Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Physics and chemistry of snowfall and snow distribution T.L. Richards A tmosphe rie Enviranment Servie@, Environment Crmada, Toronto, Onta2rio ABSTRACT: Snow, whether falling through the air or accumulating on the ground, is a most important phase of the hydrologic cycle. The initial snowfall is produced almost entirely by means of synoptic scale or large mesoscale physical processes associated with travelling low pressure areas or orographic or convective lifting. The ultimate distribution and physical characteristics of the snow cover on the ground is, however, highly dependent upon local variations of wind caused by small-scale topographic features and by even smaller scale energy processes in the snowpack itself. Although there are chemical aspects to the nucleation process the major chemical constituents of the snow cover are the result of the scavenging effects of the falling snow and dry fallout on the snow itself. ' , RESUME: La neige est une des plus importantes phases du cycle hydrologique. La première chute de neige qui est produite presqu' entièrement au moyen de processus physiques d'échelle synoptique ou de large mésoéchelle, est associée avec une aire de basse pression ou avec une ascendance orographique ou avec une ascendance de convection. La distribution finale et les caractéristiques physiques de la couche de neige,sont grandement dépendantes des effets locaux du vent causés par de's aspects topographiques de petite échelle et aussi mdme par des processus d'énergie de plus petite échelle dans l'accumulation de la neige elle-même. Bien qu'il y ait des aspects chimiques dans le processus de nucléation, les constituants chimiques de la couche de neige sont le résultat de l'effet de lavage de la neige tombante et de retombées de particules sur la neige elle-même. 1. INTRODUCTION Snow, whether falling through the air or accumulating on the ground, is a most important phase of the hydrologic cycle and is a major source of moisture which affects both the physical quantity and the chemical quality of the earth's fresh water supply. In addition, the depth, density and melting characteristics of the snow cover dictate the flow regimes of most of the rivers of the temperate latitudes of the world. The rather complex and all-inclgsive subject of the physics and chemistry of snowfall and snow distribution falls naturally into several separate and, in some cases, almost independent divisions. First is the evident one between falling snow and snow on the ground or snow cover, and second is the even more distinct division between physical and chemical processes and properties. Such divisions suggest an approach that would first consider the physical and chemical aspects of the natural production of snowfall to be followed by discussions of the physical, and then the chemical, characteristics of the snow cover or older snow on the ground. Because of the broad scope of the subject it is apparent that a theme 1 paper must, of necessity, be in the nature of an introductory review of the state of the science. It is left for ensuing papers to undertake more detailed discussions of specific aspects of the subject or to push forward towards new horizons. 2. PHYSICS OF CLOUD FORMATION It is recognized that the physics of snowfall is a special case of the more general subject of the physics of precipitation. For this reason it is necessary to first introduce the broader subject of the physical processes involved in the formation of clouds and precipitation in order to reach the special case of snow. Clouds, and the resulting precipitation which may be either liquid or solid, form in the free atmosphere almost entirely as a result of the lifting and consequent expansion and cooling of ascending air. In the simplest of terms, a parcel of air as it is lifted, expands and cools to temperatures lower than the air surrounding it. This adiabatic cooling process may continue until the dew-point temperature of the parcel of air is reached and condensation takes place. The required vertical motion for such a process may be found in the atmosphere under four general and relatively well-known conditions: (i) Widespread gradual lifting of low pressure areas and frontal systems. This type of vertical motion is prevalent with the travelling synoptic-scale cyclonic storms or low pressure areas most frequently found in temperate latitudes. As illustrated in Figure 1 such lifting is actually the result of two separate actions: - the convergent flow found associated