Abstract. In a minute proportion of angiosperm species, rehydrating foliage can revive from airdryness or even from equilibration with air of~0% RH. Such desiccation tolerance is known from vegetative cells of some species of algae and of major groups close to the evolutionary path of the angiosperms. It is also found in the reproductive structures of some algae, moss spores and probably the aerial spores of other terrestrial cryptogamic taxa. The occurrence of desiccation tolerance in the seed plants is overwhelmingly in the aerial reproductive structures; the pollen and seed embryos. Spatially and temporally, pollen and embryos are close ontogenetic derivatives of the angiosperm microspores and megaspores respectively. This suggests that the desiccation tolerance of pollen and embryos derives from the desiccation tolerance of the spores of antecedent taxa and that the basic pollen/embryo mechanism of desiccation tolerance has eventually become expressed also in the vegetative tissue of certain angiosperm species whose drought avoidance is inadequate in microhabitats that suffer extremely xeric episodes. The protective compounds and processes that contribute to desiccation tolerance in angiosperms are found in the modern groups related to the evolutionary path leading to the angiosperms and are also present in the algae and in the cyanobacteria. The mechanism of desiccation tolerance in the angiosperms thus appears to have its origins in algal ancestors and possibly in the endosymbiotic cyanobacteria-related progenitor of chloroplasts and the bacteria-related progenitor of mitochondria. The mechanism may involve the regulation and timing of the accumulation of protective compounds and of other contributing substances and processes.

The South African flora contains a unique abundance of higher plants which withstand virtually complete desiccation. Water potentials of fielddry leaves corresponded to 30 to 40 percent relative humidity. Mature leaves survived from 15 to approximately 0 percent relative humidity. Known examples were increased from 4 to 15 species, which for the first time included grasses.

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Drought tolerance limits are given for 36 new 'resurrection plants', sufficient to double the number of desiccation tolerant plants reported from southern Africa. Tolerance limits for angiosperm examples are usually better than those for ferns. Air-dry foliage survives for 1/2 to 5 years or more, unless stored in humidities above 50% RH Abbreviation: RH = relative humidity . Dehydration is sufficiently slow (usually 2-3 days) to allow the possibility of a tolerance induction process, like that found in Borya nitida. Rehydration after rain is usually complete in 1/2 to 1 day. A significant proportion of rain is absorbed through the leaf surface, but there is no evidence of appreciable rehydration from dew.Resurrection plants are usually pioneers in xeroseres, but they often lack xeromorphic characteristics. Anthocyanin pigmentation during drying is a reliable indicator of viability in some species.

A modification of the ‘cold plaque’ screening technique (Hodge et al., Plant Journal1992, 2, 257–260) was used to screen a cDNA library constructed from drought‐stressed leaf tissue of the desiccation tolerant (‘resurrection’) grass Sporobolus stapfianus. This technique allowed a large number of clones representing genes expressed at low abundance to be isolated. An examination of expression profiles revealed that several of these genes are induced in desiccation‐tolerant tissue experiencing severe drought stress. Further characterization indicated that the gene products encoded include an eIF1 protein translation initiation factor and a glycine‐ and proline‐rich protein which have not previously been associated with drought stress. In addition, genes encoding a serine/threonine phosphatase type 2C, a tonoplast‐intrinsic protein (TIP) and an early light‐inducible protein (ELIP) were isolated. A number of these genes are expressed differentially in desiccation‐tolerant and desiccation‐sensitive tissues, suggesting that they may be associated with the desiccation tolerance response of S. stapfianus. The results indicate that there may be unique gene regulation processes occurring during induction of desiccation tolerance in resurrection plants which allow different drought‐responsive genes to be selectively expressed at successive levels of water loss.