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a particular geological level. Discrete heterogeneities are sharply demarcated
from the matrix by their texture, whereas cryptic heterogeneities are not. Dia-
genetic heterogeneities represent recrystallized cement accompanying burrow
fabrics. Below, the permeability classifications are expanded upon case stud-
ies from the literature and are summarized with each example.
4.3.1 Surface-Constrained Discrete Heterogeneities
This class of biogenically enhanced flow media is characteristic of trace-fossil
assemblagesassociatedwiththe
Glossifungites
Ichnofacies.The
Glossifungites
Ich-
nofaciescomprisesunlinedburrows thatdescendfromasinglesurface.Theburrows
commonly exceed 10 cm in diameter and show little or no evidence of post-
depositional compaction.Thesecharacteristicsareassociatedwith thedevelopment
of
Glossifungites
assemblages, which dominantly result from animals burrowing
into firm sediment (i.e., compacted substrates). The most common expression of
the
Glossifungites
Ichnofacies is sand-filled burrows within a mud matrix (e.g.,
Gingras et al., 2001; MacEachern et al., 1992; Pemberton and Frey, 1985
).
Trace-fossil assemblages that constitute the
Glossifungites
Ichnofacies typ-
ically penetrate as little as a few centimeters and as much as approximately
70 cm below their surface of origin. Some commonly associated ichnogenera
include isolated burrows such as
Skolithos
,
Diplocraterion,
and clavate bivalve
burrows (e.g.,
Gingras et al., 2001
), and burrows that potentially interpenetrate
one another such as
Thalassinoides
(e.g.,
Pemberton and Frey, 1985
) and
Zoophycos
(
MacEachern and Burton, 2000
). Deeply emplaced burrows that
interpenetrate, such as
Thalassinoides
-dominated
Glossifungites
assemblages,
can constitute flow units that are, broadly speaking, isotropic in character.
Owing to the presence of sand-filled burrows within the muddy matrix, SCD
normally represent dual-permeability flow media (
Fig. 5
). The proportion of
burrowing ranges from 10% to 80% of the volume. Notably, horizontal connec-
tivity is limited until burrow volumes approach 20-30% (depending on the
burrow architecture;
La Croix et al., 2012
).
Glossifungites
-associated SCD are typically limited in their distribution.
Due to their association with a single surface, the thickness of the permeability-
enhanced zone is typically
1 m (e.g.,
Gingras et al., 2001; MacEachern et al.,
1992
). Additionally, the colonization of firmgrounds depends upon a number of
factors, so their stratigraphic expression is discontinuous (cf.
Gingras et al.,
2001; Pemberton and Gingras, 2005
); SCD are generally limited in scale to
some hundreds of square meters, with a maximum areal extent of about a square
kilometer (
Pemberton and Gingras, 2005
).
Surface-constrained permeability enhancement is probably not limited
to
Glossifungites
-Ichnofacies-demarcated surfaces. For example, short-term
colonization windows in deep-water environments (e.g., a turbidite fan) may
promote the emplacement of sand-filled burrows along singular bedding planes.
The porosity and permeability distributions in such occurrences are likely
similar, but no case studies have as yet been conducted on such media.
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