Mapping the vulnerability of crop production to drought in Ghana using rainfall, yield and socioeconomic data

This study evaluates new multi-scale, multi-indicator methods for assessing the vulnerability of crop production to drought at a national and regional scale. It does this by identifying differences across and within ten regions of Ghana, a country that faces many climate and crop production challenges typical of sub-Saharan Africa. In particular, we illustrate how a quantitative national and regional study is a critical first step in assessing differences in the drought sensitivity of food production systems and show how such an assessment enables the formulation of more targeted district and community level research that can explore the drivers of vulnerability and change on a local-scale. Finally, we propose methodological steps that can improve drought sensitivity and vulnerability assessments in dynamic dryland farming systems where there are multiple drivers of change and thresholds of risk that vary in both space and time. Results show that the vulnerability of crop production to drought in Ghana has discernible geographical and socioeconomic patterns, with the Northern, Upper West and Upper East regions being most vulnerable. Partly, this is because these regions have the lowest adaptive capacity due to low socioeconomic development and have economies based on rain-fed agriculture. Within these regions we find considerable differences between districts that can be explained only partly by socioeconomic variables with further community and household-scale research required to explain the causes of differences in vulnerability status. Our results highlight that national and regional scale multi-indicator vulnerability assessments are a vital (and often ignored) first step in assessing vulnerability across a large area. These inputs can guide both local-level research and also demonstrate the need for region-specific policies to reduce vulnerability and to enhance drought preparedness within dryland farming communities.     

A Global Inventory of Burned Areas at 1 Km Resolution for the Year 2000 Derived from Spot Vegetation Data

Biomass burning constitutes a major contribution to global emissions of carbon dioxide, carbon monoxide, methane, greenhouse gases and aerosols. Furthermore, biomass burning has an impact on health, transport, the environment and land use. Vegetation fires are certainly not recent phenomena and the impacts are not always negative. However, evidence suggests that fires are becoming more frequent and there is a large increase in the number of fires being set by humans for a variety of reasons. Knowledge of the interactions and feedbacks between biomass burning, climate and carbon cycling is needed to help the prediction of climate change scenarios. To obtain this knowledge, the scientific community requires, in the first instance, information on the spatial and temporal distribution of biomass burning at the global scale. This paper presents an inventory of burned areas at monthly time periods for the year 2000 at a resolution of 1 kilometer (km) and is available to the scientific community at no cost. The burned area products have been derived from a single source of satellite-derived images, the SPOT VEGETATION S1 1 km product, using algorithms developed and calibrated at regional scales by a network of partners. In this paper, estimates of burned area, number of burn scars and average size of the burn scar are described for each month of the year 2000. The information is reported at the country level. This paper makes a significant contribution to understanding the effect of biomass burning on atmospheric chemistry and the storage and cycling of carbon by constraining one of the main parameters used in the calculation of gas emissions.     

Nutrient loss and water quality under extensive grazing in the upper Burdekin river catchment, North Queensland

Increased sediment and nutrient losses resulting from unsustainable grazing management in the Burdekin River catchment are major threats to water quality in the Great Barrier Reef Lagoon. To test the effects of grazing management on soil and nutrient loss, five 1 ha mini-catchments were established in 1999 under different grazing strategies on a sedimentary landscape near Charters Towers. Reference samples were also collected from watercourses in the Burdekin catchment during major flow events. Soil and nutrient loss were relatively low across all grazing strategies due to a combination of good cover, low slope and low rainfall intensities. Total soil loss varied from 3 to 20 kg ha(-1) per event while losses of N and P ranged from 10 to 1900 g ha(-1) and from 1 to 71 g ha(-1) per event respectively. Water quality of runoff was considered moderate across all strategies with relatively low levels of total suspended sediment (range: 8-1409 mg l(-1)), total N (range: 101-4000 microg l(-1)) and total P (range: 14-609 microg l(-1)). However, treatment differences are likely to emerge with time as the impacts of the different grazing strategies on land condition become more apparent. Samples collected opportunistically from rivers and creeks during flow events displayed significantly higher levels of total suspended sediment (range: 10-6010 mg l(-1)), total N (range: 650-6350 microg l(-1)) and total P (range: 50-1500 microg l(-1)) than those collected at the grazing trial. These differences can largely be attributed to variation in slope, geology and cover between the grazing trial and different catchments. In particular, watercourses draining hillier, grano-diorite landscapes with low cover had markedly higher sediment and nutrient loads compared to those draining flatter, sedimentary landscapes. These preliminary data suggest that on relatively flat, sedimentary landscapes, extensive cattle grazing is compatible with achieving water quality targets, provided high levels of ground cover are maintained. In contrast, sediment and nutrient loss under grazing on more erodable land types is cause for serious concern. Long-term empirical research and monitoring will be essential to quantify the impacts of changed land management on water quality in the spatially and temporally variable Burdekin River catchment.     

Geology of the platanares geothermal area, Departamento de Copán, Honduras

The Platanares geothermal area, Departamento de Copán, Honduras, is located within a graben that is complexly faulted. The graben is bounded on the north by a highland composed of Paleozoic (?) metamorphic rocks in contact with Cretaceous - Tertiary redbeds of unknown thickness. These are unconformably overlain by Tertiary andesitic lavas, rhyolitic ignimbrites, and associated sedimentary rocks. The volcanic rocks are mostly older than 14 Ma, and thus are too old to represent the surface expression of an active crustal magma body. Thermal fluids that discharge in the area are heated during deep circulation of meteoric water along faults in a region of somewhat elevated heat flow. Geothermometry based upon the chemical composition of thermal fluids from hot springs and from geothermal gradient coreholes suggests that the reservoir equilibrated at temperatures as high as 225 to 240°C, within the Cretaceous redbed sequence. Three continuously cored geothermal gradient holes have been drilled; fluids of about 165°C have been produced from two drilled along a NW-trending fault zone, from depths of 250 to 680 m. A conductive thermal gradient of 139°C/km, at a depth of 400 m, was determined from the third well, drilled 0.6 km west of that fault zone. These data indicate that the Platanares geothermal area holds considerable promise for electrical generation by moderate- to hightemperature geothermal fluids.     

