Ice

Ice is water that is frozen into a solid state, typically forming at or below temperatures of 0 °C, 32 °F, or 273.15 K.[4] As a naturally occurring crystalline inorganic solid with an ordered structure, ice is considered to be a mineral.[5][6] Depending on the presence of impurities such as particles of soil or bubbles of air, it can appear transparent or a more or less opaque bluish-white color.

This article is about water ice. For the broader concept of "ices" as used in the planetary sciences, see Volatile (astrogeology). For other uses, see Ice (disambiguation).

Ice
A picture of ice
An ice block, photographed at the Duluth Canal Park in Minnesota
Physical properties
Density (ρ)0.9167[1]–0.9168[2] g/cm3
Refractive index (n)1.309
Mechanical properties
Young's modulus (E)3400 to 37,500 kg-force/cm3[2]
Tensile strength (σt)5 to 18 kg-force/cm2[2]
Compressive strength (σc)24 to 60 kg-force/cm2[2]
Poisson's ratio (ν)0.36±0.13[2]
Thermal properties
Thermal conductivity (k)0.0053(1 + 0.0015 θ) cal/(cm s K), θ = temperature in °C[2]
Linear thermal expansion coefficient (α)5.5×10−5[2]
Specific heat capacity (c)0.5057 − 0.001863 θ cal/(g K), θ = absolute value of temperature in °C[2]
Electrical properties
Dielectric constant (εr)~3.15[3]
The properties of ice vary substantially with temperature, purity and other factors.

In the Solar System, ice is abundant and occurs naturally from as close to the Sun as Mercury to as far away as the Oort cloud objects. Beyond the Solar System, it occurs as interstellar ice. It is abundant on Earth's surface – particularly in the polar regions and above the snow line[7] – and, as a common form of precipitation and deposition, plays a key role in Earth's water cycle and climate. It falls as snowflakes and hail or occurs as frost, icicles or ice spikes and aggregates from snow as glaciers and ice sheets.

Ice exhibits at least eighteen phases (packing geometries), depending on temperature and pressure. When water is cooled rapidly (quenching), up to three types of amorphous ice can form depending on its history of pressure and temperature. When cooled slowly, correlated proton tunneling occurs below −253.15 °C (20 K, −423.67 °F) giving rise to macroscopic quantum phenomena. Virtually all ice on Earth's surface and in its atmosphere is of a hexagonal crystalline structure denoted as ice Ih (spoken as "ice one h") with minute traces of cubic ice, denoted as ice Ic and, more recently found, Ice VII inclusions in diamonds. The most common phase transition to ice Ih occurs when liquid water is cooled below 0 °C (273.15 K, 32 °F) at standard atmospheric pressure. It may also be deposited directly by water vapor, as happens in the formation of frost. The transition from ice to water is melting and from ice directly to water vapor is sublimation.

Ice is used in a variety of ways, including for cooling, for winter sports, and ice sculpting.

Physical properties
The three-dimensional crystal structure of H2O ice Ih (c) is composed of bases of H2O ice molecules (b) located on lattice points within the two-dimensional hexagonal space lattice (a).[8][9]

Ice possesses a regular crystalline structure based on the molecule of water, which consists of a single oxygen atom covalently bonded to two hydrogen atoms, or H–O–H. However, many of the physical properties of water and ice are controlled by the formation of hydrogen bonds between adjacent oxygen and hydrogen atoms; while it is a weak bond, it is nonetheless critical in controlling the structure of both water and ice.

An unusual property of water is that its solid form—ice frozen at atmospheric pressure—is approximately 8.3% less dense than its liquid form; this is equivalent to a volumetric expansion of 9%. The density of ice is 0.9167[1]–0.9168[2] g/cm3 at 0 °C and standard atmospheric pressure (101,325 Pa), whereas water has a density of 0.9998[1]–0.999863[2] g/cm3 at the same temperature and pressure. Liquid water is densest, essentially 1.00 g/cm3, at 4 °C and begins to lose its density as the water molecules begin to form the hexagonal crystals of ice as the freezing point is reached. This is due to hydrogen bonding dominating the intermolecular forces, which results in a packing of molecules less compact in the solid. Density of ice increases slightly with decreasing temperature and has a value of 0.9340 g/cm3 at −180 °C (93 K).[10]

When water freezes, it increases in volume (about 9% for fresh water).[11] The effect of expansion during freezing can be dramatic, and ice expansion is a basic cause of freeze-thaw weathering of rock in nature and damage to building foundations and roadways from frost heaving. It is also a common cause of the flooding of houses when water pipes burst due to the pressure of expanding water when it freezes.

The result of this process is that ice (in its most common form) floats on liquid water, which is an important feature in Earth's biosphere. It has been argued that without this property, natural bodies of water would freeze, in some cases permanently, from the bottom up,[12] resulting in a loss of bottom-dependent animal and plant life in fresh and sea water. Sufficiently thin ice sheets allow light to pass through while protecting the underside from short-term weather extremes such as wind chill. This creates a sheltered environment for bacterial and algal colonies. When sea water freezes, the ice is riddled with brine-filled channels which sustain sympagic organisms such as bacteria, algae, copepods and annelids, which in turn provide food for animals such as krill and specialised fish like the bald notothen, fed upon in turn by larger animals such as emperor penguins and minke whales.[13]

When ice melts, it absorbs as much energy as it would take to heat an equivalent mass of water by 80 °C. During the melting process, the temperature remains constant at 0 °C. While melting, any energy added breaks the hydrogen bonds between ice (water) molecules. Energy becomes available to increase the thermal energy (temperature) only after enough hydrogen bonds are broken that the ice can be considered liquid water. The amount of energy consumed in breaking hydrogen bonds in the transition from ice to water is known as the heat of fusion.

As with water, ice absorbs light at the red end of the spectrum preferentially as the result of an overtone of an oxygen–hydrogen (O–H) bond stretch. Compared with water, this absorption is shifted toward slightly lower energies. Thus, ice appears blue, with a slightly greener tint than liquid water. Since absorption is cumulative, the color effect intensifies with increasing thickness or if internal reflections cause the light to take a longer path through the ice.[14]

Other colors can appear in the presence of light absorbing impurities, where the impurity is dictating the color rather than the ice itself. For instance, icebergs containing impurities (e.g., sediments, algae, air bubbles) can appear brown, grey or green.[14]

Because ice in natural environments is usually close to its melting temperature, its hardness shows pronounced temperature variations. At its melting point, ice has a Mohs hardness of 2 or less, but the hardness increases to about 4 at a temperature of −44 °C (−47 °F) and to 6 at a temperature of −78.5 °C (−109.3 °F), the vaporization point of solid carbon dioxide (dry ice).[15]

Phases
Pressure dependence of ice melting

Ice may be any one of the nineteen known solid crystalline phases of water, or in an amorphous solid state at various densities.[16]

Most liquids under increased pressure freeze at higher temperatures because the pressure helps to hold the molecules together. However, the strong hydrogen bonds in water make it different: for some pressures higher than 1 atm (0.10 MPa), water freezes at a temperature below 0 °C, as shown in the phase diagram below. The melting of ice under high pressures is thought to contribute to the movement of glaciers.[17]

