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Water availability for plant growth is becoming increasingly limited, whereas rising atmospheric carbon dioxide concentration may have interactive effects with drought stress. The objectives of this study were to determine whether elevated CO₂ would mitigate drought-induced water deficit and photosynthesis inhibition and enhance recovery from drought damages on rewatering and to determine whether the mitigating effects during drought stress and the recovery in photosynthesis during rewatering by elevated CO₂ were the result of the regulation of stomatal movement or carboxylation activities in tall fescue (Festuca arundinacea Schreb. cv. Rembrandt). Plants were grown in controlled-environment chambers with ambient CO₂ concentration (400 μmol·mol⁻¹) or elevated CO₂ concentration (800 μmol·mol⁻¹) and maintained well watered (control) or subjected to drought stress and subsequently rewatered. Elevated CO₂ reduced stomatal conductance (g _S) and transpiration rate of leaves during both drought stress and rewatering. Osmotic adjustment and soluble sugar content were enhanced by elevated CO₂. Elevated CO₂ enhanced net photosynthetic rate with lower g _S but higher Rubisco and Rubisco activase activities during both drought and rewatering. The results demonstrated that elevated CO₂ could improve leaf hydration status and photosynthesis during both drought stress and rewatering, and the recovery in photosynthesis from drought damages on rewatering was mainly the result of the elimination of metabolic limitation from drought damages associated with carboxylation enzyme activities.

Microbial fertilizers can activate and promote nutrient absorption and help inflorescence elongation. To understand the molecular mechanisms governing grape (Vitis vinifera) inflorescence elongation after microbial fertilizer application, we comprehensively analyzed the transcriptome dynamics of ‘Summer Black’ grape inflorescence at different leaf stages. With the development of ‘Summer Black’ grape inflorescence, gibberellic acid content gradually increased and was clearly higher in the microbial fertilizer group than in the corresponding control group. In addition, the microbial fertilizer and control groups had 291, 487, 490, 287, and 323 differentially expressed genes (DEGs) at the 4-, 6-, 8-, 10-, and 12-leaf stages, respectively. Kyoto Encyclopedia of Genes and Genomes pathway annotation revealed that most upregulated DEGs were enriched in starch and sucrose metabolism pathways at the 6-, 8-, and 10-leaf stages. Weighted gene coexpression network analysis identified stage-specific expression of most DEGs. In addition, multiple transcription factors and phytohormone signaling-related genes were found at different leaf stages, including basic helix-loop-helix proteins, CCCH zinc finger proteins, gibberellin receptor GID1A, 2-glycosyl hydrolases family 16, protein TIFY, MYB transcription factors, WRKY transcription factors, and ethylene response factor, suggesting that many transcription factors play important roles in inflorescence elongation at different developmental stages. These results provide valuable insights into the dynamic transcriptomic changes of inflorescence elongation at different leaf stages.

Abscisic acid (ABA) and glycine betaine (GB) may regulate plant responses to drought or salinity stress. The objectives of this controlled-environment study were to determine whether foliar application of ABA or GB improves turf quality under drought or salinity and whether improved stress responses were associated changes in antioxidant metabolism in two C3 turfgrass species, creeping bentgrass (Agrostis stolonifera) and kentucky bluegrass (Poa pratensis). Physiological parameters evaluated included turf quality, leaf relative water content, membrane electrolyte leakage (EL), membrane lipid peroxidation [expressed as malondialdehyde (MDA) content], and activity of superoxide dismutase (SOD), peroxidase (POD), and ascorbate peroxidase (APX). Abscisic acid and GB were both effective in mitigating physiological damage resulting from drought or salinity for both grass species, but effects were more pronounced on kentucky bluegrass. The most notable effects of ABA or GB application were the suppression of EL and MDA accumulation and an increase in APX, POD, and SOD activities after prolonged periods of drought (21 days) or salinity stress (35 days). These results suggest foliar application of ABA or GB may alleviate physiological damage by drought or salinity stress in turfgrass and the maintenance of membrane stability and active antioxidant metabolism could contribute to the positive effects in the stress mitigation effects.

Heat is a major factor limiting growth of C₃ grass species. Elevated CO₂ may mitigate the adverse effects of heat stress or enhance heat tolerance. The objective of this study was to determine metabolic changes associated with improvement of heat tolerance by elevated atmospheric CO₂ concentration in tall fescue (Festuca arundinacea). Plants (cv. Rembrandt) were exposed to ambient day/night temperature (25/20 °C) or heat stress (35/30 °C) and ambient CO₂ concentration (400 ± 10 μmol·mol⁻¹) or double ambient CO₂ concentration (800 ± 10 μmol·mol⁻¹) in growth chambers. Turf quality (TQ), shoot growth rate, and leaf electrolyte leakage results demonstrated that heat stress at ambient CO₂ concentration inhibits turf growth and reduces cell membrane stability, whereas heat-stressed plants under elevated CO₂ concentration exhibit improved TQ, shoot growth rate, and membrane stability. Plants exposed to heat stress under elevated CO₂ exhibited a significantly greater amount of several organic acids (shikimic acid, malonic acid, threonic acid, glyceric acid, galactaric acid, and citric acid), amino acids (serine, valine, and 5-oxoproline), and carbohydrates (sucrose and maltose) compared with heat-stressed plants at ambient CO₂. The increased production or maintenance of metabolites with important biological functions such as those involved in photosynthesis, respiration, and protein metabolism could play a role in elevated CO₂ mitigation of heat stress damage. Therefore, elevated CO₂ conditions may contribute to improved heat stress tolerance as exhibited by better TQ and shoot growth of heat-stressed plants. Practices to harness the power of CO₂ may be incorporated into turfgrass management for plant adaptation to increasing temperatures, particularly during summer months.

