In seasonal climates, germination timing is mainly controlled by temperature, especially in species with physiological seed dormancy. The germination response to temperature may, however, vary among populations across the distribution range of species. Understanding how populations along climate gradients vary in their sensitivity to temperature is important for determining their vulnerability to climate variability and change. Here, we investigated the germination response of two Erica species with physiological seed dormancy (E. australis and E. umbellata) to changes in temperature throughout the seasons (simulated autumn through to spring) and to the local climate in six localities across a latitudinal gradient in western Iberia. Effects were studied with and without exposing the seeds to a heat shock. The local climate of seed provenance emerged as a key factor in modifying the germination sensitivity to germination temperature and their variation through the seasons. Although each species showed idiosyncratic germination responses to temperature treatments and across the gradient, germination of both species was sensitive to warmer temperatures and to a heat shock. Both showed similar seasonal germination patterns: as we moved from south to north, populations tended to have a larger germination peak in spring, which was greater at colder temperatures. We conclude that rising temperatures associated with climate change will affect these species, particularly at their northern ranges, where many seeds will remain dormant during warmer winters. Arguably, models aiming at assessing climate change impacts in these species need to include such variability across latitude.

Seed germination, one aspect of fitness, of chlorsulfuron-resistant (R) and -susceptible (S) kochia biotypes collected in North Dakota and Kansas was compared at 8, 18, and 28 C. Cumulative germination, characterized for each biotype using a Weibull function, was different at 8 and 18 C but not at 28 C. The Kansas R biotype reached 50% and maximum germination 70 and 300 h before Kansas S biotype at 8 C and 12 and 100 h before the S biotype at 18 C, respectively. The North Dakota R biotype reached 50% and maximum germination 12 and 100 h before the North Dakota S biotype at 8 C, respectively, and they were not different at 18 C. The resistance trait affects the cumulative germination process of kochia and may affect resistant-weed management strategies implemented early in the growing season when temperatures are lowest.

The allelopathic potential of wheat [Triticum aestivum (L.) ‘Doublecrop′] straw residue was evaluated on weed-seed germination and seedling growth. The inhibition of weed-seed germination and seedling growth was extract-, species-, and temperature-dependent. The extracts prepared by agitating and soaking caused greater inhibition than those obtained by leaching. The descending order of species susceptibility was ivyleaf morningglory [Ipomoea hederacea (L.) Jacq.], velvetleaf (Abutilon theophrasti Medic.), pitted morningglory (Ipomoea lacunosa L.), hemp sesbania [Sesbania exaltata (Raf.) Cory], sicklepod (Cassia obtusifolia L.), and Japanese barnyard millet [Echinochloa crus-galli var. frumetaceae (Roxb.) Link]. Incubation at 35 C caused the greatest inhibition of germination and growth.

Timing of seed germination influences plant lifetime fitness and can affect the ability of plant populations to colonize and persist in changing environments. However, the genetic variation of the seed germination response remains poorly understood. The amplified restriction fragment polymorphism (AFLP) technique was applied to characterize the genetic variation of germinated seeds collected from three Festuca hallii populations in the Canadian prairie. Three subpopulations with early, intermediate and late germination were identified from each population, based on germination tests at 10, 15 and 20°C in controlled growth chambers. Three AFLP primer pairs were employed to screen a total of 540 assayed seedling samples and 188 polymorphic AFLP bands were scored for each sample. None of the assayed AFLP bands were significantly associated with seed germination, but marked differences in estimates of mean band frequency were observed for various groups of germinating seeds under different test temperatures. Partitioning of the total AFLP variation showed that 5.9% AFLP variation was present among seeds of the three populations, 0.3% among seeds of three germination subpopulations, and 0.5% among seeds grouped for germination temperature. Genetic differentiation was significant among 27 groups of seeds representing population, germination timing and test temperature. Subpopulations with early and intermediate germination shared similar genetic backgrounds and were genetically differentiated from the late germination subpopulation. These results indicate that seed genotypes respond slightly differently to environmental variation, resulting in significant but weak genetic differentiation in the germination of F. hallii seeds. Implications for plant establishment and fescue restoration are discussed.

We studied dormancy and germination requirements of seeds of Acacia aroma, A. caven and A. furcatispina from a semi-arid region of central Argentina. Imbibition experiments were performed to determine the rate of water uptake in seeds. To determine optimal temperature for germination, seeds were incubated at three temperature regimes (15/5, 25/15 and 35/20°C) with a 12/12 h daily photoperiod or in total darkness. Additionally, differences in dormancy and germination in seed colour morphs of A. aroma were studied. Seeds of A. aroma and A. caven had impermeable coats, while those of A. furcatispina did not. Seeds of the three species showed the same pattern of germination. Germination percentages were significantly lower at 15/5°C than at 25/15 or 35/20°C. The germination temperature pattern found for these species is probably related to the summer seasonal nature of rainfall in the study area. In A. aroma, seeds of the two colour morphs showed a similar pattern of dormancy and germination.