Effects of the combination of hydrophobic polypeptides, iso-alpha acids, and malto-oligosaccharides on beer foam stability

The influence of hydrophobic polypeptides concentrated in beer foam, together with the composition of iso-alpha acids and the content of malto-oligosaccharides in beer on foam stability, has been investigated. The objective was to find out whether a shortage of one of these positive contributors to foam stability could be compensated for by an increased presence of another or whether optimum levels of each contributor is necessary. For that purpose, an image analysis method to evaluate beer foam quality was developed. The foam collapse time was the parameter chosen to group beers according to their foam stability. Profiles of hydrophobic polypeptides that concentrate in beer foam, iso-alpha acids, and malto-oligosaccharides of 14 beer brands were acquired by high-performance liquid chromatography. Principal component analysis (PCA) was performed to show the relationship between beer brands and its composition. Beers that contained propylene glycol alginate as a foam enhancer showed high foam stability except for one beer, which had a low content of hydrophobic polypeptides, thereby highlighting the requirement of threshold levels of hydrophobic polypeptides to obtain stable foam. The data of samples that were devoid of a foam additive were subjected to a discriminant statistical analysis. Foam stability declined in proportion to decreases in hydrophobic polypeptides and to a lesser extent to decreases in iso-alpha-acid contents. Apparently, the content of malto-oligosaccharides were found to have no major influence on foam stability. The model of discriminate analysis was found to explain 100% of the variance in data with 85.2% success in classifying all samples according to the model, suggesting that foam stability is mainly governed by the beer constituents evaluated in this study.     

New insights into the origins and evolution of rhizobia that nodulate common bean (Phaseolus vulgaris) in Brazil

It is generally accepted that there are two major centers of genetic diversification of common beans (Phaseolus vulgaris L.): the Mesoamerican (Mexico, Colombia, Ecuador and north of Peru, probably the primary center), and the Andean (southern Peru to north of Argentina) centers. Wild common bean is not found in Brazil, but it has been grown in the country throughout recorded history. Common bean establishes symbiotic associations with a wide range of rhizobial strains and Rhizobium etli is the dominant microsymbiont at both centers of genetic diversification. In contrast, R. tropici, originally recovered from common bean in Colombia, has been found to be the dominant species nodulating field-grown common-bean plants in Brazil. However, a recent study using soil dilutions as inocula has shown surprisingly high counts of R. etli in two Brazilian ecosystems. In the present study, RFLP-PCR analyses of nodABC and nifH genes of 43 of those Brazilian R. etli strains revealed unexpected homogeneity in their banding patterns. The Brazilian R. etli strains were closely similar in 16S rRNA sequences and in nodABC and nifH RFLP-PCR profiles to the Mexican strain CFN 42^T, and were quite distinct from R. etli and R. leguminosarum strains of European origin, supporting the hypothesis that Brazilian common bean and their rhizobia are of Mesoamerican origin, and could have arrived in Brazil in pre-colonial times. R. tropici may have been introduced to Brazilian soils later, or it may be a symbiont of other indigenous legume species and, due to its tolerance to acidic soils and high temperature conditions became the predominant microsymbiont of common bean.     

Demographic threats to the sustainability of Brazil nut exploitation

A comparative analysis of 23 populations of the Brazil nut tree (Bertholletia excelsa) across the Brazilian, Peruvian, and Bolivian Amazon shows that the history and intensity of Brazil nut exploitation are major determinants of population size structure. Populations subjected to persistent levels of harvest lack juvenile trees less than 60 centimeters in diameter at breast height; only populations with a history of either light or recent exploitation contain large numbers of juvenile trees. A harvesting model confirms that intensive exploitation levels over the past century are such that juvenile recruitment is insufficient to maintain populations over the long term. Without management, intensively harvested populations will succumb to a process of senescence and demographic collapse, threatening this cornerstone of the Amazonian extractive economy.     

