Relationship between microstructures and resistance in mafic assemblages that deform and transform
- 1Institut des Sciences de la Terre d'Orléans (ISTO), UMR 7327, CNRS/BRGM, Université d'Orléans, 45071 Orléans, France
- 2Department of Geology, University of Tromsø, Dramsveien 201, 9037 Tromsø, Norway
- 3BRGM, 45060 Orléans, France
Correspondence: Nicolas Mansard (email@example.com)
Syn-kinematic mineral reactions play an important role for the mechanical properties of polymineralic rocks. Mineral reactions (i.e., nucleation of new phases) may lead to grain size reduction, producing fine-grained polymineralic mixtures, which have a strongly reduced viscosity because of the activation of grain-size-sensitive deformation processes. In order to study the effect of deformation–reaction feedback(s) on sample strength, we performed rock deformation experiments on “wet” assemblages of mafic compositions in a Griggs-type solid-medium deformation apparatus. Shear strain was applied at constant strain rate (10−5 s−1) and constant confining pressure (1 GPa) with temperatures ranging from 800 to 900 ∘C. At low shear strain, the assemblages that react faster are significantly weaker than the ones that react more slowly, demonstrating that reaction progress has a first-order control on rock strength. With increasing strain, we document two contrasting microstructural scenarios: (1) the development of a single throughgoing high-strain zone of well-mixed, fine-grained aggregates, associated with a significant weakening after peak stress, and (2) the development of partially connected, nearly monomineralic shear bands without major weakening. The lack of weakening is caused by the absence of interconnected well-mixed aggregates of fine-grained reaction products. The nature of the reaction products, and hence the intensity of the mechanical weakening, is controlled by the microstructures of the reaction products to a large extent, e.g., the amount of amphibole and the phase distribution of reaction products. The samples with the largest amount of amphibole exhibit a larger grain size and show less weakening. In addition to their implications for the deformation of natural shear zones, our findings demonstrate that the feedback between deformation and mineral reactions can lead to large differences in mechanical strength, even at relatively small initial differences in mineral composition.
Mafic rocks constitute a large part of the oceanic crust and may be one of the main components of the lower continental crust (Rudnick and Fountain, 1995). The major constituents of mafic rocks, i.e., pyroxene and plagioclase, are mechanically strong minerals that show crystal plastic deformation only at high temperatures in natural systems (e.g., Rutter and Brodie, 1985; Brodie and Rutter, 1985, 1992). However, there are abundant examples of strongly deformed mafic rocks, even at relatively low temperatures, but invariably these rocks show metamorphic retrogression (Rutter and Brodie, 1985). For instance, concomitant deformation and metamorphism are observed along oceanic detachments, where deep levels of the oceanic mafic crust are exhumed (Harigane et al., 2008; Schroeder and John, 2004). Strongly sheared meta-gabbros are also present in exhumed subduction belts (Imon et al., 2004; Shelley, 1994; Soret et al., 2019) or in large-scale transcurrent shear zones (Jolivet and Miyashita, 1985; Shelley, 1994). In most cases, the decreasing temperature conditions during deformation result in coeval mineral reactions, often causing strong grain size reduction. The coupling between deformation and reaction is therefore essential to understand the process of strain localization, as observed in mafic mylonites (Brodie et al., 1992).
The pyroxenes typically deform by crystal plasticity at high temperatures and high stresses (e.g., Borg and Handin, 1966; Coe, 1970; Coe and Kirby, 1975; Bystricky and Mackwell, 2001; Bystricky et al., 2016). Mechanical data from high-temperature deformation experiments with mafic rocks are relatively scarce (e.g., Dimanov et al., 2003, 2007; Dimanov and Dresen, 2005; Marti et al., 2017, 2018; Mansard et al., 2020), but the existing studies indicate that weakening processes are dependent on the “deformation history”. The study of mylonitic deformation of natural mafic rocks provides insights, at small scale, into the deformation mechanisms and strain localization processes and, at large scale, into the strength of the lower crust (e.g., Rutter and Brodie, 1992; Kanagawa et al., 2008). There are two main mechanisms of rock deformation in the viscous deformation regime: (1) dislocation creep (crystal plasticity; e.g., Paterson, 2013) and (2) diffusion creep. The latter includes grain-scale diffusion creep, whereby diffusive mass transfer either occurs through the volume or phase boundaries of individual grains (e.g., Wheeler, 1992) and is the main strain-producing process, and diffusion-accommodated grain boundary sliding (GBS), whereby diffusive mass transfer adjusts grain shapes and asperities during cohesive, frictionless sliding (e.g., Ashby and Verrall, 1973; Paterson, 1990; Langdon, 2006, and references therein). If a fluid is involved and material is dissolved and reprecipitated, the process is often referred to as dissolution–precipitation creep (DPC). Grain boundary sliding and diffusive mass transfer are both always involved, so the terms diffusion creep and DPC are collective terms involving GBS and diffusive mass transfer. Diffusion creep is a grain-size-sensitive (GSS) deformation mechanism and may operate at low or high temperature, as well as typically at low stresses (e.g., Paterson, 1995).
Many researchers have pointed out the close relationship between strain or reaction-dependent grain size reduction and the activation of GSS creep in a variety of mafic assemblages (e.g., Kruse and Stünitz, 1999; Kenkmann and Dresen, 2002; Baratoux et al., 2005; Kanagawa et al., 2008; Mehl and Hirth, 2008; Menegon et al., 2015; Okudaira et al., 2015; Degli Alessandrini et al., 2017). For this reason, grain size reduction is recognized as one of the most significant mechanisms that controls rheological properties (e.g., Elyaszadeh et al., 2018; Brodie and Rutter, 1987; Bercovici and Ricard, 2012; Montési, 2013, Platt, 2015). Grain-size-controlling processes usually include dynamic recrystallization (e.g., Schmid, 1982; Brodie and Rutter, 1987; Behrmann, 1985; Fliervoet and White, 1995; Vissers et al., 1997) and/or metamorphic reactions (e.g., Rubie, 1983; Fitz Gerald and Stünitz, 1993; Stünitz and Fitz Gerald, 1993; Newman et al., 1999), but while dynamic recrystallization is only considered to have transient mechanical effects (Brodie and Rutter, 1987), a small grain size can be stabilized by new phases in phase mixtures wherein grain growth is inhibited by the pinning of grain boundaries (e.g., Olgaard and Evans, 1986, 1988; Fliervoet et al., 1997; Herwegh et al., 2011; Herwegh and Berger, 2004). Furthermore, phase separation and compositional layering commonly form or develop during crystal plastic deformation (dislocation creep) of minerals. During metamorphic reactions and nucleation of new phases, minerals are spatially rearranged so that fine-grained mixed-phase zones and polyphase shear bands may develop (e.g., Stünitz and Tullis, 2001; De Ronde et al., 2004, 2005; Kilian et al., 2011; Platt, 2015; Mansard et al., 2018, 2020). Such a spatial rearrangement controls the bulk strength of the rock, particularly when these phases have a large mechanical contrast. In particular, the interconnection of weak materials is necessary to induce a significant drop in bulk strength (e.g., Jordan, 1988; Handy, 1994; Dell'Angelo and Tullis, 1996; Holyoke and Tullis, 2006a, b).
The principal objective of this contribution is to study the effect of initial rock composition on the feedback processes between reaction and deformation. To do so, we have performed rock deformation experiments on “wet” assemblages of plagioclase–pyroxene assemblages in a Griggs-type solid-medium deformation apparatus. As representative of the lower crust, the starting material was composed of plagioclase (labradorite; plag) and either Mg-rich orthopyroxene (opx) (from peridotite) or Fe-rich opx (from a granulite-facies anorthosite) in order to investigate the effect of different mineral compositions on rock deformation. In this system, the opx deformation properties are assumed to be the same for Mg- and Fe-rich opx. We also performed deformation experiments on amphibole (amph) + plag and pure amph assemblages at similar conditions to extend the study to typical amphibolite facies conditions. All these assemblages were deformed to varying amounts of strain, including at the early stages of deformation. These early stages can be challenging to access when studying natural cases because of successive overprints of deformation stages. In this contribution, we suggest that viscous strain localization is primarily dependent on the ability of minerals to react and that the feedback between deformation and mineral reactions can lead to large differences in mechanical strength and deformation processes.
