Diagnóstico de la fertilidad de suelos en dos parcelas para cultivo de cacao (Theobroma cacao) y café (Coffea arábica) en el municipio de San Buenaventura

En el norte del departamento de La Paz, la frontera agrícola fue incrementándose vertiginosamente por el ingreso del cultivo de caña de azúcar, actividades ganaderas, asentamientos en áreas para la extracción ilegal de la madera, entre otras, que van en desmedro de la biodiversidad; el trabajo consistió en diagnosticar la fertilidad de suelos para la implementación de cultivos con cacao y café, en dos comunidades (San Silvestre y Esmeralda), tomando como base los datos obtenidos por Miranda et al. (2021) sobre análisis físico-químico de suelos. El procedimiento fue: a) sistematización de información secundaria y primaria, b) análisis de ingresos y salidas de nutrientes del suelo y c) dosificación de nutrientes en base al balance de los mismos para el cultivo de cacao y café. De acuerdo al análisis realizado, En la comunidad Esmeralda para tener adecuados rendimientos en cacao se debe adicionar 738.5 kg N ha-1 y 76.07 kg P2O5 ha-1 y en café 212.5 kg N ha-1, los mismos por su bajo porcentaje de saturación de acidez no requieren encalado. En la comunidad San Silvestre, se requiere adición de 788.09 kg N ha-1, 229.03 kg P2O5 ha-1 y 403.86 kg K2O para el cultivo de cacao y para el cultivo de café 262.09 kg N ha-1 21.20 kg P2O5. Por otro lado, los suelos presentan un alto porcentaje de saturación de acidez recomendado con 46.73 %, mayor al porcentaje de saturación de cultivo de cacao (20 %) y café (25 %) sugiriendo la adición de 4.327 kg de cal agrícola para el cultivo de cacao por planta y 0.439 kg para el cultivo de café, sugiriendo los mismos ser aplicados en dos etapas

Computation Provides Chemical Insight into the Diverse Hydride NMR Chemical Shifts of [Ru(NHC)₄(L)H]^0/+ Species (NHC = N-heterocyclic carbene; L = vacant, H₂, N₂, CO, MeCN, O₂, P₄, SO₂, H^-, F^- and Cl^-) and their [Ru(R₂PCH₂CH₂PR₂)₂(L)H]⁺ Congeners

Relativistic density functional theory calculations, both with and without the effects of spin–orbit coupling, have been employed to model hydride NMR chemical shifts for a series of [Ru(NHC)4(L)H]0/+ species (NHC = N-heterocyclic carbene; L = vacant, H2, N2, CO, MeCN, O2, P4, SO2, H−, F− and Cl−), as well as selected phosphine analogues [Ru(R2PCH2CH2PR2)2(L)H]+ (R = iPr, Cy; L = vacant, O2). Inclusion of spin–orbit coupling provides good agreement with the experimental data. For the NHC systems large variations in hydride chemical shift are shown to arise from the paramagnetic term, with high net shielding (L = vacant, Cl−, F−) being reinforced by the contribution from spin–orbit coupling. Natural chemical shift analysis highlights the major orbital contributions to the paramagnetic term and rationalizes trends via changes in the energies of the occupied Ru dπ orbitals and the unoccupied σ*Ru–H orbital. In [Ru(NHC)4(η2-O2)H]+ a δ-interaction with the O2 ligand results in a low-lying LUMO of dπ character. As a result this orbital can no longer contribute to the paramagnetic shielding, but instead provides additional deshielding via overlap with the remaining (occupied) dπ orbital under the Lz angular momentum operator. These two effects account for the unusual hydride chemical shift of +4.8 ppm observed experimentally for this species. Calculations reproduce hydride chemical shift data observed for [Ru(iPr2PCH2CH2PiPr2)2(η2-O2)H]+ (δ = −6.2 ppm) and [Ru(R2PCH2CH2PR2)2H]+ (ca. −32 ppm, R = iPr, Cy). For the latter, the presence of a weak agostic interaction trans to the hydride ligand is significant, as in its absence (R = Me) calculations predict a chemical shift of −41 ppm, similar to the [Ru(NHC)4H]+ analogues. Depending on the strength of the agostic interaction a variation of up to 18 ppm in hydride chemical shift is possible and this factor (that is not necessarily readily detected experimentally) can aid in the interpretation of hydride chemical shift data for nominally unsaturated hydride-containing species. The synthesis and crystallographic characterization of the BArF4− salts of [Ru(IMe4)4(L)H]+ (IMe4 = 1,3,4,5-tetramethylimidazol-2-ylidene; L = P4, SO2; ArF = 3,5-(CF3)2C6H3) and [Ru(IMe4)4(Cl)H] are also reported

