Advances in Plant Sulfur Research

A special issue of Plants (ISSN 2223-7747).

Deadline for manuscript submissions: closed (1 March 2019) | Viewed by 51936

Printed Edition Available!
A printed edition of this Special Issue is available here.

Special Issue Editors


E-Mail Website
Guest Editor
Plant Physiology Laboratory, Crop Science Department, Agricultural University of Athens, Iera Odos 75, 11855 Athens, Greece
Interests: plant physiology; plant nutrition physiology; sulfur physiology; sulfur nutrition; sulfur use efficiency; fertilization with sulfur-containing fertilizers; sulfur interactions with iron, nitrogen, and phosphorus, focusing on graminaceous species
Special Issues, Collections and Topics in MDPI journals
Institute for Crop and Soil Science, Julius Kühn-Institut (JKI), Federal Research Centre for Cultivated Plants, Bundesallee 69 (Gebäude 250), D-38116 Braunschweig, Germany
Interests: sulfur nutrition; glucosinolates; sulfur-containing metabolites; gaseous S compounds; hydrogensulfide; cysteine; glutathione; biotic stress; abiotic stress; sulfur and fungal pathogens; medicinal plants

E-Mail Website
Guest Editor
Department of Agronomy Food Natural resources Animals and Environment, University of Padova, Agripolis, 35020 Legnaro PD, Italy
Interests: plant physiology; plant nutrition; sulfur nutrition; sulfur and abiotic stresses; sulfur fertilization; sulfur and tolerance to heavy metals; sulfur in grapevine cultivation
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
UMR INRA-UCBN 950 Ecophysiologie Végétale, Agronomie & Nutritions N.C.S., UFR des Sciences, FED 4277 Normandie Végétal, Université de Caen Normandie, F-14032 Caen, France
Interests: nutrient use efficiency; plant nutrition; nitrogen and sulfur fertilization; plant responses to abiotic stress; plant senescence; seed quality; remobilization of nutrients; proteolytic mechanisms

Special Issue Information

Dear Colleagues,

Sulfur is an essential nutrient required for plant growth and development, therefore sulfur containing fertilizers are nowadays used worldwide to increase crop yield and quality. Crops can suffer from sulfur deficiency due to environmental protection and decreased emission of sulfur dioxide to the atmosphere which limited the availability of sulfate as input in the large scale agriculture. The emergence of sulfur deficiency in such productive systems attracted the scientific attention and triggered significant research interest. As a consequence, in the last 25 years a tremendous boost has taken place in all aspects of plant sulfur research. Milestones in this field include so far the central role of sulfate transporters in response to sulfur availability, sulfur as a part of plant metabolic network, sulfotranferases, impact of sulfur on N2 fixation of legumes, role of sulfur-compounds in abiotic and biotic stress tolerance, sulfur nutrition and assimilation in crop plants, sulfur interactions in crop ecosystems, sulfur in biotic interactions of plant, the concept of sulfur-induced-resistance, the molecular links between metals in the environment and plant sulfur metabolism, role of sulfate and sulfur-rich compounds in heavy metal tolerance and accumulation.

Despite the amazing amount of the rapidly accumulating information, there are still open questions and challenges on this fascinating field. For example, the regulation of gene expression in response to sulfur regime is an important aspect of sulfur metabolism in plants and it is still subject of intense research. On the other hand, S contributes to plant tolerance under stressful agricultural conditions. For instance, NO acts as a signal molecule and induces salt tolerance in plants by enhancing S assimilation and synthesis of S compounds and modulating the activity of antioxidant enzymes. Interactions between NO and S assimilation regulates GSH synthesis for the adaptation of plants to stressful environments. The physiological and molecular mechanisms with which NO induces S assimilation and how it interacts with other plant hormones and nutrients to achieve plant salt tolerance are among the open research topics.

