AH1 - Magma Properties

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    Volcanology

    Key Reading

    Volcanoes(2ndEdition) (2004)

    P. Francis & C. Oppenheimer, Oxford Univ. Press, 521 p.

    Volcanoes: Global Perspectives(2010)

    J.P. Lockwood &. R.W. Hazlett, Wiley-Blackwell, 541 p.

    Le Volcanisme(1994)

    J.L. Bourdier, BRGM dition, Manuels et Mthodes n25, 420 p.

    Volcans, source de vie, cause de mor t(2003)

    C. Jaupart et al., 2003, Vuibert, 328 p.

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    Outline

    Basic definitions and concepts, classification

    Magma and Volcanic rock properties

    Melt properties I: goechemistry, SiO2 Melt properties II: temperature

    Vesicles, bubbles and control on viscosity

    Magma properties III: crystals

    After A. Harris et rfrences cites

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    So we need to consider the properties of:

    (1) Melt (chemistry, temperature)

    (2) Crystals

    (3) Volatiles, gas and bubbles (vesicles)

    Magma at depth is a mixture of:

    = Melt (liquid) + crystals (solids) + volatiles

    Magma (upon reaching the surface) is a mix of:

    = Melt (liquid) + crystals (solids) + bubbles

    Together these define the magma rheological (e.g., viscosity) &

    physical (e.g., density) properties

    Magma and Volcanic Rock Properties

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    Magma and Volcanic Rock Properties:

    Basic Definitions & Concepts

    (1) Magma:

    Molten rock containing volatiles + crystals;

    Volatiles will, however, exsolve at shallow depths to

    create bubbles (vesicles);

    The term is maintained as long as the molten rock

    remains below the Earths surface.

    (2) Lava and pyroclasts:

    The term lava (or pyroclast) is applied to molten rock thathas been erupted onto the Earths surface.

    Molten rock from which the volatiles have largely exsolved;

    Contains bubbles (otherwise termed vesicles in lava);

    Lava = effusive product; pyro-clast = explosive product

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    Melt Properties I, Chemistry:

    SiO2

    Term SiO2(wt%) (Note)

    Acid (felsic/salic) >63 (High silica)

    Intermediate 52-63 (Intermediate silica)

    Basic (mafic) 45-52 (Low silica)

    Ultrabasic

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    Felsic Rock Type: Properties

    End Member Type I : - FELSIC (or Salic / ACID):

    Magmas composed of minerals that melt (faire fondre)

    at the lowest temperatures.

    Felsic magma is K- and Na-rich, and contain plagioclase

    feldspars.

    While K- and Na-rich plagioclase feldspars are rich in

    aluminum (Al), feldspars and quartz are rich in silicon (Si).

    The presence of these elements give Felsic rocks a light(clair) color.

    The presence of the feldspar and silica gives rise to the

    name of these magmas: Felsic (fels for feldspar; sic for silica)

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    Mafic Rock Type: Properties

    End Member Type I I : - MAF IC (BASIC):

    Magmas composed of minerals that melt (faire fondre)

    at the highest temperatures.

    Mafic magma is Ca-rich, and contains olivine and

    pyroxene.

    Olivine and pyroxene are rich in iron (Fe) and/or

    magnesium (Mg).

    These elements give Mafic rocks a dark (fonce/sombre) color.

    The high Mg and Fe contents give rise to the name of these

    magmas: Mafic [ma for magnesium; fic for ferric (2+)

    iron].

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    Classification of MacDonald (1972):

    Table A2-2, Page 462

    Rhyolite

    Rhyo-

    dacite Dacite Trachyte Phonolite Andesite

    Tholeiitic

    Basalt Pyroxenite

    Alkalic

    Basalt Peridotite Serpentine Nephelinite Dunite

    SiO2 73.6 66.3 63.6 58.3 56.9 54.2 50.8 50.5 45.8 43.5 40.4 40.3 40.2

    TiO2 0.2 0.7 0.6 0.7 0.6 1.3 2.0 0.5 2.6 0.8 tr 2.9 0.2

    Al2O3 13.4 15.4 16.7 18.0 20.2 17.2 14.1 4.1 14.6 4.0 1.9 11.3 0.8

    Fe2O3 1.2 2.1 2.2 2.5 2.3 3.5 2.9 2.4 3.2 2.5 2.8 4.9 1.9

    FeO 0.8 2.2 3.0 2.0 1.8 5.5 9.1 7.4 8.7 9.8 4.3 7.7 11.9

    MgO 0.3 1.6 2.1 2.1 0.6 4.4 6.3 21.7 9.4 34.0 36.0 13.3 43.2MnO 0.3 0.1 0.1 0.1 0.2 0.1 0.2 0.1 0.2 0.2 - 0.2 0.2

