2010
DOI: 10.1071/bt10144
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Effects of soil temperature regimes after fire on seed dormancy and germination in six Australian Fabaceae species

Abstract: M. (2010). Effects of soil temperature regimes after fire on seed dormancy and germination in six Australian Fabaceae species. Australian Journal of Botany, 58 (7), 539-545.Effects of soil temperature regimes after fire on seed dormancy and germination in six Australian Fabaceae species AbstractIn addition to direct fire cues such as heat, smoke and charred wood, the passage of fire leads indirectly to changes in environmental conditions which may be able to break physical dormancy in hard-coated seeds. After … Show more

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Cited by 78 publications
(71 citation statements)
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“…Plant count done at 40 DAP had the higher number of plants m −2 than at 20 DAP ( Table 3) among all planting dates and genotypes in both years. Temperature plays an important role in facilitating the germination of seed legumes [43]. Soil temperature greater than 30˚C accelerates guar seed germination [9].…”
Section: Stand Establishmentmentioning
confidence: 99%
“…Plant count done at 40 DAP had the higher number of plants m −2 than at 20 DAP ( Table 3) among all planting dates and genotypes in both years. Temperature plays an important role in facilitating the germination of seed legumes [43]. Soil temperature greater than 30˚C accelerates guar seed germination [9].…”
Section: Stand Establishmentmentioning
confidence: 99%
“…With few exceptions (for example, Dolan et al, 2008;Ayre et al, 2009), we know little about the genetic composition of soil-stored seedbanks and their likely interaction with the potentially patchy effects of fire, or indeed, in general, the extent to which the genetic structure of standing adults reflects structure within groups of post-germination seedlings or the effects of natural selection (Honnay et al, 2008). However, it is known that the likelihood of seedling emergence varies with factors such as the age of the seed, depth of seed burial, and the timing, intensity and duration of fire (Ooi et al, 2004;Santana et al, 2010;Anderson et al, 2012) and for many species, seeds are likely to be aggregated in full and half-sib clusters representing the seed shadow of pre-fire adults (for example, Ayre et al, 2009) or in seed caches (Chung et al, 2003).…”
Section: Introductionmentioning
confidence: 99%
“…), suggesting that resprouting may be the dominant mechanism for persistence after fire in these species, as in many Cerrado species (Simon et al 2009;Simon & Pennington 2012). On the other hand, germination percentage of U. parviflorus and C. albidus seeds were enhanced with F treatments, suggesting that temperatures reached with the passage of fire are effective in breaking seed dormancy and enabling germination in these species, which is particularly important for obligate seeder species, whose regenerating strategy after fire relays exclusively on seed germination and establishment (Bond & Midgley 2001;Pausas et al 2004), as is the case for both these species (Baeza & Vallejo 2006;Santana et al 2010).…”
Section: Talita Zupo M Jaime Baeza and Alessandra Fidelismentioning
confidence: 90%
“…50-55 o C) and wide temperature fluctuations. Recent studies have indicated that these temperature fluctuations also act as germination cues in hard-seeded species, breaking physical dormancy and enabling germination (Baeza & Roy 2008;Santana et al 2010;Jaganathan 2015). Moreover, in non-dormant seeds, daily temperature fluctuations may affect the rate of germination (Musso et al 2015;Le Stradic et al 2015).…”
mentioning
confidence: 99%