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flashes. II. Proton deposition. Aust J Plant Physiol 11:176–267CrossRef Hope AB, Matthews DB (1985) Adsorption of amines to thylakoids and estimations of ΔpH. Aust J Plant Physiol 12:9–19CrossRef Hope AB, Doherty G, Stainer P (1985) Proton motive force and phosphorylation potential in thylakoids. Aust J Plant Physiol 12:21–26CrossRef Hope AB, Matthews DB (1988) BYL719 Electron and proton transfers around the b/f complex in chloroplasts: modelling the constraints on Q-cycle activity. Aust J Plant Physiol 15:567–583CrossRef Hope AB, Rich PR (1989) Proton uptake by the chloroplast cytochrome bf complex. Biochim Biophys Acta 975:96–103CrossRef Hope AB, Liggins J, Matthews DB (1989) The kinetics of reactions in and near the cytochrome b/f complex of chloroplasts. II. Cytochrome b-563 reduction. Aust J Plant Physiol 16:353–364CrossRef Hope AB, Huilgol RR, Panizza M, Thompson M, Matthews DB (1992) The flash-induced turnover of cytochrome b-563, Luminespib cytochrome f and plastocyanin in chloroplasts. Models and estimation of kinetic parameters. Biochim Biophys Acta 1100:15–26CrossRef Jia H, Oguchi R, Hope AB, Barber J, Chow WS (2008) Differential effects of severe water stress on linear and cyclic electron fluxes through photosystem I in spinach leaf discs in CO2-enriched air. Planta 228:803–812CrossRefPubMed
Kim S-J, Lee
C-H, Hope AB, Chow WS (2001) Inhibition of photosystem I and II and enhanced back flow of photosystem I electrons in cucumber leaf discs chilled in the light. Plant Cell Physiol 42:842–848CrossRefPubMed Losciale P, Oguchi R, Hendrickson L, Hope AB, Corelli-Grappadelli L, Chow WS (2008) A rapid, whole-tissue determination of the functional fraction of photosystem II after photoinhibition TCL of leaves based on flash-induced P700 redox kinetics. Physiol Plant 132:23–32PubMed Mercer FV, Hodge AJ, Hope AB, McLean JD (1955) The structure and swelling properties of Nitella chloroplasts. Aust J Biol Sci 8:1–18 Robertson RN (1992) A dilettante Australian plant physiologist. Annu Rev Plant Physiol Plant Mol Biol 43:1–24CrossRef”
“Introduction Although iron (Fe) is the fourth most Selleckchem SNS-032 abundant element in the Earth’s crust, its low bioavailability makes it a limiting nutrient for life. In nature, iron is mostly found as stable Fe3+-oxides, which are insoluble in aerobic environments at biological pH (Guerinot and Yi 1994). Iron’s control on photosynthetic systems has been notably demonstrated by the stimulation of algal blooms following the addition of nanomolar concentrations of iron to several open ocean locations that receive very low natural iron inputs (e.g., Martin et al. 1994; Boyd et al. 2000). Besides oceanic plankton communities, iron-deficiency has been well documented in plants and in heterotrophs.