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UPSC Mains Answer PYQ 2022: Geology Paper 2 (Section- A) | Geology Optional Notes for UPSC PDF Download

How are Miller Indices of a crystal face calculated ? Calculate Miller Indices of following two crystal faces : (i)    A face intersects all three crystallographic axes at 3-unit distance. (ii)    A face intersects a-axis at 4-unit distance and is parallel to b and c axes.
Ans:

Introduction:

Miller Indices are a set of notation used to describe the orientation of crystallographic planes or faces within a crystal lattice. They are essential in crystallography and materials science for identifying and characterizing different crystallographic facets. The Miller Indices system was developed by the British mineralogist William Hallowes Miller in the 19th century.

Miller Indices are represented as (hkl), where h, k, and l are integers that represent the reciprocals of the intercepts of the plane with the crystallographic axes a, b, and c. The steps to calculate Miller Indices are as follows:

Calculating Miller Indices:

  1. Intercept Method:

    • Determine the intercepts of the plane with the three crystallographic axes (a, b, and c).
    • Take the reciprocals of these intercepts and simplify the ratios to the smallest integers.
    • Enclose the resulting indices in parentheses (hkl).
  2. Example (i): A face intersects all three crystallographic axes at 3-unit distance.

    • In this case, the plane intersects all axes at 3 units, so the Miller Indices are (111).
  3. Example (ii): A face intersects a-axis at 4-unit distance and is parallel to b and c axes.

    • The plane is parallel to the b and c axes, so their intercepts are infinity (represented as 0).
    • The intercept along the a-axis is 4.
    • Therefore, the Miller Indices are (400).

Conclusion:

Miller Indices are a vital tool for crystallographers to describe and communicate the orientation of crystallographic planes within a crystal structure. They provide a concise and standardized way to represent these orientations, making it easier to study and understand the properties and behavior of crystalline materials.

Examples:

  1. Diamond Crystal Structure: In a diamond crystal, the (111) plane represents the top face of the tetrahedral unit cell. It has a close-packed arrangement of carbon atoms and plays a significant role in diamond's exceptional hardness.

  2. Calcite Crystal Structure: In the calcite crystal structure, the (104) plane represents one of the cleavage planes. When calcite crystals are cleaved along this plane, they break into rhombohedron-shaped pieces. The Miller Indices (104) help identify this cleavage plane.

Geological Significance:

Geologists use Miller Indices to study the crystallographic properties of minerals and rocks. For instance, understanding the orientation of mineral cleavage planes can provide insights into the ease of splitting rocks along specific directions, which has implications for quarrying and geological engineering.

In summary, Miller Indices are a fundamental concept in crystallography and materials science, providing a standardized notation system for describing crystallographic planes within a crystal lattice. They are essential for understanding the properties and behavior of crystalline materials and have practical applications in various fields, including geology and materials engineering.

Explain the phenomena of solid solution and exsolution in minerals.
Ans:

Introduction:

Solid solution and exsolution are two important phenomena in mineralogy that describe the composition and structure of minerals. Understanding these processes is crucial for geologists and materials scientists as they shed light on the formation, properties, and behavior of minerals within Earth's crust. This explanation will delve into the concepts of solid solution and exsolution, differentiating between them and providing examples to illustrate their significance.

Solid Solution:

Solid solution refers to the homogeneous blending of two or more chemical elements within a mineral's crystal structure. It occurs when ions or atoms of similar size and charge substitute for one another without altering the overall crystal lattice. Key points about solid solution:

  1. Substitution of Elements: Solid solution happens when ions or atoms of different elements substitute for each other in the crystal structure. These substitutions maintain the mineral's crystal symmetry.

  2. Complete vs. Partial Solid Solution: Solid solution can be complete, where one element fully substitutes another, or partial, where only a fraction of the ions are replaced. The degree of solid solution depends on factors like temperature, pressure, and the size and charge of ions.

  3. Examples:

    • Olivine, a common mineral in the Earth's mantle, shows solid solution between the iron-magnesium end-members (forsterite and fayalite).
    • The mineral plagioclase feldspar exhibits solid solution between sodium-rich albite and calcium-rich anorthite.

Exsolution:

Exsolution is the opposite of solid solution. It occurs when a previously homogeneous mineral, typically as a result of changes in temperature or pressure, undergoes phase separation, leading to the formation of distinct, often lamellar, phases within the mineral. Key points about exsolution:

  1. Phase Separation: Exsolution occurs when a mineral phase that was initially homogenous separates into two or more distinct phases. These phases may have different compositions.

  2. Lamellar Structures: In many cases, exsolution results in the formation of lamellar (layered) structures within the mineral. These layers are composed of different phases and often exhibit distinctive optical properties.

  3. Examples:

    • The mineral feldspar often undergoes exsolution, forming lamellar structures. In alkali feldspar, the phases of potassium feldspar (K-feldspar) and sodium feldspar (Na-feldspar) can exsolve from a homogeneous phase.
    • Exsolution of iron-titanium oxides (ilmenite and hematite) can occur in the mineral pyroxene, creating distinctive lamellar patterns called exsolution lamellae.

Conclusion:

Solid solution and exsolution are essential concepts in mineralogy, influencing the composition, structure, and properties of minerals. Understanding these phenomena helps geologists interpret the conditions under which minerals formed and provides insights into their behavior when subjected to geological processes. Solid solution maintains homogeneity, while exsolution leads to the separation of phases, often resulting in unique visual patterns within minerals. These concepts are fundamental for the study of Earth's geology and materials science.

Describe with suitable sketches ‘intergranular’ and ‘sub-ophitic’ textures. How do you explain presence of both these textures in a mafic rock ?
Ans:
Introduction:

In the field of geology, the texture of a rock refers to the size, shape, and arrangement of mineral grains or crystals within it. Two common textures found in igneous rocks, such as mafic rocks, are intergranular and sub-ophitic textures. In this explanation, we will describe these textures with suitable sketches, explain their presence in mafic rocks, and provide examples to illustrate these concepts.

