Introduction
The basal ice of glaciers and ice sheets has been widely studied to understand the inaccessible ice–bed interface (e.g. Reference Gow, Epstein and SheehyGow and others, 1979; Reference LawsonLawson, 1979; Reference KnightKnight, 1994; Reference Hubbard and SharpHubbard and Sharp, 1995). Various formation processes of the basal ice have been proposed from various types of glaciers and ice sheets: shear (Reference Tison, Petit, Barnola and MahaneyTison and others, 1993), regelation (Reference WeertmanWeertman, 1964), congelation related to change in the basal thermal regime (Reference KnightKnight, 1987) and freezing of supercooled water (Reference Lawson, Strasser, Evenson, Alley, Larson and ArconeLawson and others, 1998). The processes change from one glacier to another, or even from one part to another within the same glacier. In East Antarctica there have been only a few studies of basal ice (Reference GoodwinGoodwin, 1993; Reference Tison, Petit, Barnola and MahaneyTison and others, 1993; Reference FitzsimonsFitzsimons, 1996; Reference Bouzette and SouchezBouzette and Souchez, 1999; Reference Kluiving, Bartek and van der WaterenKluiving and others, 1999), and these have proposed different formation processes in each region.
Stable-isotopic analysis is one of the most promising techniques used to study the basal ice. Co-isotopic analyses based on δ 18O and δD are especially useful since they reveal not only the possibility of liquid-water existence (Reference Jouzel and SouchezJouzel and Souchez, 1982) but also the refreezing condition at the base of glaciers and ice sheets (Reference Souchez and JouzelSouchez and Jouzel, 1984; Reference Souchez and de GrooteSouchez and de Groote, 1985). However, the technique has been applied solely to bulk measurements of the basal ice. Such studies have either discussed bulk processes of refreezing or compared bulk isotopic values of basal ice and those of meteoric glacier ice on the basis of slopes of δ 18O vs δD diagrams (e.g. Reference SugdenSugden and others, 1987; Reference Zdanowicz, Michel and ShiltsZdanowicz and others, 1996; Reference Lawson, Strasser, Evenson, Alley, Larson and ArconeLawson and others, 1998). It is unlikely, however, that basal ice several meters thick could be formed by one refreezing cycle. More detailed treatment of the basal ice is necessary to detect single freezing events in basal ice.
In contrast to the analyses of basal ice from glaciers and ice sheets, past theoretical and experimental isotopic studies of this problem describe the single-event melting and refreezing process (Reference Jouzel and SouchezJouzel and Souchez, 1982; Reference Souchez and JouzelSouchez and Jouzel, 1984; Reference Souchez, Tison and JouzelSouchez and others, 1987; Reference Lehmann and SiegenthalerLehmann and Siegenthaler, 1991). Theoretical studies of formation processes of basal ice have also considered a single refreezing process (e.g. Reference WeertmanWeertman, 1964; Reference RobinRobin, 1976; Reference LliboutryLliboutry, 1993; Reference Alley, Lawson, Evenson, Strasser and LarsonAlley and others, 1998). In order to compare the theoretical and experimental results so far obtained, isotopic analyses of ice from glaciers and ice sheets should be performed for a single refreezing process. Reference Jansson, Kohler and PohjolaJansson and others (1996) presented a study with this goal. However, their rough sampling interval (15 mm) prevented them from discussing the refreezing process at the base of the glacier. Multiple isotopic values from a single refrozen ice layer are needed to investigate the refreezing process at the base by curve-fitting for ice samples on δ 18O vs δD diagrams.
In this paper, we present a detailed co-isotopic study from the basal ice of Hamna Glacier, Dronning Maud Land, East Antarctica. Vertical profiles formed by basal ice samples on δ 18O and δD were used to deduce the processes occurring beneath the East Antarctic ice sheet on the basis of past theoretical and experimental studies.
Study Site and Analytical Procedures
The sampling site is located on the left bank of Hamna Glacier, one of the outlet glaciers from the East Antarctic ice sheet, 30 km south of Syowa station, Sôya Coast, Dronning Maud Land (Fig. 1). The figure shows the ice sheet to the southeast and a bedrock hill to the northwest whose summit is 141 m a.s.l.
