The Cambrian is a short period in earth
history, starting approximately 545 m.y. ago and ending about 490 m.y. ago.
Nevertheless, it was without any doubt one of the most important and dramatic
periods. The lower boundary of the Cambrian is not only the beginning of a new
system but also the start of the Paleozoic and the Phanerozoic. And the Early
Cambrian saw the extremely rapid diversification of multicellular animals, the
Cambrian Explosion, that determined the animal evolution and is indirectly
responsible for the present-day wildlife.
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Mostly for practical reasons, any system in
earth history needs to be subdivided into smaller portions. However, any period
has different aspects: The subdivision of the rock successions leads to the
distinction of Groups, Formations, and Members, which are lithostratigraphic
units. Short-lived fossils permit to recognize rocks of certain ages. They
establish Biozones, which are biostratigraphic units. The pure time aspect
leads to chronostratigraphy and a subdivision of systems into Series and
Stages. The choice of subdivision at a particular locality or in a certain region
is normally without any problem. Globally useful units, however, are generally
extremely difficult to establish. All these hierarchically ordered units need
to be fixed by sound boundaries that should be easily correlatable over large
distances. Ideally, a boundary should be recognizable on a global scale by the
sudden and synchronous appearence of a significant and short living fossil that
occurs abundantly in the rocks and/or by a significant change of physical
parameters in a rock succession (e.g., a dramatic change in the oxygen or
carbonate isotopic composition). However, those are lucky events and rarely
found, or they are at places in the successions that are unsuitable for global
subdivisions for historical and other reasons. Stratigraphical subdivision is
hence a difficult task, and this is the reason why the International Subcommission on Cambrian Stratigraphy (see I.U.G.S.) exists.
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As it seems, the subdivision of the Cambrian is
particularly difficult. The Cambrian System is currently without formally
agreed international subdivisions, such as stages. This partly reflects the
scarcity of suitable biostratigraphic markers for intercontinental correlation
at the stage level and a strong faunal provincialism. However, research in
progress on trilobites and conodonts (for the latter half of the Late Cambrian)
shows promise for long range correlation and definition of stages. The Cambrian
time interval is of growing international interest and research is being
actively pursued by ISCS members. A number of suggested correlations was
published in recent years by members of the Cambrian Subcommission, but usually
they differ from each other in several aspects. Nevertheless, they depart
markedly from correlations suggested some twenty or even ten years ago and
indicate a steady progress in stratigraphical research.
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The choice of a formal Cambrian lower boundary
started in the 1970s and finally ended by the ratification of the
Proterozoic-Cambrian boundary stratotype in 1991. The decision was officially
driven forward by the I.G.C.P. Working Group 29 on the Precambrian-Cambrian
boundary, which became the longest active of all I.G.C.P. working groups. The
major reason for this delay of a formal decision was the growing amount of data
on strata and fossils from the Proterozoic-Cambrian transition that lead to
steady change of the opinions where the boundary should be drawn. Starting in
the 1970s with the correlation of strata the earliest shelly macrofossils, small shelly fossils of Tommotian aspect came into focus shortly after. However, this
episode ended when it became clear that the correlation potential of the
earliest SSFs is insufficient. Finally, it became evident that the
stratigraphical occurrence of trace-fossils depicts an evolution to more complicated traces, which, in turn, proves
the progressive evolution to more anatomically complicated animals that were
able to perform a progressively complex behaviour. The first trace with a
somewhat complicated pattern is Trichophycus pedum (formerly known as "Phycodes pedum"). It occurs nearly
worldwide, and its first occurrence is with the late fossils of Ediacaran
aspect or, usually, in strata above them, whereas the first shelly fossils
appeared clearly later. Hence, the ichnofossil assemblage with Trichophycus
pedum marks the first occurrence of well-developed, fairly complex metazoan
animals, and this is today regarded as the most useful landmark to characterize
the Cambrian lower boundary. The best section to study the stacked appearance
of various ichnofossils, SSFs, and finally shelled macrofossils is the section
at Fortune Head, southeastern Newfoundland, which belonged to the Cambrian
continent Avalonia. Accordingly, the International Subcommission on Cambrian
Stratigraphy (through its Working Group on the Precambrian-Cambrian Boundary) made
the official decision in 1991 to draw the base on the Cambrian at the first
appearence date (FAD) of Trichophycus pedum in the reference section at
Fortune Head.
