Microatoll microbialites of Lake Clifton, Western Australia: Morphological analogues of Cryptozoön proliferumHall, the first formally-named stromatolite

The Linnaean name Cryptozoön proliferumHall was proposed in 1883 for a previously undescribed life-form preserved in spectacular exposures of Cambrian limestones in New York State, USA. It is now recognised that these are exposures of stromatolitic microbialites, laminated organosedimentary structur...

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Published in:Facies
Main Authors: Burne, Robert V., Moore, Linda S.
Format: Article in Journal/Newspaper
Language:English
Published: Springer Nature 1993
Subjects:
Online Access:https://espace.library.uq.edu.au/view/UQ:77001cd
id ftunivqespace:oai:espace.library.uq.edu.au:UQ:77001cd
record_format openpolar
institution Open Polar
collection The University of Queensland: UQ eSpace
op_collection_id ftunivqespace
language English
topic Cambrian
Cryptozoon
Ecomorphs
Lake Clifton (Australia)
Microatolls
Microbialites
Recent
Reef Platform
Saratoga springs
Stromatolites
Thrombolites
1907 Geology
1911 Palaeontology
1913 Stratigraphy
spellingShingle Cambrian
Cryptozoon
Ecomorphs
Lake Clifton (Australia)
Microatolls
Microbialites
Recent
Reef Platform
Saratoga springs
Stromatolites
Thrombolites
1907 Geology
1911 Palaeontology
1913 Stratigraphy
Burne, Robert V.
Moore, Linda S.
Microatoll microbialites of Lake Clifton, Western Australia: Morphological analogues of Cryptozoön proliferumHall, the first formally-named stromatolite
topic_facet Cambrian
Cryptozoon
Ecomorphs
Lake Clifton (Australia)
Microatolls
Microbialites
Recent
Reef Platform
Saratoga springs
Stromatolites
Thrombolites
1907 Geology
1911 Palaeontology
1913 Stratigraphy
description The Linnaean name Cryptozoön proliferumHall was proposed in 1883 for a previously undescribed life-form preserved in spectacular exposures of Cambrian limestones in New York State, USA. It is now recognised that these are exposures of stromatolitic microbialites, laminated organosedimentary structures formed from interaction between a benthic microbial community (BMC) and the environment. Microbialites are neither fossil organisms nor trace fossils. These complex structures are the products of dissipative, self-organising systems involving a BMC, the external environment and the accreting microbialite. Functionally analogous BMCs of different species compositions may build similar structures in similar environments in quite separate periods. The type exposures of Cryptozoön proliferum show objects composed of complex, concentric rings, up to a metre in diameter, that have grown laterally without any restriction other than that provided by neighbouring structures. They are not the relicts of domes truncated by penecontemporaneous erosion or Pleistocene glaciation, but depositional forms in which upward growth was restricted. Analogous modern structures occur on a reef platform along the north east shore of hyposaline Lake Clifton, Western Australia. These are tabular thrombolitic microbialites that vary lakeward across the reef platform from low, compound structures to discrete, concentric structures up to 50 cm high. The Lake Clifton forms are, in turn, morphological analogues of microatolls found on coral reef platforms. Coral microatolls are coral colonies with flat, dead tops and living perimeters in which upward growth is constrained by the sea surface. In shallow water they form circular rims of laterally growing coral around a dead centre. In deeper water they form coral heads that develop flat tops on reaching sea level. It is concluded that both the tabular microbialites of Lake Clifton and the type exposures of Cryptozoön proliferum are analogous to coral microatolls in both form and origin-structures that have been able to grow laterally, but in which upward growth is restricted by subaerial exposure. Similar microatoll microbialites have been described from other modern environments, including Great Salt Lake, Utah, USA and Stocking Island, Exuma Cays, Bahamas. Ancient examples may include some of the “tufa” deposits of the Basal Purbeck Formation in Dorset, UK, as well as the coalesced domal bioherms of the Upper Cambrian Arrinthrunga Formation of the Georgina Basin, Central Australia, and the “washbowl” structures described from the Båtsfjord Formation of the Varanger Peninsula, north Norway. Progress towards a reliable interpretation of ancient microbialites depends on an understanding of modern environments in which analogous structures are forming. This study of microatolls has demonstrated that other sessile life forms may create colonial ecomorphs that, used cautiously, can serve as analogues for understanding the factors controlling the growth and form of microbialites. The surprising lack of pre-Pleistocene examples of microatolls recorded to date has simply been due to their lack of recognition in the geological record. They occur in sequences from the Proterozoic onwards, and provide powerful environmental indicators of ancient reef platforms on which biological growth was adjusted to contemporary sea level.
format Article in Journal/Newspaper
author Burne, Robert V.
Moore, Linda S.
author_facet Burne, Robert V.