K/Ar dates of hydrothermal clays from core hole VC-2B, Valles caldera, New Mexico and their relation to alteration in a large hydrothermal system

Seventeen K/Ar dates were obtained on illitic clays within Valles caldera (1.13 Ma) to investigate the impact of hydrothermal alteration on Quaternary to Precambrian intracaldera and pre-caldera rocks in a large, long-lived hydrothermal system ( 1.0 Ma to present). Clay samples came from scientific core hole VC-2B (295°C at 1762 m) which was spudded in the Sulphur Springs thermal area and drilled into the boundary between the central resurgent dome and the western ring-fracture zone. Six illitic clays within Quaternary caldera-fill debris flow, tuffaceous sediment, and ash-flow tuff (48 to 587 m depth) yield ages from 0.35 to 1.09 Ma. Illite from Miocene pre-caldera sandstone (765 m) gives an age of 6.74 Ma. Two dates on illite from sandstones in Permian red beds (1008 and 1187 m) are 4.33 and 4.07 Ma, respectively. Surprisingly, three dates on illites from altered andesite pebbles within the red beds (1010–1014 m) are 0.95 to 1.06 Ma. Four illite dates on variably altered Precambrian quartz monzonite (1615–1762 m) range from 2.90 to 276 Ma.Post-Valles age illite is not correlated with alteration style (argillic to propylitic). Rather, post-Valles ages are uniformly obtained from illites in highly fractured, intensely altered, caldera-fill rocks and the Permian volcanic clasts. Generally, finer clay fractions from identical samples yield younger ages. Plots of ⁴⁰Ar/³⁶Ar versus ⁴⁰K/³⁶Ar and ⁴⁰Ar* versus ⁴⁰K for the illites in caldera-fill rocks lie close to a 1-Ma isochron. Most illite dates older than Valles caldera are difficult to interpret because they correspond to the ages of pre-Valles volcanic and hydrothermal episodes in the Jemez volcanic field ( 13 Ma). In addition, older dates may be caused by co-mingling of different illites during sample preparation, or by inherited argon or lost argon in illites from rocks with potentially complex hydrothermal histories. However, the range of ages obtained from illites in Permian sands and pebbles and from Precambrian crystalline rocks indicates that Valles hydrothermal activity is overwhelming illite produced by earlier geologic events.     

Measurements of trace gases emitted by Australian savanna fires during the 1990 dry season

During 18–23 July 1990, 31 smoke samples were collected from an aircraft flying at low altitudes through the plumes of tropical savanna fires in the Northern Territory, Australia. The excess (above background) mixing ratios of 17 different trace gases including CO₂, CO, CH₄, several non-methane hydrocarbons (NMHC), CH₃CHO, NO _x (– NO + NO₂), NH₃, N₂O, HCN and total unspeciated NMHC and sulphur were measured. Emissionratios relative to excess CO₂ and CO, and emissionfactors relative to the fuel carbon, nitrogen or sulphur content are determined for each measured species. The emission ratios and factors determined here for carbon-based gases, NO _x , and N₂O are in good agreement with those reported from other biomass burning studies. The ammonia data represent the first such measurements from savanna fires, and indicate that NH₃ emissions are more than half the strength of NO _x emissions. The emissions of NO _x , NH₃, N₂O and HCN together represent only 27% of the volatilised fuel N, and are primarily NO _x (16%) and NH₃ (9%). Similarly, only 56% of the volatilised fuel S is accounted for by our measurements of total unspeciated sulphur.     

Carbon tetrachloride lifetimes and emissions determined from daily global measurements during 1978–1985

Seven years of daily gas chromatographic measurements of CCl₄ at the five globally distributed ALE/GAGE surface sites are reported. It is determined that CCl₄ has been accumulating in the atmosphere at a rate of 1.3±0.1%/yr over the period 1978–1985 and that the releases of CCl₄ into the atmosphere have remained fairly constant, with the smallest releases in 1981–1982. Using an inversion scheme based on a nine box model of the atmosphere, we infer a CCl₄ lifetime of approximately 40 yr, an inventory on 1 July 1978 of (2.08±0.07)×10⁹ kg and an average rate of release over the period 1978–1985 of (0.9±0.9)×10⁷ kg/yr. These results produce excellent agreement with a release scenario derived from global production estimates for CCl₄ and the major CCl₄ byproduct, the chlorofluorocarbons. However, to obtain this consistency, it is necessary that our current ALE/GAGE absolute calibration standard be reduced approximately 25% thus bringing it into agreement with measurements by Yokohata et al. (1985) and Hanst et al. (1975).     

Determination of activities in silicate melts by Knudsen cell mass spectrometry—I. The system NaAlSi3O8-KAlSi3O8

The mixing properties of aluminosilicate melts in the pseudobinary system NaAlSi₃O₈-KAlSi ₃O₈ have been determined by measuring the compositions of their saturated vapours by hightemperature Knudsen cell mass spectrometry. The melts mix close to ideally over most of the composition range with small positive deviations from ideality for K-rich compositions. These may be related to incipient partial ordering of melt constituents into leucite-like and SiO₂-like structures above the feldspar liquidus.