Allelic losses and gains during translocations of a high conservation value fish,Coregonus lavaretus

1. The use of translocations to establish new or ‘refuge’ populations for species with high conservation value is controversial but widely used in conservation management. One of the risks of this approach is that an establishing population does not adequately capture the genetic diversity of the donor gene pool. This effect, rarely examined, is tested here.
2. In this study the genetic consequences of two conservation translocations after five generations (16 years) of the European whitefish, Coregonus lavaretus, were quantified. Both translocations were made using almost the same genetic groups and thus represent a partly replicated natural study.
3. Analysis of 12 informative microsatellites showed that expected heterozygosity, the mean number of alleles per locus and allelic richness did not differ between donor and translocated populations. There was also no loss of heterozygosity in the translocated populations, nor deviations from Hardy–Weinberg equilibrium expectations, nor signs of linkage disequilibrium.
4. All populations were genetically differentiated but pairwise F_ST values were low, indicating that the magnitude of divergence was small.
5. There was no evidence of inbreeding but there were significant differences in private allelic richness between donor and translocated populations. Of 50 alleles found in the donor population, 16% of the rarer alleles were lost in one translocated population and 8% in the other.
6. Allele loss without a reduction in heterozygosity strongly points to stochastic drift effects having occurred following translocation. The evidence indicates that alleles that were not detected in the donor population have arisen de novo in the translocated populations.
7. It is concluded that conservation translocations comprising even a modest number of propagules can successfully capture a high proportion of genetic variation of the host population, and that reduced genetic variation in the translocated population may be mitigated by the emergence of new variation over short time periods.

     

Opportunity costs: Who really pays for conservation?

Designing conservation areas entails costs that, if considered explicitly, can be minimized while still achieving conservation targets. Here we focus on opportunity costs which measure forgone benefits from alternative land uses. Conservation planning studies often use partial estimates of costs, but the extent to which these result in actual efficiencies has not been demonstrated. Our study partitions land costs into three distinct opportunity costs to smallholder agriculture, soybean agriculture and ranching. We demonstrate that opportunity costs to single stakeholder groups can be inaccurate measures of true opportunity costs and can inadvertently shift conservation costs to affect groups of stakeholders disproportionately. Additionally, we examine how spatial correlations between costs as well as target size affect the performance of opportunity costs to single stakeholder groups as surrogate measures of true opportunity costs. We conclude that planning with opportunity costs to single stakeholder groups can result in cost burdens to other groups that could undermine the long-term success of conservation. Thus, an understanding of the spatial distributions of opportunity costs that are disaggregated to groups of stakeholders is necessary to make informed decisions about priority conservation areas.     

Toll-like receptor triggering of a vitamin D-mediated human antimicrobial response

In innate immune responses, activation of Toll-like receptors (TLRs) triggers direct antimicrobial activity against intracellular bacteria, which in murine, but not human, monocytes and macrophages is mediated principally by nitric oxide. We report here that TLR activation of human macrophages up-regulated expression of the vitamin D receptor and the vitamin D-1-hydroxylase genes, leading to induction of the antimicrobial peptide cathelicidin and killing of intracellular Mycobacterium tuberculosis. We also observed that sera from African-American individuals, known to have increased susceptibility to tuberculosis, had low 25-hydroxyvitamin D and were inefficient in supporting cathelicidin messenger RNA induction. These data support a link between TLRs and vitamin D-mediated innate immunity and suggest that differences in ability of human populations to produce vitamin D may contribute to susceptibility to microbial infection.     

Evaluation of L-selectin expression and assessment of protein tyrosine phosphorylation in bovine polymorphonuclear neutrophil leukocytes around parturition

Impaired polymorphonuclear neutrophil leukocyte (PMN) function around parturition has been associated with increased clinical mastitis in dairy cows. Rolling and attachment of PMN to the endothelium is the first step in the recruitment process and is accomplished by interaction between L-selectin on PMN and its ligand on endothelial cells. Furthermore, tyrosine phosphorylation is involved in the initiation of many PMN functions. The objective of this work was to determine changes in expression of L-selectin and tyrosine phosphorylation in the perinatal period. Eight clinically healthy Holstein cows were used as PMN donors at d-21, -14, -7,0 (calving), +1, +2, +7, +14, +28. Evaluation of L-selectin expression was carried out on activated and resting PMN. Anti-bovine L-selectin monoclonal antibody (MAB) and flow cytometric analysis were used to measure the percentage of PMN fluorescing and receptor expression (log mean fluorescent channel, LMFC). Activated and resting PMN showed similar trends in % PMN fluorescence and LM FC. The percentage of PMN fluorescing tended to decrease at parturition, followed by a significant increase at d +14 and +28 (P < 0.02). For LMFC a decrease was observed on d +1 followed by an increase through d +28 (P < 0.01). Protein tyrosine phosphorylation of lysates prepared from PMN isolated throughout the study was detected by electrophoresis and western blotting using anti-phosphotyrosine MAB. Several protein bands were tyrosine phosphorylated. Two of these bands (42-44 kDa and 90 kDa) varied in intensity over time. The intensity of the 42-44 kDa band gradually increased from d -7, peaked at d +7 (P < 0.03), and steadily decreased to d +28 (P < 0.02). Antibody to activated mitogen protein kinase reacted with the 42-44 kDa band. Reduced PMN function during the periparturient period could be related to reduced L-selectin adhesion molecules on the cell surface, and to modulation in the phosphorylation of functionally important molecules.     

