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Modification of three ice-core δ18O records from an area of high melt

Published online by Cambridge University Press:  14 September 2017

Hou Shugui
Affiliation:
Laboratory of Cryosphere and Environment, Cold and Arid Regions Environmental and Engineering Research Institute, Chinese Academy of Sciences, 260 Donggang West Road, Lanzhou 730000, China E-mail: [email protected]
Ren Jiawen
Affiliation:
Laboratory of Cryosphere and Environment, Cold and Arid Regions Environmental and Engineering Research Institute, Chinese Academy of Sciences, 260 Donggang West Road, Lanzhou 730000, China E-mail: [email protected]
Qin Dahe
Affiliation:
Laboratory of Cryosphere and Environment, Cold and Arid Regions Environmental and Engineering Research Institute, Chinese Academy of Sciences, 260 Donggang West Road, Lanzhou 730000, China E-mail: [email protected]
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Abstract

Stable oxygen isotope ratios (δ18O) of three shallow ice cores (extending back to 1963) from Urümqi glacier No. 1 at the headwater of Urümqi river, Tien Shan, northwest China, were used to test the relationship between δ18O and contemporaneous surface air temperature (Ta). The ice cores were dated using the seasonal stable-isotopic signals, and seven insoluble particulate β-activity horizons associated with known nuclear tests. Although a strong positive relationship exists between δ18O in precipitation and Ta at our study site, this relationship is not preserved between the annually averaged ice-core δ18O records and the local temperature due to post-depositional modification. These results indicate that the processes forming the ice-core chemical records in areas of high melt must be understood before the δ18O record can be confidently interpreted as a climatic indicator.

Type
Research Article
Copyright
Copyright © The Author(s) [year] 2006

1. Introduction

Ice-core chemical records from areas experiencing high melt have attracted more and more attention for paleoclimatic construction because of their widespread occurrence in the world (Reference KoernerKoerner, 1997; Reference Grumet, Wake, Zielinski, Fisher, Koerner and JacobsGrumet and others, 1998; Reference Vehviläinen, Isaksson and MooreVehvilainen and others, 2002). However, such valuable ice-core records might be more-or-less modified by post-depositional processes. Reference Hou and QinHou and Qin (2002) compared the chemical profiles from two snow pits sampled successively at the same spot on Urumqi glacier No. 1 (UG1) at the head of Ürumqi river, Tien Shan, northwest China, and reported the striking effect of post-depositional processes on the chemical profiles. This phenomenon is also evident for an ice core drilled from Far East Rongbuk Glacier in the Himalaya (Reference HouHou and others, 2002).

Historically, three independent precipitation-sampling experiments for δ18O were performed at the Daxigou meteorological station (43.05˚ N, 86.49˚ E; 3539ma.s.l.; shown as DMS in Fig. 1) located near UG1. The daily mean δ18O values of precipitation samples collected from 9 July to 17 August 1981 became more negative with a reduction in daily mean air temperature (Reference Watanabe, Wu, Ikegami and AgetaWatanabe and others, 1983). For all the precipitation events sampled from June 1995 to June 1996, a strong temporal relationship was also found between the monthly δ18O in precipitation and monthly Ta, with linear fits as high as 0.95%˚C−1 (R = 0.98; p<0.001; Reference HouHou and others, 1999). This was further confirmed by Reference Yao, Masson, Jouzel, Stiévenard, Sun and JiaoYao and others (1999) based on continuous precipitation sampling from May 1997 to August 1998, with a linear fit of 0.92%˚C−1 (R = 0.96; p<0.001) for monthly averages.

Fig. 1. Sketch map showing our study site and the locations of the Daxigou meteorological station (DMS) and the ice-core drilling sites (TS-1, TS-2 and TS-3).

During May 1996, two shallow ice cores (6.03 and 6.81 m long, ∼2 km away from DMS) were recovered from the accumulation zone of UG1 at an elevation of 4040 m, and another 14.08 m core was recovered near the previous drilling sites in October 1998 (shown as TS-1 , TS-2 and TS-3 in Fig. 1). In this paper, δ18O of these shallow ice cores was used to examine the relationship between δ18O and the contemporaneous surface air temperature recorded at DMS which has been in continuous operation since 1959.