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. The
Proterozoic-Cambrian boundary GSSP: The
Fortune Head section near Fortune, southeastern Newfoundland. Exposed are
rocks of the Chapel Island Formation, members 1 and 2. Copyright (c) G. Geyer, 1997 |
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Definition of the Cambrian-Ordovician boundary was a
basic problem dealt with by the Cambrian-Ordovician Boundary Working Group
for a long period. Traditional concepts of the Cambrian-Ordovician boundary
based on the occurrence of the graptolite Rhabdinopora flabelliforme,
which has a limited regional distribution. Strata with Rhabdinopora
flabelliforme are often difficult to correlate precisely so that
different species (and subspecies) of conodonts were favored for definition
of the Cambrian-Ordovician boundary. The Cambrian-Ordovician Boundary Working
Group finally decided in 1998 by majority that the base of the Ordovician
should be placed at the base of the zone with Iapetognathus fluctivagus,
which approximates the Cordylodus lindstromi Zone, the Rhabdinopora
flabelliforme Zone and the FAD of the trilobite Jujuyaspis. The
GSSP for this boundary was chosen at the Green Point section, Newfoundland. |
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.. The Cambrian-Ordovician transition near Port
Cerriad, North Wales: Arenigian rocks (thick unit)
overlie Copyright (c) G. Geyer,
1997 |
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The restriction of faunal groups to particular
climatic belts and facies confined many genera and species of Cambrian
organisms to single Cambrian continents, and diachronous occurrences of key
groups between the continents often limits the precision the precision of
biostratigraphy in global correlation, especially in the Early Cambrian.
Correlations based on international comparison of improved geochronologic
dating techniques will improve correlations, particularly of the uppermost
Proterozoic to sub-trilobitic Lower Cambrian interval.
About a decade ago it became evident that most
of the published age data on the Cambrian were irrelevant because they were
based on Rubidium-Strontium ages that deviated from the true values and gave
ages that were up to 50 m.y. too high. This created a remarkable changes in the
age assignment of the Cambrian in general, particularly in its lower boundary
as portrait in the figure below.
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Changing views of late Neoproterozoic to
earliest Ordovician time. The figure shows estimated dates from Harland et
al., 1982, the Decade of North American Geology (DNAG) issues (1983),
Harland et al., 1990, the International Union of Geological Sciences
(IUGS) table generated by Cowie and Brasier (1989), and the data presented by
Bowring & Erwin, 1998. Open circles denote poorly constrained
geochronologic tie-points and the black circles better contrained tie-points.
Error bars are shown for the Harland et al., 1982 and 1989 time scales. The
543.9±1.0 m.y. at the Proterozoic-Cambrian boundary cames from ashes in the Rusophycus
avalonensis assemblage zone of southeastern Newfoundland so that the base
of the Cambrian is slightly older than shown in the figure and would be
roughly at 545 m.y.The Manykaian stage of Siberia and its equivalents were
added to the Cambrian in 1992. Note that Neoproterozoic subdivisions are not
yet firmly established. Slightly modified after Bowring & Erwin (GSA
today, vol. 8, September 1998, Fig. 2). |
New datings focus particularly on the latest Proterozoic-earliest Cambrian interval, from which no readily correlatable biostratigraphic data are available. A number of recent age data with relatively reliable numbers are listed below.
Latest
Proterozoic and base of the Cambrian
595±15
m.y. mid-Dahai Mb.,
Meishucun, South China (Rb-Sr whole rock age; Zhang et al., 1984)
575±7.6
m.y. volcanics, Carolina Slate
Belt, eastern United States (U-Pb age, Kozuch et al., 198)
550±26 m.y. volcanics,
Puncoviscana Foldbelt, northwestern Argentina (K-Ar age, Omarini et al., 1996)
551.4±5.8 m.y. rhyolite flow,
Mooring Cove Fm., Fortune Bay, Nfld. (isotope dilution U-Pb age; Tucker and McKerrow,
1995)
543.6±0.24 m.y. volcanic breccias,
Lessyusa Fm., Nemakit-Dal'dyn Stage, Khorbusuonka, Olenek uplift, Siberia (U-Pb
zircon age; Bowring et al., 1993)
535±7 m.y. granitoids, Puncoviscana
Foldbelt, northwestern Argentina (U-Pb age, Bachmann et al., 1987)
534.6±0.4 fluvial
conglomerates, between Nemakit-Dal'dyn and Tommotian stages, Kharaulakh
Mountains, Siberia (U-Pb zircon age; Bowring et al., 1993)
525±7
m.y., max. 539±34 m.y. K-bentonite,
Zhongyicun Mb., Dengying Fm., Meishucun, South China (SHRIMP zircon ages;
Compston et al., 1992)
Middle Early Cambrian
530.7±0.9 m.y.