Ice, water, and water vapour can coexist at the triple point, which is exactly 273.16 K (0.01 °C) at a pressure of 611.657 Pa.[18][19] The kelvin was defined as 1/273.16 of the difference between this triple point and absolute zero,[20] though this definition changed in May 2019.[21] Unlike most other solids, ice is difficult to superheat. In an experiment, ice at −3 °C was superheated to about 17 °C for about 250 picoseconds.[22]

Subjected to higher pressures and varying temperatures, ice can form in nineteen separate known crystalline phases. With care, at least fifteen of these phases (one of the known exceptions being ice X) can be recovered at ambient pressure and low temperature in metastable form.[23][24] The types are differentiated by their crystalline structure, proton ordering,[25] and density. There are also two metastable phases of ice under pressure, both fully hydrogen-disordered; these are IV and XII. Ice XII was discovered in 1996. In 2006, XIII and XIV were discovered.[26] Ices XI, XIII, and XIV are hydrogen-ordered forms of ices Ih, V, and XII respectively. In 2009, ice XV was found at extremely high pressures and −143 °C.[27] At even higher pressures, ice is predicted to become a metal; this has been variously estimated to occur at 1.55 TPa[28] or 5.62 TPa.[29]

As well as crystalline forms, solid water can exist in amorphous states as amorphous solid water (ASW) of varying densities. Water in the interstellar medium is dominated by amorphous ice, making it likely the most common form of water in the universe. Low-density ASW (LDA), also known as hyperquenched glassy water, may be responsible for noctilucent clouds on Earth and is usually formed by deposition of water vapor in cold or vacuum conditions. High-density ASW (HDA) is formed by compression of ordinary ice Ih or LDA at GPa pressures. Very-high-density ASW (VHDA) is HDA slightly warmed to 160 K under 1–2 GPa pressures.

In outer space, hexagonal crystalline ice (the predominant form found on Earth) is extremely rare. Amorphous ice is more common; however, hexagonal crystalline ice can be formed by volcanic action.[30]

Ice from a theorized superionic water may possess two crystalline structures. At pressures in excess of 500,000 bars (7,300,000 psi) such superionic ice would take on a body-centered cubic structure. However, at pressures in excess of 1,000,000 bars (15,000,000 psi) the structure may shift to a more stable face-centered cubic lattice. It is speculated that superionic ice could compose the interior of ice giants such as Uranus and Neptune.[31]

Log-lin pressure-temperature phase diagram of water. The Roman numerals correspond to some ice phases listed below.
An alternative formulation of the phase diagram for certain ices and other phases of water[32]
Phase Characteristics
Amorphous ice Amorphous ice is ice lacking crystal structure. Amorphous ice exists in four forms: low-density (LDA) formed at atmospheric pressure, or below, medium-density (MDA), high-density (HDA) and very-high-density amorphous ice (VHDA), forming at higher pressures. LDA forms by extremely quick cooling of liquid water ("hyperquenched glassy water", HGW), by depositing water vapour on very cold substrates ("amorphous solid water", ASW) or by heating high density forms of ice at ambient pressure ("LDA"). Recently, a medium-density amorphous form ("MDA") has been shown to exist, created by ball-milling ice Ih at low temperatures.[33]
Ice Ih Normal hexagonal crystalline ice. Virtually all ice in the biosphere is ice Ih, with the exception only of a small amount of ice Ic.
Ice Ic A metastable cubic crystalline variant of ice. The oxygen atoms are arranged in a diamond structure. It is produced at temperatures between 130 and 220 K, and can exist up to 240 K,[34][35] when it transforms into ice Ih. It may occasionally be present in the upper atmosphere.[36] More recently, it has been shown that many samples which were described as cubic ice were actually stacking disordered ice with trigonal symmetry.[37] The first samples of ice I with cubic symmetry (i.e. cubic ice) were only reported in 2020.[38]
Ice II A rhombohedral crystalline form with highly ordered structure. Formed from ice Ih by compressing it at temperature of 190–210 K. When heated, it undergoes transformation to ice III.
Ice III A tetragonal crystalline ice, formed by cooling water down to 250 K at 300 MPa. Least dense of the high-pressure phases. Denser than water.
Ice IV A metastable rhombohedral phase. It can be formed by heating high-density amorphous ice slowly at a pressure of 810 MPa. It does not form easily without a nucleating agent.[39]
Ice V A monoclinic crystalline phase. Formed by cooling water to 253 K at 500 MPa. Most complicated structure of all the phases.[40]
Ice VI A tetragonal crystalline phase. Formed by cooling water to 270 K at 1.1 GPa. Exhibits Debye relaxation.[41]
Ice VII A cubic phase. The hydrogen atoms' positions are disordered. Exhibits Debye relaxation. The hydrogen bonds form two interpenetrating lattices.
Ice VIIt Forms at around 5 GPa, when Ice VII becomes tetragonal.[42]
Ice VIII A more ordered version of ice VII, where the hydrogen atoms assume fixed positions. It is formed from ice VII, by cooling it below 5 °C (278 K) at 2.1 GPa.
Ice IX A tetragonal phase. Formed gradually from ice III by cooling it from 208 K to 165 K, stable below 140 K and pressures between 200 MPa and 400 MPa. It has density of 1.16 g/cm3, slightly higher than ordinary ice.
Ice X Proton-ordered symmetric ice. Forms at pressures around 70 GPa,[43] or perhaps as low as 30 GPa.[42]
Ice XI An orthorhombic, low-temperature equilibrium form of hexagonal ice. It is ferroelectric. Ice XI is considered the most stable configuration of ice Ih.[44]
Ice XII A tetragonal, metastable, dense crystalline phase. It is observed in the phase space of ice V and ice VI. It can be prepared by heating high-density amorphous ice from 77 K to about 183 K at 810 MPa. It has a density of 1.3 g·cm−3 at 127 K (i.e., approximately 1.3 times denser than water).
Ice XIII A monoclinic crystalline phase. Formed by cooling water to below 130 K at 500 MPa. The proton-ordered form of ice V.[45]
Ice XIV An orthorhombic crystalline phase. Formed below 118 K at 1.2 GPa. The proton-ordered form of ice XII.[45]
Ice XV A proton-ordered form of ice VI formed by cooling water to around 80–108 K at 1.1 GPa.
Ice XVI The least dense crystalline form of water, topologically equivalent to the empty structure of sII clathrate hydrates.
Square ice Square ice crystals form at room temperature when squeezed between two layers of graphene. The material was a new crystalline phase of ice when it was first reported in 2014.[46][47] The research derived from the earlier discovery that water vapor and liquid water could pass through laminated sheets of graphene oxide, unlike smaller molecules such as helium. The effect is thought to be driven by the van der Waals force, which may involve more than 10,000 atmospheres of pressure.[46]
Ice XVII A porous hexagonal crystalline phase with helical channels, with density near that of ice XVI.[48][49][50] Formed by placing hydrogen-filled ice in a vacuum and increasing the temperature until the hydrogen molecules escape.[48]
Ice XVIII A form of water also known as superionic water or superionic ice in which oxygen ions develop a crystalline structure while hydrogen ions move freely.
Ice XIX Another phase related to ice VI formed by cooling water to around 100 K at approximately 2 GPa.[16]

