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A R T I C L E I N FO A B S T R A C T
Keywords: Ediacaran– The Ediacaran–Cambrian transition was a time of marked biological and sedimentary changes, representing a
Cambrian boundarySequence significant evolutionary breakthrough in Earth’s history. Numerous explanations have been posited for these
stratigraphy dramatic changes. One view emphasizes an extensive period of widespread continental denudation during the
Sea-level changes
Neoproterozoic followed by extensive reworking of the basement during the early Cambrian, resulting in the
Macroevolution
formation of what is known as the “Great Unconformity”. Geologic events leading to the formation of this
Cambrian explosion
Great Unconformity unconformity have been hypothesized as an environmental trigger for the Cambrian explosion. H ere we review
seventeen key Ediacaran-Cambrian successions around the globe with a focus on their sedimentary facies and
sequence-stratigraphic architecture. Based on this information, we explore the relationship of the Ediacaran–
Cambrian boundary to this unconformity, underscoring a more nuanced scenario. We consider each section in a
chemostratigraphic and chronostratigraphic framework, and consider the hypothesized origin of this
unconformity at each locale—for example, whether it was eustatic in origin and therefore of global stratigraphic
significance or whether it resulted from local tectonics, implying marked inter-basin diachronism. Our sys-
tematic review shows that significant diachronism was involved in the generation of the Great Unconformity,
suggesting that the sea-level fall reflects overprint of local tectonics on pure eustasy. In most places, the Great
Unconformity is actually a composite sequence boundary resulting from successive eustatic episodes of sea-level
rise and fall overprinted by multiple tectonic events of subsidence and uplift. Thus this surface should not be
used for inter-basin correlations. Although the general proximity and common co-occurrence of the Ediacaran–
Cambrian boundary with a sequence boundary (SB) in places resulting in fluvial valley incision, has proved
challenging for biostratigraphic sampling, by mapping this unconformity and its associated facies, there are new
opportunities. In particular, paleontological work in terminal Ediacaran deposits located in inter fluve positions
may be promising because these areas may have preserved thick shallow-marine strata below the SB. Such strata
could hold additional clues to help fill in gaps in our understanding of the Ediacaran roots of the Cambrian
explosion.
1. Introduction ichnotaxa as well (Landing et al., 2013). This view has been subse-
quently challenged (Babcock et al., 2014), making detailed integrated
The Ediacaran–Cambrian boundary (541.0 ± 1.0 Ma; but see analysis of the boundary remarkably timely (see Buatois, 2018 for
Linnemann et al., 2019 for the proposal of a younger age of approxi- discussion).
mately 538.8 Ma) is one of the most important points of the geological A series of studies have emphasized the importance of the so-called
time scale because it encompasses a critical period in the history of life. “Great Unconformity”, which separates Precambrian from Cambrian
This boundary is defined by the first appearance of the ichnospecies strata (Peters and Gaines, 2012; Keller et al., 2019; Wan et al., 2019).
Treptichnus pedum (Brasier et al., 1994; Narbonne et al., 2012; Peng Based on an extensive analysis of the expression of the Great Un-
et al., 2012; Buatois et al., 2013; Buatois, 2018), although further re- conformity in North America, Peters and Gaines (2012) proposed that
finements suggest using a T. pedum zone, which includes other an extended period of continental denudation during the
⁎ Corresponding author.
E-mail address: luis.buatois@usask.ca (L.A. Buatois).
https://doi.org/10.1016/j.precamres.2020.105721
Received 30 October 2019; Received in revised form 16 March 2020; Accepted 30 March 2020
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Neoproterozoic followed by extensive physical reworking of soil, re- 2.1. Southeast Newfoundland, Canada
golith and basement rocks during the first continental-scale Phaner-
ozoic marine transgression resulted in worldwide occurrence of this The Chapel Island Formation at Fortune Head, Burin Peninsula of
surface. These authors suggested that the Great Unconformity might southeastern Newfoundland was deposited in a transtensional basin
“have been an environmental trigger for the evolution of biominer- (Smith and Hiscott, 1984; Myrow and Hiscott, 1993; Landing, 1996,
alization and the ‘Cambrian explosion’ of ecologic and taxonomic di- 2004). The base of the T. pedum zone, 2.4 m above the base of member
versity following the Neoproterozoic emergence of animals” (Peters and 2, has been ratified as the Global Standard Stratotype-section and Point
Gaines, 2012). Further work in North America has attributed the Great (GSSP) for the Ediacaran–Cambrian boundary (Narbonne et al., 1987;
Unconformity to heterogeneous Neoproterozoic glacial erosion of un- Landing, 1994) (Fig. 2). Recent carbon isotope studies show a positive
precedented scale (Keller et al., 2019). Also, recent work has refined excursion of δ13 coincident with the Ediacaran–Cambrian boundary
our knowledge of this unconformity in other areas of the world, such as (Hantsoo et al., 2018).
the North China Craton (Wan et al., 2019). Subsequently, T. pedum was recorded 3.11 and 4.4 m below the
Many explanations have been put forward to account for the dra- GSSP (Gehling et al., 2001). The uppermost part of member 1 in the
matic changes that took place during the Ediacaran-Cambrian transi- Fortune Head area contains red and green sandstone and shale de-
tion, including environmental, geochemical, and biotic factors posited in tidal-flat and shallow subtidal environments, and grey to
(Marshall, 2006; Squire et al., 2006; Budd, 2008; Maloof et al., 2010; black parallel-laminated sandstone and shale deposited in semi-re-
Erwin and Tweedt, 2012; Laflamme et al., 2013; Mángano and Buatois, stricted low-energy environment (Myrow et al., 1988). The pro-
2014; Schiffbauer et al., 2016; Zhuravlev & Wood, 2018; Darroch et al., blematicum Harlaniella podolica is present in these deposits (Gehling
2018; Muscente et al., 2018; Linnemann et al., 2019; Wood et al., 2019; et al., 2001). The lowermost part of member 2 spanning the Ediacar- an–
Bowyer et al., 2020). Despite its importance, the precise location of the Cambrian boundary consists primarily of very thin to thin-bedded gray-
Ediacaran–Cambrian boundary has been a highly contentious issue, green sandstone and siltstone deposited in a storm-influenced shallow-
further complicating evaluation of the chronostratigraphic framework marine environment, probably with some deltaic influence (Myrow et al.,
of major evolutionary events (Buatois et al., 2013; Babcock et al., 2014; 1988; Myrow and Hiscott, 1993). The problematicum Harlaniella
Linnemann et al., 2019). The Great Unconformity is in many places a podolica occurs in the lowermost part of member 2 together with
diachronous surface that spans as much as 1.2 billion years, even within Palaeopascichnus delicatus (Gehling et al., 2001). Recent ichnologic work
the same basin (e.g., Karlstrom et al., 2003; 2018; Matthews et al., further supports the notion of significant evolutionary innovations
2017). Moreover, within the presumably well-defined “Cambrian” coincident with this transition (Laing et al., 2018) and subsequently
epicratonic sheet sandstones that cap this unconformity, emerging between the Fortunian and Cambrian Stage 2 (Gougeon et al., 2018).