Clinical and histopathological study on reproductive lesions caused by Pasteurella multocida type B2 immunogens in buffalo heifers

Hemorrhagic septicemia (HS) is a globally renowned disease that affects cattle and buffaloes. Its effects on the reproductive system have not been previously studied. Thus, the present study aims to evaluate the pathological responses in pre-pubertal female buffalo infected with immunogens; lipopolysaccharide (LPS) and outer membrane protein (OMP) derived from P. multocida type B: 2. Fifteen healthy pre-pubertal female buffaloes of approximately 8 months old were selected and divided into five equal groups of 3 buffaloes each. Buffaloes in groups 1 and 2 were intravenously and orally inoculated with 10 mL of P. multocida LPS at 1× 1012 colony forming unit (cfu) ,while those in group 3 and group 4 were subcutaneously and orally inoculated with10 mL of P. multocida OMP at 1× 1012 colony forming unit (cfu). Buffaloes in group 5 were inoculated with 10mL of sterile phosphate buffered saline (PBS) PH7 and served as the negative control. During the post infection period, all buffaloes were examined for clinical signs throughout 21 days and surviving buffaloes were euthanized for postmortem evaluation. Histopathological evaluation of buffaloes inoculated with LPS showed a significantly higher occurrence (p<0.05) of necrosis and degeneration in the uterine horn and supramammary glands of buffaloes inoculated intravenously. Following inoculation with OMP, hemorrhage and congestion was significantly higher (p<0.05) in the ovaries, cervix, vagina, mammary and supra-mammary glands of buffaloes inoculated subcutaneously, while necrosis and degeneration and inflammatory cell infiltration in different organs was also significantly increased in the same inoculation group. The findings of this study have shown that both P. multocida bacterial LPS and OMP affect the uterine horn, ovaries, cervix, mammary gland and supramammary lymph nodes of buffalo calves inoculated either intravenously or subcutaneously, as compared to those inoculated orally

Computation Provides Chemical Insight into the Diverse Hydride NMR Chemical Shifts of [Ru(NHC)₄(L)H]^0/+ Species (NHC = N-heterocyclic carbene; L = vacant, H₂, N₂, CO, MeCN, O₂, P₄, SO₂, H^-, F^- and Cl^-) and their [Ru(R₂PCH₂CH₂PR₂)₂(L)H]⁺ Congeners