with low pressure areas; and the lifting of the warm moist air of the warm sector provided by the associated warm and cold fronts. In the typical warm front situation the somewhat warmer and lighter air is lifted very gradually over the heavier cooler air. With a cold front the warm air is lifted much more vigorously by the advancing colder air. Both these processes will produce snow under the proper set of circumstances primarily below freezing temperatures and a sufficient supply of moisture. (ii) Orographic lifting. When an airmass is thrust against a mountain barrier, or even against a line of lesser hills, some of the air is forced to rise and this can result in the same adiabatic lifting and cooling which will form an extensive sheet of cloud and may ultimately provide rain or snow, a prime example is the large snowfall on the windward side of the Rocky Mountains of North America (Figure 2). (iii) Convective lifting. Convective currents resulting from a warming of the lowest layer of the atmosphere lead to the heaped-up cumuliform clouds most readily identified with thunderstorm activity. However, under freezing conditions these clouds can also produce heavy showery or squally types of snowfall that in some areas form a large part of the annual snow production (Figure 2). Frêquently such low-level warming comes from the passage of cold air over large bodies of relatively warm water. Very often this snowfall is intensified by orographic lifting just to the lee of the open water; for example, the greatest snowfalls in the United States east of the Rocky Mountain areas may be found in the Tug Hill snowbelt area south and east of Lake Ontario. There, heavy snowfalls are - - due to convective lifting of the atmosphere resulting from the passage of cold air over open, and therefore relatively warm, Lake Ontario and further orographic lifting caused by the Adirondak Mountains. (iv) Lifting of mechanical turbulence. Another cloud forming mechanism may be found in the random stirring by ground friction of a layer of air below an inversion of temperature. This cloud is typically very thin and rarely yields more than a light drizzle or fine snow. 3.1 3. THE PHYSICS AND CHEMISTRY OF NUCLEATION The Physics of Condensation As indicated earlier, when air expands and is cooled adiabatic- ally its relative humidity is increased. When the process continues to the point of 100 per cent (or higher) saturation, condensation and cloud formation begins. Condensation is a process that does not occur easily in the pure environment. For pure water vapour at room temperature the vapour pressure must be about four times its saturation value before condensation occurs. Fortunately, however, the atmosphere is not an entirely pure environment. Invariably it contains very small particles (aerosols) some of which are hygroscopic crystals or droplets of various chemical solutions. Condensation occurs very readily upon such aerosols with only a very small degree of supersaturation required. 3.2 The FnemicaZ Composition of Condensation Nuclei Although there is still much to be learned relative to the chemistry of condensation nuclei it appears evident that there is an adequate supply available in the earth's atmosphere. In this connection the following sources have been identified: (i) Sea salt nuclei. These are prevalent not only over the sea but also over the continents. Recent investigations have revealed that salt nuclei are readily formed by bursting of salt water bubbles in the form of breaking waves. (ii) Continental dust particles. Soil and dust particles from the e m r s surface are prevalent throughout the atmosphere. (iii) Nuclei created by combustion and chemical reaction i.e., sulphur, ammonia, oxides of nitrogen, chlorine and sodium. 3.3 The Physics of SzcbZimation and Freezing When dealing exclusively with snow, prime interest is naturally restricted to the cloud forming processes that take place in belowfreezing temperatures. Just as pure water vapour, when it becomes supersaturated, does not condense spontaneously until a very large degree of supersaturation has been reached, so also a pure liquid will not freeze spontaneously until supercooled well below its equilibrium freezing temperature. In the case of water, supercooling to -40°C is required for such homogeneous freezing. However, as in the case of condensation, suspended particles may act as nuclei for the freezing process and if such nuclei are present freezing may occur with only a few degrees of supercooling. There is also another process