stratigraphic and geochronometric work is revealing that many of these The marine succession comprises both transgressive (TST) and high-
“Cambrian” sandstones to be, at least in part, Ediacaran (e.g., Sanford stand systems tract (HST) deposits, and passes upward into a red-bed
and Arnott, 2010; Hagadorn et al., 2011), Furongian (“Late”) Cambrian interval consisting of thin- to thick-bedded, massive and parallel-lami-
and Early Ordovician (e.g., Amato and Mack, 2012; Holm-Denoma nated sandstone, siltstone, and shale with abundant syneresis and de-
et al., 2016; Lowe and Arnott, 2016). Such records imply that up to 150 siccation cracks formed in a fluvial environment (Myrow et al., 1988)
million years of time is represented by units previously thought to re- (Fig. 3a-g). This sharp basinward facies change suggests that the base of
present entirely Cambrian onlap. Thus, it has been challenging to de- the red-bed interval represents a SB resulting in the establishment of a
cipher the precise timing of the Cambrian portion of the Great Un- lowstand systems tract (LST) fluvial system dissecting the shelf (Fig. 2),
conformity event. indicating a period of subaerial exposure later in the early Fortunian.
In addition, there is robust sedimentologic and sequence-strati- The depositional history of the Chapel Island Formation has been
graphic evidence indicating that in many areas of the world a sea-level considered as a transitional stage from deposition in tectonically active
fall took place around the Ediacaran-Cambrian transition (e.g. Saylor, fault-bounded basins related to strike-slip tectonics to a more quiet
2003; Wilson et al., 2012). However, correlation of this erosional sur- tectonic condition (Smith and Hiscott, 1984; Myrow and Hiscott, 1993).
face from basin to basin and differentiation of the role of eustasy and Many strike-slip basins form adjacent to uplifted blocks with pro-
local tectonics as controlling factors on associated relative sea-level fall nounced topographic relief, which leads to deposition of very coarse-
have been equally challenging. All of these are key elements in our grained sedimentary facies along some basin margins and to abrupt
understanding of the biologic and oceanographic changes surrounding lateral facies changes. Local vertical movements of blocks result in lo-
the Ediacaran–Cambrian transition. calized unconformities (Christie-Blick and Biddle, 1985).
The objectives of this paper are to (1) evaluate the precise position
of these large unconformities in key Ediacaran–Cambrian successions; 2.2. Northwest Canada
and (2) examine if these discontinuities were eustatic in origin, or if on
the contrary, some of them are the result of local tectonics, implying The Ediacaran–Cambrian succession of the Mackenzie Mountains,
marked inter-basin diachronism. These results are a starting point for northwest Canada records the break-up of Rodinia and the early evo-
evaluating which strata might be used to test hypotheses about the links lution of the passive continental margin of Laurentia (Fritz et al., 1991;
between tectonics, eustasy, and biotic changes of the Ediacaran– Levy and Christie-Blick, 1991; Yonkee et al., 2014; Moynihan et al.,
Cambrian transition. 2019), and consists, in ascending order, of the Sheepbed, June beds,
Gametrail, Blueflower, and Risky formations (all in the upper Wind-
ermere Supergroup), and the overlying Ingta, Backbone Ranges, and
2. The great unconformity and the Ediacaran–Cambrian boundary Vampire formations (Narbonne and Aitken, 1995; MacNaughton et al.,
2000; Turner et al., 2011). The Sheepbed Formation is a shale-domi-
In this section we summarize and assess seventeen key successions nated unit deposited on a continental slope (Dalrymple and Narbonne,
(Fig. 1), focusing on sedimentary facies and sequence-stratigraphic ar- 1996; Carbone and Narbonne, 2014), and is unconformably overlain by
chitecture in order to evaluate the precise stratigraphic location of the thin-bedded carbonate and siliciclastic strata of the June Beds Forma-
Ediacaran–Cambrian boundary with respect to the sequence boundary tion (Macdonald et al., 2013), which gradationally passes up into the
(SB). The best estimate of the Ediacaran–Cambrian boundary is in- Gametrail Formation.
dicated in each section based on the latest available radiometric dating, The Gametrail Formation consists of dolomitized, evenly-bedded
chemostratigraphic information, and biostratigraphic data. The tectonic limestone, and is conformably overlain by the Blueflower Formation.
setting for each section is also assessed. The Blueflower Formation consists of two members, a lower, carbonate
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Fig. 1. Paleogeographic map during the Ediacaran-Cambrian transition showing the locations of the studied sections (base map after Scotese, 2016).
dominated member and an upper, siliciclastic-dominated member Narbonne (2014) have subsequently reported examples of Treptichnus
(MacNaughton et al., 2000), and contains simple trace fossils, such as cf. T. pedum, T. bifurcus, and other undetermined ichnospecies of
Archaeonassa, Gordia, Helminthopsis, Helminthoidichnites, Palaeophycus, Treptichnus, arthropod tracks and trails, and other Cambrian-type trace
Planolites, and Torrowangea (Hofmann, 1981; Aitken, 1989; Narbonne fossils, including possible U-shaped vertical burrows and Psammichnites
and Aitken, 1990; Carbone and Narbonne, 2014). A number of Edia- cara- below the originally proposed Ediacaran–Cambrian boundary. The oc-
type body fossils have been documented from the June Beds and currence of these trace fossils suggests that the Ediacaran–Cambrian
Blueflower formations, including Annulatubus flexuosus, Aspidella sp., boundary in NW Canada is tentatively placed within the lower interval
Charniodiscus sp., Ediacara sp., Eoporpita sp., Hiemalora sp., Inkrylovia of the Ingta Formation at the abrupt incoming of ichnospecies of
sp., Pteridinium sp., Sekwitubulus annularis, Sekwia excentrica, and Treptichnus, thereby co-occurring with or immediately overlying the
Windermeria sp. (Hofmann, 1981; Narbonne and Aitken, 1990; prominent negative carbon isotope excursion (Fig. 4). These authors
Narbonne, 1994; Carbone and Narbonne, 2014; Carbone et al., 2015). also suggested that the Ediacaran–Cambrian boundary might lie in the
Macdonald et al. (2013) inferred an age somewhere between 553 and prominent unconformity at the top of the underlying Risky Formation.
541 Ma for the Blueflower Formation. The Risky Formation consists of However, trace fossils, although present in these strata, are highly di-
dolostone to sandy dolostone (MacNaughton et al., 2000), and lies minutive relative to trace fossils elsewhere in the Ingta Formation,
gradationally upon the Blueflower Formation and unconformably be- which may suggest either an Ediacaran age or a significant environ-
neath siliciclastic and minor carbonate rocks of the Ingta, Backbone mental limiting factor (Carbone and Narbonne, 2014).