Friction properties
Frozen waterfall in southeast New York

The low coefficient of friction ("slipperiness") of ice has been attributed to the pressure of an object coming into contact with the ice, melting a thin layer of the ice and allowing the object to glide across the surface.[51] For example, the blade of an ice skate, upon exerting pressure on the ice, would melt a thin layer, providing lubrication between the ice and the blade. This explanation, called "pressure melting", originated in the 19th century. However, it does not account for skating on ice temperatures lower than −4 °C (25 °F; 269 K), which is often skated upon. Also, the effect of pressure melting is too small to account for the reduced friction as commonly experienced.[52]

A second theory describing the coefficient of friction of ice suggested that ice molecules at the interface cannot properly bond with the molecules of the mass of ice beneath (and thus are free to move like molecules of liquid water). These molecules remain in a semi-liquid state, providing lubrication regardless of pressure against the ice exerted by any object. However, the significance of this hypothesis is disputed by experiments showing a high coefficient of friction for ice using atomic force microscopy.[52]

A third theory is "friction heating", which suggests that friction of the material is the cause of the ice layer melting. However, this theory does not sufficiently explain why ice is slippery when standing still even at below-zero temperatures.[51]

A comprehensive theory of ice friction takes into account all the above-mentioned friction mechanisms.[53] This model allows quantitative estimation of the friction coefficient of ice against various materials as a function of temperature and sliding speed. In typical conditions related to winter sports and tires of a vehicle on ice, melting of a thin ice layer due to the frictional heating is the primary reason for the slipperiness. The mechanism controlling the frictional properties of ice is still an active area of scientific study.[54]

Natural formation
Feather ice on the plateau near Alta, Norway. The crystals form at temperatures below −30 °C (−22 °F).

The term that collectively describes all of the parts of the Earth's surface where water is in frozen form is the cryosphere. Ice is an important component of the global climate, particularly in regard to the water cycle. Glaciers and snowpacks are an important storage mechanism for fresh water; over time, they may sublimate or melt. Snowmelt is an important source of seasonal fresh water. The World Meteorological Organization defines several kinds of ice depending on origin, size, shape, influence and so on.[55] Clathrate hydrates are forms of ice that contain gas molecules trapped within its crystal lattice.

On the oceans
Main article: Sea ice

Ice that is found at sea may be in the form of drift ice floating in the water, fast ice fixed to a shoreline or anchor ice if attached to the sea bottom. Ice which calves (breaks off) from an ice shelf or glacier may become an iceberg. Sea ice can be forced together by currents and winds to form pressure ridges up to 12 metres (39 ft) tall. Navigation through areas of sea ice occurs in openings called "polynyas" or "leads" or requires the use of a special ship called an "icebreaker".

On land and structures
Ice on deciduous tree after freezing rain

Ice on land ranges from the largest type called an "ice sheet" to smaller ice caps and ice fields to glaciers and ice streams to the snow line and snow fields.

Aufeis is layered ice that forms in Arctic and subarctic stream valleys. Ice, frozen in the stream bed, blocks normal groundwater discharge, and causes the local water table to rise, resulting in water discharge on top of the frozen layer. This water then freezes, causing the water table to rise further and repeat the cycle. The result is a stratified ice deposit, often several meters thick.

Freezing rain is a type of winter storm called an ice storm where rain falls and then freezes producing a glaze of ice. Ice can also form icicles, similar to stalactites in appearance, or stalagmite-like forms as water drips and re-freezes.

The term "ice dam" has three meanings (others discussed below). On structures, an ice dam is the buildup of ice on a sloped roof which stops melt water from draining properly and can cause damage from water leaks in buildings.

On rivers and streams
A small frozen rivulet

Ice which forms on moving water tends to be less uniform and stable than ice which forms on calm water. Ice jams (sometimes called "ice dams"), when broken chunks of ice pile up, are the greatest ice hazard on rivers. Ice jams can cause flooding, damage structures in or near the river, and damage vessels on the river. Ice jams can cause some hydropower industrial facilities to completely shut down. An ice dam is a blockage from the movement of a glacier which may produce a proglacial lake. Heavy ice flows in rivers can also damage vessels and require the use of an icebreaker to keep navigation possible.

Ice discs are circular formations of ice surrounded by water in a river.[56]

Pancake ice is a formation of ice generally created in areas with less calm conditions.

On lakes

Ice forms on calm water from the shores, a thin layer spreading across the surface, and then downward. Ice on lakes is generally four types: primary, secondary, superimposed and agglomerate.[57][58] Primary ice forms first. Secondary ice forms below the primary ice in a direction parallel to the direction of the heat flow. Superimposed ice forms on top of the ice surface from rain or water which seeps up through cracks in the ice which often settles when loaded with snow.

Shelf ice occurs when floating pieces of ice are driven by the wind piling up on the windward shore.

Candle ice is a form of rotten ice that develops in columns perpendicular to the surface of a lake.

An ice shove occurs when ice movement, caused by ice expansion and/or wind action, occurs to the extent that ice pushes onto the shores of lakes, often displacing sediment that makes up the shoreline.[59]

In the air
Ice formation on exterior of vehicle windshield

Rime

Rime is a type of ice formed on cold objects when drops of water crystallize on them. This can be observed in foggy weather, when the temperature drops during the night. Soft rime contains a high proportion of trapped air, making it appear white rather than transparent, and giving it a density about one quarter of that of pure ice. Hard rime is comparatively dense.

Pellets
Main article: Ice pellets
An accumulation of ice pellets

Ice pellets are a form of precipitation consisting of small, translucent balls of ice. This form of precipitation is also referred to as "sleet" by the United States National Weather Service.[60] (In British English "sleet" refers to a mixture of rain and snow.) Ice pellets are usually smaller than hailstones.[61] They often bounce when they hit the ground, and generally do not freeze into a solid mass unless mixed with freezing rain. The METAR code for ice pellets is PL.[62]

Ice pellets form when a layer of above-freezing air is located between 1,500 and 3,000 metres (4,900 and 9,800 ft) above the ground, with sub-freezing air both above and below it. This causes the partial or complete melting of any snowflakes falling through the warm layer. As they fall back into the sub-freezing layer closer to the surface, they re-freeze into ice pellets. However, if the sub-freezing layer beneath the warm layer is too small, the precipitation will not have time to re-freeze, and freezing rain will be the result at the surface. A temperature profile showing a warm layer above the ground is most likely to be found in advance of a warm front during the cold season,[63] but can occasionally be found behind a passing cold front.