Intergranular Texture:

Intergranular texture is characterized by mineral grains that do not touch or partially touch each other within a rock. There are open spaces or voids between the mineral grains, allowing for the presence of interstitial material. This texture is often associated with slower cooling rates during the formation of the rock.

Sub-ophitic Texture:

Sub-ophitic texture is a finer-grained variation of the ophitic texture. In this texture, larger mineral grains (usually pyroxenes or amphiboles) called phenocrysts are surrounded by smaller, closely packed mineral grains called groundmass. The term "sub-ophitic" indicates that the groundmass grains are not as well-formed or closely packed as in a true ophitic texture.

Presence of Both Textures in Mafic Rocks:

Mafic rocks are primarily composed of dark-colored minerals such as pyroxenes, amphiboles, and sometimes olivine. The presence of both intergranular and sub-ophitic textures in mafic rocks can be explained by their cooling history and the crystallization process. Here's how:

  1. Cooling Rate: Mafic rocks, which are rich in iron and magnesium, often solidify from molten magma at relatively high temperatures. The rate of cooling influences the texture:

    • Intergranular Texture: Slower cooling rates, as found in larger magma bodies or when magma ascends slowly to the Earth's surface, can result in intergranular textures. The minerals have more time to grow, and there are spaces between them.
    • Sub-ophitic Texture: Faster cooling rates, as in smaller intrusions or when magma cools rapidly upon reaching the surface, favor the formation of sub-ophitic textures. In this case, the minerals crystallize quickly and may not have enough time to grow as large as in intergranular textures.
  2. Mineral Composition: Mafic rocks contain minerals like pyroxenes and amphiboles, which can exhibit both intergranular and sub-ophitic textures depending on cooling conditions. For example, pyroxenes may form larger, distinct grains (intergranular) or smaller, finer grains (sub-ophitic) based on cooling rates.

Examples:

  1. Basalt: Basalt, a common mafic rock, often exhibits a sub-ophitic texture with small, densely packed mineral grains surrounding larger phenocrysts of pyroxene or olivine. In some cases, slower-cooling basalts in larger magma chambers may show intergranular texture.

  2. Gabbro: Gabbro, another mafic rock, typically displays an intergranular texture due to slower cooling within plutonic intrusions beneath the Earth's surface. However, variations in cooling rates can lead to sub-ophitic patches within a gabbroic rock.

Conclusion:

Intergranular and sub-ophitic textures are important features in mafic rocks, reflecting the cooling history and mineral composition of the rocks. Their presence provides valuable information about the conditions under which these rocks formed and solidified. Understanding these textures aids geologists in interpreting the geological history of rock formations.

How do increasing pressure and temperature either singularly or jointly, metamorphose a rock ?
Ans:
Introduction:

Metamorphism is a geological process that involves the transformation of pre-existing rocks (protoliths) into new rocks, typically under the influence of increased temperature and pressure. The combination of these two factors, either singly or jointly, can bring about significant changes in the mineral composition, texture, and overall character of a rock. In this explanation, we will explore how increasing pressure and temperature affect rocks, individually and together, and provide examples to illustrate these processes.

Effects of Increasing Pressure on Rocks:

  1. Recrystallization: As pressure increases, minerals in a rock can undergo recrystallization, which means the minerals' crystal structures change without changing their chemical composition. This can lead to the development of more compact and stable minerals.

  2. Texture Changes: High-pressure conditions can cause changes in the texture of a rock. For example, grains may become more closely packed, resulting in a denser, finer-grained rock.

  3. Phase Changes: Under high pressure, certain minerals may undergo phase changes, converting from one mineral phase to another stable phase. For instance, the high-pressure form of quartz (coesite) can form from ordinary quartz under extreme pressure conditions.

Effects of Increasing Temperature on Rocks:

  1. Recrystallization and Growth: Increasing temperature allows mineral grains in a rock to grow larger as atoms or ions migrate within the crystal lattice. This recrystallization often leads to the development of larger, well-formed crystals.

  2. Texture Changes: Higher temperatures can cause minerals to become more equidimensional, resulting in coarser-grained textures. Rocks may transition from fine-grained to coarse-grained as temperature increases.

  3. Chemical Reactions: Elevated temperatures can facilitate chemical reactions between minerals, leading to the formation of new minerals. For example, the alteration of feldspars into micas is common during metamorphism due to temperature-driven reactions.

Effects of Increasing Pressure and Temperature Together (Metamorphism):

  1. Regional Metamorphism: When rocks experience both increased pressure and temperature over large areas, it results in regional metamorphism. This process typically occurs in the Earth's crust during tectonic events like mountain building. Examples include the transformation of shale into slate, then phyllite, and finally schist as pressure and temperature increase.

  2. Contact Metamorphism: Contact metamorphism occurs when rocks are heated by the intrusion of molten magma (igneous intrusions). In this case, the increase in temperature is the dominant factor, causing changes primarily in the rocks adjacent to the intrusion. For example, limestone can metamorphose into marble in the presence of high-temperature fluids from magma.

Examples:

  1. Slate Formation: Under moderate pressure and temperature conditions, shale can transform into slate. The increased pressure causes recrystallization and the alignment of minerals, resulting in a foliated texture.

  2. Marble Formation: Limestone, a sedimentary rock, can metamorphose into marble when subjected to high temperatures and moderate pressure. The calcite in limestone recrystallizes into larger, interlocking grains of calcite in marble.

Conclusion:

The transformation of rocks under increasing pressure and temperature, either singularly or jointly, is a fundamental aspect of metamorphism in geology. These processes can lead to the development of new minerals, changes in texture, and the formation of distinct rock types. Understanding the effects of pressure and temperature on rocks is essential for interpreting geological history, understanding rock formation, and predicting the behavior of Earth's crust under various conditions.

Describe the classification of sandstones on the basis of their composition and matrix.
Ans:

Introduction:

Sandstone is a sedimentary rock primarily composed of sand-sized mineral, rock, or organic particles that are cemented together. These rocks can vary significantly in composition and appearance, and geologists classify sandstones based on their composition and the nature of the matrix material. This classification provides valuable insights into the origin and characteristics of these rocks. In this explanation, we will describe the classification of sandstones based on composition and matrix, providing examples to illustrate each category.