The terminus of Hamna Glacier forms an ice cliff about 30 m high. The lower part of the ice cliff is an exposed debrisladen basal ice layer 6.8 m thick (hereafter called Hamna Basal Ice; Fig. 2). The sequence of the basal layer extends laterally, without any stratigraphic disturbances, for more than 500 m from the sampling site to an ice-marginal lake to the west. The debris has probably originated from subglacial bedrock, since there are no nunataks on the upper reaches of Hamna Glacier. The basal ice is considered to have preserved features formed in the inland area in the Sôya drainage basin, because outflow of water due to basal melting has not been observed in this area. The basal ice is composed of two parts: the upper stratified bubble-free and bubbly layers, and the lower massive bubble-free layer containing several debris-rich horizons. The lower layer rests directly on the crystalline basement rock. Above the basal ice, we observed white bubble-rich ice to the top of the ice cliff. Since there is no indication of visible disturbance in this ice, we consider it ordinary ice-sheet ice.
The basal ice was sampled in winter 1994 during the 35th Japanese Antarctic Research Expedition. Using a chain-saw, a columnar section was cut from the ice cliff. It covers the lower 9 m of the cliff, so the sample includes not only the Hamna Basal Ice but also the upper undisturbed ice-sheet ice. The samples were transported frozen to a cold laboratory in the Institute of Low Temperature Science, Sapporo, Japan, and preserved there at −20°C.
Two kinds of laboratory analyses, which have different measurement intervals for isotope analysis, were conducted. The first was a general analysis of the entire basal ice layer. Analyses included stratigraphy, ice-crystal orientation, debris concentration (percentage in weight) and stable isotopes (δ 18O and δD). Stable-isotopic analyses were performed continuously every 100 mm in thickness. The second was a detailed analysis focusing on particular stratigraphic sections. Several characteristic parts about 100–200 mm long were used for detailed stable-isotopic analyses, which were done every 1.5–5 mm in thickness. Isotope analyses were carried out with a mass spectrometer (PRISM) at Toyama University, Japan. The CO2- and H2-water equilibration method was adopted for the measurement of isotopic ratios using a Pt catalyst for H2-water (Reference Ohba and HirabayashiOhba and Hirabayashi, 1996). Analyses of δD were performed twice for each sample, and means of two measurements are given. Errors are estimated to be less than ±0.1‰ for δ 18O, and ±1.4‰ for δD (1σ error).
Results
Figure 3 shows the entire stratigraphy of bubbly ice, bubble-free ice and debris layers observed on the Hamna Basal Ice, together with the debris concentration in each layer. The vertical axis represents height measured upward from the base of the ice sheet. Hereafter, we take the height in this way. The Hamna Basal Ice exhibits two peculiar stratigraphic features. The upper part of the basal ice (height: 1.3–6.8 m) consists of alternating layers of bubble-free and bubbly ice of order mm to cm in thickness and has low concentration (< 1% in weight) of debris. The lower part of the basal ice (height: 0–1.3 m) consists predominantly of bubble-free ice and has high concentration (up to 4% in weight) of debris. The stratigraphic features of the upper part are described by contemporary terminology such as dispersed facies (Reference LawsonLawson, 1979), clotted ice (Reference KnightKnight, 1987) and clear or laminated facies (Reference Hubbard and SharpHubbard and Sharp, 1995). Features of the lower part are classified as stratified facies (Reference LawsonLawson, 1979; Reference Hubbard and SharpHubbard and Sharp, 1995) and stratified or debris-banded facies (Reference KnightKnight, 1987).
Figure 3 also shows Schmidt plots of the c-axis orientation of the basal ice and the upper ice-sheet ice. Ice fabrics of Hamna Basal Ice (0.9, 2.5 and 6.5 m high) have different patterns from that of the overlying ice-sheet ice (7.8 m high), which shows an ambiguous single-maximum pattern. The upper and lower parts of the basal ice have a similar pattern of multiple-maximum fabrics. Reference KizakiKizaki (1962) proved that such multiple-maximum fabrics can be produced by ice being subjected to long-continued strain under strong shear stress.
