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Seed production (mean ? SE) of C 4 grass species in the central Monte desert during growing seasons 2001–2002 (GS1), 2002–2003 (GS2) and 2003–2004 (GS3). Seed production is measured as the mean number of seeds per plant (n = 10) for the summer months February and April. Different letters indicate significant differences between growing seasons' seed production (Kruskal–Wallis tests and a posteriori Dunn's tests)  

Seed production (mean ? SE) of C 4 grass species in the central Monte desert during growing seasons 2001–2002 (GS1), 2002–2003 (GS2) and 2003–2004 (GS3). Seed production is measured as the mean number of seeds per plant (n = 10) for the summer months February and April. Different letters indicate significant differences between growing seasons' seed production (Kruskal–Wallis tests and a posteriori Dunn's tests)  

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In desert regions, water availability triggers primary production, which determines seed production, the composition and size of soil seed reserves and the abundance and behaviour of seed-eating animals. In the central Monte desert, large precipitation events (≥10mm) account for a high proportion of growing season’s rainfall. Our first objective he...

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... Hampton et al. [28] found that tiller production of perennial ryegrass was optimal at 18-24℃ but that higher temperatures depressed tiller production and seed yield. Pol et al. [33] suggested that perenniality could enable perennial grasses to make large reproductive investments despite harsh environmental conditions. However, little is known about the year-to-year variation in seed yield of L. chinensis growing in a finite space within the same habitat [34,35]. ...
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... Usually, both dormant and non-dormant seeds are present in soil seed banks and consequently increases the chances of species persistence by synchronizing the germination timing with favorable seasons or in the absence of enough seed production during a particular year [17][18][19]. Since seed production in the desert is usually inconsistent and low due to scanty and irregular rainfall events [20,21], understanding the ability of desert species to form a soil seed bank could be important for designing restoration and conservation plans. Here the natural vegetation has been already degraded as a result of several factors such as overgrazing, off-road driving, and camping [22]. ...
... Additionally, retaining dormancy could promote species persistence under desert conditions by assisting in (i) synchronizing the germination timing with favorable seasons, (ii) the formation of seedbanks, and (iii) reducing the competition for resources (i.e., nutrients and water) at the seedling proliferation stage [51,54]. Generally, seed production in deserts is erratic and low due to scanty and irregular rainfall events [21]; therefore, forming seed banks could be the adaptation strategy to survive under such conditions, especially when the production of seeds may be reduced for long periods. Moreover, the lower germination of fresh seeds has been suggested as a survival strategy that ensures species persistence by the formation of soil seed banks, even with the repeated droughts that usually occur in desert environments [55,56]. ...
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... Continuous and extensive grazing causes minor changes in the cover and structure of woody vegetation, but it significantly reduces the cover and seed abundance of herbaceous species, especially perennial grasses consumed by livestock (Gonnet, 2001;Marone et al., 2017;Pol et al., 2014Pol et al., , 2017Sagario et al., 2020). In addition, high rainfall variability is associated with inter-annual changes in herbaceous plant cover and seed production, resulting in marked temporal fluctuations in the abundance and composition of the soil seed bank (Blendinger & Ojeda, 2001;Marone & Pol, 2021;Pol et al., 2010). The combined effect of grazing and rainfall variability may further reduce the availability of seeds in the soil bank, particularly of perennial grasses that are highly consumed and preferred by granivorous ants (Marone & Pol, 2021;Pirk, di Pasquo, & Lopez de Casenave, 2009;Pirk & Lopez de Casenave, 2006. ...
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... The findings for MaxEnt indicated that the precipitation of the warmest quarter (Bio 18) had the greatest effect on the distribution of all Meconopsis species amongst the 11 environmental variables involved in modeling, and this is consistent with our previous study in Minjiang headwater region [42]. Since precipitation can affect plant growth, morphology, phenology, and biomass accumulation [62][63][64][65][66], in particular for seedling emergence and establishment [67], an appropriate degree of precipitation can supply sufficient water and promote plant growth; however, excessive rainfall can deteriorate the soil permeability [68], creating an anaerobic environment that inhibits the regular respiration of roots [69], and limits plant growth and development by influencing their metabolism [70]. Moreover, waterlogging can also cause stomata to close and photosynthesis to decrease, and increases the energy consumption for respiration, affecting the accumulation of organic matter [71]. ...