by which ice crystals are formed in the atmosphere. This is by direct sublimation from the vapour in the same way that condensation droplets are formed. This process can 3 occur spontaneously and when suitable nuclei are present it is thought to be an important one. 3.4 The Chemical Composition of Ice-Forming Nuclei Although ice-forming nuclei occur naturally in the atmosphere their origin and composition are far from clearly established. One reason for this is that they are relatively scarce and difficult to identify since a cubic metre of atmospheric air at -10°C may contain as few as ten ice nuclei among perhaps 1O1I other particles. The following three quite different approaches have been taken by investigators to study ice-forming nuclei: (i) Samples of naturally occurring dust and smoke have been examined for nucleation ability. Most investigators suggest that clay-silicate particles (mainly kaolinite) play a large part in ice nucleation. Industrial sources are also available but are not considered to be more than locally importmt. (ii) Snow crystals have been examined and studies have been made of particles contained within them. Weickmann [l] using aircraft observations was a pioneer in this field. Again in this approach, clay particles appear as the most likely agents. (iii) Alternatively, Bowen [Z] in 1953 suggested that nuclei enter the top of the atmosphere as meteoric dust. Although this theory has drawn much public and scientific attention Mason [3] and others have suggested that conclusive evidence is still lacking. It should perhaps also be noted that artificial nuclei, such as silver iodide, are well known and widely used in precipitationinducing attempts. However they are not considered to be part of the natural process of snow production and so will not be discussed further. 4. THE FORMATION OF SNOWFLAKES Recent studies have classified the predominant ice crystal forms found in different atmospheric temperature ranges and cloud types. One such classification by Mason [3] considers the results of a number of investigations and may be seen in Table 1. Beyond this point, however, it must be admitted that in spite of considerable experimental and theoretical work, the physical mechanisms underlying the formation of intricate snowflake patterns from the original ice crystals are still largely unknown. About all that can be said at this time is that the growth occurs by either direct vapour transfer from a cloud droplet to the crystal because of the difference in vapour pressures over ice and water or by the interaction between ice crystals to form aggregate snow known as snowflakes. The overall result is that the snowflake is an aglomerate of individual crystals in which the star-shaped dendrites are generally predominant but in which needle and plate forms may also be found. TABLE 1 CRYSTAL TYPES ASSOCIATED WITH TEMPERATURE RANGES (from Mason [3]) Temperature Range - - 3 to 8°C - 8 to -25°C -10 to -20°C -20°C -30°C 4 Crystal Types Needles Plates, sector stars Stellar dendrites Prisms, single crystals, twins Clusters of hollow prisms Collecting, photographing and classifying snowflakes is a science to some and an art form to others and is well reported in the literature. However, a review of this aspect of the subject would be lengthy and is not considered to be a necessary part of this paper. 5. THE PHYSICS OF SNOWFALL In summary, the formation of snow, whether ít be a flake, a flurry or a full-blown storm requires several well known prerequisites: (i) An atmospheric lifting process must be available either in the form of a low pressure area or convection or orography, or any combination of these processes. As a result, greater than average snowfall should be expected along favoured s t o n tracks, to the windward side of mountain barriers and to the lee of open water. (ii) A sufficient amount of water vapour must be available so that saturation or supersaturation may be reached in the lifting process. If all other conditions are equal it is evident that the greater the water vapour content of the lifted air, the greater will be the snowfall. (iii) Nuclei must be available in the atmosphere to ensure condensation and the formation of ice crystals and snowflakes. Although relatively little is known of this process in nature it may be assumed that heavier snowfalls will be associated with greater numbers of nuclei. (iv) Finally, temperatures must be at, or below, freezing. Since temperature is a function of both latitude and altitude it follows that if all other conditions were