Hail
Main article: Hail
A large hailstone, about 6 cm (2.4 in) in diameter

Like other precipitation, hail forms in storm clouds when supercooled water droplets freeze on contact with condensation nuclei, such as dust or dirt. The storm's updraft blows the hailstones to the upper part of the cloud. The updraft dissipates and the hailstones fall down, back into the updraft, and are lifted up again. Hail has a diameter of 5 millimetres (0.20 in) or more.[64] Within METAR code, GR is used to indicate larger hail, of a diameter of at least 6.4 millimetres (0.25 in) and GS for smaller.[62] Stones of 19 millimetres (0.75 in), 25 millimetres (1.0 in) and 44 millimetres (1.75 in) are the most frequently reported hail sizes in North America.[65] Hailstones can grow to 15 centimetres (6 in) and weigh more than 0.5 kilograms (1.1 lb).[66] In large hailstones, latent heat released by further freezing may melt the outer shell of the hailstone. The hailstone then may undergo 'wet growth', where the liquid outer shell collects other smaller hailstones.[67] The hailstone gains an ice layer and grows increasingly larger with each ascent. Once a hailstone becomes too heavy to be supported by the storm's updraft, it falls from the cloud.[68]

Hail forms in strong thunderstorm clouds, particularly those with intense updrafts, high liquid water content, great vertical extent, large water droplets, and where a good portion of the cloud layer is below freezing 0 °C (32 °F).[64] Hail-producing clouds are often identifiable by their green coloration.[69][70] The growth rate is maximized at about −13 °C (9 °F), and becomes vanishingly small much below −30 °C (−22 °F) as supercooled water droplets become rare. For this reason, hail is most common within continental interiors of the mid-latitudes, as hail formation is considerably more likely when the freezing level is below the altitude of 11,000 feet (3,400 m).[71] Entrainment of dry air into strong thunderstorms over continents can increase the frequency of hail by promoting evaporational cooling which lowers the freezing level of thunderstorm clouds giving hail a larger volume to grow in. Accordingly, hail is actually less common in the tropics despite a much higher frequency of thunderstorms than in the mid-latitudes because the atmosphere over the tropics tends to be warmer over a much greater depth. Hail in the tropics occurs mainly at higher elevations.[72]

Snow
Main articles: Snow and Snowflake
Snowflakes by Wilson Bentley, 1902

Snow crystals form when tiny supercooled cloud droplets (about 10 μm in diameter) freeze. These droplets are able to remain liquid at temperatures lower than −18 °C (255 K; 0 °F), because to freeze, a few molecules in the droplet need to get together by chance to form an arrangement similar to that in an ice lattice; then the droplet freezes around this "nucleus". Experiments show that this "homogeneous" nucleation of cloud droplets only occurs at temperatures lower than −35 °C (238 K; −31 °F).[73] In warmer clouds an aerosol particle or "ice nucleus" must be present in (or in contact with) the droplet to act as a nucleus. Our understanding of what particles make efficient ice nuclei is poor – what we do know is they are very rare compared to that cloud condensation nuclei on which liquid droplets form. Clays, desert dust and biological particles may be effective,[74] although to what extent is unclear. Artificial nuclei are used in cloud seeding.[75] The droplet then grows by condensation of water vapor onto the ice surfaces.

Diamond dust
Main article: Diamond dust

So-called "diamond dust", also known as ice needles or ice crystals, forms at temperatures approaching −40 °C (−40 °F) due to air with slightly higher moisture from aloft mixing with colder, surface-based air.[76] The METAR identifier for diamond dust within international hourly weather reports is IC.[62]

Ablation
Main article: Ablation

Ablation of ice refers to both its melting and its dissolution.

The melting of ice means entails the breaking of hydrogen bonds between the water molecules. The ordering of the molecules in the solid breaks down to a less ordered state and the solid melts to become a liquid. This is achieved by increasing the internal energy of the ice beyond the melting point. When ice melts it absorbs as much energy as would be required to heat an equivalent amount of water by 80 °C. While melting, the temperature of the ice surface remains constant at 0 °C. The rate of the melting process depends on the efficiency of the energy exchange process. An ice surface in fresh water melts solely by free convection with a rate that depends linearly on the water temperature, T∞, when T∞ is less than 3.98 °C, and superlinearly when T∞ is equal to or greater than 3.98 °C, with the rate being proportional to (T∞ − 3.98 °C)α, with α = 5/3 for T∞ much greater than 8 °C, and α = 4/3 for in between temperatures T∞.[77]

In salty ambient conditions, dissolution rather than melting often causes the ablation of ice. For example, the temperature of the Arctic Ocean is generally below the melting point of ablating sea ice. The phase transition from solid to liquid is achieved by mixing salt and water molecules, similar to the dissolution of sugar in water, even though the water temperature is far below the melting point of the sugar. Thus the dissolution rate is limited by salt transport whereas melting can occur at much higher rates that are characteristic for heat transport.[78]

Role in human activities

Humans have used ice for cooling and food preservation for centuries, relying on harvesting natural ice in various forms and then transitioning to the mechanical production of the material. Ice also presents a challenge to transportation in various forms and a setting for winter sports.

Cooling

Ice has long been valued as a means of cooling. In 400 BC Iran, Persian engineers had already mastered the technique of storing ice in the middle of summer in the desert. The ice was brought in from ice pools or during the winters from nearby mountains in bulk amounts, and stored in specially designed, naturally cooled refrigerators, called yakhchal (meaning ice storage). This was a large underground space (up to 5000 m3) that had thick walls (at least two meters at the base) made of a special mortar called sarooj, composed of sand, clay, egg whites, lime, goat hair, and ash in specific proportions, and which was known to be resistant to heat transfer. This mixture was thought to be completely water impenetrable. The space often had access to a qanat, and often contained a system of windcatchers which could easily bring temperatures inside the space down to frigid levels on summer days. The ice was used to chill treats for royalty.

Harvesting
Main article: Ice cutting
Gwrych Castle, North Wales, with 18 towers, one of which is called the 'Ice Tower' designed specifically to store ice, the construction of the tower was completed in 1822.
Harvesting ice on Lake St. Clair in Michigan, c. 1905

There were thriving industries in 16th–17th century England whereby low-lying areas along the Thames Estuary were flooded during the winter, and ice harvested in carts and stored inter-seasonally in insulated wooden houses as a provision to an icehouse often located in large country houses, and widely used to keep fish fresh when caught in distant waters. This was allegedly copied by an Englishman who had seen the same activity in China. Ice was imported into England from Norway on a considerable scale as early as 1823.[79]

In the United States, the first cargo of ice was sent from New York City to Charleston, South Carolina, in 1799,[79] and by the first half of the 19th century, ice harvesting had become a big business. Frederic Tudor, who became known as the "Ice King", worked on developing better insulation products for long distance shipments of ice, especially to the tropics; this became known as the ice trade.

Between 1812 and 1822, under Lloyd Hesketh Bamford Hesketh's instruction, Gwrych Castle was built with 18 large towers, one of those towers is called the 'Ice Tower'. Its sole purpose was to store Ice.[80]

Trieste sent ice to Egypt, Corfu, and Zante; Switzerland, to France; and Germany sometimes was supplied from Bavarian lakes.[79] The Hungarian Parliament building used ice harvested in the winter from Lake Balaton for air conditioning.

Ice houses were used to store ice formed in the winter, to make ice available all year long, and an early type of refrigerator known as an icebox was cooled using a block of ice placed inside it. In many cities, it was not unusual to have a regular ice delivery service during the summer. The advent of artificial refrigeration technology has since made delivery of ice obsolete.

Ice is still harvested for ice and snow sculpture events. For example, a swing saw is used to get ice for the Harbin International Ice and Snow Sculpture Festival each year from the frozen surface of the Songhua River.[81]

Artificial production

The earliest known written process to artificially make ice is by the 13th-century writings of Arab historian Ibn Abu Usaybia in his book Kitab Uyun al-anba fi tabaqat-al-atibba concerning medicine in which Ibn Abu Usaybi’a attributes the process to an even older author, Ibn Bakhtawayhi, of whom nothing is known.[82]

Mechanical production
Layout of a late 19th-century ice factory

Ice is now produced on an industrial scale, for uses including food storage and processing, chemical manufacturing, concrete mixing and curing, and consumer or packaged ice.[83] Most commercial icemakers produce three basic types of fragmentary ice: flake, tubular and plate, using a variety of techniques.[83] Large batch ice makers can produce up to 75 tons of ice per day.[84] In 2002, there were 426 commercial ice-making companies in the United States, with a combined value of shipments of $595,487,000.[85] Home refrigerators can also make ice with a built in icemaker, which will typically make ice cubes or crushed ice. Stand-alone icemaker units that make ice cubes are often called ice machines.

Transportation

Ice can present challenges to safe transportation on land, sea and in the air.

Land travel
Loss of control on ice by an articulated bus

Ice forming on roads is a dangerous winter hazard. Black ice is very difficult to see, because it lacks the expected frosty surface. Whenever there is freezing rain or snow which occurs at a temperature near the melting point, it is common for ice to build up on the windows of vehicles. Driving safely requires the removal of the ice build-up. Ice scrapers are tools designed to break the ice free and clear the windows, though removing the ice can be a long and laborious process.

Far enough below the freezing point, a thin layer of ice crystals can form on the inside surface of windows. This usually happens when a vehicle has been left alone after being driven for a while, but can happen while driving, if the outside temperature is low enough. Moisture from the driver's breath is the source of water for the crystals. It is troublesome to remove this form of ice, so people often open their windows slightly when the vehicle is parked in order to let the moisture dissipate, and it is now common for cars to have rear-window defrosters to solve the problem. A similar problem can happen in homes, which is one reason why many colder regions require double-pane windows for insulation.

When the outdoor temperature stays below freezing for extended periods, very thick layers of ice can form on lakes and other bodies of water, although places with flowing water require much colder temperatures. The ice can become thick enough to drive onto with automobiles and trucks. Doing this safely requires a thickness of at least 30 cm (11+3⁄4 in).

Water-borne travel
Channel through ice for ship traffic on Lake Huron with ice breakers in background

For ships, ice presents two distinct hazards. First, spray and freezing rain can produce an ice build-up on the superstructure of a vessel sufficient to make it unstable, and to require it to be hacked off or melted with steam hoses. Second, icebergs – large masses of ice floating in water (typically created when glaciers reach the sea) – can be dangerous if struck by a ship when underway. Icebergs have been responsible for the sinking of many ships, the most famous being the Titanic. For harbors near the poles, being ice-free, ideally all year long, is an important advantage. Examples are Murmansk (Russia), Petsamo (Russia, formerly Finland), and Vardø (Norway). Harbors which are not ice-free are opened up using icebreakers.

Air travel
Main article: Icing conditions
Rime ice on the leading edge of an aircraft wing, partially released by the black pneumatic boot

For aircraft, ice can cause a number of dangers. As an aircraft climbs, it passes through air layers of different temperature and humidity, some of which may be conducive to ice formation. If ice forms on the wings or control surfaces, this may adversely affect the flying qualities of the aircraft. During the first non-stop flight across the Atlantic, the British aviators Captain John Alcock and Lieutenant Arthur Whitten Brown encountered such icing conditions – Brown left the cockpit and climbed onto the wing several times to remove ice which was covering the engine air intakes of the Vickers Vimy aircraft they were flying.

One vulnerability effected by icing that is associated with reciprocating internal combustion engines is the carburetor. As air is sucked through the carburetor into the engine, the local air pressure is lowered, which causes adiabatic cooling. Thus, in humid near-freezing conditions, the carburetor will be colder, and tend to ice up. This will block the supply of air to the engine, and cause it to fail. For this reason, aircraft reciprocating engines with carburetors are provided with carburetor air intake heaters. The increasing use of fuel injection—which does not require carburetors—has made "carb icing" less of an issue for reciprocating engines.

Jet engines do not experience carb icing, but recent evidence indicates that they can be slowed, stopped, or damaged by internal icing in certain types of atmospheric conditions much more easily than previously believed. In most cases, the engines can be quickly restarted and flights are not endangered, but research continues to determine the exact conditions which produce this type of icing, and find the best methods to prevent, or reverse it, in flight.

Recreation and sports
Main article: Ice sports
Skating fun by 17th century Dutch painter Hendrick Avercamp

Ice also plays a central role in winter recreation and in many sports such as ice skating, tour skating, ice hockey, bandy, ice fishing, ice climbing, curling, broomball and sled racing on bobsled, luge and skeleton. Many of the different sports played on ice get international attention every four years during the Winter Olympic Games.

A sort of sailboat on blades gives rise to ice yachting. Another sport is ice racing, where drivers must speed on lake ice, while also controlling the skid of their vehicle (similar in some ways to dirt track racing). The sport has even been modified for ice rinks.

As thermal ballast
  • Ice is used to cool and preserve food in iceboxes.
  • Ice cubes or crushed ice can be used to cool drinks. As the ice melts, it absorbs heat and keeps the drink near 0 °C (32 °F).
  • Ice can be used as part of an air conditioning system, using battery- or solar-powered fans to blow hot air over the ice. This is especially useful during heat waves when power is out and standard (electrically powered) air conditioners do not work.
  • Ice can be used (like other cold packs) to reduce swelling (by decreasing blood flow) and pain by pressing it against an area of the body.[86]

As structural material
Ice pier during 1983 cargo operations. McMurdo Station, Antarctica.
  • Engineers used the substantial strength of pack ice when they constructed Antarctica's first floating ice pier in 1973.[87] Such ice piers are used during cargo operations to load and offload ships. Fleet operations personnel make the floating pier during the winter. They build upon naturally occurring frozen seawater in McMurdo Sound until the dock reaches a depth of about 22 feet (6.7 m). Ice piers have a lifespan of three to five years.
    An ice-made dining room of the Kemi's SnowCastle ice hotel in Finland
  • Structures and ice sculptures are built out of large chunks of ice or by spraying water[88] The structures are mostly ornamental (as in the case with ice castles), and not practical for long-term habitation. Ice hotels exist on a seasonal basis in a few cold areas. Igloos are another example of a temporary structure, made primarily from snow.
  • In cold climates, roads are regularly prepared on iced-over lakes and archipelago areas. Temporarily, even a railroad has been built on ice.[88]
  • During World War II, Project Habbakuk was an Allied programme which investigated the use of pykrete (wood fibers mixed with ice) as a possible material for warships, especially aircraft carriers, due to the ease with which a vessel immune to torpedoes, and a large deck, could be constructed by ice. A small-scale prototype was built,[89] but the need for such a vessel in the war was removed prior to building it in full-scale.
  • Ice has even been used as the material for a variety of musical instruments, for example by percussionist Terje Isungset.[90]

Non-water
Main article: Volatile (astrogeology)

The solid phases of several other volatile substances are also referred to as ices; generally a volatile is classed as an ice if its melting point lies above or around 100 K. The best known example is dry ice, the solid form of carbon dioxide.

