Does biomass production depend on plant community diversity?

In order to ensure the sustainability of agroecosystems, biodiversity must be a priority. Agroforestry, which includes trees, is an example of such diverse systems. We evaluated plant diversity and aboveground biomass production to assess whether areas under fallow following traditional cultivation return to their initial condition. Also, plant diversity and aboveground biomass production were assessed in agroforestry systems (AFS) to determine if these were similar to unmanaged ecosystems. Another objective of the study was to observe the influence of plant diversity on aboveground biomass production in plant communities and also in the population of the dominant species, Cordia oncocalyx. Plant diversity was evaluated by assessing species richness, as well as using Shannon’s (H′) and Pielou’s (J′) indices. Aboveground plant biomass was evaluated in two AFS: agrosilvopastoral (ASP) and silvopastoral (SP), and also in a traditionally managed agricultural system (AG), areas that had been under fallow for six years (F6) and nine years (F9) and an area of unmanaged caatinga (CAT) vegetation. We observed that the ASP system had a lower diversity and number of species, especially tree species. However, it sustained the same total biomass production as CAT and fallow areas. The SP system, despite having lower H′ and J′ indices as well as lower total biomass production, had a similar number of species to CAT and cropped and fallow systems AG, F6 and F9. Plant biomass in F6 and F9 had recovered to productivity levels of unmanaged CAT vegetation; however the diversity indices were not restored to the same level. Plant diversity did not have an effect on the productivity of the agroecosystems. Likewise, annual biomass production by C. oncocalyx is not dependent upon diversity, but it is influenced by the growth stage of individuals.     

Interaction of common beans cultivars of the black group with years, locations and sowing seasons

The objectives of this study were to assess which environmental factors (local, season or years) are the most important to contribute for the interactions with genotypes of common black beans and to verify the existence of genotypes with broad and/or specific adaptation to the diverse planting seasons in Central Brazil. Data of grain yields for 13 genotypes in 18 field trials used for cultivar registration were utilized, across 2?years (2003 and 2004). Analyses of variance were carried out with decomposition of the genotype x environment interactions. Firstly, data of 18 trials were used, allowing a partial isolation of factors and, subsequently, eight trials were used to allow a complete isolation of the factors. The genotype x sowing seasons (R²?=?4.2?%) and genotype x year (R²?=?4.1?%) interactions were of the greatest important, while genotype x location was less important (R²?=?3.0?%). It was concluded that is more important to conduct evaluations of genotypes in different seasons and years rather than in different locations. The majority of the genotypes tested presented specific adaptation, although it was possible to identify superior lines with wide adaptation.     

The Effects of the Decaffeination of Coffee Samples on Platelet Aggregation in Hyperlipidemic Rats

The effect of coffee on cardiovascular diseases is still controversial. It is known that the process of decaffeination may influence the chemical constitution and, therefore, the biological effects of coffee. This study thus evaluated the effects of decaffeination on the levels of total phenols and chlorogenic acids in Coffea arabica L. samples, as well as the effects of ingesting both integral and decaffeinated coffee on the lipid profile and hemostatic and hematological parameters in normal and hyperlipidemic rats. Samples of integral and decaffeinated lyophilized coffee (Coffea arabica L., planted in Brazil) were used for chemical analysis (total phenols, chlorogenic acid and caffeine contents). For the bioassays, coffee beverages were prepared with non-lyophilized samples (10 % w/v) and were filtered and administered to animals by gavage (7.2 mL/kg/day) over 30 days. On the 31st day after beginning the treatment with coffee beverages, hyperlipidemia was induced to the animals by administering Triton WR-1339 (300 mg/kg body weight). On day 32, blood was taken to determine the lipid profile, platelet aggregation, prothrombin time, partially activated thromboplastin time and hemogram. The contents of both phenolic compounds and chlorogenic acid in the integral coffee beverage were significantly lower than those in the decaffeinated coffee beverage. The animals treated with Triton WR-1339 presented a mixed hyperlipidemia. Although the decaffeination process caused a relative increase in total phenols and chlorogenic acids, the coffee drinks were unable to change the lipid profile or the hemostatic and hematological parameters in the studied animals.     

Factors associated with seroprevalence of Neospora caninum in dairy cattle in southeastern Brazil

Neosporosis is an infectious disease caused by Neospora caninum, an obligate intracellular cyst-forming protozoan considered a major cause of miscarriage in dairy cattle in many parts of the world. This cross-sectional study evaluated the relationship between reproductive abnormalities and seropositivity to N. caninum in 1,204 dairy cows from 40 farms located in the state of Minas Gerais, southeastern Brazil. Producers were interviewed, and blood samples were collected to perform indirect immunofluorescence tests (IFAT 1:200). Association between reproductive abnormalities and seropositivity in cattle was evaluated with generalized estimating equations. The true herd-level seroprevalence of N. caninum was 95 % (83.3–99.1), while the individual-level true seroprevalence was 21.6 % (19.2–24.2). Several reproductive abnormalities were significantly associated with seropositivity to N. caninum: occurrence of repeated estrus (p?=?0.02; OR?=?3.84; 95 % CI?=?1.239–11.893), repeated miscarriages (p?=?0.001; OR?=?2.54; 95 % CI?=?1.423–5.402), and temporary anestrus (p?=?0.001; OR?=?3.44; 95 % CI?=?1.976–5.994). Furthermore, loose dogs (p?=?0.041; OR?=?2.20; 95 % CI?=?1.033–4.672) when fed raw meat (p?=?0.001; OR?=?1.91; 95 % CI?=?1.443–2.519) are risk factors for N. caninum infection. We observed that seropositivity to N. caninum in cattle increases risk of miscarriage by almost twice throughout the reproductive life of cows (p?=?0.004; OR?=?1.978; 95 % CI?=?1.249–3.131). Serologic evidence in this study indicates that N. caninum infection is widely distributed among dairy herds and significantly associated with reproductive disorders, especially miscarriage, repeated estrus, and temporary anestrus.     

