Carbon dioxide removal (CDR) from the atmosphere has been proposed as a measure for mitigating global warming and ocean acidification. To assess the extent to which CDR might eliminate the long-term consequences of anthropogenic CO2 emissions in the marine environment, we simulate the effect of two massive CDR interventions with CO2 extraction rates of 5 GtC yr(-1) and 25 GtC yr(-1), respectively, while CO2 emissions follow the extended RCP8.5 pathway. We falsify two hypotheses: the first being that CDR can restore pre-industrial conditions in the ocean by reducing the atmospheric CO2 concentration back to its pre-industrial level, and the second being that high CO2 emissions rates (RCP8.5) followed by CDR have long-term oceanic consequences that are similar to those of low emissions rates (RCP2.6). Focusing on pH, temperature and dissolved oxygen, we find that even after several centuries of CDR deployment, past CO2 emissions would leave a substantial legacy in the marine environment.

Climate change in response to a change in external forcing can be understood in terms of fast response to the imposed forcing and slow feedback associated with surface temperature change. Previous studies have investigated the characteristics of fast response and slow feedback for different forcing agents. Here we examine to what extent that fast response and slow feedback derived from time-mean results of climate model simulations can be used to infer total climate change. To achieve this goal, we develop a multivariate regression model of climate change, in which the change in a climate variable is represented by a linear combination of its sensitivity to CO2 forcing, solar forcing, and change in global mean surface temperature. We derive the parameters of the regression model using time-mean results from a set of HadCM3L climate model step-forcing simulations, and then use the regression model to emulate HadCM3L-simulated transient climate change. Our results show that the regression model emulates well HadCM3L-simulated temporal evolution and spatial distribution of climate change, including surface temperature, precipitation, runoff, soil moisture, cloudiness, and radiative fluxes under transient CO2 and/or solar forcing scenarios. Our findings suggest that temporal and spatial patterns of total change for the climate variables considered here can be represented well by the sum of fast response and slow feedback. Furthermore, by using a simple 1-D heat-diffusion climate model, we show that the temporal and spatial characteristics of climate change under transient forcing scenarios can be emulated well using information from step-forcing simulations alone.

Anthropogenic emissions of carbon dioxide (CO2) are causing ocean acidification, lowering seawater aragonite (CaCO3) saturation state (Omega(arag)), with potentially substantial impacts on marine ecosystems over the 21st Century. Calcifying organisms have exhibited reduced calcification under lower saturation state conditions in aquaria. However, the in situ sensitivity of calcifying ecosystems to future ocean acidification remains unknown. Here we assess the community level sensitivity of calcification to local CO2-induced acidification caused by natural respiration in an unperturbed, biodiverse, temperate intertidal ecosystem. We find that on hourly timescales nighttime community calcification is strongly influenced by Omega(arag), with greater net calcium carbonate dissolution under more acidic conditions. Daytime calcification however, is not detectably affected by Omega(arag). If the short-term sensitivity of community calcification to Omega(arag) is representative of the long-term sensitivity to ocean acidification, nighttime dissolution in these intertidal ecosystems could more than double by 2050, with significant ecological and economic consequences.

Approximately one-quarter of the anthropogenic carbon dioxide released into the atmosphere each year is absorbed by the global oceans, causing measurable declines in surface ocean pH, carbonate ion concentration ([CO32-]), and saturation state of carbonate minerals (Omega)(1). This process, referred to as ocean acidification, represents a major threat to marine ecosystems, in particular marine calcifiers such as oysters, crabs, and corals. Laboratory and field studies(2,3) have shown that calcification rates of many organisms decrease with declining pH, [CO32-], and Omega. Coral reefs are widely regarded as one of the most vulnerable marine ecosystems to ocean acidification, in part because the very architecture of the ecosystem is reliant on carbonate-secreting organisms(4). Acidification-induced reductions in calcification are projected to shift coral reefs from a state of net accretion to one of net dissolution this century(5). While retrospective studies show large-scale declines in coral, and community, calcification over recent decades(6-12), determining the contribution of ocean acidification to these changes is difficult, if not impossible, owing to the confounding effects of other environmental factors such as temperature. Here we quantify the net calcification response of a coral reef flat to alkalinity enrichment, and show that, when ocean chemistry is restored closer to pre-industrial conditions, net community calcification increases. In providing results from the first seawater chemistry manipulation experiment of a natural coral reef community, we provide evidence that net community calcification is depressed compared with values expected for pre-industrial conditions, indicating that ocean acidification may already be impairing coral reef growth.

Many previous studies have shown that a solar forcing must be greater than a CO2 forcing to cause the same global mean surface temperature change but a process-based mechanistic explanation is lacking in the literature. In this study, we investigate the physical mechanisms responsible for the lower efficacy of solar forcing compared to an equivalent CO2 forcing. Radiative forcing is estimated using the Gregory method that regresses top-of-atmosphere (TOA) radiative flux against the change in global mean surface temperature. For a 2.25% increase in solar irradiance that produces the same long term global mean warming as a doubling of CO2 concentration, we estimate that the efficacy of solar forcing is similar to 80% relative to CO2 forcing in the NCAR CAM5 climate model. We find that the fast tropospheric cloud adjustments especially over land and stratospheric warming in the first four months cause the slope of the regression between the TOA net radiative fluxes and surface temperature to be steeper in the solar forcing case. This steeper slope indicates a stronger net negative feedback and hence correspondingly a larger solar forcing than CO2 forcing for the same equilibrium surface warming. Evidence is provided that rapid land surface warming in the first four months sets up a land sea contrast that markedly affects radiative forcing and the climate feedback parameter over this period. We also confirm the robustness of our results using simulations from the Hadley Centre climate model. Our study has important implications for estimating the magnitude of climate change caused by volcanic eruptions, solar geoengineering and past climate changes caused by change in solar irradiance such as Maunder minimum.