Therefore, in this special issue articles (original research papers, perspectives, hypotheses, opinions, reviews, modeling approaches and methods) that focus on S metabolism and its regulation including biochemistry, physiology, genes, proteins, metabolites, nutrition and environment, at all levels comprising transcriptome, proteome, metabolome and epigenome studies, plant microbiome, sulfur use efficiency, sulfur interaction with nutrients and/or hormones, sulfur-status and plant health, senescence, whole plant studies, field trials and agronomics in model plants, crop plants, trees, aquatic plants and native species are most welcome.

Prof. Dr. Dimitris L. Bouranis
Prof. Dr. Mario Malagoli
Prof. Dr. Jean-Christophe Avice
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Plants is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • sulfur metabolism
  • regulation of sulfur metabolism
  • sulfur in signalling systems
  • sulfur deficiency
  • sulfur nutrition physiology
  • reactive sulfur species
  • sulfur use efficiency
  • sulfur uptake efficiency
  • sulfur utilization efficiency
  • sulfur remobilization
  • sulfur interactions

Published Papers (12 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Editorial

Jump to: Research

6 pages, 215 KiB  
Editorial
Advances in Plant Sulfur Research
by Dimitris L. Bouranis, Mario Malagoli, Jean-Christophe Avice and Elke Bloem
Plants 2020, 9(2), 256; https://doi.org/10.3390/plants9020256 - 17 Feb 2020
Cited by 25 | Viewed by 3668
Abstract
As an essential nutrient required for plant growth and development, sulfur (S) deficiency in productive systems limits yield and quality. This special issue hosts a collection of original research articles, mainly based on contributions from the 11th International Plant Sulfur Workshop held on [...] Read more.
As an essential nutrient required for plant growth and development, sulfur (S) deficiency in productive systems limits yield and quality. This special issue hosts a collection of original research articles, mainly based on contributions from the 11th International Plant Sulfur Workshop held on 16–20 September 2018 in Conegliano, Italy, focusing on the following topics: (1) The germinative and post-germinative behaviour of Brassica napus seeds when severe S limitation is applied to the parent plants; (2) the independence of S deficiency from the mRNA degradation initiation enzyme PARN in Arabidopsis; (3) the glucosinolate distribution in the aerial parts of sel1-10, a disruption mutant of the sulfate transporter SULTR1;2, in mature Arabidopsis thaliana plants; (4) the accumulation of S-methylcysteine as its γ-glutamyl dipeptide in Phaseolus vulgaris; and (5) the role of ferric iron chelation-strategy components in the leaves and roots of maize, have provided new insights into the effect of S availability on plant functionality. Moreover, the role of S deficiency in root system functionality has been highlighted, focusing on (6) the contribution of root hair development to sulfate uptake in Arabidopsis, and (7) the modulation of lateral root development by the CLE-CLAVATA1 signaling pathway under S deficiency. The role of S in plants grown under drought conditions has been investigated in more detail focusing (8) on the relationship between S-induced stomata closure and the canonical ABA signal transduction machinery. Furthermore, (9) the assessment of S deficiency under field conditions by single measurements of sulfur, chloride, and phosphorus in mature leaves, (10) the effect of fertilizers enriched with elemental S on durum wheat yield, and (11,12) the impact of elemental S on the rhizospheric bacteria of durum wheat contributed to enhance the scientific knowledge on S nutrition under field conditions. Full article
(This article belongs to the Special Issue Advances in Plant Sulfur Research)

