Carbon allocation, osmotic adjustment, antioxidant capacity and growth in cotton under long-term soil drought during flowering and boll-forming period

2016 ◽  
Vol 107 ◽  
pp. 137-146 ◽  
Author(s):  
Rui Wang ◽  
Min Gao ◽  
Shu Ji ◽  
Shanshan Wang ◽  
Yali Meng ◽  
...  
2018 ◽  
Vol 373 (1760) ◽  
pp. 20170315 ◽  
Author(s):  
Cleiton B. Eller ◽  
Lucy Rowland ◽  
Rafael S. Oliveira ◽  
Paulo R. L. Bittencourt ◽  
Fernanda V. Barros ◽  
...  

The current generation of dynamic global vegetation models (DGVMs) lacks a mechanistic representation of vegetation responses to soil drought, impairing their ability to accurately predict Earth system responses to future climate scenarios and climatic anomalies, such as El Niño events. We propose a simple numerical approach to model plant responses to drought coupling stomatal optimality theory and plant hydraulics that can be used in dynamic global vegetation models (DGVMs). The model is validated against stand-scale forest transpiration ( E ) observations from a long-term soil drought experiment and used to predict the response of three Amazonian forest sites to climatic anomalies during the twentieth century. We show that our stomatal optimization model produces realistic stomatal responses to environmental conditions and can accurately simulate how tropical forest E responds to seasonal, and even long-term soil drought. Our model predicts a stronger cumulative effect of climatic anomalies in Amazon forest sites exposed to soil drought during El Niño years than can be captured by alternative empirical drought representation schemes. The contrasting responses between our model and empirical drought factors highlight the utility of hydraulically-based stomatal optimization models to represent vegetation responses to drought and climatic anomalies in DGVMs. This article is part of a discussion meeting issue ‘The impact of the 2015/2016 El Niño on the terrestrial tropical carbon cycle: patterns, mechanisms and implications’.


2021 ◽  
Vol 2021 ◽  
pp. 1-22
Author(s):  
Xiaohan Yang ◽  
Degao Liu ◽  
Haiwei Lu ◽  
David J. Weston ◽  
Jin-Gui Chen ◽  
...  

A grand challenge facing society is climate change caused mainly by rising CO2 concentration in Earth’s atmosphere. Terrestrial plants are linchpins in global carbon cycling, with a unique capability of capturing CO2 via photosynthesis and translocating captured carbon to stems, roots, and soils for long-term storage. However, many researchers postulate that existing land plants cannot meet the ambitious requirement for CO2 removal to mitigate climate change in the future due to low photosynthetic efficiency, limited carbon allocation for long-term storage, and low suitability for the bioeconomy. To address these limitations, there is an urgent need for genetic improvement of existing plants or construction of novel plant systems through biosystems design (or biodesign). Here, we summarize validated biological parts (e.g., protein-encoding genes and noncoding RNAs) for biological engineering of carbon dioxide removal (CDR) traits in terrestrial plants to accelerate land-based decarbonization in bioenergy plantations and agricultural settings and promote a vibrant bioeconomy. Specifically, we first summarize the framework of plant-based CDR (e.g., CO2 capture, translocation, storage, and conversion to value-added products). Then, we highlight some representative biological parts, with experimental evidence, in this framework. Finally, we discuss challenges and strategies for the identification and curation of biological parts for CDR engineering in plants.


Author(s):  
Daniel G. Milchunas ◽  
William K. Lauenroth

Although livestock are the most obvious consumers on the shortgrass steppe, they are certainly not the only consumers. However, livestock may influence the other consumers in a number of different ways. They may directly compete for food resources with other aboveground herbivores. There is behavioral interference between livestock and some species of wildlife (Roberts and Becker, 1982), but not others (Austin and Urness, 1986). The removal of biomass by livestock alters canopy structure (physiognomy) and influences microclimate. Bird, small-mammal, and insect species can be variously sensitive to these structural alterations (Brown, 1973; Cody, 1985; MacArthur, 1965; Morris, 1973; Rosenzweig et al., 1975; Wiens, 1969). There are both short- and long-term effects of grazing on plant community species composition, primary production, and plant tissue quality. Belowground consumers can also be affected by the effects of grazing on soil water infiltration, nutrient cycling, carbon allocation patterns of plants, litter accumulation, and soil temperature. The overall effects of livestock on a particular component of the native fauna can be negative or can be positive through facilitative relationships (Gordon, 1988). In this chapter we assess the effects of cattle grazing on other above- and belowground consumers, on the diversity and relative sensitivity of these groups of organisms, and on their trophic structure. We first present some brief background information on plant communities of the shortgrass steppe and on the long-term grazing treatments in which many of the studies reported herein were conducted. Details on the plant communities are presented by Lauenroth in chapter 5 (this volume), grazing effects on plant communities by Milchunas et al. in chapter 16 (this volume); and grazing effects on nutrient distributions and cycling by Burke et al. in chapter 13 (this volume). The physiognomy of the shortgrass steppe is indicated in its name. The dominant grasses (Bouteloua gracilis and Buchloë dactyloides), forb (Sphaeralcea coccinea), and carex (Carex eleocharis) have the majority of their leaf biomass within 10 cm of the ground surface. A number of less abundant midheight grasses and dwarf shrubs are sparsely interspersed among the short vegetation, but usually much of their biomass is within 25 cm of the g round. Basal cover of vegetation typically totals 25% to 35%, and is greater in long-term grazed than in ungrazed grassland. Bare ground (more frequent on grazed sites) and litter-covered ground (more frequent on ungrazed sites) comprise the remainder of the soil surface (Milchunas et al., 1989).


