首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 259 毫秒
1.
Abstract Most porphyroblasts never rotate during ductile deformation, provided they do not internally deform during subsequent events, with the exception of relatively uncommon but spectacular examples of spiralling garnets. Instead, the surrounding foliation rotates and reactivates due to partitioning of the deformation around the porphyroblast. Consequently, porphyroblasts commonly preserve the orientation of early foliations and stretching lineations within strain shadows or inclusion trails, even where these structures have been rotated or obliterated in the matrix due to subsequent deformation. These relationships can be readily used to help develop an understanding of the processes of foliation development and they demonstrate the prominent role of reactivation of old foliations during subsequent deformation. They can also be used to determine the deformation history, as porphyroblasts only rotate when the deformation cannot partition and involves progressive shearing with no combined bulk shortening component.  相似文献   

2.
Porphyroblast inclusion trails: the key to orogenesis   总被引：8，自引：0，他引：8  
Detailed microstructural analysis of inclusion trails in hundreds of garnet porphyroblasts from rocks where spiral-shaped inclusion trails are common indicates that spiral-shaped trails did not form by rotation of the growing porphyroblasts relative to geographic coordinates. They formed instead by progressive growth by porphyroblasts over several sets of near-orthogonal foliations that successively overprint one another. The orientations of these near-orthogonal foliations are alternately near-vertical and near-horizontal in all porphyroblasts examined. This provides very strong evidence for lack of porphyroblast rotation.
The deformation path recorded by these porphyroblasts indicates that the process of orogenesis involves a multiply repeated two-stage cycle of: (1) crustal shortening and thickening, with the development of a near-vertical foliation with a steep stretching lineation; followed by (2) gravitational instability and collapse of this uplifted pile with the development of a near-horizontal foliation, gravitational spreading, near-coaxial vertical shortening and consequent thrusting on the orogen margins. Correlation of inclusion trail overprinting relationships and asymmetry in porphyroblasts with foliation overprinting relationships observed in the field allows determination of where the rocks studied lie and have moved within an orogen. This information, combined with information about chemical zoning in porphyroblasts, provides details about the structural/metamorphic ( P-T-t ) paths the rocks have followed.
The ductile deformation environment in which a porphyroblast can rotate relative to geographic coordinates during orogenesis is spatially restricted in continental crust to vertical, ductile tear/transcurrent faults across which there is no component of bulk shortening or transpression.  相似文献   

3.
Detailed 3‐D analysis of inclusion trails in garnet porphyroblasts and matrix foliations preserved around a hand‐sample scale, tight, upright fold has revealed a complex deformation history. The fold, dominated by interlayered quartz–mica schist and quartz‐rich veins, preserves a crenulation cleavage that has a synthetic bulk shear sense to that of the macroscopic fold and transects the axis in mica‐rich layers. Garnet porphyroblasts with asymmetric inclusion trails occur on both limbs of the fold and display two stages of growth shown by textural discontinuities. Garnet porphyroblast cores and rims pre‐date the macroscopic fold and preserve successive foliation inflection/intersection axes (FIAs), which have the same trend but opposing plunges on each limb of the fold, and trend NNE–SSW and NE–SW, respectively. The FIAs are oblique to the main fold, which plunges gently to the WSW. Inclusion trail surfaces in the cores of idioblastic porphyroblasts within mica‐rich layers define an apparent fold with an axis oblique to the macroscopic fold axis by 32°, whereas equivalent surfaces in tabular garnet adjacent to quartz‐rich layers define a tighter apparent fold with an axis oblique to the main fold axis by 17°. This potentially could be explained by garnet porphyroblasts that grew over a pre‐existing gentle fold and did not rotate during fold formation, but is more easily explained by rotation of the porphyroblasts during folding. Tabular porphyroblasts adjacent to quartz‐rich layers rotated more relative to the fold axis than those within mica‐rich layers due to less effective deformation partitioning around the porphyroblasts and through quartz‐rich layers. This work highlights the importance of 3‐D geometry and relative timing relationships in studies of inclusion trails in porphyroblasts and microstructures in the matrix.  相似文献   

