How does a petrologist distinguish between high-T
minerals characterizing a high grade of metamorphism
from low-T and low-grade?
In Figure 14.25c and d, the major difference in the
mineral assemblage in the Onawa contact hornfelses is
the presence of muscovite and quartz in the outer,
lower T part of the aureole and the absence of this
mineral pair in the higher grade hornfels closer to the
intrusion that instead contain alkali feldspar and an
Al
2
SiO
5
polymorph. This change in mineral assem-
blage can be modeled by the mineralogical reaction
14.1 thermal energy (K,Na)Al
2
AlSi
3
O
10
(OH)
2
muscovite
SiO
2
(K,Na)AlSi
3
O
8
Al
2
SiO
5
H
2
O
quartz alkali feldspar
Al
2
SiO
5
can be any of the polymorphs andalusite,
sillimanite, or kyanite, depending on P–T conditions.
Breakdown of muscovite quartz is an endothermic
dehydration reaction, consuming heat and liberating
water. (Because of excess quartz in the Onawa aureole
rock relative to muscovite, it was not entirely con-
sumed in the reaction and higher grade hornfelses still
contain quartz.)
Thus, a general rule is that lower-grade metamorphic
mineral assemblages contain more volatile-rich phases
whereas higher-grade assemblages equilibrated at higher
T are made of less volatile-rich or volatile-free minerals.
Remember that in considerations of metamorphic
grade we compare rocks of similar bulk chemical com-
position: pelites with pelites, metabasites with meta-
basites, and so on; we don’t attempt to compare toads
with horses!
Devolatilizing prograde reactions liberate volatiles
with increasing T. Dehydrating prograde reactions,
such as the breakdown of muscovite, give off water as
T increases; the hydrous mineral assemblage, in effect,
“dries out” at higher T as a result of the endothermic
reaction. Prograde decarbonation reactions liberate
CO
2
from calcite, dolomite, and other CO
2
-bearing
minerals. A metamorphic path that progresses toward
a peak or maximum T is referred to as prograde meta-
morphism. Thus the aureole rocks toward the intru-
sion at Onawa experienced prograde metamorphism,
as did the sequence of mafic rocks in Figure 14.6a to d.
After a peak T is reached during prograde meta-
morphism, there must logically be a reversal going
down T. This is clearly the case for rocks now exposed
at the surface. Reversal may happen soon (in a geolo-
gical sense), or many, possibly tens or hundreds of, mil-
lions of years after attaining the peak T. But high-grade
metamorphic mineral assemblages (and also magmatic
rocks made of high-T minerals) exposed at the surface
all over the world indicate that retrograde reactions
during the decreasing T of retrograde metamorphism
do not generally occur. Prograde mineral reactions are
not automatically reversed during cooling and uplift to
the surface for two apparent reasons. The first follows
from the nature of reaction kinetics (Section 3.6.2)
whereby phases formed at high T typically persist
metastably at falling T because of slowing kinetic rates
of equilibrating reactions. The second is that prograde
reactions progressively liberate volatile fluids, which
migrate out of the metamorphosing body. As T falls
after the peak metamorphic event, no volatiles are avail-
able within the system and little can enter into typically
impermeable bodies. Without available water, hydrous
phases more stable at lower T cannot replace high-T
anhydrous minerals. Primary magmatic minerals in
granitic rocks are typically only partially replaced (e.g.
Plate IV), if at all, during the excursion of the rock
system from the solidus to lower temperatures. In
metamorphic rocks, high-T anhydrous silicates, such
as garnet, are commonly incompletely replaced by a
hydrous Mg–Fe alumino-silicate, such as chlorite, if at
all. Retrogressive metamorphism (or alteration, as it
might be called by some geologists) is commonly local-
ized along fractures or shear zones in aggregates of
high-T minerals. Shearing not only produces a higher
energy state in the strained grains, making them less
stable and more amenable to replacement, but also
provides an avenue for advective influx of volatile fluid
into the otherwise impermeable rock body. Planar
veins of hydrous Ca–Al silicates, especially epidote, are
common in granitic rocks (Figure 14.26) and form by
reaction between plagioclase and water that invaded a
fracture, possibly during cooling below the solidus. In
Figure 14.27, an anhydrous eclogite assemblage has
been retrograded to a lower T hydrous assemblage in a
vein.
14.2.5 Metamorphic Zones
Terranes of metamorphosed rock commonly display
geographically limited, or mappable, metamorphic
zones. Each zone is defined by some distinctive fabric
attribute or mineral assemblage in rocks derived from
compositionally similar protoliths. The sequence of
zones reflects the existence of gradients, or spatial vari-
ations, in conditions of metamorphism. Zones range in
dimension from that of an outcrop, or small portions of
it, to terranes measured in hundreds of square kilome-
ters. Zones are of considerable significance in the elu-
cidation of transfers of heat that caused changes in the
T of metamorphism, of changes in P that were caused
by variations in depth of burial, and of changes in the
nature of advecting fluids from different potential
sources. Where successive zones in a regional terrane
or contact aureole correspond essentially to a thermal
gradient they will be of different grade. Zones based
on some fabric attribute can be used to infer something
of states of stress and deformation. Zones and the
Metamorphic Rocks and Metamorphism: An Overview
431