–desorption processes in soil. Sorption–desorption of p-coumaric acid (4-hydroxycinnamic acid), ferulic acid (3-methoxy-4-hydroxycinnamic acid), veratric acid (3,4-dimethoxybenzoic acid), vanillic acid (3-methoxy-4-hydroxybenzoic acid), and p-hydroxybenzoic acid (4-hydroxybenzoic acid) was characterized on soils with varying physicochemical properties. The phenolic acids sorbed quickly (<8 h) and in high proportions to the amount applied (average 84% of applied was sorbed). Sorption was irreversible with the batch desorption method used (0.01 N CaCl₂ extraction). Pretreatment of soils to remove organic matter and free metal oxides from the soils decreased sorption, particularly in soils with free oxides removed. Statistical analysis suggested that sorption of p-coumaric and ferulic acids was correlated with soil clay content and veratric acid sorption was correlated with several soil factors. In contrast, no consistent relationship between soil characteristics and vanillic and p-hydroxybenzoic acid sorption was found. Based on the results of these experiments, i.e. the high reactivity of the phenolic acids, it is unlikely that these chemicals would be transported far from their point of origin, limiting their range of influence. It appears that, for phenolic acids to have allelopathic effects on plants, they would have to persist in the soil for long periods, resulting in a buildup of the chemical to high enough levels so that sufficient chemical would be in solution to cause the allelopathic effects, even though they may be strongly sorbed at lower concentrations.     

2种昆虫病原真菌对草地贪夜蛾体表侵染模式的扫描电镜观察

【目的】在前期筛选获得对草地贪夜蛾高效致病真菌球孢白僵菌（Beauveria bassiana）菌株GZSL-1和玫烟色虫草（Cordyceps fumosorosea）菌株IFCF01的基础上,进一步明确2株菌株在草地贪夜蛾体表的侵染模式,为阐明菌株致病机理,提高昆虫病原真菌对草地贪夜蛾的防效提供理论依据。【方法】利用扫描电镜观察草地贪夜蛾2龄幼虫分别接种菌株GZSL-1和IFCF01（孢子悬浮液浓度为1.0×107孢子/mL）后分生孢子在幼虫体表附着、萌发、穿透和增殖的过程。【结果】菌株GZSL-1和IFCF01萌发后均可形成附着胞,草地贪夜蛾幼虫体表结构对2株菌株分生孢子萌发、附着和穿透芽管长度有不同程度的影响。2株菌株在各结构区均有较高的萌发率（> 90.00%）和附着胞率（> 80.00%）,在平缓结构区比瘤状突起结构区观察到更短的穿透芽管。在各结构区,菌株GZSL-1形成的穿透芽管长度均短于菌株IF-CF01相应的芽管长度,在平缓结构区,菌株GZSL-1的穿透芽管长度显著短于菌株IFCF01（P<0.05）。菌株GZSL-1和IFCF01分生孢子接种后分别在16和8 h内萌发,在24和32 h内普遍出现穿透结构穿透草地贪夜蛾幼虫体壁。2株菌株的初级和次级分生孢子分别在接种后72和96 h内出现。【结论】扫描电镜观察证实球孢白僵菌菌株GZSL-1和玫烟色虫草菌株IFCF01对草地贪夜蛾具有高致病性,揭示了病原真菌分生孢子在草地贪夜蛾虫体上的侵染过程,结果为后续2株菌株的改良及田间应用打下理论基础。     

Comparison of net ecosystem CO2 exchange in two peatlands in western Canada with contrasting dominant vegetation, Sphagnum and Carex

Net ecosystem carbon dioxide exchange was measured in two contrasting peatlands in northern Alberta, Canada using the eddy covariance technique during the growing season (May–October). Sphagnum spp. made up approximately 66% of the total LAI (1.52 m² m⁻²) at the poor fen and the total N content of Sphagnum capitula was 7.8 mg g⁻¹ at the peak of the growing season. In contrast, the dominant plant species at the extreme-rich fen site, the perennial sedge, Carex lasiocarpa, accounted for approximately 60% of the total LAI (1.09 m² m⁻²), and had leaf total N content of 19.3 mg g⁻¹ at peak biomass. In addition, the peak aboveground biomass was higher at the poor fen (230.9 g m⁻²) than at the extreme-rich fen (157.1 g m⁻²). Both sites had maximum daily rates of net CO₂ uptake of approximately 5 μmol m⁻² s⁻¹, and typical nighttime rates of CO₂ loss of approximately 2 μmol m⁻² s⁻¹ during the peak of the growing season. Calculations of maximum photosynthetic and respiratory capacity were consistently higher at the extreme-rich fen. The poor fen was a net sink for CO₂ during 4 of the 6 months (peaking at 44 g C m⁻² in July), while only slight net losses of CO₂ (3 g C m⁻²) occurred in May and September. In contrast, the extreme-rich fen was calculated to be a significant net sink for CO₂ only during 2 months of the growing season (peaking at 30 g C m⁻² in August), while significant net losses of CO₂ occurred in May (8 g C m⁻²) and in October (13 g C m⁻²). The plant species at the poor fen site were active earlier and later in the growing season, while it took longer for C. lasiocarpa to develop leaf tissue, and leaf senescence and reduction in photosynthetic activity occurred earlier in the fall at the extreme-rich fen. When integrated over the 6-month growing season, the poor fen was a net sink (90 g C m⁻²) that was three times larger than the extreme-rich fen (31 g C m⁻²). The ratio of cumulative total ecosystem respiration to gross primary production was 0.7 at the poor fen and 0.9 at the extreme-rich fen.     

