RESUMEN
Nutrient management on US dairy farms must balance an array of priorities, some of which conflict. To illustrate nutrient management challenges and opportunities across the US dairy industry, the USDA Agricultural Research Service Dairy Agroecosystems Working Group (DAWG) modeled 8 confinement and 2 grazing operations in the 7 largest US dairy-producing states using the Integrated Farm System Model (IFSM). Opportunities existed across all of the dairies studied to increase on-farm feed production and lower purchased feed bills, most notably on large dairies (>1,000 cows) with the highest herd densities. Purchased feed accounted for 18 to 44% of large dairies' total operating costs compared with 7 to 14% on small dairies (<300 milk cows) due to lower stocking rates. For dairies with larger land bases, in addition to a reduction in environmental impact, financial incentives exist to promote prudent nutrient management practices by substituting manure nutrients or legume nutrients for purchased fertilizers. Environmental priorities varied regionally and were principally tied to facility management for dry-lot dairies of the semi-arid western United States (ammonia-N emissions), to manure handling and application for humid midwestern and eastern US dairies (nitrate-N leaching and P runoff), and pasture management for dairies with significant grazing components (nitrous oxide emissions). Many of the nutrient management challenges identified by DAWG are beyond slight modifications in management and require coordinated solutions to ensure an environmentally and economically sustainable US dairy industry.
Asunto(s)
Alimentación Animal/normas , Fenómenos Fisiológicos Nutricionales de los Animales , Bovinos/fisiología , Industria Lechera/métodos , Animales , Femenino , Estiércol , Necesidades Nutricionales , Fósforo , Estados Unidos , United States Department of AgricultureRESUMEN
Reliable estimates of N excretion in the urine and feces of beef cattle are essential for developing cost-effective and environmentally sound nutrient management plans. A meta-analysis dataset was compiled that included data for starting live BW, DMI, N intake, dietary CP and RDP concentrations, urine N excretion, and feces N excretion. The data were taken from 12 individual feeding trials that included N balance data, and represented a total of 47 different dietary treatments and 255 animals. Correlation analysis was used to determine the animal and dietary parameters that were most closely related to N excretion in urine and feces by beef cattle. A multivariate mixed modeling approach was used to develop empirical equations to predict excretion of urine N, feces N, and the partitioning of total N excretion between urine and feces, as a function of N intake and the concentration of dietary CP. Univariate, regression, and mean difference comparisons indicated 46 to 95% agreement between observed and predicted values for the developed equations. Evaluation of the equations with an independent dataset taken from 6 studies, and 2 random subsets of the meta-analysis dataset showed moderate agreement (P < 0.05, r(2) = 0.34 to 0.86) for urine N excretion as a function of both N intake and %CP, and the partitioning of total N excretion into urine as a function of %CP. There was less agreement between predictions and observations for feces N excretion as a function of %CP (r(2) = 0.003 to 0.14) than N intake (r(2) = 0.52 to 0.75), indicating that %CP is not a good predictor of fecal N excretion. The empirical equations provide a simple tool that, if used with caution, could predict N excretion characteristics for a wide range of dietary and animal characteristics and could improve ammonia emissions estimates by process-based models.
Asunto(s)
Bovinos/fisiología , Proteínas en la Dieta/metabolismo , Nitrógeno/metabolismo , Fenómenos Fisiológicos Nutricionales de los Animales , Animales , Bovinos/crecimiento & desarrollo , Dieta/veterinaria , Heces/química , Modelos Biológicos , Nitrógeno/orinaRESUMEN
Interspecific hybrids and backcrossed organisms generally suffer from reduced viability and/or fertility. To identify and genetically map these defects, we introgressed regions of the Drosophila sechellia genome into the D. simulans genome. A female-biased sex ratio was observed in 24 of the 221 recombinant inbred lines, and subsequent tests attributed the skew to failure of Y-bearing sperm to fertilize the eggs. Apparently these introgressed lines fail to suppress a normally silent meiotic drive system. Using molecular markers we mapped two regions of the Drosophila genome that appear to exhibit differences between D. simulans and D. sechellia in their regulation of sex chromosome segregation distortion. The data indicate that the sex ratio phenotype results from an epistatic interaction between at least two factors. We discuss whether this observation is relevant to the meiotic drive theory of hybrid male sterility.