Research

Jump to: Editorial

16 pages, 3698 KiB  
Article
The Recovery from Sulfur Starvation Is Independent from the mRNA Degradation Initiation Enzyme PARN in Arabidopsis
by Laura Armbruster, Veli Vural Uslu, Markus Wirtz and Rüdiger Hell
Plants 2019, 8(10), 380; https://doi.org/10.3390/plants8100380 - 27 Sep 2019
Cited by 3 | Viewed by 3275
Abstract
When plants are exposed to sulfur limitation, they upregulate the sulfate assimilation pathway at the expense of growth-promoting measures. Upon cessation of the stress, however, protective measures are deactivated, and growth is restored. In accordance with these findings, transcripts of sulfur-deficiency marker genes [...] Read more.
When plants are exposed to sulfur limitation, they upregulate the sulfate assimilation pathway at the expense of growth-promoting measures. Upon cessation of the stress, however, protective measures are deactivated, and growth is restored. In accordance with these findings, transcripts of sulfur-deficiency marker genes are rapidly degraded when starved plants are resupplied with sulfur. Yet it remains unclear which enzymes are responsible for the degradation of transcripts during the recovery from starvation. In eukaryotes, mRNA decay is often initiated by the cleavage of poly(A) tails via deadenylases. As mutations in the poly(A) ribonuclease PARN have been linked to altered abiotic stress responses in Arabidopsis thaliana, we investigated the role of PARN in the recovery from sulfur starvation. Despite the presence of putative PARN-recruiting AU-rich elements in sulfur-responsive transcripts, sulfur-depleted PARN hypomorphic mutants were able to reset their transcriptome to pre-starvation conditions just as readily as wildtype plants. Currently, the subcellular localization of PARN is disputed, with studies reporting both nuclear and cytosolic localization. We detected PARN in cytoplasmic speckles and reconciled the diverging views in literature by identifying two PARN splice variants whose predicted localization is in agreement with those observations. Full article
(This article belongs to the Special Issue Advances in Plant Sulfur Research)
Show Figures

Figure 1

21 pages, 4256 KiB  
Article
Impact of Elemental Sulfur on the Rhizospheric Bacteria of Durum Wheat Crop Cultivated on a Calcareous Soil
by Dimitris L. Bouranis, Anastasia Venieraki, Styliani N. Chorianopoulou and Panagiotis Katinakis
Plants 2019, 8(10), 379; https://doi.org/10.3390/plants8100379 - 27 Sep 2019
Cited by 19 | Viewed by 3421
Abstract
Previous experiments have shown that the application of fertilizer granules containing elemental sulfur (S0) as an ingredient (FBS0) in durum wheat crops produced a higher yield than that produced by conventional ones (F), provided that the soils of the [...] Read more.
Previous experiments have shown that the application of fertilizer granules containing elemental sulfur (S0) as an ingredient (FBS0) in durum wheat crops produced a higher yield than that produced by conventional ones (F), provided that the soils of the experimental fields (F vs. FBS0) were of comparable quality and with the Olsen P content of the field’s soil above 8 mg kg−1. In this experiment the FBS0 treatment took place in soil with Olsen P at 7.8 mg kg−1, compared with the F treatment’s soil with Olsen P of 16.8 mg kg−1, aiming at reducing the imbalance in soil quality. To assess and evaluate the effect of FBS0 on the dynamics of the rhizospheric bacteria in relation to F, rhizospheric soil at various developmental stages of the crops was collected. The agronomic profile of the rhizospheric cultivable bacteria was characterized and monitored, in connection with the dynamics of phosphorus, iron, organic sulfur, and organic nitrogen, in both the rhizosoil and the aerial part of the plant during development. Both crops were characterized by a comparable dry mass accumulation per plant throughout development, while the yield of the FBS0 crop was 3.4% less compared to the F crop’s one. The FBS0 crop’s aerial part showed a transient higher P and Fe concentration, while its organic N and S concentrations followed the pattern of the F crop. The incorporation of S0 into the conventional fertilizer increased the percentage of arylsulfatase (ARS)-producing bacteria in the total bacterial population, suggesting an enhanced release of sulfate from the soil’s organic S pool, which the plant could readily utilize. The proportion of identified ARS-producing bacteria possessing these traits exhibited a maximum value before and after topdressing. Phylogenetic analysis of the 68 isolated ARS-producing bacterial strains revealed that the majority of the isolates belonged to the Pseudomonas genus. A large fraction also possessed phosphate solubilization, and/or siderophore production, and/or ureolytic traits, thus improving the crop’s P, Fe, S, and N balance. The aforementioned findings imply that the used FBS0 substantially improved the quality of the rhizosoil at the available phosphorus limiting level by modulating the abundance of the bacterial communities in the rhizosphere and effectively enhancing the microbially mediated nutrient mobilization towards improved plant nutritional dynamics. Full article
(This article belongs to the Special Issue Advances in Plant Sulfur Research)
Show Figures

