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Several studies have attempted to determine the lower limit of atmospheric oxygen under which combustion can occur; however, none have been conducted within a fully controlled and realistic atmospheric environment. We performed experimental burns (using pine wood, moss, matches, paper, and a candle) at 20°C in O₂ concentrations ranging from 9 to 21% and at ambient and high CO₂ (2000 parts per million) in a controlled environment room, which was equipped with a thermal imaging system and full atmospheric, temperature, and humidity control. Our data reveal that the lower O₂ limit for combustion should be increased from 12 to 15%. These results, coupled with a record of Mesozoic paleowildfires, are incompatible with the prediction of prolonged intervals of low atmospheric O₂ levels (10 to 12%) in the Mesozoic.

The Triassic-Jurassic boundary marks a major faunal mass extinction, but records of accompanying environmental changes are limited. Paleobotanical evidence indicates a fourfold increase in atmospheric carbon dioxide concentration and suggests an associated 3° to 4°C \"greenhouse\" warming across the boundary. These environmental conditions are calculated to have raised leaf temperatures above a highly conserved lethal limit, perhaps contributing to the >95 percent species-level turnover of Triassic-Jurassic megaflora.

Climate change is likely to have altered the ecological functioning of past ecosystems, and is likely to alter functioning in the future; however, the magnitude and direction of such changes are difficult to predict. Here we use a deep-time case study to evaluate the impact of a well-constrained CO 2 -induced global warming event on the ecological functioning of dominant plant communities. We use leaf mass per area (LMA), a widely used trait in modern plant ecology, to infer the palaeoecological strategy of fossil plant taxa. We show that palaeo-LMA can be inferred from fossil leaf cuticles based on a tight relationship between LMA and cuticle thickness observed among extant gymnosperms. Application of this new palaeo-LMA proxy to fossil gymnosperms from East Greenland reveals significant shifts in the dominant ecological strategies of vegetation found across the Triassic–Jurassic transition. Late Triassic forests, dominated by low-LMA taxa with inferred high transpiration rates and short leaf lifespans, were replaced in the Early Jurassic by forests dominated by high-LMA taxa that were likely to have slower metabolic rates. We suggest that extreme CO 2 -induced global warming selected for taxa with high LMA associated with a stress-tolerant strategy and that adaptive plasticity in leaf functional traits such as LMA contributed to post-warming ecological success. Leaf cuticle thickness can infer leaf mass area (LMA) of fossil plants. Gymnosperms from East Greenland show forests of low LMA taxa being replaced by high LMA taxa across the Triassic–Jurassic boundary as a result of CO 2 -induced global warming.

Studies have indicated that plant stomatal conductance (gs) decreases in response to elevated atmospheric CO2, a phenomenon of significance for the global hydrological cycle. However, gs increases across certain CO2 ranges have been predicted by optimization models. The aim of this work was to demonstrate that under certain environmental conditions, gs can increase in response to elevated CO2. Using (1) an extensive, up-to-date synthesis of gs responses in free air CO2 enrichment (FACE)experiments, (2) in situ measurements across four biomes showing dynamic gs responses to a CO2 rise of ~50 ppm (characterizing the change in this greenhouse gas over the past three decades) and (3) a photosynthesis-stomatal conductance model, it is demonstrated that gs can in some cases increase in response to increasing atmospheric CO2. Field observations are corroborated by an extensive synthesis of gs responses in FACE experiments showing that 11.8 % of gs responses under experimentally elevated CO2 are positive. They are further supported by a strong data-model fit (r2 = 0.607) using a stomatal optimization model applied to the field gs dataset. A parameter space identified in the Farquhar-Ball-Berry photosynthesis-stomatal conductance model confirms field observations of increasing gs under elevated CO2 in hot dry conditions. Contrary to the general assumption, positive gs responses to elevated CO2, although relatively rare, are a feature of woody taxa adapted to warm, low-humidity conditions, and this response is also demonstrated in global simulations using the Community Land Model (CLM4). The results contradict the over-simplistic notion that global vegetation always responds with decreasing gs to elevated CO2, a finding that has important implications for predicting future vegetation feedbacks on the hydrological cycle at the regional level.

Fluctuations in [CO 2 ] have been widely studied as a potential driver of plant evolution; however, the role of a fluctuating [O 2 ]:[CO 2 ] ratio is often overlooked. The present study aimed to investigate the inherent physiological plasticity of early diverging, extant species following acclimation to an atmosphere similar to that across the Triassic-Jurassic mass extinction interval (TJB, approx. 200 Mya), a time of major ecological change. Mature plants from two angiosperm ( Drimys winteri and Chloranthus oldhamii ), two monilophyte ( Osmunda claytoniana and Cyathea australis ) and one gymnosperm ( Ginkgo biloba ) species were grown for 2 months in replicated walk-in Conviron BDW40 chambers running at TJB treatment conditions of 16 % [O 2 ]-1900 ppm [CO 2 ] and ambient conditions of 21 % [O 2 ]-400 ppm [CO 2 ], and their physiological plasticity was assessed using gas exchange and chlorophyll fluorescence methods. TJB acclimation caused significant reductions in the maximum rate of carboxylation ( V Cmax ) and the maximum electron flow supporting ribulose-1,5-bisphosphate regeneration ( J max ) in all species, yet this downregulation had little effect on their light-saturated photosynthetic rate ( A sat ). Ginkgo was found to photorespire heavily under ambient conditions, while growth in low [O 2 ]:[CO 2 ] resulted in increased heat dissipation per reaction centre ( DI o / RC ), severe photodamage, as revealed by the species' decreased maximum efficiency of primary photochemistry ( F v / F m ) and decreased in situ photosynthetic electron flow ( Jsitu ). It is argued that the observed photodamage reflects the inability of Ginkgo to divert excess photosynthetic electron flow to sinks other than the downregulated C 3 and the diminished C 2 cycles under low [O 2 ]:[CO 2 ]. This finding, coupled with the remarkable physiological plasticity of the ferns, provides insights into the underlying mechanism of Ginkgoales' near extinction and ferns' proliferation as atmospheric [CO 2 ] increased to maximum levels across the TJB.

Leaf stomatal density and index of Ginkgo biloba L. were both significantly (P<0.05) reduced after 3 years growth at elevated CO2 (560 ppm), with values comparable to those of cuticles prepared from Triassic and Jurassic fossil Ginkgo leaves thought to have developed in the high CO2 ‘greenhouse world’ of the Mesozoic. A reciprocal transfer experiment indicated that reductions in stomatal density and index irreversibly reduced stomatal conductance, particularly at low leaf-to-air vapour pressure deficits and low internal leaf CO2 concentrations (Ci). These effects probably contributed to the high water-use efficiency of Ginkgo spp. in the Mesozoic relative to those of the present, as determined from carbon isotope measurements of extant and fossil cuticles.

Several studies have attempted to determine the lower limit of atmospheric oxygen under which combustion can occur; however, none have been conducted within a fully controlled and realistic atmospheric environment. We performed experimental burns (using pine wood, moss, matches, paper, and a candle) at 20°C in O 2 concentrations ranging from 9 to 21% and at ambient and high CO 2 (2000 parts per million) in a controlled environment room, which was equipped with a thermal imaging system and full atmospheric, temperature, and humidity control. Our data reveal that the lower O 2 limit for combustion should be increased from 12 to 15%. These results, coupled with a record of Mesozoic paleowildfires, are incompatible with the prediction of prolonged intervals of low atmospheric O 2 levels (10 to 12%) in the Mesozoic.

This corrects the article DOI: 10.1038/nplants.2017.104.