This paper describes the contents of the 2016 edition of the HITRAN molecular spectroscopic compilation. The new edition replaces the previous HITRAN edition of 2012 and its updates during the intervening years. The HITRAN molecular absorption compilation is composed of five major components: the traditional line-by-line spectroscopic parameters required for high-resolution radiative-transfer codes, infrared absorption cross-sections for molecules not yet amenable to representation in a line-by-line form, collision-induced absorption data, aerosol indices of refraction, and general tables such as partition sums that apply globally to the data. The new HITRAN is greatly extended in terms of accuracy, spectral coverage, additional absorption phenomena, added line-shape formalisms, and validity. Moreover, molecules, isotopologues, and perturbing gases have been added that address the issues of atmospheres beyond the Earth. Of considerable note, experimental IR cross-sections for almost 300 additional molecules important in different areas of atmospheric science have been added to the database. The compilation can be accessed through www.hitran.org. Most of the HITRAN data have now been cast into an underlying relational database structure that offers many advantages over the long-standing sequential text-based structure. The new structure empowers the user in many ways. It enables the incorporation of an extended set of fundamental parameters per transition, sophisticated line-shape formalisms, easy user-defined output formats, and very convenient searching, filtering, and plotting of data. A powerful application programming interface making use of structured query language (SQL) features for higher-level applications of HITRAN is also provided.

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The HITRAN 2008 molecular spectroscopic database

Changes in Atmospheric Constituents and in Radiative Forcing

Using inorganic carbon measurements from an international survey effort in the 1990s and a tracer-based separation technique, we estimate a global oceanic anthropogenic carbon dioxide (CO2) sink for the period from 1800 to 1994 of 118 19 petagrams of carbon. The oceanic sink accounts for48% of the total fossil-fuel and cement-manufacturing emissions, implying that the terrestrial biosphere was a net source of CO 2 to the atmosphere of about 39 28 petagrams of carbon for this period. The current fraction of total anthropogenic CO2 emissions stored in the ocean appears to be about one-third of the long-term potential. Since the beginning of the industrial period in the late 18th century, i.e., over the anthropocene (1), humankind has emitted large quantities of CO2 into the atmosphere, mainly as a result of fossil-fuel burning, but also because of land-use practices, e.g., deforestation (2). Measurements and reconstructions of the atmospheric CO2 history reveal, however, that less than half of these emissions remain in the atmosphere (3). The anthropogenic CO2 that did not accumulate in the atmosphere must have been taken up by the ocean, by the land biosphere, or by a combination of both. The relative roles of the ocean and land biosphere as sinks for anthropogenic CO2 over the anthropocene are currently not known. Although the anthropogenic CO2 budget for the past two decades, i.e., the 1980s and 1990s, has been investigated in detail (3), the estimates of the ocean sink have not been based on direct measurements of changes in the oceanic inventory of dissolved inorganic carbon (DIC). Recognizing the need to constrain the oceanic uptake, transport, and storage of anthropogenic CO 2 for the anthropocene and to provide a baseline for future estimates of oceanic CO 2 uptake, two international ocean research programs, the World Ocean Circulation Experiment (WOCE) and the Joint Global Ocean Flux Study (JGOFS), jointly conducted a comprehensive survey of inorganic carbon distributions in the global ocean in the 1990s (4). After completion of the U.S. field program in 1998, a 5-year effort was begun to compile and rigorously quality-control the U.S. and international data sets, in

/pdf/the-oceanic-sink-for-anthropogenic-co2-480zoye29p.pdf

The oceanic sink for anthropogenic CO2.

We present the greenhouse gas concentrations for the Representative Concentration Pathways (RCPs) and their extensions beyond 2100, the Extended Concentration Pathways (ECPs). These projections include all major anthropogenic greenhouse gases and are a result of a multi-year effort to produce new scenarios for climate change research. We combine a suite of atmospheric concentration observations and emissions estimates for greenhouse gases (GHGs) through the historical period (1750-2005) with harmonized emissions projected by four different Integrated Assessment Models for 2005-2100. As concentrations are somewhat dependent on the future climate itself (due to climate feedbacks in the carbon and other gas cycles), we emulate median response characteristics of models assessed in the IPCC Fourth Assessment Report using the reduced-complexity carbon cycle climate model MAGICC6. Projected 'best-estimate' global-mean surface temperature increases (using inter alia a climate sensitivity of 3°C) range from 1.5°C by 2100 for the lowest of the four RCPs, called both RCP3-PD and RCP2.6, to 4.5°C for the highest one, RCP8.5, relative to pre-industrial levels. Beyond 2100, we present the ECPs that are simple extensions of the RCPs, based on the assumption of either smoothly stabilizing concentrations or constant emissions: For example,

