Foraging behavior of Melipona rufiventris Lepeletier (Apinae; Meliponini) in Ubatuba, SP, Brazil.

This study describes how the foraging activity of Melipona rufiventris is influenced by the environment and/or by the state of a colony. Two colonies were studied in Ubatuba, SP (44 degrees 48 W and 23 degrees 22 S) from July/2000 to June/2001. These colonies were classified as strong (Colony 1) and intermediate (Colony 2) according to their general conditions: population and brood comb size and number of food pots. The bees were active from dawn to dusk. The number of pollen loads presented a positive correlation with relative humidity (r(s) = 0.401; p <0.01) and was highest between 70 and 90%. However, it was negatively correlated with temperature (r(s) = -0.228; p <0.01) showing a peak between 18 and 23 degrees C. The number of nectar loads presented a positive correlation with temperature (r(s) = 0.244; p <0.01) and light intensity (r(s) = 0.414; p <0.01); it was greater between 50 and 90% of relative humidity and 20 and 30 degrees C of temperature. They collected more nectar than pollen throughout the day, and were more active between 6 and 9 hours. Workers from Colony 1 (strong) collected nectar in greater amounts and earlier than those from Colony 2 (intermediate). The number of pollen, nectar and resin loads varied considerably between the study days. Peaks of pollen collection occurred earlier in months with longer days and in a hotter and more humid climate. The foraging behavior of M. rufiventris is probably affected by the state of the colony and by environmental conditions, notably temperature, relative humidity, light intensity and length of the day.     

pkc-1 regulates daf-2 insulin/IGF signalling-dependent control of dauer formation in Caenorhabditis elegans

In Caenorhabditis elegans, the insulin/IGF pathway participates in the decision to initiate dauer development. Dauer is a diapause stage that is triggered by environmental stresses, such as a lack of nutrients. Insulin/IGF receptor mutants arrest constitutively in dauer, an effect that can be suppressed by mutations in other elements of the insulin/IGF pathway or by a reduction in the activity of the nuclear hormone receptor daf‐12. We have isolated a pkc‐1 mutant that acts as a novel suppressor of the dauer phenotypes caused by insulin/IGF receptor mutations. Interactions between insulin/IGF mutants and the pkc‐1 suppressor mutant are similar to those described for daf‐12 or the DAF‐12 coregulator din‐1. Moreover, we show that the expression of the DAF‐12 target daf‐9, which is normally elevated upon a reduction in insulin/IGF receptor activity, is suppressed in a pkc‐1 mutant background, suggesting that pkc‐1 could link the daf‐12 and insulin/IGF pathways. pkc‐1 has been implicated in the regulation of peptide neurosecretion in C. elegans. Although we demonstrate that pkc‐1 expression in the nervous system regulates dauer formation, our results suggest that the requirement for pkc‐1 in neurosecretion is independent of its role in modulating insulin/IGF signalling. pkc‐1 belongs to the novel protein kinase C (nPKC) family, members of which have been implicated in insulin resistance and diabetes in mammals, suggesting a conserved role for pkc‐1 in the regulation of the insulin/IGF pathway.     

Natural regeneration of Spanish black pine [Pinus nigra Arn. ssp. salzmannii (Dunal) Franco] at contrasting altitudes in a Mediterranean mountain area

Information on plant seed dispersal, natural loss dynamics of seeds and germination are critical for understanding natural regeneration mechanisms. The aim of this study was to assess the effect of different forest stand densities on seedfall, seed predation, and seedling germination of two populations of the endangered Spanish black Pine forests located at lower (Central population) and higher elevation near the limit of the species?? range (peripheral population) in the Cuenca Mountains of Central Spain. The seed predation and germination experiment also included a nested site preparation treatment. Seed fall varied significantly between 2006 and 2005 or 2007 in both populations. During the only mast year of 2006, higher seedfall was observed at lower elevation and in higher density stands. Predation rates were influenced by the seed crop since predators consumed more than 75?% of seeds in years with lower production and less than 15?% in a mast year. Seed germination is influenced by forest habitat, stand density and soil scalping. For common habitat types, and in a high seed production year, better seed germination rates were observed in medium and dense stands (25?C30 and 35?C40?m²?ha^?1, respectively, in terms of basal area). No statistical difference in seed germination rate was found for Spanish black pine forest at its ecological distribution limit between lower and higher densities (15?C20 and 35?C40?m²?ha^?1, in terms of basal area). In both sites, closed stands with soil scalping exhibited higher germination rates.     

Salt stress affects glutamine synthetase activity and mRNA accumulation on potato plants in an organ-dependent manner

Ammonium assimilation into glutamine and glutamate is vital for plant growth as these are precursors for almost all nitrogenous compounds. Ammonium can be assimilated onto nitrogenous organic compounds by the concerted action of two enzymes that compose the glutamine synthetase (GS, EC 6.3.1.2) – glutamate synthase (Fd-GOGAT, EC 1.4.7.1; NADH–GOGAT, EC 1.4.1.14) cycle. Ammonium may also be directly incorporated into glutamate by the glutamate dehydrogenase (GDH, EC 1.4.1.2) aminating reaction. However, as GDH reversibly deaminates glutamate, its physiological role in vivo remains controversial. Potato has been classified as moderately tolerant to salinity. Potato GS is encoded by a small multigene family which is differentially regulated in an organ and age-dependent way. In this study, the effect of increasing concentrations of salinity in the soil in GS activity and gene-specific mRNA accumulation levels were studied on potato leaves and roots, as well as the biochemical parameters protein, chlorophyll, lipid peroxidation and proline levels, in order to evaluate the severity of the imposed stress. The data obtained suggests that when potato plants are subjected to salt stress, increased ammonium assimilation occurs in roots, due to an increased GS accumulation, along with a decreased assimilation in leaves. Regarding GS gene-specific mRNA accumulation, an organ-dependent response was also observed that contributes for the detected alteration in the ammonium assimilatory metabolism. This response may be a key feature for future genetic manipulations in order to increase crop productivity in salty soils. The possible contribution of GDH for ammonia assimilation was also investigated.     