2.1 Experimental procedures
2.1.1 Starting material and sample preparation
We have performed a series of shear deformation experiments in two Griggs-type deformation apparatuses at the University of Tromsø (Norway) and at the University of Orléans (France). Experiments were conducted on mineral powders separated from natural materials. Four different starting materials were prepared from different mineral sources: (1) gem-quality labradorite (An60–Ab38–Or2) from Sonora (Mexico) mixed with orthopyroxene (Wo1–En88–Fs11) from Damaping peridote (China), here referred to as Mg-opx; (2) labradorite (An55–Ab44–Or1) mixed with orthopyroxene (Wo2–En62–Fs36) from Hidaka granulite (Japan), here referred to as Fe-opx; (3) amphibole (Mg-rich hornblende; composition available in Table 1) from the Massif Central (France) mixed with Sonora labradorite; and (4) pure Mg-rich hornblende. The pre-separated minerals were crushed in an alumina mortar, then sieved to <100 µm, handpicked, and finally sorted in a distilled water column to obtain grain sizes between 10 and 20 µm. Powders were mixed in a 50:50 vol. % ratio in acetone using an ultrasonic stirrer to avoid density and/or grain size separation (De Ronde et al., 2004, 2005).
To perform experiments, we used a conventional solid-salt, non-coaxial (“general shear”) sample assembly with alumina pistons (Précigout et al., 2018). After adding 0.1 wt. % of distilled H2O, the powder was placed between alumina forcing blocks along a 45∘ precut so that a shear zone ∼ 1 mm thick is formed when the deformation experiment starts (Fig. 1). The assembly was wrapped into a nickel foil 25 µm thick and then inserted into a weld-sealed platinum jacket. NaCl pieces were used as solid confining medium for both the inner and outer furnace assembly. The temperature was measured by S-type (Pt ∕ Pt–Rh) thermocouples centered on the sample. Readers are invited to refer to Pec et al. (2012b) and Précigout et al. (2018) for further details and descriptions of sample assemblies and experimental protocols employed.
2.1.2 Experiments and mechanical data processing
Deformation experiments were conducted at a constant shear strain rate of ∼ 2 × 10−5 s−1 to varying amounts of shear strain (see Table 2 for a summary of experimental conditions), at temperatures of 800, 850, and 900 ∘C, and at a confining pressure of 1 GPa. To bring the samples to the desired pressure–temperature (P–T) conditions, both the σ1 and σ3 pistons are alternatingly advanced between steps of increasing temperature. At the desired P–T conditions, a period of hydrostatic hot-pressing was applied, and the deformation was started by advancing the σ1 piston first through the lead piece (“lead run-in”) to bring it into contact with the upper forcing block (hit point). During the lead run-in stage, the sample is maintained in a more or less isostatic stress state, as the lead protects the sample from becoming deformed. Two series of experiments on Mg-rich opx-bearing assemblages have been performed: one series with a short run-in period and a second one with a longer period (Table 2).
At the end of experiments, samples were quenched to 200 ∘C within 2 to 3 min (∼ 150 to 300 ∘C per minute) so that the deformation microstructures and grain size were preserved. Subsequently, the force and confining pressure were decreased simultaneously to room pressure and temperature conditions. During initial stages of the decompression, the differential stress is kept above the confining pressure (∼ 100 to 200 MPa) to reduce the formation of unloading cracks.
Experimental data were acquired and recorded using catman® Easy and then processed after the experiment with a MATLAB-based program following the “rig” program of Matej Pec (Pec et al., 2016; available at https://sites.google.com/site/jacquesprecigout/telechargements-downloads, last access: 21 March 2020). The hit point is defined by intersecting the run-in and loading curve tangent lines. After this point, several corrections are then applied to consider the rig distortion and changes in thickness and surface due to the sample compaction and piston overlap, respectively. The corrected mechanical data are represented in stress vs. strain graphs from the hit point.
2.2 Analytical methods
Double-polished thick sections (∼ 150–200 µm) of the starting materials were prepared for Fourier transform infrared (FTIR) analysis. Thick sections were prepared from mineral powders for the Mg-rich opx + plag sample and from a natural section of mylonite for the Fe-rich opx + plag sample. For each sample, only grains larger than 100 µm were used for FTIR analysis. Infrared absorption spectra were collected for Mg-opx, Fe-opx, and plag using a Nicolet 6700 FTIR instrument at the ISTO (Orléans, France); 128 scans were acquired for each spectrum at a resolution of 4 cm−1 with a spot size of 40 × 40 µm2. Only grain interiors were analyzed by FTIR. The integrated areas of the absorption bands measured between 3750 and 3000 cm−1 were used to calculate the H2O contents using the calibration of Bell et al. (1995) for opx and of Johnson and Rossmann (2003) for plag.
After the experiments, samples were cut parallel to the shear direction and impregnated under vacuum with low-viscosity epoxy to prepare thin sections. Sample microstructures were analyzed using a scanning electron microscope (SEM – TESCAN MIRA 3 XMU) at ISTO-BRGM (Orléans, France). All SEM analyses have been performed on carbon-coated (20 nm thickness) thin sections at 12–15 kV and a working distance of ∼ 8 mm. Mineral compositions were collected using a CAMECA SX Five electron microprobe analyzer (EPMA) at ISTO-BRGM (Orléans, France). We adopted the following analytical condition: an acceleration voltage of 12–15 kV, a beam current of ∼ 6 nA, and a beam diameter of ∼ 1µm.
Thin sections were additionally polished with colloidal silica and then coated with a thin carbon coat ∼ 2 nm thick for electron backscatter diffraction (EBSD) analysis. The EBSD analyzes were carried out using an EDAX PEGASUS EDS/EBSD system and the OIM DC 6.4 software (manufacturer EDAX; Mahwah, USA) at ISTO-BRGM (Orléans, France). The operating conditions involved an accelerating voltage of 20–25 kV and a working distance of 15–18 mm. Post-acquisition treatments, which include plotting equal-area lower-hemisphere pole figures of amphibole lattice preferred orientation (LPO), were performed using the open-source MTEX toolbox for MATLAB. For the definition of a grain, five adjacent indexed points were required. Texture strength is expressed through the J index and M index (Bunge, 1982; Skemer et al., 2005).
2.3 Microstructural analysis
SEM backscattered electron (BSE) images were used to produce manually digitized grain maps. Grain sizes were measured from these grain maps by using the public domain software ImageJ (http://rsb.info.nih.gov/ij/, last access: 11 March 2020). By extracting the area-equivalent diameter from these maps, the grain size is defined as the diameter of equivalent circular diameter . From these grain maps, the grain shape preferred orientation (SPO) and the modal proportion of phases can be analyzed. In the case in which grain boundaries are indistinguishable within amphibole aggregates, EBSD maps have been processed with MTEX to determine the grain size.
In order to estimate the proportion of phases we used SEM BSE images to produce manually digitized grain maps with the illustrator software when it was possible to distinguish the grain boundaries (e.g., Fe-rich opx + plag assemblages). From these phase maps we could separate the phases with the ImageJ software and estimate their proportion. This is how the amount of amphibole in the Fe-rich opx + plag assemblages is estimated. When it was impossible to distinguish the grains individually, we drew areas that corresponded either to a set of grains of the same phase or to several phases that could not be separated. Some grains are too small to be separated with enough confidence from other grains. For this reason, we have included all reaction products together and have not separated the amphibole from the plagioclase2 and the pyroxene2 in the Mg-rich opx + plag assemblages.
