Changes in the concentration of mRNAs for the inhibin subunits in ovarian follicles after administration of gonadotropins to progestin treated ewes.

RNA was extracted from single or small groups of ovine ovarian follicles after treatment of ewes with FSH and/or LH. The content of mRNA for the alpha-inhibin and beta A-inhibin subunits was analyzed by hybridization with specific cDNA probes. All ewes were treated with progestin vaginal pessaries to suppress spontaneous preovulatory follicle maturation and ewes were given three intramuscular injections of gonadotropins at 8-hr intervals starting 24 hr prior to collection of ovaries. In experiment I, both Schering-FSH and NIDDK-oFSH-17 (oFSH) significantly increased alpha- and beta A-inhibin mRNA per ewe in 2-5 mm follicles and tended to increase alpha- and beta A-inhibin mRNA in large (greater than 5 mm) follicles. In experiment II, oFSH and NIDDK-oLH-25 (oLH) were administered in a 2X2 factorial arrangement. Separate administration of oFSH or oLH increased (P less than .05) the alpha-inhibin mRNA concentration in large follicles. alpha-inhibin mRNA concentration in 4-5 mm follicles was also increased by oFSH but was decreased by oLH. Concomitant treatment with oFSH and oLH did not change alpha-inhibin mRNA concentrations from those measured in oFSH treated ewes. In experiment II, beta A mRNA concentrations followed a pattern similar to that of alpha A mRNA, but the differences were not statistically significant. We conclude that, in the ewe, exogenous FSH increases the concentration of inhibin mRNA in the whole follicle. The ability of exogenous oLH to alter expression of the inhibin subunit genes may depend upon the stage of follicle maturation.     

Structural Characterisation of the Interaction between Triticum aestivum and the Dothideomycete Pathogen Stagonospora nodorum

The interaction between Stagonospora nodorum and a susceptible wheat cultivar was investigated using a range of microscopic techniques. Germination of pycnidiospores occurred approximately 3 h after making contact with the leaf surface and was followed by attempted penetration 8–12 h later. Penetration was observed through stomata and also directly through periclinal and anticlinal epidermal cell walls. Penetration down the anticlinal cell walls appeared to occur without a differentiated penetrating structure whilst structures identified as either lateral appressoria or hyphopodia were typically present when penetrating over a periclinal cell wall. Once inside the leaf, the fungus continued to grow for the next 4–5 days colonising all parts of the leaf except the vascular bundles. Only in the later phase of the infection was total host cell collapse apparent. Evidence of polyphenolic compounds was observed. The infection cycle was completed within 7 days as indicated by sporulation on the leaf surface. These results have allowed us to understand how the fungus physically interacts with the leaf and will help the overall understanding of the infection process.     

Integrated disease management of ascochyta blight in pulse crops

Ascochyta blight causes significant yield loss in pulse crops worldwide. Integrated disease management is essential to take advantage of cultivars with partial resistance to this disease. The most effective practices, established by decades of research, use a combination of disease-free seed, destruction or avoidance of inoculum sources, manipulation of sowing dates, seed and foliar fungicides, and cultivars with improved resistance. An understanding of the pathosystems and the inter-relationship between host, pathogen and the environment is essential to be able to make correct decisions for disease control without compromising the agronomic or economic ideal. For individual pathosystems, some components of the integrated management principles may need to be given greater consideration than others. For instance, destruction of infested residue may be incompatible with no or minimum tillage practices, or rotation intervals may need to be extended in environments that slow the speed of residue decomposition. For ascochyta-susceptible chickpeas the use of disease-free seed, or seed treatments, is crucial as seed-borne infection is highly effective as primary inoculum and epidemics develop rapidly from foci in favourable conditions. Implemented fungicide strategies differ according to cultivar resistance and the control efficacy of fungicides, and the effectiveness of genetic resistance varies according to seasonal conditions. Studies are being undertaken to develop advanced decision support tools to assist growers in making more informed decisions regarding fungicide and agronomic practices for disease control.     

