Small wetlands in Kenya and Tanzania cover about 12 million ha and are increasingly converted for agricultural production. There is a need to provide guidelines for their future protection or use, requiring their systematic classification and characterisation. Fifty-one wetlands were inventoried in 2008 in four contrasting sites, covering a surveyed total area of 484 km 2 . Each wetland was subdivided into sub-units of 0.5-458 ha based on the predominant land use. The biophysical and socio-economic attributes of the resulting 157 wetland sub-units were determined. The wetland sub-units were categorized using multivariate analyses into five major cluster groups. The main wetland categories comprised: (1) narrow permanently flooded inland valleys that are largely unused; (2) wide permanently flooded inland valleys and highlands floodplains under extensive use; (3) large inland valleys and lowland floodplains with seasonal flooding under medium use intensity; (4) completely drained wide inland valleys and highlands floodplains under intensive food crop production; and (5) narrow drained inland valleys under permanent horticultural production. The wetland types were associated with specific vegetation forms and soil attributes.Electronic supplementary material The online version of this article (

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SUMMARYTo assess genotype adaptability to variable environments, we evaluated five irrigated rice genotypes, three new varieties, WAS161, a NERICA, IR32307 and ITA344, and two controls: Sahel 108, the most popular short-duration variety in the region, and IR64. In a field experiment conducted at two locations, Ndiaye and Fanaye, along the Senegal River, rice was sown on 15 consecutive dates at one month intervals starting in February 2006. Yield (0-12.2 t ha −1 ) and crop cycle duration (117-190 days) varied with sowing date, genotype and site. Rice yield was very sensitive to sowing date and the associated temperature regimes. Spikelet sterility due to cold stress (T < 20 • C) was observed when the crops were sown in August (Ndiaye), September (Ndiaye and Fanaye) and October (Ndiaye and Fanaye), and heat stress (T > 35 • C) resulted in spikelet sterility when sowing took place in April (Ndiaye and Fanaye) and May (Fanaye). For all experiments the source and sink balance was quantified and showed that yield was most limited by sink size when sowing between July and October. Variety WAS 161 was least affected by genotype × environment interactions, resulting in lower interactive principal component values. An increase in minimum temperature of 3 • C could decrease spikelet sterility from 100 to 45%. These changes in temperature are likely to force rice farmers in the Senegal River to adjust the cropping calendar, e.g. to delay planting or to use heat-tolerant genotypes.