Assessment of Bioconcentration Factor of Chromium by Instrumental Neutron Activation Analysis in Argyrodiaptomus falcifer Daday, a Subtropical Freshwater Copepod

The objectives of this study were to determine the capacity of the freshwater calanoid copepod Argyrodiaptomus falcifer (Daday, 1905) to accumulate Cr from water, to know the bioconcentration factors in order to evaluate its potential as a biomonitor, and to compare this with data previously obtained with Daphnia magna Straus under identical conditions. By static bioassays using triplicates and a control, a pool of A. falcifer was exposed to three concentrations of Cr (VI): 150 μg/L (T1), 280 μg/L (T2), and 350 μg/L (T3) for 48 h to later determine by Instrumental Neutron Activation Analysis the amount of Cr accumulated. A. falcifer accumulated Cr in all the three concentrations tested. The comparison of T1, T2, and T3 and the control showed significant differences (p?<?0.05) but not between the treatments (p?>?0.05). On the other hand, A. falcifer accumulated more Cr than D. magna, but these differences were not significant (p?>?0.05). Almost no information is available about metal toxicity in freshwater copepods so the reported results are of high importance in order to detect good biomonitors of freshwater Cr-polluted environments.     

Habitat fragmentation alters the structure of dung beetle communities in the Atlantic Forest

Habitat loss and fragmentation have turned into the most important threats to biodiversity and ecosystem function worldwide. Here we investigate the effects of habitat fragmentation and drastic changes in tree communities on dung beetle richness and community structure. This study was carried out in a severely fragmented 670-km² forest landscape of the Atlantic Forest of north-eastern Brazil. Sampling was carried out in 19 forest fragments between September 2007 and March 2008 with the use of pitfall traps and flight interception traps. A total of 5893 individuals and 30 species of dung beetle were collected. Fragment area and isolation were the most significant explanatory variables for predictable and conspicuous changes in dung beetle species richness. Smaller and isolated fragments presented lower number of species, but fragments with lower tree species richness and lower proportion of shade-tolerant species were also considerably impoverished in terms of dung beetle species richness. The body mass of dung beetles were explained by fragment area and the percentage of emergent trees with smaller and less stratified fragments being dominated by small-bodied dung beetles. An ordination analysis segregated dung beetle communities between small fragments (<100 ha) and the control area. Seventy-seven percent of the species were recorded in the control area and 22% of all species were unique to this habitat. Our findings indicate that large fragments in the Atlantic Forest appear to consist in a sort of irreplaceable habitats for particular groups of dung beetle species, as well as for the integrity of their communities.     

Induced nutrient deficiencies in Catharanthus roseus impact ajmalicine bioproduction

Plants are key sources to obtain drugs and related medical compounds. In the species Catharanthus roseus L.G. Don, ordinarily known as vinca, contains significant amounts of the alkaloid ajmalicine, which is used as an anti-hypertension drug. The aim of this research was to verify the effect of macro-nutrient deficiencies and boron over ajmalicine bioproduction in vinca roots. The experiment was performed in random blocks with eight treatments: complete, nitrogen deficient (-N), phosphorus deficient (-P), potassium deficient (-K), calcium deficient (-Ca), magnesium deficient (- Mg), sulfur deficient (-S) and boron deficient (-B), with four replicates. Seedlings were initially watered once a day with a complete solution and after 55 days after germination the treatments were started. Plants were collected 135 days after germination and evaluated in relation to root's dry matter, concentration of N, P, K, Ca, Mg, S, B and ajmalicine. Concentration of N, P, K, Ca, Mg, S and B within the root's dry matter of the vinca plants in deficient treatments were respectively of 62, 61, 93, 52, 70, 61 and 44% lower when compared with complete treatment. Potassium deficiency resulted in ajmalicine increment of 19% within roots, while deficiencies in N, P, Mg and S reduced ajmalicine concentration in 55, 33, 22 and 26% respectively when compared with complete treatment. Deficiencies in Ca and B had no significant effect in ajmalicine concentration within the plant roots. Within plants with the complete treatment, nutrient contents of ajmalicine from the roots’ dry matter were respectively of 18,5 g kg^?1 N, 1,46 g kg^?1 P, 13,5 g kg^?1 K, 4,47 g kg^?1 Ca, 1,43 g kg^?1 Mg, 1,53 g kg^?1 S, 61 mg kg^?1 B and 1,28 mg g^?1 of vitexin.     

