Farm-SAFE: the process of developing a plot- and farm-scale model of arable,forestry, and silvoarable economics

Financial feasibility and financial return are two key issues that farmers and land owners consider when deciding between alternative land uses such as arable farming, forestry and agroforestry. Moreover regional variations in yields, prices and government grants mean that the relative revenue and cost of such systems can vary substantially within Europe. To aid our understanding of these variations, the European Commission sponsored a research project called “Silvoarable Agroforestry For Europe” (SAFE). This paper describes the process of developing a new economic model within that project. The initial stages included establishing criteria for the model with end-users and reviewing the literature and existing models. This indicated that the economic model needed to allow comparison of arable farming, forestry and agroforestry systems at a plot- and a farm-scale. The form of comparisons included net margins, net present values, infinite net present values, equivalent annual values, and labour requirements. It was decided that the model would operate in a spreadsheet format, and the effect of phased planting patterns would be included at a farm-scale. Following initial development, additional user feedback led to a final choice on a model name, a final method of collating input data, and the inclusion of field-based operations such as varying the cropped area, replacing dead trees, and pruning. In addition options in terms of improved graphical outputs and the ability to undertake sensitivity analysis were developed. Some of the key lessons learnt include the need to establish clear model criteria and the benefits of developing a working prototype at an early stage to gain user-feedback.     

Lecithin aerosols generated ultrasonically above 25 degrees C

Dl-Dipalmitoyl-alpha-lecithin, suspended in 0.15-molar sodium chloride solution by sonic cavitation at 20 kilohertz, can be aerosolized by an 800-kilohertz ultrasonic generator only at temperatures above 25 degrees C. The aerosol thus produced is exceptionally stable against evaporation even at particle radii of 0.1 to 0.6 micron; this suggests applicability to the therapy of pulmonary disorders.     

Initiation and synergistic fibrillization of tau and alpha-synuclein

Alpha-synuclein (alpha-syn) and tau polymerize into amyloid fibrils and form intraneuronal filamentous inclusions characteristic of neurodegenerative diseases. We demonstrate that alpha-syn induces fibrillization of tau and that coincubation of tau and alpha-syn synergistically promotes fibrillization of both proteins. The in vivo relevance of these findings is grounded in the co-occurrence of alpha-syn and tau filamentous amyloid inclusions in humans, in single transgenic mice that express A53T human alpha-syn in neurons, and in oligodendrocytes of bigenic mice that express wild-type human alpha-syn plus P301L mutant tau. This suggests that interactions between alpha-syn and tau can promote their fibrillization and drive the formation of pathological inclusions in human neurodegenerative diseases.     

Sawfish,read in tooth and saw: Rostral teeth as endogenous chemical records of movement and life-history in a critically endangered species

1. The ecology of endangered and rare species can be difficult to study owing to their low abundances and legal limits on scientist’s ability to catch, sample, and track them. This is particularly true of sawfish (family Pristidae), whose numbers have declined precipitously, placing all five species on the IUCN Red List of Threatened Species worldwide. Best known for their distinctive, toothed rostrum, the ecology, movement and life-history of sawfish are poorly understood.
2. Sawfish rostral teeth are modified placoid scales, which grow continuously throughout the life of the fish. This continuous growth, combined with their stable calcified makeup, makes sawfish rostral teeth a potential source of temporal records of chemical and isotopic changes through the life of the fish.
3. Rostral teeth are often preserved in museums and as curios, potentially providing a source of life-history data to inform conservation actions without the need for field study, or as an important compliment to it. This is the first study to recover temporally explicit chemical data from sawfish rostral teeth.
4. Using archived samples of largetooth sawfish (Pristis pristis) we show that multiple chemical tracers can be recovered from sawfish rostral teeth, and that these tracers can be used to understand movement across salinity gradients. We further show that sawfish rostral teeth contain repeated structures and indistinct banding which could potentially be used for ageing or growth analysis of fish.

     

Distribution of K and L cells in the feline intestinal tract

Glucose-dependent insulinotropic peptide (GIP), glucagon-like peptide (GLP)-1 and GLP-2 are hormones secreted from specialized K cells (GIP) and L cells (GLP-1, GLP-2) in the intestinal mucosa. These hormones play major roles in health and disease by modulating insulin secretion, satiety, and multiple intestinal functions. The aim of this study was to describe the distribution of K cells and L cells in the intestines of healthy cats. Samples of duodenum, mid-jejunum, ileum, cecum, and colon were collected from 5 cats that were euthanized for reasons unrelated to this study and had no gross or histologic evidence of gastrointestinal disease. Samples stained with rabbit-anti-porcine GIP, mouse-anti-(all mammals) GLP-1, or rabbit-anti-(all mammals) GLP-2 antibodies were used to determine the number of cells in 15 randomly selected 400× microscopic fields. In contrast to other mammals (eg, dogs) in which K cells are not present in the ileum and aborally, GIP-expressing cells are abundant throughout the intestines in cats (>6/high-power field in the ileum). Cells expressing GLP-1 or GLP-2 were most abundant in the ileum (>9/high-power field) as in other mammals, but, although GLP-1–expressing cells were abundant throughout the intestines, GLP-2–expressing cells were rarely found in the duodenum. In conclusion, the distribution of GIP-secreting K cells in cats is different from the distribution of K cells that is described in other mammals. The difference in distribution of GLP-2– and GLP-1–expressing cells suggests that more than 1 distinct population of L cells is present in cats.     

Influence of a bovine respiratory disease vaccine with a temperature‐sensitive modified live or killed infectious bovine rhinotracheitis component on oestrous cycle parameters and anti‐Müllerian hormone concentration in nulliparous heifers

The objective of this study was to examine the impact of a bovine respiratory disease complex (BRDC) vaccine with a temperature‐sensitive modified live vaccine (MLV) infectious bovine rhinotracheitis (IBR) component on oestrous cycle parameters and the follicular pool. Twenty‐four Holstein heifers (12.4 ± 0.5 months) previously calfhood vaccinated with an IBR MLV component were enrolled in two replicates (Spring; n = 10 and Fall; n = 14) and were blocked by pre‐vaccination bovine viral diarrhoea (BVD) serum neutralizing (SN) titres. Upon enrolment, heifers were oestrous synchronized with sampling beginning at detected oestrus. At their second heat, heifers were vaccinated with a BRDC calfhood vaccine with a MLV (MLV; n = 12) or killed (K; n = 12) IBR component and sampled for two additional cycles. Serum samples for oestrogen (E2) and progesterone (P4) as well as ultrasound data of ovarian structures were collected every other day. Serum samples for anti‐Müllerian hormone (AMH) were collected at oestrus and mid‐cycle for each cycle, and serum for titres was collected prior to and following vaccination. Data were analysed with the PROC MIXED and GLM procedures of SAS. There was no difference in pre‐ or post‐vaccination titres between MLV and K heifers (p > .5). Vaccination had no impact on P4 concentrations, P4 area under the curve, luteal tissue area, peak E2 production or oestrous cycle length (p > .05). Cycle number did impact AMH concentration (p < .05). In MLV heifers, AMH concentration was highest in cycle 1 (p < .05) while cycles 2 and 3 did not differ (p > .05). This was also true for the K heifers in the Fall replicate (p < .05). Within cycle 2, AMH concentrations were numerically lower between vaccine types (K = 308.22 ± 33.3 pg/ml, MLV = 181.13 ± 32.9 pg/ml; p > .05). Although no differences were seen in overall cycle parameters, differences in AMH concentrations may indicate a reduction of the follicular pool following vaccination and requires further investigation.