a b s t r a c tTolerance to drought remains poorly described for Jatropha curcas accessions from different geographical and climatic origins. To address this issue we studied the response of two J. curcas accessions, one from Indonesia (wet tropical climate) and the other from Cape Verde islands (semi-arid climate). Potted seedlings (with 71 days) of both accessions were subjected to continuous well watered conditions (control) or to a drought stress period followed by re-watering. To mimic natural conditions in which drought stress develops gradually, stress was imposed progressively by reducing irrigation (10% reduction every 2 days, on a weight base), for a period of 28 days, until a field capacity of 15% (maximum stress) was achieved, followed by one week under well-watered conditions. We measured soil and plant water status, growth and biomass partitioning, leaf morphology, leaf gas exchange and chlorophyll a fluorescence. Both accessions maintained high leaf relative water content (70-80%) even at maximum stress. Net photosynthesis (A n ) was not affected by mild to moderate stress but it abruptly dropped at severe stress. This was due to reduced stomatal conductance, which showed earlier decline than A n . Plant growth (stem elongation, leaf emergence and total leaf area) was reduced, minimizing water loss, but no significant differences were found between accessions. Drought stress did not reduce chlorophyll contents but led to reduced chlorophyll a/b. Both accessions showed fast recovery of both stomatal and photochemical parameters suggesting a good tolerance to water stress. Both J. curcas accessions showed a-dehydrationavoidant behaviour, presenting a typical water saving strategy due to strict stomatal regulation, regardless of their provenance.

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Current efforts to grow the tropical oilseed crop Jatropha curcas L. economically are hampered by the lack of cultivars and the presence of toxic phorbol esters (PE) within the seeds of most provenances. These PE restrict the conversion of seed cake into animal feed, although naturally occurring ‘nontoxic’ provenances exist which produce seed lacking PE. As an important step towards the development of genetically improved varieties of J. curcas, we constructed a linkage map from four F2 mapping populations. The consensus linkage map contains 502 codominant markers, distributed over 11 linkage groups, with a mean marker density of 1.8 cM per unique locus. Analysis of the inheritance of PE biosynthesis indicated that this is a maternally controlled dominant monogenic trait. This maternal control is due to biosynthesis of the PE occurring only within maternal tissues. The trait segregated 3 : 1 within seeds collected from F2 plants, and QTL analysis revealed that a locus on linkage group 8 was responsible for phorbol ester biosynthesis. By taking advantage of the draft genome assemblies of J. curcas and Ricinus communis (castor), a comparative mapping approach was used to develop additional markers to fine map this mutation within 2.3 cM. The linkage map provides a framework for the dissection of agronomic traits in J. curcas, and the development of improved varieties by marker-assisted breeding. The identification of the locus responsible for PE biosynthesis means that it is now possible to rapidly breed new nontoxic varieties.

The resistance gene H1 confers resistance to the potato cyst nematode Globodera rostochiensis and is located at the distal end of the long arm of chromosome V of potato. For marker enrichment of the H1 locus, a bulked segregant analysis (BSA) was carried out using 704 AFLP primer combinations. A second source of markers tightly linked to H1 is the ultra-high-density (UHD) genetic map of the potato cross SH x RH. This map has been produced with 387 AFLP primer combinations and consists of 10,365 AFLP markers in 1,118 bins (http://www.dpw.wageningen-ur.nl/uhd/). Comparing these two methods revealed that BSA resulted in one marker/cM and the UHD map in four markers/cM in the H1 interval. Subsequently, a high-resolution genetic map of the H1 locus has been developed using a segregating F(1) SH x RH population consisting of 1,209 genotypes. Two PCR-based markers were designed at either side of the H1 gene to screen the 1,209 genotypes for recombination events. In the high-resolution genetic map, two of the four co-segregating AFLP markers could be separated from the H1 gene. Marker EM1 is located at a distance of 0.2 cM, and marker EM14 is located at a distance of 0.8 cM. The other two co-segregating markers CM1 (in coupling) and EM15 (in repulsion) could not be separated from the H1 gene.

We have studied the effect of various in-vitro conditions on dormancy of bulblets generated on scale explants of Lilium speciosum Thunb. cv. 'Rubrum' nr. 10. The bulblets were harvested after 11 weeks of culture. Dormancy was measured by determining the percent emergence in soil of viable, non-cold-treated bulblets.