Analizzatore di efficienza degli impianti
Capace di misurare completamente la clorofillaOJIPAnalizzatore di fluorescenza ad eccitazione continua per curva cinetica indotta da fluorescenza
Campo di applicazione principale:
Campi quali fisiologia vegetale, ecologia vegetale, agricoltura, orticoltura, silvicoltura, scienze ambientali, patologia vegetale, biologia algale, ecc.
Parametri di misura:
Il nuovo software può calcolare direttamenteFO,Fm,Fv,Fv/Fm,Ft,FJ,FI,FP,Tm, ψO, φEo, φDo,Vt,VJ,WK,PIABS,PICS,ABS/RC,TRO/RC,ETO/RC,DIO/RC,RC/CSO,RC/CSMAspettate cinquanta parametri di fluorescenza clorofillica. Registrare accuratamente la fase veloce della curva cinetica di induzione della fluorescenza clorofillica, che può essere registrata continuamente ogni secondo10Diecimila dati sulle tracce di fluorescenza, in1Determinazione completa della clorofilla entro pochi secondiOJIPCurva cinetica indotta dalla fluorescenza.
Una nuova interpretazione della teoria della fluorescenza della clorofilla
Handy PEAL'analisi di efficienza delle piante è un tipo di analizzatore di fluorescenza della clorofilla, che appartiene all'analizzatore di fluorescenza di eccitazione continua.Handy PEAcorrettoPEALa serie di analizzatori di efficienza dell'impianto ha funzioni potenti, prezzi moderati e un numero molto elevato di utenti domestici.
Figura 1 Curva cinetica tipica di induzione della fluorescenza della clorofilla Figura 2 Curva cinetica rapida di induzione della fluorescenza della clorofilla
A differenza dei tradizionali misuratori di fluorescenza modulati a impulsi,Handy PEADotato di risoluzione temporale ultra-alta, con una risoluzione fino a105Può registrare accuratamenteO-J-I-PStrumento per la curva cinetica rapida di induzione della fluorescenza clorofillica.OJIPLa curva può essere1Misurazioni accurate complete in pochi secondi.OJIPL'analisi dei dati delle curve si basa suJIP-TestIl metodo di analisi è sviluppato daPEAFondatore dell'analizzatore di efficienza degli impiantiStrasserIl professore ha creato.
passa attraversoOJIPPossiamo analizzare con precisione se il meccanismo fotosintetico è danneggiato sotto avversità analizzando la curva? Quale parte del sistema fotosintetico è danneggiata? Qual è l'entità della lesione? Può essere utilizzato sia per l'analisi qualitativa che per l'analisi quantitativa del grado di pregiudizio.
Inventore di strumentiStrasserIntroduzione del professore:
Figura 3 Professor Strasser al lavoro Figura 4 Professor Strasser invitato a guidare gli esperimenti degli utenti presso Lufthansa Technology Group
R.T.StrasserÈ professore presso l'Università di Ginevra in Svizzera, esperto di ricerca sulla fotosintesi di fama internazionale, direttore del Laboratorio Chiave di Bioenergia e Microbiologia dell'Università di Ginevra e membro del team di esperti di valutazione del Progetto di Restauro Vegetativo nel Deserto Mediterraneo delle Nazioni Unite, impegnato principalmente nella ricerca di fotosintesi e simulazione fotosintetica.
Strumento fluorescente comunemente usato per piante e alghe superiori
Figura 5 Sonda PEA pratica per piante superiori Figura 6 Sonda PEA pratica per campioni di alghe
Handy PEAAnalizzatore di efficienza dell'impianto, dotato di sonde avanzate dell'impianto come standard, molto conveniente per l'analisi delle foglieO-J-I-PDeterminazione rapida della curva cinetica di induzione di fluorescenza clorofillica e la sonda facoltativa del campione di alghe può anche essere utilizzata per misurare l'attività delle algheOJIPCurva.