Natural gas has been suggested as a "bridge fuel" in the transition from coal to a near-zero emission energy system. However, the expansion of natural gas risks a delay in the introduction of near-zero emission energy systems, possibly offsetting the potential climate benefits of a gas-for-coal substitution. We use a schematic climate model to estimate CO2 and CH4 emissions from integrated energy systems and the resulting changes in global warming over various timeframes. Then we evaluate conditions under which delayed deployment of near-zero emission systems would result in loss of all net climate benefit (if any) from using natural gas as a bridge. Considering only physical climate system effects, we find that there is potential for delays in deployment of near-zero-emission technologies to offset all climate benefits from replacing coal energy systems with natural gas energy systems, especially if natural gas leakage is high, the natural gas energy system is inefficient, and the climate change metric emphasizes decadal time scale changes. (C) 2015 The Authors. Published by Elsevier Ltd.

Solar geoengineering has been proposed as a potential means to counteract anthropogenic climate change, yet it is unknown how such climate intervention might affect the Earth's climate on the millennial time scale. Here we use the HadCM3L model to conduct a 1000year sunshade geoengineering simulation in which solar irradiance is uniformly reduced by 4% to approximately offset global mean warming from an abrupt quadrupling of atmospheric CO2. During the 1000year period, modeled global climate, including temperature, hydrological cycle, and ocean circulation of the high-CO2 simulation departs substantially from that of the control preindustrial simulation, whereas the climate of the geoengineering simulation remains much closer to that of the preindustrial state with little drift. The results of our study do not support the hypothesis that nonlinearities in the climate system would cause substantial drift in the climate system if solar geoengineering was to be deployed on the timescale of a millennium.

Ocean acidification has the potential to adversely affect marine calcifying organisms, with substantial ocean ecosystem impacts projected over the 21st century. Characterizing the in situ sensitivity of calcifying ecosystems to natural variability in carbonate chemistry may improve our understanding of the long-term impacts of ocean acidification. We explore the potential for intensive temporal sampling to isolate the influence of carbonate chemistry on community calcification rates of a coral reef and compare the ratio of organic to inorganic carbon production to previous studies at the same location. Even with intensive temporal sampling, community calcification displays only a weak dependence on carbonate chemistry variability. However, across three years of sampling, the ratio of organic to inorganic carbon production is highly consistent. Although further work is required to quantify the spatial variability associated with such ratios, this suggests that these measurements have the potential to indicate the response of coral reefs to ongoing disturbance, ocean acidification, and climate change.

Nearly 17% of people in an international survey said they believed the existence of a secret large-scale atmospheric program (SLAP) to be true or partly true. SLAP is commonly referred to as 'chemtrails' or 'covert geoengineering', and has led to a number of websites purported to show evidence of widespread chemical spraying linked to negative impacts on human health and the environment. To address these claims, we surveyed two groups of experts-atmospheric chemists with expertize in condensation trails and geochemists working on atmospheric deposition of dust and pollution-to scientifically evaluate for the first time the claims of SLAP theorists. Results show that 76 of the 77 scientists (98.7%) that took part in this study said they had not encountered evidence of a SLAP, and that the data cited as evidence could be explained through other factors, including well-understood physics and chemistry associated with aircraft contrails and atmospheric aerosols. Our goal is not to sway those already convinced that there is a secret, large-scale spraying program-who often reject counter-evidence as further proof of their theories-but rather to establish a source of objective science that can inform public discourse.

Projections of ocean acidification have often been based on ocean carbon cycle models that do not represent deep-sea sedimentation and terrestrial weathering. Here we use an Earth system model of intermediate complexity to quantify the effect of sedimentation and weathering on projections of ocean acidification under an intensive CO2 emission scenario that releases 5000 Pg C after year 2000. In our simulations, atmospheric CO2 reaches a peak concentration of 2123 ppm near year 2300 with a maximum reduction in surface pH of 0.8. Consideration of deep-sea sedimentation and terrestrial weathering has negligible effect on these peak changes. Only after several millenniums, sedimentation and weathering feedbacks substantially affect projected ocean acidification. Ten thousand years from today, in the constant-alkalinity simulation, surface pH is reduced by similar to 0.7 with 95% of the polar oceans undersaturated with respect to calcite, and no ocean has a calcite saturation horizon (CSH) that is deeper than 1000 m. With the consideration of sediment feedback alone, surface pH is reduced by similar to 0.5 with 35% of the polar oceans experiencing calcite undersaturation, and 8% global ocean has a CSH deeper than 1000 m. With the addition of weathering feedback, depending on the weathering parameterizations, surface pH is reduced by 0.2-0.4 with no polar oceans experiencing calcite undersaturation, and 30-80% ocean has a CSH that is deeper than 1000 m. Our results indicate that deep-sea sedimentation and terrestrial weathering play an important role in long-term ocean acidification, but have little effect on mitigating ocean acidification in the coming centuries.