4.
变斑晶晶内包体径迹在变质地质学和构造地质学中具有广泛的用途。尤其在造山带研究、PTt轨迹、变质与变形关系及历史、变形机制及褶皱和剪切带运动学、变质变形程度、变斑晶生长率、应变量、应变速率等方面的应用取得许多重大进展。其中所有变斑晶都是同运动的、未旋转的“固定论”新观点、新应用,值得重视和深入综合研究。另外,在任何应用之前都宜首先确定变斑晶旋转与否。  相似文献   

5.
Abstract The main porphyroblastic minerals in schists and phyllites of the Foothills terrane, Western Metamorphic Belt, central Sierra Nevada, California, are cordierite and andalusite (mostly chiastolite). Less commonly, biotite, muscovite, chlorite, garnet or staurolite are also present as porphyroblasts. The variety of porphyroblast and matrix microstructures in these rocks makes them suitable for testing three modern hypotheses on growth and deformation of porphyroblasts: (1) porphyroblast growth is always syndeformational; (2) porphyroblasts nucleate only in low-strain, largely coaxially deformed, quartz-rich (Q) domains of a crenulation foliation and are dissolved in active high-strain, non-coaxially deformed, mica-rich (M) domains, the spacing between which limits the size of the porphyroblasts; and (3) porphyroblasts generally do not rotate, with respect to geographical coordinates, during deformation, provided they do not deform internally, so that they may be used as reliable indicators of the orientation of former regional structural surfaces, even on the scale of orogenic belts. Some porphyroblast–matrix relationships in the Foothills terrane are inconsistent with hypotheses 1 and 2, and others are equivocal. For example, in many rocks it cannot be determined whether the porphyroblasts grew where the strain had already been partitioned into M and Q domains, whether the porphyroblasts caused this partitioning, or both. Although most porphyroblasts appear to be syndeformational, as predicted by hypothesis 1, observations that do not support the general application of hypotheses 1 and 2 to rocks of the Foothills terrane include: (a) lack of residual crenulations in many strain-shadows and alternative explanations where they are present; (b) absence of porphyroblasts smaller than the distance between nearest mica-rich domains; (c) nucleation of crenulations on existing porphyroblasts, rather than nucleation of porphyroblasts between existing crenulations; (d) presence of micaceous ‘arcs’in an undifferentiated matrix against some porphyroblasts, suggesting static growth; (e) absence of crenulations in porphyroblastic rocks showing sedimentary bedding; and (f) porphyroblasts with very small, random inclusions, which are probably pre-deformational. Similarly, porphyroblasts that have overgrown sets of crenulations and porphyroblasts with micaceous ‘arcs’are probably post-deformational, at least on the scale of a large thin section and probably over much larger areas, judging from mesoscopic structural evidence. Some porphyroblasts in rocks of the Foothills terrane do not appear to have rotated, with respect to geographical coordinates, during matrix deformation, in accordance with hypothesis 3, at least on the scale of a large thin section. However, other porphyroblasts evidently have rotated. In some instances, this appears to be due to mutual interference, but many apparently rotational porphyroblasts are too far apart to have interfered with each other, which indicates that the rotation was associated with deformation of the matrix. The occurrence of planar bedding surfaces adjacent to porphyroblasts about which bedding and/or foliation surfaces are folded suggests rotation of the porphyroblasts during non-coaxial flow parallel to bedding, rather than crenulation of the matrix foliation around static porphyroblasts. It appears that porphyroblasts may rotate during deformation if the matrix is relatively homogeneous, so that the strain is effectively non-coaxial. This may occur after homogenization of a matrix in response to the strongest degree of crenulation folding, whereas the same porphyroblasts may have been inhibited from rotating previously, when strain accumulation was partitioned in the matrix.  相似文献   