3.1 Mechanical data
Depending on the starting material, the mechanical data differ significantly with respect to each other (Fig. 2). At 850 and 900 ∘C, the Mg-rich opx + plag samples (Fig. 2b–c) are characterized by a pronounced peak stress at shear strains of less than γ ∼ 1, whereas the Fe-rich opx + plag ones do not show a pronounced peak stress but a steady-state flow after yield or, at 900 ∘C, a constant strain-hardening behavior (Fig. 2d). At 800 ∘C, the peak stresses of all opx + plag samples are above the Goetze criterion (Δσ≤Pconf), which provides an empirical upper limit for viscous creep. Above this limit, samples are expected to deform by brittle mechanisms (Kohlstedt et al., 1995). The abrupt stress drop in Fe-rich opx + plag samples at 800 ∘C and short run-in samples at 800 and 850 ∘C indicates that slip has occurred at the interface between the sample and one forcing block (Fig. 2b, d; 557NM, 559NM, and 538NM). The slip is confirmed by sample microstructures and suggests that peak stress might have been higher without the slip event. In contrast, two Mg-rich opx + plag samples at 900 ∘C show a pronounced strain weakening after peak stress. In one case, the sample falls substantially below the Goetze criterion as a result of slip along the forcing block interface and stabilizes around 800 MPa (OR49NM). In the other case, the sample weakens continuously after peak stress and reaches almost steady state for γ ∼ 6.5 (OR41NM). One way to vary the time of reaction in different experiments is to keep the sample at hydrostatic conditions at given pressure and temperature before starting to deform it (long or short run-in periods of the piston). In the experiments with longer run-in periods, the Mg-rich opx + plag assemblages weaken systematically after peak stress. They reach stresses lower than 400 MPa at 850 and 900 ∘C, corresponding to ∼ 64 % (OR38NM) and ∼ 78 % (OR34NM) of the peak stress before reaching a quasi-steady-state shear stress near γ ∼ 6.5 for OR34NM and γ ∼ 7.7 for OR38NM (Fig. 2c). At 850 ∘C, the Fe-rich opx + plag sample behavior is no longer comparable to that of the mixed Mg-rich assemblages, as no weakening occurs after peak stress and a quasi-steady-state shear stress is reached at low shear strain (γ ∼ 2). At 900 ∘C, the sample remains weak but hardens continuously until γ ∼ 5, unlike the other experiments (Fig. 2d).
Compared to the opx + plag assemblages, the amph + plag and pure amph assemblages do not reach the same strength, regardless of the deformation temperature (Fig. 2e). At 800 ∘C, the amph + plag assemblage reaches a peak stress of ∼ 563 MPa and then slightly weakens to ∼ 483 MPa at γ ∼ 5.8. The pure amph assemblages deformed at 800 and 900 ∘C show stress–strain curves with a significant weakening after peak stress at γ ∼ 0.5 to 1.0. However, the sample at 800 ∘C documents a peak stress of ∼ 450 MPa higher than the sample deformed at 900 ∘C.
Our set of experiments reveals two distinct types of mechanical behavior: one that shows a pronounced weakening after high peak stress (Mg-rich opx + plag and pure amph assemblages) and one without weakening (Fe-rich opx + plag and amph + plag assemblages) or even hardening (Fe-rich sample at 900 ∘C, 532NM; Fig. 2d) but that deforms at considerably lower stresses (all Fe-rich samples; Fig. 2d).
3.2 Mineral reactions and microstructures
Mineral reactions occur pervasively in deformed portions of the samples – there is a clear correlation between strain and reaction progress (Mansard et al., 2020). The pervasive occurrence of mineral reactions induces substantial changes in the grain size and spatial distribution of phases. This is particularly prominent in the development of shear bands within the deformed assemblages. For the sake of clarity, the term “bulk shear zone” refers to the whole sample deformed between the two alumina forcing blocks, while the term “shear bands” refers to a localized zone of variable thickness of high shear strain accommodation within the bulk shear zone. In addition, the term “high-strain zone” is also used to refer to the domain of coalescence of fine-grained shear bands that are connected as a more or less single zone through the bulk shear zone.
In the two main systems studied, the Fe-rich and Mg-rich opx + plag assemblages, the opx deformation features are the same. In these deformed assemblages, similar reaction products are observed, with the formation of amphibole, pyroxene, plagioclase, and, to a minor extent, quartz.
In these assemblages the mineral compositions were analyzed if the grain size was sufficiently large because in mixture zones, individual grains are typically too small to be analyzed. Thus, the very small grain size precludes an exact compositional analysis of the actual reaction products.
The Mg-rich opx + plag assemblages deformed to high shear strain are characterized by the development of low-strain zones and a high-strain zone in the center of the bulk shear zone (Fig. 3a). Mineral reactions are localized within this single connected zone that traverses the sample from one interface of the forcing block to the other (at 850 ∘C; Fig. 3a) as fine-grained mixed zones and C-geometry shear bands subparallel to the shear plane (or forcing block interface; Figs. 4a–c, 5a–f). The C-type shear bands are mainly composed of fine opx2, plag2, and amph that are present as equant grains; their identification is possible by EDS analysis in the SEM (Fig. 4). The original large grains of plag1 and opx1 form porphyroclasts embedded in a mixture of reaction products (Fig. 3a). In contrast to the high-strain zone, the reaction products in the low-strain zones usually occur as coronas or rims surrounding opx1 clasts (Fig. 4d–e). The main difference between the assemblages deformed at 850 and 900 ∘C is the degree of strain localization. At 850 ∘C, strain is highly localized in a ∼ 250–300 µm wide single zone, while strain is more distributed throughout the sample at 900 ∘C, and therefore local strain appears lower. Otherwise, the microstructural features are similar to those of the high-strain zone (Fig. 4f–g).
At the scale of the bulk shear zone, both the Fe-rich opx + plag and amph + plag assemblages are banded and show a locally developed, nonconnected mylonitic foliation characterized by the development of amph-rich shear bands and tails at opx1 porphyroclasts (Fig. 3b–c). These bands wrap around the original and large opx1 porphyroclasts in Fe-rich opx + plag assemblages (Fig. 3b) and in amph + plag assemblages (Fig. 3c). The reaction products in shear bands alternate with aggregates of original grains. The mylonitic foliation is better defined in the amph + plag assemblage because of more pervasive deformation and strain localization (Fig. 3c). The shear bands are more heterogeneously distributed in the Fe-rich opx + plag assemblage deformed at 850 ∘C (Fig. 3b). This results in the development of an anastomosing network of amph-rich shear bands that are less connected (Fig. 3b), without forming any throughgoing high-strain zone (Fig. 3a).
The reaction products in the Fe-rich opx + plag assemblages contain less opx2 than the Mg-rich opx + plag assemblages, and amph + plag2 represents the main reaction products (Figs. 5g–j, 6). From site to site in the Fe-rich opx + plag sample deformed at 850 ∘C, a variable proportion of opx and plag has reacted. Mineral reactions preferentially occur in strongly deformed areas and form only locally interconnected separate aggregates and shear bands consisting of amph + opx2 ∕ cpx or plag (Fig. 6a–b), while in less deformed areas, the reaction products typically occur as thick rims at grain boundaries of extensional sites of opx1 and plag1 clasts (Fig. 6c). The amph grains are elongated and typically form tails extending from opx1 porphyroclasts (Fig. 6b, c). At 900 ∘C, the Fe-rich opx + plag sample is more homogeneously deformed with a similar distribution of reaction products as observed at 850 ∘C (Fig. 6d–e).
