Early Metazoan Evolution and the Meaning of Its Fossil Record

1993 ◽  
pp. 339-386 ◽  
Author(s):  
Jerzy Dzik
2007 ◽  
Vol 3 (3) ◽  
pp. 314-317 ◽  
Author(s):  
Christian B Skovsted ◽  
Glenn A Brock ◽  
Anna Lindström ◽  
John S Peel ◽  
John R Paterson ◽  
...  

Predation is arguably one of the main driving forces of early metazoan evolution, yet the fossil record of predation during the Ediacaran–Early Cambrian transition is relatively poor. Here, we present direct evidence of failed durophagous (shell-breaking) predation and subsequent shell repair in the Early Cambrian (Botoman) epibenthic mollusc Marocella from the Mernmerna Formation and Oraparinna Shale in the Flinders Ranges, South Australia. This record pushes back the first appearance of durophagy on molluscs by approximately 40 Myr.


Paleobiology ◽  
2019 ◽  
Vol 45 (02) ◽  
pp. 235-245 ◽  
Author(s):  
Seth Finnegan ◽  
James G. Gehling ◽  
Mary L. Droser

AbstractRecent excavations of Ediacaran assemblages have revealed striking bed-to-bed variation in diversity–abundance structure, offering potential insight into the ecology and taphonomy of these poorly understood early Metazoan ecosystems. Here we compare faunal variability in Ediacaran assemblages to that of younger benthic assemblages, both fossil and modern. We decompose the diversity of local assemblages into within-collection (α) and among-collection (β) components and show that β diversity in Ediacaran assemblages is unusually high relative to younger assemblages. Average between-bed ecological dissimilarities in the Phanerozoic fossil record are comparable to within-habitat dissimilarities typically observed over meter to kilometer scales in modern benthic marine habitats, but dissimilarities in Ediacaran assemblages are comparable to those typically observed over 10–100 km scales in modern habitats. We suggest that the unusually variable diversity–abundance structure of Ediacaran assemblages is due both to their preservation as near snapshots of benthic communities and to original ecological differences, in particular the paucity of motile taxa and the near lack of predation and infaunalization.


1985 ◽  
Vol 122 (1) ◽  
pp. 77-81 ◽  
Author(s):  
S. Conway Morris

The unique appearance of Vendian metazoans in the Precambrian fossil record is controlled not only by taphonomic and ecological factors, but also by the level of morphological and physiological organization of these animals. The peculiar nature of these factors means that the Vendian represents an important stage in metazoan evolution. This notion is supported by the Bauplan analysis of Vendian forms, many of which have a bodyplan (architectonics) that is most unusual in comparison with animals from later periods. This new information allows a revision of the systematics of Precambrian metazoans at a high taxonomic level. The new classes Cyclozoa, Inordozoa, and Trilobozoa are recognized among Vendian Coelenterata. The phylum Proarticulata, with classes Dipleurozoa and Vendiamorpha, represents the most primitive Vendian Bilateria. These, the oldest faunas on Earth, provide indication of the earliest modes of metazoan evolution that have not been part of the theoretical predictions of neontologists, and they also serve as a tool to check certain phylogenetic models.


2004 ◽  
Vol 132 (1-2) ◽  
pp. 123-132 ◽  
Author(s):  
Duo Fu Chen ◽  
Wei Quan Dong ◽  
Bin Quan Zhu ◽  
Xian Pei Chen

2000 ◽  
Vol 74 (5) ◽  
pp. 979-982 ◽  
Author(s):  
Xingliang Zhang ◽  
Jian Han ◽  
Degan Shu

The early Cambrian Chengjiang Lagerstatte, generally regarded as late Atdabanian (Qian and Bengtson, 1989; Bengtson et al., 1990), has become celebrated for perhaps the earliest biota of soft-bodied organisms known from the fossil record and has proven to be critical to our understanding of early metazoan evolution. The Sirius Passet fauna from Peary Land, North Greenland, another important repository of soft-bodied and poorly sclerotized fossils, was also claimed as Early Cambrian (Conway Morris et al., 1987; Budd, 1995). The exact stratigraphic position of the Sirius Passet fauna (Buen Formation) is still uncertain, although the possibility of late Atdabanian age was proposed (Vidal and Peel, 1993). Recent work dates it in the “Nevadella” Biozone (Budd and Peel, 1998). It therefore appears to be simultaneous with or perhaps slightly younger than Chengjiang Lagerstatte, Eoredlichia Biozone (Zhuravlev, 1995). The Emu Bay Shale of Kangaroo Island, South Australia, has long been famous as a source of magnificent specimens of the trilobites Redlichia takooensis and Hsunaspis bilobata. It is additionally important as the only site in Australia so far to yield a Burgess-Shale-type biota (Glaessner, 1979; Nedin, 1992). The Emu Bay Shale was considered late Early Cambrian in age (Daily, 1956; Öpik, 1975). But Zhang et al.(1980) reassessed its age based on data from the Chinese Early Cambrian. The occurrence of Redlichia takooensis and closely related species of Hsunaspis indicates an equivalence to the Tsanglangpuian in the Chinese sequence, and the contemporary South Australia fauna correlate with the Botomian of Siberia (Bengtson et al., 1990). Thus the Emu Bay Shale is younger than the upper Atdabanian Chengjiang Lagerstatte, Chiungchussuian.


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