2019 ◽  
Vol 44 (1) ◽  
Author(s):  
Fayçal Boughalleb ◽  
Maher Mahmoudi ◽  
Raoudha Abdellaoui ◽  
Boutheina Yahia ◽  
Slah Zaidi ◽  
...  

2009 ◽  
Vol 64 (2) ◽  
pp. 102-107 ◽  
Author(s):  
Jara Pérez-Jiménez ◽  
José Serrano ◽  
Maria Tabernero ◽  
Sara Arranz ◽  
M. Elena Díaz-Rubio ◽  
...  

2010 ◽  
Vol 158 (8) ◽  
pp. 2604-2609 ◽  
Author(s):  
Christian P. Andersen ◽  
Wilma Ritter ◽  
Jillian Gregg ◽  
Rainer Matyssek ◽  
Thorsten E.E. Grams

2021 ◽  
Author(s):  
Leonie Schönbeck ◽  
Charlotte Grossiord ◽  
Arthur Gessler ◽  
Jonas Gisler ◽  
Katrin Meusburger ◽  
...  

SummaryThe future climate will be characterized by an increase in frequency and duration of drought and warming that exacerbates atmospheric evaporative demand. How trees acclimate to long-term soil moisture changes and whether these long-term changes alter trees’ sensitivity to short-term (day to months) variations of vapor pressure deficit (VPD) and soil moisture is largely unknown.Leaf gas exchange measurements were performed within a long-term (17 years) irrigation experiment in a Scots pine-dominated forest in one of Switzerland’s driest areas on trees in naturally dry (control), irrigated, and‘irrigation-stop’ (after 11 years of irrigation) conditions.Seventeen years of irrigation increased photosynthesis (A) and stomatal conductance (gs) and reduced the gs sensitivity to increasing VPD but not to soil drying. Following irrigation-stop, gas exchange did not decrease immediately, but after three years, had decreased significantly in irrigation-stop trees. Vcmax and Jmax recovered after five years.These results suggest that long-term release of soil drought reduces the sensitivity to atmospheric evaporative demand and that atmospheric constraints may play an increasingly important role in combination with soil drought. In addition, they suggest that structural adjustments lead to an attenuation of initially strong leaf-level acclimation to strong multiple-year drought.


2015 ◽  
Vol 69 (5) ◽  
pp. 469-483 ◽  
Author(s):  
Marijana Sakac ◽  
Ivana Sedej ◽  
Anamarija Mandic ◽  
Aleksandra Misan

Buckwheat is grown primarily because of its grain which, after undergoing the processes of dehulling, grinding and sieving, is used to produce buckwheat flour which is characterized by a considerable content of antioxidants, especially polyphenols and tocopherols. Buckwheat polyphenols are represented by phenolic acids and flavonoids, mainly rutin, a proven potent antioxidant. The content of polyphenols and tocopherols in buckwheat grain primarily depends on the buckwheat species, growing area, climate and growing conditions. Common buckwheat (Fagopyrum esculentum M?ench), which is often used for the production of light and wholegrain buckwheat flour, contains less polyphenols than tartary buckwheat. The content of polyphenols in common buckwheat grain varies depending on the grain part. As their largest amount is contained in the hull and the outer layers of the grain, the wholegrain buckwheat flour is superior in polyphenols than the light buckwheat flour. Therefore, the wholegrain buckwheat flour is characterized by a higher antioxidant capacity. Polyphenols in buckwheat flour exist in free and bound forms, where the contribution of free polyphenols ranges between 48-64%. Due to a relatively high content of antioxidants in light and wholegrain buckwheat flour, they are used for substitution of wheat or other cereal flours in bakery, pasta and confectionary formulations in order to create either added value or gluten-free products. The aim of a long-term consumption of buckwheat flours is to achieve health benefits and protect from many chronic diseases. Technological procedures and some treatments used during the food preparation influence polyphenol composition and content and consequently the functionality of food. Therefore, in order to minimize polyphenol losses and preserve the antioxidant capacity of the final products it is necessary to understand the thermal treatments and their mechanisms.


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