Ranges, and Vampire formations (MacNaughton et al., 2000) (Fig. 4). In short, the precise position of the Ediacaran–Cambrian boundary
The Ingta Formation is dominated by green, purple, and red colored in northwest Canada is still unclear. However, both proposed positions
shale with minor sandstone beds, and a limestone cap deposited in an for the boundary are between two major unconformities, one at the
offshore to shelf environment (Aitken, 1989; Carbone and Narbonne, base of the Ingta Formation and the other within the lower interval of
2014). The Ingta Formation is overlain by the Backbone Ranges For- the Backbone Ranges Formation. Initially it was believed that the
mation consisting of two members, a lower member containing near- terminal Ediacaran to basal Cambrian succession of the Mackenzie
shore siltstone and sandstone similar to those of the underlying Ingta Mountains was deposited on a passive margin, and therefore contains a
Formation, and an upper member, containing deposits encompassing fairly sensitive record of eustatic sea-level changes (MacNaughton and
various shallow-marine to non-marine environments, including wave- Narbonne, 1999). However, Macdonald et al. (2013) argued that major
influenced braid-delta systems. The uppermost unit, the Vampire For- facies changes (Aitken, 1989; Narbonne and Aitken, 1995) and large
mation, is dominated by siltstone and sandstone of wave-dominated overlapping unconformities within Ediacaran strata (MacNaughton
offshore and prodelta origin, and contains the lowest occurrence of et al., 2000), coupled with the ∼570 Ma late Ediacaran syn-rift volca-
trilobite body fossils (MacNaughton and Narbonne, 1999). nics in the southeastern Canadian Cordillera (Colpron et al., 2002),
The Ediacaran–Cambrian boundary in the Mackenzie Mountains indicate a more complex tectonostratigraphic architecture and probably
was recognized by the first occurrence of T. pedum in the upper interval a more nuanced subsidence history (see also Moynihan et al., 2019).
of the Ingta Formation (MacNaughton and Narbonne, 1999) (Fig. 4).
The proposed position for the boundary was supported by the first
occurrence of Cambrian-type small shelly fossil Protohertzina in carbo- 2.3. Death Valley, Eastern California, United States
nate strata at the top of the Ingta Formation (Conway and Fritz, 1980;
Narbonne and Aitken, 1995), coupled with a pronounced negative The Ediacaran–Cambrian succession in Death Valley, southeastern
carbon isotopic excursion ∼−10‰ in the basal beds of the Ingta California, includes in ascending order, the Johnnie Formation, Stirling
Formation (Narbonne et al., 1994) (Fig. 4). However, Carbone and Quartzite, Wood Canyon Formation, and the Zabriskie Quartzite. The
Johnnie Formation, Stirling Quartzite, and the lower member of the
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Fig. 2. Generalized stratigraphy of the Ediacaran–Cambrian succession in the Chapel Island Formation, southeastern Newfoundland, Canada (GSSP) (modi fied from
Myrow et al., 1988). The presence of Treptichnus pedum below the GSSP Ediacaran–Cambrian boundary was recorded after the official decision was made (Gehling
et al., 2001).
Wood Canyon Formation represent early development of a passive et al., 2017, 2020). The lower member of the Wood Canyon Formation
continental margin along the western margin of Laurentia (Link et al., consists of siltstone and sandstone abruptly overlaying the LST deposit
1993; Fedo and Cooper, 2001), whereas the middle member of the of the underlying Stirling Quartzite (Fedo and Cooper, 2001) (Fig. 5).
Wood Canyon Formation and younger strata are interpreted to re- The lower interval of the lower member consists of TST deposits,
present a mature passive-margin phase of dominantly fluvial sedi- whereas the rest were formed as part of a prograding HST (Hogan et al.,
mentation (Fedo and Cooper, 2001; Hogan et al., 2011; Muhlbauer 2011). The LST deposit of the middle member comprises trough cross-
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Fig. 3. Sedimentary facies and stratal stacking patterns in the Chapel Island Formation of Burin Peninsula, Newfoundland; (a) Red bed interval; (b) Ripple cross
lamination; (c) Convolute lamination; (d) Convolute lamination; (e) Syneresis cracks; (f) Contact between the red-beds and overlying transgressive shoreface. TS is
transgressive surface. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
bedded, pebbly medium- to very coarse-grained feldespatic quartzite middle member of the Wood Canyon Formation occurs above the
and interbedded siltstone interpreted as braid-plain deposits (Fedo and Ediacaran–Cambrian boundary, and lacks evidence for significant in-
Cooper, 1990). Progradation of fluvial deposits of the middle member cision. Given that the Ediacaran–Cambrian strata in Eastern California
of the Wood Canyon Formation over the shallow-water deposits of the represent deposition along a craton margin hinge zone, formed on a
lower member at the onset of sea level fall has caused a minor amount thermally subsiding passive margin following late Neoproterozoic
of incision at the contact between the lower and middle members rifting, Fedo and Cooper (2001) proposed that the main unconformities
(Fig. 6a-d). The erosive base of this fluvial unit is regarded as a SB in this section, including the one at the base and top of lower member of
(Fig. 5). the Wood Canyon Formation, were formed mostly by eustatic processes
Radiometric age constraints are not available for these successions; that were possibly modified by the effects of differential subsidence
therefore, the exact position of the Ediacaran–Cambrian boundary is across the hinge zone (Fedo and Cooper, 2001; Hogan et al., 2011).
unclear. The first occurrence of T. pedum suggests an approximate po-
sition of the boundary within the middle interval of the lower member 2.4. White Inyo Mountains and Esmeralda County, western Nevada, United
of the Wood Canyon Formation (Hagadorn and Waggoner, 2000) States
(Fig. 5). This is also supported by the report of Ediacaran fossils in the
lower portion of the lower member of the Wood Canyon Formation and The Ediacaran-Cambrian in the White Inyo Mountains and
the underlying Stirling Quartzite, including iconic representatives of Esmeralda County of western Nevada is the distal equivalent of those
the Ediacara biota, such as Swartpuntia and erniettomorphs, as well as successions exposed in the Death Valley. The White Inyo Mountains and
Archaeichnium, Cloudina, Corumbella, Nimbia, Onuphionella, Gaojia- Esmeralda County succession includes, from base to top, the Wyman
shania, and Conotubus (Hagadorn and Waggoner, 2000; Smith et al., Formation, Reed Dolomite, Deep Spring Formation, Campito
2016, 2017; Selly et al., 2020). This is consistent with information from Formation, Poleta Formation, and Harkless Formation (Nelson, 1962;
carbon isotope stratigraphy, which shows a negative excursion of Stewart, 1970; Link et al., 1993; Smith et al., 2016) (Fig. 7). The Deep
δ13Ccarb coincident with the first occurrence of T. pedum (Corsetti and Spring Formation is subdivided into the Dunfee, Esmeralda, and Gold
Hagadorn, 2000; Smith et al., 2016) and overlying trace-fossil assem- Point members (Corsetti and Kaufman, 1994; Ahn et al., 2012). As in
blages (Mata et al., 2012). the case of the coeval successions in Death Valley, strata in Nevada
The Ediacaran–Cambrian boundary in Death Valley is placed be- record deposition along a passive margin.
tween two major unconformities, a major one at the top of the Stirling The Dunfee Member is dominated by dolomitic limestone with
Quartzite and another one at the base of the middle member of the subordinate siltstone, sandstone and quartzite. The Esmeralda Member
Wood Canyon Formation (Hogan et al., 2011). The SB at the base of the is dominated by sandstone, quartzite, and stromatolitic and oolitic
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clastics of this unit but bona fide trace fossils are thus far lacking (Hagadorn, 2009; Hogan et al., 2011).
