Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP - Wikidata - awgldk - TriplyDB

Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP

Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP

http://www.wikidata.org/entity/Q59064143

about

Enhancing drought tolerance in C(4) crops Photosynthetic complex stoichiometry dynamics in higher plants: biogenesis, function, and turnover of ATP synthase and the cytochrome b6f complex Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell An algorithm to derive the fraction of photosynthetically active radiation absorbed by photosynthetic elements of the canopy (FAPAR(ps)) from eddy covariance flux tower data.Effects of elevated [CO2] and low soil moisture on the physiological responses of Mountain Maple (Acer spicatum L.) seedlings to light.Patterns and variability in seedling carbon assimilation: implications for tree recruitment under climate change.A physiological and biophysical model of coppice willow (Salix spp.) production yields for the contiguous USA in current and future climate scenarios.Long-term water stress leads to acclimation of drought sensitivity of photosynthetic capacity in xeric but not riparian Eucalyptus species Photosynthetic limitation of several representative subalpine species in the Catalan Pyrenees in summer.Physiological responses of forest trees to heat and drought.Delayed autumn phenology in the Northern Hemisphere is related to change in both climate and spring phenology.The crucial role of plant mitochondria in orchestrating drought tolerance.Identification and Comparative Analysis of Differential Gene Expression in Soybean Leaf Tissue under Drought and Flooding Stress Revealed by RNA-Seq.Are plant growth and photosynthesis limited by pre-drought following rewatering in grass?Photosynthesis and drought: can we make metabolic connections from available data?Elevated CO2 reduces stomatal and metabolic limitations on photosynthesis caused by salinity in Hordeum vulgare.Physiological and biochemical responses of Quercus pubescens to air warming and drought on acidic and calcareous soils.Sink regulation of photosynthesis.Coordinated regulation of photosynthesis in rice increases yield and tolerance to environmental stress.Comparative analysis of barley leaf proteome as affected by drought stress.Improved tolerance to drought stress after anthesis due to priming before anthesis in wheat (Triticum aestivum L.) var. Vinjett.Wheat proteomics: proteome modulation and abiotic stress acclimation.Variation in Rubisco content and activity under variable climatic factors.The impact of environmental stress on male reproductive development in plants: biological processes and molecular mechanisms.Short-term water stress impacts on stomatal, mesophyll and biochemical limitations to photosynthesis differ consistently among tree species from contrasting climates.Diffusive and metabolic limitations to photosynthesis under drought and salinity in C(3) plants.A meta-analysis of leaf gas exchange and water status responses to drought.Root-Zone Warming Differently Benefits Mature and Newly Unfolded Leaves of Cucumis sativus L. Seedlings under Sub-Optimal Temperature Stress.Leaf Gas Exchange and Fluorescence of Two Winter Wheat Varieties in Response to Drought Stress and Nitrogen Supply Chloroplast proteome response to drought stress and recovery in tomato (Solanum lycopersicum L.).Delayed leaf senescence induces extreme drought tolerance in a flowering plant.Physiological and proteomic analyses of the drought stress response in Amygdalus Mira (Koehne) Yü et Lu roots.Molecular responses of genetically modified maize to abiotic stresses as determined through proteomic and metabolomic analyses.Different adaptation strategies of two citrus scion/rootstock combinations in response to drought stress.Transcriptomic Changes Drive Physiological Responses to Progressive Drought Stress and Rehydration in Tomato Sulfur Use Efficiency Is a Significant Determinant of Drought Stress Tolerance in Relation to Photosynthetic Activity in Brassica napus Cultivars.The relationship of drought-related gene expression in Arabidopsis thaliana to hormonal and environmental factors.Genotypically Identifying Wheat Mesophyll Conductance Regulation under Progressive Drought Stress.Divergence in Eco-Physiological Responses to Drought Mirrors the Distinct Distribution of Chamerion angustifolium Cytotypes in the Himalaya-Hengduan Mountains Region.Transcription factors and regulation of photosynthetic and related metabolism under environmental stresses.