Classification of Sandstones by Composition:

  1. Quartz Arenite (Orthoquartzite):

    • Composition: More than 90% of the grains are quartz. Minimal amounts of feldspar, rock fragments, and other minerals.
    • Appearance: Generally light-colored and homogeneous.
    • Example: White Sands in New Mexico is composed mainly of pure quartz sand.
  2. Lithic Arenite:

    • Composition: Composed primarily of lithic fragments (rock fragments) such as shale, granite, or basalt, along with some quartz and feldspar grains.
    • Appearance: Varied in color and texture, depending on the nature of the lithic fragments.
    • Example: Greywacke, which contains a mix of lithic fragments and mineral grains.
  3. Arkose:

    • Composition: Rich in feldspar grains (more than 25%) with quartz, rock fragments, and other minerals.
    • Appearance: Often pink or red due to the presence of feldspar. The texture can range from fine- to coarse-grained.
    • Example: Fountain Formation in Colorado is an example of arkose.

Classification of Sandstones by Matrix:

  1. Silica Cemented Sandstone:

    • Matrix: The grains are cemented together by silica minerals, mainly quartz.
    • Appearance: Typically hard, well-consolidated, and resistant to weathering.
    • Example: Many quartz arenites fall into this category.
  2. Calcareous Cemented Sandstone (Calcarenite):

    • Matrix: The cementing material is predominantly calcium carbonate (calcite). May contain shells or shell fragments.
    • Appearance: Often light-colored and may effervesce (fizz) when exposed to dilute hydrochloric acid (HCl).
    • Example: Coquina is a type of calcareous sandstone composed of shell fragments.
  3. Iron Oxide Cemented Sandstone (Ferrarenite):

    • Matrix: The cementing material is iron oxide minerals, typically hematite or goethite.
    • Appearance: Red or brown in color due to the presence of iron oxides.
    • Example: Navajo Sandstone in the southwestern United States is often iron oxide cemented.

Conclusion:

The classification of sandstones based on composition and matrix provides a systematic way to categorize these sedimentary rocks. It helps geologists understand the origin, depositional environment, and characteristics of different sandstone types. Examples of each category illustrate the diversity of sandstones found in geological formations worldwide. This classification is essential for both geological research and practical applications in fields such as construction and hydrocarbon exploration.

Describe the crystallographic, physical, optical and chemical properties of garnet group of minerals. Give examples of rocks in which each species of garnet occurs as an essential mineral.
Ans:
Introduction:

The garnet group of minerals is a diverse family of silicate minerals with a wide range of crystallographic, physical, optical, and chemical properties. These minerals are commonly found in a variety of rock types and have both industrial and geological significance. In this explanation, we will describe the key properties of the garnet group and provide examples of rocks in which each species of garnet occurs as an essential mineral.

Crystallographic Properties:

  1. Crystal System: Garnets belong to the isometric (cubic) crystal system, characterized by three mutually perpendicular axes of equal length.
  2. Hardness: Garnets are relatively hard minerals with a hardness ranging from 6.5 to 7.5 on the Mohs scale.
  3. Cleavage: Garnets typically lack cleavage, which means they do not break along specific planes but instead fracture irregularly.
  4. Fracture: They exhibit conchoidal to uneven fracture patterns.

Physical Properties:

  1. Color: Garnets occur in a wide range of colors, including red, brown, green, yellow, orange, and even black. The most well-known garnet color is deep red, but this can vary due to different elements substituting in the crystal lattice.
  2. Luster: Garnets have a vitreous (glassy) luster.
  3. Transparency: They can be transparent to opaque, depending on the type and quality of the garnet.
  4. Specific Gravity: Garnets have a specific gravity that typically ranges from 3.5 to 4.3.

Optical Properties:

  1. Refractive Index (RI): The refractive index of garnets ranges from approximately 1.72 to 1.94, making them highly dispersive and responsible for their striking brilliance.
  2. Birefringence: Garnets are isotropic minerals, which means they do not exhibit birefringence under polarized light.
  3. Pleochroism: Some garnet varieties can show weak to moderate pleochroism, where the color changes when viewed from different angles.

Chemical Properties:

  1. Chemical Composition: The general formula for garnets is A3B2(SiO4)3, where A represents divalent cations (e.g., calcium, magnesium, ferrous iron) and B represents trivalent cations (e.g., aluminum, iron, chromium).
  2. Solid Solution: Garnets often form solid solutions, where different elements can substitute into the crystal structure, leading to a wide range of garnet species and varieties.
  3. Mineral Associations: Garnets are commonly associated with other minerals such as mica, feldspar, quartz, and amphiboles in a variety of rock types.

Examples of Garnet Species in Rocks:

  1. Almandine: Almandine garnet, known for its deep red color, occurs in metamorphic rocks like schist and gneiss. It is often associated with minerals like biotite and quartz.

  2. Pyrope: Pyrope garnet, which ranges from red to purplish-red, is commonly found in kimberlite pipes, which are sources of diamonds. It can also occur in serpentinite and eclogite.

  3. Spessartine: Spessartine garnet, with an orange to reddish-brown color, is associated with manganese-rich rocks and occurs in pegmatites, schists, and skarns.

  4. Grossular: Grossular garnet comes in various colors, including green, brown, and yellow. It is found in metamorphic rocks like marble and skarns. Green grossular is known as tsavorite.

Conclusion:

The garnet group of minerals exhibits a wide range of crystallographic, physical, optical, and chemical properties. These properties, along with their various species and colors, make garnets valuable both geologically and commercially. They are commonly found in a variety of rock types and provide insights into the geological history and processes of their host rocks.

What are symmetry elements present in normal class of orthorhombic system ? Show the stereographic projection of a crystal face (hkl) for normal class of orthorhombic system. Write down Hermann-Mauguin notations of all classes of orthorhombic system. 
Ans:Introduction:

The orthorhombic crystal system is one of the seven crystal systems in crystallography. It is characterized by three mutually perpendicular axes of different lengths (a, b, c) and right angles between them. In the normal class of the orthorhombic system, the crystal possesses certain symmetry elements that define its structure. These symmetry elements are crucial for understanding the crystal's properties and behavior. Additionally, the Hermann-Mauguin notations describe the symmetry elements and operations for all classes of the orthorhombic system.