A "magnetic analogue" of ice is also realized in some insulating magnetic materials in which the magnetic moments mimic the position of protons in water ice and obey energetic constraints similar to the Bernal-Fowler ice rules arising from the geometrical frustration of the proton configuration in water ice. These materials are called spin ice.

See also
  • Density of ice versus water – Physical and chemical properties of pure water
  • Ice famine – Historical scarcity of commercial ice
  • Ice jacking – Structural damage caused by freezing water
  • Ice road – Path made over frozen water rather than land
  • Jumble ice – Irregular jagged ice formed over water
  • Pumpable ice technology – Type of technology to produce and use fluids or secondary refrigerants
  • Ice crystal – Water ice in symmetrical shapes

References
  1. Harvey, Allan H. (2017). "Properties of Ice and Supercooled Water". In Haynes, William M.; Lide, David R.; Bruno, Thomas J. (eds.). CRC Handbook of Chemistry and Physics (97th ed.). Boca Raton, FL: CRC Press. ISBN 978-1-4987-5429-3.
  2. Voitkovskii, K. F., Translation of: "The mechanical properties of ice" ("Mekhanicheskie svoistva l'da"), Academy of Sciences (USSR), DTIC AD0662716
  3. This applies in a range only, roughly 1 MHz to 300 GHz
  4. "CK-12 Chemistry for High School 15.2 Structure of Ice". ck12.org. Retrieved 17 August 2023.
  5. Demirbas, Ayhan (2010). Methane Gas Hydrate. Springer Science & Business Media. p. 90. ISBN 978-1-84882-872-8.
  6. "The Mineral Ice". minerals.net. Retrieved 9 January 2019.
  7. Prockter, Louise M. (2005). "Ice in the Solar System" (PDF). Johns Hopkins APL Technical Digest. 26 (2): 175. Archived from the original (PDF) on 19 March 2015. Retrieved 21 December 2013.
  8. Physics of Ice, V. F. Petrenko, R. W. Whitworth, Oxford University Press, 1999, ISBN 9780198518945
  9. Bernal, J. D.; Fowler, R. H. (1933). "A Theory of Water and Ionic Solution, with Particular Reference to Hydrogen and Hydroxyl Ions". The Journal of Chemical Physics. 1 (8): 515. Bibcode:1933JChPh...1..515B. doi:10.1063/1.1749327.
  10. Lide, D. R., ed. (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton (FL): CRC Press. ISBN 0-8493-0486-5.
  11. Sreepat, Jain. Fundamentals of Physical Geology. New Delhi: Springer, India, Private, 2014. 135. Print. ISBN 978-81-322-1538-7
  12. Tyson, Neil deGrasse. "Water, Water". haydenplanetarium.org. Archived from the original on 26 July 2011.
  13. Sea Ice Ecology Archived 21 March 2012 at the Wayback Machine. Acecrc.sipex.aq. Retrieved 30 October 2011.
  14. Lynch, David K.; Livingston, William Charles (2001). Color and light in nature. Cambridge University Press. pp. 161–. ISBN 978-0-521-77504-5.
  15. Walters, S. Max (January 1946). "Hardness of Ice at Low Temperatures". Polar Record. 4 (31): 344–345. doi:10.1017/S003224740004239X. S2CID 250049037.
  16. Metcalfe, Tom (9 March 2021). "Exotic crystals of 'ice 19' discovered". Live Science.
  17. "The Life of a Glacier". National Snow and Data Ice Center. Archived from the original on 15 December 2014.
  18. Wagner, Wolfgang; Saul, A.; Pruss, A. (May 1994). "International Equations for the Pressure Along the Melting and Along the Sublimation Curve of Ordinary Water Substance". Journal of Physical and Chemical Reference Data. 23 (3): 515–527. Bibcode:1994JPCRD..23..515W. doi:10.1063/1.555947.
  19. Murphy, D. M. (2005). "Review of the vapour pressures of ice and supercooled water for atmospheric applications". Quarterly Journal of the Royal Meteorological Society. 131 (608): 1539–1565. Bibcode:2005QJRMS.131.1539M. doi:10.1256/qj.04.94. S2CID 122365938.
  20. "SI base units". Bureau International des Poids et Mesures. Archived from the original on 16 July 2012. Retrieved 31 August 2012.
  21. "Information for users about the proposed revision of the SI" (PDF). Bureau International des Poids et Mesures. Archived from the original (PDF) on 21 January 2018. Retrieved 6 January 2019.
  22. Iglev, H.; Schmeisser, M.; Simeonidis, K.; Thaller, A.; Laubereau, A. (2006). "Ultrafast superheating and melting of bulk ice". Nature. 439 (7073): 183–186. Bibcode:2006Natur.439..183I. doi:10.1038/nature04415. PMID 16407948. S2CID 4404036.
  23. La Placa, S. J.; Hamilton, W. C.; Kamb, B.; Prakash, A. (1972). "On a nearly proton ordered structure for ice IX". Journal of Chemical Physics. 58 (2): 567–580. Bibcode:1973JChPh..58..567L. doi:10.1063/1.1679238.
  24. Klotz, S.; Besson, J. M.; Hamel, G.; Nelmes, R. J.; Loveday, J. S.; Marshall, W. G. (1999). "Metastable ice VII at low temperature and ambient pressure". Nature. 398 (6729): 681–684. Bibcode:1999Natur.398..681K. doi:10.1038/19480. S2CID 4382067.
  25. Dutch, Stephen. "Ice Structure". University of Wisconsin Green Bay. Archived from the original on 16 October 2016. Retrieved 12 July 2017.
  26. Salzmann, Christoph G.; Radaelli, Paolo G.; Hallbrucker, Andreas; Mayer, Erwin; Finney, John L. (24 March 2006). "The Preparation and Structures of Hydrogen Ordered Phases of Ice". Science. 311 (5768): 1758–1761. Bibcode:2006Sci...311.1758S. doi:10.1126/science.1123896. PMID 16556840. S2CID 44522271.
  27. Sanders, Laura (11 September 2009). "A Very Special Snowball". Science News. Archived from the original on 14 September 2009. Retrieved 11 September 2009.
  28. Militzer, Burkhard; Wilson, Hugh F. (2 November 2010). "New Phases of Water Ice Predicted at Megabar Pressures". Physical Review Letters. 105 (19): 195701. arXiv:1009.4722. Bibcode:2010PhRvL.105s5701M. doi:10.1103/PhysRevLett.105.195701. PMID 21231184. S2CID 15761164.
  29. MacMahon, J. M. (1970). "Ground-State Structures of Ice at High-Pressures". Physical Review B. 84 (22): 220104. arXiv:1106.1941. Bibcode:2011PhRvB..84v0104M. doi:10.1103/PhysRevB.84.220104. S2CID 117870442.