Immunocytochemical study of Ki-67 as a prognostic marker in canine mammary neoplasia

Background: Canine mammary tumors are challenging for clinicians and pathologists because of complex histologic classification, low specificity of cytologic diagnosis, and unpredictable biological behavior. In histologic specimens, expression of tumor proliferation marker Ki‐67, a nuclear nonhistone protein, has been shown to have prognostic value for canine mammary tumors and to correlate with malignancy and low survival rates. Objective: The objective of this study was to measure the proliferation index of canine mammary tumors by immunochemical detection of Ki‐67 in cytologic specimens and to determine its relationship to clinical and pathologic variables and patient outcome. Methods: Spontaneous mammary tumors from 31 female dogs were surgically excised. Imprint specimens for cytologic evaluation were wet‐fixed in ethanol; histologic specimens were prepared routinely. Immunostaining was performed with the PH 177 monoclonal antibody against Ki‐67; proliferation index was graded from negative to +++. Dogs were followed for 18 months. Multivariate logistic regression analysis was used to determine correlations between immunocytochemical results, tumor and clinical variables, and patient outcome. Results: Ki‐67 proliferation indices in cytologic specimens were significantly lower for nonmalignant tumors than for malignant tumors. High index values of Ki‐67 were positively correlated with metastasis, death from neoplasia, low disease‐free survival rates, and low overall survival rate. With the exception of 4 specimens for which cellularity was insufficient, positive expression of Ki‐67 in cytologic specimens correlated with that of histologic specimens. Conclusions: The prognostic value of the Ki‐67 index in canine mammary tumors by using wet‐fixed cytology imprint specimens was similar to that observed previously for histologic specimens. Immunocytochemical detection of Ki‐67 could improve the accuracy and value of cytology by providing safe and rapid information about malignancy and patient outcome.     

Efficiency of entomopathogenic fungi in the control of eggs and larvae of the horn fly Haematobia irritans (Diptera: Muscidae)

The present study assessed the pathogenic effect of isolates E9, IBCB425 and IBCB159 of the Metarhizium anisopliae fungus, JAB06, JAB07 and AM09 of Beauveria bassiana, IBCB133 and CB75 of Isaria fumosorosea (=Paecilomyces fumosoroseus) and CG189 and CG195 of Isaria farinosa (=Paecilomyces farinosus) against eggs and larvae of the horn fly Haematobia irritans. Eggs were inoculated with suspensions containing 10⁶, 10⁷ and 10⁸ conidia ml⁻¹ of the fungal isolates and observed after 48 h to determine viability. In the larvae study, eggs were allowed to hatch into fresh bovine feces that had been treated with 10⁸, 10⁷ or 10⁶ conidia mg feces⁻¹. In both studies, 5 days after initial procedures, all formed pupae were transferred to an incubator at 27 ± 0.5 °C until the emergence of the adult flies was complete. The M. anisopliae isolates did not cause the death of H. irritans eggs, but they did promote the death of larvae that hatched from treated eggs, and therefore increased the total mortality. Isolate E9 promoted 100% mortality of treated larvae at a concentration of 10⁸ conidia ml⁻¹. For the B. bassiana isolates, no activity was observed against insect eggs or larvae. Both I. fumosorosea isolates promoted significant mortality (p < 0.05) of eggs at every concentration of conidia. Isolate CG195 of I. farinosa increased the mortality of larvae and pupae that hatched from treated eggs and promoted significant total mortality (p < 0.05) of the insect at every concentration of conidia.