Figure 4 shows photographs of a thin section of the upper part at about 5.6 m height. The stratification formed by different air-bubble concentrations in the transparent figures corresponds to the difference in crystal size in the cross-polarized figure. Table 1 shows statistical values of crystal size observed in the thin sections. The average diameter of the ice crystals in the bubble-free ice layers is one and a half times larger than that in the bubbly ice layers.
A bulk measurement of stable isotopes of the basal ice is shown in Figure 5. Both δ 18O and δD show lower values (−45.6‰ and −364‰ on average, respectively) than precipitation in the marginal region of the Sôya drainage basin where seasonal δ 18O values range from −33‰ to −10‰ at present (Reference KatoKato, 1979). The result indicates that the basal ice originated from precipitation in inland regions of the ice sheet. If we assume that the present spatial distribution of δ 18O values in the Sôya drainage basin (Reference Satow and WatanabeSatow and Watanabe, 1992) does not change, the Hamna Basal Ice could have originated from precipitation in the inland area around 3000 m a.s.l., about 150 km southeast from Mizuho station (70°42′ S, 44°20′ E). The excess d value (2‰ on average) is lower than the value for the ice-sheet ice (5‰ on average) or meteoric line (10‰; Reference CraigCraig, 1961).
In order to examine the formation mechanism of the alternating layers, we selected four particular parts, each 100–200 mm thick, for detailed isotopic analyses in which the sampling interval is 5 mm. One of these was selected from the upper undisturbed ice-sheet ice above the basal ice (Ice Sheet Ice), two were from the upper part of the basal ice (Basal Ice-A and -B), and one was from the lower part (Basal Ice-C). Only Basal Ice-A and -B have the alternating layers. Stratigraphy and vertical distributions of δ 18O and δD in the four parts are shown in Figure 6. In order to acquire more detailed information, we selected two particular parts in the upper part of the basal ice: one is about 100 mm thick with sampling resolution of 3 mm (Basal Ice-D), and the other is about 200 mm thick with sampling resolution of 1.5 mm (Basal Ice-E). Basal Ice-D and -E also have alternating layers. Stratigraphy and vertical distributions of δ 18O in Basal Ice-D and -E are shown in Figures 7 and 8.
δ values in the Ice Sheet Ice and in Basal Ice-A, -B, -C, -D and -E are the same as in the bulk measurements plotted in Figure 5, ranging from −47‰ to −40‰ for δ 18O, and −380‰ to −320‰ for δD. But δ 18O and δD vertical profiles between the Ice Sheet Ice and Basal Ice-A, -B, -C, -D and -E have different patterns. Variations in δ 18O and δD values in the Ice Sheet Ice are so small (<2.2‰ and 13‰ for δ 18O and δD, respectively) that it is difficult to find any features caused by seasonal or climatic changes in δ values of precipitation. On the other hand, variations in the Basal Ice-A, -B, -C, -D and -E are large, as much as 6.0‰ and 50‰, for δ 18O and δD, respectively.
Isotopic curves of Basal Ice-A, -B, -D and -E, which belong to the upper part of the basal ice, are closely related to the alternating layers of bubble-free and bubbly ice. In each alternating layer, almost all the δ values of the bubble free ice layers are heavier than those of the neighboring bubbly ice layers. The average values of isotopic fluctuations between the bubble-free and the neighboring bubbly ice layers observed in Basal Ice-A and -B are 2.4 ± 1.0‰ (standard deviation) and 19 ± 8‰ for δ 18O and δD, respectively. In the cases of Basal Ice-D and -E, the average differences defined by the maxima in the bubble-free ice layers and minima in the neighboring bubbly ice layers are 2.6 ± 1.2 (standard deviation) and 21 ±9‰ for δ 18O and δD. In some cases, they are enriched by 5–6‰ for δ 18O and by 45–50% for δD (e.g. at 4.86 m in Basal Ice-A and at 40 mm in Basal Ice-E shown in Figs 6 and 8).