Figure 1

10 pages, 1993 KiB  
Article
An Exploration of the Roles of Ferric Iron Chelation-Strategy Components in the Leaves and Roots of Maize Plants
by Georgios Saridis, Styliani N. Chorianopoulou, Yannis E. Ventouris, Petros P. Sigalas and Dimitris L. Bouranis
Plants 2019, 8(5), 133; https://doi.org/10.3390/plants8050133 - 18 May 2019
Cited by 7 | Viewed by 3161
Abstract
Plants have developed sophisticated mechanisms for acquiring iron from the soil. In the graminaceous species, a chelation strategy is in charge, in order to take up ferric iron from the rhizosphere. The ferric iron chelation-strategy components may also be present in the aerial [...] Read more.
Plants have developed sophisticated mechanisms for acquiring iron from the soil. In the graminaceous species, a chelation strategy is in charge, in order to take up ferric iron from the rhizosphere. The ferric iron chelation-strategy components may also be present in the aerial plant parts. The aim of this work was to search for possible roles of those components in maize leaves. To this end, the expression patterns of ferric iron chelation-strategy components were monitored in the leaves and roots of mycorrhizal and non-mycorrhizal sulfur-deprived maize plants, both before and after sulfate supply. The two levels of sulfur supply were chosen due to the strong impact of this nutrient on iron homeostasis, whilst mycorrhizal symbiosis was chosen as a treatment that forces the plant to optimize its photosynthetic efficiency, in order to feed the fungus. The results, in combination with the findings of our previous works, suggest a role for the aforementioned components in ferric chelation and/or unloading from the xylem vessels to the aerial plant parts. It is proposed that the gene expression of the DMA exporter ZmTOM1 can be used as an early indicator for the establishment of a mycorrhizal symbiotic relationship in maize. Full article
(This article belongs to the Special Issue Advances in Plant Sulfur Research)
Show Figures

Figure 1

15 pages, 8888 KiB  
Article
Common Bean (Phaseolus vulgaris L.) Accumulates Most S-Methylcysteine as Its γ-Glutamyl Dipeptide
by Elham Saboori-Robat, Jaya Joshi, Aga Pajak, Mahmood Solouki, Motahhareh Mohsenpour, Justin Renaud and Frédéric Marsolais
Plants 2019, 8(5), 126; https://doi.org/10.3390/plants8050126 - 14 May 2019
Cited by 7 | Viewed by 3440
Abstract
The common bean (Phaseolus vulgaris) constitutes an excellent source of vegetable dietary protein. However, there are sub-optimal levels of the essential amino acids, methionine and cysteine. On the other hand, P. vulgaris accumulates large amounts of the γ-glutamyl dipeptide of S [...] Read more.
The common bean (Phaseolus vulgaris) constitutes an excellent source of vegetable dietary protein. However, there are sub-optimal levels of the essential amino acids, methionine and cysteine. On the other hand, P. vulgaris accumulates large amounts of the γ-glutamyl dipeptide of S-methylcysteine, and lower levels of free S-methylcysteine and S-methylhomoglutathione. Past results suggest two distinct metabolite pools. Free S-methylcysteine levels are high at the beginning of seed development and decline at mid-maturation, while there is a biphasic accumulation of γ-glutamyl-S-methylcysteine, at early cotyledon and maturation stages. A possible model involves the formation of S-methylcysteine by cysteine synthase from O-acetylserine and methanethiol, whereas the majority of γ-glutamyl-S-methylcysteine may arise from S-methylhomoglutathione. Metabolite profiling during development and in genotypes differing in total S-methylcysteine accumulation showed that γ-glutamyl-S-methylcysteine accounts for most of the total S-methylcysteine in mature seed. Profiling of transcripts for candidate biosynthetic genes indicated that BSAS4;1 expression is correlated with both the developmental timing and levels of free S-methylcysteine accumulated, while homoglutathione synthetase (hGS) expression was correlated with the levels of γ-glutamyl-S-methylcysteine. Analysis of S-methylated phytochelatins by liquid chromatography and high resolution tandem mass spectrometry revealed only small amounts of homophytochelatin-2 with a single S-methylcysteine. The mitochondrial localization of phytochelatin synthase 2—predominant in seed, determined by confocal microscopy of a fusion with the yellow fluorescent protein—and its spatial separation from S-methylhomoglutathione may explain the lack of significant accumulation of S-methylated phytochelatins. Full article
(This article belongs to the Special Issue Advances in Plant Sulfur Research)
Show Figures

