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Relationship: 2333
Title
Decrease, Photosystem II efficiency leads to Decrease, Photosynthesis
Upstream event
Downstream event
Key Event Relationship Overview
AOPs Referencing Relationship
| AOP Name | Adjacency | Weight of Evidence | Quantitative Understanding | Point of Contact | Author Status | OECD Status |
|---|---|---|---|---|---|---|
| Deposition of ionizing energy leading to population decline via inhibition of photosynthesis | adjacent | High | High | Knut Erik Tollefsen (send email) | Under development: Not open for comment. Do not cite | |
| Oxygen-evolving complex damage leading to population decline via inhibition of photosynthesis | adjacent | High | High | Knut Erik Tollefsen (send email) | Under development: Not open for comment. Do not cite | |
| Binding to plastoquinone B site leading to decreased population growth rate via photosystem II inhibition | adjacent | High | High | Li Xie (send email) | Under development: Not open for comment. Do not cite |
Taxonomic Applicability
Sex Applicability
| Sex | Evidence |
|---|---|
| Unspecific | High |
Life Stage Applicability
| Term | Evidence |
|---|---|
| All life stages | High |
Key Event Relationship Description
The decrease in photosystem II (PSII) efficiency impairs the effectiveness of light-driven electron transport in thylakoid membranes, thereby limiting the reduction of plastoquinone, weakening proton gradient formation, and consequently reducing ATP and NADPH production. Since these energy carriers are crucial for carbon fixation, diminished PSII efficiency directly leads to reduced photosynthetic rates. This relationship exhibits direct mechanistic causality and has been consistently validated across all photosynthetic oxygen-producing organisms.
Evidence Collection Strategy
A systematic literature search will be conducted in Web of Science, Scopus, and PubMed using combinations of terms related to PSII efficiency (e.g., Fv/Fm, ΦPSII, ETR, chlorophyll fluorescence) and photosynthesis (e.g., oxygen evolution, CO₂ fixation, ¹⁴C uptake). Studies will be included if they report paired measurements of PSII performance and photosynthetic rate in oxygenic phototrophs under controlled exposure conditions. Priority will be given to experiments demonstrating temporal or dose-response concordance. Extracted data will include species, exposure details, endpoints, effect magnitude, and methodological quality to support WoE evaluation and potential quantitative linkage.
Evidence Supporting this KER
Strong empirical evidence supports the relationship between decreased PSII efficiency and reduced photosynthesis. Declines in chlorophyll fluorescence parameters (e.g., Fv/Fm) are consistently associated with reduced oxygen evolution and carbon fixation rates in plants and algae (Maxwell and Johnson, 2000; DELIEU and WALKER, 1981). PSII-inhibiting herbicides such as atrazine and terbutryn directly impair electron transport at the D1 protein QB site, leading to decreased photosynthetic performance (Alfonso et al., 1996; Broser et al., 2011). These studies demonstrate mechanistic causality, dose-response concordance, and cross-taxa consistency, providing strong support for this KER.
Biological Plausibility
Biological plausibility was considered as high. Photosystem II (PSII) is the primary site of light-driven charge separation and water oxidation in oxygenic photosynthesis, and its photochemical efficiency governs electron entry into the photosynthetic electron transport chain (Maxwell and Johnson, 2000). Reduced PSII efficiency limits electron transfer from QA to QB, decreasing plastoquinone reduction and proton gradient formation across the thylakoid membrane, thereby constraining ATP and NADPH production (Broser et al., 2011). Because ATP and NADPH drive the Calvin–Benson cycle, impaired PSII function mechanistically results in decreased carbon fixation and overall photosynthetic rate.
Empirical Evidence
The empirical support of this KER is considered high.
Rationale: A substantial body of experimental evidence demonstrates strong incidence, dose, and temporal concordance between decreased Photosystem II (PSII) efficiency and reduced photosynthetic performance across cyanobacteria, algae, aquatic macrophytes, and higher plants. Reductions in chlorophyll fluorescence parameters (e.g., Fv/Fm, ΦPSII) are consistently accompanied by declines in oxygen evolution and carbon fixation, with few inconsistencies reported.