The co-isotopic profile of Basal Ice-C, which belongs to the lower part of the basal ice, shows that a sudden isotopic change (3.2‰ and 30‰ for δ 18O and δD, respectively) occurs at the boundary between the bubble-free and bubbly ice layers, and 8 values decrease downward with height in the bubble-free ice. Values of excess d of Basal Ice-A, -B, -C, -D and -E are similar to the values of the whole basal ice (2‰ on average), and fluctuations of excess d are unrelated to the stratigraphy of bubbles.
Discussion
Formation processes of bubble-free and bubbly ice layers in the upper part of the Hamna Basal Ice
The isotopic variations found in the upper part of Basal Ice-A, -B, -D and -E (Figs 6–8) are suggested to have been formed when the alternating layers of bubble-free and bubbly ice were created at the base in the inland Sôya drainage basin. This idea is justified first by the fact that significant variations in stable isotopes were not observed in the undisturbed bubbly ice overlying the Hamna Basal Ice (Ice Sheet Ice in Fig. 6). Second, the bubble-free layers exist only in the basal ice. Third, the isotopic variations correspond closely to the alternating layers.
Stable isotopes have been used as an indicator of phase change in H2O (e.g. Reference Jouzel and SouchezJouzel and Souchez, 1982). Theoretical considerations show that freezing of water induces isotopic enrichment of 3.0‰ for δ 18O and 18.7‰ for δD (Reference O’NeilO’Neil, 1968) from initial water to ice formed by freezing of the water for the first time. In alternating layers in the upper part of the Hamna Basal Ice, similar variations in δ values were found; heavier δ values of 2.4 ± 1.0‰ and 19 ± 8‰ for δ 18O and δD were observed in the bubble-free ice layers as compared with the neighboring bubbly ice layers. This suggests that the bubble-free layers in the upper part were formed by freezing at the base of the ice sheet. The water that was frozen must have been meltwater from inland ice, because δ values as low as −45.6‰ (δ 18O) and −364‰ (δD) are only available from the inland ice.
Relatively larger grain-size observed in the bubble-free layers as compared to that in the bubbly layers (Table 1; Fig. 4) supports the statement above because the grain-size of sheared layers is relatively smaller than that of associated bubbly layers if the bubble-free layers were formed by a mechanical process such as shearing (Reference Tison, Petit, Barnola and MahaneyTison and others, 1993). Our measurements do not fit this idea, so the bubble-free layers are considered to have been formed by freezing of meltwater at the base.
On the other hand, the bubbly layers in the upper part of the Hamna Basal Ice could have been formed by two different processes. The isotopic profiles obtained for the Basal Ice-D and -E showed see-saw-type variations consisting of multiple “>” shapes in which two kinds of patterns were observed (Figs 7 and 8).
The first is a neutral profile found in Basal Ice-E as indicated by thick white arrows in Figure 8. In the bubbly layers, the δ values are as constant as those observed in the overlying ice-sheet ice (Fig. 5). Such bubbly layers are suggested to be ice not affected by the melting and refreezing process, and are considered to be the same as the overlying ice-sheet ice. The neutral profile can most likely be explained by assuming that the bubbly layers were folded/sheared and embedded within the bubble-free layers without suffering any isotopic fractionations.
The second type of pattern is indicated by thick black arrows where the δ values decrease gradually from the neighboring bubble-free layers without any significant breaks (Figs 7 and 8). Each pattern of the second type could be formed by a single meltwater-refreezing event associated with formation of the neighboring bubble-free layer, resulting in dissolved gas being trapped in frozen ice (Reference HubbardHubbard, 1991).
From the interpretation of the mechanisms acting on the formation of both bubble-free and bubbly layers in the upper part of the Hamna Basal Ice, we believe that two different mechanisms, refreezing of meltwater (i.e. regelation or congelation) and tectonic deformation, were important in formation of the upper part. The two processes could only occur in the same profile if a subglacial tectonic disturbance was predated by multiple regelation/congelation layers, which will be explained in the final subsection of the discussion.
