scholarly journals Sinks for Plant Surplus Carbon Explain Several Ecological Phenomena

Author(s):  
Cindy E. Prescott

Abstract Plants engage in many processes and relationships that appear to be wasteful of the high-energy compounds that they produce through carbon fixation and photosynthesis. For example, living trees keep leafless tree stumps alive (i.e. respiring) and support shaded understory trees by sharing carbohydrates through root grafts or mycorrhizal fungal networks. Plants exude a variety of organic compounds from their roots and leaves, which support abundant rhizosphere and phyllosphere microbiomes. Some plants release substantial amounts of sugar via extra-floral nectaries, which enrich throughfall and alter lichen communities beneath the canopy. Large amounts of photosynthetically fixed carbon are transferred to root associates such as mycorrhizal fungi and N-fixing micro-organisms. In roots, some fixed C is respired through an alternative non-phosphorylating pathway that oxidizes excess sugar. Each of these processes is most prevalent when plants are growing under mild-to-moderate deficiencies or nutrients or water, or under high light or elevated atmospheric CO2. Under these conditions, plants produce more fixed carbon than they can use for primary metabolism and growth, and so have ‘surplus carbon’. To prevent cellular damage, these compounds must be transformed into other compounds or removed from the leaf. Each of the above phenomena represents a potential sink for these surplus carbohydrates. The fundamental ‘purpose’ of these phenomena may therefore be to alleviate the plant of surplus fixed C.

2008 ◽  
Vol 25 (2) ◽  
pp. 66-72 ◽  
Author(s):  
Kevin Lewis ◽  
Brian McCarthy

Abstract Tree-of-heaven (Ailanthus altissima Miller [Swingle]) can be managed easily with herbicide injection. However, the potential herbicide translocation to neighboring trees must be evaluated before widespread recommendations for herbicide injections. We assessed the nontargettranslocation of imazapyr (Arsenal), an herbicide commonly used to manage woody vegetation in forests, from injected tree-of-heaven to neighboring noninjected stems. Targeted imazapyr injections not only killed all injected tree-of-heaven, but also killed 17.5% of neighboring (within 3 m) noninjected tree-of-heaven and eight other tree species 62 weeks after treatment. Nontarget mortality from herbicide translocation decreased as the distance from injected tree-of-heaven increased (up to 3 m) and as stem diameter of noninjected plants increased. The plausible modes ofinter- and intraspecific herbicide translocation include root grafts, mutually shared mycorrhizal fungi, root exudation and absorption, and/or leaf senescence. Because tree-of-heaven is clonal, patch size and vegetation heterogeneity will be an important determinant of herbicide injectionprotocols. In forest environments with many small patches (i.e., high edge to interior ratio) or mixed species stands, nontarget hardwoods are at an increased risk of mortality. In isolated large patches (with lower edge to interior ratio) or dense monospecific clones, injection risk to nontarget species will be relatively low.


1983 ◽  
Vol 244 (3) ◽  
pp. H328-H334
Author(s):  
S. W. Schaffer ◽  
K. P. Burton ◽  
H. P. Jones ◽  
H. H. Oei

The effect of several phenothiazines on the extent of cellular damage resulting from the calcium paradox was examined. Hearts treated with trifluoperazine, a potent calmodulin inhibitor, exhibited less cellular damage than untreated myocardium as reflected by light microscopy, high-energy phosphate content and the loss of protein and creatine phosphokinase into the perfusate. A dose response of this effect revealed a maximal response at about 1 microM trifluoperazine, a concentration which lies well within the range generally attributed to calmodulin inhibition. Several other lines of evidence were also obtained suggesting a possible role for calmodulin in calcium-overload induced necrosis. First, the phenothiazines had little influence on membrane changes believed responsible for altered calcium permeability. Second, trifluoperazine was without major effect unless included in the reperfusion buffer, indicating that the drug is only effective during the phase associated with calcium overload. Finally, less protection was afforded hearts exposed to phenothiazines such as chlorpromazine and promethazine, which are weaker inhibitors of calmodulin, than those treated with the potent inhibitor trifluoperazine. While other interpretations are possible, these studies are consistent with a role for calmodulin in calcium overload-induced heart failure.


2002 ◽  
Vol 1 (4) ◽  
pp. 295-304 ◽  
Author(s):  
Lynn J. Rothschild ◽  
Lorraine J. Giver

The discovery of subsurface communities has encouraged speculation that such communities might be present on planetary bodies exposed to harsh surface conditions, including the early Earth. While the astrobiology community has focused on the deep subsurface, near-subsurface environments are unique in that they provide some protection while allowing partial access to photosynthetically active radiation. Previously we identified near-surface microbial communities based on photosynthesis. Here we assess the productivity of such an ecosystem by measuring in situ carbon fixation rates in an intertidal marine beach through a diurnal cycle, and find them surprisingly productive. Gross fixation along a transect (99×1 m) perpendicular to the shore was highly variable and depended on factors such as moisture and mat type, with a mean of ~41 mg C fixed m−2 day−1. In contrast, an adjacent well-established cyanobacterial mat dominated by Lyngbya aestuarii was ~12 times as productive (~500 mg C fixed m−2 day−1). Measurements made of the Lyngbya mat at several times per year revealed a correlation between total hours of daylight and gross daily production. From these data, annual gross fixation was estimated for the Lyngbya mat and yielded a value of ~1.3×105 g m−2 yr−1. An analysis of pulse-chase data obtained in the study in conjunction with published literature on similar ecosystems suggests that subsurface interstitial mats may be an overlooked endogenous source of organic carbon, mostly in the form of excreted fixed carbon.