Figure 1

14 pages, 1730 KiB  
Article
Contribution of Root Hair Development to Sulfate Uptake in Arabidopsis
by Yuki Kimura, Tsukasa Ushiwatari, Akiko Suyama, Rumi Tominaga-Wada, Takuji Wada and Akiko Maruyama-Nakashita
Plants 2019, 8(4), 106; https://doi.org/10.3390/plants8040106 - 19 Apr 2019
Cited by 20 | Viewed by 4133
Abstract
Root hairs often contribute to nutrient uptake from environments, but the contribution varies among nutrients. In Arabidopsis, two high-affinity sulfate transporters, SULTR1;1 and SULTR1;2, are responsible for sulfate uptake by roots. Their increased expression under sulfur deficiency (−S) stimulates sulfate uptake. Inspired [...] Read more.
Root hairs often contribute to nutrient uptake from environments, but the contribution varies among nutrients. In Arabidopsis, two high-affinity sulfate transporters, SULTR1;1 and SULTR1;2, are responsible for sulfate uptake by roots. Their increased expression under sulfur deficiency (−S) stimulates sulfate uptake. Inspired by the higher and lower expression, respectively, of SULTR1;1 in mutants with more (werwolf [wer]) and fewer (caprice [cpc]) root hairs, we examined the contribution of root hairs to sulfate uptake. Sulfate uptake rates were similar among plant lines under both sulfur sufficiency (+S) and −S. Under −S, the expression of SULTR1;1 and SULTR1;2 was negatively correlated with the number of root hairs. These results suggest that both −S-induced SULTR expression and sulfate uptake rates were independent of the number of root hairs. In addition, we observed (1) a negative correlation between primary root lengths and number of root hairs and (2) a greater number of root hairs under −S than under +S. These observations suggested that under both +S and −S, sulfate uptake was influenced by the root biomass rather than the number of root hairs. Full article
(This article belongs to the Special Issue Advances in Plant Sulfur Research)
Show Figures