Symmetry Elements in the Normal Class of Orthorhombic System:

In the normal class of the orthorhombic system, the following symmetry elements are present:

  1. Three Perpendicular 2-Fold Rotation Axes (C2): These axes pass through the center of each face of the unit cell, parallel to the crystallographic axes a, b, and c. They indicate a 180-degree rotation.

  2. Center of Symmetry (i): This symmetry element is located at the center of the unit cell and represents an inversion operation. It is absent in many other classes of the orthorhombic system.

Stereographic Projection of a Crystal Face (hkl) for the Normal Class of Orthorhombic System:

To draw a stereographic projection of a crystal face (hkl) in the orthorhombic system, you can follow these steps:

  1. Determine the Miller indices (hkl) of the crystal face.

  2. Find the reciprocal lattice vectors for the given face using the formula:
    bash Copy code
    1/d(hkl) = h/a* + k/b* + l/c*
    Here, a*, b*, and c* are the reciprocal lattice parameters.
  3. Plot the reciprocal lattice points corresponding to the face (hkl) on a stereographic projection sphere. These points will lie on the intersections of circles representing the reciprocal lattice planes.

  4. Connect the reciprocal lattice points with lines to outline the projection of the crystal face (hkl) on the stereographic projection.

Hermann-Mauguin Notations for All Classes of Orthorhombic System:

The Hermann-Mauguin notations describe the symmetry elements and operations for all classes of the orthorhombic system. There are four classes in the orthorhombic system, each represented by a unique notation:

  1. Class mm2 (222): This class has two perpendicular mirror planes and a 2-fold rotation axis perpendicular to both mirror planes.

  2. Class mmm (mmm): This class has three mutually perpendicular mirror planes.

  3. Class 222 (mm2): This class has three mutually perpendicular 2-fold rotation axes.

  4. Class 2/m2/m2/m (mmm2): This class has three mutually perpendicular mirror planes and three perpendicular 2-fold rotation axes.

Conclusion:

The normal class of the orthorhombic system exhibits specific symmetry elements, including perpendicular 2-fold rotation axes and a center of symmetry. Stereographic projections are essential tools for visualizing crystal faces, and Hermann-Mauguin notations provide a concise way to describe the symmetry of crystals in the orthorhombic system. These elements and notations are fundamental in crystallography for the characterization and study of orthorhombic crystals.

Why does an anisotropic mineral, viewed under crossed polars, suffer four times of complete extinction during a 360° rotation of microscope stage ? What is pleochroism and how is it determined?
Ans:

Introduction:

In optical mineralogy, anisotropic minerals are those that exhibit different optical properties in different crystallographic directions. When viewed under crossed polarized light, these minerals undergo four times of complete extinction during a 360° rotation of the microscope stage. This phenomenon is due to the mineral's anisotropic nature, which causes changes in the orientation of its optical properties as it is rotated. Additionally, pleochroism is a property of some anisotropic minerals that causes them to absorb different colors of light when viewed along different crystallographic directions. In this explanation, we will explore why anisotropic minerals experience four times of extinction and discuss pleochroism and its determination.

Four Times of Complete Extinction in Anisotropic Minerals:

  1. Uniaxial vs. Biaxial Minerals: Anisotropic minerals can be classified as uniaxial or biaxial based on the number of optic axes they possess. Uniaxial minerals have one optic axis (also known as the c-axis), while biaxial minerals have two optic axes (a- and b-axes).

  2. Rotation of Optic Axes: When an anisotropic mineral is placed between crossed polarizers and the microscope stage is rotated, the mineral's optic axis or axes change their orientation relative to the polarized light.

  3. Complete Extinction: Complete extinction occurs when the optic axis of a uniaxial mineral or one of the optic axes of a biaxial mineral aligns parallel to one of the polarizers (i.e., when it is perpendicular to the other polarizer). At this point, the mineral becomes dark and exhibits no birefringence.

  4. Four Extinction Positions: Anisotropic minerals have four extinction positions during a 360° rotation because they have two optic axes, and each optic axis can align with one of the polarizers to cause extinction. Therefore, they undergo complete extinction four times during a full rotation.

Pleochroism and Its Determination:

Pleochroism is the property of some anisotropic minerals to exhibit different colors when viewed along different crystallographic directions. It occurs due to variations in the absorption of light by mineral grains.

Determination of Pleochroism:

  1. Sample Preparation: To determine pleochroism, a thin section of the mineral is prepared, which involves slicing the mineral into very thin sections and mounting them on glass slides.

  2. Microscope Observation: The thin section is placed under a petrographic microscope with crossed polarizers. When the mineral is rotated, the observer can notice changes in color as the mineral's optic axes align differently with the polarized light.

  3. Comparison: The colors observed are compared as the mineral is rotated. Typically, minerals with pleochroism exhibit different colors when viewed parallel to the crystallographic axes, and these colors change as the stage is rotated.

  4. Documentation: The colors observed, along with their orientation relative to crystallographic axes, are documented. This information is valuable for mineral identification and characterization.

Examples:

  1. Mineral with Pleochroism: Augite, a common pyroxene mineral, exhibits pleochroism. When viewed along different crystallographic directions, it may appear green, brown, or yellow.

  2. Mineral with Four Extinction Positions: Hypersthene, a pyroxene mineral, has two optic axes, leading to four extinction positions during a 360° rotation when viewed under crossed polarized light.

Conclusion:

Anisotropic minerals exhibit four times of complete extinction during a 360° rotation due to their optical properties and the changing orientation of their optic axes. Pleochroism, the phenomenon of displaying different colors when viewed along different crystallographic directions, is determined by observing these color changes under a microscope. Understanding these optical properties is crucial in mineral identification and the study of mineral behavior under polarized light.

