FluorPen FP110手持式葉綠素?zé)晒鈨x用于實(shí)驗(yàn)室、溫室和野外快速測量植物葉綠素?zé)晒鈪?shù)，具有便攜性強(qiáng)、度高、性價(jià)比高等特點(diǎn)；雙鍵操作，具圖形顯示屏，內(nèi)置鋰電和數(shù)據(jù)存儲(chǔ)，廣泛應(yīng)用于研究植物的光合作用、脅迫監(jiān)測、除草劑檢測或突變體篩選，還可用于生態(tài)毒理的生物檢測，如通過不同植物對(duì)土壤或水質(zhì)污染的葉綠素?zé)晒忭憫?yīng)，找出敏感植物作為生物傳感器用于生物檢測。FP110配備多種葉夾型號(hào)，用于不同的樣品與研究 

●參考文獻(xiàn)

1. JA Pérez-Romero, et al. 2018. Atmospheric CO2 enrichment effect on the Cu-tolerance of the C4 cordgrass Spartina densiflora. Journal of Plant Physiology 220: 155-166.

2. SK Yadav, et al. 2018. Physiological and Biochemical Basis of Extended and Sudden Heat Stress Tolerance in Maize.Proceedings of the National Academy of Sciences 88(1): 249-263.

3. D Balfagón, et al. 2018. Involvement of ascorbate peroxidase and heat shock proteins on citrus tolerance to combined conditions of drought and high temperatures. Plant Physiology and Biochemistry 127: 194-199.

4. JI Vílchez, et al. 2018. Protection of Pepper Plants from Drought by Microbacterium sp. 3J1 by Modulation of the Plant's Glutamine and α-ketoglutarate Content: A Comparative Metabolomics Approach. Front. Microbiol. 9: 284.

5. MC Sorrentino, et al. 2018. Performance of three cardoon c*rs in an industrial heavy metal-contaminated soil: Effects on morphology, cytology and photosynthesis. Journal of Hazardous Materials 351: 131-137.

6. E Niewiadomska, et al. 2018. Lack of tocopherols influences the PSII antenna and the functioning of photosystems under low light. Journal of Plant Physiology 223: 57-64.

7. S Singh, et al. 2018. Cadmium toxicity and its amelioration by kinetin in tomato seedlings vis-à-vis ascorbate-glutathione cycle. Journal of Photochemistry and Photobiology B: Biology 178: 76-84.

8. EL Fry, et al. 2018. Drought neutralises plant–soil feedback of two mesic grassland forbs. Oecologia 186(4): 1113–125.

9. B Duarte, et al. 2017. Disentangling the photochemical salinity tolerance in Aster tripolium L.: connecting biophysical traits with changes in fatty acid composition. Plant Biology,19(2): 239-248

10. OO Ajigboye, et al. 2017. Altered gene expression by sedaxane increases PSII efficiency, photosynthesis and growth and improves tolerance to drought in wheat seedlings. Pesticide Biochemistry and Physiology 137: 49-61.

附：OJIP參數(shù)及計(jì)算公式

Bckg = background

Fo = F50μs; fluorescence intensity at 50 μs

Fj = fluorescence intensity at j-step (at 2 ms)

Fi = fluorescence intensity at i-step (at 60 ms)

Fm = maximal fluorescence intensity

Fv = Fm - Fo (maximal variable fluorescence)

Vj = (Fj - Fo) / (Fm - Fo)

Fm / Fo = Fm / Fo

Fv / Fo = Fv / Fo

Fv / Fm = Fv / Fm

Mo = TRo / RC - ETo / RC

Area = area between fluorescence curve and Fm

Sm = area / Fm - Fo (multiple turn-over)

Ss = the smallest Sm turn-over (single turn-over)

N = Sm . Mo . (I / Vj) turn-over number QA

Phi_Po = (I - Fo) / Fm (or Fv / Fm)

Phi_o = I - Vj

Phi_Eo = (I - Fo / Fm) . Phi_o

Phi_Do = 1 - Phi_Po - (Fo / Fm)

Phi_Pav = Phi_Po - (Sm / tFM); tFM = time to reach Fm (in ms)

ABS / RC = Mo . (I / Vj) . (I / Phi_Po)

TRo / RC = Mo . (I / Vj)

ETo / RC = Mo . (I / Vj) . Phi_o)

DIo / RC = (ABS / RC) - (TRo / RC)