(Fig. 9). The base of the Cambrian in Sonora, Mexico is defined based on the
The overlying Cerro Rajón Formation (formerly Unit 1 of the Puerto first occurrence of T. pedum at the lower interval of the Cerro Rajón
Blanco Formation) consists of interfingering volcaniclastic sandstone Formation. However, underlying clastics can be continental in origin,
and conglomerate, basalt, tuff, quartzite, siltstone, and silty dolostone, and Loyd et al. (2012) suggested that considering the environmental
and contains abundant trace fossils (Stewart et al., 1984; McMenamin, range of T. pedum and the carbon isotope excursion correlation between
1984; Sour-Tovar et al., 2007; Barrón-Díaz et al., 2019a). Although the the lower member of the Wood Canyon Formation and the La Ciénega/
lowest occurrence of T. pedum is ∼20 m above the base of this unit, tens Cerro Rajón formations, the Ediacaran–Cambrian boundary could occur
of meters of the basal trace-fossil-bearing part of this unit is in places lower in the section, coincident with the large negative carbon isotope
removed by local incision, and a Cambrian-aspect assemblage of ich- excursion within the upper interval of La Ciénega Formation. Indeed,
nofossils, including Archaeonassa, Diplichnites, Gordia, Mono- the magnitude and biostratigraphic position of the nadir of this carbon
morphichnus, Palaeophycus, Planolites, and Treptichnus, occur in these isotopic excursion (over −7 per mil; Hagadorn, 2011; Loyd et al., 2012)
sub-incision strata (Sour-Tovar and Hagadorn, 2008; Barrón-Díaz et al., indicates it is the basal Cambrian carbon isotope excursion, or BACE
2019a). The Puerto Blanco Formation is subdivided into three units (Zhu et al., 2019). This excursion occurs in unit 3, ∼50 m below the top
(Stewart et al., 1984; Barrón-Díaz et al., 2019a). The lower unit (Unit 2) of the La Ciénega Formation (Fig. 8).
is predominantly siltstone with minor quartzite and limestone. Trace The Ediacaran–Cambrian boundary interval in Sonora occurs below
fossils are abundant in the siliciclastic strata, and carbonate lenses near the SB that extends to the base of the Cerro Rajón Formation. The
the base of the unit bear non-age-diagnostic brachiopods, such as Sonoran succession reflects a depositional and paleogeographic history
Obolella and Lingulella, and rare Fallotaspis zone trilobites including similar to the Death Valley succession, with depocenters occurring
Parafallotaspis (Hagadorn, 2011). Nevadella zone trilobites, such as along the same margin (Stewart et al., 1984). The extent to which re-
Nevadia, occur near the top of the unit (Hagadorn et al., 2016). The gional versus widespread rift-related volcanism is occurring in the
middle unit (Unit 3) is dominated by archaeocyathan-bearing limestone Ediacaran-Cambrian portion of these successions is challenging to de-
and siltstone, and Nevadella zone trilobites (Pope et al., 2012). The cipher (Stewart, 1972; Stewart et al., 1990, 2002), despite rift-related
upper unit (Unit 4) is dominantly interbedded limestone, dolostone, geochemical signatures of the basalts in the succession (Centeno-García
quartzite, and siltstone, and contains Skolithos piperock, trilobite trace et al., 2002; Hagadorn and Holm-Denoma, 2016; Barrón-Díaz et al.,
fossils, and abundant biomineralized fossil coquinas that bear trilobites 2019b). The intercalation of rift-related mafic extrusive and intrusive
of the Bonnia-Olenellus zone (Stewart et al., 1984; Pope et al., 2012; volcanics in the Sonoran succession, together with evidence for local
Hernández-Barbosa and Sour-Tovar, 2018). uplift and associated incision, suggests the margin was tectonically
The contact between the La Ciénega and Cerro Rajón formations is active during the Ediacaran-Cambrian transition (Barrón-Díaz et al.,
transitional. However, an erosional unconformity occurs within the 2019a).
latter above the first occurrence of T. pedum-like trace fossils, and lo-
cally cuts out portions of the lowermost Cerro Rajón Formation (Fig. 8
2.6. South Australia
and 9a-e). This erosional unconformity has been correlated with the
cratonal nonconformity at the top of the lower member of the Wood
The Ediacaran–Cambrian strata in Flinders Ranges, South Australia
Canyon Formation (Loyd et al., 2012), but other authors suggested that
comprise the Rawnsley Quartzite and Uratanna formations representing
the Sonoran contact may reflect local volcanic doming and uplift
deposition in a passive margin setting followed by a rifting event
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Zang et al., 2007), and passes up into the shallow marine, shoreface and
lagoonal Parachilna Formation (Gehling and Droser, 2012) (Fig. 11).
This erosive surface at the base of the Uratanna Formation is a SB as-
sociated with a marked basinward shift in the facies.
Treptichnus pedum first appears in sandy facies more than 200 m
above the base of the Uratanna Formation (Jensen et al., 1998)
(Fig. 10). Kullingia concentrica, sabelliditids, and Swartpuntia-like fronds
have been reported within or close to the beds containing T. pedum
Fig. 7. Generalized stratigraphy and carbon isotope chemostratigraphy of
Ediacaran–Cambrian succession in White Inyo Mountains and Esmerald
(Jensen et al., 1998; Droser et al., 1999) (Fig. 10), which may indicate
County, Western Nevada, United States (modified from Smith et al., 2016). See the extension of Ediacara-type organisms into the Cambrian period
Fig. 2 for symbols. (Jensen et al., 1998; but for the origin of Kullingia, see Jensen et al.,
2002). Other trace fossils reported from the Uratanna Formation in-
clude Curvolithus isp., Hormosiroidea isp. (probably Saerichnites isp.),
(Powell et al., 1994). The Rawnsley Quartzite is subdivided into three
Phycodes cf. palmatus, Phycodes coronatum, Rusophycus avalonensis, and
members, in ascending order, Chace Quartzite, Ediacara, and Upper
Taphrhelminthopsis circularis (now included in Psammichnites) (Jensen
Rawnsley Quartzite (Gehling, 2000). The Ediacara Member contains
et al., 1998; Droser et al., 1999). The base of the Cambrian succession is
fossils of the classic Ediacara biota, and is interpreted as the distal part
considered to be at the basal unconformity that sits at top of the
of a shallowing-upward, prograding delta sequence (Goldring and
Rawnsley Quartzite, 200 m below the first occurrence of T. pedum
Curnow, 1967; Gehling and Rigby, 1996; Droser et al., 1999, 2006;
(Daily, 1973; Zang et al., 2007; Gehling and Droser, 2012) (Fig. 10).