What are different types of metamorphism and what are their controlling factors ? State characteristic mineral assemblages which appear under different facies during regional metamorphism of pelitic rocks.
Ans:

Introduction:

Metamorphism is a geological process that involves the alteration of rocks due to changes in temperature, pressure, and fluid composition. There are different types of metamorphism, each with its controlling factors and characteristic mineral assemblages. One common type is regional metamorphism, which occurs over large areas and is associated with tectonic plate interactions. In regional metamorphism of pelitic rocks (rich in clay minerals), specific mineral assemblages called metamorphic facies are observed, and these facies reflect the temperature and pressure conditions at depth. In this explanation, we will discuss the different types of metamorphism and their controlling factors, followed by the characteristic mineral assemblages in pelitic rocks during regional metamorphism.

Different Types of Metamorphism:

  1. Regional Metamorphism:

    • Controlling Factors: High pressure and temperature conditions over large areas, typically associated with tectonic plate convergence.
    • Examples: Formation of schist and gneiss in mountain-building regions.
  2. Contact Metamorphism:

    • Controlling Factors: High temperature but relatively low pressure due to the intrusion of molten magma into country rocks.
    • Examples: Formation of hornfels around igneous intrusions.
  3. Dynamic Metamorphism:

    • Controlling Factors: High pressure associated with fault zones, often accompanied by shearing and deformation.
    • Examples: Formation of mylonites along fault zones.
  4. Hydrothermal Metamorphism:

    • Controlling Factors: Elevated temperature and pressure due to hot, chemically active fluids circulating through rocks.
    • Examples: Formation of ore deposits in hydrothermal veins.

Characteristic Mineral Assemblages in Regional Metamorphism of Pelitic Rocks:

Pelitic rocks, which are rich in clay minerals, undergo a series of mineral transformations during regional metamorphism. These transformations are grouped into metamorphic facies, each associated with specific temperature and pressure conditions:

  1. Zeolite Facies:

    • Conditions: Low to moderate temperature and low pressure.
    • Mineral Assemblage: Chlorite, albite, quartz, and sometimes zeolites. No new minerals are formed.
  2. Blueschist Facies:

    • Conditions: Low temperature and high pressure.
    • Mineral Assemblage: Glauconite, lawsonite, and blue amphiboles (e.g., glaucophane). These minerals are indicators of high-pressure, low-temperature conditions.
  3. Greenschist Facies:

    • Conditions: Moderate temperature and pressure.
    • Mineral Assemblage: Chlorite, albite, epidote, and actinolite. These minerals are characteristic of greenschist facies and indicate moderate metamorphic conditions.
  4. Amphibolite Facies:

    • Conditions: High temperature and moderate pressure.
    • Mineral Assemblage: Hornblende, plagioclase feldspar, biotite, and garnet. Formation of garnet is a key indicator of the amphibolite facies.
  5. Granulite Facies:

    • Conditions: Very high temperature and moderate to high pressure.
    • Mineral Assemblage: Orthopyroxene, garnet, and plagioclase feldspar. These rocks have undergone high-grade metamorphism.

Conclusion:

Metamorphism occurs in various forms, each driven by different temperature, pressure, and geological conditions. Regional metamorphism of pelitic rocks results in the development of distinct metamorphic facies, characterized by specific mineral assemblages that reflect the depth and temperature conditions during their formation. Understanding these facies is essential for interpreting the geological history and tectonic processes of the Earth's crust.

Define different types of zoning observed in minerals. Discuss processes of formation of different types of zoning in plagioclase with the help of Albite-Anorthite system.
Ans:

Introduction:

Zoning in minerals refers to the occurrence of systematic compositional variations within a single crystal. These variations can take different forms and are often a result of changing environmental conditions during the crystal's growth. In plagioclase feldspar minerals, such as those in the Albite-Anorthite system, various zoning types can be observed due to processes like fractional crystallization and diffusion. In this explanation, we will define different types of zoning in minerals and discuss the processes of formation of these zoning types in plagioclase using the Albite-Anorthite system as an example.

Types of Zoning in Minerals:

  1. Simple Zoning: In this type, the mineral exhibits concentric zones with distinct compositions, typically in a continuous manner from the core to the rim of the crystal.

  2. Oscillatory Zoning: Oscillatory zoning consists of alternating bands or layers of different compositions within a crystal. This type is often associated with periodic changes in the surrounding conditions.

  3. Sector-Zoning: Sector zoning is characterized by irregularly shaped regions within a crystal, each with a different composition. These regions can be oriented in various directions.

  4. Normal Zoning: Normal zoning occurs when the central part of the crystal is less calcic (contains more sodium) than the outer parts. This is commonly seen in plagioclase feldspars.

  5. Reverse Zoning: Reverse zoning is the opposite of normal zoning, where the core of the crystal is more calcic (contains more calcium) than the outer zones.

Formation of Zoning in Plagioclase (Albite-Anorthite System):

The Albite-Anorthite system encompasses a range of plagioclase feldspar compositions from pure albite (NaAlSi3O8) to pure anorthite (CaAl2Si2O8). Zoning in plagioclase occurs due to changes in the cooling rate, pressure, and composition of the surrounding magma during crystallization. Here are the processes leading to different zoning types:

  1. Simple Zoning: Simple zoning in plagioclase results from changes in magma composition. As the magma cools, plagioclase crystals may form, and their composition may vary with time. Continuous changes in the ratio of sodium to calcium in the magma lead to concentric zones in the crystal.

  2. Oscillatory Zoning: Oscillatory zoning is linked to periodic variations in the magma composition or temperature. As the crystal grows, fluctuations in the surrounding conditions cause alternating bands of albite-rich and anorthite-rich plagioclase to form.

  3. Normal and Reverse Zoning: Normal zoning occurs when the magma becomes progressively more sodium-rich during cooling, causing the plagioclase to have a calcium-rich core and sodium-rich rim. Reverse zoning happens if there is a sudden influx of calcium-rich magma, leading to a calcium-rich core surrounded by sodium-rich zones.

  4. Sector-Zoning: Sector zoning can develop when crystals experience changes in growth direction due to changes in flow patterns or stress within the magma chamber. This can result in irregular regions of different composition within the crystal.

