Financial analysis of shaded cocoa in Ghana

The cultivation of cocoa has been an important driver of tropical deforestation globally. Efforts to reverse this trend are focusing on the reintroduction of shade trees to cocoa plantations. Shade trees are valuable in enhancing biophysical conditions on cocoa (Theobroma cacao) fields and contribute to biodiversity and product diversification for smallholder producers. Participatory trials of cocoa agroforests planted with indigenous shade tree species were undertaken with farmers in the Atwima District of the Ashanti Region of Ghana, to increase tree volume on cocoa fields while improving rural livelihoods and enhancing environmental sustainability. An ex ante financial analysis of the technology was undertaken to assess its economic viability. Input–output data were collected from farmer experiments over three seasons and supplemented with data from traditional cocoa fields of varying rotation ages, and secondary data on production in later years of an eighty-year cocoa rotation. A discounted cash flow analysis was carried out to estimate the benefit-cost (B/C) ratio, net present value (NPV), internal rate of return (IRR) and land expectation value (LEV) as well as the sensitivity to a 20% decline in cocoa prices and additional chemical costs for various shade scenarios at a 10% discount rate. It was observed that cocoa production is, in general, profitable. The change from the traditional system to one with hybrid cocoa raised the IRR from 31% to 57% with planted shade and 67% without, although extra agrochemical costs would tend to reduce the profitability of unshaded hybrid cocoa in particular. The age of maximum LEV for the various scenarios suggests that the optimum economic rotation for the hybrid cocoa is between 18 and 29 years, much less than the traditional system.     

Preliminary study on differentiation of Leptospira grippotyphosa and Leptospira sejroe from other common pathogenic leptospiral serovars in canine urine by polymerase chain reaction assay.

A multiplex polymerase chain reaction (PCR) method using primer sets of G1/G2 and B64-I/B64-II was validated to detect pathogenic leptospira serovars from canine urine samples. The PCR method was found to be specific and sensitive with a detection limit of 100 cells of Leptospira icterohaemorrhagiae per milliliter of urine. The primer set previously designated and erroneously transcribed B64-I/B64-II amplified a DNA fragment of 352 base pairs from Leptospira grippotyphosa and Leptospira sejroe but not from Leptospira autumnalis, Leptospira bratislava, Leptospira canicola, Leptospira hardjo, Leptospira icterohaemorrhagiae, and Leptospira pomona. From 100 diagnostic canine urine samples, 5 were found positive for Leptospira grippotyphosalsejroe with a PCR product of 352 base pairs and 6 were positive for other pathogenic leptospira serovars with a PCR product of 285 base pairs. One 285-base pair product was sequenced and found to be 99.3% homologous to the G1/G2 PCR fragment sequence reported previously. All 352-base pair PCR products of clinical samples and pure cultures of L. grippotyphosa and L. sejroe were sequenced. The 352-base pair fragment sequences of L. grippotyphosa and L sejroe were identical. Only 2 base pairs were found different between the sequences from pure cultures and those from clinical samples. Serum samples from 3 positive cases that generated a PCR product of 352 base pairs were tested by the microscopic agglutination test, and 2 were found to be positive for L. grippotyphosa (1:10,240 and 1:5,120), 1 was positive for L. grippotyphosa (1:320) or L. icterohaemorrhagiae (1:320). The results of this study suggest that the multiplex PCR with the primer set G1/G2 and the erroneously transcribed B64-I/B64-II may be able to differentiate L. grippotyphosa or L. sejroe from other pathogenic leptospira serovars commonly tested for in Canadian diagnostic laboratories.     

Genetic correlations among pulpwood and solid-wood selection traits in Eucalyptus globulus

New Forests - Eucalyptus globulus is widely grown for pulpwood production in temperate regions of the world. However, there is increasing interest in using it for solid-wood products. We studied...     