The study site is surrounded by large deserts on the north, south and east sides. The nearest sea is located >3000km away, so the region is dominated by classic continental climate conditions. The weather conditions in the study area are influenced by the blocking effect of the Qinghai–Tibetan Plateau. Since the jet stream maintains its west-to-east orientation along the Tien Shan on the northern side of the Qinghai–Tibetan Plateau (Reference ReiterReiter, 1981), it carries moisture originating from the Atlantic Ocean and/or the Mediterranean Sea to the study site (Reference LiLi, 1991). The annual average surface air temperature and precipitation at DMS are –5.3˚C and 440.6 mm w.e., respectively, for the period 1959–96 (Chinese Meteorological Administration, unpublished data).

2. Methodology

The ice-core samples were processed in the field by scraping with a clean stainless knife to obtain a contamination-free center sample. The TS-1 , TS-2 and TS-3 ice cores were cut into disks roughly at 3, 5 and 4cm intervals, respectively. Samples were then transferred into polyethylene bags, melted at about 20˚C and poured into pre-cleaned high-density polyethylene bottles. The tops were sealed in wax to avoid evaporation or diffusion. Bottled samples were transported to the Laboratory of Cryosphere and Environment, and kept in a cold room at −20˚C until δ18O analyses were performed with a Finnigan MAT-252 Spectrometer (precision 0.05%). The results are expressed as the relative deviation of the heavy isotope content of Standard Mean Ocean Water (SMOW).

The β-activity samples are from the TS-3 core, with sample lengths ranging from 0.52 to 0.61 m for the upper 5.69 m section, and from 0.26 to 0.34 m below 5.69 m. The sample masses vary from 0.56 to 1.93 kg. The radionuclides are concentrated from the melted samples onto cation exchange filters after adding concentrated HCl (0.333 mL kg−1). Each sample was filtered twice. Afterwards the filters were dried and measured for the activity of insoluble particulates in a gas-flow proportional counter (Reference DibbDibb, 1992). Since retention of activity depends upon the total quality of the insoluble matter (Reference Picciotto and WilgainPicciotto and Wilgan, 1963), we measured the insoluble matter of each sample by combusting the filter, and then divided the bulk activity measurement of each sample by its corresponding insoluble matter quantity. This might eliminate the influence of the dust layers occurring at seven places from top to bottom: 0−0.06, 0.62−0.64, 4.604.64, 5.03−5.10, 6.89−6.97, 8.50−8.59 and 13.00−13.17 m, respectively. The β-activity profiles are plotted with and without the normalization to insoluble matter (Table 1; Fig. 2).

Table 1. Non-normalized and normalized β-activity values of the TS-3 ice core

Fig. 2. The annual layers in the ice cores are indicated by the light dashed lines that include the seven radioactivity horizons of 1963, 1967, 1968, 1970, 1973, 1976 and 1986, respectively, indicated by the stars.

3. Ice-Core Dating

The β-activity, major-ionic and δ18O profiles of the cores are shown in Figure 2, together with the yields of the atmospheric nuclear tests conducted at Lop Nur (∼440 km south of our study site) before 1980 (Reference Norris, Burrows and FieldhouseNorris and others, 1994). The close proximity and similar geographic environment of the test area and our study site, along with the regional atmospheric circulation system (Reference LiLi, 1991), create favorable conditions for the artificial nuclear fallout to reach UG1. For both non-normalized and normalized β-activity profiles, the β-activity peaks at 12.92−13.24 m and at 3.46−3.98 m are evident. We suspect that the peak at 12.92−13.24 m is a 1963 reference horizon, because 57% of the total atmospheric nuclear-test yields (or some 244 Mt) were concentrated in the 16 month period September 1961-December 1962. The peak at 3.46−3.98 m is very likely associated with the Chernobyl nuclear power station accident in April 1986, as UG1 and the accident site are located close together in central Asia. Moreover, the Chernobyl horizon is also evident in the snow layers of the Greenland ice sheet (Reference DibbDibb, 1989). In addition to the β-activity peaks of regional or hemispherical importance, five peaks of the normalized β-activity profiles from 10.35 to 6.57m are likely to correspond to the five atmospheric nuclear tests at Lop Nur between 1967 and 1976. However, only two peaks are evident in the non-normalized β-activity profiles, and we attribute this to dilution by the high concentration of insoluble dust.