Examples:

  1. In a granite intrusion, plagioclase feldspar crystals can exhibit oscillatory zoning due to periodic changes in magma composition.

  2. In volcanic rocks, plagioclase crystals can show normal zoning if the magma gradually evolves from a calcium-rich composition to a sodium-rich composition during cooling.

Conclusion:

Zoning in minerals, including plagioclase in the Albite-Anorthite system, arises from variations in environmental conditions during crystal growth. The type of zoning observed depends on the specific processes, such as fractional crystallization and diffusion, that affect the mineral's composition over time. Understanding zoning provides valuable insights into the geological history and conditions of rock formation.

State the petrographic characters of different types of anorthosites. Write a note on petrogenesis of anorthosites.
Ans:

Introduction:

Anorthosites are a type of intrusive igneous rock composed predominantly of the mineral anorthite, a variety of plagioclase feldspar. These rocks are known for their unique petrographic characteristics and are associated with specific petrogenetic processes. In this explanation, we will state the petrographic characters of different types of anorthosites and discuss the petrogenesis of anorthosites.

Petrographic Characters of Different Types of Anorthosites:

  1. Monzodioritic Anorthosites:

    • Mineral Composition: Dominated by plagioclase feldspar (anorthite) with minor amounts of pyroxenes (augite and orthopyroxene) and olivine.
    • Texture: Typically coarse-grained with well-developed crystals. May exhibit a cumulate texture, where plagioclase crystals settle out and accumulate.
  2. Leucoanorthosites:

    • Mineral Composition: Composed almost entirely of anorthite plagioclase feldspar.
    • Texture: Very coarse-grained, often pegmatitic in appearance, with large, clear, and colorless plagioclase crystals.
  3. Gabbroic Anorthosites:

    • Mineral Composition: Consist of plagioclase feldspar (anorthite) with significant amounts of pyroxenes (augite) and sometimes olivine.
    • Texture: Coarse-grained with well-developed crystals, similar to monzodioritic anorthosites.
  4. Troctolitic Anorthosites:

    • Mineral Composition: Composed of plagioclase feldspar (anorthite) with minor to trace amounts of olivine and orthopyroxene.
    • Texture: Typically medium- to coarse-grained with a cumulate texture, showing distinct layering.

Petrogenesis of Anorthosites:

The formation of anorthosites is associated with specific petrogenetic processes and geological settings:

  1. Magmatic Differentiation: Anorthosites are often associated with layered intrusions, where magmatic differentiation plays a crucial role. As a magma chamber cools and evolves, plagioclase feldspar (anorthite) crystals can settle out and accumulate at the bottom, forming anorthosites.

  2. Fractional Crystallization: In some cases, anorthosites result from the fractional crystallization of a magma. As the magma cools, certain minerals, including plagioclase, crystallize out in sequence, leading to the enrichment of anorthite.

  3. Postcumulus Processes: Postcumulus processes, such as the reaction between residual melt and previously crystallized minerals, can also contribute to the formation of anorthosites.

Examples:

  1. Bushveld Complex (South Africa): This layered intrusion is famous for its anorthosite layers, including leucoanorthosites. These anorthosites are believed to have formed through magmatic differentiation.

  2. Adirondack Mountains (New York, USA): The Adirondack Mountains contain gabbroic anorthosites associated with the Grenville Orogeny. These rocks are thought to have formed as part of large igneous intrusions.

Conclusion:

Anorthosites exhibit distinct petrographic characters, including their mineral composition and texture. They are often associated with layered intrusions and can form through processes like magmatic differentiation and fractional crystallization. The study of anorthosites provides valuable insights into the geological history and petrogenesis of these intriguing rocks.

What do you understand by sedimentary depositional environment ? Describe fluvial environment in detail.
Ans:

Introduction:

Sedimentary depositional environments refer to specific geological settings or conditions where sediments accumulate and are later lithified into sedimentary rocks. These environments are characterized by distinct physical, chemical, and biological factors that influence the type and arrangement of sediments. One common sedimentary environment is the fluvial environment, which pertains to rivers and their associated features. In this explanation, we will provide a detailed description of the fluvial environment.

Fluvial Environment:

The fluvial environment, also known as a riverine or river system environment, is a sedimentary depositional environment associated with the flow of water in rivers and streams. It is a dynamic and ever-changing environment that plays a crucial role in the transportation and deposition of sediments. Here are the key characteristics and features of the fluvial environment:

  1. Flowing Water: Fluvial environments are characterized by the presence of flowing water, primarily in the form of rivers and streams. The flow of water can vary from slow-moving meandering rivers to fast-flowing mountain streams.

  2. Sediment Transport: Rivers transport a wide range of sediment sizes, from clay and silt to sand, gravel, and even larger boulders. The type and size of sediment depend on factors like the velocity of the water and the geology of the river's drainage basin.

  3. Sediment Sorting: Within a river system, sediments are naturally sorted by size, with larger, coarser particles settling closer to the riverbed, and finer particles being transported further downstream. This sorting process is known as sedimentary grading.

  4. Channel Morphology: Rivers can exhibit various channel morphologies, including meandering channels with gentle curves, braided channels with multiple interconnected channels, and straight channels with minimal curvature.

  5. Depositional Features: Fluvial environments are associated with specific depositional features, including point bars (sediment deposition on the inner curve of a meandering river), levees (raised banks along river channels), and alluvial fans (fan-shaped deposits at the base of mountainous regions).

  6. Erosion and Sediment Supply: The erosive power of flowing water in rivers is responsible for the removal of sediments from one location and their transport downstream. Factors like precipitation, vegetation, and geology influence sediment supply.

  7. Sedimentary Rocks: Over time, sediments transported and deposited in fluvial environments become lithified into sedimentary rocks. Common fluvial sedimentary rocks include sandstones and conglomerates.

  8. Biological Activity: Fluvial environments support various forms of aquatic life, including fish, aquatic plants, and benthic organisms. Biological activity can influence sediment dynamics and the deposition of organic-rich layers.

Examples:

  1. Amazon River (South America): The Amazon River is a classic example of a fluvial environment, known for its vast size, meandering channels, and extensive floodplains. It transports enormous amounts of sediment and plays a crucial role in shaping the Amazon Basin.

