Effects of charcoal production on maize yield,chemical properties and texture of soil

The effects of charcoal production on soil textural and chemical properties were investigated in Ejura, Ghana. The aim was to study the effects of heating and charcoal residue on maize yield, soil texture and soil chemical properties. Composite samples were taken from the 0–10 cm layer of soil at charcoal-making sites and from adjacent fields (control). Twelve sites were randomly selected for the study across the range of the Kotokosu watershed. Maize was planted in four selected locations on charcoal site soils (CSS) and adjacent field soils (AFS) to assess the impact of charcoal production on crop yield. There was a significant increase in soil pH, base saturation, electrical conductivity, exchangeable Ca, Mg, K, Na and available P in the soil at the kiln sites as compared to the adjacent soils. A relative change of up to 329% was observed in K while organic C and total N decreased by 9.8% and 12.8%, respectively. Organic C and total N were highly correlated ( P <0.01) and both parameters significantly ( P <0.05) depended on clay minerals in the soils. Soil texture was also modified with a significantly higher sand content and lower clay fraction in the CSS. The grain and biomass yield of maize increased by 91% and 44%, respectively, on CSS as compared to AFS. Further research to ascertain the long-term effects of charcoal production on the soil environment and the fertility of tropical soils is needed.     

Above- and belowground ecosystem biomass and carbon pools in an age-sequence of temperate pine plantation forests

We assessed the successional development of above- and belowground ecosystem biomass and carbon (C) pools in an age-sequence of four White pine (Pinus strobus L.) plantation stands (2-, 15-, 30-, and 65-years-old) in Southern Ontario, Canada. Biomass and C stocks of above- and belowground live and dead tree biomass, understorey and forest ground vegetation, forest floor C (LFH-layer), and woody debris were determined from plot-level inventories and destructive tree sampling. Small root biomass (<5 mm) and mineral soil C stocks were estimated from soil cores. Aboveground tree biomass became the major ecosystem C pool with increasing age, reaching 0.5, 66, 92, and 176 t ha⁻¹ in the 2-, 15-, 30-, and 65-year-old stands, respectively. Tree root biomass increased from 0.1 to 10, 18, 38 t ha⁻¹ in the 2-, 15-, 30-, and 65-year-old stands, respectively, contributing considerably to the total ecosystem C in the three older stands. Forest floor C was 0.8, 7.5, 5.4, and 12.1 t C ha⁻¹ in the 2-, 15-, 30-, and 65-year-old stands, respectively, indicating an increase during the first two decades, but no further age-effect during the later growth phase. Mineral soil C was age-independent with 37.2, 33.9, 39.1, and 36.7 t C ha⁻¹ in the 2-, 15-, 30-, and 65-year-old stands, respectively. Aboveground ecosystem C increased with age from 3 to 40, 52, and 100 t C ha⁻¹ in the 2-, 15-, 30-, and 65-year-old stands, respectively, due to an increase in aboveground tree biomass. Belowground ecosystem C remained similiar in the early decades after establishment with 37, 39, and 39 t C ha⁻¹ in the 2-, 15-, and 30-year-old stands, but increased to 56 t C ha⁻¹ in the 65-year-old stand due to an increase in root biomass. The difference in total ecosystem C between the 2- and 65-year-old stand was 116 t C ha⁻¹. Our results highlight the importance of considering the successional development of forest ecosystem C pools, when estimating C sink potentials over their complete life cycle.     

Short internode,double podding and early flowering effects on maturity and other agronomic characters in chickpea