Evidence:
Dose concordance: Increasing concentrations of PSII inhibitors (e.g., diuron, atrazine, terbutryn) cause progressive declines in Fv/Fm and ΦPSII, which are quantitatively paralleled by reductions in oxygen evolution and CO₂ assimilation rates. In controlled experiments, decreases in fluorescence-based PSII efficiency strongly correlate with inhibition of electron transport and reduced photosynthetic activity (Maxwell and Johnson, 2000; Delieu and Walker, 1981).
Incidence concordance: Impaired PSII photochemistry, reflected by altered QA reoxidation kinetics and reduced quantum yield, is consistently associated with diminished photosynthetic oxygen evolution in functional assays across taxa (Sundby et al., 1993; Broser et al., 2011).
Temporal concordance: Reductions in PSII efficiency occur rapidly (minutes to hours) after herbicide exposure or photoinhibitory stress, followed by measurable decreases in carbon fixation and net photosynthesis, supporting upstream–downstream sequence consistency (Macinnis-Ng and Ralph, 2003; Wilkinson et al., 2015).
Genetic/functional concordance: Mutations or damage affecting PSII reaction center components reduce photochemical efficiency and are directly accompanied by decreased photosynthetic capacity, supporting causal linkage between PSII impairment and reduced photosynthesis (Ohad and Hirschberg, 1992; Alfonso et al., 1996).
Uncertainties and Inconsistencies
Some variability exists across species, light regimes, and exposure conditions. PSII efficiency reductions do not always translate proportionally to decreased whole-organism photosynthesis due to compensatory mechanisms, alternative electron pathways, or short-term acclimation. Differences in measurement methods and recovery dynamics may also introduce variability in observed effect magnitude.
Known modulating factors
| Modulating Factor (MF) | MF Specification | Effect(s) on the KER | Reference(s) |
|---|---|---|---|
| Light intensity | Low vs. high irradiance; fluctuating light | High light amplifies PSII photoinhibition and accelerates decline in photosynthesis; low light may partially mask PSII impairment | Maxwell and Johnson, 2000 |
| Temperature | Suboptimal vs. optimal thermal range | Alters membrane fluidity and enzyme kinetics, modifying electron transport and recovery capacity | Sundby et al., 1993 |
| Nutrient status | Nitrogen or iron limitation | Reduces chlorophyll content and D1 repair capacity, strengthening coupling between PSII decline and photosynthesis reduction | Maxwell and Johnson, 2000 |
| Species-specific traits | NPQ capacity, cyclic electron flow, antenna size | Enhanced photoprotective mechanisms buffer translation of PSII impairment into reduced photosynthesis | Maxwell and Johnson, 2000 |
| Exposure duration | Acute vs. chronic exposure | Short-term inhibition may be reversible; prolonged exposure leads to sustained reduction in photosynthesis | Macinnis-Ng and Ralph, 2003 |
Quantitative Understanding of the Linkage
The quantitative understanding is high. PSII efficiency endpoints consistently show equal or greater sensitivity than whole-photosynthesis measurements, reflecting upstream positioning in the pathway. In Rhodomonas salina, the EC₅₀ for PSII photoinhibition (ΔF/Fm′) was 1.71 µg/L diuron, compared to 6.27 µg/L for growth (Thomas et al., 2020). Oxygen evolution in Synechococcus elongatus was inhibited by 50% at 20 µg/L diuron and 65 µg/L atrazine (Jones et al., 2003). Regulatory assessments report similar EC₅₀ values for atrazine based on fluorescence (232 µg/L) and oxygen evolution (222 µg/L), demonstrating quantitative concordance (USEPA, n.d.).
Response-response Relationship
A strong response–response relationship exists between PSII efficiency and photosynthetic. Declines in Fv/Fm or ΦPSII correlate proportionally with reductions in electron transport, oxygen evolution, and CO₂ fixation. This quantitative alignment supports a mechanistically consistent, predictive linkage between upstream photochemical impairment and downstream photosynthetic performance.
Time-scale
The time-scale of this KER is rapid and sequential. Decreases in PSII efficiency typically occur within minutes to hours following exposure to PSII inhibitors or photoinhibitory stress. Reductions in oxygen evolution and carbon fixation follow shortly thereafter, while longer-term decreases in growth emerge under sustained exposure conditions.