6.
In the metamorphic cores of many orogenic belts, large macroscopic folds in compositional layering also appear to fold one or more pervasive matrix foliations. The latter geometry suggests the folds formed relatively late in the tectonic history, after foliation development. However, microstructural analysis of four examples of such folds suggests this is not the case. The folds formed relatively early in the orogenic history and are the end product of multiple, near orthogonal, overprinting bulk shortening events. Once large macroscopic folds initiate, they may tighten further during successive periods of sub-parallel shortening, folding or reactivation of foliations that develop during intervening periods of near orthogonal shortening. Reactivation of the compositional layering defining the fold limbs causes foliation to be rotated into parallelism with the limbs.Multiple periods of porphyroblast growth accompanied the multiple phases of deformation that postdated the initial development of these folds. Some of these phases of deformation were attended by the development of large numbers of same asymmetry spiral-shaped inclusion trails in porphyroblasts on one limb of the fold and not the other, or larger numbers of opposite asymmetry spirals on the other limb, or similar numbers of the same asymmetry spirals on both limbs. Significantly, the largest disparity in numbers from limb to limb occurred for the first of these cases. For all four regional folds examined, the structural relationships that accompanied these large disparities were identical. In each case the shear sense operating on steeply dipping foliations was opposite to that required to originally develop the fold. Reactivation of the folded compositional layering was not possible for this shear sense. This favoured the development of sites of approximately coaxial shortening early during the deformation history, enhancing microfracture and promoting the growth of porphyroblasts on this limb in comparision to the other. These distributions of inclusion trail geometries from limb to limb cannot be explained by porphyroblast rotation, or folding of pre-existing rotated porphyroblasts within a shear zone, but can be explained by development of the inclusion trails synchronous with successive sub-vertical and sub-horizontal foliations.  相似文献   

7.
In the Littleton Formation, garnet porphyroblasts preserve three generations of growth that occurred before formation of the Bolton Syncline. Inclusion trails of foliations overgrown by these porphyroblasts are always truncated by the matrix foliation suggesting that garnet growth predated the matrix foliation. In contrast, many staurolite porphyroblasts grew synchronously with formation of the Bolton Syncline. However, local rim overgrowths of the matrix foliation suggest that some staurolite porphyroblasts continued to grow after development of the fold during younger crenulation producing deformations. The axes of curvature or intersection of foliations defined by inclusion trails inside the garnet porphyroblasts lie oblique to the axial plane of the Bolton Syncline but do not change orientation across it. This suggests the garnets were not rotated during the subsequent deformation associated with fold development or during even younger crenulation events. Three samples also contain a different set of axes defined by curvature of inclusion trails in the cores of garnet porphyroblasts suggesting a protracted history of garnet growth. Foliation intersection axes in staurolite porphyroblasts are consistently orientated close to the trend of the axial plane of the Bolton Syncline on both limbs of the fold. In contrast, axes defined by curvature or intersection of foliations in the rims of staurolite porphyroblasts in two samples exhibit a different trend. This phase of staurolite growth is associated with a crenulation producing deformation that postdated formation of the Bolton Syncline. Measurement of foliation intersection axes defined by inclusion trails in both garnet and staurolite porphyroblasts has enabled the timing of growth relative to one another and to the development of the Bolton Syncline to be distinguished in rocks where other approaches have not been successful. Consistent orientation of foliation intersection axes across a range of younger structures suggests that the porphyroblasts did not rotate relative to geographical coordinates during subsequent ductile deformation. Foliation intersection axes in porphyroblasts are thus useful for correlating phases of porphyroblastic growth in this region.  相似文献   

8.
Three periods of mineral growth and three generations of spiral‐shaped inclusion trails have been distinguished within folded rocks of the Qinling‐Dabie Orogen, China, using the development of three successive and differently trending sets of foliation intersection axes preserved in porphyroblasts (FIAs). This progression is revealed by the consistent relative sequence of changes in FIA trends from the core to rim of garnet porphyroblasts in samples with multiple FIAs. The first and second formed sets of FIAs trend oblique to the axial planes of macroscopic folds that dominate the outcrop pattern in this region. The porphyroblasts containing these FIAs grew prior to the development of the macroscopic folds, yet the FIAs do not change orientation across the fold hinges. The youngest formed FIAs (set 3) lie subparallel to the axial planes of these folds and the porphyroblasts containing these FIAs formed in part as the folds developed. The deformation associated with all three generations of spiral‐shaped inclusion trails in garnet porphyroblasts involved the formation of subhorizontal and subvertical foliations against porphyroblast rims accompanied by periods of garnet growth; pervasive structures have not necessarily formed in the matrix away from the porphyroblasts. The macroscopic folds are heterogeneously strained from limb to limb, doubly plunging and have moderately dipping axial planes. The consistent orientation of Set 1 FIAs indicates that the development of spiral‐shaped inclusion trails in porphyroblasts with FIAs belonging to Set 2 did not involve rotation of the previously formed porphyroblasts. The consistent orientation of Sets 1 and 2 FIAs indicate that the development of spiral‐shaped inclusion trails in porphyroblasts with FIAs belonging to Set 3 did not involve rotation of the previously formed porphyroblasts during folding. This requires a fold mechanism of progressive bulk inhomogeneous shortening and demonstrates that spiral‐shaped inclusion trails can form outside of shear zones.  相似文献   