La sonda per la misurazione delle piante più alte non è influenzata dalla superficie fogliare,HPEA/LCClip di adattamento scuro (clip a foglia), con un diametro misurato di4mmPer meno di4mmLe foglie delle piante,Handy PEAL'elaborazione attraverso la standardizzazione dei dati non influisce sull'accuratezza dei dati.
Sonda campione per la misurazione delle algheHPEA/LPA2Con una risoluzione estremamente elevata, è possibile effettuare misurazioni accurate su campioni di alghe molto basse, come i diatomi, che possono essere determinati completamente e accuratamente anche quando la loro presenza è quasi indistinguibile ad occhio nudoOJIPCurva.
Esperienza utente portatile
Figura 7 Pratico PEA con eccellente portabilità per test sul campo
Handy PEAPeso insufficiente del set completo di apparecchiature per l'analizzatore di efficienza dell'impianto1kgCon le cinghie, è conveniente per le operazioni sul campo, anche le ricercatrici possono completare tutte le operazioni da sole.
Misurazione rapida dei dati, apparecchiature standard20A dark adaptation clip(6g)Può essere fatto almeno una volta20Il trattamento di adattamento scuro di un campione, misurando il tempo di un campione2scirca. Può completare un gran numero di misurazioni in un periodo di tempo molto breve e ottenere una ricchezza di dati preziosi. Nell'era dei big data,Handy PEAEssa dimostrerà inevitabilmente ulteriormente la sua potente funzionalità.
Software potente con funzioni potenti
Figura 8 Interfaccia software PEA amichevole
L'interfaccia software è facile da usare, facile da usare e ha una funzione di filtraggio, che può essere utilizzata per lo screening di varietà eccellenti e resistenti nell'era dei big data. Condurre analisi quali raggruppamento, classificazione, media e regolarità.
Potente team di assistenza post-vendita
Tutti gli ingegneri del servizio post-vendita guidati dal Dr. Luo Bing hanno un master o superiore e sono in grado di utilizzare lo strumento per esperimenti3Più di anni di esperienza pratica.
Il servizio post vendita può fornire lezioni teoriche sugli strumenti, nonché introduzioni specialistiche a possibili errori e soluzioni di prevenzione durante l'uso dello strumento, può anche introdurre una ricchezza di preziose esperienze o testare materiali esistenti degli utenti per l'analisi dei dati, aiutando gli utenti a utilizzare strumenti per il lavoro di ricerca scientifica in un breve periodo di tempo.
Abbondante supporto alla letteratura
2015anno
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Lv Sansan,Du Guodong,Liu Zhikun,classe. L'effetto della copertura dell'erba sulla microstruttura e sulla funzione fotosistemica delle foglie di mela[J].Scienze agricole in Cina, 2015, 48(1): 130-139.
Qilin,Mana,Wu Wenwen,classe. Risposta fisiologica e valutazione della tolleranza di waterlogging delle piantine di fichi sotto stress waterlogging[J].Acta Horticulturae Sinisca, 2015, 42(7): 1273-1284.
Yan Yujing,Bai Jian,Fu Chunxia,classe. L'effetto della regolazione dello stoccaggio dell'acqua nella zona radicolare sulle caratteristiche fotosintetiche e sull'attività enzimatica antiossidante delle foglie di mela[J].Acta Horticulturae Sinisca, 2015, 42(5): 817-825.
Yan Kun,Zhao Shijie,Xu Hualing,classe. L'effetto dello stress salino sulle caratteristiche fotosintetiche dell'oro e dell'argento con diversi livelli di ploidy[J].Scienze agricole in Cina, 2015, 48(16): 3275-3286.
Yang Ye,Chen Ke,Zhu Jing. Effetti dell'applicazione del calcio sulla crescita e biochimica fisiologica di Jatropha curcas sotto stress di stronzio[J].Journal of Nuclear Agriculture, 2015, 29(2): 405-411.
2016anno
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Bhar A, Gupta S, Chatterjee M, et al. Differential expressions of photosynthetic genes provide clues to the resistance mechanism during Fusarium oxysporum f. sp. ciceri race 1 (Foc1) infection in chickpea (Cicer arietinum L.)[J]. European Journal of Plant Pathology, 2016: 1-17.
