Introduction
The rate of change in mechanical strength of a snow cover is a parameter of considerable usefulness in glaciological engineering. Intuitively we all recognize that it is a function of the rate of bond growth between individual ice grains which, with their complementary pore spaces, comprise a snow-pack. Unfortunately, the extreme fragility and thermal instability of low density seasonal snow makes the study of bonding extremely difficult.
Studies of the nature of the intergranular bond in snow have been conducted in a laboratory environment (Reference Hobbs and MasonHobbs and Mason, 1964) and both field and laboratory studies have investigated the strength changes in snow (Reference MellorRamseier and Sander, 1966; Reference Ramseier and KeelerRamseier and Keeler, 1966). This paper describes simultaneous measurements on both strength and bonding in a natural, dry, seasonal snow cover, made during the winter of 1966 at Alta, Utah.
Field Methods
Strength properties
Brittle fracture stress was measured using shear boxes, shear vanes and a centrifugal tensile apparatus, all of which are fully described in Reference Keeler and WeeksKeeler and Weeks (1968). Whether or not brittle behavior is a correct assumption in all cases is conjectural, but in any event the measured values provide suitable indices for correlation with other snow properties. The effect of temperature has not been considered in the analysis of these data. It is recognized that this is a fundamental weakness of this study, however, in a field situation, temperature variations are not systematic. In any case, the range of temperatures encountered were rather limited, being between −5°C and —10°C.
Figure 1 is a plot of shear-vane failure stress versus porosity and density. The open circles represent data obtained from a snow with high densities but low cohesion. These data typify the depth-hoar layers of these snow-packs which, from the standpoint of snow-slope stability, represent very important exceptions to most strength-density relationships. The laboratory data is from direct shear tests conducted by Reference BallardBallard and others (1965). Unfortunately, these were the only two points in the appropriate density range.
The data were fitted by an expression derived theoretically by Reference Ballard and FeldtBallard and Feldt (1966):
where σ f is the failure strength of the sample, σ i is the strength (for the same test procedure) of bubble-free polycrystalline ice with a random crystallographic orientation, and n is the porosity. The value ofσ i ; is unknown and obtained by regressing σ f on exp [−2n/(1−n)]. In this case σ i = 3.42 × 105 N m −2 with a correlation coefficient of 0.83. This value of σ i is approximately 20% less than the σ i of 4.05 × 105 N m −2 obtained by Reference Keeler and WeeksKeeler and Weeks (1968) for data from Goose Lake, Montana. Considering the scatter in both sets of data this is considered to be in reasonably close agreement.
Centrifugal tensile test data were fitted with the same expression yielding a value forσ i; of 22.14 × 105 N m−2 with a correlation coefficient of 0.86. By way of comparison ai for tension using the Goose Lake data was 27.3 × 105 N m−2 (Reference Keeler and WeeksKeeler and Weeks, 1968). The fact that the tensile strength of these snows should exceed their shear strength has been reported on before (Reference RochRoch, 1966) but has not as yet been explained. It is likely that the methods of testing may be in part responsible, however, the persistence of the difference suggests that it is worth further study.
Structural properties
Intergranular bonding in snow samples taken in close proximity to the location of the strength measurements (presumably from snow of similar density, age, etc.) was studied in thin sections prepared using the aniline technique. For this purpose a small walk-in freezer was used. Measurements were made on microphotographs similar to those shown in Figure 2.
The absolute accuracy of linear measurements made on such photographs is limited by a number of factors. First, when very porous, poorly cohesive snow is impregnated with aniline, the forces created by the movement of the liquid through the snow tend to destroy whatever tenuous bonding exists. Second, it is very difficult, if not impossible, to section a sample consisting largely of voids and irregularly shaped grains lying in various planes in such a manner that the section yields accurate values of grain dimensions. The problem is complex enough for aggregates of randomly packed unbonded spherical particles (Reference Krumbein and PettijohnKrumbein and Pettijohn, 1938). As proof of probable errors is the fact that “two-dimensional” densities determined by point count on the photographs differed by a factor of from 1.8 to 2 from the bulk density determination on the same sample. The “two-dimensional” density was always the larger value indicating an overly thick thin section despite the fact that the section was presumably microtomed to approximately one-half the average grain size as previously determined by sieve analysis. This error has been previously discussed by Reference Nakaya, Kuroiwa and BuraNakaya and Kuroiwa (1967) who found that for Greenland snow, a 0.3 mm difference in thin-section thickness could result in a two-dimensional density difference from the bulk density of a factor of 2. The achievement of identical densities using both bulk and thin-section techniques would appear fortuitous. Fortunately, however, the difference between the two values for the Alta samples was constant from section to section (within 10%) because the section thickness was not kept the same but was varied as the average grain size of the sample varied. Therefore, the data can be used to show rates of change despite the fact that the absolute values may not be correct.