Drought stress is one of the most important abiotic stresses limiting plant growth, while high recuperative capacity of plants from drought damages is critical for plant survival in periods of drought stress and rewatering. The objective of our study was to determine physiological and growth factors in association with drought tolerance and recuperative capacity of cool-season kentucky bluegrass (Poa pratensis cv. Excursion II) and warm-season zoysigrass (Zoysia matrella cv. Diomand), which were grown in controlled environment chambers and maintained well watered (control) or subjected to drought stress and subsequently rewatering. Compared with kentucky bluegrass, zoysiagrass maintained higher leaf hydration level during drought stress, as shown by greater relative water content (RWC), improved osmotic adjustment (OA), increased leaf thickness, and more extensive root system at deeper soil layers. Turf quality (TQ) and photosynthesis recovered to a greater level and sooner in response to rewatering for zoysiagrass, compared with kentucky bluegrass, which could be due to more rapid reopening of stomata [higher stomatal conductance (g _S)] and leaf rehydration (higher RWC). The aforementioned physiological factors associated with leaf dehydration tolerance during drought and rapid resumption in turf growth and photosynthesis in zoysiagrass could be useful traits for improving drought tolerance in turfgrasses.

The accumulation of different types of metabolites may reflect variations in plant adaptation to different severities or durations of drought stress. The objectives of this project are to examine changes in metabolomic profiles and determine predominant metabolites in response to short-term (6 days) and long-term (18 days) drought stress with gas chromatography–mass spectrometry analysis in a C₄ perennial grass species. Plants of hybrid bermudagrass (Cynodon dactylon × C. transvaalensis cv. Tifdwarf) were unirrigated for 18 days to induce drought stress in growth chambers. Physiological responses to drought stress were evaluated by visual rating of grass quality, relative water content, photochemical efficiency, and electrolyte leakage (EL). All parameters decreased significantly at 6 and 18 days of drought stress, except EL, which increased with the duration of drought stress. Under short-term drought stress (6 days), the content did not change significantly for most metabolites, except methionine, serine, γ-aminobutyric acid (GABA), isoleucine, and mannose. Most metabolites showed higher accumulation under long-term drought stress compared with that under the well-watered conditions, including three organic acids (malic acid, galacturonic acid, and succinic acid), 10 amino acids (proline, asparagine, phenylalanine, methionine, serine, 5-hydroxynorvaline, GABA, glycine, theorine, valine), seven sugars (sucrose, glucose, galactose, fructose, mannose, maltose, xylose), one nitrogen compound (ethanolamine), and two-sugar alcohol (myo-inositol). The accumulation of those metabolites, especially malic acid, proline, and sucrose, could be associated with drought adaptation of C₄ hybrid bermudagrass to long-term or severe drought stress.

Cold stress is a major factor limiting the growth of warm-season turfgrass species. Cold tolerance in warm-season turfgrass species could be improved through in vitro selection for somaclonal variations. The objectives of this study were to establish an effective in vitro culture protocol for generating plants from calli using mature seeds of seashore paspalum (Paspalum vaginatum) and to determine whether in vitro cold selection of somaclonal variations would lead to improved cold tolerance in seashore paspalum. The optimal concentrations of supplemental compounds in the culture medium for callus induction, embryogenic callus formation, and plant regeneration were determined. The supplemental compounds included 2,4–dichlorophenoxy acetic acid (2,4-D), 6-benzylaminopurine (6-BA), kinetin (KT), naphthalene-1-acetic acid (NAA), CuSO₄, and acidic hydrolysis casein (AHC). The highest rates of callus induction (97.50%), embryogenic callus formation (66.88%), and regeneration (55.94%) were obtained with the supplemental compounds of 3.0 mg·L⁻¹ 2,4-D and 10.0 mg·L⁻¹ CuSO₄ for callus induction; with 3.0 mg·L⁻¹ 2,4-D, 15 mg·L⁻¹ CuSO₄, and 1.0 g·L⁻¹ AHC for embryogenic callus formation; and with 8.0 mg·L⁻¹ 6-BA, 0.2 mg·L⁻¹ KT, 0.5 mg·L⁻¹ NAA, and 10 mg·L⁻¹ CuSO₄ for plant regeneration. Embryogenic calli were subjected to 2 or 6 °C treatment for 90 days for in vitro cold selection of somaclonal variation. Plants regenerated from calli surviving cold treatment (cold-selected) for 45 or 60 days were then exposed to low temperatures [15/10 or 5/3 °C (day/night)]. Plant variants derived from cold-selected calli exhibited significant improvement in their tolerance to low temperature of either 15/10 or 5/3 °C (day/night), as manifested by higher turf quality, leaf chlorophyll content, and membrane stability as well as lower levels of lipid peroxidation compared with the control plants. This study demonstrated the feasibility of in vitro selection for cold tolerance in seashore paspalum. The cold-tolerant variants could be useful germplasm for breeding programs and further molecular characterization of cold tolerance mechanisms.