Purification of fusaproliferin from cultures of Fusarium subglutinans by preparative high-performance liquid chromatography

Thirty-six Fusarium strains were grown on cracked yellow corn and evaluated for optimum fusaproliferin production, with Fusarium subglutinans E-1583 producing the highest levels (1600 microg/g). Three solvent systems were tested for extracting fusaproliferin from the cultures of F. subglutinans E-1583. Methanol gave the highest fusaproliferin recovery, followed by methanol/1% aqueous NaCl (55:45, v/v) and acetonitrile/methanol/H(2)O (16:3:1, v/v/v). Hexane partitioning was effective in removing many impurities from the crude fusaproliferin extracts prior to the liquid chromatography step. Fusaproliferin samples were further purified by high-performance liquid chromatography (HPLC) with a C18 preparatory column using a mobile phase of acetonitrile/H(2)O (80:20, v/v). The purity of the fusaproliferin was verified by analytical HPLC, GC/MS, (1)H NMR spectroscopy, and electrospray ionization (ESI) MS. The isolated fusaproliferin was shown to be free of impurities and can be used as a standard for routine analysis. Fusaproliferin was shown to be temperature-sensitive when samples were stored at room temperature (20-24 degrees C) for more than several days. After 30 days at 4 degrees C, approximately 8% of the fusaproliferin had been transformed to deacetyl-fusaproliferin; however, samples stored at -20 degrees C for 1 year contained only trace amounts of the deacetylated form.     

Survival rates for a declining population of bottlenose dolphins in Doubtful Sound,New Zealand: an information theoretic approach to assessing the role of human impacts

• 1. The bottlenose dolphins of Doubtful Sound, New Zealand are a declining population at the southern limit of the species' range, exposed to impacts from tourism and habitat modification. Patterns in apparent annual survival were analysed from photographic resightings of naturally marked adults (1990 to 2008) and calves within the first year of life (1994 to 2008) using capture‐recapture models.
• 2. The most parsimonious model for adults provided a time‐invariant, sex‐invariant estimate of survival (?_{a(1990–2008)}=0.9374; 95% CI: 0.9170–0.9530), marginally lower than prior estimates for wild bottlenose dolphins.
• 3. The most parsimonious model for calves indicated a significant time‐variant decline in survival from an estimate similar to other populations (?_{c(1994–2001)}=0.8621; 95% CI: 0.6851–0.9473) to a current estimate that is, to our knowledge, the lowest recorded for free‐ranging bottlenose dolphins (?_{c(2002–2008)}=0.3750; 95% CI: 0.2080–0.5782).
• 4. Information theoretic evidence ratios suggested that observed patterns in calf survival were 22 times more likely to be explained by a decline coincident with the opening of a second tailrace tunnel for a hydroelectric power station than by a decline in any other year or across multiple years.
• 5. Projections using an age‐structured stochastic population model indicated that the current level of calf survival was unsustainable (population decline: 100% of model runs; population extinction: 41.5% of model runs) and was a key factor in the observed population decline in Doubtful Sound.

Copyright © 2008 John Wiley & Sons, Ltd.     

Enabling natural resource managers to self-assess their adaptive capacity

We describe the development of a low cost, repeatable self-assessment process enabling community-based natural resource management (CBNRM) groups to set priorities for building their capacity to adopt sustainable farming practices and adapt to global change. Regional measures of adaptive capacity derived from rural livelihoods analysis were populated with secondary data and used to communicate the multiple dimensions of adaptive capacity to groups of landowners. This conceptual framework was then used to derive locally relevant measures of adaptive capacity via focus groups drawn from pre-existing networks of land managers. The key issue discussed at the workshop was what constrained or enabled private land managers to effectively manage natural resources. This self-assessment process was designed to support dialogue between CBNRM groups, industry and governments to prioritise collective action for building adaptive capacity. The approach was piloted with CBNRM groups across New South Wales, Australia.     