Figure 1

11 pages, 1567 KiB  
Article
CLE-CLAVATA1 Signaling Pathway Modulates Lateral Root Development under Sulfur Deficiency
by Wei Dong, Yinghua Wang and Hideki Takahashi
Plants 2019, 8(4), 103; https://doi.org/10.3390/plants8040103 - 18 Apr 2019
Cited by 26 | Viewed by 4968
Abstract
Plant root system architecture changes drastically in response to availability of macronutrients in the soil environment. Despite the importance of root sulfur (S) uptake in plant growth and reproduction, molecular mechanisms underlying root development in response to S availability have not been fully [...] Read more.
Plant root system architecture changes drastically in response to availability of macronutrients in the soil environment. Despite the importance of root sulfur (S) uptake in plant growth and reproduction, molecular mechanisms underlying root development in response to S availability have not been fully characterized. We report here on the signaling module composed of the CLAVATA3 (CLV3)/EMBRYO SURROUNDING REGION (CLE) peptide and CLAVATA1 (CLV1) leucine-rich repeat receptor kinase, which regulate lateral root (LR) development in Arabidopsis thaliana upon changes in S availability. The wild-type seedlings exposed to prolonged S deficiency showed a phenotype with low LR density, which was restored upon sulfate supply. In contrast, the clv1 mutant showed a higher daily increase rate of LR density relative to the wild-type under prolonged S deficiency, which was diminished to the wild-type level upon sulfate supply, suggesting that CLV1 directs a signal to inhibit LR development under S-deficient conditions. CLE2 and CLE3 transcript levels decreased under S deficiency and through CLV1-mediated feedback regulations, suggesting the levels of CLE peptide signals are adjusted during the course of LR development. This study demonstrates a fine-tuned mechanism for LR development coordinately regulated by CLE-CLV1 signaling and in response to changes in S availability. Full article
(This article belongs to the Special Issue Advances in Plant Sulfur Research)
Show Figures

Figure 1

10 pages, 2061 KiB  
Article
Glucosinolate Distribution in the Aerial Parts of sel1-10, a Disruption Mutant of the Sulfate Transporter SULTR1;2, in Mature Arabidopsis thaliana Plants
by Tomomi Morikawa-Ichinose, Sun-Ju Kim, Alaa Allahham, Ryota Kawaguchi and Akiko Maruyama-Nakashita
Plants 2019, 8(4), 95; https://doi.org/10.3390/plants8040095 - 10 Apr 2019
Cited by 14 | Viewed by 3686
Abstract
Plants take up sulfur (S), an essential element for all organisms, as sulfate, which is mainly attributed to the function of SULTR1;2 in Arabidopsis. A disruption mutant of SULTR1;2, sel1-10, has been characterized with phenotypes similar to plants grown under sulfur deficiency [...] Read more.
Plants take up sulfur (S), an essential element for all organisms, as sulfate, which is mainly attributed to the function of SULTR1;2 in Arabidopsis. A disruption mutant of SULTR1;2, sel1-10, has been characterized with phenotypes similar to plants grown under sulfur deficiency (−S). Although the effects of −S on S metabolism were well investigated in seedlings, no studies have been performed on mature Arabidopsis plants. To study further the effects of −S on S metabolism, we analyzed the accumulation and distribution of S-containing compounds in different parts of mature sel1-10 and of the wild-type (WT) plants grown under long-day conditions. While the levels of sulfate, cysteine, and glutathione were almost similar between sel1-10 and WT, levels of glucosinolates (GSLs) differed between them depending on the parts of the plant. GSLs levels in the leaves and stems were generally lower in sel1-10 than those in WT. However, sel1-10 seeds maintained similar levels of aliphatic GSLs to those in WT plants. GSL accumulation in reproductive tissues is likely to be prioritized even when sulfate supply is limited in sel1-10 for its role in S storage and plant defense. Full article
(This article belongs to the Special Issue Advances in Plant Sulfur Research)
Show Figures