The amph + plag assemblage (Figs. 5k–l, 7a–c) deformed at 800 ∘C produced a large quantity of reaction products composed of amph2, plag2, clinopyroxene (cpx), and minor zoisite (zo). There is a spatial relationship between amph and cpx, the latter occurring as small grains, predominantly around amph porphyroclasts (amph1) mixed with small grains of new amph2 (Fig. 7a–b). Unlike Fe-rich opx + plag assemblages, the shear bands involve several phases (amph and cpx) in the amph + plag assemblages (Fig. 5k–l). Regarding the pure amph assemblages deformed at 800 and 900 ∘C (Figs. 5m–n, 7d–e), mineral reactions are homogeneously distributed with the formation of amph2, cpx and minor zo, quartz (qtz), and garnet (grt). Reaction induces the development of mixture zones of amph2 and cpx and unmixed zones of grt, zo, and qtz (Fig. 5m–n). No melt was detected in the microstructures.
3.3 Chemical composition
The chemical composition of new grains is systematically different compared to that of the original ones. In each assemblage, the original plag1 composition is An55–60. These grains are rimmed by more albite-rich plag2 (An38–45 in Fe-rich opx + plag samples, An48–55 in Mg-rich opx + plag samples; Figs. 4, 5, 7, 8a–a′). The fine grains in mixed zones are also more albite-rich than the starting plag1 (Fig. 8a–a′). For the opx2, the ferrosilite content increases with respect to the original opx1, regardless of the original opx1 composition (Fig. 8b). The XMg ratio ranges between ∼ 0.85 and ∼ 0.89 in the Mg-rich opx2 and between ∼ 0.64 and ∼ 0.68 in the Fe-rich opx2 (with XMg = Mg ∕ (Mg+Fe2+)). The newly formed cpx in the amph + plag and pure amph assemblages has an augite composition (Fig. 8b). It is worth mentioning that the composition of the main reaction products (orthopyroxene and plagioclase) in the Fe-rich opx + plag assemblages are farther away from the starting composition compared to those of the Mg-rich opx + plag assemblages.
The composition of the original amph used in both amph + plag and pure amph experiments is not constant and varies in the magnesio-hornblende field (Fig. 8c). The newly formed amph for all assemblages has a composition ranging from magnesio-hornblende to tschermakite (Fig. 8c). There are nonetheless four chemically distinct populations of new amph, depending on the composition of the starting mixture, as shown in the plot of Si vs. XMg (Fig. 8c).
3.4 OH content and thermodynamic modeling
Fe-rich opx and plag grains from Hidaka granulite show a broad and asymmetric infrared (IR) water absorption, with a maximum amplitude at ∼ 3580–3590 cm−1 (Fig. 9). The average H2O contents (ppm H2O by weight), calculated between 3750 and 3000 cm−1, are 451 ± 35 ppm for Fe-rich opx and 226 ± 24 ppm for plag. In contrast, there are no H2O IR absorption bands for Mg-rich opx grains from Damaping peridotite and plag grains from Sonora (Fig. 9).
Pseudo-sections for the Mg-rich opx + plag and Fe-rich opx + plag assemblages were calculated for different H2O contents in the simplified but representative system of our experiments (Na2O–CaO–FeO–MgO–Al2O3–SiO2–H2O) using the Perple_X 6.6.8 package (Connolly, 2009) combined with the updated database of Holland and Powell (1998) and the following solution model: amphibole (Dale et al., 2005), orthopyroxene (Powell and Holland, 1999), garnet, clinopyroxene (Holland and Powell, 1998), and feldspar (Newton et al., 1980).
At the experimental P–T conditions, plag, opx, amph, qtz, cpx, and grt are expected to be stable phases in the Fe-rich opx + plag assemblage; plag, opx, amph, and qtz are expected to be stable phases in the Mg-rich opx + plag assemblage. The modeling of the Fe-rich opx + plag assemblage agrees rather well with the observed reaction product assemblage, whereas the modeling of the Mg-rich opx + plag assemblage does not match the observed reaction product assemblage.
3.5 Initial shear localization
In the Mg-rich opx assemblages, shear deformation is initially localized between the boundaries of original opx1 and plag1, where the nucleation of fine-grained tails of mixed phases that define the general shear foliation occurs (Fig. 10a). Everywhere, the new grains of opx2 are pervasively mixed with plag2 and amph grains (Fig. 10a). In contrast, the initial strain localization in the Fe-rich opx + plag assemblages predominantly forms amph + less opx2 shear bands or tails extending from opx1 porphyroclasts. Amph + opx2 nucleates at boundaries between opx1 and plag, preferentially at extensional ends of opx1 grains, defining σ-type tails that stay connected to the original opx1 grains (Figs. 6b, 10b). In the samples of amph + plag starting material, the reaction products cpx + amph2 + plag2 + zo nucleate at the boundaries between original amph1 and plag1 grains (Figs. 8a–c, 10c). Amph2 + cpx tends to form mixed layers that surround and stay connected to amph1 porphyroclasts (Figs. 7a, b, 10c), while plag2 + zo forms separate aggregates that tend to surround the amp2 + cpx aggregates (Figs. 8c, 10c). Both types of reaction products organize into an anastomosing network of thin amph2 + cpx and plag2 + zo in which layers become progressively more parallel to the shear plane (Fig. 10c).
To summarize, two types of reaction products and related microstructures form in the two different starting material assemblages: (1) in the Mg-rich opx + plag samples, fine-grained phase mixtures are produced by nucleation of reaction products and localize into more or less contiguous bands approximately parallel to the forcing block interface, i.e., the shear plane. (2) In the Fe-rich opx + plag and amph + plag samples, predominantly amph + opx2 and plag2 + zo shear bands and tails develop from opx1 porphyroclasts and stay connected with these. While fine-grained reaction products in case (1) produce C-type shear bands, the sample fabrics of case (2) develop S–C'-type shear band geometries in strongly deformed areas, the C' bands of which are predominantly formed amph and plag2.
3.6 Abundance and grain size of reaction products
The transition from low-strain to high-strain zones in the Mg-rich opx + plag assemblages is accompanied by a significant grain size reduction (mode of the distribution as the dominant grain size) from ∼ 15 µm to ∼ 0.2 µm (Fig. 11a). The high-strain zones concentrate most of the reconstituted material with roughly ∼ 65 % and locally more than ∼ 80 % of reaction products. This proportion is substantially higher compared to that in the low-strain zones (∼ 25 %), where no mixed-phase layers develop. Similarly, in the mixed-phase reacted zones of the original pure amph assemblages, the new grains are very small (∼ 0.6 µm) and they represent nearly ∼ 61 % of the assemblage (Fig. 11b). The amph grain size is also reduced in Fe-rich opx + plag assemblages compared to the starting material (Fig. 11c), but the reaction products are not as pervasively mixed and show a grain size that is approximately 1 order of magnitude larger (1.9 µm) than that in the Mg-rich opx + plag samples (0.2 µm; Fig. 11a). In the 850 ∘C sample, the reaction products are largely connected to opx1 porphyroclasts, and their proportion increases with increasing proximity to higher-strained portions of the shear zone (∼ 26 %). In these Fe-rich opx + plag assemblages, amph is the main reaction product (∼ 17 %). In contrast, the quantity of reaction products at 900 ∘C remains roughly constant at approximately ∼ 29 % and there is no strain gradient. Finally, in the amph + plag starting material, the nucleation in amph-rich shear bands is more extensive (∼ 36 %) and the grain size of cpx reaction products decreases to ∼ 1.3 µm (Fig. 11d).
