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.
The essential oils obtained from rosemary (Rosmarinus officinalis L.), thyme (Thymus vulgaris L.), and savory (Satureja montana L.) and the four monoterpenes that are their major constituents have been analyzed by GC and GC-MS and tested for their allelopathic properties on the seeds of three different annual weeds (Chenopodium album, Portulaca oleracea, and Echinochloa crus-galli) and three crops (Raphanus sativus, Capsicum annuum, and Lactuca sativa), with the aim to evaluate in vitro their potential as germination inhibitors. The essential oil composition varied with the species, thymol being the main constituent (44%) of thyme and carvacrol (57%) that of savory oil. Differences in essential oil composition were observed within two different rosemary ecotypes, type A, with alpha-pinene (37%) and 1,8-cineole (23%), and type B, characterized by a 2-fold content of 1,8-cineole (47%). This latest essential oil inhibited completely the germination of weeds while concurrently displaying little effect on pepper. The other two oils showed less selective action. S. montana essential oil, with 57% carvacrol, is the most active compound, completely inhibiting germination both of crops and weeds. Borneol, one of the main constituents of the oil of rosemary type B, showed an activity comparable to that of the whole oil. Crop and weed seeds treated with 1,8-cineole showed germination values that were not significantly different from controls, even if a slowing of the germination process expressed in terms of a significant increase in mean germination time was observed. Monoterpene compounds also present in the essential oils mainly represented the volatile fraction released from the crops and their residues into the soil.
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.
Predicting weed emergence dynamics can help farmers to plan more effective weed control. The hydrothermal time concept has been used to model emergence as a function of temperature and water potential. Application of this concept is possible if the specific biological thresholds are known. This article provides a data set of base temperature and water potential of eight maize weeds (velvetleaf, redroot pigweed, common lambsquarters, large crabgrass, barnyardgrass, yellow foxtail, green foxtail, and johnsongrass). For five of these species, two ecotypes from two extreme regions of the predominant maize-growing area in Italy (Veneto and Tuscany), were collected and compared to check possible differences that may arise from using the same thresholds for different populations. Seedling emergence of velvetleaf and johnsongrass were modeled using three different approaches: (1) thermal time calculated assuming 5 C as base temperature for both species; (2) thermal time using the specific estimated base temperatures; and (3) hydrothermal time using the specific, estimated base temperatures and water potentials. All the species had base temperatures greater than 10 C, with the exception of velvetleaf (3.9 to 4.4 C) and common lambsquarters (2.0 to 2.6 C). All species showed a calculated base-water potential equal or up to 21.00 MPa. The thresholds of the two ecotypes were similar for all the studied species, with the exception of redroot pigweed, for which the Veneto ecotype showed a water potential lower than 20.41 MPa, whereas it was 20.62 MPa for the Tuscany ecotype. Similar thresholds have been found to be useful in hydrothermal time models covering two climatic regions where maize is grown in Italy. Furthermore, a comparison between the use of specific, estimated, and common thresholds for modeling weed emergence showed that, for a better determination of weed control timing, it is often necessary to estimate the specific thresholds
Summary Trials were carried out in order to investigate the effect of hypoxia on seed germination of Datura stramonium L. in Petri dishes and when buried at various depths in soil. Hypoxia was found to cause a decrease in germination capacity and germination rate. This inhibition was partially alleviated by daily exchange of hypoxic gas surrounding the seeds during incubation. Similarly, seed scarification allowed maintenance of a higher germination capacity under conditions of low oxygen availability, showing that the seed coat was only partially gas permeable. Oxygen deficiency led to a decrease in respiratory capacity. However, this was probably compensated for by induction of fermentation metabolism. The possibility of removing the final products of fermentation exerts a decisive influence on seed germination, especially in an environment such as soil, where their diffusion into the surrounding environment is restricted. Thus daily nitrogen flushing partially eliminated this inhibition, even under conditions of low external oxygen availability. It was therefore postulated that the main depth–derived inhibition was not caused directly by oxygen deficiency but by the increasing difficulty in eliminating toxic fermentation products, which was found to be proportional to the degree of hypoxia. Finally, incubation for several days under completely anaerobic conditions induced secondary dormancy. This was probably due to an ecological adaptation mechanism that prevents germination under conditions that are unfavourable for survival.
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