P2860

Q26809994-334AE679-C625-449F-9219-46186A2F0C79 Q28254615-EC4685B8-6F5C-446B-9BEF-974022825FEE Q28288904-2B78B498-7080-4D52-8850-1F06739A778A Q30578247-CD6202BD-7986-458F-AD88-AA97C5614AE9 Q30681827-A48EA6F3-6188-499E-9E69-6DE49AFF0129 Q30883902-99D46150-7794-4A53-AFA1-CEEF98A6EC43 Q30949496-1CF70BA1-65CB-4005-8DC4-3278F75A6833 Q31009901-C85FA0DF-B4C0-4483-A88F-21FFA81F54B7 Q31042020-8AB68413-A736-4A69-98BE-86C7AD6008C9 Q31044204-A3D89AD0-3799-45EB-8C2E-5E8B24E5B488 Q31072525-61713E36-8353-4199-AEBB-C3088F7F704C Q31159109-A0DCF72F-9A92-400A-8143-486153FD8A58 Q33363626-DAA71FEC-868C-4C04-8C20-41A161DB15CB Q33481545-B4D4AB64-5739-4573-B364-96D4063D0945 Q33776494-FFCCCC6A-CA89-4EA8-B4A1-7EF8FD675D2D Q34143954-D226F813-8554-4D58-8D34-D455EC666AA2 Q34294302-051BF10D-D282-4971-8212-B0687558D41A Q34310380-D33010F7-0B05-41F3-9205-F728D9DB1B5D Q34453812-4B114912-CC3C-4B78-8824-C8AED406BD8A Q34467955-4678D665-CDB3-4C60-B9A7-00BC2463CE91 Q34580656-92CFE4A4-07A9-4688-B6A5-00928E0BC054 Q34652148-929C3D5D-0AC8-4C01-B30E-E03C5E325D9B Q34763494-D3EFBA05-D13D-4CF0-8DFF-B6027E8D61A3 Q34795263-1724DAA2-FF1D-4170-8A92-418D1231E84F Q35240261-E54EB508-7135-4618-936C-4191F3AD7771 Q35773272-90EED711-B3BB-4E33-B24E-D96D83CEF9D5 Q35921299-4E853306-2287-469E-A54A-1648D9859352 Q36010562-90E2BDB2-66F1-4D5D-81EC-CEA8F4BFA093 Q36179384-1CD18BC8-E1DA-4030-B5DB-0E9B683A7BC3 Q36276056-B4215898-D5B2-4F7B-BC8B-9DB275BDDFDF Q36288769-46707122-B008-4C43-A625-0166D022B3E4 Q36292155-86804D65-63F2-4A29-9E94-26F325993A9F Q36292770-6D179629-BA04-4ED6-9D60-E8383A3C9CD4 Q36381569-0D0AB71B-B21E-47B7-A0C0-E2016FF1875D Q36747710-7876D4E4-25C2-4161-8D9A-F6FA53094A5D Q36778017-E009FD7E-4F3E-4C2B-B5DD-37AE9898C123 Q36824119-B68DD6B4-E9E9-43BE-82DC-4D088EB911C0 Q37156804-A48FCC26-0106-40EE-85CE-5831639FD1EE Q37218198-B9F55EAF-3F14-48EA-A111-068C8CE0AB5A Q37326097-B6F70907-6D09-4352-B383-FF81DD86A7BB

P2860

Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP

http://www.wikidata.org/entity/Q59064143

description

article publié dans la revue scientifique Nature

@fr

scientific article published in Nature

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована в Nature в жовтні 1999

@uk

name

Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP

@en

Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP

@nl

type

label

Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP

@en

Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP

@nl

prefLabel

Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP

@en

Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP

@nl

P1433

Q59064143-E907B0CB-C533-4003-BBAF-8A4C3A86DF04

P1476

Q59064143-CF6D2554-B937-49B6-85E9-1D1F6CA1F6F8

P2093

Q59064143-2D827E35-212F-4AEE-8CFA-756227C27F9B

Q59064143-3E25E4E3-F51C-4B1B-9D52-9BFB03572C55

Q59064143-40286FDD-8863-4915-B19C-4CAD3E135971

Q59064143-6867F64A-A44A-4DB9-B9BC-7323215721AF

P2860

Q59064143-1475A162-9251-4D94-94C5-3FB778806412

Q59064143-15026296-8105-4FEE-BEC6-529AAEE5B0FA

Q59064143-61C76300-4294-48BD-8411-DF2B91FE7C50

Q59064143-B421BE42-A147-476F-B97A-7E4F14A58CF6

Q59064143-C68D6049-61A8-4965-82B8-B0A5585B1CD6

Q59064143-EDDBDA32-76CE-43FB-B706-7866D6F6DBD5

P2888

Q59064143-66A5BC9D-3B3F-4568-AA1A-BEA87D0A5D40

P304

Q59064143-C96E11CC-86F9-4B52-BAFA-6353ACBB1EB8

P31

Q59064143-2440E279-6901-4BCA-AAB4-BE13D02B6930

P356

Q59064143-78684862-4F98-46FF-83E8-3F8ABCFD48FB

P407

Q59064143-18C28E08-0071-47F1-A4B3-91FB74B2BEED

P433

Q59064143-A74A3429-79B8-428E-B535-CC5DE0A1E9D7

P478

Q59064143-5787395F-C51A-443B-9F76-6CFA4F104165

P577

Q59064143-D1CBFF33-8043-4DF4-B0E4-96931F7677A8

P6179

Q59064143-C940DEC2-D877-4DAF-B4E4-F75891BE5D68

P921

Q59064143-F57D571A-628B-4F23-BE42-047DA5CCDA45

P356

P1433

P1476

Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP

@en

P2093

D. W. Lawlor

http://www.w3.org/2001/XMLSchema#string

S. D. Driscoll

http://www.w3.org/2001/XMLSchema#string

V. J. Mitchell

http://www.w3.org/2001/XMLSchema#string

W. Tezara

http://www.w3.org/2001/XMLSchema#string

P2860

The in-vivo response of the ribulose-1,5-bisphosphate carboxylase activation state and the pool sizes of photosynthetic metabolites to elevated CO2 inPhaseolus vulgaris L.

Conformation and activity of chloroplast coupling factor exposed to low chemical potential of water in cells.

Dependence of photosynthesis of sunflower and maize leaves on phosphate supply, ribulose-1,5-bisphosphate carboxylase/oxygenase activity, and ribulose-1,5-bisphosphate pool size.

Protein changes in response to progressive water deficit in maize . Quantitative variation and polypeptide identification

Regulation of Photosynthetic Rate of Two Sunflower Hybrids under Water Stress.

Photorespiration protects C3 plants from photooxidation

P2888

P304

914-917

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/44842

http://www.w3.org/2001/XMLSchema#string

P407

P433

6756

http://www.w3.org/2001/XMLSchema#string

P478

401

http://www.w3.org/2001/XMLSchema#string

P577

1999-10-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P6179

1036613446

http://www.w3.org/2001/XMLSchema#string

P921