The data taken from the photographs were:
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joint order: the number of intersections of lines halving connecting grains (Reference Yosida and KingeryYosida, 1963);
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bond diameter: the width of bonds connecting grains;
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number of bonds per grain.
The data were averaged for each thin section. Thin-section studies were made of samples collected at various depths in a single snow pit (Table I) and at successive time intervals on a stratigraphically identifiable layer (Table II).
The data from Table I can also be used to study the time rate of change of these parameters by assuming that each layer had somewhat similar initial properties and determining the interval from the time of deposition for each depth increment. In other words, time can be substituted for depth if the accumulation rate is known.
In Table I two sections at 0.40 m are included to give some idea of the errors involved in replication. In this case they do not appear large.
The joint order is quite constant. Yosida (1963) theorized that this indicates that the basic structure of the network is preserved during metamorphism despite changes in grain and bond sizes. This may well be the case within the limited range of stresses found in a seasonal snow cover, The exception to this is the breakdown of intergranular bonding which occurs during the formation of depth hoar. The mean number of bonds per grain is the measurement least subject to error and consequently a valuable index of structure.
A further parameter calculated from the measured data is bond area per unit area of section. This was calculated from bond diameter and numbers of bonds per unit area of section, using the assumption that the bonds are circular in cross-section and that bonding is spatially uniform (i.e. that thin-section orientation does not affect the number of bonds in the section).
Relationship Between Snow Strength and Snow Structure
While empirical correlations between snow strength and density, grain size, depth, time, etc. are useful as predictors they are rarely explanatory. Ultimately, at constant temperature, snow strength is a direct function of the number and size of intergranular bonds, a fact intuitively recognized by most people and quantitatively described to some extent by Reference NakayaNakaya (1961), Reference ButkovichButkovich (1962), Reference Anderson, Benson and KingeryAnderson and Benson (1963), Reference HobbsHobbs (1965), Reference Ballard and McCawBallard and McGaw (1966), Reference Ramseier and SanderRamseier and Sander (1966), Reference Ramseier and KeelerRamseier and Keeler (1966), and Reference Ballard and FeldtBallard and Feldt (1966).
Figure 3 shows a plot of shear-vane strength versus unit bond area. Reference Ballard and McCawBallard and McGaw (1966) described a failure condition in which failure occurred under uniform stress when bonds were stressed to the ultimate strength of ice, σ i. A geometric analysis of the resulting failure surface gave an effective porosity, n f, which is equal to (1 —unit bond area). n f generally exceeds the bulk porosity n and does so to the greatest degree in low density (high porosity) snow. Ballard and McGaw consider n f to be a linear function of bulk porosity n, and this agreed well with data for bulk porosity less than 50%.
The data in Figure 3 can be fitted with the expression:
which is similar in form to Equation (1), the more general expression for strength derived by Reference Ballard and FeldtBallard and Feldt (1966) for the entire porosity range. σ i predicted by Equation (2) is 1.2 × 105 N m−2 which is at least of the same order of magnitude as the value of 3.42 × 105 N m−2 predicted by Equation (1), which used bulk porosity. This Iends credence to the notion that Equation (1) is a workable expression for the strength-density relation for snow over a wide range of densities.
Time Dependence of Strength and Bonding
The classical theory of sintering predicts that bond growth between particles will occur at a rate which may be expressed as
where X is the bond neck radius, R the radius of the particles, f(T) a temperature term, t is time and n and m are constants which depend on the mechanism by which sintering occurs. There is considerable evidence that, at the temperatures normal to most snow-packs, this mechanism is one of mass transport by diffusion through the environmental vapor (Reference Hobbs and MasonHobbs and Mason, 1964; Reference Krumbein and PettijohnRamseier and Keeler, 1966). In this case the value of n should be about 3 (Reference Hobbs and MasonHobbs and Mason, 1964). Most of the experimental work in this field has involved observing the behavior of small ice spheres placed together in a uniform environment. Needless to say, the situation in a snow-pack where there may be gross mass transport in and out of the system and repeated temperature cycling is considerably less amenable to formalization. A plot of the logarithm of (X/R) against the logarithm of time is shown in Figure 4 using the data of bond diameter and grain diameter from Table II. While errors in determining R for irregularly shaped particles must be taken into account, the rising portion of the curve has a slope of 0.75 (n = 1.3). After 47 d × ceases to increase and the ratio (X/R) decreases slightly due to general grain growth. The significantly higher rate of bond growth than that predicted by the sintering equation may possibly be attributed to convective circulation within the void spaces of the snow-pack, temperature cycling, or viscous creep induced by overburden pressures (the exponent for this particular mechanism should be about 2 (Reference Hobbs and MasonHobbs and Mason, 1964)). While the overburden pressures are not high for a bulk sample they may impose a considerable absolute stress at points of contact because of the relatively small area of the contact surfaces. It is suggested that the rather static X/R ratio occurring from 47 d and thereafter indicates that bond growth has reached its limit for snow in this environment. The value of the ratio (X/R≈0.25) is approximately that predicted for the initial stages of sintering of powder compacts, i.e. prior to grain growth and pore-shape change (Reference CobleCoble, 1961). To substantiate this, reference should also be made to the constancy of joint order referred to earlier, which suggests that the geometry of pores and solids does not change greatly within this density range.