  30. Chang, Kenneth (9 December 2004). "Astronomers Contemplate Icy Volcanoes in Far Places". The New York Times. Archived from the original on 9 May 2015. Retrieved 30 July 2012.
  31. Zyga, Lisa (25 April 2013). "New phase of water could dominate the interiors of Uranus and Neptune". Phys.org.
  32. David, Carl (8 August 2016). "Verwiebe's '3-D' Ice phase diagram reworked". Chemistry Education Materials.
  33. Rosu-Finsen, Alexander; Davies, Michael B.; Amon, Alfred; Wu, Han; Sella, Andrea; Michaelides, Angelos; Salzmann, Christoph G. (3 February 2023). "Medium-density amorphous ice". Science. 379 (6631): 474–478. Bibcode:2023Sci...379..474R. doi:10.1126/science.abq2105. ISSN 0036-8075. PMID 36730416. S2CID 256504172.
  34. Murray, Benjamin J.; Bertram, Allan K. (2006). "Formation and stability of cubic ice in water droplets". Physical Chemistry Chemical Physics. 8 (1): 186–192. Bibcode:2006PCCP....8..186M. doi:10.1039/b513480c. hdl:2429/33770. PMID 16482260.
  35. Murray, Benjamin J. (2008). "The Enhanced formation of cubic ice in aqueous organic acid droplets". Environmental Research Letters. 3 (2): 025008. Bibcode:2008ERL.....3b5008M. doi:10.1088/1748-9326/3/2/025008.
  36. Murray, Benjamin J.; Knopf, Daniel A.; Bertram, Allan K. (2005). "The formation of cubic ice under conditions relevant to Earth's atmosphere". Nature. 434 (7030): 202–205. Bibcode:2005Natur.434..202M. doi:10.1038/nature03403. PMID 15758996. S2CID 4427815.
  37. Malkin, Tamsin L.; Murray, Benjamin J.; Salzmann, Christoph G.; Molinero, Valeria; Pickering, Steven J.; Whale, Thomas F. (2015). "Stacking disorder in ice I". Physical Chemistry Chemical Physics. 17 (1): 60–76. doi:10.1039/c4cp02893g. PMID 25380218.
  38. Salzmann, Christoph G.; Murray, Benjamin J. (June 2020). "Ice goes fully cubic". Nature Materials. 19 (6): 586–587. Bibcode:2020NatMa..19..586S. doi:10.1038/s41563-020-0696-6. PMID 32461682. S2CID 218913209.
  39. Chaplin, Martin (10 April 2012). "Ice-four (Ice IV)". Water Structure and Science. London South Bank University. Archived from the original on 12 August 2011. Retrieved 27 May 2022.
  40. Chaplin, Martin (10 April 2012). "Ice-five (Ice V)". Water Structure and Science. London South Bank University. Archived from the original on 12 October 2003. Retrieved 30 July 2012.
  41. Chaplin, Martin (10 April 2012). "Ice-six (Ice VI)". Water Structure and Science. London South Bank University. Archived from the original on 23 September 2012. Retrieved 30 July 2012.
  42. Grande, Zachary M.; et al. (2022). "Pressure-driven symmetry transitions in dense H2O ice". APS Physics. 105 (10): 104109. Bibcode:2022PhRvB.105j4109G. doi:10.1103/PhysRevB.105.104109. S2CID 247530544.
  43. Chaplin, Martin (10 April 2012). "Ice-seven (Ice VII)". Water Structure and Science. London South Bank University. Archived from the original on 2 November 2011. Retrieved 30 July 2012.
  44. Chaplin, Martin (17 February 2017). "Ice-eleven (ice XI)". Water Structure and Science. London South Bank University. Archived from the original on 23 March 2017. Retrieved 11 March 2017.
  45. Chaplin, Martin (10 April 2012). "Ice-twelve (Ice XII)". Water Structure and Science. London South Bank University. Archived from the original on 2 November 2011. Retrieved 30 July 2012.
  46. "Sandwiching water between graphene makes square ice crystals at room temperature". ZME Science. 27 March 2015. Retrieved 2 May 2018.
  47. Algara-Siller, G.; Lehtinen, O.; Wang, F. C.; Nair, R. R.; Kaiser, U.; Wu, H. A.; Geim, A. K.; Grigorieva, I. V. (26 March 2015). "Square ice in graphene nanocapillaries". Nature. 519 (7544): 443–445. arXiv:1412.7498. Bibcode:2015Natur.519..443A. doi:10.1038/nature14295. PMID 25810206. S2CID 4462633.
  48. del Rosso, Leonardo; Celli, Milva; Ulivi, Lorenzo (7 November 2016). "New porous water ice metastable at atmospheric pressure obtained by emptying a hydrogen-filled ice". Nature Communications. 7 (1): 13394. arXiv:1607.07617. Bibcode:2016NatCo...713394D. doi:10.1038/ncomms13394. PMC 5103070. PMID 27819265.
  49. Chaplin, Martin. "Ice-seventeen (Ice XVII)". Archived from the original on 11 September 2022. Retrieved 12 September 2022.{{cite web}}: CS1 maint: bot: original URL status unknown (link)
  50. Liu, Yuan; Huang, Yingying; Zhu, Chongqin; Li, Hui; Zhao, Jijun; Wang, Lu; Ojamäe, Lars; Francisco, Joseph S.; Zeng, Xiao Cheng (25 June 2019). "An ultralow-density porous ice with the largest internal cavity identified in the water phase diagram". Proceedings of the National Academy of Sciences. 116 (26): 12684–12691. Bibcode:2019PNAS..11612684L. doi:10.1073/pnas.1900739116. PMC 6600908. PMID 31182582.
  51. Rosenberg, Robert (2005). "Why Is Ice Slippery?". Physics Today. 58 (12): 50–54. Bibcode:2005PhT....58l..50R. doi:10.1063/1.2169444.
  52. Chang, Kenneth (21 February 2006). "Explaining Ice: The Answers Are Slippery". The New York Times. Archived from the original on 11 December 2008. Retrieved 8 April 2009.
  53. Makkonen, Lasse; Tikanmäki, Maria (June 2014). "Modeling the friction of ice". Cold Regions Science and Technology. 102: 84–93. Bibcode:2014CRST..102...84M. doi:10.1016/j.coldregions.2014.03.002.
  54. Canale, L. (4 September 2019). "Nanorheology of Interfacial Water during Ice Gliding". Physical Review X. 9 (4): 041025. arXiv:1907.01316. Bibcode:2019PhRvX...9d1025C. doi:10.1103/PhysRevX.9.041025.
  55. "WMO SEA-ICE NOMENCLATURE" Archived 5 June 2013 at the Wayback Machine (Multi-language Archived 14 April 2012 at the Wayback Machine) World Meteorological Organization / Arctic and Antarctic Research Institute. Retrieved 8 April 2012.
  56. Moore, Judith; Lamb, Barbara (2001). Crop Circles Revealed. Light Technology Publishing. p. 140. ISBN 978-1-62233-561-9.