felsic volcanic ash, near top of the Chapel Island Fm., R. avalonensis
Zone, New Brunswick (U-Pb dilution age; Isachsen et al., 1994)
521±7 m.y. tuff layer fom the upper Lie de vin Formation, Morocco (SHRIMP zircon age; Compston et al., 1992)
522±1
m.y. ash layer fom the
upper Lie de vin Formation, Morocco (isotope dilution U-Pb age; Landing et al.,
1998)
Late Early Cambrian
526±4 m.y. felsic
tuff, Heatherdale Shale, mid-Botomian, Sellick's Hill, Fleurieu Peninsula,
South Australia (SHRIMP zircon ages, Cooper et al., 1992)
525±8 m.y. felsic tuff,
Cymbric Vale Fm., western New South Wales (SHRIMP zircon ages, Zhou and
Whitford, 1994)
517±1
m.y. ash layer from uppermost
Issafen Formation, Sectigena Zone, Morocco (isotope dilution U-Pb
age; Landing et al., 1998)
511±1
m.y. volcanic ash layer
from "Protolenus Zone", southern New Brunswick (isotope
dilution U-Pb age; Landing et al., 1998)
Latest
Middle Cambrian
505.1±1.3 m.y. ignimbrites and
crystal tuffs, Taylor Formation, probable equivalent of Floran/Undillan,
Antarctica (U-Pb zircon age; Encarnación et al. 1999)
494.4±3.8 m.y. Comstock Tuff, Lejopyge
laevigata Zone, mid-Boomerangian, Tasmania (U-Pb zircon age; Perkins and
Walshe, 1993)
Latest
Late Cambrian
501±7 m.y. mudstones, base
of Cordylodus proavus Zone, Xiaoyangqiao section, Dayangcha, Northeast
China (Rb-Sr age; Chen et al., 1988)
491±1 m.y. ash bed, top of
Upper Cambrian, North Wales (U-Pb zircon age; Davidek et al., 1998)
.A diagrammatic summary of biostratigraphically and geochronologically
well constraint samples of late Vendian and Cambrian age was provided by Sam
Bowring and Doug Erwin (GSA today, vol. 8, September 1998, Fig. 3), which is
presented below. This figure presents data from Bowring et al., 1993,
Grotzinger et al., 1995, Compston et al., 1995, Landing et al., 1998, and
Davidek et al., 1998. MIT IDTIMS data were isotope dilution-thermal mass
spectrometry data from the Massachusetts Institute of Technology; ANU SHRIMP
are super-high resolution ion microprobe data from the Australian National
University; ROM IDTIMS are isotope dilution-thermal mass spectrometry data from
the Royal Ontario Museum, Toronto. Note that the stages Nemakit-Daldynian,
Tommotian, Atdabanian and Botoman used in the figure are Siberian regional
stages. The 543.9±1.0 m.y. at the Proterozoic-Cambrian boundary cames from
ashes in the Rusophycus avalonensis assemblage zone of southeastern
Newfoundland so that the base of the Cambrian is slightly older than shown in
the figure and would be roughly at 545 m.y.

Significant changes of physical parameters in a
rock succession theoretically have a great potential, and studies on the
oxygen, carbon and strontium isotopes have growing value, especially for
regional studies of facies and stratigraphy. This is particularly interesting,
when faunal groups are restricted to climate belt and magnafacies and are
confined to single Cambrian continents, or when the first occurrence of key
faunal groups is diachronous. Comparison of stable isotopic signatures and
paleomagnetic variations have already improved correlations of the uppermost
Proterozoic and sub-trilobitic Early Cambrian and will allow a precise
intercontinental correlation when more data and improved techniques are
available. Especially paleomagnetic data still suffer from uncertainties, such
as diagenetic overprint, rates of sedimentation or paleolatitude.
Isotopic research has made good progress in the
last decade, mainly studies on carbon and strontium isotopes, and plenty of
data are now available for the Cambrian lower and upper boundary intervals (further reading).
For most of the Cambrian, no meaningful
paleomagnetic data have been published (further reading). The latest Cambrian appears to be characterized by mainly reversed
polarity. The earliest Ordovician, by contrast, is characterized by periods of
normal polarity (Ripperdan and Kirschvink, 1992).
Kirschvink (1976, 1978a, 1978b) investigated
polarity fluctuations in the Early Cambrian of the Amadeus Basin, Australia and
showed that the Cambrian portion of the Arumbera Sandstone is an interval of
mixed polarity following normal polarity in the Late Proterozoic lower Arumbera
Sandstone. This interval of mixed polarity extend into the Todd River Dolomite
and Eninta Sandstone. Biostratigraphic data give evidence for an Early Cambrian
age of the Todd River Dolomite. Data from the Early Cambrian of South Australia
and from the Middle and Late Cambrian of central Australia summarized by
Klootwijk (1980) suggest that the Lower Cambrian Ajax Limestone (Flinders
Ranges) indicates a mixed polarity while the coeval Wilkawillina Limestone and
Oraparinna Shale has a reversed. The Middle Cambrian Wirrealpa Limestone, the
Moodlatana Formation and parts of the Balcoracana Formation appear to have a
reversed, but the Pantapinna Sandstone has a mixed polarity. The upper Giles
Creek and the lower Shannon formations have a reversed polarity (see Shergold,
1995).
Latest update: March 13, 2001