Chickpea is an indeterminate species, which continues to flower and set new pods over a long period under wet and cool growing conditions, resulting in excessive canopy development and delayed maturity. We hypothesized that the chickpea's long season requirement could be reduced through introgression of short internode, double podding and early flowering. Four populations E100Ym/CDC Anna, 272-2/CDC Anna, 298T-9/CDC Anna, and 298T-9/CDC Frontier were developed to test this hypothesis with the first parents of each cross being the donor of the short internode, double podding and early flowering traits, respectively. Also, the donor parents E100Ym, 272-2 and 298T-9 were intercrossed. Segregating populations of F₂ to F_3:6 generations were then evaluated under greenhouse and field conditions. When expressed well, double podding significantly reduced time to maturity as compared to the single podding counterparts. The best double podding lines were about 1 week earlier maturing than the early parent and standard checks. Days to flowering (DF) was positively associated with days to maturity (DM) (r = 0.44, P < 0.001), and partial path analysis revealed that DF contributed to DM mainly via days to first pod maturity (DFPM). In the two early flowering populations 298T-9/CDC Anna and 298T-9/CDC Frontier, DF determined about 32% of the variation in DFPM. Conversely, the short internode trait had an undesirable effect, in that all the short internode segregants were too late to mature. In conclusion, the alleles for double podding and early flowering may be used to improve early maturity in chickpea and subsequently minimize the risks associated with the production of this crop in environments where the growing conditions allow excessive crop canopy development, as in the Canadian prairies.     

Defining output-based standards to achieve and maintain tuberculosis freedom in farmed deer, with reference to member states of the European Union

Within the European Union (EU), detailed legislation has been developed for cattle, but not deer, to minimise disease risks associated with trade in animals and animal products. This legislation is expressed as input-based standards, providing a detailed outline of the activity required (for example, testing of animals and application of defined control measures), on the expectation that an adequate output (for example, confidence in freedom) will be achieved. Input-based standards are at odds with the increasing shift towards output-based standards, particularly in OIE rules governing international trade. In this paper, we define output-based standards to achieve and maintain freedom from tuberculosis (TB) in farmed deer, with reference to EU member states. After considering the probability of freedom achieved for cattle under existing EU legislation, we defined a ‘free farmed deer holding’ as one with a probability of freedom from infection of at least 99%. We then developed an epidemiological model of TB surveillance systems for deer holdings, incorporating different surveillance strategies, including combinations of diagnostic tests, and a variety of different scenarios relating to the potential for introduction of infection. A range of surveillance strategies were identified to achieve and maintain a free farmed deer holding, and worked examples are presented. The surveillance system sensitivity for varying combinations of screening and confirmatory tests in live animals, animals at slaughter and on-farm deaths is also presented. Using a single test at a single point in time, none of the TB tests routinely used in farmed deer is able to achieve an acceptable probability of TB freedom. If repeat testing were undertaken, an acceptable probability of TB freedom could be achieved, with differing combinations of the surveillance system sensitivity, frequency of testing and risk of introduction. The probability of introduction of infection through the importation of infected deer was influenced by the use of a pre-movement test (assumed 90% test sensitivity and negative test results), the TB prevalence in the source herd and the number of animals imported. A surveillance system sensitivity of at least 81% was achieved with different combinations of annual live animal surveillance and surveillance of animals at slaughter or on-farm deaths. This methodology has broad applicability and could also be extended to other diseases in both deer and other species with relevance to trade in animals and animal products.     

Anti-Leishmania IgA in urine samples from dogs with clinical leishmaniasis

Recently, anti-Leishmania IgG has been detected in urine samples from Leishmania-infected dogs and its concentrations have been correlated with impairment of renal function. The presence and relationship with other anti-Leishmania Ig isotypes in urine have not yet been investigated. The current study analyzed the concentrations of anti-Leishmania IgA and IgG in sera (Ig-S) and urine (Ig-U) samples by ELISA in 64 untreated dogs with clinical leishmaniasis. All 64 serum samples tested were positive for anti-Leishmania IgG. Fifty of them (78.1%) were also positive for anti-Leishmania IgA. The results showed the presence of anti-Leishmania IgA-U in 38% of the 50 dogs that were positive for specific IgA-S. Thirty-eight of the 64 dogs positive for Leishmania-specific IgG-S (59.4%) were also positive for Leishmania-specific IgG in urine (IgG-U). The concentrations of anti-Leishmania IgA-U were significantly correlated with urine protein/creatinine (uP/C) ratio (ρ = 0.542; P < 0.001) and with serum biochemical parameters, such as γ-globulins, urea and creatinine. Goldmann–Witmer coefficient (C value) indicated that detection of specific IgA in urine samples from dogs with leishmaniasis might not only be due to impairment of filtration of the glomerular barrier but also be due to local production of this isotype, which might reflect a local immunological response to the presence of the parasite in the genitourinary tract. Anti-Leishmania IgG-U concentrations were highly correlated with uP/C ratio (ρ = 0.779; P < 0.001) and C value did not support in any case local production of this isotype. IgG isotype might be a more suitable and specific tool to evaluate renal damage due to the lower IgA-U sensitivity and correlation coefficients and evidence of IgA local production. However, dogs found positive for both Ig isotypes in urine presented significantly higher specific IgG-U concentrations and higher uP/C ratios than dogs found positive only for IgG-U, thus suggesting that the first group suffered more severe renal damage. This fact makes it necessary to evaluate the prognosis of dogs showing both anti-Leishmania IgA-U and IgG-U in future studies.     

