Seasonal diet changes in elephant and impala in mopane woodland

Elephant and impala as intermediate feeders, having a mixed diet of grass and browse, respond to seasonal fluctuations of forage quality by changing their diet composition. We tested the hypotheses that (1) the decrease in forage quality is accompanied by a change in diet from more monocots in the wet season to more dicots in the dry season and that that change is more pronounced and faster in impala than in elephant; (2) mopane (Colophospermum mopane), the most abundant dicot species, is the most important species in the elephant diet in mopane woodland, whereas impala feed relatively less on mopane due to the high condensed tannin concentration; and (3) impala on nutrient-rich soils have a diet consisting of more grass and change later to diet of more browse than impala on nutrient-poor soils. The phosphorus content and in vitro digestibility of monocots decreased and the NDF content increased significantly towards the end of the wet season, whereas in dicots no significant trend could be detected. We argue that this decreasing monocot quality caused elephant and impala to consume more dicots in the dry season. Elephant changed their diet gradually over a 16-week period from 70% to 25% monocots, whereas impala changed diets rapidly (2-4 weeks) from 95% to 70% monocots. For both elephants and impala, there was a positive correlation between percentage of monocots and dicots in the diet and the in vitro digestibility of these forage items. Mopane was the most important dicot species in the elephant diet and its contribution to the diet increased significantly in the dry season, whereas impala selected other dicot species. On nutrient-rich gabbroic soils, impala ate significantly more monocots than impala from nutrient-poor granitic soils, which was related to the higher in vitro digestibility of the monocots on gabbroic soil. Digestibility of food items appears to be an important determinant of diet change from the wet to the dry season in impala and elephants

Detection of genetic incompatibilities in non-model systems using simple genetic markers: hybrid breakdown in the haplodiploid spider mite Tetranychus evansi

When two related species interbreed, their hybrid offspring frequently suffer from reduced fitness. The genetics of hybrid incompatibility are described by the Bateson–Dobzhansky–Muller (BDM) model, where fitness is reduced by epistatic interactions between alleles of heterospecific origin. Unfortunately, most empirical evidence for the BDM model comes from a few well-studied model organisms, restricting our genetic understanding of hybrid incompatibilities to limited taxa. These systems are predominantly diploid and incompatibility is often complete, which complicates the detection of recessive allelic interactions and excludes the possibility to study viable or intermediate stages. Here, we advocate research into non-model organisms with haploid or haplodiploid reproductive systems and incomplete hybrid incompatibility because (1) dominance is absent in haploids and (2) incomplete incompatibility allows comparing affected with unaffected individuals. We describe a novel two-locus statistic specifying the frequency of individuals for which two alleles co-occur. This approach to studying BDM incompatibilities requires genotypic characterization of hybrid individuals, but not genetic mapping or genome sequencing. To illustrate our approach, we investigated genetic causes for hybrid incompatibility between differentiated lineages of the haplodiploid spider mite Tetranychus evansi, and show that strong, but incomplete, hybrid breakdown occurs. In addition, by comparing the genotypes of viable hybrid males and inviable hybrid male eggs for eight microsatellite loci, we show that nuclear and cytonuclear BDM interactions constitute the basis of hybrid incompatibility in this species. Our approach opens up possibilities to study BDM interactions in non-model taxa, and may give further insight into the genetic mechanisms behind hybrid incompatibility

A sensitive non-radioactive in situ hybridization method for the detection of chicken IgG γ-chain mRNA: a technique suitable for detecting of variety of mRNAs in tissue sections

We established a sensitive non-radioactive in situ hybridization (ISH) method for the detection of chicken IgG γ-chain mRNA in paraffin sections. RNA probes were transcribed in vitro from cloned chicken IgG CH1 nucleotide sequences with SP6/T7 RNA polymerases in the presence of DIG-UTP. These probes were used for hybridization and were immunodetected using anti-DIG antibodies conjugated to horseradish peroxidase. The immunoreactive products were visualized with DAB-H(2)O(2). IgG γ-chain mRNA-expressing cells were localized in both the spleen and oviductal tissues. This method demonstrated an excellent sensitivity since the ISH signal was clear and the background was negligible. We found that in the spleen IgG γ-chain mRNA-expressing cells were present mainly in the red pulp, whereas in the oviduct they appeared mainly in the mucosal stroma and not in the mucosal epithelium

