共查询到20条相似文献,搜索用时 15 毫秒
1.
2.
3.
4.
5.
C. C. W. LEE J. H. SAVARINO H. CACHIER M. H. THIEMENS 《Tellus. Series B, Chemical and physical meteorology》2002,54(3):193-200
The recent discovery of an anomalous enrichment in 17 O isotope in atmospheric sulfate has opened a new way to investigate the oxidation pathways of sulfur in the atmosphere. From laboratory investigations, it has been suggested that the wet oxidation of sulfur in rain droplets was responsible for the excess 17 O. In order to confirm this theory, sulfur and oxygen isotope ratios of different primary sulfates produced during fossil fuel combustion have been investigated and are reported. None of these samples exhibits any anomalous oxygen or sulfur isotopic content, as compared to urban sulfate aerosols. These results, in agreement with the laboratory investigations, reinforce the idea of an aqueous origin for the oxygen-17 anomaly found in tropospheric sulfates. 相似文献
6.
The relationship between 18 O/16 O and 13 C/12 C ratios of ambient CO2 in two Amazonian tropical forests
LEONEL DA S. L. STERNBERG MARCELO Z. MOREIRA LUIZ A. MARTINELLI REYNALDO L. VICTORIA EDELCILIO M. BARBOSA LUIZ C. M. BONATES DANIEL NEPSTAD 《Tellus. Series B, Chemical and physical meteorology》1998,50(4):366-376
7.
8.
W. J. M. VAN DER KEMP C. ALDERLIESTEN K. VAN DER BORG A. F. M. DE JONG R. A. N. LAMERS J. OERLEMANS M. THOMASSEN R. S. W. VAN DE WAL 《Tellus. Series B, Chemical and physical meteorology》2002,54(2):186-192
Samples of a core (52 m) of ablating Antarctic ice were analysed for 14 CO and 14 CO2 by accelerator mass spectrometry. The data were compared with a 14 C in situ production model that includes muon capture in addition to oxygen spallation by neutrons. The analysis reveals significant in situ 14 C at depths below 10 m, which we attribute to 14 C production by cosmic ray muons. The age of the ice was determined as 9.3±0.4 14 C ka BP. 相似文献
9.
10.
By TOBIAS NAEGLER 《Tellus. Series B, Chemical and physical meteorology》2009,61(2):372-384
Oceanic excess radiocarbon data is widely used as a constraint for air–sea gas exchange. However, recent estimates of the global mean piston velocity 〈 k 〉 from Naegler et al., Krakauer et al., Sweeney et al. and Müller et al. differ substantially despite the fact that they all are based on excess radiocarbon data from the GLODAP data base. Here I show that these estimates of 〈 k 〉 can be reconciled if first, the changing oceanic radiocarbon inventory due to net uptake of CO2 is taken into account; second, if realistic reconstructions of sea surface Δ14 C are used and third, if 〈 k 〉 is consistently reported with or without normalization to a Schmidt number of 660. These corrections applied, unnormalized estimates of 〈 k 〉 from these studies range between 15.1 and 18.2 cm h−1 . However, none of these estimates can be regarded as the only correct value for 〈 k 〉 . I thus propose to use the 'average' of the corrected values of 〈 k 〉 presented here (16.5 ± 3.2 cm h−1 ) as the best available estimate of the global mean unnormalized piston velocity 〈 k 〉 , resulting in a gross ocean-to-atmosphere CO2 flux of 76 ± 15 PgC yr−1 for the mid-1990s. 相似文献
11.
12.
13.
14.
15.
16.
By HEATHER D. GRAVEN † BRITTON B. STEPHENS THOMAS P. GUILDERSON TERESA L. CAMPOS DAVID S. SCHIMEL J. ELLIOTT CAMPBELL RALPH F. KEELING 《Tellus. Series B, Chemical and physical meteorology》2009,61(3):536-546
Measurements of Δ14 C in atmospheric CO2 are an effective method of separating CO2 additions from fossil fuel and biospheric sources or sinks of CO2 . We illustrate this technique with vertical profiles of CO2 and Δ14 C analysed in whole air flask samples collected above Colorado, USA in May and July 2004. Comparison of lower tropospheric composition to cleaner air at higher altitudes (>5 km) revealed considerable additions from respiration in the morning in both urban and rural locations. Afternoon concentrations were mainly governed by fossil fuel emissions and boundary layer depth, also showing net biospheric CO2 uptake in some cases. We estimate local industrial CO2 :CO emission ratios using in situ measurements of CO concentration. Ratios are found to vary by 100% and average 57 mole CO2 :1 mole CO, higher than expected from emissions inventories. Uncertainty in CO2 from different sources was ±1.1 to ±4.1 ppm for addition or uptake of −4.6 to 55.8 ppm, limited by Δ14 C measurement precision and uncertainty in background Δ14 C and CO2 levels. 相似文献
17.
Hiroshi A. Takahashi Eiichi Konohira Tetsuya Hiyama Masayo Minami Toshio Nakamura Naohiro Yoshida 《Tellus. Series B, Chemical and physical meteorology》2002,54(2):97-109
Diurnal variation in the atmospheric CO2 concentration and the carbon isotopic composition (Δ14 C and δ13 C) was measured in a forest in an urban area on 9 February 1999. The carbon isotope approach used in the present study differentiated between the quantitative contributions from anthropogenic and biogenic CO2 sources in the urban atmosphere. The anthropogenic (fossil fuel) and biogenic (soil respiration) contributions was estimated, and they ranged from 1 to 16% and from 2 to 8% of the total atmospheric CO2 . The diurnal variation of the anthropogenic CO2 was the major cause of the total atmospheric CO2 variation, while the biogenic CO2 remained relatively constant throughout the day. Estimating the contribution of soil respired CO2 provided the mean residence time of soil respired CO2 within the forest atmosphere. 相似文献
18.
19.