Gehling, 2000; Gehling and Droser, 2012; Tarhan et al., 2015; Coutts
The delayed appearance of T. pedum could result from inhospitable
et al., 2016) (Fig. 10). The Rawnsley Quartzite, above and below the
conditions, notably marked dilution of marine salinity, during deposi-
Ediacara Member, is unfossiliferous, and features barren, shoreface and
tion of the lower part of the Uratanna Formation, which took place
tidal sand-flat facies with distinctive petee lamination, the latter formed
within the context of an estuary system; only the estuary mouth (the
by buckling and desiccation of cyanobacterial mats (Gehling, 1999;
upper interval of Uratanna Formation) may have experienced near-
Droser et al., 1999; Gehling, 2000; Gehling and Droser, 2012). The
marine salinity conditions in this area.
overlying Uratanna Formation consists of massive, channel-filling
The proposed Ediacaran–Cambrian boundary in the Flinders Ranges
sandstone of fluvio-estuarine origin, followed by a single coarsening-
coincides with a major unconformity forming an incised valley at the
upward succession of monotonous, laminated siltstone that grades into
base of the Uratanna Formation. The same situation has been observed
estuary mouth trace-fossil-bearing, thinly bedded sandstone beds, and
in the Amadeus Basin, Central Australia, where the unconformity at the
shoreface hummocky cross-stratified and cross-bedded sandstone base of Member III of the Arumbera Formation marks the Ediacaran–
(Droser et al., 1999). The Uratanna Formation cuts down and forms
Cambrian boundary. However, the lack of quantitative temporal
erosive channels into the underlying Rawnsley Quartzite (Daily, 1973;
constraint on the position of the Ediacaran–Cambrian
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Fig. 11. The incised valley at the contact between the Uratanna Formation and the underlying Rawnsley Quartzite.
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and Poprawa, 2005). The Lublin Slope succession comprises the Polesie,
Sławatycze, Białopole (or Siemiatycze), Lublin, Włodawa, Mazowsze,
Kaplonosy, and Radzyn formations (Moczydłowska, 1991). The LST
deposits of the Sławatycze Formation consist of basalt, tuff, agglom-
erate, and conglomerate, unconformably overlying the feldspathic and
quartzitic continental sandstone of the Polesie Formation. The Sława-
tycze Formation has yielded a U–Pb zircon date of 551 ± 4 Ma
(Compston et al., 1995).
The erosive base of the Sławatycze Formation marks a major un-
conformity at the beginning of the Ediacaran (Pacześna and Poprawa,
2005) (Fig. 17). The Białopole Formation comprises quartzite inter-
calated with mudstone and shale, representing lagoonal to coastal-
marine facies of an embayment, with tidal-flat, channels, and shoreface
environments (Moczydłowska, 1991; Poprawa and Pacześna, 2002).
Characteristic marine cyanobacteria and vendotaenids occur in this
formation (Moczydłowska, 1991). The succeeding Lublin, Włodawa,
and Mazowsze formations consist of shallow-marine sandstone, silt-
stone, and shale, representing deposition as part of a TST to HST
(Pacześna and Poprawa, 2005). A rich and diverse acritarch assemblage
was recovered from the Mazowsze Formation together with the earliest
shelly fossils (Lendzion, 1983). The lowermost occurrence of Torro-
wangea rosei and Gordia isp. is in the Lublin Formation (Pacześna,
1986); these two ichnotaxa are known in Ediacaran strata (Mángano
and Buatois, 2014). The first occurrence of T. pedum and an increased
diversity of trace fossils are recorded at the base of the Mazowsze
Formation (Pacześna, 1986) (Fig. 17). The HST deposits of the Ma-
zowsze Formation are overlain by TST deposits of the Kaplonosy For-
mation; the contact between the two formations is marked by a co-
planar surface (amalgamated flooding surface and sequence boundary)
revealed by the presence of the Glossifungites Ichnofacies (Pacześna and
Poprawa, 2005) (Fig. 17). The base of Cambrian in the Lublin region is
Fig. 15. Generalized stratigraphy of Ediacaran–Cambrian succession in defined within the uppermost part of the Włodawa Formation on the
Vanrhynsdorp Group, South Africa (modified from Gresse, 1992; and Buatois basis of the stratigraphically lowest occurrence of a diagnostic early
et al., 2007). See Fig. 2 for symbols. Cambrian acritarch (Moczydłowska, 2008) (Fig. 17).
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A large negative carbon isotope excursion at the base of the Innerelv, and Manndraperelv members. The LST deposits of the Lille-
Mazowsze Formation (Fig. 17), that elsewhere in the world is taken as vatn Member consist of a mixed siltstone and sandstone lower unit and
approximating the Ediacaran–Cambrian boundary (Maloof et al., a sandstone-dominated upper unit, which have been regarded as fluvial
2010), further supports the proposed position for the Ediacaran–Cam- in origin (Högström et al., 2013; McIlroy and Brasier, 2017). The TST
brian boundary (Strauss et al., 1997). The Ediacaran–Cambrian deposits of the Innerelv Member consist of stacked coarsening-upward
boundary has been convincingly correlated with successions elsewhere successions, ranging from parallel-laminated mudstone to sandstone,
on Baltica (Moczydłowska, 1991), with the Global Stratotype Section recording deposition in a storm-influenced offshore (Banks, 1973;
and Point of the base of Cambrian in Newfoundland, and with succes- Högström et al., 2013). The Manndraperelv Member comprises three
sions elsewhere (Moczydłowska, 1999, 2002; Vidal et al., 1999; coarsening-upward successions, ranging from mudstone to sandstone,
Moczydłowska and Zang, 2006). representing offshore to shoreface deposition (Banks et al., 1971;
In the Lublin slope, the Ediacaran–Cambrian boundary interval is Högström et al., 2013; McIlroy and Brasier, 2017) as part of HST.
positioned between two major unconformities, at the base of the The Breivik Formation conformably overlies the Stappogiedde
Sławatycze Formation and at the top of the Mazowsze Formation. The Formation (Reading and Walker, 1966; Banks et al., 1971). This for-
SB at the base of the Sławatycze Formation indicates a period of relative mation is divided into two members; the Lower Breivik and Upper
sea-level fall in the early Ediacaran, whereas the SB at the top of the Breivik. The Lower Breivik Member contains common sandstone in-
Kaplonosy Formation, which is marked by a co-planar surface, was terbedded with mudstone, and is interpreted to have been deposited in
formed at the onset of transgression in the early Fortunian (Pacześna offshore to shoreface settings (Högström et al., 2013; McIlroy and
and Poprawa, 2005). These authors suggested that a complex interplay Brasier, 2017). The Upper Breivik Member is mudstone-dominated, and
between tectonic and eustatic process were major controls on basin is interpreted to have been deposited in an offshore to shelf setting
evolution. Considering the significant role of local tectonics in the Lu- (Nielsen and Schovsbo, 2011; Högström et al., 2013). The base of a
blin region, it is most likely that the development of the basin was sandstone unit near the top of the Lower Breivik Member represents a
mainly controlled by an Ediacaran (to earliest Cambrian) rifting event regional unconformity (Nielsen and Schovsbo, 2011) (Fig. 18).