/pdf/the-rcp-greenhouse-gas-concentrations-and-their-extensions-2lai11z83a.pdf

The RCP greenhouse gas concentrations and their extensions from 1765 to 2300

Soil carbon sequestration to mitigate climate change

A record of atmospheric CO2 mixing ratios from 1006 A.D. to 1978 A.D. has been produced by analysing the air enclosed in three ice cores from Law Dome, Antarctica. The enclosed air has unparalleled age resolution and extends into recent decades, because of the high rate of snow accumulation at the ice core sites. The CO2 data overlap with the record from direct atmospheric measurements for up to 20 years. The effects of diffusion in the firn on the CO2 mixing ratio and age of the ice core air were determined by analyzing air sampled from the surface down to the bubble close-off depth. The uncertainty of the ice core CO2 mixing ratios is 1.2 ppm (1 σ). Preindustrial CO2 mixing ratios were in the range 275–284 ppm, with the lower levels during 1550–1800 A.D., probably as a result of colder global climate. Natural CO2 variations of this magnitude make it inappropriate to refer to a single preindustrial CO2 level. Major CO2 growth occurred over the industrial period except during 1935–1945 A.D. when CO2 mixing ratios stabilized or decreased slightly, probably as a result of natural variations of the carbon cycle on a decadal timescale.

Natural and anthropogenic changes in atmospheric CO2 over the last 1000 years from air in Antarctic ice and firn

The air occluded in ice sheets and glaciers has, in general, a younger age (defined as the time after its isolation from the atmosphere) than the surrounding ice matrix because snow is first transformed into open porous firn, in which the air can exchange with the atmosphere. Only at a certain depth (firn-ice transition) the pores are pinched off and the air is definitely isolated from the atmosphere. The firn-ice transition depth is at around 70 m under present climatic conditions at Summit, central Greenland. The air at this depth is roughly 10 years old due to diffusive mixing, whereas the ice is about 220 years old. This results in an age difference between the air and the ice of 210 years. This difference depends on temperature and accumulation rate and did thus not remain constant during the past. We used a dynamic firn densification model to calculate the firn-ice transition depth and the age of the ice at this depth and an air diffusion model to determine the age of the air at the transition. Past temperatures and accumulation rates have been deduced from the δ18O record using time independent functions. We present the results of model calculations of two paleotemperature scenarios yielding a record of the age difference between the air and the ice for the Greenland Ice Core Project (GRIP) and the Greenland Ice Sheet Project Two (GISP2) ice cores for the last 100,000 years. During the Holocene, the age difference stayed rather stable around 200 years, while it reached values up to 1400 years during the last glaciation for the colder scenario. The model results are compared with age differences obtained independently by matching corresponding climate events in the methane and δ18O records assuming a very small phase lag between variations in the Greenland surface temperature and the atmospheric methane. The past firn-ice transition depths are compared with diffusive column heights obtained from δ15N of N2 measurements. The results of this study corroborate the large temperature change of 20 to 25 K from the coldest glacial to Holocene climate found by evaluating borehole temperature profiles.

https://agupubs.onlinelibrary.wiley.com/doi/pdf/10.1029/97JD01309

Age scale of the air in the summit ice: Implication for glacial-interglacial temperature change

The atmospheric histories of two potent greenhouse gases, tetrafluoromethane (CF4) and hexafluoroethane (C2F6), have been reconstructed for the 20th century based on firn air measurements from both hemispheres. The reconstructed atmospheric trends show that the mixing ratios of both CF4 and C2F6 have increased during the 20th century by factors of ∼2 and ∼10, respectively. Initially, the increasing mixing ratios coincided with the rise in primary aluminum production. However, a slower atmospheric growth rate for CF4 appears to be evident during the 1990s, which supports recent aluminum industry reports of reduced CF4 emissions. This work illustrates the changing relationship between CF4 and C2F6 that is likely to be largely the result of both reduced emissions from the aluminum industry and faster growing emissions of C2F6 from the semiconductor industry. Measurements of C2F6 in the older firn air indicate a natural background mixing ratio of <0.3 parts per trillion (ppt), demonstrating that natural sourc...

Jean-Marc Barnola

Papers

Natural and anthropogenic changes in atmospheric CO2 over the last 1000 years from air in Antarctic ice and firn

Age scale of the air in the summit ice: Implication for glacial-interglacial temperature change

Atmospheric trends and radiative forcings of CF4 and C2F6 inferred from firn air.

Comment on ¿Greenland-Antarctic phase relations and millennial time-scale climate fluctuations in the Greenland ice-cores¿ by C. Wunsch

High-resolution carbon dioxide concentration records from the EPICA Dome C ice core (EDC99)