    CaO 1.1 3.7 5.5 4.2 1.9 7.9 10.4 12.0 10.7 3.5 0.7 13.0 0.8

    Na2O 3.0 4.1 4.0 3.8 8.7 3.7 2.2 0.4 2.6 0.6 3.1 0.3

    K2O 5.4 3.0 1.4 7.4 5.4 1.1 0.8 0.2 1.0 0.2 0.2 1.4 0.1

    H2O+ 0.8 0.7 0.6 0.5 1.0 0.9 0.9 0.5 0.8 0.8 10.5 1.1 0.4

    P2O5 0.1 0.2 0.2 0.2 0.2 0.3 0.2 0.1 0.4 0.1 tr 0.8 0.1

    after Nockolds SR (1954): Average chemical compositions of some igneous rocks

    Geol Soc Am Bull, 65, 1007-1032.

    Name of volcanic rock with

    Characteristic (or case type) composition

    Place into 4 classes: Felsic, Intermediate, Mafic & Ultra-Basic

    Define the oxide amounts that define each class: are there anomalies?

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    Rhyolite Rhyodacite Dacite Trachyte

    SiO2 73.6 66.3 63.6 58.3

    TiO2 0.2 0.7 0.6 0.7Al2O3 13.4 15.4 16.7 18.0

    Fe2O3 1.2 2.1 2.2 2.5

    FeO 0.8 2.2 3.0 2.0

    MgO 0.3 1.6 2.1 2.1MnO 0.3 0.1 0.1 0.1

    CaO 1.1 3.7 5.5 4.2

    Na2O 3.0 4.1 4.0 3.8

    K2O 5.4 3.0 1.4 7.4

    Classification of MacDonald (1972):

    Acid-to-Intermediate (Felsic) End

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    Classification of MacDonald (1972):

    Intermediate-to-Basic (Mafic) End

    Andesite Tholeiite Pyroxenite Alkali

    Basalt Basalt

    SiO2 54.2 50.8 50.5 45.8

    TiO2 1.3 2.0 0.5 2.6Al2O3 17.2 14.1 4.1 14.6

    Fe2O3 3.5 2.9 2.4 3.2

    FeO 5.5 9.1 7.4 8.7

    MgO 4.4 6.3 21.7 9.4MnO 0.1 0.2 0.1 0.2

    CaO 7.9 10.4 12.0 10.7

    Na2O 3.7 2.2 0.4 2.6

    K2O 1.1 0.8 1.4 1.0

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    Classification of MacDonald (1972):

    Ultra-Basic (Ultra-Mafic) End

    Peridotite Serpentine Nephelinite Dunite

    SiO2 43.5 40.4 40.3 40.2

    TiO2 0.8 tr. 2.9 0.2Al2O3 4.0 1.9 11.3 0.8

    Fe2O3 2.5 2.8 4.9 1.9

    FeO 9.8 4.3 7.7 11.9

    MgO 34.0 36.0 13.3 43.2MnO 0.2 - 0.2 0.2

    CaO 3.5 0.7 13.0 0.8

    Na2O 0.6 3.1 0.3

    K2O 0.2 1.4 0.10.2

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    Al2O3Saturation Classes

    Peraluminous:

    Molecular Al2O3> (CaO + Na2O + K2O)

    Metaluminous:

    Molecular Al2O3< (CaO + Na2O + K2O)

    but

    Molecular Al2O3> (Na2O + K2O)

    Subaluminous:

    Molecular Al2O3~ (Na2O + K2O)

    Peralkaline:

    Molecular Al2O3< (Na2O + K2O)

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    Simple Chemical Classification for

    the Common Volcanic Rock Types

    Rock Type SiO2 Al2O3Saturation Class Class(wt%)

    Rhyolite >68 Peraluminous+Metaluminous Acid (silicic, salic)

    (FELSIC)

    Dacite 63-68 Peraluminous+Metaluminous

    Andesite 57-63 Metaluminous Intermediate

    Basalt

    Tholeiitic 52-57 Metaluminous-to-Subaluminous

    Hawaiite

    Alkali Basalt 45-52 Metaluminous-to-Subaluminous Basic

    (MAFIC)

    Leucite

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    Some physical properties of magma (or lava) related to differences

    in chemical composition. Basaltic lavas have lower SiO2contents,

    higher temperatures, and lower viscosity when compared to more

    evolved lavas such as dacites and rhyolites.

    Credit: J. Johnson, U.S. Geological Survey Photoglossary of Volcanic Terms.

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    Density

    The density of a magma is determined by its temperature, pressure, and

    composition. Increasing temperature causes magma to expand, which decreases its

    density, while increasing pressure causes magma to compress, which

    increases its density.