and subsequent Cambrian to middle Ordovician post-thermal sub- The trace fossil T. pedum was first reported 3 m above the base of the
sidence (Pacześna and Poprawa, 2005). Breivik Formation (Banks, 1970), which together with the presence of
the zone fossil Platysolenites antiquissimus from the top of the Lower
Breivik Member, suggest an early Cambrian age for the unit (Føyn and
2.11. Eastern Finnmark Glaessner, 1979). More recently, Högström et al. (2013) and Jensen
et al. (2018a) have reported T. pedum 20 m and 30 m below the top of
The Ediacaran–Cambrian succession of the Vestertana Group, the Manndraperelv Member, respectively, suggesting that the transition
eastern Finnmark, northern Norway consists of five formations, in as- between the Ediacaran and the Cambrian is most likely placed at the
cending order, Smalfjord, Nyborg, Mortensnes, Stappogiedde upper part of the Manndraperelv Member (Fig. 18). Abundant Sabelli-
(=Stáhpogieddi), and Breivik (=Breidvika). The Smaltjord, Nyborg, dites cambriensis occur close to the base of the Lower Breivik Member
and Mortensnes formations were deposited in an extensional tectonic (Högström et al., 2013). The presence of the problematicum Palaeo-
setting (Røe, 2003), and contain Cryogenian–Ediacaran acritarchs of a pascichnus from transitional beds between the Lillevannet and Indreelva
wide stratigraphic range (Gorokhov et al., 2001), whereas the other members and in the second cycle of the Manndrapselva Member pro-
units represent deposition in a foreland basin (Røe, 2003). Multicellular vides further evidence of an Ediacaran age for these units (Jensen et al.,
eukaryotes have been recovered recently from the Nyborg Formation 2018b).
(Agić et al., 2019). The two tillite-bearing formations (Smalfjord and Similar to the Lublin slope, the Ediacaran–Cambrian strata of the
Mortensnes) are separated by interglacial turbiditic deposits of the Vestertana Group of eastern Finnmark do not record subaerial exposure
Nyborg Formation, and overlain by shoreface and offshore deposits of at the exact timing of Ediacaran–Cambrian transition. The Ediacaran–
the Stappogiedde Formation (Banks et al., 1971; Edwards, 1975, 1984; Cambrian boundary in this region is best located between two major
Högström et al., 2013). A major unconformity between the Nyborg and unconformities at the top of the Nyborg Formation and within the
Mortensnes formations is signaled by both a microfossil assemblage and Lower Breivik Member. The lower unconformity is placed at the base of
a mappable erosional relief (Vidal, 1981; Edwards, 1984) (Fig. 18). The glacial deposits of the Mortensnes Formation hundreds of
Stappogiedde Formation is divided into three members, the Lillevatn,
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Fig. 19. Generalized stratigraphy and carbon isotope chemostratigraphy in Zavkhan terrane, western Mongolia (modified from Smith et al., 2015). See Fig. 2 for
symbols.
miocenica (probably Psammichnites isp.), Hormosiroidea isp. (probably first occurrence of small shelly fossils (∼250 m below the first ap-
Saerichnites isp.), Monomorphichnus isp., Oldhamia radiata, Palaeophycus pearance of T. pedum) (Smith et al., 2015), and a report of early ar-
tubularis, Treptichnus pedum, Planolites isp., Psammichnites isp. (Plagi- thropod trace fossils from the middle part of BG3, which suggest that
ogmus isp. in original papers), Rusophycus avalonensis, Treptichnus bi- the Ediacaran–Cambrian boundary is actually much lower in the sec-
furcus, Treptichnus triplex, and Zoophycos isp. (Goldring and Jensen, tion, probably at the base of the Bayangol Formation, above the large
1996; Smith et al., 2015). The small shelly fossils were originally negative excursion of δ13Ccarb in the Zuun-Arts Formation (Smith et al.,
thought to first appear near the base of the Zuun-Arts Formation 2015) (Fig. 19).
(Brasier et al., 1996). However, Smith et al. (2015) suggested that the Based on the available evidence, the Ediacaran–Cambrian boundary
first appearance of small shelly fossils occurs 200–300 m strati- in the Zavkhan terrane, western Mongolia, is most likely placed at the
graphically higher at the base of Bayangol Formation (Fig. 19). base of the Bayangol Formation, coincident with a co-planar surface
The flooding surface at the base of the BG2, which overlies the HST marking the SB. The SB is overlain by transgressive phosphatic marine
deposit of the Zuun-Arts Formation, is overlain by transgressive phos- shale of the Bayangol Formation, recording a large positive carbon
phatic marine shale of BG2, thus denoting a SB, represented by a co- isotope excursion. Smith et al. (2015) applied the correlation between
planar surface (Fig. 19). The Ediacaran–Cambrian boundary was ori- positive carbon isotope excursions and occurrence of major SB in the
ginally defined based on the first occurrence of T. pedum at the contact Bayangol Formation to suggest that the larger-scale transgressions as-
between BG3 and BG4 of the Bayangol Formation (Goldring and sociated with positive carbon isotope excursions, such as the one at the
Jensen, 1996) (Fig. 19). However, the first appearance of T. pedum in base of the Bayangol Formation (coincide with positive carbon isotope
the Zavkhan terrane contradicts other lines of evidence, including the excursion B of Brasier et al., 1996), are products of local tectonism.
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Given that Ediacaran to early Cambrian strata in the Zavkhan terrane pedum occurs within the upper interval of the Syhargalakh Formation,
were deposited in a foreland basin (Macdonald et al., 2009), tectoni- slightly below the lowermost occurrence of R. avalonensis, which is in
cally driven changes of sea level seem to be the most plausible scenario. the lower part of the Mattaia Formation (Rogov et al., 2015) (Fig. 20).
The base of Cambrian in Russia has been historically placed at the
beginning of the Tommotian Stage at the first appearance of small
2.13. Northeastern Siberia
skeletal fossils of the Nochoroicyathus sunnaginicus Assemblage zone in
the middle of the Mattaia Formation (Peng et al., 2012). The Nema-kit–
The Ediacaran–Cambrian succession in the Olenek Uplift, north-
Daldynian Stage of Siberia is characterized by the appearance of the first
eastern Siberia includes the Khorbusuonka and Kessyusa groups, both
skeletal fossils belonging to the Anabarites trisulcatus zone at or just
containing mixed siliciclastic and carbonate rocks. The carbonates re-
beneath the base of the Kessyusa Group (Knoll et al., 1995; Peng et al.,
present part of a passive-margin succession that developed along the
2012), which is consistent with the markedly negative carbon isotope
eastern margin of the Siberian craton during Neoproterozoic time.
excursion in the upper Turkut Formation (Knoll et al., 1995). The SB in
Traditionally the siliciclastic succession has been considered as re-
the Ediacaran–Cambrian succession of the Olenek Uplift is defined by a
cording an early Cambrian rift event (Pelechaty et al., 1996). However,
regionally extensive paleokarst unconformity at the base of the Sy-
a foreland basin setting has been proposed more recently (Grazhdankin
hargalakh Formation. Available evidence suggests that the Ediacar-an–
et al., 2020). The uppermost formation of the Khorbusuonka Group, the
Cambrian boundary in this section occurs near the top of the Sy-
Turkut Formation, consists of thickly laminated dolostone and minor
hargalakh Formation, approximately 20 m above the SB (Fig. 20).
thinly laminated limestone, overlain by dolomitic intraclast-ooid
grainstone and stromatolitic biostromes (Vishnevskaya et al., 2013). It
is interpreted to represent a HST shallowing from basinal to shallow 2.14. Northern Iran
ramp environments (Knoll et al., 1995; Pelechaty et al., 1996). The
overlying Kessyusa Group consists of siliciclastic and minor limestone, The Ediacaran–Cambrian succession of the Alborz Mountains, in
and is subdivided into the Syhargalakh, Mattaia, and Chuskuna for-
northern Iran comprises mixed siliciclastic–carbonate deposits of the
mations (Rogov et al., 2015; Nagovitsin et al., 2015). The boundary
Soltanieh Formation. The Soltanieh Formation was developed in the
between the Syhargalakh and Turkut formations is irregular and fills
Proto-Paleotethys passive margin of northwestern Gondwana (Alavi,
paleokarst caverns (Rogov et al., 2015). This paleokarst unconformity
1996). This formation consists of five members, from bottom to top: the
represents a SB (Fig. 20). A tuff breccia at the base of the Syhargalakh
Lower Dolomite, Lower Shale, Middle Dolomite, Upper Shale, and
Formation has yielded a U–Pb zircon date of 543.9 ± 0.24 Ma
Upper Dolomite members (Hamdi et al., 1989) (Figs. 21 and 22).