Formation process of the lower part of the Hamna Basal Ice
It is clear that the lower part of the Hamna Basal Ice has long been affected by the underlying bedrock since the concentration of debris in the layer is significantly higher than in the upper part (Fig. 3). The development of multiple-maximum fabric found in the lower part also indicates that the lower part of the basal ice has long been subjected to strong shear stress, which is typical at the base of the ice sheet. In the co-isotopic profile of the lower part (Basal Ice-C in Fig. 6), the major variation corresponds to the stratigraphy of bubbles, and the range of the fluctuation in δ values is 3.2‰ (δ 18O) and 30‰ (δD), which is again similar to the fluctuations observed in the upper part. This suggests that the lower part was also formed by refreezing of meltwater. Since the isotopic change occurred over a wider thickness than in the upper part, the refreezing of the lower part is considered to have occurred on a larger scale (> 100 mm thickness) than that of the upper part (1–10 mm thickness).
Possible freezing conditions deduced from δ 18O vs δD plots
Reference Jouzel and SouchezJouzel and Souchez (1982) showed that for a closed system, where there is no water input or output, the slope gradient defined by δ 18O vs δD (hereinafter we call this the freezing slope) depends on the initial composition of the liquid admitted to freeze (equation 1 in Reference Souchez and de GrooteSouchez and de Groote, 1985) and takes the value 4.2 in the case of −45.6‰ (δ 18O) and −364‰ (δD). In contrast, the freezing slope depends on (1) the isotopic composition of the initial and input water, and (2) the ratio of input to freezing-rate coefficient, if the system is open (equation 3 in Reference Souchez and de GrooteSouchez and de Groote, 1985). The freezing slope becomes similar between open and closed systems when the isotopic composition of the input water is not significantly different from that of the initial water or when the freezing rate is much higher than the input rate. On the other hand, the freezing slope is nearly 8 when the isotopic composition of the input water is significantly different from that of the initial water and when the ratio of input to freezing-rate coefficient is high.
The freezing slopes obtained for the various parts of the Hamna Basal Ice were as follows: 8.6 (entire profile; Fig. 5), 7.5 (Basal Ice-D; Fig. 7A) and 8.0 (Basal Ice-E; Fig. 8A). The latter two values are more significant because the correlation coefficients for the two cases were high (r = 0.97–0.99) as compared with that obtained for the entire profile (r = 0. 83). This lower coefficient results from the rough sampling interval (100 mm) in the analysis of the entire profile. Namely, the scale of analysis containing several sets of the alternating layers is too coarse to investigate the causes of the isotopic fluctuation. Besides, even if we select the data solely from the bubble-free layers, the slopes become 7.6 (Basal Ice-D; Fig. 7B) and 7.9 (Basal Ice-E; Fig. 8B). Furthermore, the freezing slope of 7.5 was also obtained when we calculated it in the single decreasing profile from an interval 72–80 mm thick in Basal Ice-E (Fig. 8C). Therefore, we conclude that the bubble-free layers and part of bubbly layers were formed by the melting–refreezing process in an open system in which the input water is isotopically different from the initial water. The input water is considered to be isotopically lighter than the initial water, because almost all of the measured isotopic enrichments in the bubble-free ice layers should be much larger than those of the theoretical fractionation by freezing, if the input water was isotopically heavier.
Now a question may arise as to how the meltwater was produced and supplied to the production of the bubble-free and part of the bubbly layers in the Hamna Basal Ice. As far as the radio-echo soundings and model simulation applied to Sôya drainage basin are concerned, the basal temperature is below the pressure-melting point (e.g. Reference Mae and YoshidaMae and Yoshida, 1987; Reference Hansen and GreveHansen and Greve, 1996). The modeled basal temperature is, however, very close to the fusion temperature and there might be a possibility of melting area in relation to either enhanced local stresses or impurities. One example is that Reference Mae and NaruseMae and Naruse (1978) attributed the recent rapid thinning of the ice sheet to local melting at the bottom of nearby Shirase drain age basin. We cannot determine the origin of the meltwater at the moment, but we expect that study of the basal ice from a chemical viewpoint may shed light on it.