3.7 Analysis of SPO and amphibole LPO
Amph formed during deformation of Fe-rich opx + plag assemblages exhibits a distinct SPO oriented at ∼ 30∘ to the shear direction (Fig. 12a–b). These amph aggregates occur as reaction rims around original opx1 grains and form in strongly deformed areas partly interconnected to aggregates that define S–C' fabrics (Fig. 12c). Plag2 and opx2 also reveal a well-defined SPO similarly oriented to amph. The preferred orientation of amph forms an angle of ∼ 30∘ with the shear plane, slightly greater than that of plagioclase and original opx (Fig. 12a–b). In addition, the amph reaction seams in high-stress sites of opx porphyroclasts are significantly thinner compared to those in low-stress or extensional sites, indicating that amph grows preferentially in strain shadows. In the higher-strained portions of the shear zone deformed at 850 ∘C, the foliation defined by amph-dominated layers rotates and is now well-oriented subparallel to the boundaries of C' shear bands or the shear plane (Fig. 12c). Within these shear bands, amph grains show a moderate LPO with  axes aligned subparallel to the boundaries of C' shear bands and poles (100) normal to the shear plane (Fig. 12c–d). In the mixed zones of Mg-rich opx + plag samples, the fine grains are characterized by equant grain shapes with an aspect ratio of 1.23 (Fig. 13) and a weak preferred orientation either parallel or at 45∘ to the shear plane (Fig. 13).
4.1 Nucleation, grain size reduction, and phase mixing
In this study, the deformation of two-phase assemblages is accompanied by the nucleation of new grains with (1) systematic differences in composition between new grains and parent grains (Fig. 8), (2) significant grain size reduction (Fig. 11), and (3) a new spatial arrangement of reaction products into fine-grained mixture zones (Fig. 5). Based on these observations, we infer that grain size reduction and phase mixing both result from the nucleation of new phases (e.g., Kruse and Stünitz, 1999; Kenkmann and Dresen, 2002; Kilian et al., 2011; Linckens et al., 2015; Platt, 2015; Précigout and Stünitz, 2016; Mansard et al., 2018). Despite common features, our samples have developed two sets of microstructures distinguished mainly by the size and spatial arrangement of reaction products and the degree of phase mixing. We discuss these differences below.
In the Mg-rich opx + plag assemblages, a strain gradient is clearly observed and expressed by the development of low- and high-strain zones (Figs. 3a, 4). This is particularly notable in the sample deformed at 850 ∘C. The transition from a low- to high-strain zone is accompanied by drastic grain size reduction and an increase in reaction products within localized mixed zones by a factor of more than 2 (Fig. 11a). The grain size of reaction products in the mixed high-strain zones (∼ 0.2 µm) is about 2 orders of magnitude smaller than the opx grain size of the starting material and the low-strain regions (∼ 10–20 µm; Fig. 11a). Similarly, an extensive nucleation of reaction products within mixed-phase zones is documented in the pure amph starting material (Fig. 7d–e). The reaction products are also very small, far below 1 µm (∼ 0.6 µm; Fig. 11b). As documented in Mansard et al. (2020), such a correlation between deformation, mineral reactions, and related grain size reduction in Mg-rich assemblages has been also observed in experimentally deformed fine-grained gneiss (Holyoke and Tullis, 2006a, b), plagioclase + olivine samples (De Ronde et al., 2005; De Ronde and Stünitz, 2007), and plagioclase + pyroxene samples (Marti et al., 2018).
In the Fe-rich opx + plag assemblages, amph is by far the more abundant product, and there is less phase mixing (Fig. 5g–j). The reaction products consist mainly of thick rims around the opx1 (Fig. 6c) or amph-dominated tails and shear bands (Fig. 6a–b). The abundance of reaction products increases with increasing proximity to strongly deformed portions of the shear zone. The reaction products have a grain size about 1 order of magnitude smaller than the starting material (∼ 1.9 µm) but 1 order of magnitude larger than the mixed reaction products in the Mg-rich opx + plag assemblages (Fig. 11). Similarly to the Fe-rich opx + plag assemblages, amph-rich shear bands have developed in the amph + plag assemblages (Fig. 7a–c), and the grain size, reduced by about 1 order of magnitude compared to the starting material, is 1 order of magnitude larger than in the mixed zones in the Mg-rich opx + plag assemblages (Fig. 11).
Two types of major microstructures can be distinguished: (1) in one case, intense grain size reduction by 2 orders of magnitude is produced by nucleation of reaction products in pervasive and layered phase mixtures (Mg-rich opx + plag and pure amph starting materials); (2) in the other case, the reaction products are less pervasively mixed and develop aggregates that are dominated by amph extending from opx porphyroclasts. These aggregates have a grain size 1 order of magnitude larger than (1) and may form C' shear bands or tails connected to opx porphyroclasts.
4.2 Deformation processes
As the reaction products in Mg-rich opx + plag samples occur in pervasively mixed high-strain zones and layers with equant grains of a size far below 1 µm, the dominant deformation mechanism is inferred to be one of grain-size-sensitive creep. The absence of well-developed layering of separate phases and absence of strong elongation of individual grains during GSS creep suggest that grain boundary sliding makes the dominant kinematic contribution to the finite strain (Rachinger sliding; e.g., Langdon, 2006). Such a deformation mechanism should probably be termed diffusion-accommodated grain boundary sliding (GBS) or, more generally, as a fluid has been present and solution precipitation is the probable transfer mechanism, dissolution–precipitation creep (DPC). The pronounced weakening of the samples in combination with localization of strain made strain rate stepping tests problematic in our samples, so the deformation mechanism is primarily identified based on microstructures. At first, the microstructures are similar to other cases in which such deformation mechanisms have been identified (e.g., Marti et al., 2017, 2018; De Ronde et al., 2005; Stünitz and Tullis, 2001; Holyoke and Tullis, 2006a, b; Tasaka et al., 2016, 2017; Getsinger and Hirth, 2014). The transition from low- to high-strain zones in the Mg-rich opx + plag assemblages marks the transition from a two-phase aggregate with strong phases (starting material) potentially deforming by dislocation creep to a material deforming by grain-size-sensitive mechanisms, including DPC and/or GBS (e.g., Boullier and Gueguen, 1975; Kerrich et al., 1980; Schmid, 1982; Brodie and Rutter, 1987; Kilian et al., 2011), whereby samples deform by low bulk stresses (Fig. 2).
The spatial arrangement of mineral phases in mixed aggregates by nucleation impedes grain growth (e.g., Olgaard and Evans, 1986, 1988). As documented by Mansard et al. (2020), the mixing of mineral phases is homogeneous and starts from peak stress, in favor of GBS accommodated by DPC (e.g., Fliervoet et al., 1997; Kilian et al., 2011; Linckens et al., 2011, 2015). The original plag1 almost completely disappeared in the high-strain zones of Mg-rich samples, while the original opx1 remains as small clasts embedded in fine-grained mixed zones (Figs. 3a, 4a–c). Although the opx1 is still present, its proportion, aspect ratio, and size decrease compared to that in the low-strain zones (Fig. 4). These microstructures suggest that opx1 grains act as rigid particles affected by dissolution and, together with plag1, represent a source of elements required for the development of the ductile fine-grained zone deformed by diffusion-accommodated GBS.
In the Fe-rich opx + plag samples, the deformation mechanism is also assumed to be predominantly DPC, as demonstrated by the fact that (1) the samples deform at lower stresses well below the Goetze criterion, and (2) the microstructures that consist of elongate mineral aggregates of reaction products dominantly grow in the extension direction, shear bands, or dilatant sites (Figs. 2, 6, 12). The nucleation of reaction products, anisotropic growth, and local dilatancy could also require the operation of GBS (Lifshitz sliding; Paterson, 1990; Langdon, 2006). The grain sizes of the reaction products in the Fe-rich opx + plag samples are larger, resulting in higher flow stresses compared to the final stresses – after weakening – of the Mg-rich opx + plag samples (Figs. 2, 11; e.g., Mansard et al., 2020).