Moore, Linda S.
author_sort Burne, Robert V.
title Microatoll microbialites of Lake Clifton, Western Australia: Morphological analogues of Cryptozoön proliferumHall, the first formally-named stromatolite
title_short Microatoll microbialites of Lake Clifton, Western Australia: Morphological analogues of Cryptozoön proliferumHall, the first formally-named stromatolite
title_full Microatoll microbialites of Lake Clifton, Western Australia: Morphological analogues of Cryptozoön proliferumHall, the first formally-named stromatolite
title_fullStr Microatoll microbialites of Lake Clifton, Western Australia: Morphological analogues of Cryptozoön proliferumHall, the first formally-named stromatolite
title_full_unstemmed Microatoll microbialites of Lake Clifton, Western Australia: Morphological analogues of Cryptozoön proliferumHall, the first formally-named stromatolite
title_sort microatoll microbialites of lake clifton, western australia: morphological analogues of cryptozoön proliferumhall, the first formally-named stromatolite
publisher Springer Nature
publishDate 1993
url https://espace.library.uq.edu.au/view/UQ:77001cd
geographic Norway
geographic_facet Norway
genre Båtsfjord
North Norway
Varanger
genre_facet Båtsfjord
North Norway
Varanger
op_relation doi:10.1007/BF02536926
issn:1612-4820
issn:0172-9179
orcid:0000-0003-0689-4298
op_doi https://doi.org/10.1007/BF02536926
container_title Facies
container_volume 29
container_issue 1
container_start_page 149
op_container_end_page 168
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spelling ftunivqespace:oai:espace.library.uq.edu.au:UQ:77001cd 2023-05-15T15:39:55+02:00 Microatoll microbialites of Lake Clifton, Western Australia: Morphological analogues of Cryptozoön proliferumHall, the first formally-named stromatolite Burne, Robert V. Moore, Linda S. 1993-01-01 https://espace.library.uq.edu.au/view/UQ:77001cd eng eng Springer Nature doi:10.1007/BF02536926 issn:1612-4820 issn:0172-9179 orcid:0000-0003-0689-4298 Cambrian Cryptozoon Ecomorphs Lake Clifton (Australia) Microatolls Microbialites Recent Reef Platform Saratoga springs Stromatolites Thrombolites 1907 Geology 1911 Palaeontology 1913 Stratigraphy Journal Article 1993 ftunivqespace https://doi.org/10.1007/BF02536926 2020-08-06T12:04:32Z The Linnaean name Cryptozoön proliferumHall was proposed in 1883 for a previously undescribed life-form preserved in spectacular exposures of Cambrian limestones in New York State, USA. It is now recognised that these are exposures of stromatolitic microbialites, laminated organosedimentary structures formed from interaction between a benthic microbial community (BMC) and the environment. Microbialites are neither fossil organisms nor trace fossils. These complex structures are the products of dissipative, self-organising systems involving a BMC, the external environment and the accreting microbialite. Functionally analogous BMCs of different species compositions may build similar structures in similar environments in quite separate periods. The type exposures of Cryptozoön proliferum show objects composed of complex, concentric rings, up to a metre in diameter, that have grown laterally without any restriction other than that provided by neighbouring structures. They are not the relicts of domes truncated by penecontemporaneous erosion or Pleistocene glaciation, but depositional forms in which upward growth was restricted. Analogous modern structures occur on a reef platform along the north east shore of hyposaline Lake Clifton, Western Australia. These are tabular thrombolitic microbialites that vary lakeward across the reef platform from low, compound structures to discrete, concentric structures up to 50 cm high. The Lake Clifton forms are, in turn, morphological analogues of microatolls found on coral reef platforms. Coral microatolls are coral colonies with flat, dead tops and living perimeters in which upward growth is constrained by the sea surface. In shallow water they form circular rims of laterally growing coral around a dead centre. In deeper water they form coral heads that develop flat tops on reaching sea level. It is concluded that both the tabular microbialites of Lake Clifton and the type exposures of Cryptozoön proliferum are analogous to coral microatolls in both form and origin-structures that have been able to grow laterally, but in which upward growth is restricted by subaerial exposure. Similar microatoll microbialites have been described from other modern environments, including Great Salt Lake, Utah, USA and Stocking Island, Exuma Cays, Bahamas. Ancient examples may include some of the “tufa” deposits of the Basal Purbeck Formation in Dorset, UK, as well as the coalesced domal bioherms of the Upper Cambrian Arrinthrunga Formation of the Georgina Basin, Central Australia, and the “washbowl” structures described from the Båtsfjord Formation of the Varanger Peninsula, north Norway. Progress towards a reliable interpretation of ancient microbialites depends on an understanding of modern environments in which analogous structures are forming. This study of microatolls has demonstrated that other sessile life forms may create colonial ecomorphs that, used cautiously, can serve as analogues for understanding the factors controlling the growth and form of microbialites. The surprising lack of pre-Pleistocene examples of microatolls recorded to date has simply been due to their lack of recognition in the geological record. They occur in sequences from the Proterozoic onwards, and provide powerful environmental indicators of ancient reef platforms on which biological growth was adjusted to contemporary sea level. Article in Journal/Newspaper Båtsfjord North Norway Varanger The University of Queensland: UQ eSpace Norway Facies 29 1 149 168