9.
The behaviour of spherical versus highly ellipsoidal rigid objects in folded rocks relative to one another or the Earth’s surface is of particular significance for metamorphic and structural geologists. Two common porphyroblastic minerals, garnet and staurolite, approximate spherical and highly ellipsoidal shapes respectively. The motion of both phases is analysed using the axes of inflexion or intersection of one or more foliations preserved as inclusion trails within them (we call these axes FIAs, for foliation inflexion/intersection axes). For staurolite, this motion can also be compared with the distribution of the long axes of the crystals. Schists from the regionally shallowly plunging Bolton syncline commonly contain garnet and staurolite porphyroblasts, whose FIAs have been measured in the same sample. Garnet porphyroblasts pre-date this fold as they have inclusion trails truncated by all matrix foliations that trend parallel to the strike of the axial plane. However, they have remarkably consistent FIA trends from limb to limb. The FIAs trend 175° and lie 25°NNW from the 020° strike of the axial trace of the Bolton syncline. The plunge of these FIAs was determined for six samples and all lie within 30° of the horizontal. Eleven of these samples also contain staurolite porphyroblasts, which grew before, during and after formation of the Bolton syncline as they contain inclusion trails continuous with matrix foliations that strike parallel to the axial trace of this fold. The staurolite FIAs have an average trend of 035°, 15°NE from the 020° strike of the axial plane of this fold. The total amount of inclusion trail curvature in staurolite porphyroblasts, about the axis of relative rotation between staurolite and the matrix (i.e. the FIA), is greater than the angular spread of garnet FIAs. Although staurolite porphyroblasts have ellipsoidal shapes, their long axes exhibit no tendency to be preferentially aligned with respect to the main matrix foliation or to the trend of their FIA. This indicates that the axis of relative rotation, between porphyroblast and matrix (the FIA), was not parallel to the long axis of the crystals. It also suggests that the porphyroblasts were not preferentially rotated towards a single stretch direction during progressive deformation. Five overprinting crenulation cleavages are preserved in the matrix of rocks from the Bolton syncline and many of these result from deformation events that post-date development of this fold. Staurolite porphyroblast growth occurred during the development of all of these deformations, most of which produced foliations. Staurolite has overgrown, and preserved as helicitic inclusions, crenulated and crenulation cleavages; i.e. some inclusion trail curvature pre-dates porphyroblast growth. The deformations accompanying staurolite growth involved reversals in shear sense and changing kinematic reference frames. These relationships cannot all be explained by current models of rotation of either, or both, the garnet and staurolite porphyroblasts. In contrast, we suggest that the relationships are consistent with models of deformation paths that involve non-rotation of porphyroblasts relative to some external reference frame. Further, we suggest there is no difference in the behaviour of spherical or ellipsoidal rigid objects during ductile deformation, and that neither garnet nor staurolite have rotated in schists from the Bolton syncline during the multiple deformation events that include and post-date the development of this fold.  相似文献   

10.
变质岩中变斑晶成核生长及旋转问题的述评   总被引：3，自引：0，他引：3  
发生递进变形的变质岩中,斑晶成核生长于变形分解作用的递进缩短带内,斑晶的大小受两侧递进剪切变形带的限制。除少数螺旋状石榴石外,产于共轴或非共轴递进不均匀缩短变形过程中的斑晶不发生旋转,斑晶内部包体形迹(Si)反映外部面理(Se)的再活化。利用未旋转斑晶中的包体形迹可以确定早期面理的取向,寻找构造演化的时间标志,确定褶皱轴迹等,本文给出了斑晶中包体形迹弯曲的成因模式图。  相似文献   