Investigating the effect of Azospirillum brasilense and Rhizobium pisi on agronomic traits of wheat (Triticum aestivum L.)

ABSTRACT

Plant growth-promoting rhizobacteria (PGPR) play an important role in improving crop growth but have not been studied sufficiently. A wire house experiment was conducted in Pakistan to determine the combined effect of inoculating wheat seeds with PGPR on the subsequent growth and yield of the wheat. The experiment included four treatments: T_{0 –} no-inoculation (control), T₁ – Azospirillum brasilense inoculation, T₂ – Rhizobium pisi inoculation and T₃ – co-inoculation with A. brasilense and R. pisi. Development and growth attributes, as well as final yield of wheat, were studied. Co-inoculation of seeds with both strains increased significantly wheat grain yield, the number of grains per plant and 1000-grain weight by 36%, 11% and 17%, respectively, compared to non-inoculated control. While crop growth rate increased for, respectively, 5.5% and 33% at tillering and flag leaf stages, corresponding values for T₃ were about 9% and 14% higher than values for sole inoculations in T₁ and T₂. Co-inoculation also significantly increased leaf epicuticular wax and relative water content as compared to the control treatment. Thus, inoculation of wheat seeds with A. brasilense and R. pisi and their combination is a promising method to improve growth, yield and quality of wheat.     

The possible role of organic acids as allelochemicals in Tamarindus indica L. leaves

Tamarindus indica L. is well known for its acidic nature and allelopathic potential, but to date, little is known about its organic acids playing their role as allelochemicals. Hence, in the present study, identification, quantification, and contribution of organic acids present in its leaf extract were conducted using the principle of bioassay-guided procedure. High pressure liquid chromatography identified four organic acids, viz. citric, malic, oxalic, and tartaric acids, in its leaf aqueous extract with the predominance of oxalic acid (7.5 g kg^?1 leaves fresh weight) followed by tartaric acid (7.3 g kg^?1). The allelopathic activity of identified acids and aqueous extract was evaluated on lettuce seedlings growth based on the specific activity (EC₅₀). The crude extract reduced radicle growth more adversely than hypocotyl at the concentration of 2.5 g L^?1 (EC₅₀). It hindered the normal physiological growth process through weak and curly seedlings, and necrosis of their tips. Among the identified acids, oxalic acid had the highest specific activity (40 mg L^?1) and citric acid had the lowest (>1000 mg L^?1). As a consequence of its high contents, the total activity, a function of specific activity and concentration, of oxalic acid (188) was found higher followed by tartaric acid (146). The contribution of both acids influencing the specific activity of the crude extract was then turned out to be 74%. To the best of our knowledge, this is the first report identifying the oxalic and tartaric acids as growth inhibitors in tamarind leaves and quantifying their contribution in its allelopathic expression. Based on the total activity, the results suggested that oxalic and tartaric acids are the major allelochemicals in tamarind leaves. The allelopathic potential of these acids might promote the development of natural herbicides as an alternative to the synthetic ones in a most sustainable manner.     

Immunodetection of coproantigens for the diagnosis of amphistomosis in naturally infected Indian Water Buffalo,Bubalus bubalis

The infection of gastrointestinal helminths in livestock is routinely diagnosed by microscopical examination of faecal samples for the presence of ova/eggs but this approach becomes ineffective for the seasonally egg producing trematodes. Therefore, an alternative approach to detect the coproantigens of liver and rumen amphistomes, Gigantocotyle explanatum and Gastrothylax crumenifer respectively, infecting Indian water buffalo Bubalus bubalis, was undertaken using ELISA, immunodot and countercurrent immunoelectrophoresis (CCIEP). The hyperimmune polyclonal antisera were separately raised in rabbits against excretory/secretory (ES) antigens of both the flukes under study. An overall 70% buffalo faecal samples were tested positive for G. crumenifer and 75% for G. explanatum in Aligarh region. The ELISA results reflected higher infection intensity among individual buffaloes that was also observed at necropsy. Using the respective homologous hyperimmune antiserum, 55% buffaloes tested positive for G. crumenifer and 65% positive for G. explanatum in immunodot assay. Further, the faecal samples with high absorbance values in ELISA and strong immunodot reaction tested positive in CCIEP. The analysis of CCIEP result revealed two and one precipitin bands in G. crumenifer and G. explanatum respectively, indicating prominent antigenic differences in the coproantigens of these two parasites. Taken together, it is suggested that polyclonal antibodies could be conveniently used for the detection of coproantigens by ELISA and immunodot methods, particularly during the non-egg producing phase of the seasonally regulated reproductive cycle of the rumen amphistome G. crumenifer. It is concluded that the coproantigen detection is a good alternative over conventional method for the diagnosis of amphistomosis in livestock; however, further studies are required on a larger sample size of field buffaloes to augment the reproducibility of the present results.