There are a few examples of bubble-free layers enriched by 5–6‰ (for δ 18O) and 45–50‰ (for δD) compared with the overlying bubbly layers. The enrichment values are much larger than those expected from theoretical considerations for the single melt–freeze process. The larger enrichment values can be ascribed to multiple melting and refreezing processes (Reference Hubbard and SharpHubbard and Sharp, 1993) in the single bubble-free layer.
Formation history of the Hamna Basal Ice
The most probable interpretation of the origin of the Hamna Basal Ice is that it was formed by either regelation or congelation of meltwater in an open system at the base of the ice sheet in the inland region. Bulk co-isotopic analyses of the Hamna Basal Ice showed that the average isotopic values are −45.6‰ (δ 18O) and −364‰ (δD), which are nearly equivalent to those obtained for the overlying ice-sheet ice (Fig. 5). This fact excludes the possibility that it is fossil ice like that found in the Greenland ice sheet (Reference SouchezSouchez and others, 1994). In addition to similar δ values, the lower part of the Hamna Basal Ice has similar crystal-orientation fabrics to the upper parts. Therefore, the lower part is not ice that accreted at the sampled point in the Hamna Glacier region like that reported for Glacier de Tsanfleuron, Switzerland (Reference Tison and LorrainTison and Lorrain, 1987).
Regelation is possible when the ice-sheet sole meets a bedrock bump (Reference WeertmanWeertman, 1964; Reference RobinRobin, 1976) or within a watervein network in the basal layer above a bump (Reference LliboutryLliboutry, 1993). Congelation can be caused by either a difference in the basal thermal regime (Reference Boulton, Price and SugdenBoulton, 1972), cooling in a water-filled cavity (Reference ShoemakerShoemaker, 1990) or by supercooled water (Reference Lawson, Strasser, Evenson, Alley, Larson and ArconeLawson and others, 1998). As mentioned above, the bottom of the ice sheet in the Sôya drainage is supposed to be frozen. This means that regelation or congelation, which produces the Hamna Basal Ice, can only be caused by local “stress” or “impurity”-induced melting and freezing.
Reference WeertmanWeertman (1964) showed that regelation thickness by single refreezing cannot exceed several hundred mm. The thickness of each bubble-free layer in the Hamna Basal Ice was at most 100 mm for the upper part and more than several hundred mm for the lower part. Therefore, the upper part of the Hamna Basal Ice was probably formed either by the Weertman-type or by the Lliboutry-type regelations. The massive lower part of the Hamna Basal Ice was probably formed by congelation related to either a water-filled cavity or a change in the thermal regime on the local scale.
Field observations on the Lliboutry-type regelation within a vein network were reported at Engabreen (Reference Jansson, Kohler and PohjolaJansson and others, 1996) and Glacier de Tsanfleuron (Reference Hubbard, Tison, Janssens and SpiroHubbard and others, 2000). They interpreted an ice layer with little debris and with high content of dissolved cations as a Lliboutry-type regelation layer. Since the bubble-free ice layers in the upper part of the Hamna Basal Ice contain debris, they are considered to be formed by Weertman-type regelation with the help of input water.
Now, we must consider how the upper part of the Hamna Basal Ice became as thick as 5.5 m. Successive accretion by multiple regelations from the bottom cannot be a complete explanation because some of the bubbly layers are thought to have originated from the ice-sheet ice without suffering from isotopic fractionations. Such a process is only possible by mechanical deformation, i.e. shearing/thrusting or folding.