Postharvest changes in pigment concentrations in ‘Fuji’ apples with ‘Fuji’ stain

’Fuji’ apples (Malus domestica Borkh cv. ‘Fuji’) sometimes develop a discolouration in the peel during cold storage, typically in the periphery of sunburned peel. We refer to this particular postharvest disorder as ‘Fuji’ stain as we have not observed it in any cultivar other than ‘Fuji’ and the discolouration looks like a stain on the peel. Because peel discolouration occurs, peel pigments are thought to be involved. Hence the concentrations of anthocyanins, epicatechin, quercetin glycosides, chlorogenic acid, chlorophylls, and carotenoids in peel disks taken from areas exhibiting ‘Fuji’ stain were compared to concentrations observed in peel disks not exhibiting ‘Fuji’ stain. In 2005, peel from sunburned apples exhibiting ‘Fuji’ stain was compared to peel from three areas of sunburned apples not exhibiting stain [i.e. sunburned peel, the area around the sunburned peel (halo), and the area around the halo (OH)]. Additionally, stained peel was compared to the sun-exposed side of non-stained non-sunburned apples (NSNB). The second year, 2006, we compared stained peel to NSNB peel and the area outside the stained area (OS) on those fruit with stain. The concentrations of idaein, epicatechin, and quercetin glycosides were consistently low in the stained peel both years. This is in contrast to our earlier studies in which sunburned ‘Fuji’ apples had high concentrations of quercetin glycosides and epicatechin and low concentrations of idaein, and non-sunburned apples had low concentrations of quercetin glycosides and epicatechin and high concentrations of idaein. The consistent and unique characteristic of stained peel reported here indicates an association of these compounds with the incidence of stain. In 2005, chlorogenic acid concentrations in the stain peel were lower than other peel types, but in 2006 they were higher. Differences in chlorophyll and carotenoid concentrations were observed among many of the peel types. However, there is not a clear association between stain development and changes in chlorophyll and carotenoid concentrations due to significant differences not being observed in both years. While our research provides insight into pigment changes associated with ‘Fuji’ stain formation, more work is needed to help clarify the inconsistencies observed between the 2 years.     

Degradation Studies of the Non-lethal Bird Repellent,Methyl Anthranilate

Methyl anthranilate (MA), a food grade flavor and fragrance additive, has been reported to be an effective non-lethal bird repellent in a variety of situations. Despite the experimental success of MA, field studies have yielded widely differing levels of efficacy. Diminished efficacy in some field trials probably results from the failure of specific formulations to retain or protect the active ingredient under natural conditions. Therefore, a clearer understanding of the physical and chemical factors affecting the stability of MA is needed. We undertook a series of laboratory studies on hydrolysis, photolysis and microbial degradation of MA, the results of which could be useful in the development of appropriate formulation strategies and residue analyses. We found the n-octanol:water partition coefficient, (P) to be 84. MA is not subject to hydrolysis at 25°C in phosphate buffer media at pH 5·0, 7·0 and 9·0. MA slowly photodegrades under simulated UV ‘sunlight’. Forty-four percent of MA is lost after 432 h illuminance at 1·25 mW cm⁻², which is equivalent to approximately 1200 h natural sunlight (40°N, noontime, June). Kinetic data indicate that the initial step of photolysis, subsequent to excitation, is a second-order reaction with respect to MA. A major photodegradation product appeared in an amount of about 10% of the mass balance and was determined to be an oxidized trimer of MA. MA is primarily affected by aerobic microbial degradation. For a 12:12 h light:dark, under laboratory illumination, 12% of water-solubilized material can be lost in the first seven days. Losses were 30% and 42% at 16 and 27 days, respectively. Under conditions of optimal bacterial growth (warmth and darkness) loss of MA was 22% at nine days and 100% by 20 days. The susceptibility of MA to microbial degradation is promising for the prospects of developing formulated, environmentally safe, bird repellents.     

European stone fruit yellows phytoplasmas associated with a decline disease of apricot in southern England

Phytoplasmas detected by fluorescence microscopy and polymerase chain reaction (PCR) have been discovered infecting Prunus trees at a site in south-east England. The pathogens were detected in tissue samples taken in autumn and also in spring. The symptoms in infected trees varied from severe decline to absence. PCR experiments using group-specific primers to amplify regions of the 16S RNA gene indicated that the phytoplasmas are similar to European stone fruit yellows isolates occurring in southern and eastern Europe. This is the first record of phytoplasmas in Prunus species in the UK. The origin of the infection is unknown. The implications of this new disease for the fruit industry are discussed.     

Microtechnique for quantitative platelet isolation from blood enabling electronic counting and sizing of animal and human platelets

A technique for rapidly separating platelets from small quantities of whole blood is described. The isolation method allowed for counting and sizing platelets by electronic means, and counts with this new method were closely correlated with those obtained by phase microscopy. Platelet sizing was possible because of the inert and isotonic nature of the density-gradient medium used in the procedure. The technique was applicable to samples of blood from persons, horses, cattle, sheep, goats, pigs, dogs, mice, rats, guinea pigs, and rabbits. The isolation of platelets from whole blood of various species of animals was necessary for electronic counting because of the great variation in sizes of platelets and erythrocytes and the variable sedimentation properties of animal blood.