Ephemeral wetland vegetation (EWV) in the Mediterranean Basin appears in temporary wetlands where favourable hydrological conditions exist only for a short time and year-to-year variability is high. Here, we report results of the seed germination, dormancy and desiccation tolerance of eight annual species living in this vulnerable habitat. Experiments were performed in laboratory conditions under constant and alternating temperatures and using a 12-h daily photoperiod or continuous darkness. Whilst germination and dormancy differed between the species, seeds demonstrated an absolute light requirement and prefer cool temperatures to germinate (mean a parts per thousand currency sign15 A degrees C). Logistic regression analysis showed significant effects of alternating temperature in all the species except in Tillaea vaillantii whose germination was stimulated by constant temperature. Mean temperature was a significant term in the logistic models for the dormant species Cicendia filiformis, Linum radiola and T. vaillantii for which after-ripening was an effective dormancy-breaking treatment. From these results we infer three strategies of regeneration by seeds: (1) species germinating during the whole vegetative season (2) species germinating in a narrow temperature niche and (3) species requiring flooding (T. vaillantii). Seeds possessed orthodox storage behaviour (tolerating drying to 15 % relative humidity) and may be amenable to seed banking as a means of ex-situ conservation. We conclude that EWV species are adapted to the irregular presence of water with characteristics that are typical of neither truly aquatic nor wetland plants. These EWV species showed a more plastic germination response based on alternating and constant temperature sensitivity and a low proportion of dormant seeds

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The aim of this work was to examine whether seed ecophysiological traits in three closely related Crocus species were associated with ecological niche differentiation and species divergence. Seeds of the temperate tetraploid cytotype of Crocus neapolitanus, the sub-Mediterranean C. etruscus and the Mediterranean C. ilvensis were placed either on agar in the laboratory under different periods of simulated seasonal conditions or in nylon mesh bags buried outdoors to examine embryo growth, radicle and shoot emergence. In agreement with the phenology observed outdoors, in the laboratory embryos required a cool temperature (ca. 10 °C) to grow to full size (embryo length:seed length, E:S ratio ca. 0.75) but only after seeds received a warm stratification; radicle emergence then followed immediately (November). Shoot emergence is a temporally separated phase (March) that was promoted by cold stratification in C. neapolitanus while in the other two species this time lag was attributed to a slow continuous developmental process. These species have similar embryo growth and radicle phenology but differ in their degree of epicotyl dormancy, which is related to the length of local winter. Conclusions from laboratory experiments that only consider root emergence could be misleading; evaluating the phenology of both root and shoot emergence should be considered in order to demonstrate ecologically meaningful differences in germination behaviour and to develop effective propagation protocols. Although these taxa resulted from recent speciation processes, the outcomes suggest an early onset of adaptation to local ecological factors and that phylogeny may represent a significant constraint in the evolution and expression of seed traits in Crocus.

Chromosome number and genome variation in flowering plants have stimulated growing speculation about the ancestral chromosome number of angiosperms, but estimates so far remain equivocal. We used a probabilistic approach to model haploid chromosome number (n) changes along a phylogeny embracing more than 10 000 taxa, to reconstruct the ancestral chromosome number of the common ancestor of extant angiosperms and the most recent common ancestor for single angiosperm families. Independently, we carried out an analysis of 1C genome size evolution, including over 5000 taxa. Our analyses revealed an ancestral haploid chromosome number for angiosperms of n = 7, a diploid status, and an ancestral 1C of 1.73 pg. For 160 families, inferred ancestral n are provided for the first time. Both descending dysploidy and polyploidy played crucial roles in chromosome number evolution. While descending dysploidy is equally distributed early and late across the phylogeny, polyploidy is detected mainly towards the tips. Similarly, 1C genome size also increases (or decreases) significantly in late-branching lineages. Therefore, no evidence exists of a clear link between ancestral chromosome numbers and ancient polyploidization events, suggesting that further insights are needed to elucidate the organization of genome packaging into chromosomes.

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