11.
Abstract Reactivation of early foliations accounts for much of the progressive strain at more advanced stages of deformation. Its role has generally been insufficiently emphasized because evidence is best preserved where porphyroblasts which contain inclusion trails are present. Reactivation occurs when progressive shearing, operating in a synthetic anastomosing fashion parallel to the axial planes of folds, changes to a combination of coarse- and finescale zones of progressive shearing, some of which operate antithetically relative to the bulk shear on a fold limb. Reactivation of earlier foliations occurs in these latter zones. Reactivation decrenulates pre-existing or just-formed crenulations, generating shearing along the decrenulated or rotated pre-existing foliation planes. Partitioning of deformation within these foliation planes, such that phyllosilicates and/or graphite take up progressive shearing strain and other minerals accommodate progressive shortening strain, causes dissolution of these other minerals. This results in concentration of the phyllosilicates in a similar, but more penetrative manner to the formation of a differentiated crenulation cleavage, except that the foliation can form or intensify on a fold limb at a considerable angle to the axial plane of synchronous macroscopic folds. Reactivation can generate bedding-parallel schistosity in multideformed and metamorphosed terrains without associated folds. Heterogeneous reactivation of bedding generates rootless intrafolial folds with sigmoidal axial planes from formerly through-going structures. Reactivation causes rotation or ‘refraction’of axial-plane foliations (forming in the same deformation event causing reactivation) in those beds or zones in which an earlier foliation has been reactivated, and results in destruction of the originally axial-plane foliation at high strains. Reactivation also provides a simple explanation for the apparently ‘wrong sense’, but normally observed ‘rotation’of garnet porphyroblasts, whereby the external foliation has undergone rotation due to antithetic shear on the reactivated foliation. Alternatively, the rotation of the external foliation can be due to its reactivation in a subsequent deformation event. Porphyroblasts with inclusion trails commonly preserve evidence of reactivation of earlier foliations and therefore can be used to identify the presence of a deformation that has not been recognized by normal geometric methods, because of penetrative reactivation. Reactivation often reverses the asymmetry between pre-existing foliations and bedding on one limb of a later fold, leading to problems in the geometric analysis of an area when the location of early fold hinges is essential. The stretching lineation in a reactivated foliation can be radically reoriented, potentially causing major errors in determining movement directions in mylonitic schistosities in folded thrusts. Geometric relationships which result from reactivation of foliations around porphyroblasts can be used to aid determination of the timing of the growth of porphyroblasts relative to deformation events. Other aspects of reactivation, however, can lead to complications in timing of porphyroblast growth if the presence of this phenomenon is not recognized; for example, D2-grown porphyroblasts may be dissolved against reactivated S1 and hence appear to have grown syn-D1.  相似文献   

12.
Abstract Porphyroblast textures in a Karakorum phyllite reveal that porphyroblast growth was syn-tectonic with respect to a cleavage forming deformation. During and after porphyroblast growth it partitions the deformation such that zones of intensified cleavage are developed which wrap around the porphyroblast whilst the porphyroblast and its strain shadow undergo little deformation. Porphyroblast strain shadows comprise quartz, calcite and felspar with little mica, and are probably formed by solution transfer during deformation. Unless the deformation is so strongly partitioned that no deformation of the porphyroblasts and their immediate surrounds occurs, inequidimensional porphyroblasts will rotate. Porphyroblasts undergo some dissolution after they have finished growing.  相似文献   

13.
剪切带中变斑晶的生长及包裹体痕迹的演化   总被引：6，自引：0，他引：6       下载免费PDF全文
李海兵  曾令森 《地质科学》1997,32(2):181-192
韧性剪切带中,由于变形分解作用的存在,岩石发生递进变形过程中,产于共轴或非共轴递进缩短带内的变斑晶不发生旋转,而变斑晶内的包裹体痕迹是递进变形过程中遗留在变斑晶内的变形变质痕迹。利用未旋转斑晶中的包裹体痕迹可以确定早期面理的取向,寻找构造演化的时间标志,确定变形变质的关系及其演化史。对北祁连托勒牧场大型走滑韧性剪切带中石榴石、黑云母等变斑晶及包裹体痕迹的研究,揭示了变斑晶的生长和包、裹体痕迹与褶劈理的演化有着重要联系以及剪切变形过程中变形变质演化史、应变速率的变化。递进变形相应地发生递增变质,但两者存在着一定的差异性。  相似文献   