Identification of recombination hotspots and quantitative trait loci for recombination rate in layer chickens

Background: The frequency of recombination events varies across the genome and between individuals, which may be related to some genomic features. The objective of this study was to assess the frequency of recombination events and to identify QTL(quantitative trait loci) for recombination rate in two purebred layer chicken lines.Methods: A total of 1200 white-egg layers(WL) were genotyped with 580 K SNPs and 5108 brown-egg layers(BL)were genotyped with 42 K SNPs(single nucleotide polymorphisms). Recombination events were identified within half-sib families and both the number of recombination events and the recombination rate was calculated within each0.5 Mb window of the genome. The 10% of windows with the highest recombination rate on each chromosome were considered to be recombination hotspots. A BayesB model was used separately for each line to identify genomic regions associated with the genome-wide number of recombination event per meiosis. Regions that explained more than 0.8% of genetic variance of recombination rate were considered to harbor QTL.Results: Heritability of recombination rate was estimated at 0.17 in WL and 0.16 in BL. On average, 11.3 and 23.2 recombination events were detected per individual across the genome in 1301 and 9292 meioses in the WL and BL,respectively. The estimated recombination rates differed significantly between the lines, which could be due to differences in inbreeding levels, and haplotype structures. Dams had about 5% to 20% higher recombination rates per meiosis than sires in both lines. Recombination rate per 0.5 Mb window had a strong negative correlation with chromosome size and a strong positive correlation with GC content and with CpG island density across the genome in both lines. Different QTL for recombination rate were identified in the two lines. There were 190 and 199 non-overlapping recombination hotspots detected in WL and BL respectively, 28 of which were common to both lines.Conclusions: Differences in the recombination rates, hotspot locations, and QTL regions associated with genomewide recombination were observed between lines, indicating the breed-specific feature of detected recombination events and the control of recombination events is a complex polygenic trait.     

AMPK is a direct adenylate charge-regulated protein kinase

The adenosine monophosphate (AMP)-activated protein kinase (AMPK) regulates whole-body and cellular energy balance in response to energy demand and supply. AMPK is an αβγ heterotrimer activated by decreasing concentrations of adenosine triphosphate (ATP) and increasing AMP concentrations. AMPK activation depends on phosphorylation of the α catalytic subunit on threonine-172 (Thr(172)) by kinases LKB1 or CaMKKβ, and this is promoted by AMP binding to the γ subunit. AMP sustains activity by inhibiting dephosphorylation of α-Thr(172), whereas ATP promotes dephosphorylation. Adenosine diphosphate (ADP), like AMP, bound to γ sites 1 and 3 and stimulated α-Thr(172) phosphorylation. However, in contrast to AMP, ADP did not directly activate phosphorylated AMPK. In this way, both ADP/ATP and AMP/ATP ratios contribute to AMPK regulation.     

Long-term stability in core habitat of an endangered population of bottlenose dolphins (Tursiops truncatus): Implications for spatial management

1. A small population of approximately 68 bottlenose dolphins, Tursiops truncatus, resident in Doubtful Sound, New Zealand, is subject to physiologically challenging conditions, and is exposed to anthropogenic pressure from tourism.
2. A voluntary Code of Management incorporating dolphin protection zones (DPZs), in which tour boat access is limited, was established in 2008.
3. Kernel density estimation (KDE) was used to quantify dolphin habitat use over a 13-year period in order to describe seasonal variation in habitat use and consistency of habitat use over a decadal period, and to provide quantitative estimates of the extent of overlap between DPZs and core areas (50% volume contour) of habitat use.
4. Habitat use varied seasonally, with the inner fjord area used more frequently in warmer months, and with a shift in use to the outer fjord in colder months. Patterns in habitat use were highly consistent over the 13-year duration of the study.
5. The spatial overlap between the area of core dolphin habitat and DPZs was low (<18%) overall, and some DPZs were rarely used during colder periods.
6. Consistency in habitat use through time vindicates spatial management, but low overlap between core habitat and current DPZs suggests that an expansion of the DPZ areas would confer greater protection.