  2. Mississippi River (USA): The Mississippi River and its tributaries exhibit various fluvial features, including levees, point bars, and the formation of the Mississippi Delta, which is a prime example of fluvial sediment deposition.

Conclusion:

The fluvial environment is a dynamic and complex sedimentary depositional environment shaped by the flow of water in rivers and streams. It plays a significant role in the geological and geomorphological processes of the Earth's surface, leading to the formation of various sedimentary rocks and distinctive landforms. Understanding fluvial environments is essential for interpreting the Earth's history and the interactions between water, sediment, and landscapes.

Explain different processes of diagenesis in clastic sedimentary rocks. Describe common diagenetic structures.

Ans:

Introduction:

Diagenesis is the collection of physical, chemical, and biological processes that transform sediments into sedimentary rocks over geological time. Clastic sedimentary rocks, which originate from the accumulation and lithification of loose clasts or fragments, undergo various diagenetic processes that modify their texture, mineralogy, and properties. In this explanation, we will discuss different processes of diagenesis in clastic sedimentary rocks and describe common diagenetic structures.

Processes of Diagenesis in Clastic Sedimentary Rocks:

  1. Compaction:

    • Process: As sediments accumulate, the weight of overlying material compresses the lower layers, reducing pore spaces and increasing sediment density.
    • Effect: Compaction decreases porosity and permeability, leading to the expulsion of pore water.
  2. Cementation:

    • Process: Groundwater carrying dissolved minerals, such as silica (SiO2), calcium carbonate (CaCO3), or iron oxide (Fe2O3), precipitates these minerals in pore spaces, binding sediment grains together.
    • Effect: Cementation strengthens the rock, enhancing its durability.
  3. Recrystallization:

    • Process: Minerals within sediment grains may undergo recrystallization, where unstable minerals transform into more stable forms.
    • Effect: This process can change the mineral composition of the rock, often improving its quality. For example, unstable aragonite may recrystallize into stable calcite.
  4. Pressure Solution:

    • Process: In areas of high stress, minerals at grain-to-grain contacts can dissolve under pressure and precipitate in regions of lower stress, leading to grain contact dissolution and growth.
    • Effect: Pressure solution contributes to compaction and can create stylolites, discussed later.
  5. Chemical Alteration:

    • Process: Minerals in sedimentary rocks can chemically react with pore fluids, leading to mineral alteration. For instance, feldspars can alter to clay minerals through chemical weathering.
    • Effect: Chemical alteration can change the rock's mineral composition and color.

Common Diagenetic Structures:

  1. Cementation Bonds: Cementation often produces mineral cements that bind sediment grains together. For example, silica cement in sandstone forms quartz overgrowths that bridge between sand grains.

  2. Nodules and Concretions: Diagenesis can result in the formation of nodules or concretions within sedimentary rocks. These are rounded masses of minerals or cement that often have different properties than the surrounding rock.

  3. Stylolites: Stylolites are irregular, jagged surfaces that form due to pressure solution. They occur at grain-to-grain contacts where minerals have dissolved under pressure and reprecipitated.

  4. Dissolution Porosity: In some cases, diagenesis may create dissolution porosity where minerals have been selectively removed. This can result in vuggy or cavernous textures in the rock.

  5. Replacement Structures: Replacement structures occur when one mineral replaces another without significant change in the original texture. Examples include the replacement of calcite by quartz in limestone.

Examples:

  1. Sandstone cemented with silica cement (quartz) forming quartz overgrowths.
  2. The formation of iron nodules in a shale, giving it a distinctive spotted appearance.
  3. Stylolites in a limestone bed, where pressure solution has occurred along grain contacts.
  4. The development of dissolution porosity in a limestone, creating a network of interconnected pores.
  5. The replacement of original shell material by pyrite in a fossiliferous shale.

Conclusion:

Diagenesis in clastic sedimentary rocks involves a series of processes that transform loose sediments into solid sedimentary rocks. These processes can create various diagenetic structures and significantly impact the rock's properties, mineral composition, and texture. Understanding diagenesis is essential for interpreting the history and characteristics of sedimentary rocks.

Enumerate the sedimentary basins of India based on their petroleum prospects.
Ans:

Introduction:

Sedimentary basins are geological depressions or regions where sediments have accumulated over geological time. These basins play a critical role in the exploration and production of hydrocarbons, including oil and natural gas. India is home to several sedimentary basins with varying petroleum prospects. In this explanation, we will enumerate the major sedimentary basins in India based on their petroleum prospects.

Sedimentary Basins in India with Petroleum Prospects:

  1. Mumbai Offshore Basin (Bombay High):

    • Location: Located off the west coast of India in the Arabian Sea.
    • Petroleum Prospects: Bombay High is one of the most prolific petroleum basins in India, known for significant oil and gas reserves. It has numerous oil and gas fields, making it a major contributor to India's hydrocarbon production.
  2. Cauvery Basin:

    • Location: Situated in the southeastern part of India, primarily offshore in the Bay of Bengal.
    • Petroleum Prospects: The Cauvery Basin has seen both onshore and offshore exploration activities. It contains several oil and gas fields, contributing to India's hydrocarbon production.
  3. Assam Basin:

    • Location: Located in northeastern India, covering parts of Assam, Arunachal Pradesh, Nagaland, and Meghalaya.
    • Petroleum Prospects: The Assam Basin is known for its oil and natural gas reserves, and it hosts numerous oilfields. Digboi, one of the oldest oilfields in India, is situated in this basin.
  4. Krishna-Godavari Basin:

    • Location: Located off the east coast of India in the Bay of Bengal.
    • Petroleum Prospects: The Krishna-Godavari Basin is one of India's major offshore basins, known for significant hydrocarbon discoveries. It contains several oil and gas fields, with the Krishna-Godavari Delta being a key area of interest.
  5. Rajasthan Basin (Barmer Basin):

    • Location: Located in northwestern India, primarily in the state of Rajasthan.
    • Petroleum Prospects: The Rajasthan Basin, particularly the Barmer Basin, has emerged as a significant oil-producing region in India. The Mangala oilfield in Barmer is one of the largest onshore oilfields in the country.
  6. Cambay Basin:

    • Location: Situated in western India, covering parts of Gujarat.
    • Petroleum Prospects: The Cambay Basin is known for both onshore and offshore oil and gas reserves. It hosts several oilfields and gas fields.
  7. Andaman Basin:

    • Location: Located in the Andaman Sea, to the southeast of the Indian mainland.
    • Petroleum Prospects: While exploration activities in the Andaman Basin are ongoing, it has shown potential for oil and gas discoveries, particularly in deepwater areas.