Effects of Saccharomyces cerevisiae and monensin on digestion, ruminal parameters, and balance of nitrogenous compounds of beef cattle fed diets with different starch concentrations

This study was carried out aiming to evaluate the effects of yeast or monensin supplementation on dry matter intake, nutrients digestibility, ruminal volatile fatty acids profile, ruminal pH and ammonia concentration, microbial protein synthesis, and the balance of nitrogen compounds of cattle fed high concentrate diet (80 % dry matter (DM) basis) with two different levels of starch. Eight crossbred beef steers fitted with rumen cannula were assigned to two simultaneous 4?×?4 Latin squares arranged in a 4?×?2 factorial design. Two different starch levels (23 and 38 % of DM) were assigned to each Latin square, independently. Within each Latin square, four treatments were randomly assigned to the experimental animals (control; monensin; 1-g yeast [1 g/100 kg body weight (BW)/day] treatment; and 2.5-g yeast [2.5 g/100 kg BW/day] treatment). Feed additives did not influence ruminal pH (P?>?0.05). Total ruminal volatile fatty acids (VFA) concentration was greater (P?<?0.05) in the diet with the lowest starch level. Similarly, monensin and 1-g yeast treatments resulted in greater (P?<?0.05) VFA concentration in the rumen. Monensin inclusion in the diet with the highest starch level led to a decrease (P?<?0.05) in lactate concentration in the rumen. However, acetate levels were increased (P?<?0.05) by the inclusion of 1 g of yeast in the diet with lowest starch level. Ruminal concentrations of propionate and butyrate, and ammonia-N were not influenced (P?>?0.05) by none of the additives evaluated. However, propionate concentration was greater (P?<?0.05) in the low-starch diets. Low-starch diets resulted in lower ruminal ammonia-N concentration and greater neutral detergent fiber digestibility (P?<?0.05). The excretion of urinary nitrogenous compounds, purine derivatives, synthesis of microbial protein, microbial efficiency, and balance of nitrogenous compounds were not affected by treatments evaluated (P?>?0.05). Monensin or yeast inclusion in high concentrate beef cattle diets in tropical regions as in Brazil is not justified by do not alter nutrient digestibility, nitrogen balance, and main ruminal parameters.     

Protein nutrition of dairy cattle

Abstract

In the June 1998 issue of the New Zealand Veterinay Journal, a clinical review was published focusing on aspects of the protein nutrition of dairy cattle (Westwood et al., 1998 Westwood, CT,, Lean, IJ, and Kellaway, RC. 1998. Indications and implications for testing milk urea in dairy cattle: A quantitative review. Part 1. Dietary protein sources and metabolism. New Zealand Veterinary Journal, 46: 87–96. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]). The authors wrote: “Most species of rumen bacteria can use ammonia for growth, but some, particularly bacteria which ferment cell wall carbohydrates, use or have obligate requirements for amino acids and peptides (Russel et al., 1992 Russel, JB,, O’Connor, JD,, Fox, DG,, Soest, PJ, van and Sniffen, CJ. 1992. A net carbohydrate and protein system for evaluating cattle diets. I. Ruminal fermentation. Journal of Animal Science, 70: 3551–61. [PubMed], [Web of Science ®] , [Google Scholar])”.     

IGF-I,GHR and UCP mRNA expression in the liver and muscle of high- and low-feed-efficiency laying Japanese quail at different environmental temperatures

In this study, we analyzed insulin-like growth factor I (IGF-I), growth hormone receptor (GHR) and uncoupling protein (UCP) mRNA expression in the muscle and liver of high- (0.23 g/g) and low- (0.17 g/g) feed-efficiency (FE) Japanese quail at three different air temperatures: comfortable (25 °C), heat stress (38 °C) for 12 h or cold stress (10 °C) for 12 h. Total RNA was extracted from the liver and breast muscle of each quail, and cDNA was amplified using specific primers for the target genes. Expression was analyzed using quantitative real-time PCR (qRT-PCR). IGF-I mRNA expression was higher in the livers of high-FE quail than in the livers of low-FE quail under both heat and cold stress conditions. High-FE birds also showed higher GHR mRNA expression independent of temperature. UCP mRNA expression in the liver was lower in high-FE birds and higher under heat stress compared with the other conditions. IGF-I mRNA expression was higher in the muscle of high-FE quail under the three conditions tested, and UCP mRNA expression was higher under cold stress. Our results suggest that air temperature affects the expression of genes related to growth and mitochondrial energy production, and quail with different feed efficiencies respond differently to environmental stimuli.