In addition, the amphibole fabric displays a fairly moderate but consistent LPO with  axes aligned subparallel to the boundaries of C' shear bands (Fig. 12). This type of LPO is typical for naturally deformed amphibole (e.g., Berger and Stünitz, 1996). It is generally accepted that significant LPO of minerals is attributed to viscous deformation dominated by dislocation creep (e.g., Nicolas and Christensen, 1987; Knipe, 1989; Wenk and Christie, 1991). However, an increasing number of studies have found that LPOs can develop without the dominance of dislocation creep, as shown in olivine (e.g., Sundberg and Cooper, 2008; Miyazaki et al., 2013, Précigout and Hirth, 2014), plagioclase (e.g., Barreiro et al., 2007), and amphibole (e.g., Getsinger and Hirth, 2014). The amph LPOs presented here are similar to the ones documented in experimentally deformed amphibolite by Getsinger and Hirth (2014) and to those of natural samples deformed at lower crustal conditions (e.g., Berger and Stünitz, 1996; Getsinger et al., 2013; Menegon et al., 2015; Okudaira et al., 2015). These studies have demonstrated that oriented grain growth of pyroxenes and amphibole can lead to consistent amphibole–pyroxene LPO, even though diffusion creep is the dominant deformation mechanism. We thus interpret the presence of amphibole LPO in our samples as resulting from oriented growth with the fastest growth direction (c axis) in the flow direction. This supports an important contribution of metamorphic re-equilibration, chemical transport, and hence DPC in the development of amph mylonitic foliation in the Fe-rich and amph + plag assemblages (e.g., Bons and Den Brok, 2000; Berger and Stünitz, 1996).
4.3 Formation of polyphase vs. monophase shear bands and implications for the degree of rheological weakening
4.3.1 Polyphase shear bands
In Mg-rich opx + plag assemblages at 850 ∘C, the mixture zones are strongly connected to form a single high-strain zone that traverses the sample through the center from one interface of the forcing block to the other (Fig. 3). The deformation microstructures at early stages of our experiments suggest that phase mixing occurs at phase boundaries with the nucleation of small equant grains in polyphase aggregates and layers (Fig. 10a). These polyphase aggregates, into which strain is partitioned, are composed of opx2, plag2, and amph. It has been documented by many authors (e.g., Kruse and Stünitz, 1999; Kenkmann and Dresen, 2002; Linckens et al., 2015) that phase mixing can be produced by the nucleation of new phases within clast tails. The effect of mixing on grain size is significant as grain growth is impeded by the nucleation of second phases and preserves a small grain size in the mixture zones (Fig. 11a), producing stable microstructures (e.g., Olgaard and Evans, 1986; 1988; Olgaard, 1990; Stünitz and Fitz Gerald, 1993; Herwegh and Berger, 2004; Warren and Hirth, 2006; Farla et al., 2013). The opening of cavities and the formation of dilatant sites in which material can nucleate (e.g., Fusseis et al., 2009; Platt, 2015; Menegon et al., 2015; Précigout and Stünitz, 2016; Précigout et al., 2017; Gilgannon et al., 2017) may be additional factors to promote mixing and lead to the stabilization of small grain sizes.
4.3.2 Amphibole-dominated σ tails and shear bands
In the Fe-rich opx + plag samples, the majority of reaction products occurs in strongly deformed portions of the shear zones, indicating a close relationship between deformation and mineral reactions (Fig. 3b). These portions are not characterized by the development of intensely mixed zones with C-type mylonite geometries, as in the Mg-rich opx + plag assemblages. Instead, deformation and reaction have induced the formation of shear bands or, more frequently, σ tails at the tip of elongated amph or amph + opx2 (Figs. 5, 6). These tails stay connected with the original porphyroclasts, forming S–C or S–C' fabrics. Similarly, the amph + plag assemblage is banded and shows a subhorizontal mylonitic foliation characterized by the development of amph-rich shear bands (Fig. 3c). These shear bands have a similar geometry as those of the amph + opx2 bands and σ clasts of the Fe-rich opx + plag assemblages.
4.3.3 Effects of shear band interconnection on the degree of rheological weakening
Shear bands connect differently depending on the composition of the starting material. In the Mg-rich opx + plag samples, strain tends to produce mixed and connected fine-grained bands with C-type geometry in high-strain zones (Figs. 3a, 4, 10a, 11a). This gave rise to the development of a single throughgoing high-strain zone that probably contributed to strongly weakening the samples after peak stress (Figs. 2, 3a). And the samples are so weak that we consider the fine-grained aggregate of reaction products to be sustaining almost the whole sample strength. In contrast, the Fe-rich opx + plag and amph + plag mixtures tend to form clusters and only locally connected amph-rich σ tails at porphyroclasts (S–C- or S–C'-type geometries; Figs. 3b–c, 5g–l, 6, and 10b). When the shear bands and tails of clasts are only partially connected or nonconnected, there is no peak stress and hence no subsequent weakening (Fig. 3b; Fe-rich opx + plag assemblages). This feature may be caused by two aspects: (1) the absence of highly connected aggregates of reaction products and (2) the fact that reaction products have a larger grain size and are less intensely mixed so that GSS creep occurs at lower strain rate. The connectivity of the reaction products appears to also be affected by their geometry; the fine-grained C-type bands are parallel to the shear plane and seem to connect much more easily than the local S–C- and S–C'-type tails and shear bands.
The fact that the connectivity of weak zones has a major effect on the bulk sample strength has been documented by, e.g., Pec et al. (2012a, b, 2016), Palazzin et al. (2018), and Richter et al. (2018) and is definitely a major rheological factor in these mafic samples. However, in addition to the connectivity, we also documented different microstructures in the weak parts of each sample, pointing to a difference in GBS–DPC mechanisms. The less intensely mixed layers, tails, and shear bands in the Fe-rich assemblages display higher aspect ratios of the reaction products, i.e., more fiber-like grains (Figs. 6c, 10b, 12a–b). These microstructures constitute a type of DPC that tends more towards grain-scale DPC, whereby ideally (in the end-member case) the grain shapes would reflect the finite strain, and grain boundary sliding is more a type of Lifshitz sliding. We cannot consider the Fe-rich opx + plag samples to be representative of the end-member case, but they approach this situation far more than the fine-grained, well-mixed mylonitic bands of equant grains in Mg-rich opx + plag samples (Figs. 4a–b, 13), wherein DPC is probably dominated by GBS or Rachinger sliding. The combination of relatively fast strain rates in the fine-grained layers and strong connectivity of the reaction product zones causes the pronounced weakening in the Mg-rich opx + plag samples, emphasizing the importance of grain size for material strength (Mansard et al., 2020). Such expected higher strain rates in aggregates dominated by Rachinger sliding have been pointed out by Paterson (1990).
4.4 OH speciation and concentration in the starting material
Our absorption spectra have been compared with reference spectra available for plagioclase (Johnson and Rossmann, 2003, 2004; Johnson, 2006) and orthopyroxene (Skogby, 2006) in the literature. While the IR spectra we obtained in plagioclase and opx are very similar to one another, they strongly differ from the reference spectra, which correspond to structural OH or H2O, i.e., to molecules with specific position and orientation in the structure of the host mineral. The spectra in plagioclase bear the largest similarities to reference measurements of fluid inclusions and alteration products (Johnson and Rossman, 2004), i.e., OH or H2O molecules not structurally bound to the host solid. This interpretation is also favored by the very similar shape of the spectra in plag and opx (Fig. 9), whereas structural OH or H2O in these minerals yields different spectra.
According to this interpretation, the calibration coefficient for the H2O content should be different from that of the mineral-specific ones we have used. However, using the general coefficient from Paterson (1982) would not significantly affect the estimates of H2O concentration in the starting material: the integrated absorption coefficient used in Fig. 9 is 80 600 L ∕ (mol H2O cm2) for opx (Bell et al., 1995) and 107 000 L ∕ (mol H2O cm2) for plag, i.e., relatively similar to the estimate of 82 200 L ∕ (mol cm2) for quartz and other silicates (Paterson, 1982).