14.
Inclusion trails in garnet and albite porphyroblasts in the Fleur de Lys Supergroup preserve successive generations of microstructures, some of which correlate with equivalent microstructures in the matrix. Microstructure–porphyroblast relationships provide timing constraints on a succession of seven crenulation cleavages (S1–S7) and five stages of porphyroblast growth. Significant destruction and alteration of early fabrics has occurred during the microstructural development of the rock mass. Garnet porphyroblasts grew episodically through four growth stages (G1–G4) and preserve a succession of five fabrics (S1–S5) as inclusion trails. Garnet growth during each of the four growth phases did not occur on all pre-existing porphyroblasts, resulting in contrasting growth histories between individual garnet porphyroblasts from the same outcrop. Albite porphyroblasts grew during a single stage of growth and have overgrown microstructures continuous with the matrix. The garnet and albite porphyroblast inclusion trails record a succession of crenulation cleavages without any rotation of the porphyroblasts relative to other porphyroblasts in the population.
Complex microstructural histories are best resolved by preparing multiple oriented thin sections from a large number of samples of different rock types within the area of study. The succession of matrix foliations must be understood, as it provides the most useful time-frame against which to measure the relative timing of phases of porphyroblast growth. Comparable microstructures must be identified in different porphyroblasts and in the rock matrix.  相似文献   

15.
Porphyroblast inclusion trails provide important information about the tectonometamorphic evolution of a metamorphic rock. However, there remains considerable controversy over whether porphyroblasts rotate during bulk non-coaxial deformation.
With reference to an area of the Scandinavian Caledonides and utilizing existing data from theoretical and experimental modelling, this study demonstrates that both 'straight' and 'S-shaped' inclusion trails are consistent with an interpretation in terms of syndeformational porphyroblast growth in a regime approximating to Newtonian simple shear. At crustal strain rates of 10-14 s-1 and porphyroblast growth times of 0.1–1.0 Ma, it is shown that a maximum of 5-9 angular rotation would occur during growth. At faster strain rates of 10-12 s-1 (e.g. those in a shear zone) porphyroblast angular rotations of 90 are shown to occur in 0.1–0.25 Ma (i.e. times comparable with or faster than porphyroblastesis). In view of this, 'S-shaped' inclusion trails are to be expected in porphyroblasts growing in active shear zones or other situations of high shear strain, whereas 'straight' inclusion trails can be interpreted as static overgrowth of an existing fabric or as syndeformational porphyroblastesis at low strain rates.  相似文献   

16.
变斑晶包体形迹研究的几个问题   总被引：1，自引：0，他引：1  
变斑晶是联系变质与变形的重要媒介。变斑晶内的包体按几何形态可分为９大类。在发生递进变形的变质岩中，斑晶成核生长于变形分解作用的递进缩短带内。除少数螺旋状石榴石外，产于共轴或非共轴递进不均匀缩短变形过程中的斑晶不发生旋转。在韧性剪切带中，由于存在变形分解作用，在岩石发生递进变形过程中，产于共轴或非共轴递进缩短带内的变斑晶也不发生旋转。利用未旋转斑晶中包体形迹可以确定早期面理的取向，寻找构造演化时间标志，确定变形变质关系及其演化史。如在大背坞地区，根据黄铁矿变斑晶的旋转演化，可以恢复韧性剪切带的成生演化历史。近十几年来由于计算机模拟的引人，使变斑晶微构造研究从定性步入定量阶段。  相似文献   

17.
It has been claimed that rigid porphyroblasts which grow before or during folding and concurrent cleavage development do not rotate with respect to the geographical reference frame (GRF), even if the straining is non-coaxial (Bell, 1985, Bell and Johnson, 1990). The explanation offered is based on strain partitioning. It is argued that the initial orientations of early fabrics included as internal foliations (Si) in the porphyroblasts have been preserved after polyphase deformation, and even after successive orogenies. According to the strain partitioning model, the porphyroblasts are fixed in domains of coaxial straining (microlithons) and are isolated from the non-coaxial straining associated with the enveloping septa (Se). This hypothesis, and also its discussions both pro and contra, suffer from insufficient attention to reference frames. We therefore attempt to demonstrate: (a) the need for rigorous treatment of reference frames in geological interpretations; (b) that, in a folding situation, grains that do not rotate with respect to their immediate matrix generally rotate with respect to the GRF; (c) that lack of porphyroblast rotation with respect to the GRF demands a rare folding mechanism (slip fold model); and (d) that the non-rotation hypothesis is in conflict with heterogeneous deformation (cleavage refraction). Finally, we question the validity of the evidence in a study by Fyson (1980), cited in support of non-rotation with respect to the GRF during folding. Fyson reported orientations of Si that are constant, after folding, over a large area; this scenario is a product of selective data acquisition. In summary, our investigation shows that the lack of porphyroblast rotation with respect to a GRF during folding, while possible, is not universal. The development of microstructures (e.g. curved Si) is only related to the local deformation path, the characterisation of which does not rely on the GRF.  相似文献   