equal, more snow would be expected at higher latitudes and higher elevations. The importance of the above-noted prerequisites may be verified by inspecting the accompanying snowfall maps of the North American continent (Figures 3 and 4). It is readily noted that there is more snow in the north than in the south a temperature (latitude) effect. More snow is also to;be found in the mountain areas. This is the effect of both tempeqature (elevation) and orography. More snow is indicated in mid-northern latitudes than in the far north, this is due partly to favourea storm tracks being in mid-latitudes and partly I to a general deficiency in the moisture supply in the far north. More snow may also be ',foundto the lee of open waters and in the upslope areas such as the west slopes of the Rockies and the snowbelt areas of the Great Lakes. As indicated earlier this is the result of both convective and orographic lifting. - - 6. THE PHYSICAL PROPERTIES AND PROCESSES OF SNOW COVER 6.1 S n m Depth On the synoptic or very broad scale the distribution of snow cover as measured by depth is a function of the meteorological controls of snowfall just outlined. However, superimposed upon the above-noted relatively large scale distribution of snow cover are patterns of snow depth that may be described as small meso-scale. These are due to the modifying influence of transport by wind and to variations in energy exchange within the snow cover itself. Transport Transport by blowing and/or drifting snow may result in a decrease or increase in snow cover depending on the relative local 5 wind speed which, in turn, is determined by local obstructions to airflow. Wherever surface winds increase, as between hills or on the crest of a ridge, erosion occurs. Conversely, wherever winds decrease, snow is deposited by the air stream. Favoured deposition areas are the lee sides of ridges, in depressions and along the edges of forests and urban areas. As might be expected, different surfaces of the earth exhibit quite different abilities to catch and retain snowfall. Kuzmin [6] has made extensive studies in this area finding for example that there is 30 to 40 per cent greater depth of snow cover in forest areas than on open virgin soil. A summary of his findings is shown in Table 2. The same author has also found variations of snow accumulation in forest areas which are related to the specific kinds of trees found in the forest; for example he reports a 15-year average of 134 mm (water equivalent) of snow in a birch forest as compared to only 85 mm in a fir forest. TABLE 2 SNOW RETENTION COEFFICIENTS FOR VARIOUS SURFACES RELATIVE TO VIRGIN SOIL (Kuzmin, 1960 [6]) Surface Coefficient Virgin soil Open ,ice Arable land Hilly land Large forest tracts River beds 1.0 0.4 to 0.5 0.9 1.2 1.3 to 1.4 3.0 Although possibly not directly related to hydrology, a survey of the subject of drifting snow cannot be considered complete without reference to Theakston's [7] laboratory investigations in which he employs scale models exposed to simulated snowstorms created by light white sand in an open-channel water flume. This work relates the degree and pattern of drifting directly to the local physical characteristics of the topography and of man-made obstructions, as well as, of course, to the speed and direction of the local winds. Energy exchange Variations in the energy exchange within the snowpack and at the snow-atmosphere interface may also result in major variations in the snow cover. Shading, variations in slope, unequal pollution on the snowpack by dust, variations in vegetative cover, and differences in the depth of snow cover can all affect the uniformity of the energy balance. MacKay [8] and others have discussed this process in detail and the subject will no doubt receive further attention later in these Symposia. 6.2 Snow Cover Densitg An indication of depth alone does not provide an adequate measure of snow cover because of the variability of the density of the snowpack on the ground. Even in freshly fallen snow densities vary markedly in both time and space. Potter [9] reports that although annual averages of snow-water equivalent for observing sites across Canada fall within the relatively narrow range of .O74 to .lo7 the water equivalent of individual snowfalls ranged all the way from .O2 to .28. 