Effect of carotenoids and background colour on the skin pigmentation of Australian snapper Pagrus auratus (Bloch & Schneider, 1801)

Three 2‐factor experiments were conducted to determine the effects of background colour and synthetic carotenoids on the skin colour of Australian snapper Pagrus auratus. Initially, we evaluated the effects on skin colour of supplementing diets for 50 days with 60 mg kg^?1 of either astaxanthin (LP; Lucantin^® Pink), canthaxanthin (LR; Lucantin^® Red), apocarotenoic acid ethyl ester (LY; Lucantin^® Yellow), selected combinations of the above or no carotenoids and holding snapper (mean weight=88 g) in either white or black cages. In a second experiment, all snapper (mean weight=142 g) from Experiment 1 were transferred from black to white, or white to white cages to measure the short‐term effects of cage colour on skin L^*, a^* and b^* colour values. Skin colour was measured after 7 and 14 days, and total carotenoid concentrations were determined after 14 days. Cage colour was the dominant factor affecting the skin lightness of snapper with fish from white cages much lighter than fish from black cages. Diets containing astaxanthin conferred greatest skin pigmentation and there were no differences in redness (a^*) and yellowness (b^*) values between snapper fed 30 or 60 mg astaxanthin kg^?1. Snapper fed astaxanthin in white cages displayed greater skin yellowness than those in black cages. Transferring snapper from black to white cages increased skin lightness but was not as effective as growing snapper in white cages for the entire duration. Snapper fed astaxanthin diets and transferred from black to white cages were less yellow than those transferred from white to white cages despite the improvement in skin lightness (L^*), and the total carotenoid concentration of the skin of fish fed astaxanthin diets was lower in white cages. Diets containing canthaxanthin led to a low level of deposition in the skin while apocarotenoic acid ethyl ester did not alter total skin carotenoid content or skin colour values in snapper. In a third experiment, we examined the effects of dietary astaxanthin (diets had 60 mg astaxanthin kg^?1 or no added carotenoids) and cage colour (black, white, red or blue) on skin colour of snapper (mean weight=88 g) after 50 days. Snapper fed the astaxanthin diet were more yellow when held in red or white cages compared with fish held in black or blue cages despite similar feed intake and growth. The skin lightness (L^* values) was correlated with cage L^* values, with the lightest fish obtained from white cages. The results of this study suggest that snapper should be fed 30 mg astaxanthin kg^?1 in white cages for 50 days to increase lightness and the red colouration prized in Australian markets.     

From both sides: Dire demographic consequences of carnivorous mice and longlining for the Critically Endangered Tristan albatrosses on Gough Island

The IUCN recently uplisted the Tristan albatross (Diomedea dabbenena) to Critically Endangered. Here we present new data indicating negative population trends on Gough Island arising from low adult survival (∼91%, ascribed to accidental mortality on fishing gear) and low breeding success (averaging 32%, due to mouse predation). Fledgling production from 1979 to 2007 and numbers of incubating adults from 1956 to 2007 have both decreased by ∼1% p.a. Consecutive annual counts of incubating adults and a population model permit the first reliable estimates of the Tristan albatross population, presently 5400 breeding adults and 11,300 birds in all age- and stage-classes. Population models explore scenarios of likely demographic trends using combinations of hypothetical best-case estimates vs. observed estimates for two key parameters: adult survival and breeding success. These scenarios highlight the relative benefits to the species of eradicating mice or mitigating bycatch. The model scenario using observed estimates predicts annual growth rate at −2.85%. Adult survival rates have probably decreased in recent years, concomitant with increased longline fishing effort, which might explain the discrepancy between counts and modelled trends. Negative trends cannot be reversed by improving breeding success alone, and adult survival must exceed an improbable 97% to balance the current chick production. A worst-case scenario including a fixed number of adult deaths annually predicted a catastrophic 4.2% p.a. decrease and extinction in ∼30 years. Population growth was most sensitive to adult survival, but even using an adult survival estimate without fishery mortality, current breeding success is insufficient to maintain the population. These findings do not support the ‘compensatory mitigation of bycatch’ model (offsetting bycatch impacts by eradicating invasive species), and the impacts of both fishery mortality and mouse predation must be addressed to improve the conservation status of the Critically Endangered Tristan albatross.