2019 ◽  
Vol 31 (3) ◽  
pp. 123-132 ◽  
Author(s):  
Trista J. Vick-Majors ◽  
John C. Priscu

AbstractInorganic carbon fixation, usually mediated by photosynthetic microorganisms, is considered to form the base of the food chain in aquatic ecosystems. In high-latitude lakes, lack of sunlight owing to seasonal solar radiation limits the activity of photosynthetic plankton during the polar winter, causing respiration-driven demand for carbon to exceed supply. Here, we show that inorganic carbon fixation in the dark, driven by organisms that gain energy from chemical reactions rather than sunlight (chemolithoautotrophs), provides a significant influx of fixed carbon to two permanently ice-covered lakes (Fryxell and East Bonney). Fryxell, which has higher biomass per unit volume of water, had higher rates of inorganic dark carbon fixation by chemolithoautotrophs than East Bonney (trophogenic zone average 1.0 µg C l−1 d−1vs 0.08 µg C l−1 d−1, respectively). This contribution from dark carbon fixation was partly due to the activity of ammonia oxidizers, which are present in both lakes. Despite the potential importance of new carbon input by chemolithoautotrophic activity, both lakes remain net heterotrophic, with respiratory demand for carbon exceeding supply. Dark carbon fixation increased the ratio of new carbon supply to respiratory demand from 0.16 to 0.47 in Fryxell, and from 0.14 to 0.22 in East Bonney.


Metabolites ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 335 ◽  
Author(s):  
Sukhmanpreet Kaur ◽  
Vidya Suseela

Arbuscular mycorrhizal fungi (AMF) is among the most ubiquitous plant mutualists that enhance plant growth and yield by facilitating the uptake of phosphorus and water. The countless interactions that occur in the rhizosphere between plants and its AMF symbionts are mediated through the plant and fungal metabolites that ensure partner recognition, colonization, and establishment of the symbiotic association. The colonization and establishment of AMF reprogram the metabolic pathways of plants, resulting in changes in the primary and secondary metabolites, which is the focus of this review. During initial colonization, plant–AMF interaction is facilitated through the regulation of signaling and carotenoid pathways. After the establishment, the AMF symbiotic association influences the primary metabolism of the plant, thus facilitating the sharing of photosynthates with the AMF. The carbon supply to AMF leads to the transport of a significant amount of sugars to the roots, and also alters the tricarboxylic acid cycle. Apart from the nutrient exchange, the AMF imparts abiotic stress tolerance in host plants by increasing the abundance of several primary metabolites. Although AMF initially suppresses the defense response of the host, it later primes the host for better defense against biotic and abiotic stresses by reprogramming the biosynthesis of secondary metabolites. Additionally, the influence of AMF on signaling pathways translates to enhanced phytochemical content through the upregulation of the phenylpropanoid pathway, which improves the quality of the plant products. These phytometabolome changes induced by plant–AMF interaction depends on the identity of both plant and AMF species, which could contribute to the differential outcome of this symbiotic association. A better understanding of the phytochemical landscape shaped by plant–AMF interactions would enable us to harness this symbiotic association to enhance plant performance, particularly under non-optimal growing conditions.


2000 ◽  
Vol 27 (6) ◽  
pp. 507 ◽  
Author(s):  
Charlotte E. Lewis ◽  
Graham Noctor ◽  
David Causton ◽  
Christine H. Foyer

Concepts of the regulation of assimilate partitioning in leaves frequently consider only the allocation of carbon between sucrose and starch synthesis, storage and export. While carbohydrate metabolism accounts for a large proportion of assimilated carbon, such analyses provide only a restricted view of carbon metabolism and partitioning in leaf cells since photosynthetic carbon fixation provides precursors for all other biosynthetic pathways in the plant. Most of these precursors are required for biosynthesis of amino acids that form the building blocks for many compounds in plants. We have used leaf carbon : nitrogen ratios to calculate the allocation of photosynthetic electrons to the assimilation of nitrogen necessary for amino acid formation, and conclude that this allocation is variable but may be higher than values often quoted in the literature. Respiration is a significant fate of fixed carbon. In addition to supplying biosynthetic precursors, respiration is required for energy production and may also act, in both light and dark, to balance cellular energy budgets. We have used growth CO2 concentration and irradiance to modify source activity in Lolium temulentum in order to explore the interactions between photosynthetic carbon and nitrogen assimilation, assimilate production, respiration and export. It is demonstrated that there is a robust correlation between source activity and foliar respiration rates. Under some conditions concomitant increases in source activity and respiration may be necessary to support faster growth. In other conditions, increases in respiration appear to result from internal homeostatic mechanisms that may be candidate targets for increasing yield.