Table I indicates that a similar situation exists with respect to the number of bonds per grain. During the initial stages of sintering the snow is being stressed by overburden pressures which push grains together and mechanically increase the number of intergranular contacts. At some point densification has proceeded far enough so that the snow is in equilibrium with the stress imposed upon it. In the absence of greatly increased overburden pressures the mechanical arrangement of grains will not change and at this point there is no tendency to create new bonds.
Figure 5 is a plot of tensile strength against time for various snow layers. These layers were dated stratigraphically using natural and colored-yarn horizons. The plot is on logarithmic paper to accommodate the large changes in both variables. The snow temperatures during this time were between –10 and –5°C and varied many times for each particular layer.
Reference HobbsHobbs (1965) found that for certain sets of strength data a power function of time appeared to give the best fit. He explained this as being due to the fact that strength should be linearly related to bond growth which he also found to be a power function of time. The slopes of his strength versus time curves were of the order of 0.3 to 0.4 whereas those of Figure 5 are 1.2 for curve a and 2.9 for curve b. Regardless of whether a power law represents the physical case or is simply a convenient way of presenting these data, the great disparity in the rates of strengthening deserves comment.
The most notable difference between the data analysed by Hobbs and the Alta data is the density at the start of sintering. Hobbs used data from prepared samples with initial densities of 550 kg m−3 (Reference JellinekJellinek, 1959), processed snow with densities of 430 to 580 kg m−3 (Reference NakayaNakaya, 1959), and compacted snow with densities of 350 to 650 g m−3 (Reference Wuori and KingeryWuori, 1963) whereas the Alta snow plotted in Figure 5 has initial densities on the order of 150 kg m−3. Furthermore, the Alta snow, under conditions of constantly increasing overburden pressure, was densifying continuously and rapidly. A second obvious difference is the much lower strength of Alta samples. Even less than 1 h after the preparation of his samples Jellinek found compressive strengths two orders of magnitude higher than the shear strength of 20 d old Alta snow (shear and compressive strength are generally considered to be of the same order of magnitude for the same sample (Reference MellorMellor, 1966)).
The most likely explanation for the difference in rate of strengthening between various snow types appears to lie in the nature of the snow itself. It is suggested that the same factors which produce rapid densification in the Alta snow samples produce the rapid increases in strength. Despite the fact that Equation (1) and experimental evidence (see Fig. 1) predict a very low dependence of strength on density for low-density samples, new snow with its many irregular and sharply curved surfaces and high surface energies rapidly compacts and strengthens until some semblance of stability is achieved. It is quite likely that rapid fluctuations in temperature play a role in this process (Butkovich, 1959). This appears to be substantiated by the higher rate for curve b (Fig. 5) which was for snow existing near the surface under warmer ambient temperatures than any of the other layers plotted.
More fundamental proof of the fact that differences in rates of strengthening are due to snow structure is demonstrated in Figure 6 which is a plot of unit bond area versus time based on the data of Table II. The initial slope of the curve is 3.3 and the second portion has a slope of 0.25. At the point of discontinuity the snow density is 350 kg m−3 at an age of 50 d. A density of 350 kg m−3 represents a reasonable level of compaction for the normal overburden pressure in deep, dry alpine snow-packs at their greatest accumulation and at this point the rate of densification is very slow (Reference KeelerKeeler, 1967). At this time the X/R ratio (bond diameter to grain diameter) was approximately 0.2 which, as has been discussed, is approximately the ratio which marks the end of the initial period of sintering (neck growth only). Both these facts suggest that this is the point beyond which geometrical relationships will change slowly and grain boundaries have somewhat stabilized. It is, therefore, reasonable to expect that processes related to these changes will likewise be slowed.
Conclusions
It would be presumptuous to suggest that a bond growth law can be derived from these data. The interrelation of a number of variables; time, temperature, temperature gradient, and overburden stress is extremely complex in a natural snow pack and there is no way in which their individual effects can be systematically studied.
It is apparent, however, that existing theories, including the classical sintering equations, do not accurately fit the whole range of properties found in natural snow. Both the growth of existing bonds and the creation of new bonds are very much more rapid in low density, new snow than seems to be the case in older, denser snow.
The fact that the relationship between bond size and strength properties agrees reasonably well with relationships derived using macroscopic properties (e.g. bulk density) is encouraging as it indicates that the fundamental assumptions used are correct. If, as suggested, there is a strength—density relationship which is applicable over a broad range of densities then it is likely that other phenomena, including the increase of snow strength with time, can also be described as a continuous process.