    The most important factor controlling magma density is composition.

    In particular iron, which is relatively abundant in basalts, has a highermass-to-radius ratio than elements like potassium and silicon, which

    are enriched in evolved magmas.

    The density of most magmas ranges from 2.2 to 3.1 g/cm3, with basalts

    being densest and rhyolites being least dense.

    Viscosity

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    Viscosity

    One of the most important physical properties of magma in terms of determining its

    behavior is its viscosity.

    Viscosity is a measure of resistance to flow, i.e. the thickness or stickiness of a liquid.

    A low-viscosity liquid is runny(water). A high-viscosity liquid is thicker and lessrunny(honey or caramel). The viscosity of a silicate liquid is determined by its

    composition.

    Viscosity is typically expressed in units of Pas (Pascal-seconds) or P (poises), where

    1 Pas = 10 P

    Silica (SiO2) in a melt tends to form an interconnectednetwork of ions, like a polymer. The more silica there

    is in a melt, the more developed the network becomes,

    giving the liquid a higher viscosity. Conversely,

    increasing the temperature of a melt has the effect of

    decreasing its viscosity.

    Because basaltic liquids are characterized by both

    higher temperatures and lower SiO2contents than

    rhyolitic liquids, basaltic liquids will also have lower

    viscosities.

    .

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    Viscosity, or the resistance of magma to flow when

    subjected to a force.

    Viscosity is measured in the units of Poise and there

    is a tremendous rangedisplayed by magmas erupted

    on Earth.

    In general, the viscosity of magma increases as the

    silica content increases from basalt to rhyolite.

    Magmatic viscosities are much larger than fluids that

    we are familiar with, such as water or olive oil.

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    A natural magma or lava is more complex than a pure silicate melt. A

    magma (or lava) is typically a mixture of melt and crystals. Thus, the

    viscosity of a magma also depends on the degree of crystallization.

    The greater the percentage of crystals, the higher the viscosity. We

    refer to this as the effective viscosity of the magma. The effectiveviscosity is related to the liquid viscosity by the relationship

    eff=0(11.35)2.5

    where heffis the effective viscosity, h0is the crystal-free liquid

    viscosity, andfis the fractional volume of crystals.

    Viscosity of silicate liquids plotted as a

    function of SiO2content and

    temperature.Note that magmas at lower temperature

    are more viscous than those at higher

    temperature for any given SiO2content. For a

    given temperature, the viscosity increases

    with SiO2content.

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    SiO2: Control on Viscosity

    Viscosity is a measure of the resistance of a fluid to flow

    Viscosity (h) increases logarithmically with SiO2

    Log(h)

    SiO2(wt%)

    1 Pa s

    1015Pa s

    50

    wt%

    70

    wt%

    Lava lakes (10-103Pa s)Lava flows (100105Pa s)

    Lava domes (>109pa s)

    Silicic lava flows (108-1010Pa s)

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    Density increases with decreased SiO2Why?

    McBirney (2007), Fig. 2.11

    Because:(i) silica is one of the lightest

    oxides, and

    (ii) silica is the most dominant

    oxide:

    density decreaseswith

    increasedSiO2

    Basaltis the most densemelt(least SiO2).

    Rhyoliteis the least densemelt

    (most SiO2).

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    Melt Properties II, Temperature

    Melt temperature varies with composition

    Generally, the lower the SiO2content, the higher the melt T

    (Plus le taux de silice est bas plus la temprature est leve)

    Rock Type Temperature (C)

    Rhyolite 700900

    Dacite 8001100

    Andesite 9501200

    Basalt 10001200

    From Cas & Wright (1987)

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    Location Date Temp, C Technique (source)

    Santiaguito 1940 725 Pyrometer (1)Santiaguito 1990 850 Chemistry (2)

    Etna 1043-1111 Chemistry (3)

    Etna 2001 1074 Radiometer

    Etna 1975 1070-90 Thermocouple (4)Etna 1991-93 1080 Thermocouple (5)

    Mauna Loa 1984 1143 Thermocouple (6)

    Stromboli 1901 1150 Thermocouple (7)

    Kilauea 1999 1150 Thermocouple (h)

    Erta Ale 1970 1175 Thermocouple (8)

    Vesuvius 1913 1200 Thermocouple (7)

    Mauna Loa 1859 1205 Chemistry (9)

    (1) Zies (1941); (2) Scaillet et al. (1998); (3) Pompilio et al. (1998); (4) Pinkerton & Sparks (1976); (5) Calvari et

    al. (1994); (6) Lipman and Banks (1987); (7) from Table 4.2 of MacDonald (1972); (8) Le Guern et al. (1979); (9)Riker et al. (2009); (h) field-measurement.