Known Feedforward/Feedback loops influencing this KER
PSII impairment activates feedback mechanisms such as increased non-photochemical quenching (NPQ) and cyclic electron flow, which transiently compensate for reduced photochemical efficiency (Maxwell and Johnson, 2000). However, sustained PSII inhibition enhances reactive oxygen species (ROS) formation, leading to oxidative damage of the D1 protein and amplifying photosynthetic decline through feedforward stress pathways (Sundby, Chow and Anderson, 1993; Alfonso et al., 1996).
Domain of Applicability
Taxonomic applicability: This KER applies to all oxygenic photosynthetic taxa possessing Photosystem II (PSII), including cyanobacteria, chlorophytes (green algae), diatoms, macrophytes (e.g., Lemna spp.), seagrasses, and higher terrestrial plants. The mechanistic linkage is conserved because PSII structure and electron transport function are highly evolutionarily conserved across these groups.
Sex applicability: Not sex-specific. Photosynthesis is not sexually dimorphic; therefore, the KER is applicable to both male and female individuals in dioecious plant species, as well as hermaphroditic or clonal organisms.
Life-stage applicability: Applicable across all photosynthetically active life stages, including vegetative growth stages, juvenile and adult plants, and algal exponential growth phases. Sensitivity may vary with developmental stage due to differences in chloroplast density, metabolic demand, and repair capacity, but the mechanistic relationship remains consistent.
Chemical applicability: Most relevant for PSII-targeting chemicals (e.g., triazines, phenylureas, triazinones) and stressors causing photoinhibition, oxidative damage to D1 protein, or disruption of thylakoid electron transport.
Environmental applicability: Relevant under light-exposed conditions in freshwater, marine, and terrestrial ecosystems. The linkage may be modulated by irradiance, temperature, and nutrient status.
References
Alfonso, M., Pueyo, J.J., Gaddour, K., Etienne, A.-L., Kirilovsky, D. and Picorel, R., 1996. Induced new mutation of D1 serine-268 in soybean photosynthetic cell cultures produced atrazine resistance, increased stability of S2QB⁻ and S3QB⁻ states, and increased sensitivity to light stress. Plant Physiology, 112(4), pp.1499–1508.
Broser, M., Glöckner, C., Gabdulkhakov, A., Guskov, A., Buchta, J., Kern, J., Müh, F., Dau, H., Saenger, W. and Zouni, A., 2011. Structural basis of cyanobacterial Photosystem II inhibition by the herbicide terbutryn. Journal of Biological Chemistry, 286(18), pp.15964–15972.
Delieu, T. and Walker, D.A., 1981. Polarographic measurement of photosynthetic oxygen evolution by leaf discs. New Phytologist, 89(2), pp.165–178.
Macinnis-Ng, C.M.O. and Ralph, P.J., 2003. Short-term response and recovery of the seagrass Zostera capricorni to the herbicide diuron. Marine Environmental Research, 55(2), pp.153–166.
Maxwell, K. and Johnson, G.N., 2000. Chlorophyll fluorescence—A practical guide. Journal of Experimental Botany, 51(345), pp.659–668.
Ohad, N. and Hirschberg, J., 1992. Mutations in the D1 protein of photosystem II affect herbicide binding and electron transport properties. Plant Cell, 4(3), pp.273–282.
Sundby, C., Chow, W.S. and Anderson, J.M., 1993. Effects on Photosystem II function, photoinhibition, and herbicide binding caused by mutation of the D1 protein. Photosynthesis Research, 36(2), pp.123–135.
Wilkinson, A.D., Collier, C.J., Flores, F. and Ralph, P.J., 2015. Assessing the toxicity of herbicides to tropical seagrasses using chlorophyll fluorescence. Marine Pollution Bulletin, 95(2), pp.449–455.
Jones, R.J., Muller, J., Haynes, D. and Schreiber, U., 2003. Effects of herbicides diuron and atrazine on corals of the Great Barrier Reef, Australia. Marine Ecology Progress Series, 251, pp.153–167.
Thomas, M.C. et al., 2020. Toxicity of ten herbicides to the tropical marine microalgae Rhodomonas salina. Scientific Reports, 10, Article 7521.
U.S. Environmental Protection Agency (EPA), n.d. Ambient Aquatic Life Water Quality Criteria for Atrazine