Metabolism, physiology and stress defense in three aging Ins/IGF-1 mutants of the nematode Caenorhabditis elegans

The insulin/insulin-like growth factor-1 (Ins/IGF-1) pathway regulates the aging rate of the nematode Caenorhabditis elegans. We describe other features of the three Ins/IGF-1 mutants daf-2, age-1 and aap-1. We show that the investigated Ins/IGF-1 mutants all have a reduced body volume, reduced reproductive capacity, increased ATP concentrations and an elevated stress resistance. We also observed that heat production is lower in these mutants, although the respiration rate was similar or higher compared with wild-type individuals, suggesting a metabolic shift in these mutants.     

DNA polymerase proofreading: active site switching catalyzed by the bacteriophage T4 DNA polymerase

DNA polymerases achieve high-fidelity DNA replication in part by checking the accuracy of each nucleotide that is incorporated and, if a mistake is made, the incorrect nucleotide is removed before further primer extension takes place. In order to proofread, the primer-end must be separated from the template strand and transferred from the polymerase to the exonuclease active center where the excision reaction takes place; then the trimmed primer-end is returned to the polymerase active center. Thus, proofreading requires polymerase-to-exonuclease and exonuclease-to-polymerase active site switching. We have used a fluorescence assay that uses differences in the fluorescence intensity of 2-aminopurine (2AP) to measure the rates of active site switching for the bacteriophage T4 DNA polymerase. There are three findings: (i) the rate of return of the trimmed primer-end from the exonuclease to the polymerase active center is rapid, >500 s⁻¹; (ii) T4 DNA polymerase can remove two incorrect nucleotides under single turnover conditions, which includes presumed exonuclease-to-polymerase and polymerase-to-exonuclease active site switching steps and (iii) proofreading reactions that initiate in the polymerase active center are not intrinsically processive.     

Comparative floral preferences in nectar and pollen foraging by Scaptotrigona postica (Latreille 1807) in two different biomes in São Paulo (Brazil)

To describe the trophic resources used by Scaptotrigona postica, honey and bee bread samples were taken monthly from May 2015 to December 2016 at two different localities. Fontes do Ipiranga State Park (PEFI), an urban remnant of the Atlantic Forest, and the Mogi Guaçu Biological Reserve (RBMG), in the Cerrado. Two colonies were kept in each site. Samples were analysed with the melissopalynological method in order to calculate the relative frequencies. Principal component analysis was used to compare the similarity between the samples and to examine the influence of quantitative and qualitative data on the ordination of the pollen types. Similarity tests were performed to compare the pollen spectra of the bee bread and honey samples between the study sites and seasons. Hence, 69 and 61 pollen types were identified in 33 honey and 29 bee bread samples. The main families in honey were Asteraceae, Euphorbiaceae and Fabaceae; in bee bread Fabaceae, Myrtaceae and Sapindaceae were the main families for both localities, followed by Asteraceae, Euphorbiaceae and Solanaceae at the RBMG. The results showed that the species maintains its floral preferences regardless of the biome in which it occurs. Also, demonstrates that the bees make use of nectariferous and polliniferous sources available in the preserved areas as well as in its surroundings. There is a risk of pesticides exposure caused by the use of trophic resources of cultivated plants by this bee. This points to the need for further studies.     

Comparison of Methods for Detection of Erysipelothrix spp. and Their Distribution in Some Australasian Seafoods

For many years, Erysipelothrix rhusiopathiae has been known to be the causative agent of the occupationally related infection erysipeloid. A survey of the distribution of Erysipelothrix spp. in 19 Australasian seafoods was conducted, and methodologies for the detection of Erysipelothrix spp. were evaluated. Twenty-one Erysipelothrix spp. were isolated from 52 seafood parts. Primary isolation of Erysipelothrix spp. was most efficiently achieved with brain heart infusion broth enrichment followed by subculture onto a selective brain heart infusion agar containing kanamycin, neomycin, and vancomycin after 48 h of incubation. Selective tryptic soy broth, with 48 h of incubation, was the best culture method for the detection of Erysipelothrix spp. with PCR. PCR detection was 50% more sensitive than culture. E. rhusiopathiae was isolated from a variety of different fish, cephalopods, and crustaceans, including a Western rock lobster (Panulirus cygnus). There was no significant correlation between the origin of the seafoods tested and the distribution of E. rhusiopathiae. An organism indistinguishable from Erysipelothrix tonsillarum was isolated for the first time from an Australian oyster and a silver bream. Overall, Erysipelothrix spp. were widely distributed in Australasian seafoods, illustrating the potential for erysipeloid-like infections in fishermen.