Feline leukaemia. ABCD guidelines on prevention and management

OverviewFeline leukaemia virus (FeLV) is a retrovirus that may induce depression of the immune system, anaemia and/or lymphoma. Over the past 25 years, the prevalence of FeLV infection has decreased considerably, thanks both to reliable tests for the identification of viraemic carriers and to effective vaccines.InfectionTransmission between cats occurs mainly through friendly contacts, but also through biting. In large groups of non-vaccinated cats, around 30–40% will develop persistent viraemia, 30–40% show transient viraemia and 20–30% seroconvert. Young kittens are especially susceptible to FeLV infection.Disease signsThe most common signs of persistent FeLV viraemia are immune suppression, anaemia and lymphoma. Less common signs are immune-mediated disease, chronic enteritis, reproductive disorders and peripheral neuropathies. Most persistently viraemic cats die within 2–3 years.DiagnosisIn low-prevalence areas there may be a risk of false-positive results; a doubtful positive test result in a healthy cat should therefore be confirmed, preferably by PCR for provirus. Asymptomatic FeLV-positive cats should be retested.Disease managementSupportive therapy and good nursing care are required. Secondary infections should be treated promptly. Cats infected with FeLV should remain indoors. Vaccination against common pathogens should be maintained. Inactivated vaccines are recommended. The virus does not survive for long outside the host.Vaccination recommendationsAll cats with an uncertain FeLV status should be tested prior to vaccination. All healthy cats at potential risk of exposure should be vaccinated against FeLV. Kittens should be vaccinated at 8–9 weeks of age, with a second vaccination at 12 weeks, followed by a booster 1 year later. The ABCD suggests that, in cats older than 3–4 years of age, a booster every 2–3 years suffices, in view of the significantly lower susceptibility of older cats.     

Feline rabies. ABCD guidelines on prevention and management

OverviewRabies virus belongs to the genus Lyssavirus, together with European bat lyssaviruses 1 and 2. In clinical practice, rabies virus is easily inactivated by detergent-based disinfectants.InfectionRabid animals are the only source of infection. Virus is shed in the saliva some days before the onset of clinical signs and transmitted through a bite or a scratch to the skin or mucous membranes. The average incubation period in cats is 2 months, but may vary from 2 weeks to several months, or even years.Disease signsAny unexplained aggressive behaviour or sudden behavioural change in cats must be considered suspicious. Two disease manifestations have been identified in cats: the furious and the dumb form. Death occurs after a clinical course of 1–10 days.DiagnosisA definitive rabies diagnosis is obtained by post-mortem laboratory investigation. However, serological tests are used for post-vaccinal control, especially in the context of international movements.Disease managementPost-exposure vaccination of cats depends on the national public health regulations, and is forbidden in many countries.Vaccination recommendationsA single rabies vaccination induces a long-lasting immunity. Kittens should be vaccinated at 12–16 weeks of age to avoid interference from maternally derived antibodies and revaccinated 1 year later. Although some vaccines protect against virulent rabies virus challenge for 3 years or more, national or local legislation may call for annual boosters.