In the case of the Hamna Basal Ice, our analytical evidence favors a folding mechanism rather than thrusting/shearing. Not all of the maxima of the isotopic profiles, which means the positions of frozen ice in the first stage, were observed at the uppermost part of the bubble-free layers as indicated by the thin arrows in Figures 7 and 8. This fact excludes the thrusting/shearing mechanism in which the bubble-free layers forming isotopic maxima at the uppermost part (Reference Hubbard and SharpHubbard and Sharp, 1993) should thrust from the bottom of the ice sheet onto the overlying ice-sheet ice (see fig. 6 of Reference Tison, Petit, Barnola and MahaneyTison and others, 1993). Moreover, a part of the isotopic profiles in Basal Ice-D and -E shows symmetrical patterns across layers with respect to the thick horizontal axes indicated at thicknesses of 50 mm in Figure 7, and 48 and 90 mm in Figure 8. These features strongly suggest that Basal Ice-D and -E are examples of folding.
Finally, we propose a hypothesis for the formation history of the Hamna Basal Ice (Fig. 9). At first, bubble-free ice and part of the bubbly layers were formed somewhere inland in the Sôya drainage basin, probably related to the bedrock bump with the help of input water at the base of the ice sheet (Fig. 9-①). The layers flowed downward beyond the bedrock bumps, and suffered shear stress and folded without significant shearing/thrusting (Fig. 9-②). The folded layers suffered from compression, due probably to bedrock undulation or cold stiff ice at the terminus (Fig. 9-③). Then the layers suffered strong shear stress after the accretion of the massive lower part by congelation, as we observed at the ice cliff at the terminus (Fig. 9-④). Since the fabric in the lower part shows the same features as that in the upper part (Fig. 3), the lower part is suggested to have been formed before the action of strong shear stress.
Conclusions
The Hamna Basal Ice exhibits two peculiar stratigraphic features. One is the upper part of the basal ice (height: 1.3–6.8 m), which consists of alternating layers of bubble-free and bubbly ice of the order of mm to cm in thickness and has a low concentration (< 1% in weight) of dispersed debris. The other is the lower part of the basal ice (height: 0–1.3 m), which consists predominantly of bubble-free ice and has a high concentration (<4% in weight) of stratified debris. Isotopic analyses of the bulk samples show that the Hamna Basal Ice originated from precipitation in inland regions of the ice sheet. Based on estimation from the δ values, the Hamna Basal Ice could have originated from precipitation in the inland area around 3000 m a.s.l., about 150 km southeast of Mizuho station (70°42′ S, 44°20′ E).
We have presented the formation processes of the alternating layers in the upper part using detailed co-isotopic values. The bubble-free ice layers show smooth profiles for stable isotopes, with variations closely corresponding to values for theoretical fractionation of water to ice (Reference Jouzel and SouchezJouzel and Souchez, 1982), i.e. heavier δ values of 2.4 ± 1.0‰ and 19 ± 8‰ for δ 18O and δD, respectively, were observed in the bubble-free ice layers as compared with the neighboring bubbly ice layers. Since the freezing slopes of the layers are close to 8, such layers are suggested to have been formed by refreezing of meltwater in an open system (Reference Souchez and JouzelSouchez and Jouzel, 1984; Reference Souchez and de GrooteSouchez and de Groote, 1985). The mechanism of the freezing is probably regelation at a bed bump. On the other hand, a part of the bubbly layers shows neutral profiles for stable isotopes, with values closely corresponding to the overlying ice-sheet ice. Such bubbly layers are suggested not to have been affected by the melt-freezing process. The alternating layers are considered to have been formed by piling up of freezing layers and non-melted layers followed by folding.
The profile of stable isotopes in the lower part shows variations similar to those observed in the upper part. The range of the fluctuation in δ values was 3.2‰ for δ 18O and 30‰ for δD. Since the isotopic fluctuation was found to have occurred on a larger scale in the lower part (>100 mm thickness), the freezing mechanism of the lower part is probably congelation in a water-filled cavity or congelation by a change in the basal thermal regime on a local scale.
Acknowledgements
We would like to thank K. Yokoyama of Hokuriku National Agricultural Experiment Station and the members of the 35th Japanese Antarctic Research Expedition for their support in the field operation and sampling of ice. We are grateful to O. Watanabe and Y. Fujii of the National Institute of Polar Research for useful discussion of this study. The paper was significantly improved as a result of comments by M.J. Sharp and an anonymous referee to whom we are greatly indebted.