The DOI matches its Crossref record; 58 of the 58 references it cites were found in a registry or an index.
The water–water cycle as alternative photon and electron sinks
Open accessAbstract
The water–water cycle in chloroplasts is the photoreduction of dioxygen to water in photosystem I (PS I) by the electrons generated in photosystem II (PS II) from water. In the water–water cycle, the rate of photoreduction of dioxygen in PS I is several orders of magnitude lower than those of the disproportionation of superoxide catalysed by superoxide dismutase, the reduction of hydrogen peroxide to water catalysed by ascorbate peroxidase, and the reduction of the resulting oxidized forms of ascorbate by reduced ferredoxin or catalysed by either dehydroascorbate reductase or monodehydroascorbate reductase. The water–water cycle therefore effectively shortens the lifetimes of photoproduced superoxide and hydrogen peroxide to suppress the production of hydroxyl radicals, their interactions with the target molecules in chloroplasts, and resulting photoinhibition. When leaves are exposed to photon intensities of sunlight in excess of that required to support the fixation of CO 2 , the intersystem electron carriers are over–reduced, resulting in photoinhibition. Under such conditions, the water–water cycle not only scavenges active oxygens, but also safely dissipates excess photon energy and electrons, in addition to downregulation of PS II and photorespiration. The dual functions of the water–water cycle for protection from photoinhibition under photon excess stress are discussed, along with its functional evolution.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Hydrogen Peroxide is Scavenged by Ascorbate-specific Peroxidase in Spinach Chloroplasts
Nakano, Y., & Asada, K. (1981) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a076232 · Cited by 10,809
Self-citationAsada, K. (1999) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.50.1.601 · Cited by 4,061
Self-citationFoyer, C. H., & Halliwell, B. (1976) · Planta · doi:10.1007/bf00386001 · Cited by 2,629
CAKMAK, I. (2000) · New Phytologist · doi:10.1046/j.1469-8137.2000.00630.x · Cited by 1,280
Oxidative stress and the molecular biology of antioxidant defenses.
Scandalios, J. G. (1997) · Cited by 1,027
Photosynthesis and the Environment
(1996) · Advances in Photosynthesis and Respiration · doi:10.1007/0-306-48135-9 · Cited by 972
Studies on reactions of illuminated chloroplasts
Mehler, A. H. (1951) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(51)90082-3 · Cited by 814
(1984) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a076726 · Cited by 733
Photorespiration protects C3 plants from photooxidation
Kozaki, A., & Takeba, G. (1996) · Nature · doi:10.1038/384557a0 · Cited by 593
Farrington, J. A., Ebert, M., Land, E. J., & Fletcher, K. (1973) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(73)90121-7 · Cited by 523
Cited by
Production and Scavenging of Reactive Oxygen Species in Chloroplasts and Their Functions
Asada, K. (2006) · Plant Physiology · doi:10.1104/pp.106.082040 · Cited by 2,752
Self-citationThe role of potassium in alleviating detrimental effects of abiotic stresses in plants
Cakmak, I. (2005) · Journal of Plant Nutrition and Soil Science · doi:10.1002/jpln.200420485 · Cited by 1,300
Making the life of heavy metal-stressed plants a little easier
Gratão, P. L., Polle, A., Lea, P. J., & Azevedo, R. A. (2005) · Functional Plant Biology · doi:10.1071/fp05016 · Cited by 1,156
Davletova, S., Rizhsky, L., Liang, H., Shengqiang, Z., Oliver, D. J., Coutu, J., Shulaev, V., Schlauch, K., & Mittler, R. (2005) · The Plant Cell · doi:10.1105/tpc.104.026971 · Cited by 990
Lawlor, D. W., & Tezara, W. (2009) · Annals of Botany · doi:10.1093/aob/mcn244 · Cited by 852
Metadata
- Authors
- Asada, K.
- Venue
- Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences
- Publisher
- The Royal Society
- Published
- 2000-10-29
- Volume
- 355
- Issue
- 1402
- Pages
- 1419-1431
- ISSN
- 0962-8436 (ISSN-L)
- 1471-2970
- OpenAlex
- W2098243282
- Cited by
- 622
- References
- 58
- FWCI
- 4.06
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: The water–water cycle as alternative photon and electron sinks. https://app.cochat.ai/papers/10.1098/rstb.2000.0703
- The paper
- Asada, K. (2000). The water–water cycle as alternative photon and electron sinks. Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences. https://doi.org/10.1098/rstb.2000.0703
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.