Mangroves are one of the most important ecosystems in the world being found in the tropical–subtropical belt. Despite their significance, they have been highly disturbed due to many anthropogenic and natural causes. A significant effort has been made to restore mangroves around the world. However, a lack of information on the seed biology of mangrove species has impeded restoration. Thus, this study aimed to produce a seed dormancy profile for selected plant species of mangroves in Sri Lanka. This profile would allow restoration ecologists to better understand what kinds of dormancy are present, how to alleviate dormancy and how to best stimulate germination to generate seedlings for nursery stock or out-planting. Mature fruits/seeds were collected from coastal zone mangroves in Sri Lanka. Germination and imbibition of non-scarified and manually scarified seeds and embryo:seed length (E:S) ratio of fresh and radicle-emerged seeds were evaluated to assess the class of dormancy. Of the 30 species, seeds from 12 (40%) were non-dormant and 18 (60%) were dormant. Three dormancy classes [physiological (PD), physical (PY) and morphophysiological (MPD)] and presence of epicotyl dormancy were identified. Among species producing dormant seeds, most of them showed PD (44%). PY, MPD and presence of epicotyl dormancy were represented by 28, 17 and 11% of the species, respectively. These findings aid practitioners to craft strategies to effectively break dormancy and germinate seeds for conservation and restoration activities of mangroves.

The Asteraceae with up to 30,000 species occurs on all continents except Antarctica and in all major vegetation zones on earth. Our primary aim was to consider cypselae dormancy-break and germination of Asteraceae in relation to ecology, vegetation zones and evolution. Cypselae are desiccation-tolerant and in various tribes, genera, species and life forms of Asteraceae are either non-dormant (ND) or have non-deep physiological dormancy (PD) at maturity. All six types of non-deep PD are found among the Asteraceae, and dormancy is broken by cold or warm stratification or by afterripening. Soil cypselae banks may be formed but mostly are short-lived. Much within-species variation in dormancy-break and germination has been found. Using data compiled for 1192 species in 373 genera and 35 tribes of Asteraceae, we considered ND and PD in relation to life form, vegetation zone and tribe. Senecioneae and Astereae had the best representation across the vegetation zones on earth. In evergreen and semi-evergreen rainforests, more species have ND than PD, but in all other vegetation zones, except alpine/high-latitude tundra (where ND and PD are equal), more species have PD than ND. Tribes in the basal and central grades and those in the Heliantheae Alliance have both ND and PD. The high diversity and lability of non-deep PD may have enhanced the rate of species diversification by promoting the survival of new species and/or species in new habitats that became available following globally disruptive events since the origin of the Asteraceae in the Late Cretaceous.

Seeds of legumes are generally considered to have physical dormancy and to be orthodox, but most seed biologists are unaware of the various kinds and combinations of dormancy and storage behaviour in seeds of this family. The aim of our study was to document the dormancy and storage behaviour of seeds of 100 native and introduced tropical Fabaceae species in Sri Lanka and classify them into germination/storage behaviour categories. Moisture content (MC) was < 16% for fresh seeds of 94 species and >29% for those of six. Seeds of these six species had low tolerance for desiccation and for low temperatures. Thus, seeds of six species are non-orthodox and 94 species orthodox. Nine of the 100 species were non-dormant, and 2, 3 and 86 had physiological, physiological epicotyl and physical dormancy, respectively. Six germination/storage behaviour categories were identified among the 100 species. However, as in extratropical regions of the world, orthodox storage behaviour and physical dormancy are characteristic of seeds of the majority of species of Fabaceae in tropical Sri Lanka.