1984 ◽  
Vol 222 (1227) ◽  
pp. 215-230 ◽  

Colony morphology, rates of production and respiration, translocation of carbon from symbiotic algae to host, and the daily contribution of carbon fixed by zooxanthellae to animal respiration demands (CZAR) in phenotypes of Stylophora pistillata from 3 and 35 m were compared. Corals from 35 m showed an increase in branch density, a decrease in zooxanthellae density, and an increase in chlorophyll a per algal cell when compared to colonies from 3m. These changes are explained as adaptations to limited photosynthetically active radiation at the deeper depth. Photosynthetic efficiency was higher at 35 m, as evidenced by a production rate 25% that at 3 m, but with light only about 8% that of shallow water irradiance. Respiration of deeper corals decreased by a half. A depth-specific respiratory decline was displayed by both the algae and the animal fractions. Decreased coral animal respiration appears to be a direct function of decreased photosynthetically fixed carbon availability, and to be an immediate response to daily carbon input. Decreased carbon availability to the host animal at 35 m was a consequence of both decreased net carbon fixation and decreased percentage of net fixed carbon translocated to the host. The daily CZAR at 35 m was less than half that at 3m. Mean CZAR at 35 m was 78%, suggesting that deeper corals have an obligate requirement for heterotrophically obtained carbon. By contrast, corals from 3m, which displayed a mean CZAR of 157%, appeared to be photo trophic with respect to carbon required for respiration. Altered trophic strategies with depth were confirmed by daily carbon budgets calculated for average size corals from both depths. Multiple correlation tests of all parameters confirmed the utility of expressing production and respiration measures in terms of unit surface area. However, significant correlations with other normalizing parameters were found, and their usefulness discussed.


2013 ◽  
Vol 164 (2) ◽  
pp. 100-109 ◽  
Author(s):  
Min Zhang ◽  
Rongrong Zhu ◽  
Mingfeng Zhang ◽  
Bo Gao ◽  
Dongmei Sun ◽  
...  

2021 ◽  
Vol 11 ◽  
Author(s):  
Chikae Tatsumi ◽  
Fujio Hyodo ◽  
Takeshi Taniguchi ◽  
Weiyu Shi ◽  
Keisuke Koba ◽  
...  

Nitrogen (N) is an essential plant nutrient, and plants can take up N from several sources, including via mycorrhizal fungal associations. The N uptake patterns of understory plants may vary beneath different types of overstory trees, especially through the difference in their type of mycorrhizal association (arbuscular mycorrhizal, AM; or ectomycorrhizal, ECM), because soil mycorrhizal community and N availability differ beneath AM (non-ECM) and ECM overstory trees (e.g., relatively low nitrate content beneath ECM overstory trees). To test this hypothesis, we examined six co-existing AM-symbiotic understory tree species common beneath both AM-symbiotic black locust (non-ECM) and ECM-symbiotic oak trees of dryland forests in China. We measured AM fungal community composition of roots and natural abundance stable isotopic composition of N (δ15N) in plant leaves, roots, and soils. The root mycorrhizal community composition of understory trees did not significantly differ between beneath non-ECM and ECM overstory trees, although some OTUs more frequently appeared beneath non-ECM trees. Understory trees beneath non-ECM overstory trees had similar δ15N values in leaves and soil nitrate, suggesting that they took up most of their nitrogen as nitrate. Beneath ECM overstory trees, understory trees had consistently lower leaf than root δ15N, suggesting they depended on mycorrhizal fungi for N acquisition since mycorrhizal fungi transfer isotopically light N to host plants. Additionally, leaf N concentrations in the understory trees were lower beneath ECM than the non-ECM overstory trees. Our results show that, without large differences in root mycorrhizal community, the N uptake patterns of understory trees vary between beneath different overstory trees.


2020 ◽  
Vol 5 (6) ◽  
Author(s):  
Waleed Fouad Abobatta

Plant stimulants is an organic substance and micro-organisms, used by small quantities, Biostimulants categorize according to their nature, modes of action, and types of effects on crops, there are main groups of plant stimulants include Protein hydrolysates, Humate substances, Seaweed extracts, Biopolymers (Chitosan and other polymers), and Microbial biostimulants like mycorrhizal, non-mycorrhizal fungi, Rhizobium, and Trichoderma. Horticulture crop production facing several challenges particularly abiotic stresses and malnutrition resulting in yield loss and affects negatively fruit quality. The main effects of plant stimulants due to its working as the auxin-like effect, enhancing Nitrogen uptake, and stimulate plant growth. There is various stimulation effects on horticulture crops including promote plant growth, increase plant tolerance for biotic and abiotic stresses. Applying plant stimulants to plants or the rhizosphere stimulating plant metabolic processes, increase the efficiency of the nutrients, and increase plant tolerance to abiotic stress, consequently, improving plant growth increases yield, and enhancing fruit quality.


Sign in / Sign up

Export Citation Format

Share Document