|
|
||||||||
1 Department of Geological Sciences, University of Saskatchewan, 114 Science Place, Saskatoon, Saskatchewan, S7N 5E2, Canada; luis.buatois{at}usask.ca
2 Department of Earth and Atmospheric Sciences, 126 Earth Sciences Building, University of Alberta, Edmonton, Alberta, T6G 2E3, Canada
3 Earth Sciences, Simon Fraser University, Burnaby, British Columbia, V5A 1S6, Canada
4 Department of Geological Sciences, University of Saskatchewan, 114 Science Place, Saskatoon, Saskatchewan, S7N 5E2, Canada
5 Geological Survey of Canada, 3303-33rd Street N.W., Calgary, Alberta, T2L 2A7, Canada
6 Department of Earth and Atmospheric Sciences, 1-26 Earth Sciences Building, University of Alberta, Edmonton, Alberta, T6G 2E3, Canada
7 Núcleo de Estudos Sedimentológicos e EstratigráficosNESE UNISINOS, Av. Unisinos 950, 93022-000 São Leopoldo RS, Brazil
8 Department of Environmental Studies, Emory University, Atlanta, Georgia 30322
Trace fossils in estuarine deposits of different ages have been compared to evaluate colonization history of brackish-water ecosystems and to calibrate trace-fossil, brackish-water models with respect to geologic time. This comparative analysis reveals that, although the colonization of marginal-marine, brackish-water environments was a long-term process that spanned most of the Phanerozoic, this process of invasion of fully marine organisms into restricted, marginal-marine habitats did not occur at a constant rate.
Five major colonization phases can be distinguished. The first phase (EdiacaranOrdovician) represents a prelude to the major invasion that occurred during the rest of the Paleozoic. While EdiacaranCambrian ichnofaunas seem to be restricted to the outermost zones of marginal-marine depositional systems, Ordovician assemblages show some degree of landward expansion within brackish-water ecosystems. Intensity of bioturbation and ichnodiversity levels were relatively low during this phase. The second phase (SilurianCarboniferous) is marked by the appearance of more varied morphologic patterns and behavioral strategies, resulting in a slight increase in ichnodiversity. While previous assemblages were arthropod dominated, brackish-water SilurianCarboniferous ichnofaunas include structures produced by bivalves, ophiuroids, and polychaetes. Ichnofaunas from the third phase (PermianTriassic) seem to be characterized by the presence of crustacean burrows, reflecting the late Paleozoic crustacean radiation and adaptation of some groups to brackish-water conditions. The fourth phase (JurassicPaleogene) is typified by a remarkable increase in ichnodiversity and intensity of bioturbation of estuarine facies. Colonization occurred not only in softgrounds and firmgrounds, but also in hardgrounds and xylic substrates. The fifth phase (NeogeneRecent) records the onset of modern brackish-water benthos. Although still impoverished with respect to their fully marine counterparts, brackish-water ichnofaunas may reach moderately high diversities, particularly in middle- and outer-estuarine regions, and degree of bioturbation may be high in certain estuarine subenvironments. Comparative analysis of brackish-water ichnofaunas through geologic time provides valuable evidence to understand colonization of marginal-marine environments through the Phanerozoic, and allows for calibration of ichnologic models that may aid in the recognition of estuarine valley-fill deposits in the stratigraphic record.
This article has been cited by other articles:
![]() |
N. S. Davies and I. J. Sansom Ordovician vertebrate habitats: A Gondwanan perspective Palaios, October 1, 2009; 24(10): 717 - 722. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. E. HAUCK, S. E. DASHTGARD, S G. PEMBERTON, and M. K. GINGRAS BRACKISH-WATER ICHNOLOGICAL TRENDS IN A MICROTIDAL BARRIER ISLAND-EMBAYMENT SYSTEM, KOUCHIBOUGUAC NATIONAL PARK, NEW BRUNSWICK, CANADA Palaios, August 1, 2009; 24(8): 478 - 496. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. A. Buatois, N. Santiago, K. Parra, and R. Steel Animal-Substrate Interactions in an Early Miocene Wave-Dominated Tropical Delta: Delineating Environmental Stresses and Depositional Dynamics (Tacata Field, Eastern Venezuela) Journal of Sedimentary Research, July 1, 2008; 78(7): 458 - 479. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. A. Young, D. M. Rudkin, E. P. Dobrzanski, S. P. Robson, and G. S. Nowlan Exceptionally preserved Late Ordovician biotas from Manitoba, Canada Geology, October 1, 2007; 35(10): 883 - 886. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. J. FALCON-LANG and R. F. MILLER Palaeoenvironments and palaeoecology of the Early Pennsylvanian Lancaster Formation ('Fern Ledges') of Saint John, New Brunswick, Canada Journal of the Geological Society, September 1, 2007; 164(5): 945 - 957. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Yang, R. W. Dalrymple, M. K. Gingras, S. Chun, and H. Lee Up-Estuary Variation of Sedimentary Facies and Ichnocoenoses in an Open-Mouthed, Macrotidal, Mixed-Energy Estuary, Gomso Bay, Korea Journal of Sedimentary Research, September 1, 2007; 77(9): 757 - 771. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-P. ZONNEVELD, T. W. BEATTY, and S. G. PEMBERTON LINGULIDE BRACHIOPODS AND THE TRACE FOSSIL LINGULICHNUS FROM THE TRIASSIC OF WESTERN CANADA: IMPLICATIONS FOR FAUNAL RECOVERY AFTER THE END-PERMIAN MASS EXTINCTION Palaios, January 1, 2007; 22(1): 74 - 97. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. LOCKWOOD and L. A. WORK QUANTIFYING TAPHONOMIC BIAS IN MOLLUSCAN DEATH ASSEMBLAGES FROM THE UPPER CHESAPEAKE BAY: PATTERNS OF SHELL DAMAGE Palaios, October 1, 2006; 21(5): 442 - 450. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |