- •Contents
- •Foreword to the English translation
- •Preface
- •1 Introduction
- •1.1 Historical review
- •1.2 The birth of the concept of crystal growth
- •1.3 Morphology, perfection, and homogeneity
- •1.4 Complicated and complex systems
- •References
- •Suggested reading
- •2 Crystal forms
- •2.1 Morphology of crystals – the problems
- •References
- •Suggested reading
- •3 Crystal growth
- •3.1 Equilibrium thermodynamics versus kinetic thermodynamics
- •3.2 Driving force
- •3.3 Heat and mass transfer
- •3.4 Examples of mass transfer
- •3.6 Nucleation
- •3.7 Lattice defects
- •3.8 Interfaces
- •3.9 Spiral growth
- •3.10 Growth mechanism and morphology of crystals
- •3.11 Morphological instability
- •3.12 Driving force and morphology of crystals
- •3.13 Morphodroms
- •3.14 Element partitioning
- •3.15 Inclusions
- •References
- •Suggested reading
- •4 Factors determining the morphology of polyhedral crystals
- •4.1 Forms of polyhedral crystals
- •4.2 Structural form
- •4.3 Equilibrium form
- •4.4 Growth forms
- •4.4.1 Logical route for analysis
- •4.4.2 Anisotropy involved in the ambient phase
- •4.4.3 Whiskers
- •MAJOR FACTORS
- •METHODOLOGY
- •IMPURITIES
- •AMBIENT PHASES AND SOLVENT COMPONENTS
- •4.4.7 Factors controlling growth forms
- •References
- •Suggested reading
- •5 Surface microtopography of crystal faces
- •5.1 The three types of crystal faces
- •5.2 Methods of observation
- •5.3 Spiral steps
- •5.4 Circular and polygonal spirals
- •5.5 Interlaced patterns
- •5.6 Step separation
- •5.7 Formation of hollow cores
- •5.8 Composite spirals
- •5.9 Bunching
- •5.10 Etching
- •References
- •Suggested reading
- •6 Perfection and homogeneity of single crystals
- •6.1 Imperfections and inhomogeneities seen in single crystals
- •6.2 Formation of growth banding and growth sectors
- •6.3 Origin and spatial distribution of dislocations
- •References
- •7 Regular intergrowth of crystals
- •7.1 Regular intergrowth relations
- •7.2 Twinning
- •7.2.1 Types of twinning
- •7.2.2 Energetic considerations
- •7.2.4 Penetration twins and contact twins
- •7.2.5 Transformation twin
- •7.2.6 Secondary twins
- •7.3 Parallel growth and other intergrowth
- •7.4 Epitaxy
- •7.5 Exsolution, precipitation, and spinodal decomposition
- •References
- •Suggested reading
- •8 Forms and textures of polycrystalline aggregates
- •8.1 Geometrical selection
- •8.2 Formation of banding
- •8.3 Spherulites
- •8.4 Framboidal polycrystalline aggregation
- •References
- •Suggested reading
- •9 Diamond
- •9.1 Structure, properties, and use
- •9.2 Growth versus dissolution
- •9.3 Single crystals and polycrystals
- •9.4 Morphology of single crystals
- •9.4.1 Structural form
- •9.4.2 Characteristics of {111}, {110}, and {100} faces
- •9.4.3 Textures seen inside a single crystal
- •9.4.4 Different solvents (synthetic diamond)
- •9.4.5 Twins
- •9.4.6 Coated diamond and cuboid form
- •9.4.7 Origin of seed crystals
- •9.4.8 Type II crystals showing irregular forms
- •References
- •Suggested reading
- •10 Rock-crystal (quartz)
- •10.1 Silica minerals
- •10.2 Structural form
- •10.3 Growth forms
- •10.4 Striated faces
- •10.5 Growth forms of single crystals
- •10.5.1 Seed crystals and forms
- •10.5.2 Effect of impurities
- •10.5.3 Tapered crystals
- •10.6 Twins
- •10.6.1 Types of twins
- •10.6.2 Japanese twins
- •10.6.3 Brazil twins
- •10.7 Scepter quartz
- •10.8 Thin platy crystals and curved crystals
- •10.9 Agate
- •References
- •11 Pyrite and calcite
- •11.1 Pyrite
- •11.1.2 Characteristics of surface microtopographs
- •11.1.4 Polycrystalline aggregates
- •11.2 Calcite
- •11.2.1 Habitus
- •11.2.2 Surface microtopography
- •References
- •12 Minerals formed by vapor growth
- •12.1 Crystal growth in pegmatite
- •12.3 Hematite and phlogopite in druses of volcanic rocks
- •References
- •13 Crystals formed by metasomatism and metamorphism
- •13.1 Kaolin group minerals formed by hydrothermal replacement (metasomatism)
- •13.2 Trapiche emerald and trapiche ruby
- •13.3 Muscovite formed by regional metamorphism
- •References
- •14 Crystals formed through biological activity
- •14.1 Crystal growth in living bodies
- •14.2 Inorganic crystals formed as indispensable components in biological activity
- •14.2.1 Hydroxyapatite
- •14.2.2 Polymorphic minerals of CaCO3
- •14.2.3 Magnetite
- •14.3 Crystals formed through excretion processes
- •14.4 Crystals acting as possible reservoirs for necessary components
- •14.5 Crystals whose functions are still unknown
- •References
- •Appendixes
- •A.1 Setting of crystallographic axes
- •A.2 The fourteen Bravais lattices and seven crystal systems
- •A.3 Indexing of crystal faces and zones
- •A.4 Symmetry elements and their symbols
- •Materials index
- •Subject index
230Pyrite and calcite
face is characterized by the development of striations since layer growth does not occur on the face. A {210} face showing striations only is a crystal face of this kind. In such a crystal, the larger the normal growth rate, or the smaller the step separation, the more {hk0} or {210} faces develop, and the larger the degree of change from cubic to pentagonal dodecahedral Tracht as growth proceeds. A larger driving force condition corresponds to this situation. The observed difference in Tracht variation depending on grain size between the central portion and outer region of a deposit appears to reflect this difference. When pyrite grows under favorable conditions, such as high sulfur fugacity, pentagonal dodecahedral Tracht appears, whereas under less favorable conditions pyrite crystals maintain a cubic form. It is probably for this reason that pyrite crystals occurring further away from an ore deposit do not show distinct changes depending on grain size, and that the Trachts are different between ore deposit and the country rock, crystals formed in country rock taking exclusively simple cubic form.
Although crystallographically equivalent, the {210} faces of pyrite from a particular locality are characterized by striations perpendicular to the edge with {100}. These striations are different from the striations described above and appear due to narrow growth layers on the {210} face, indicating that, under this condition, {210} behaves as an F face. It is still to be discovered why {210} faces behave differently depending on the growth conditions.
As compared to the relation between {210} and {100}, the appearance of {111} is slightly different. It is known that octahedral crystals contain more arsenic (As) than cubic crystals in the same locality, and there is a possibility that {111} faces develop due to an impurity adsorption of As. It is observed that the internal texture of this type of crystal shows a drastic change from cubic to octahedral in association with precipitation of minerals containing As.
11.1.4 Polycrystalline aggregates
In sedimentary rocks, pyrite often occurs as nodular, spherical, irregular, massive, framboidal polycrystalline aggregates of minute crystals. It often occurs in fossils, without modifying the external fossil form, and a bacterial origin has been suggested for pyrite aggregates of this type. Among such polycrystalline aggregates, framboidal pyrites have attracted particular interest. They are spherical, they measure a few tens of micrometers across, and one framboid consists of close-packed, equal-sized idiomorphic pyrite crystals with the same Tracht. Cubic, octahedral, pentagonal dodecahedral Trachts, etc. are known. One framboid consists of a unique Tracht.
Framboidal pyrite occurs, for example, in sedimentary rocks, muddy sediments, and precipitates in hot springs; two controversial origins have been suggested, one bacterial and the other relating to agitation in hydrothermal solution. Framboidal