(Bowring et al., 1993). At the type section, the Lower Dolomite Member consists of dolo-
Tubular calcareous fossils tentatively assigned to Cambrotubulus mite to cherty dolomite and thin-bedded shale, the Lower Shale
decurvatus were recorded right above the base and below the top of the Member is dominated by black shale, the Middle Dolomite Member
Turkut Formation (Rogov et al., 2015; Markov et al., 2019), whereas
Cloudina is present near the top of the overlying Syhargalakh Formation
(Markov et al., 2019). The lowermost stratigraphic occurrence of T.
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The Neoproterozoic (Cryogenian-Ediacaran)-Cambrian succession 2.16. Eastern Yunnan Province, South China
of Oman is included in the Huqf Supergroup, which not only is re-
presented by laterally continuous outcrops, but also has been identified The Ediacaran–Cambrian succession in eastern Yunnan Province,
in the subsurface (Amthor et al., 2005; Bowring et al., 2007; Grotzinger South China was deposited in a passive continental margin (Jiang et al.,
and Al-Rawahi, 2014). This supergroup is subdivided into three groups, 2012), and comprises in ascending order, the Baiyanshao, Xiaowai-
the Abu Mahara, Nafun and Ara groups (Bowring et al., 2007) (Fig. 23). toushan (also known as Daibu) (Figs. 24 and 25a), Zhongyicun (also
known as Lower Phosphate, White Clay and Upper Phosphate
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Fig. 23. Generalized stratigraphy of the Huqf Supergroup of Oman. The illustrated portion of the Ara Group is based on subsurface data. The age-equivalent
volcaniclastic Fara Group is exposed in the Oman Mountains (modified from Schröder et al., 2003; Amthor et al., 2005; Bowring et al., 2007; and Grotzinger and Al -
Rawahi, 2014). See Fig. 2 for symbols.
members), and Dahai members (Qian et al., 2001b) (Fig. 25d). 2009a,b), and 535.2 ± 1.7 Ma (Zhu et al., 2009) obtained from the
The Baiyanshao, Xiaowaitoushan, and Dahai members are mainly middle interval of the Zhongyicun Member, together with a report of a
dolomite, whereas the Zhongyicun Member is dominantly phosphorite negative carbon isotope excursion below the first appearance of small
and tuff (Zhu et al., 2009). A karst surface occurs at the contact between shelly fossils (Brasier et al., 1990), support the proposed position of the
the Xiaowaitoushan and Zhongyicun members (Zhu, 1997) (Fig. 24b, Ediacaran–Cambrian boundary. However, small shelly fossils have also
c), representing a SB (Fig. 24). Treptichnus pedum has been reported been recovered from the underlying Xiaowaitoushan Member (Zhang
from the Meishucun section in the upper interval of the Zhongyicun Shishan, personal communication to LAB and MGM, 2015) (Fig. 24),
Member (middle interval of the Upper Phosphate Member) (Li, 1991) adding uncertainties to the position of the base of the Anabarites tri-
and near the middle interval of the Zhongyicun Member (near the top of sulcatus–Protohertzina anabarica zone (Zhu, 1997) and, therefore, of the
the Lower Phosphate Member) (Zhu, 1997), whereas small shelly fossils Ediacaran–Cambrian boundary.
first occur considerably lower in the section (Fig. 24). Therefore, the The most plausible position proposed for the Ediacaran–Cambrian
Ediacaran–Cambrian boundary has been defined by the first appearance boundary in South China co-occurs with a karst unconformity at the
of the early Cambrian small shelly fossil Anabarites trisulcatus, recording base of the Zhongyicun Member. Although the Ediacaran–Cambrian
the presence of the Anabarites trisulcatus–Protohertzina anabarica zone succession of Eastern Yunnan was deposited in the passive margin of
(Qian et al., 2001a, 2001b; Zhu et al., 1997), which coincides with the Yangtze platform, the basin was crossed by several northeast southwest
base of the Zhongyicun Member (Zhu, 1997; Zhu et al., 2001; Qian trending syn-sedimentary faults, and it seems that the activity along
et al., 2001b) (Fig. 24). these faults controlled the development of sedimentary facies and
Radiometric ages of 539.4 ± 2.9 Ma (Compston et al., 2008), stratigraphic sequences during the Ediacaran–Cambrian transition
532.3 ± 0.7 Ma (Jiang et al., 2009), 536.3 ± 5.5 Ma (Chen et al., (Qian et al., 2001b).
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Meyer et al., 2014; Cai et al., 2015; Shen et al., 2017). The ages of both
the Doushantuo and Dengying formations are also supported by U-Pb
dating (e.g., Jiang et al., 2009). The Yanjiahe Formation contains ac-
ritarchs, algae, sponges and small shelly fossils, considered of early
Cambrian age (Junfeng et al., 2008; Guo et al., 2014; Chang et al.,
2017). Specifically, sponge spicules are present in the so-called Bed 1
(Chang et al., 2017), whereas small shelly fossils corresponding to the
Anabarites trisulcatus–Protohertzina anabarica zone occur in Bed 2, the
Purella antiqua zone in Bed 3, and the Aldanella yanjiaheensis zone in
Bed 5 (Guo et al., 2014). Accordingly, Beds 1–3 are regarded as For-
tunian in age and Bed 5 as Cambrian Age 2; Bed 4 is barren precluding
the placement of the Fortunian-Cambrian Stage 2 contact (Guo et al.,
2014). A negative excursion of δ13Ccarb has been recorded at the base of
the Yanjiahe Formation (Ishikawa et al., 2008). Accordingly, the
Ediacaran-Cambrian boundary in the Three Gorges area is placed co-
incident with the contact between the Dengying and Yanjiahe forma-
tions (Guo et al., 2014; Chang et al., 2017).
Establishing a sequence stratigraphic framework for the Three
Gorges area has been historically complicated (Jiang et al., 2011).