Asunto(s)
Drosophila/genética , Cromosomas Sexuales , Animales , Secuencia de Bases , Cartilla de ADN , Femenino , Prueba de Complementación Genética , Masculino , Carácter Cuantitativo Heredable , Razón de MasculinidadRESUMEN
The bursa of Fabricius represents the primary immune organ where immature B cells undergo maturational changes in avian species. Isolation of bursal lymphocytes for analysis in cell culture results in the rapid endogenous activation of apoptosis. After 2 h of incubation, over 45% of the lymphocytes were shown to be undergoing apoptosis and by 6 h 80% were undergoing apoptosis as demonstrated by a terminal deoxynucleotidyltransferase-mediated dUTP-fluorescein isothiocynate nick end-labeling flow-cytometric analysis. These results were corroborated by a propidium iodide-staining flow-cytometric assay and by an agarose gel electrophoresis DNA fragmentation assay that demonstrated internucleosomal DNA cleavage of genomic DNA in apoptotic bursal lymphocytes. Endogenous activation of apoptosis in bursal lymphocytes could be inhibited in a dose-dependent fashion with the phorbol ester, phorbol 12-myristate 13-acetate, but not the phorbol ester antagonist 4 alpha-phorbol 12,13-didecanoate. In addition, apoptosis could be inhibited in a dose-dependent fashion with inhibitors of protein translation, cycloheximide, and puromycin, as well as the transcriptional inhibitor actinomycin D. These results suggest that endogenous activation of bursal lymphocyte apoptosis may be mediated by the protein kinase C signal transduction pathway and activation of this process appears to be dependent upon de novo protein biosynthesis.
Asunto(s)
Apoptosis/efectos de los fármacos , Apoptosis/inmunología , Linfocitos B/efectos de los fármacos , Bolsa de Fabricio/citología , Bolsa de Fabricio/efectos de los fármacos , Ésteres del Forbol/farmacología , Inhibidores de la Síntesis de la Proteína/farmacología , Animales , Apoptosis/fisiología , Linfocitos B/citología , Linfocitos B/metabolismo , Bolsa de Fabricio/metabolismo , Diferenciación Celular , Células Cultivadas , Pollos , Fragmentación del ADN , Forbol 12,13-Dibutirato/farmacología , Proteína Quinasa C/metabolismo , Transducción de Señal , Acetato de Tetradecanoilforbol/farmacologíaRESUMEN
The objective of this study was to determine the effects of an Aspergillus oryzae fermentation extract (Amaferm) as well as other factors on lactate utilization by the ruminal bacterium Megasphaera elsdenii B159. Addition of Amaferm or a filter-sterilized Amaferm filtrate stimulated L-lactate uptake by both M. elsdenii and the ruminal selenomonad strain H18. Growth of M. elsdenii in medium that contained DL-lactate (2 g/L), Trypticase, and yeast extract was only slightly stimulated by the addition of 5% (vol/vol) Amaferm filtrate after 24 h. However, growth of M. elsdenii in a similar medium lacking Trypticase and yeast extract was increased over twofold by the addition of either 2 or 5% (vol/vol) Amaferm filtrate. These results suggest that Amaferm provides growth factors (i.e., amino acids, B vitamins) to support growth of M. elsdenii on lactate. There was no inhibition of L-lactate uptake when lactate-grown cells of M. elsdenii were incubated with excess (10 mM) glucose, sucrose, or maltose. In addition, when cells were grown on glucose, sucrose, or maltose rather than lactate there was little difference in L-lactate uptake, suggesting that L-lactate transport in M. elsdenii is not subject to catabolite repression by these soluble sugars. Both K+ and Na+ had little effect on L-lactate uptake. Uptake was unaffected at extracellular pH values between 6.0 and 8.0, whereas pH values of 5.0 and 4.0 increased uptake. In addition, L-lactate uptake was inhibited between 34 and 61% by protonophores. These results suggest that protons may be involved in the uptake of L-lactate by M. elsdenii B159.