Trials were carried out to investigate the effects of seed burial depth on seedling emergence rate of 20 weed species. Marked depth-mediated variation in emergence ability of the different species was observed, together with a general pattern of decreasing emergence with increasing soil depth. At 10 cm, only johnsongrass, velvetleaf, catchweed bedstraw, and cutleaf geranium emerged, albeit only in limited numbers. Species most severely inhibited by burial depth were buckhorn plantain, large crabgrass, common purslane, chickweed, and corn spurry, none of which emerged from beyond 6 cm. In all species, depth-mediated inhibition was found to be sigmoidal (polynomial regression). In addition, the number of seedlings and rate of seedling emergence decreased when depth of burial increased. The depth at which the number of emerged seedlings was halved varied by species and ranged from 3.6 cm for common purslane and chickweed to 7 cm for velvetleaf and catchweed bedstraw. Excessive burial depth generally induced dormancy (in roughly 85% of cases) rather than suicide germination. A close inverse relation (second-degree equation) between seed unit weight and depth-mediated inhibition was observed. The physiological involvement of depth inhibition in seed bank ecology is discussed.

Trials were carried out to investigate the effects of light and temperature on germination of Rumex obtusifolius L. After several months of storage, seeds gradually lost dormancy and became photosensitive. Thermal optima for germination were between 20 °C and 25 °C in light or in darkness. At lower temperatures there was a greater demand for light, so that the greatest differences in germination percentage (between low and high temperatures) were found within the 10–15 °C temperature range. The calculated thermal minima (x‐intercept method) in light and darkness were 8.3 °C and 6.1 °C respectively. Daily temperature fluctuation increased germination even after seed irradiation with far‐red light, suggesting a lower demand for the far‐red‐absorbing form of phytochrome. Seed burial inhibited germination in proportion to depth; however, germination inhibition was independent of seed phytochrome photo‐equilibrium, which had been diversified by seed pretreatment with light. Seedlings did not emerge when seeds were buried >8 cm deep. Recovery of ungerminated seeds showed that excessive burial did not impede seedling emergence but rather prevented seed germination. However, this induction of dormancy was lost once germination processes were activated (24–48 h at 20 °C) that made germination irreversible. Temperature was also involved in inhibition, and low temperature (<15 °C) induced the least inhibition. This is discussed in terms of processes of respiration and fermentation in buried seeds.

No abstract

Arundo donax L. (Poaceae), giant reed, is a rhizomatous shrubby grass that is cultivated in subtropical and warm temperate regions for a multitude of uses. Recently, it has been identified as a leading sustainable, non-food crop for lignocellulosic biofuels due to its low ecological and agronomic demands. Lack of cold hardiness may limit its diffusion into colder areas of the transition zone. The objectives of this study were to (i) quantify freeze tolerance (LT 50 ) of coldacclimated and non-acclimated Arundo donax L. plants using reproducible, controlled environment conditions, (ii) determine the effect of prolonged exposure to freeze stress on tolerance by keeping plants at a constant, sublethal temperature and (iii) study the relationship of non-structural carbohydrates (total soluble sugars, glucose, fructose and sucrose) and proline accumulation with cold hardiness. In vitro-propagated plants of the Honduran and Hungarian ecotypes of Arundo donax L. were chosen for this study. Cold acclimation treatment was imposed for 1 week using a controlled environment chamber set at 10°C and with a 12-h photoperiod of 200 lmol m À2 s À1 photosynthetically active radiation. Freeze tolerance ranged from À12Á8°C (Honduran) to À16Á4°C (Hungarian ecotype). In all the organs analysed, total soluble sugars significantly increased during cold acclimation, with concentrations between 1Á8-and 4Á7-fold higher than in non-acclimated plants. The higher concentrations of sugars and proline in cold-acclimated plants were positively associated with enhanced giant reed freeze tolerance (2Á9°C lower). Our results confirm that during cold acclimation, metabolic changes related to increased freezing tolerance occur in giant reed.

No abstract