However, four depositional sequences have been recognized regionally
for the Ediacaran succession (Zhu et al., 2007). The SB of depositional
sequence 1 occurs at the base of the Doushantuo Formation, whereas
two other SBs were identified within this formation, one in the middle
part (depositional sequence 2) and the other one near the top (de-
positional sequence 3) (Zhu et al., 2007). The SB of depositional se-
quence 4 is present in the middle part of the Dengying Formation (Jiang
et al., 2011; Cui et al., 2019). Although the Cambrian succession has not
been explored in the same detail from a sequence stratigraphic per-
spective, a karstic surface has been identified at the top of depositional
sequence 4, in close proximity to the Ediacaran-Cambrian boundary
(Zhu et al., 2007; Cui et al., 2019).
3. Discussion
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Fig. 25. Sedimentary facies and stratal stacking patterns in Eastern Yunnan, South China. (a) Lower interval of the Xiaowaito ushan Member; (b) Contact of the
Xiaowaitoushan and Lower Phosphate members; (c) Close-up of contact between the Xiaowaitoushan and Lower Phosphate members; (d) Contact between of the
Upper Phosphate and Dahai members. See Fig. 2 for symbols.
Ediacaran–Cambrian boundary has implications that trascend the issue parasequence sets. In these sections, comparison of identical sedimen-
of correlation, and affect our ability to test evolutionary hypotheses tary facies through time allows differentiation between environmental
using stratigraphic paleobiology approaches (Buatois et al., 2013). and evolutionary factors for observed biotic changes (MacNaughton
Historically, the general proximity and common co-occurrence of the and Narbonne, 1999; Shahkarami et al., 2017a). Additionally, some of
Ediacaran–Cambrian boundary with a SB was thought to impair reliable these sections represent conformable successions (e.g., Fortune Head),
paleontologic sampling, owing to erosion, incomplete records implied displaying a more complete record of shallow-marine facies across the
hiatuses and lack of adequate facies (Mount and McDonald, 1992). Ediacaran–Cambrian transition. Thin carbonate successions, such as
However, the recognition of significant diachronism in this interval, those in South China, provide a high-resolution biostratigraphic record
coupled with decades of scrutinizing these successions for erosional (e.g., Guo et al., 2014), but are more limited to evaluate potential facies
remnants, body fossils, microfossils, trace fossils, and chemostrati- controls due to stratigraphic condensation. In other cases, the occur-
graphic evidence have increasingly allowed incomplete successions to rence of specific sedimentary facies and depositional conditions may
provide insights into the Ediacaran–Cambrian transition. Also, the fact have been detrimental for the establishment of biotas during the
that in many localities (e.g., Namibia) incision may have taken place Ediacaran-Cambrian transition. For example, the recurrence of eva-
during the earliest Cambrian underscores the importance of detailed porites in the Oman succession indicates stressful conditions and may
sampling in strata below the SB with the aim of refining the location of be responsible for the paucity of fossils near the Ediacaran-Cambrian
the Ediacaran–Cambrian transition. Specifically, exploring terminal boundary in that succession.
Ediacaran deposits located in interfluve positions (i.e., between incised Our synthesis of seventeen widely separated Ediacaran–Cambrian
valleys) may be particularly rewarding because these settings may successions suggests that significant diachronism was involved in the
preserve thick shallow-marine strata below the SB, which could have generation of the Great Unconformity. In most places, the Great
been eroded along axial positions of the paleovalleys. Integration of Unconformity is actually a composite sequence boundary recording
sequence-stratigraphic information with high-resolution age data is key various eustatic episodes of sea-level rise and fall overprinted by mul-
in evaluating competing models to explain the displacement of the tiple tectonic events of subsidence and uplift. Accordingly, the Great
Ediacara biota by the Cambrian fauna, as has been recently illustrated Unconformity cannot be attributed to a single cause, but to a result of a
in Namibia (Linnemann et al., 2019). Thick siliciclastic or mixed car- complex interplay and succession of factors. Even at the classic Tapeats
bonate-siliciclastic successions, such as those in Namibia, Iran, Oman, Sandstone exposures where this unconformity was defined, subsequent
western United States, Mackenzie Mountains, and Newfoundland are stratigraphic work (Rose, 2006) and detrital zircon geochronology
particularly useful to map and delineate parasequences and (Karlstrom et al., 2018) is showing it to be a highly diachronous surface,
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Fig. 26. Generalized stratigraphy of the Yangtze Gorges succession of Southern China (modified from Zhu et al., 2007; and Chen et al., 2013). See Fig. 2 for symbols.
with deposition often not commencing until Furongian (late Cambrian) Kaufman, 2018). More recently, the notion that these were two separate
or younger time in some parts of the craton. In short, the formation of a worlds has been questioned, and instead, an overlapping series of
SB during the Ediacaran–Cambrian transition most likely reflects evolutionary radiations is increasingly hypothesized (Schiffbauer et al.,
overprint of local tectonics on pure eustasy, implying that the SB should 2016; Zhu et al., 2017; Darroch et al., 2018; Wood et al., 2019). Ac-
not be used for inter-basin correlations. cordingly, regardless of the major geochemical changes associated with
Traditionally the Ediacaran-Cambrian boundary has been seen as weathering and erosion during the formation of the Great Un-
separating rocks containing a biota of problematic affinities from an conformity, the roots of the Cambrian explosion are in the terminal
overlying fauna dominated by representatives of almost all the main Ediacaran, and predate the sea-level fall (Schiffbauer et al., 2016;
animal body plans (Brasier et al., 1994; Landing, 1994; Narbonne et al., Buatois and Mángano, 2016; Zhu et al., 2017; Darroch et al., 2018;
2012; Peng et al., 2012; Peters and Gaines, 2012; Landing et al., 2013; Wood et al., 2019).
Table 1
Paleogeographic position, tectonic setting, and position of Ediacaran–Cambrian boundary with respect to the SB in the studied successions.
Position of the E–C boundary in relation to Section Paleogeographic position at the time of E–C Tectonic setting
SB
Below a SB Southeastern Newfoundland, Canada Northwest margin of the Avalon terrane Transtensional
Caborca terranes, northwest Mexico Southwestern Laurentia. Passive margin
Nama Group, southern Namibia Western margin of the Kalahari Craton Foreland basin
Northern Iran Northwestern margin of Gondwana Passive margin
Above a SB Olenek Uplift, northeast Siberia Northern margin of Siberian craton Passive margin/Foreland basin
In between two SB Mackenzie Mountains, Canada Western margin of Laurentia Passive margin
Death Valley, Eastern California Southwestern Laurentia Passive margin
White Inyo Mountains, western Nevada, Southwestern Laurentia passive margin
Lublin slope, southeastern Poland South western Baltica Rift
Vestertana Group, Northern Norway Northwestern Margin of Baltica (Baltoscandian Extensional/foreland basin
margin)
Huqf Supergroup, Oman Northwestern margin of Gondwana Rift
Coinciding with a SB Flinders Ranges, South Australia South eastern Australian continent Passive margin/Rift
Amadeus Basin, Central Australia Central Australian continent Intracratonic basin
Vanrhynsdorp Group, South Africa Western margin of the Kalahari Craton Foreland basin
Zavkhan terrane, western Mongolia Zavkhan terrane/adjacent to Siberian craton Foreland basin
Eastern Yunnan, South China South China Craton (Yangtze Passive margin
Yangtze Gorges, South China South China Craton (Yangtze Passive margin
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4. Conclusions
Acknowledgments
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