Enforcing Security and Safety with Proof-Carrying Code

AbstractIn an environment where more and more code cannot be trusted to behave safety it is becoming necessary to employ mechanisms for detecting and preventing unsafe program behavior. This paper first reviews various such mechanisms and then focuses on static mechanisms with an emphasis on Proof-Carrying Code and its expressiveness.Proof-Carrying Code is a technique that allows a code receiver to verify statically that the code has certain required properties, which are stated in the form of a safety policy. To make this possible the code is accompanied by a representation of an easily checkable formal proof of compliance with the safety policy. This paper discusses first the general properties of the Proof-Carrying Code technique and then explores a particular implementation of the idea using verification condition generators. As a surprising result we prove that by adopting such an implementation choice we limit ourselves to safety properties, which constitute but a subset (albeit a very important one) of all the interesting program properties. We further speculate on what it takes to extend Proof-Carrying Code to handle more that safety properties

How to label bruxism that is a sign of a disorder? That's the question! Response to letter by Meira e Cruz & Ettlin (2018)

Non peer reviewe

Nonalcoholic fatty liver disease, liver fibrosis, and structural brain imaging: The Cross-Cohort Collaboration

Background and purpose Prior studies reported conflicting findings regarding the association of nonalcoholic fatty liver disease (NAFLD) and liver fibrosis with measures of brain health. We examined whether NAFLD and liver fibrosis are associated with structural brain imaging measures in middle- and old-age adults. Methods In this cross-sectional study among dementia- and stroke-free individuals, data were pooled from the Offspring and Third Generation cohorts of the Framingham Heart Study (FHS), the Rotterdam Study (RS), and the Study of Health in Pomerania. NAFLD was assessed through abdominal imaging. Transient hepatic elastography (FibroScan) was used to assess liver fibrosis in FHS and RS. Linear regression models were used to explore the relation of NAFLD and liver fibrosis with brain volumes, including total brain, gray matter, hippocampus, and white matter hyperintensities, adjusting for potential confounders. Results were combined using fixed effects meta-analysis. Results In total, 5660 and 3022 individuals were included for NAFLD and liver fibrosis analyses, respectively. NAFLD was associated with smaller volumes of total brain (β = −3.5, 95% confidence interval [CI] = −5.4 to −1.7), total gray matter (β = −1.9, 95% CI = −3.4 to −0.3), and total cortical gray matter (β = −1.9, 95% CI = −3.7 to −0.01). In addition, liver fibrosis (defined as liver stiffness measure ≥8.2 kPa) was related to smaller total brain volumes (β = −7.3, 95% CI = −11.1 to −3.5). Heterogeneity between studies was low. Conclusions NAFLD and liver fibrosis may be directly related to brain aging. Larger and prospective studies are warranted to validate these findings and identify liver-related preventive strategies for neurodegeneration

A quantitative microbial risk assessment model for Listeria monocytogenes in RTE sandwiches

A Quantitative Microbial Risk Assessment (QMRA) was performed to estimate the expected number of listeriosis cases due to the consumption, on the last day of shelf life, of 20 000 servings of multi-ingredient sandwiches produced by a medium scale food producer in Italy, by different population strata, defined by infection susceptibility (healthy, susceptible, transplant recipients and total population). First, all the sandwich ingredients were analysed for pH, Aw, salt and organic acids content and submitted to challenge tests at three different temperatures (4, 6 and 10 \ub0C) to evaluate their suitability for L. monocytogenes growth. Next, a stochastic model was constructed simulating the contamination of the ingredients that were the best (bean cream) and worst (cheese cream) growth substrates. For each substrate, an exposure assessment was performed, estimating the number of L. monocytogenes within each serving. Then, two dose-response models were alternatively applied: the first used a fixed r value for each of the three population groups, while the second considered a variable r value (lognormal distribution), taking into account the variability in strain virulence and different host subpopulations susceptibility. The stochastic model predicted zero cases for total population for both the substrates by using the fixed r approach, while 3 cases were expected when a higher variability (in virulence and susceptibility) was considered in the model; the number of cases increased to 45\u201352 in the worst scenario (bean cream contamination) assuming all servings would be consumed by transplant recipients. An uncertainty analysis was performed by considering alternative scenarios: a higher mean bacterial concentration (+ 0.5 Log CFU/g) or higher standard deviation (+ 0.5) determined evident increases in the expected number of cases, almost doubling the risk. A similar effect was also exerted by an extended storage time (from 72 to 96 h), in particular in the worst case scenario. Finally, different protective interventions were evaluated (70/30 N2/CO2packaging, home cooking or their combination). Both the interventions resulted in a strong decrease of the risk; MAP packaging, should be regarded as the most promising one, as it can be performed by the producer, who can assure a strict control of the treatment performances