  57. Petrenko, Victor F. and Whitworth, Robert W. (1999) Physics of ice. Oxford: Oxford University Press, pp. 27–29, ISBN 0191581348
  58. Eranti, E. and Lee, George C. (1986) Cold region structural engineering. New York: McGraw-Hill, p. 51, ISBN 0070370346.
  59. Dionne, J (November 1979). "Ice action in the lacustrine environment. A review with particular reference to subarctic Quebec, Canada". Earth-Science Reviews. 15 (3): 185–212. Bibcode:1979ESRv...15..185D. doi:10.1016/0012-8252(79)90082-5.
  60. "Sleet (glossary entry)". National Oceanic and Atmospheric Administration's National Weather Service. Archived from the original on 18 February 2007. Retrieved 20 March 2007.
  61. "Hail (glossary entry)". National Oceanic and Atmospheric Administration's National Weather Service. Archived from the original on 27 November 2007. Retrieved 20 March 2007.
  62. Alaska Air Flight Service Station (10 April 2007). "SA-METAR". Federal Aviation Administration via the Internet Wayback Machine. Archived from the original on 1 May 2008. Retrieved 29 August 2009.
  63. "What causes ice pellets (sleet)?". Weatherquestions.com. Archived from the original on 30 November 2007. Retrieved 8 December 2007.
  64. Glossary of Meteorology (2009). "Hail". American Meteorological Society. Archived from the original on 25 July 2010. Retrieved 15 July 2009.
  65. Jewell, Ryan; Brimelow, Julian (17 August 2004). "P9.5 Evaluation of an Alberta Hail Growth Model Using Severe Hail Proximity Soundings in the United States" (PDF). Archived (PDF) from the original on 7 May 2009. Retrieved 15 July 2009.
  66. National Severe Storms Laboratory (23 April 2007). "Aggregate hailstone". National Oceanic and Atmospheric Administration. Archived from the original on 10 August 2009. Retrieved 15 July 2009.
  67. Brimelow, Julian C.; Reuter, Gerhard W.; Poolman, Eugene R. (2002). "Modeling Maximum Hail Size in Alberta Thunderstorms". Weather and Forecasting. 17 (5): 1048–1062. Bibcode:2002WtFor..17.1048B. doi:10.1175/1520-0434(2002)017<1048:MMHSIA>2.0.CO;2.
  68. Marshall, Jacque (10 April 2000). "Hail Fact Sheet". University Corporation for Atmospheric Research. Archived from the original on 15 October 2009. Retrieved 15 July 2009.
  69. "Hail storms rock southern Qld". Australian Broadcasting Corporation. 19 October 2004. Archived from the original on 6 March 2010. Retrieved 15 July 2009.
  70. Bath, Michael; Degaura, Jimmy (1997). "Severe Thunderstorm Images of the Month Archives". Archived from the original on 13 July 2011. Retrieved 15 July 2009.
  71. Wolf, Pete (16 January 2003). "Meso-Analyst Severe Weather Guide". University Corporation for Atmospheric Research. Archived from the original on 20 March 2003. Retrieved 16 July 2009.
  72. Downing, Thomas E.; Olsthoorn, Alexander A.; Tol, Richard S. J. (1999). Climate, change and risk. Routledge. pp. 41–43. ISBN 978-0-415-17031-4.
  73. Mason, Basil John (1971). Physics of Clouds. Clarendon Press. ISBN 978-0-19-851603-3.
  74. Christner, Brent C.; Morris, Cindy E.; Foreman, Christine M.; Cai, Rongman; Sands, David C. (29 February 2008). "Ubiquity of Biological Ice Nucleators in Snowfall". Science. 319 (5867): 1214. Bibcode:2008Sci...319.1214C. CiteSeerX 10.1.1.714.4002. doi:10.1126/science.1149757. PMID 18309078. S2CID 39398426.
  75. Glossary of Meteorology (2009). "Cloud seeding". American Meteorological Society. Archived from the original on 15 March 2012. Retrieved 28 June 2009.
  76. Glossary of Meteorology (June 2000). "Diamond Dust". American Meteorological Society. Archived from the original on 3 April 2009. Retrieved 21 January 2010.
  77. Keitzl, Thomas; Mellado, Juan Pedro; Notz, Dirk (2016). "Impact of Thermally Driven Turbulence on the Bottom Melting of Ice". J. Phys. Oceanogr. 46 (4): 1171–1187. Bibcode:2016JPO....46.1171K. doi:10.1175/JPO-D-15-0126.1.
  78. Woods, Andrew W. (1992). "Melting and dissolving". J. Fluid Mech. 239: 429–448. Bibcode:1992JFM...239..429W. doi:10.1017/S0022112092004476. S2CID 122680287.
  79. Reynolds, Francis J., ed. (1921). "Ice" . Collier's New Encyclopedia. New York: P. F. Collier & Son Company.
  80. https://www.countrylife.co.uk/architecture/gwrych-castle-217018
  81. "Ice is money in China's coldest city". The Sydney Morning Herald. AFP. 13 November 2008. Archived from the original on 2 October 2009. Retrieved 26 December 2009.
  82. Weir, Caroline; Weir, Robin (2010). Ice Creams, Sorbets & Gelati:The Definitive Guide. p. 217.
  83. ASHRAE. "Ice Manufacture". 2006 ASHRAE Handbook: Refrigeration. Inch-Pound Edition. p. 34-1. ISBN 1-931862-86-9.
  84. Rydzewski, A.J. "Mechanical Refrigeration: Ice Making." Marks' Standard Handbook for Mechanical Engineers. 11th ed. McGraw Hill: New York. pp. 19–24. ISBN 978-0-07-142867-5.
  85. U.S. Census Bureau. "Ice manufacturing: 2002." Archived 22 July 2017 at the Wayback Machine 2002 Economic Census.
  86. Deuster, Patricia A.; Singh, Anita; Pelletier, Pierre A. (2007). The U.S. Navy Seal Guide to Fitness and Nutrition. Skyhorse Publishing Inc. p. 117. ISBN 978-1-60239-030-0.
  87. "Unique ice pier provides harbor for ships", Archived 23 February 2011 at Wikiwix Antarctic Sun. 8 January 2006; McMurdo Station, Antarctica.
  88. Makkonen, L. (1994) "Ice and Construction". E & FN Spon, London. ISBN 0-203-62726-1.
  89. Gold, L.W. (1993). "The Canadian Habbakuk Project: a Project of the National Research Council of Canada". International Glaciological Society. ISBN 0946417164.
  90. Talkington, Fiona (3 May 2005). "Terje Isungset Iceman Is Review". BBC Music. Archived from the original on 24 September 2013. Retrieved 24 May 2011.
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