18.
The three-dimensional geometry of spiral inclusion trails from the Canton Schist were measured to determine whether the spirals were a product of porphyroblast rotation within a shear zone, or porphyroblast growth during a series of overprinting fold events. The spiral inclusion trails are composed of three separate, sub-planar inclusion trail surfaces occupying texturally distinct parts of the porphyroblasts. These surfaces are correlated across a >10 km2 area using textural criteria and relative timing. Measured patterns of inclusion trail orientation and asymmetry suggest they did not form by porphyroblast rotation within a non-coaxial shear zone. Rather, the porphyroblasts grew during three successive overprinting fold events (F2–F4), and the spiral inclusion trails represent the accumulated curvature associated with folding of successive axial plane foliations. The data show that spiral garnets are not peculiar to shear zones, and can form by overprinting crenulations and folds. This is consistent with the common occurrence of spiral garnets in multiply-deformed, regionally metamorphosed fold belts.  相似文献   

19.
Abstract Mica porphyroblasts in schists from several regions show nearly planar inclusion trails that are parallel over areas much larger than the wavelengths of later folds. This indicates that the porphyroblasts have not rotated, with respect to geographical co-ordinates, during deformation. Instead, the matrix has rotated, as suggested by Ramsay (1962). Even in zones of marked shortening in the matrix adjacent to large rigid porphyroblasts (e.g. of cordierite or staurolite), small biotite porphyroblasts have not rotated, but have become thinned by solution, as indicated by parallelism of inclusion trails in separate biotite grains and by evidence of truncation of inclusion trails by the matrix foliation. Less common are biotite porphyroblasts that have single asymmetrical microfolds in the matrix adjacent to the porphyroblasts and so appear to have rotated; these porphyroblasts are characterized by kinking.  相似文献   

20.
Abstract In regional metamorphic rocks, the partitioning of deformation into progressive shearing and progressive shortening components results in strain and strain-rate gradients across the boundaries between the partitioned zones. These generate dislocation density gradients and hence chemical potential gradients that drive dissolution and solution transfer. Phyllosilicates and graphite are well adapted to accommodating progressive shearing without necessarily building up large dislocation density gradients within a grain, because of their uniquely layered crystal structure. However, most silicates and oxides cannot accommodate strain transitions within grains without associated dislocation density gradients, and hence are susceptible to dissolution and solution transfer. As a consequence, zones of progressive shearing become zones of dissolution of most minerals, and of concentration of phyllosilicates and graphite. Exceptions are mylonites, where strain-rates are commonly high enough for plastic deformation to dominate over diffusion rates and therefore over dissolution and solution transfer. Porphyroblastic minerals cannot nucleate and grow in zones of active progressive shearing, as they would be dissolved by the effects of shearing strain on their boundaries. However, they can nucleate and grow in zones of progressive shortening and this is aided by the propensity for microfracturing in these zones, which allows rapid access of fluids carrying the material presumed to be necessary for nucleation and growth. Zones of progessive shortening also have a number of characteristics that help to lower the activation energy barrier for nucleation, this includes a build up of stored strain-energy relative to zones of progressive shearing, in which dissolution is occuring. Porphyroblast growth is generally syndeformational, and previously accepted criteria for static growth are not valid when the role of deformation partitioning is taken into account. Porphyroblasts in a contact aureole do not grow statically either, as microfracturing, associated with emplacement, allows access of fluids in a fashion that is similar to microfracturing in zones of progressive shortening. The criteria used for porphyroblast timing can be readily accommodated in terms of deformation partitioning, reactivation of deforming foliations, and a general lack of rotation of porphyroblasts, with the spectacular exception of genuinely spiralling garnet porphyroblasts.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号