International audienceRelativistic density functional theory calculations, both with and without the effects of spin–orbit coupling, have been employed to model hydride NMR chemical shifts for a series of [Ru(NHC)4(L)H]0/+ species (NHC = N-heterocyclic carbene; L = vacant, H2, N2, CO, MeCN, O2, P4, SO2, H−, F− and Cl−), as well as selected phosphine analogues [Ru(R2PCH2CH2PR2)2(L)H]+ (R = iPr, Cy; L = vacant, O2). Inclusion of spin–orbit coupling provides good agreement with the experimental data. For the NHC systems large variations in hydride chemical shift are shown to arise from the paramagnetic term, with high net shielding (L = vacant, Cl−, F−) being reinforced by the contribution from spin–orbit coupling. Natural chemical shift analysis highlights the major orbital contributions to the paramagnetic term and rationalizes trends via changes in the energies of the occupied Ru dπ orbitals and the unoccupied σ*Ru–H orbital. In [Ru(NHC)4(η2-O2)H]+ a δ-interaction with the O2 ligand results in a low-lying LUMO of dπ character. As a result this orbital can no longer contribute to the paramagnetic shielding, but instead provides additional deshielding via overlap with the remaining (occupied) dπ orbital under the Lz angular momentum operator. These two effects account for the unusual hydride chemical shift of +4.8 ppm observed experimentally for this species. Calculations reproduce hydride chemical shift data observed for [Ru(iPr2PCH2CH2PiPr2)2(η2-O2)H]+ (δ = −6.2 ppm) and [Ru(R2PCH2CH2PR2)2H]+ (ca. −32 ppm, R = iPr, Cy). For the latter, the presence of a weak agostic interaction trans to the hydride ligand is significant, as in its absence (R = Me) calculations predict a chemical shift of −41 ppm, similar to the [Ru(NHC)4H]+ analogues. Depending on the strength of the agostic interaction a variation of up to 18 ppm in hydride chemical shift is possible and this factor (that is not necessarily readily detected experimentally) can aid in the interpretation of hydride chemical shift data for nominally unsaturated hydride-containing species. The synthesis and crystallographic characterization of the BArF4− salts of [Ru(IMe4)4(L)H]+ (IMe4 = 1,3,4,5-tetramethylimidazol-2-ylidene; L = P4, SO2; ArF = 3,5-(CF3)2C6H3) and [Ru(IMe4)4(Cl)H] are also reported

Genetic Insight into Yield-Associated Traits of Wheat Grown in Multiple Rain-Fed Environments

Background: Grain yield is a key economic driver of successful wheat production. Due to its complex nature, little is known regarding its genetic control. The goal of this study was to identify important quantitative trait loci (QTL) directly and indirectly affecting grain yield using doubled haploid lines derived from a cross between Hanxuan 10 and Lumai 14. Methodology/Principal Findings: Ten yield-associated traits, including yield per plant (YP), number of spikes per plan

Metabolic Profiling of a Mapping Population Exposes New Insights in the Regulation of Seed Metabolism and Seed, Fruit, and Plant Relations

To investigate the regulation of seed metabolism and to estimate the degree of metabolic natural variability, metabolite profiling and network analysis were applied to a collection of 76 different homozygous tomato introgression lines (ILs) grown in the field in two consecutive harvest seasons. Factorial ANOVA confirmed the presence of 30 metabolite quantitative trait loci (mQTL). Amino acid contents displayed a high degree of variability across the population, with similar patterns across the two seasons, while sugars exhibited significant seasonal fluctuations. Upon integration of data for tomato pericarp metabolite profiling, factorial ANOVA identified the main factor for metabolic polymorphism to be the genotypic background rather than the environment or the tissue. Analysis of the coefficient of variance indicated greater phenotypic plasticity in the ILs than in the M82 tomato cultivar. Broad-sense estimate of heritability suggested that the mode of inheritance of metabolite traits in the seed differed from that in the fruit. Correlation-based metabolic network analysis comparing metabolite data for the seed with that for the pericarp showed that the seed network displayed tighter interdependence of metabolic processes than the fruit. Amino acids in the seed metabolic network were shown to play a central hub-like role in the topology of the network, maintaining high interactions with other metabolite categories, i.e., sugars and organic acids. Network analysis identified six exceptionally highly co-regulated amino acids, Gly, Ser, Thr, Ile, Val, and Pro. The strong interdependence of this group was confirmed by the mQTL mapping. Taken together these results (i) reflect the extensive redundancy of the regulation underlying seed metabolism, (ii) demonstrate the tight co-ordination of seed metabolism with respect to fruit metabolism, and (iii) emphasize the centrality of the amino acid module in the seed metabolic network. Finally, the study highlights the added value of integrating metabolic network analysis with mQTL mapping