Bearing in mind these limitations, the amount of H2O initially present in the minerals of the Fe-rich system is of the order of 451 ppm for pyroxene and 226 ppm for plagioclase, whereas it is effectively zero in the Mg-rich system. The total amount of H2O in pyroxene and plagioclase in the Fe-rich system is ∼ 677 ppm, i.e., more than half with respect to the addition of H2O to the powder. The initial amount of H2O estimated by FTIR is a lower bound as only grain interiors were analyzed by FTIR, while crushed polycrystalline aggregates include grain boundary area with additional adsorbed H2O (Palazzin et al., 2018). In summary, it is estimated that the total amount of H2O in the Fe-rich system is ∼ 50 % higher than that in the Mg-rich system.
4.5 Role of H2O availability in reaction
In the Fe-rich opx + plag samples, a large amount of amph is formed with a minor amount of opx2, whereas in the Mg-rich opx + plag samples, the nucleation of a new opx2 is more abundant. The thermodynamic modeling of the Fe-rich opx + plag system has produced a result similar to that of Okudaira et al. (2015) as an extension to higher pressures and temperatures that is rather consistent with the observed phase compositions, although the predicted garnet was not observed, and cpx is of lower abundance than predicted by the model. However, it was not possible to model the observed reactions in the Mg-rich opx + plag system in terms of phase compositions. The reason for the inadequate modeling is most likely the somewhat inadequate activity–composition relation in the Mg-rich system. Due to this issue, it is impossible to calculate differences in free energy between the two systems as a possible explanation for the different reaction kinetics.
Another difference between the two starting materials is the higher content of H2O in the Fe-rich system. Considering that amphibole contains 2 wt. % of H2O, the amount of H2O required to form 17 % of amphibole would be 3400 wt. ppm, which is a bit higher than the total amount of H2O present in the sample. Our estimation of 17 % amphibole content is also rough. In any case, it is probable that a large amount, if not all, of the H2O is used up by amphibole formation, even though the total amount of H2O in the Fe-rich system is greater to begin with. Conversely, the amount of amphibole formed in the Mg-opx + plag assemblage is subordinate so that, despite a lower total amount of H2O in the starting material, there is probably free H2O present in the Mg-rich system. It could be speculated that the presence of more H2O in the grain boundary region could lead to a more disperse nucleation of reaction products in the Mg-rich system.
4.6 Influence of reaction on material strength
4.6.1 Behavior at the onset of deformation: peak strength
Considering that the rheological behavior is strongly controlled by the reaction products, it is inferred that the Fe-rich opx + plag assemblages do not develop a peak stress behavior and initially deform at lower stresses than the Mg-rich opx + plag assemblages because in the Fe-rich assemblages reaction products nucleate faster than in the Mg-rich assemblages at early stages of the experiment (Figs. 2b–d, 14). We do not have samples of the same low strain for Mg-rich and Fe-rich compositions, but OR61 and 557NM (Fig. 2) can be compared as approximately similar strain samples. The Mg-rich material shows a slightly lower initial quantity of reaction products. The faster nucleation of reaction products in Fe-rich samples is consistent with the recent study of Mansard et al. (2020), showing that for samples wherein reaction products nucleate at an early stage with respect to the onset of deformation, the peak strength is lowered. The system that reacts faster is the Fe-rich one, which contains a greater concentration of H2O. This water is present inside the grains of the starting material, whereas the added water is located along the grain boundaries. These differences suggest that the presence of H2O in inclusions or aggregates inside grains may have triggered the onset of hydration reactions so that, possibly, the higher initial content in H2O and its location inside grains in the Fe-rich system may have had a positive effect on the kinetics of reaction. Microcracking is common in opx grains, so H2O initially stored in the grains may easily become available for reactions during deformation, as observed in Palazzin et al. (2018). The reactions commenced earlier in the Fe-rich system, presenting a weakening agent in the early stages of the deformation. The fact that sample strength is directly related to H2O content, such as in H2O weakening in olivine and quartz, is very unlikely because crystal plasticity does not contribute significantly as a deformation mechanism.
4.6.2 Behavior at large strain
During later stages of our experiments, the highest proportion of reaction products and the smallest grain size are documented for the Mg-rich opx + plag samples (Figs. 11, 14), which also record a far more pronounced weakening with respect to the Fe-rich samples (Figs. 2, 14). The phase mixing and fine grain sizes of the reaction products in Mg-rich opx + plag samples cause greater strain partitioning and suggest a faster nucleation rate after peak stress, even though the Fe-rich opx + plag samples react faster at early stages of experiment (Figs. 8, 14). Deformation and reaction products are strongly localized and connected in high-strain zones of the Mg-rich opx + plag assemblages (Figs. 3a, 10a), whereas the reaction products in the Fe-rich opx + plag samples are poorly connected or nonconnected (Figs. 3b, 10b). In the case in which the viscosity of the reaction products is very low (fine-grained mixture zones in the Mg-rich opx + plag) compared to the starting material, the reacting domains tend to connect much better during the deformation (Fig. 14). It has been demonstrated that deformation enhances the kinetics of mineral reactions (De Ronde and Stünitz, 2007; Mansard et al., 2020) so that the significant localization of deformation in the Mg-rich opx + plag samples may account for the more advanced reaction progress in those samples. In contrast, if the reaction products are stiffer – in Fe-rich opx + plag samples, amphibole appears to be one of the strongest silicates (Brodie and Rutter, 1985; Berger and Stünitz, 1996) – or harden during the reaction (see Fe-rich opx + plag at 900 ∘C; Fig. 2d), the feedback effect of enhancing reaction kinetics appears to be limited and no weakening is observed (Fig. 2). Therefore, the viscosity of the Fe-rich opx + plag and amph + plag assemblages is related to their ability to transform and connect.
The reason why the reaction products in Mg-rich samples characterized by fine-grained layers that do not stay attached to the original opx1 clasts is not clear yet, but this might be related to the difference in the amount and distribution of H2O. Indeed, in the Fe-rich system, the reaction products are dominated by a single-phase material, i.e., amphibole (Fig. 6). In contrast, although the very small grain size did not allow for any quantitative estimates of the Mg-rich reaction products, much more phase mixing occurs in the latter. The difference in the nature and proportion of reaction products between Fe- and Mg-rich systems is a major control factor for their later resistance evolution during connectivity and reaction progress. This situation illustrates that substantially more work is needed to understand the relationship between mineral reaction and mechanical behavior.
4.7 Geological application
According to the results of this study, the rheological behavior of two-phase mixtures of mafic composition is dependent on mineral reactions, as reactions can trigger strain localization and weakening, even at low shear strain. In two different starting materials, the reactions coupled with dissolution–precipitation creep (DPC) in combination with grain boundary sliding allow the mafic assemblage to be deformed. Without mineral reactions, the mafic assemblage of pyroxene and plagioclase would be too strong to be deformed by dislocation creep at the applied strain rates (Mansard et al., 2020). This situation is the same in naturally deformed rocks: below ∼700 ∘C, pyroxene and plagioclase assemblages do not show significant crystal plastic deformation (e.g., Brodie and Rutter, 1985, 1992). The partly extensive deformation of mafic rocks at lower or higher metamorphic grades appears to be dependent on mineral reactions, which can induce the development of rheologically weaker phases, on the formation of fine-grained aggregates deforming by GSS creep, or on both (e.g., Brodie and Rutter, 1985; Brodie et al., 1992; Handy and Stünitz, 2002; Brander et al., 2012; Okudaira et al., 2017; Degli Alessandrini et al., 2017).