    Some Lava Interior (Eruption) Temperatures

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    Blue glassy (p-type) pahoehoe lobe, Kilauea

    ~50 cm

    Lava Surface Temperature

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    The surface temperature of the lava is always less than that of

    the interior

    Tinterior= Terupt= 1150 C

    Active pahoehoe lobe, Kilauea, 1999

    900-950 C

    750-850 C

    Lava Interior versus Surface Temperature

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    Temperature: Control on Viscosity

    Viscosity is a measure of the resistance of a fluid to flow

    Viscosity (h) increases logarithmically as Temperature decreases

    Log(h)

    Temperature (C)

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    The large range of magmatic viscosities is related to differences in the structure of

    magmas at the molecular level, which varies as a function of silica content.

    Magmas are fluids but they possess structure in the form of silicon-oxygen building

    blocks, that are linked together to form tetrahedra.

    Magmas that are rich in silicon form many linked tetrahedra that result in the

    polymerization of the liquids. The bonds that form between shared oxygen atoms are

    strong, thus giving the liquid strength and high viscosity.

    Lower silica magmas have higher contents of anions such as Ca, Mg and Fe that form

    weaker bonds and inhibit the development of strongly linked silicon tetrahedron. Thereforelow-silica magmas have a lower viscosity.

    Structure of silicon tetrahedron (A and B)

    and the linkage of two tetrahedron by

    sharing an oxygen (C)

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    Viscosity

    increases with

    SiO2

    From Oppenheimer (2003)

    Viscosity Relations and Data

    Viscosity

    decreases with

    increased temperature

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    Vesicle Shapes: Rounded

    No shearing; bubbles can grow in all directions

    ~2 cm

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    Vesicle Shapes: Sheared

    Shearing, so bubbles are deformed, stretched and elongated

    X500 50mm 10 mm

    in the conduit in a lava flow

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    Highly Vesicular Lava: Surface

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    Vesicle Volume Fractions

    For Lava

    Location Range (%) Mean (%) Notes (Study)

    Etna 442 20 'a'a-dominated (1)

    Etna 771 32 'a'a-dominated (2)

    Kilauea 1070 4060 pahoehoe-dominated (3,4)

    Kilauea 4294 70 at-vent (1997 overflows)

    (1) Herd & Pinkerton (1997); (2) Gaonach et al. (1996);

    (3) Wilmoth & Walker (1993); Cashman et al. (1994).

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    For round bubbles: Viscosity (h) increases with number of bubbles

    For sheared bubbles: Viscosity (h) decreases with number of bubbles

    h

    Bubble Content

    Power Law

    (Einstein-Roscoe Relation)

    Round bubbles

    Sheared bubbles

    Bubbles: Control on Viscosity

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    Magma Properties III: CrystalsLavas and pyroclasts usually contain a mixture of

    glass, phenocrysts, microphenocrysts and bubbles

    Phenocrysts: >100-200 m

    microphenocrysts: 30-200 m

    microlites:

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    Crystals and Temperature

    As temperature decreases

    the relative proportions ofmelt and crystals changes

    Crystal content also

    depends on cooling rate:

    (1) Slow cooling:

    Phenocrysts

    (2) Fast Cooling:

    Micro-phenocrysts

    (3) Very Fast Cooling

    Microlites

    (4) Quenching:

    Glass

    McBirney (2007), Fig. 3.2, page 76Proportions of crystals and liquid for a basalt

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    Kilauea lava cooled to 1170 C, then quenched:

    Olivine phenocrysts + pyroxene microphenocrysts + melt (glass)

    Crystal-Glass Mix in a Cooling Lava

    (i) 1170 C

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    Kilauea lava cooled to 1130 C, then quenched:

    Olivine phenocrysts + larger pyroxene microphenocrysts

    Crystal-Glass Mix in a Cooling Lava

    (ii) 1130 C

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    Kilauea lava cooled to 1020 C, 80 % crystals:

    Small pools of Fe-poor, SiO2-rich liquid remain in a crystal mush

    Crystal-Glass Mix in a Cooling Lava

    (iii) 1020 C

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    Kilauea lava below 990 C:

    Rock is almost totally crystalline

    Crystal-Glass Mix in a Cooling Lava

    (iv) 990 C

    C l C l Vi i

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    Crystals: Control on Viscosity

    Mixture viscosity increases with crystal content

    Power Law (Einstein-Roscoe Relation)

    h

    Crystal Content (f)

    h0

    h= h0 (1 - 1.67 f)-2.5

    Offset

    viscosity of the liquid

    viscosity of the mixture