Figure 1

13 pages, 2015 KiB  
Article
Sulfate-Induced Stomata Closure Requires the Canonical ABA Signal Transduction Machinery
by Hala Rajab, Muhammad Sayyar Khan, Mario Malagoli, Rüdiger Hell and Markus Wirtz
Plants 2019, 8(1), 21; https://doi.org/10.3390/plants8010021 - 16 Jan 2019
Cited by 21 | Viewed by 7014
Abstract
Phytohormone abscisic acid (ABA) is the canonical trigger for stomatal closure upon abiotic stresses like drought. Soil-drying is known to facilitate root-to-shoot transport of sulfate. Remarkably, sulfate and sulfide—a downstream product of sulfate assimilation—have been independently shown to promote stomatal closure. For induction [...] Read more.
Phytohormone abscisic acid (ABA) is the canonical trigger for stomatal closure upon abiotic stresses like drought. Soil-drying is known to facilitate root-to-shoot transport of sulfate. Remarkably, sulfate and sulfide—a downstream product of sulfate assimilation—have been independently shown to promote stomatal closure. For induction of stomatal closure, sulfate must be incorporated into cysteine, which triggers ABA biosynthesis by transcriptional activation of NCED3. Here, we apply reverse genetics to unravel if the canonical ABA signal transduction machinery is required for sulfate-induced stomata closure, and if cysteine biosynthesis is also mandatory for the induction of stomatal closure by the gasotransmitter sulfide. We provide genetic evidence for the importance of reactive oxygen species (ROS) production by the plasma membrane-localized NADPH oxidases, RBOHD, and RBOHF, during the sulfate-induced stomatal closure. In agreement with the established role of ROS as the second messenger of ABA-signaling, the SnRK2-type kinase OST1 and the protein phosphatase ABI1 are essential for sulfate-induced stomata closure. Finally, we show that sulfide fails to close stomata in a cysteine-biosynthesis depleted mutant. Our data support the hypothesis that the two mobile signals, sulfate and sulfide, induce stomatal closure by stimulating cysteine synthesis to trigger ABA production. Full article
(This article belongs to the Special Issue Advances in Plant Sulfur Research)
Show Figures

Figure 1

13 pages, 1700 KiB  
Article
Germinative and Post-Germinative Behaviours of Brassica napus Seeds Are Impacted by the Severity of S Limitation Applied to the Parent Plants
by Philippe D’Hooghe, Dimitri Picot, Sophie Brunel-Muguet, Stanislav Kopriva, Jean-Christophe Avice and Jacques Trouverie
Plants 2019, 8(1), 12; https://doi.org/10.3390/plants8010012 - 05 Jan 2019
Cited by 5 | Viewed by 3901
Abstract
In oilseed rape (Brassica napus L.), sulphur (S) limitation leads to a reduction of seed yield and nutritional quality, but also to a reduction of seed viability and vigour. S metabolism is known to be involved in the control of germination sensu [...] Read more.
In oilseed rape (Brassica napus L.), sulphur (S) limitation leads to a reduction of seed yield and nutritional quality, but also to a reduction of seed viability and vigour. S metabolism is known to be involved in the control of germination sensu stricto and seedling establishment. Nevertheless, how the germination and the first steps of plant growth are impacted in seeds produced by plants subjected to various sulphate limitations remains largely unknown. Therefore, this study aimed at determining the impact of various S-limited conditions applied to the mother plants on the germination indexes and the rate of viable seedlings in a spring oilseed rape cultivar (cv. Yudal). Using a 34S-sulphate pulse method, the sulphate uptake capacity during the seedling development was also investigated. The rate of viable seedlings was significantly reduced for seeds produced under the strongest S-limited conditions. This is related to a reduction of germination vigour and to perturbations of post-germinative events. Compared to green seedlings obtained from seeds produced by well-S-supplied plants, the viable seedlings coming from seeds harvested on plants subjected to severe S-limitation treatment showed nonetheless a higher dry biomass and were able to enhance the sulphate uptake by roots and the S translocation to shoots. Full article
(This article belongs to the Special Issue Advances in Plant Sulfur Research)
Show Figures