At low shear strain and identical P–T conditions, the small difference in mineral reactions between the Fe-rich opx + plag and Mg-rich opx + plag assemblages induces clear differences in mechanical strength at peak stress and during subsequent weakening. These observations are crucial as shear zones are known to represent preferential regions for mineral reactions to occur, either owing to deformation (e.g., Brodie, 1980) or to the presence of fluids (e.g., Etheridge et al., 1983) during protracted shearing (e.g., Brodie, 1980; Philippot and Kienast, 1989; Newman et al., 1999). Thus, local spatial variations in mineral reactions can induce gradients in deformation due to sufficient differences in the mechanical behavior to localize strain (e.g., Holyoke and Tullis, 2006a, b). In addition, our observations suggest that the mechanical strength at peak stress is controlled by the ability of the material to react and connect to the weak material, not necessarily by the strength of the reaction products. In fact, the Fe-rich opx + plag assemblages produce intrinsically stronger reaction products (more amphibole) than the fine-grained mixed aggregates and layers in the Mg-rich opx + plag assemblages, and yet Fe-rich opx + plag assemblages are weaker at low shear strain because they react faster. It is speculated that this difference in reaction kinetics is in part controlled by the amount of H2O present. The higher H2O content in the Fe-rich opx + plag assemblages may have had a positive effect on the kinetics of reaction. This aspect of the influence of H2O availability on the strength of materials is important because shear zones have long been recognized as a preferred locus for fluid migration (e.g., Austrheim, 1987; Newton, 1990; Selverstone et al., 1991; Gueydan et al., 2004; Angiboust et al., 2011), particularly due to the development of syn-kinematic porosity resulting from dilatancy at grain boundaries (Tullis et al., 1996), creep cavitation (Fusseis et al., 2009; Menegon et al., 2015; Précigout and Stünitz, 2016; Précigout et al., 2019), or from dehydration reactions and associated fracturing (Plümper et al., 2017).
Our results suggest that small initial differences in mineral reactions in natural materials can trigger strain localization and lead to large differences in mechanical strength, regardless of the intrinsic strength of the reaction products. These observations mainly apply to the initiation and early stages of shear zone formation, as once the incipient stages of strain localization and weakening are initiated, additional mechanisms are involved and control the development of the shear zones in space and time.
The development of natural shear zones is commonly arranged into distinctive monophase layers (e.g., Berthé et al., 1979; Gapais, 1989) and/or polyphase mixtures (e.g., Fliervoet et al., 1997; Keller et al., 2004; Warren and Hirth, 2006; Kanagawa et al., 2008; Raimbourg et al., 2008; Okudaira et al., 2015) that may be found in the same shear zone as alternating layers (e.g., Kenkmann and Dresen, 2002; Kilian et al., 2011; Oliot et al., 2014; Mansard et al., 2018). In our case, the progressive deformation of two-phase assemblages also shows the development of (1) a strongly localized polyphase high-strain zone associated with a significant weakening after peak stress (Mg-rich assemblages) and (2) only locally connected σ-clast bands that do not induce major weakening (Fe-rich opx + plag and amph + plag assemblages). Strain localization into reaction-derived fine-grained mixtures is also well-documented in nature with the dominance of diffusion-accommodated GBS and/or DPC mechanisms (e.g., Newman et al., 1999; Handy and Stünitz, 2002; Kanagawa et al., 2008; Okudaira et al., 2015) and is expected to promote major rheological weakening (e.g., Fliervoet et al., 1997; Svahnberg and Piazolo, 2013; Warren and Hirth, 2006; Platt, 2015). The development of amph-rich σ-shaped aggregates and layers, notably through dissolution and precipitation processes, is also commonly documented in middle to lower crustal banded mylonites (e.g., Berger and Stünitz, 1996; Imon et al., 2002, 2004; Baratoux et al., 2005; Getsinger et al., 2013; Elyaszadeh et al., 2018; Giuntoli et al., 2018).
When applied to natural shear zones, our results suggest that (1) the ability of minerals to react controls the portions of rocks that deform, and (2) minor chemical and mineralogical variations (including the H2O available for reaction) can considerably modify the strength of deformed assemblages. Then, significant strain localization and partitioning at high shear strain, expressed by the development of interconnected high-strain zones (Mg-rich opx + plag), illustrate that fine-grained polyphase mixed zones can become weaker than coarse-grained, poorly connected ones (Fe-rich opx + plag and amph + plag). These results emphasize the importance of strain partitioning, grain size reduction, and interconnectivity of weak material as primary controls of lithospheric strength. This also suggests that the rheology of mafic rocks, which constitute a large part of the oceanic crust and may be one of the main components of the lower continental crust, cannot be summarized as being rheologically controlled by monophase materials (e.g., Dimanov and Dresen, 2005).
Shear deformation experiments with monophase and polyphase assemblages show a clear relationship between deformation and mineral reactions. A greater volume of reaction products is documented with increasing strain. This study shows that the premise of mineral reaction and strain localization has a major impact on sample strength because it conditions the resistance of the assemblage at low shear strain. Indeed, the Fe-rich opx + plag assemblages deform at lower stresses than the Mg-rich opx + plag assemblages because they react faster at early stages of experimentation. Thus, chemically similar assemblages may have significantly different strength development depending on the ability of these minerals to react. It is suggested that the availability of H2O, among other factors such as mineral composition, has a positive effect on the kinetics of reaction. With increasing strain, there are two very contrasting pathways in the material evolution, controlled by the properties of the reaction: in one case (Fe-opx + plag and amph + plag assemblages), the reaction products (mostly amphibole) have elongated grain shapes, a larger grain size, and poor connectivity. As a result, they do not show significant weakening. In such a case, the reaction products are only partially connected, the material deforms by grain-scale DPC, and the strength of the bulk sample is stable so the feedback effect of deformation on the reaction is limited. In the other cases (Mg-rich opx + plag and pure amph assemblages), the fine-grained, intensely mixed reaction products of equant grains weaken considerably during the experiment and end up much weaker than the initial material. The mechanically weak zone of reaction product deforms by GBS-dominated DPC and tends to form an interconnected zone that leads to the weakening of the bulk sample, and the drastic increase in the proportion of reaction products with strain suggests a large feedback effect. Overall, the value of the initial peak stress (that is responsible for determining where strain will start localizing) and the large weakening associated with the formation of fine-grained products (that determines whether shear bands thicken or not) seem to be mainly controlled by the chemical reactions.
Experimental data were processed using a MATLAB-based program inspired by the “rig” program of Dr. Matej Pec (Pec et al., 2016) and available at https://sites.google.com/site/jacquesprecigout/telechargements-downloads, last access: 5 August 2020.
NM, HS, HR, and JP designed the experiments. NM and JP carried them out. NM carried out the various analyses after the experiments (e.g., SEM, EPMA). AP worked on the thermodynamic modeling part, while LN contributed to the FTIR data acquisition. NM prepared the paper with contributions from all co-authors.
The authors declare that they have no conflict of interest.
This work has received funding from the European Research Council (ERC) under the Seventh Framework Programme of the European Union (ERC Advanced Grant, grant agreement no. 290864, RHEOLITH), Labex VOLTAIRE (ANR-10-LABX-100-01), and the project FluPrism (CNRS INSU, funding program SYSTER). We gratefully acknowledge the help provided by Patricia Benoist and Ida Di Carlo for analytical support, Sylvain Janiec for the preparation of thin sections, and Kai Neufeld for EBSD data acquisition. The authors wish to thank Mark Zimmerman for generously providing the Damaping peridotite and Laurent Arbaret for the Massif Central amphibolite material. We also appreciate thorough and constructive reviews by Luca Menegon and Jolien Linckens. We would like to thank Florian Fusseis for editorial handling.
This research has been supported by the European Research Council (ERC) under the Seventh Framework Programme of the European Union (ERC Advanced Grant, grant agreement no. 290864, RHEOLITH), Labex VOLTAIRE (grant no. ANR-10-LABX-100-01), EquipEx PLANEX (grant no. ANR-11-EQPX‐0036), and the project FluPrism (CNRS INSU, funding program SYSTER).
This paper was edited by Florian Fusseis and reviewed by Luca Menegon and Jolien Linckens.
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