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Meconopsis punicea is an iconic ornamental and medicinal plant whose natural habitat has degraded under global climate change, posing a serious threat to the future survival of the species. Therefore, it is critical to analyze the influence of climate change on possible distribution of M. punicea for conservation and sustainable utilization of this species. In this study, we used MaxEnt ecological niche modeling to predict the potential distribution of M. punicea under current and future climate scenarios in the southeastern margin region of Qinghai-Tibet Plateau. Model projections under current climate show that 16.8% of the study area is suitable habitat for Meconopsis. However, future projections indicate a sharp decline in potential habitat for 2050 and 2070 climate change scenarios. Soil type was the most important environmental variable in determining the habitat suitability of M. punicea, with 27.75% contribution to model output. Temperature seasonality (16.41%), precipitation of warmest quarter (14.01%), and precipitation of wettest month (13.02%), precipitation seasonality (9.41%) and annual temperature range (9.24%) also made significant contributions to model output. The mean elevation of suitable habitat for distribution of M. punicea is also likely to shift upward in most future climate change scenarios. This study provides vital information for the protection and sustainable use of medicinal species like M. punicea in the context of global environmental change. Our findings can aid in developing rational, broad-scale adaptation strategies for conservation and management for ecosystem services, in light of future climate changes.
... This can be explained by the annual die-off of the aboveground parts of Poaceae, whereas of the members of Asteraceae and Amaranthaceae are perennials (shrubs and trees). It has been reported annual parts of plants are less able to adapt to droughts during vegetation periods compared to perennial ones, which store chemical elements (Cleland et al. 2013;Pol et al. 2010). Thus, with climate desiccation, plants invest more heavily not in the biomass of annual parts (Bonser and Aarssen 2006;Van Kleunen 2007), but rather in accelerating reproductive maturation to produce seeds before the end of the favourable period (Franks et al. 2007;Hall and Willis 2006). ...
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... Pappophorum spp. Produces twice as much seeds in humid than in dry years (Pol et al., 2010). However, Pol et al. (2010) also reported that among seven warm-season perennial grass species, Trichloris crinita was the only one that significantly produced more seed in a dry than in a humid year in the region of the Central Monte in Argentina. ...
... Produces twice as much seeds in humid than in dry years (Pol et al., 2010). However, Pol et al. (2010) also reported that among seven warm-season perennial grass species, Trichloris crinita was the only one that significantly produced more seed in a dry than in a humid year in the region of the Central Monte in Argentina. ...
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Arid zones, where native rangelands are common, are essentials for millions of people livelihood. These areas support 50% of the world's livestock and are where 44% of the world's food is grown. In rangelands of Central Argentina, Pappophorum vaginatum is basically the unique, warm-season perennial grass species palatable to grazing livestock. Our major objective was to determine variability in reproductive characteristics among four spontaneous, overgrazed populations (i.e., P1, P2, P3, P4) of that species to identify promissory materials for domestication. Studies were conducted during three consecutive growing seasons within the southwestern part of the Phytogeographical Province of the Monte, in southwestern Buenos Aires, Argentina. Measured reproductive characteristics were related to flowering initiation, seed production and natural reseeding potential. Significant differences were found for flowering initiation and natural reseeding potential, but not for viable anthecia per plant among the four populations of P. vaginatum. This species fructified from the beginning to the end of the studied growing seasons with a great anthecia production per plant. The light weight of these anthecia and their awns would favor a great wind dispersal and most likely the establishment of new seedlings of P. vaginatum. This suggests that sexual reproduction might have a relatively greater importance than asexual reproduction (i.e., tillering) in the persistence of the overgrazed P. vaginatum in the plant communities of the studied region. Selection of plant materials with a late flowering initiation will allow to extend the forage production of a better quality. The variability among and within populations found on this study support the idea that would be promissory to start selection programs to obtain improved germplasm to reincorporate to grasslands of the south of the Phytogeographical Region of the Monte (Argentina) not only to increase livestock production but to recover and maintain biodiversity.
... Such full and rapid recovery of grassland communities was often triggered by an increase in the abundance of nonnative plants (Valliere et al., 2017;Xu et al., 2017b). We also found evidence for a population decline of species during an extreme event followed by either over- (Pol et al., 2010) or underrecovery (Rondeau et al., 2013;Zwicke et al., 2013). ...