Carbohydrate metabolism is important for plant adaptation to drought stress. The objective of this study was to examine major forms of carbohydrates associated with superior drought tolerance and post-drought recovery in kentucky bluegrass (Poa pratensis) by comparing responses of different forms of carbohydrates with drought stress and re-watering in two cultivars contrasting in drought tolerance. Plants of drought-tolerant ‘Midnight’ and drought-sensitive ‘Brilliant’ were maintained well watered or subjected to drought stress for 10 days by withholding irrigation, and drought-stressed plants were re-watered for 3 days. Physiological analysis (turf quality, relative water content, and electrolyte leakage) confirmed the genetic variability of the two cultivars in drought tolerance. The two cultivars exhibited differential responses to drought stress and re-watering for the content of water-soluble sugars (sucrose, fructose, and glucose) and storage carbohydrates (starch and fructan), and ‘Midnight’ maintained higher sucrose content at 10 days of drought stress and more fructan at 3 days of re-watering. The greater accumulation of sucrose in ‘Midnight’ under drought stress corresponded with higher activities of two sucrose-synthesizing enzymes (sucrose phosphate synthase and sucrose synthase) but was not related to the sucrose-degrading enzyme activity (acid invertase). These results suggested that increased sucrose accumulation resulting from the maintenance of active sucrose synthesis could be associated with superior turf performance during drought stress, whereas increased fructan accumulation could contribute to rapid re-growth and post-drought recovery on re-watering in kentucky bluegrass.

Nuclear DNA contents were estimated by flow cytometry in 18 Phalaenopsis Blume species and Doritis pulcherrima Lindl. DNA amounts differed 6.07-fold, from 2.74 pg/diploid nuclear DNA content (2C) in P. sanderiana Rchb.f. to 16.61 pg/2C in P. parishii Rchb.f. Nuclear DNA contents of P. aphrodite Rchb.f. clones, W01-38 (2n = 2x = 38), W01-41 (2n = 3x = 57), and W01-22 (2n = 4x = 76), displayed a linear relationship with their chromosome numbers, indicating the accuracy of flow cytometry. Our results also suggest that the 2C-values of the Phalaenopsis sp. correlate with their chromosome sizes. The comparative analyses of DNA contents may provide information to molecular geneticists and systematists for genome analysis in Phalaenopsis. Endoreduplication was found in various tissues of P. equestris at different levels. The highest degree of endoreduplication in P. equestris was detected in leaves.

Citrus (Citrus sp.) germplasm collections are a valuable resource for citrus genetic breeding studies, and further utilization of the resource requires knowledge of their genotypic and phylogenetic relationships. Diverse citrus accessions, including citron (Citrus medica), mandarin (Citrus reticulata), pummelo (Citrus maxima), papeda (Papeda sp.), trifoliate orange (Poncirus trifoliata), kumquat (Fortunella sp.), and related species, have been housed at the Florida Citrus Arboretum, Winter Haven, FL, but the accessions in the collection have not been genotyped. In this study, a collection of 80 citrus accessions were genotyped using 1536 sweet orange–derived single nucleotide polymorphism (SNP) markers, to determine their SNP fingerprints and to assess genetic diversity, population structure, and phylogenetic relationships, and thereby to test the efficiency of using the single genotype-derived SNP chip with relatively low cost for these analyses. Phylogenetic relationships among the 80 accessions were determined by multivariate analysis. A model-based clustering program detected five basic groups and revealed that C. maxima introgressions varied among mandarin cultivars and segregated in mandarin F₁ progeny. In addition, reciprocal differences in C. maxima contributions were observed among citranges (Citrus sinensis × P. trifoliata vs. P. trifoliata × C. sinensis) and may be caused by the influence of cytoplasmic DNA and its effect on selection of cultivars. Inferred admixture structures of many secondary citrus species and important cultivars were confirmed or revealed, including ‘Bergamot’ sour orange (Citrus aurantium), ‘Kinkoji’ (C. reticulata × Citrus paradisi), ‘Hyuganatsu’ orange (Citrus tamurana), and palestine sweet lime (Citrus aurantifolia). The relatively inexpensive SNP array used in this study generated informative genotyping data and led to good consensus and correlations with previously published observations based on whole genome sequencing (WGS) data. The genotyping data and the phylogenetic results may facilitate further exploitation of interesting genotypes in the collection and additional understanding of phylogenetic relationships in citrus.