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Wang Z X, Yang Y M, Xu P L, et al. Do Naturally Variegated Leaves have a High Photosynthetic Cost? The Case of (Rupr. & Maxim.) Maxim[J]. Agronomy Journal, 2016, 108(1): 407-414.
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Xiang L, Hu L, Xu W, et al. Exogenous γ-Aminobutyric Acid Improves the Structure and Function of Photosystem II in Muskmelon Seedlings Exposed to Salinity-Alkalinity Stress[J]. PloS one, 2016, 11(10): e0164847.
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Zhao G, Xu H, Zhang P, et al. Effects of 2, 4-epibrassinolide on photosynthesis and Rubisco activase gene expression in Triticum aestivum L. seedlings under a combination of drought and heat stress[J]. Plant Growth Regulation, 1-8.
Zhao S, Ma Q, Xu X, et al. Tomato Jasmonic Acid-Deficient Mutant spr2 Seedling Response to Cadmium Stress[J]. Journal of Plant Growth Regulation, 2016, 35(3): 603-610.
Zhong Y, Li Y, Cheng J J. Effects of selenite on chlorophyll fluorescence, starch content and fatty acid in the duckweed Landoltia punctata[J]. Journal of plant research, 2016, 129(5): 997-1004.
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Bi Huangai,Dong Xubing,Liu Peipei,classeCsRCAL'effetto di sovraespressione sulla fotosintesi delle piantine di cetriolo sotto stress ad alta temperatura[J].Journal of Applied Ecology, 2016, 27(7): 2308-2314.
Cheng Dandan,Sun Jianping,Chai Yuan,classe. L'impatto dell'infezione patogena del fuoco selvatico sugli apparecchi fotosintetici del tabacco in condizioni di luce o buio[J].Journal of Applied Ecology, 2016, 27(8): 2655-2662.
Geng Qingwei,Xing Hao,Hao Guimei,classe. La melatonina esogena risponde allo stress dell'ozono L'impatto della fotosintesi sulle foglie delle uve Cabernet Sauvignon[J].Acta Horticulturae Sinisca, 2016, 43(8): 1463-1472.
Jia Xiaohui,Wang Wenhui,Tong Wei,classe. L'effetto del confezionamento spontaneo in atmosfera modificata sulla fisiologia post raccolta e sulla qualità di conservazione della pera profumata Korla[J].Scienze agricole in Cina, 2016, 49(24): 4785-4796.
Venere,Luo Xuegang,Tang Yongjin,classe. L'effetto dell'acido borico esogeno sulla fisiologia e sull'arricchimento dell'uranio dei fagiolini sotto stress uranico[J].Bollettino cinese sulle scienze agricole, 2016, 32(33): 175-181.
Ming-Liang Lee,Li Huan,Wang Kairong,classe. CdFunghi micorrizi arbuscolari influenzano la crescita delle arachidi sotto stress,Fisiologia fotosintetica eCdL'impatto dell'assorbimento[J].chimica ambientale, 2016, 35(11): 2344-2352.
Liu Changqing,Grazie, Mu.,Zhao Jian,classe. Rilevazione cinetica della fluorescenza della clorofilla degli effetti tossici dei plastificanti su Scenedesmus obliquus[J].Acta Hydrobiologica Sinica, 2016, 40(3): 552-556.
Shao Ruixin,Li Leilei,Zheng Huifang,classe. L'effetto dell'ossido nitrico esogeno sulla fotosintesi delle piantine di mais sotto stress da siccità[J].Scienze agricole in Cina, 2016, 49(2): 251-259.
Xu Fenfen,Ke Weizhong,Wang Aibin,classeNaClIl meccanismo fisiologico fotosintetico di pre-elaborazione per alleviare lo stress ad alta temperatura nel cavolo cinese[J].Scienze ecologiche, 2016, 35(3): 161-164.
Xu Jingang,L ü Chuangen,Liu Li,classe. Mutante fotoossidativo del riso812HSProprietà fotosintetiche e antiossidanti[J].acta agronomica sinica, 2016, 42(04): 574-582.