Figure 1

15 pages, 1241 KiB  
Article
The Effect of Granular Commercial Fertilizers Containing Elemental Sulfur on Wheat Yield under Mediterranean Conditions
by Dimitris L. Bouranis, Dionisios Gasparatos, Bernd Zechmann, Lampros D. Bouranis and Styliani N. Chorianopoulou
Plants 2019, 8(1), 2; https://doi.org/10.3390/plants8010002 - 20 Dec 2018
Cited by 12 | Viewed by 4338
Abstract
The demand to develop fertilizers with higher sulfur use efficiency has intensified over the last decade, since sulfur deficiency in crops has become more widespread. The aim of this study was to investigate whether fertilizers enriched with 2% elemental sulfur (ES) via a [...] Read more.
The demand to develop fertilizers with higher sulfur use efficiency has intensified over the last decade, since sulfur deficiency in crops has become more widespread. The aim of this study was to investigate whether fertilizers enriched with 2% elemental sulfur (ES) via a binding material of organic nature improve yield when compared to the corresponding conventional ones. Under the scanning electron microscope, the granules of the ES-containing fertilizer were found to be covered by a layer of crystal-like particles, the width of which was found to be up to 60 μm. Such a layer could not be found on the corresponding conventional fertilizer granules. Several fertilization schemes with or without incorporated ES were tested in various durum wheat varieties, cultivated in commercial fields. The P-Olsen content of each commercial field was found to be correlated with the corresponding relative change in the yields (YF/YFBES) with a strong positive relationship. The content of 8 ppm of available soil phosphorus was a turning point. At higher values the incorporation of ES in the fertilization scheme resulted in higher yield, while at lower values it resulted in lower yield, compared with the conventional one. The experimental field trials that established following a randomized block design, were separated in two groups: One with P-Olsen ranging between 18–22 ppm and the other between 12–15 ppm, the results of which corroborated the aforementioned finding. The use of ES in all portions of fertilization schemes provided higher relative yields. The coexistence of ES with sulfate in the granule was more efficient in terms of yield, when compared to the granule enriched with ES alone under the same fertilization scheme and agronomic practice. The application of fertilizer mixtures containing the urease inhibitor N-(n-butyl) thiophosphoric triamide (NBPT), ES and ammonium sulfate resulted in even higher relative yields. Yield followed a positive linear relationship with the number of heads per square meter. In this correlation, the P-Olsen content separated the results of the two groups of blocks, where the applied linear trend line in each group presented the same slope. Full article
(This article belongs to the Special Issue Advances in Plant Sulfur Research)
Show Figures

Figure 1

16 pages, 1777 KiB  
Article
Assessment of Sulfur Deficiency under Field Conditions by Single Measurements of Sulfur, Chloride and Phosphorus in Mature Leaves
by Philippe Etienne, Elise Sorin, Anne Maillard, Karine Gallardo, Mustapha Arkoun, Jérôme Guerrand, Florence Cruz, Jean-Claude Yvin and Alain Ourry
Plants 2018, 7(2), 37; https://doi.org/10.3390/plants7020037 - 28 Apr 2018
Cited by 23 | Viewed by 4740
Abstract
Determination of S status is very important to detect S deficiency and prevent losses of yield and seed quality. The aim of this study was to investigate the possibility of using the ([Cl]+[NO3]+[PO43−]):[SO42− [...] Read more.
Determination of S status is very important to detect S deficiency and prevent losses of yield and seed quality. The aim of this study was to investigate the possibility of using the ([Cl]+[NO3]+[PO43−]):[SO42−] ratio as an indicator of S nutrition under field conditions in Brassica napus and whether this could be applied to other species. Different S and nitrogen (N) fertilizations were applied on a S deficient field of oilseed rape to harvest mature leaves and analyze their anion and element contents in order to evaluate a new S nutrition indicator and useful threshold values. Large sets of commercial varieties were then used to test S deficiency scenarios. As main results, this study shown that, under field conditions, leaf ([Cl]+[NO3]+[PO43−]):[SO42−] ratio was increased by lowering S fertilization, indicating S deficiency. The usefulness of this ratio was also found for other species grown under controlled conditions and it could be simplified by using the elemental ([Cl]+[P]):[S] ratio. Threshold values were determined and used for the clustering of commercial varieties within three groups: S deficient, at risk of S deficiency and S sufficient. The ([Cl]+[P]):[S] ratio quantified under field conditions, can be used as an early and accurate diagnostic tool to manage S fertilization. Full article
(This article belongs to the Special Issue Advances in Plant Sulfur Research)
Show Figures

Figure 1

Back to TopTop