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This study quantifies the potential effects of a set of technologies to address water and fertility constraints in rain-fed smallholder agriculture in South Africa, namely in situ water harvesting (WH), external WH, and ecological sanitation (Ecosan, fertilization with human urine). We used the Soil and Water Assessment Tool to model spatiotemporally differentiated effects on maize yield, river flow, evaporation, and transpiration. Ecosan met some of the plant nitrogen demands, which significantly increased maize yields by 12% and transpiration by 2% on average across South Africa. In situ and external WH did not significantly affect the yield, transpiration or river flow on the South Africa scale. However, external WH more than doubled the yields for specific seasons and locations. WH particularly increased the lowest yields. Significant water and nutrient demands remained even with WH and Ecosan management. Additional fertility enhancements raised the yield levels but also the yield variability, whereas soil moisture enhancements improved the yield stability. Hence, coupled policies addressing both constraints will likely be most effective for improving food security.

Crop production is the single largest cause of human alteration of the global nitrogen cycle. We present a comprehensive assessment of global nitrogen flows in cropland for the year 2000 with a spatial resolution of 5 arc-minutes. We calculated a total nitrogen input (IN) of 136.60 trillion grams (Tg) of N per year, of which almost half is contributed by mineral nitrogen fertilizers, and a total nitrogen output (OUT) of 148.14 Tg of N per year, of which 55% is uptake by harvested crops and crop residues. We present high-resolution maps quantifying the spatial distribution of nitrogen IN and OUT flows, soil nitrogen balance, and surface nitrogen balance. The high-resolution data are aggregated at the national level on a per capita basis to assess nitrogen stress levels. The results show that almost 80% of African countries are confronted with nitrogen scarcity or nitrogen stress problems, which, along with poverty, cause food insecurity and malnutrition. The assessment also shows a global average nitrogen recovery rate of 59%, indicating that nearly two-fifths of nitrogen inputs are lost in ecosystems. More effective management of nitrogen is essential to reduce the deleterious environmental consequences.

Cereal import has played a crucial role in compensating local water deficit. A quantitative account of water deficit and cereal import relations therefore is of significance for predicting future food import demand and formulating corresponding national and international policies. On the basis of data for countries in Asia and Africa, we estimated a water resources threshold with respect to cereal import. Below the threshold, the demand for cereal import increases exponentially with decreasing water resources. There appeared to be a declining trend in the threshold, from 2000 m3/(capita year) in the early 1980s to 1500 m3/(capita year) by the end of the 1990s. Until recently, most countries below the threshold were oil-rich and thus were able to afford cereal import. However, the next 30 yr may see many poor and populous countries dropping below the threshold in association with their rapid population growth and the depletion of fossil groundwater. Water deficit-induced food insecurity and starvation could intensify because cereal import may not be affordable for these countries.

Ralstonia eutropha JMP134 (pJP4) harbors two functional gene clusters for the degradation of chlorocatechols, i.e. tfdCDEF (in short: tfd (I)) and tfdD (II) C (II) E (II) F (II) (in short: tfd (II)), which are both present on the catabolic plasmid pJP4. In this study, we compared the function of both gene clusters for degradation of chlorocatechols by constructing isolated and hybrid tfd (I)- tfd (II) clusters on plasmids in R. eutropha, by activity assays of Tfd enzymes, and by HPLC/MS of individual enzymatic catalytic steps in chlorocatechol conversion. R. eutropha containing the tfd (II) cluster alone or hybrid tfd-clusters with tfdD (II) as sole gene for chloromuconate cycloisomerase were impaired in growth on 3-chlorobenzoate, in contrast to R. eutrophaharboring the complete tfd (I) cluster. Enzyme activities for TfdD(II) and for TfdE(II) were very low in R. eutropha when induced with 3-chlorobenzoate. By contrast, a relatively high enzyme activity was found for TfdF(II). Spectral conversion assays with extracts from R. eutropha strains expressing tfdD (II) all showed accumulation of a compound with a similar UV spectrum as 2-chloro- cis,cis-muconate from 3-chlorocatechol. HPLC analysis of in vitro assays in which each individual step in 3-chlorocatechol conversion was reproduced by sequentially adding cell extracts of an Escherichia coli expressing one Tfd enzyme only demonstrated that TfdD(II) was unable to cause conversion of 2-chloro- cis,cis-muconate. No accumulation of intermediates was observed with 4-chlorocatechol. From these results, we conclude that at least TfdD(II) is a bottleneck in conversion of 3-chlorocatechol and, therefore, in efficient metabolism of 3-chlorobenzoate. This study showed the subtle functional and expression differences between similar enzymes of the tfd-encoded pathway and demonstrated that extreme care has to be taken when inferring functionality from sequence data alone.

Transcription of the Escherichia coli aidB gene is controlled by an Esigma(S)-dependent promoter (PaidB) and is poorly transcribed by the Esigma(70) form of RNA polymerase in the absence of additional factors. In this report, we investigate the interaction between PaidB and either the Esigma(70) or the Esigma(S) forms of RNA polymerase in vitro. We show that although Esigma(70) can bind the aidB promoter, its interaction with the promoter results in the formation of an open complex inefficient in transcription initiation and sensitive to heparin challenge. Deletion of the C residue at position -13 of PaidB (Delta-13C) slightly impaired transcription initiation by Esigma(S), consistent with the role of -13C as a specific feature of Esigma(S)-dependent promoters. However, Esigma(S) could still bind and initiate transcription from the Delta-13C mutant aidB promoter more efficiently than Esigma(70), suggesting that sequence elements other than the -13C play an important role in specific promoter recognition by Esigma(S)., ((c)2002 Elsevier Science (USA).)