6 The density of freshly fallen snow depends upon both the form of the snow crystals and such meteorological factors as wind, temperature and available moisture during deposition. Mellor [lo] , quotes a density of 0.1 g/cm3 with fluffy snow and no wind as compared to a density of 0.3 g/cm3 under conditions of winds strong enough to break the crystals into small particles. Other studies suggest maximum densities at just above the freezing point'when the snow is wet and melting and again at very low temperatures when the crystals are small and readily fractured and compacted. The density of snow also changes after it lies on the ground. Prior to the spring thaw, the snowpack density is a function of the wind, the pressure of the overlying snow, and heat exchanges due to convection, condensation, radiation and conduction. However such metamorphosis of the snowpack is a subject which will receive specific attention in a later session of the Symposia. CHEMICAL COMPOSITION OF SNOW C h e ~ s t qof Falling or Freshly Fallen Snow 7. 7.1 As noted earlier, each snowflake begins its fall to earth with a chemical composition resulting from the very necessary nuclei of condensation, ice formation and/or sublimation. However as the snow falls through the air additional chemical constituents are added as the flakes pick up a share of the many aerosols present in the atmosphere. The result of this scavenging effect is a combination of chemical constituents primarily bicarbonates, sulphates, chlorides, calcium, sodium, potassium, magnesium and silicas, and clays. The actual proportions of chemicals identified in falling snow have been found to be a function of: (i) Air mass origin more salt particles are found over and near the sea, more clay particles are found over the continental areas. (ii) Physiographic effects - it is generally accepted that there are few aerosols at higher altitudes. it has been found that more aerosols are (iii) Local climate present in dry climates than in humid climates. industrial sources are important but it is (iv) Local sources thought that their effects are relatively local. Volcanoes, which may also be considered as local sources, have been known to provide widespread, but only periodic, chemical input to the atmosphere. (v) Lightening, meteoric dust and solar thermal-nuclear reaction - these have all been mentioned as possible sources of aerosols but the importance of such sources is still a matter of investigation. - - - 7.2 Chemistvy of the Snow Cover The prime difference between the chemical content of freshly fallen snow and that of the older snow on the ground is that the concentrations of chemicals present in the older snow are likely to be higher due to additions from dry fallout from the air. It is therefore not unexpected that the largest increases in chemical concentrations have been found relatively close to industrial sites. Table 3 condensed from Mellor [lo] provides an indication of the concentrations of chemicals found in snow on the ground at several widely dispersed points around the world. The very wide ranges in concentrations found in the same areas and the apparent lack of consistent geographical distribution of chemical constituents 7 8 Nja, a.m. O N d O O0 m .w. m m O d wo d w N d t r. . . M d dr. I r. I 00 I O 0 .. UJM d M 04 M M O N . . a m Nor o -.w. N I O 0 b W O N . . O 0 O .r M M O M W d d O ,-I W G O N N cn-3 m W O .. O M O . . O d W d -3N I M m o m N O d N G indicates a need for many more such observational programs distributed in both time and space. Indeed it is emphasized by scientists working in the field that there is still much to be explored in the chemistry of both falling snow and snow on the ground. In both cases extensive world-wide observing networks are a prime requisite to an improved understanding. 8. SUMMARY In general, there is little in common between the physical and chemical aspects of snow. The physical processes discussed in the paper dictate the amount of snow that will fall on any given area and the final pattern of snow distribution on the ground. The physical properties that have been considered dictate in part, the quantity and characterissic of local snowmelt runoff. The chemical composition of snowfall and snow on the ground will of course, contribute to the chemical constituents of the runoff water. Only in the nucleation phase o€ snow production do the physics and chemistry of snow become intimately associated and here there is a frontier of science that invites much further investigation. 