Based on the multiple β-activity horizons, the ice cores were further dated by counting the distinct seasonality of δ18O and major ions (Fig. 2). At our study site, the δ18O of summer precipitation is enriched, while winter precipitation is depleted (Reference HouHou and others, 1999; Reference Yao, Masson, Jouzel, Stiévenard, Sun and JiaoYao and others, 1999), and high atmospheric chemical loading is observed during spring due to the transportation of continental dust stirred up by the frequent dust storms in northwest China (Reference SunSun and others, 1998). This dating is supported by the seasonality of the major organic and inorganic ions of the TS-3 core (Reference Lee, Qin, Jiang, Duan and ZhouLee and others, 2003). We notice a large δ18O valley occurring in the 1.05–3.64m section of the TS-3 core, which matches the nearly vertical crack cutting through from one side to the other from 1.38 to 3.86 m. Reference Lee, Qin, Hou, Ren, Duan and ZhouLee and others (2002) suggest that the continuous low level of δ18O might be caused by the post-depositional changes from the crack. Therefore, we exclude the δ18O values from the 1.05–3.86m section of the TS-3 core, even though the annual variation might be still evident in the 3.56–3.84 m section (Fig. 2).

4. Ice-Core δ18O–T a Relationship

We calculate the annual mean δ18O value of each year by averaging all sample δ18O values between two adjacent annual δ18O minima, and plot the annually averaged δ18O against the contemporaneous annual mean temperature and the mean temperature of the ablation season (May– September) in Figure 3. It is apparent that the ice cores did not preserve the strong positive relationship observed between δ18O in precipitation and T a (Reference Watanabe, Wu, Ikegami and AgetaWatanabe and others, 1983; Reference HouHou and others, 1999; Reference Yao, Masson, Jouzel, Stiévenard, Sun and JiaoYao and others, 1999). We calculate the correlation coefficients between the annual mean δ18O and the annual mean temperature, the mean temperature of the ablation season, summer (June–August) and winter (December–February) at DMS. All the coefficients are negative (Table 2), implying that the ice-core δ18O records are inversely correlated with annual mean temperature and the mean temperature of the ablation season. The disappearance of a positive δ18O–T a relationship in the ice cores, as was expected from the precipitation results, might be attributed to post-depositional modification.

Fig. 3. The annual mean δ18O profiles of the TS-1, TS-2 and TS-3 ice cores, compared with the annual mean temperature and the mean temperature of the ablation season (May–September) recorded at DMS.

Table 2. Correlation coefficients between the annual mean δ18O and annual ablation season (May–September), summer half-year (April–September) and winter half-year (October–March) average temperatures

As suggested by Reference Yao, Thompson, Mosley-Thompson, Zhihong, Xingping and LinYao and others (1996), the air-temperature data reflect an equal weighting of monthly temperatures, while the ice-core δ18O record is skewed toward wet-season precipitation. Thus, it is unrealistic to expect the average δ18O from an annual layer in an ice core to record the annual average air temperature of the corresponding year. In the dry snow and firn layers, the isotopic homogenization is caused by recrystallization of the grains via the vapor phase, and diffusion in the vapor phase also causes considerable inter-stratificial mass exchange (Reference Dansgaard, Johnsen, Clausen and GundestrupDansgaard and others, 1973). In low-accumulation areas, the seasonal δ18O oscillations are simply missing due to redistribution by snowdrifting or lack of winter (or summer) snow, which introduces small-scale and local depositional noise (Reference Fisher, Koerner, Paterson, Dansgaard, Gundestrup and ReehFisher and others, 1983). When snow particles are in contact with meltwater, isotopic fractionation takes place at the interface. The effect of snowmelt percolation on the δ18O records was examined in detail by comparing the δ18O profiles of a set of successive snow pits sampled at UG1 near our drilling site during the 1996 ablation season (Reference HouHou and others, 1999).

Annual average net accumulation rates constructed from TS-1, TS-2 and TS-3 are 284, 275 and 357 mmw.e., respectively, while the annual average precipitation at DMS is 440.6 mm for the period 1959–96. The precipitation amount at the ice-core drilling sites should be larger than that at DMS owing to increase of precipitation with elevation (Reference Wang and ZhangWang and Zhang, 1985). Therefore, at least one-fifth of the accumulation has been removed as meltwater runoff. As a result, the seasonal δ18O oscillations in precipitation rapidly diminish in the presence of percolating meltwater (Reference ArnasonArnason, 1969). The δ18O values of the precipitation samples collected at DMS from June 1995 to June 1996 (Reference HouHou and others, 1999) and from May 1997 to August 1998 (Reference Yao, Masson, Jouzel, Stiévenard, Sun and JiaoYao and others, 1999) range from –38.24% to 0.97% and from –30% to near zero, respectively. However, the δ18O values of the ice-core samples have much smaller ranges: –12.57% to –7.74% for TS-1; –12.96% to –7.20% for TS-2; and –12.79% to –8.32% for TS-3 (excluding the 1.05–3.86 m section).

Reference KoernerKoerner (1997) concluded that the melting in early summer will affect the very negative winter/spring snow, which lies near the surface. The meltwater then percolates down to refreeze within, or at the base of, the current annual snowpack. Continued melting may result in the run-off of the less negative snow deposited during the early winter/fall period, leaving a snowpack that is very negative. Therefore, we speculate that the fraction of annual ablation against bulk precipitation will increase during warm summers and, as a result, the winter precipitation with more negative δ will increase its fractional contribution to the annual net accumulation. If our hypothesis is correct, then a lower annual δ18O value is expected when averaging the very negative winter snowpack and the remaining summer snow. In contrast, cool summers will preserve a thicker layer of the less negative summer snow at the surface, giving a disproportionately warm δ value for the annual layer (Reference KoernerKoerner, 1997). Therefore, we suggest that this scenario could result in an inverse relationship between the ice-core δ18O and temperature records in areas of warm temperatures and high melt.

Other post-depositional processes (e.g. evaporation or condensation) can further complicate the ice-core δ18O–Ta relationship, resulting in the low correlation coefficients between the annual mean δ18O and temperature as shown in Table 2. A quantitative analysis of the effects of all the possible post-depositional processes on the final ice-core δ18O records is beyond the scope of the current paper, but it is reasonable to conclude that post-depositional processes have the potential to compromise or even obliterate the climatological information preserved in the ice-core δ18O records from areas experiencing high melt.

5. Concluding Remarks

Ice-core δ18O records from areas of high melt might be modified by post-depositional processes. Although such effects are unlikely to have occurred during glacial stages, they could become important during interglacials or interstadials with temperatures as warm as (or warmer than) at present. For instance, the δ18O increased to its maximum (most enriched) of the whole Guliya ice core during 16.5– 13.5 kyr (Reference ThompsonThompson and others, 1997). Our results necessitate a better understanding of the processes that govern the formation of ice-core δ18O records from areas of high melt before the present-day relationship of δ18O in precipitation and temperature can be confidently applied for paleo-reconstruction. In addition, our results suggest that there is an urgent need to recover the valuable ice-core records from these mountainous ice fields before their valuable paleohistories are completely destroyed by enhanced snowmelt that will occur if temperatures continue to rise.

Acknowledgements

This work was supported by the National Natural Science Foundation of China (90411003, 40121101) and the Chinese Academy of Sciences (100 Talents Project and the 3rd Innovation Programs). Thanks are due to many scientists, technicians, graduates and porters for their hard work in the field, to C. Wake and J. Dibb for help with the /3-activity measurements, and to M. Bender and two anonymous reviewers for thoughtful comments on the manuscript.

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Figure 0

Fig. 1. Sketch map showing our study site and the locations of the Daxigou meteorological station (DMS) and the ice-core drilling sites (TS-1, TS-2 and TS-3).

Figure 1

Table 1. Non-normalized and normalized β-activity values of the TS-3 ice core

Figure 2

Fig. 2. The annual layers in the ice cores are indicated by the light dashed lines that include the seven radioactivity horizons of 1963, 1967, 1968, 1970, 1973, 1976 and 1986, respectively, indicated by the stars.

Figure 3

Fig. 3. The annual mean δ18O profiles of the TS-1, TS-2 and TS-3 ice cores, compared with the annual mean temperature and the mean temperature of the ablation season (May–September) recorded at DMS.

Figure 4

Table 2. Correlation coefficients between the annual mean δ18O and annual ablation season (May–September), summer half-year (April–September) and winter half-year (October–March) average temperatures