Conclusion:

India boasts a diverse range of sedimentary basins, each with its petroleum prospects. These basins are vital for the country's energy security and contribute significantly to its hydrocarbon production. Exploration and development activities in these basins continue to be essential for meeting India's growing energy needs.

What are the major changes in the process of formation of uranium deposits through geological time ?
Ans:

Introduction:

Uranium deposits are valuable sources of uranium, a radioactive element used primarily as fuel in nuclear reactors and for nuclear weapons production. The formation of uranium deposits has evolved over geological time, influenced by various geological processes and changes in Earth's environment. In this explanation, we will outline the major changes in the process of uranium deposit formation through geological time.

Major Changes in Uranium Deposit Formation:

  1. Precambrian and Early Paleozoic (Archean to Early Cambrian):

    • Uranium Occurrence: During the Precambrian and early Paleozoic, uranium was primarily associated with granitic rocks and high-temperature hydrothermal systems. Uranium minerals like uraninite (UO2) formed under reducing conditions.
    • Example: The Athabasca Basin in Canada contains Precambrian uranium deposits, including the high-grade McArthur River mine.
  2. Late Paleozoic to Early Mesozoic (Late Permian to Early Jurassic):

    • Uranium Occurrence: In this period, the formation of uranium deposits shifted towards sedimentary-hosted deposits. Uranium-rich fluids leached from source rocks and migrated into sandstone or limestone reservoirs, forming roll-front and tabular-type deposits.
    • Example: The Powder River Basin in the United States hosts significant sandstone-hosted uranium deposits.
  3. Late Mesozoic to Early Cenozoic (Late Cretaceous to Early Eocene):

    • Uranium Occurrence: During this time, some of the largest and richest uranium deposits formed. Uranium was deposited in sedimentary basins, often associated with organic-rich layers and reducing environments. This period saw the development of unconformity-related deposits.
    • Example: The Athabasca Basin in Canada is known for its unconformity-related uranium deposits, including the Cigar Lake and Key Lake mines.
  4. Cenozoic to Present (Eocene to Holocene):

    • Uranium Occurrence: Uranium deposits continued to form, with changes in the types of host rocks and deposit settings. This period saw the development of calcrete-hosted deposits in arid environments and the leaching of uranium from volcanic rocks.
    • Example: The Rossing Uranium Mine in Namibia contains uranium hosted in calcrete deposits.
  5. Modern Exploration and Extraction (20th Century to Present):

    • Uranium Occurrence: Modern exploration techniques, including geophysical surveys and advanced drilling methods, have led to the discovery and extraction of uranium deposits in various geological settings worldwide. This includes in-situ recovery (ISR) methods for low-grade uranium ores.
    • Example: The Olympic Dam mine in Australia utilizes ISR techniques to extract uranium from a polymetallic ore body.

Conclusion:

The formation of uranium deposits has evolved significantly over geological time, driven by changes in Earth's geology, environmental conditions, and geological processes. From early Precambrian hydrothermal deposits to the more recent sedimentary-hosted and unconformity-related deposits, uranium resources have been discovered and exploited to meet the world's energy and industrial needs. Understanding the geological history of uranium deposits is crucial for their exploration and sustainable utilization.

The document UPSC Mains Answer PYQ 2022: Geology Paper 2 (Section- A) | Geology Optional Notes for UPSC is a part of the UPSC Course Geology Optional Notes for UPSC.
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FAQs on UPSC Mains Answer PYQ 2022: Geology Paper 2 (Section- A) - Geology Optional Notes for UPSC

1. What are the topics covered in the Geology Paper 2 of UPSC Mains?
Ans. The Geology Paper 2 of UPSC Mains covers topics such as sedimentary geology, palaeontology, stratigraphy, structural geology, and applied geology. It also includes questions related to geology of fuels, ore genesis, economic geology, and environmental geology.
2. How should I prepare for the Geology Paper 2 of UPSC Mains?
Ans. To prepare for the Geology Paper 2 of UPSC Mains, it is important to have a thorough understanding of the core concepts in geology. Focus on studying the prescribed textbooks and reference materials recommended by experts. Additionally, practice solving previous year question papers and take mock tests to improve your time management and answer-writing skills.
3. What are the key areas to concentrate on while studying for the Geology Paper 2 of UPSC Mains?
Ans. While studying for the Geology Paper 2 of UPSC Mains, it is essential to concentrate on topics such as sedimentary geology, palaeontology, stratigraphy, and structural geology. Pay special attention to the principles and theories behind these areas and develop a strong foundation. Also, focus on understanding the geology of fuels, ore genesis, economic geology, and environmental geology in depth.
4. How can I improve my answer-writing skills for the Geology Paper 2 of UPSC Mains?
Ans. Improving answer-writing skills for the Geology Paper 2 of UPSC Mains requires practice and guidance. Start by analyzing the question paper patterns and understanding the demand of each question. Develop a clear and concise writing style, and ensure that your answers are well-structured and logical. Seek feedback from mentors or experienced candidates to identify areas of improvement and work on them.
5. Are there any specific resources or study materials available for the Geology Paper 2 of UPSC Mains?
Ans. Yes, there are several resources and study materials available for the Geology Paper 2 of UPSC Mains. Some recommended textbooks include "Principles of Sedimentology and Stratigraphy" by Sam Boggs Jr., "Structural Geology" by Haakon Fossen, and "Economic Geology" by Walter L. Pohl. Additionally, you can refer to geological surveys, research papers, and online resources provided by reputable institutions to supplement your preparation.
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