9. ACKNOWLEDGMENTS In developing the chemical aspects of this paper, the author is indepted to Dr. M.T. Shiomi of the Chemical Limnology Section of the Canada Centre for Inland Waters, Environment Canada, who kindly provided a number of recent references. Two o€ these, a review of Russian work by Posokhov [Il] and one of North American work by Feth et a2 [U]although not quoted directly, provided a wealth of background material. In developing the physical aspects of the paper the author also made extensive use of the well-known text books by Mason [3] and Fletcher [13]. 10. REFERENCES WEICKMA", H.K. (1947). Die Eisphase in der Atmosphare Reports and Translations No. 716, Ministry of Supply (A) Volkenrode, London. BOWEN, E.G. (1953). The influence of meteoric dust on rainfall. Aust. J. Physics 6. MASON, B.J. (1971). The physics of clouds Clarendon Press, Oxford. - second edition, VIOMAS, M.K. (1964). Snowfall in Canada. Department of Transport, Meteorological Branch, CIR-3977, TEC-503, 1964. UNITED STATES DEPARTMENT OF COMMERCE. (1968). Climatic atlas of the United States. Environmental Data Service, Environmental Science Services Administration, 80 pp. KUZMIN, P.P. (1960). Snow cover and snow reserves. Gidrometeorologicheskoe Izdatelsko, Leningrad. Translation National Science Foundation, Washington, D.C., 1633, pp. 1-84. 9 [7] THEAKSTON, F.H. (1967). Advances in the use of models to predict behaviour of snow and wind. Presented at the 60th Annual Meeting, American Soc. of Agric. Engineers meeting jointly with the Canadian Soc. of Agric. Engineering, Saskatoon, Saskatchewan, June 1967. [8] MacKAY, G.A. (1968). Problems of measuring and evaluating snow cover. Proceedings of Workshop Seminar on Snow Hydrology, sponsored by Can. Nat. Com. for the IHD , pp. 48-62. [9] POTTER, J.G. (1965). Water content of freshly fallen snow, CIR-4232, TEC-569, Meteorological Branch, Can. Dept. of Transport. [lo] MELLOR, M. (1964). Properties of snow. Cold Regions Science and Engineering, Part III Engineering, Section A: Snow Engineering. U.S. Army Material Command, Cold Regions Research on Engineering Laboratory, Hanover, N.H., pp. 1-105. [ll] POSOKHOV, E.V. (1967). Factors effekting the formation of the chemical composition of atmospheric precipitation. Gidrokhimichesky Institut (Novocherkasek) Vol. XLVI , an unedited draft translation of the Foreign Language Division of the Canada Dept. of the Secretary of State (1969). [12] FETH, J.H., ROGERS, S.M., and ROBERSON, C.E. (1964). Chemical composition of snow in the northern Sierra Nevada and other areas, Geochemistry of Water. Geol. Sun. Water Supply Paper 1535-5, U.S. Dept. of the Interior. [I31 FLETCHER, N.H. (1966). The physics of rain clouds. University Press, Cambridge, England. 10 FT M 20,000 6000 10,000 3000 O B Fig. 1. Typical low pressure area showing cross-section of warm and cold fronts Fig. 2. Orographic and convective lifting 11 Fig, 3. Snowfall Map of Canada 1931-60 (M.K. Thomas, [3]) Fig. 4. Snowfall Ma? of United States 1931-60 (U.S. Department of Commerce [5]) 12 DISCUSSION W.T. Dickinson (Canada) - Our experience in analyzing the chemical constituents of rain and snowfall near Guelph, Ontario, Canada, points out that much care is required in the sampling techniques. The samples, which were sent to a laboratory for analysis, indicated a rather high content of cadmium. This information was released to the press before it could be confirmed by further testing which showed the cadmium to be the consequence of sampling equipment and sample preparation prior to analysis. - E.J. Lmzghm (Canada) Table III of your paper mentions that samples were taken from snow on the ground. Is it possible to relate the values in this table with the chemical content of falling snow? In particular, do you believe the lead found in snow is simply a local low-level fallout or is there evidence that lead has diffused to a sufficient height in the atmosphere to have become involved in the snow formation process? T.L. Eichards (Canada) - According to the literature, the bulk of the chemical constituents in snow on the ground come from dry fallout. The longer snow remains on the ground, the higher its concentration of chemical consistuents. I have no feeling for the extent of lead diffusion in the atmosphere. Perhaps the lead comes from local sources near urban areas, from automobile exhausts. - M.C. Quick (Canada) Professor Warren of the University of British Columbia has measured lead concentrations of minute amounts, especially as related to health problems. He found large differences between lead concentrations in cities, such as Vancouver, British Columbia, and those in open country. He is also studying many other trace elements and this work might be very useful to anyone studying chemical composition of snowpacks. 13