ReviewPhotosynthesis research2011
Algal and aquatic plant carbon concentrating mechanisms in relation to environmental change.
Review in Photosynthesis research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
48 citing papers in PubMed, 1 synthesis or guideline pooled it, 267 citations in OpenAlex.
- Meta-analysis reveals enhanced growth of marine harmful algae from temperate regions with warming and elevated COGlobal change biology · 2019Pooled it
- Changes in photosynthesis and grazing facilitate growth of a mixotrophic protist under ocean acidification and warming.The New phytologist · 2026Article
- Periplasmic carbonic anhydrase CAH1 contributes to high inorganic carbon affinity in Chlamydomonas reinhardtii.Plant physiology · 2024Article
- Inorganic carbon utilization strategies of plateau aquatic plants in response to native habitats.Photosynthesis research · 2024Article
- Effects of ocean acidification on growth and photophysiology of two tropical reef macroalgae.PloS one · 2023Article
- Carbon limitation in response to nutrient loading in an eelgrass mesocosm: influence of water residence time.Marine ecology progress series · 2022Article
- Simulated ocean acidification altered community composition and growth of a coastal phytoplankton assemblage (South West coast of India, eastern Arabian Sea).Environmental science and pollution research international · 2022Article
- CO2-dependent migration and relocation of LCIB, a pyrenoid-peripheral protein in Chlamydomonas reinhardtii.Plant physiology · 2022Article
- Enhancement of diatom growth and phytoplankton productivity with reduced OCommunications biology · 2022Article
- Photorespiration in eelgrass (Frontiers in plant science · 2022Article
- Elevated COFrontiers in microbiology · 2022Article
- Acclimation and adaptation to elevated pCOThe ISME journal · 2021Article
- The Interplay of Phototrophic and Heterotrophic Microbes Under Oil Exposure: A Microcosm Study.Frontiers in microbiology · 2021Article
- Multiple global change stressor effects on phytoplankton nutrient acquisition in a future ocean.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020Review
- Contrasting responses of photosynthesis and photochemical efficiency to ocean acidification under different light environments in a calcifying alga.Scientific reports · 2019Article
- Effects of COScientific reports · 2018Article
- The organizing effects of elevated COScientific reports · 2017Article
- Effects of elevated COScientific reports · 2017Article
- Vulnerability of mixotrophic algae to nutrient pulses and UVR in an oligotrophic Southern and Northern Hemisphere lake.Scientific reports · 2017Article
- The diversity of CO2-concentrating mechanisms in marine diatoms as inferred from their genetic content.Journal of experimental botany · 2017Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors at 4 institutions in 3 countries.
Funding
Abstract
Carbon dioxide concentrating mechanisms (also known as inorganic carbon concentrating mechanisms; both abbreviated as CCMs) presumably evolved under conditions of low CO(2) availability. However, the timing of their origin is unclear since there are no sound estimates from molecular clocks, and even if there were, there are no proxies for the functioning of CCMs. Accordingly, we cannot use previous episodes of high CO(2) (e.g. the Palaeocene-Eocene Thermal Maximum) to indicate how organisms with CCMs responded. Present and predicted environmental change in terms of increased CO(2) and temperature are leading to increased CO(2) and HCO(3)(-) and decreased CO(3)(2-) and pH in surface seawater, as well as decreasing the depth of the upper mixed layer and increasing the degree of isolation of this layer with respect to nutrient flux from deeper waters. The outcome of these forcing factors is to increase the availability of inorganic carbon, photosynthetic active radiation (PAR) and ultraviolet B radiation (UVB) to aquatic photolithotrophs and to decrease the supply of the nutrients (combined) nitrogen and phosphorus and of any non-aeolian iron. The influence of these variations on CCM expression has been examined to varying degrees as acclimation by extant organisms. Increased PAR increases CCM expression in terms of CO(2) affinity, whilst increased UVB has a range of effects in the organisms examined; little relevant information is available on increased temperature. Decreased combined nitrogen supply generally increases CO(2) affinity, decreased iron availability increases CO(2) affinity, and decreased phosphorus supply has varying effects on the organisms examined. There are few data sets showing interactions amongst the observed changes, and even less information on genetic (adaptation) changes in response to the forcing factors. In freshwaters, changes in phytoplankton species composition may alter with environmental change with consequences for frequency of species with or without CCMs. The information available permits less predictive power as to the effect of the forcing factors on CCM expression than for their overall effects on growth. CCMs are currently not part of models as to how global environmental change has altered, and is likely to further alter, algal and aquatic plant primary productivity.
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Registered trials
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