Xu Lan,Gao Zhiqiang,An Wei,classe. Caratteristiche fotosintetiche delle foglie di bandiera in condizioni di semina invernale e primaverile,Modifiche dei parametri di fluorescenza clorofillica e loro rapporto con la resa[J].Journal of Applied Ecology, 2016, 27(1): 133-142.
Xu Wen,Shen Hao,Guo Jun,classe. Resistenza alla siccità del grano vicino a linee isogeniche con diverso contenuto di cera nelle foglie di bandiera[J].acta agronomica sinica, 2016, 42(11): 1700-1707.
Xu Xinglian,Song Xikun,Yue Rui,classe. Limitazione dell'azoto sul fotosistema delle alghe diatomee brune Ⅱ L'impatto delle reazioni fotochimiche[J].Journal of Ecology, 2016, 35(1): 183-188.
Yang Songqi,Shi Shaohua,Wang Lijuan,classe. Crescita di Dunaliella salina ePSⅡ Risposta a diverse fonti di fosforo[J]. Marine Sciences, 2016, 40(10): 1.
Zhang Jingzi,Bai Xinfu,Hou Yuping,classe. Confronto della competitività di crescita delle piante invasive nella fascia di protezione costiera della penisola di Shandong, compresa la terra commerciale americana e le sue specie associate[J].foresta settore di attività una branca di studi accademici o professionali studio, 2016, 52(3).
Zhao Shenglong,Zeng Fanjiang,Zhang Bo,classe. L'effetto dello stress salino sui tratti fogliari delle piantine di spine di cammello[J].Scienze del prato, 2016, 33(9): 1770-1778.
Zhao Xue,Pan Tingting,Bi Yonghong,classe. Risposta dell'attività di fluorescenza clorofillica del diatoma di Ni ai fattori ambientali[J].Acta Hydrobiologica Sinica, 2016, 40(1): 116-122.
2017anno
Alvarado-Sanabria O, Garcés-Varón G, Restrepo-Díaz H. Risposta fisiologica delle piantine di riso (Oryza sativa L.) Soggetti a diversi periodi di due temperature notturne[J]. Journal of Stress Physiology & Biochemistry, 2017, 13(1).
Amiri H, Ismaili A, Hosseinzadeh S R. Influence of Vermicompost Fertilizer and Water Deficit Stress on Morpho-Physiological Features of Chickpea (Cicer arietinum L. cv. karaj)[J]. Compost Science & Utilization, 2017: 1-14.
Bailey M F, Case A L, Caruso C M. Physiological effects of temperature do not explain prevalence of females in populations of gynodioecious Lobelia siphilitica growing in warmer climates[J]. American Journal of Botany, 2017, 104(3): 411-418.
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Cambi M, Hoshika Y, Mariotti B, et al. Compaction by a forest machine affects soil quality and Quercus robur L. seedling performance in an experimental field[J]. Forest Ecology and Management, 2017, 384: 406-414.
Chakhchar A, Lamaoui M, Aissam S, et al. Using chlorophyll fluorescence, photosynthetic enzymes and pigment composition to discriminate drought-tolerant ecotypes of Argania spinosa[J]. Plant Biosystems-An International Journal Dealing with all Aspects of Plant Biology, 2017: 1-12.
Dąbrowski P, Kalaji M H, Baczewska A H, et al. Delayed chlorophyll a fluorescence, MR 820, and gas exchange changes in perennial ryegrass under salt stress[J]. Journal of Luminescence, 2017, 183: 322-333.
Essemine J, Xiao Y, Qu M, et al. Cyclic electron flow may provide some protection against PSII photoinhibition in rice (Oryza sativa L.) leaves under heat stress[J]. Journal of Plant Physiology, 2017, 211: 138-146.
Franić M, Galić V, Ledenčan T, et al. Changes of chlorophyll a fluorescence parameters in water limited maize IBM population[J]. 52. HRVATSKI I 12. MEĐUNARODNI SIMPOZIJ AGRONOMA, 2017: 208.
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