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Evidence Found For Single-celled Animal Ancestors Print E-mail
SciMed - Biology
TS-Si News Service   
Tuesday, 27 December 2011 04:00
Single-celled Animal Ancestors.Stockholm, Sweden. Evidence of the single-celled ancestors of animals appears in 570 million-year-old South China rocks, the period in Earth's history just before the arrival of multicellular animals.

The researchers were from the University of Bristol, the Swedish Museum of Natural History, the Paul Scherrer Institut and the Chinese Academy of Geological Sciences.


A 570 million year old multicellular spore body undergoes vegetative nuclear and cell division. The background shows a cut surface through the rock — every grain (about 1 mm diameter) is an exceptionally preserved gooey ball of dividing cells turned to stone. The image is based on synchrotron x-ray tomographic microscopy of fossils recovered from rocks in South China. Image courtesy of the University of Bristol.
Click Pic for Details

Multicellular Spore Body

A 570 million year old multicellular spore body undergoes vegetative nuclear and cell division.

The background shows a cut surface through the rock — every grain (about 1 mm diameter) is an exceptionally preserved gooey ball of dividing cells turned to stone.

The image is based on synchrotron x-ray tomographic microscopy of fossils recovered from rocks in South China.

Image courtesy of the University of Bristol.
All life evolved from a single-celled universal common ancestor, and at various times in Earth history, single-celled organisms threw their lot in with each other to become larger and multicellular, resulting, for instance, in the widespread diversity of animals. However, fossil evidence of these major evolutionary transitions is extremely rare.

The fossils, reported this week in the journal Science, preserve stages in the life cycle of an amoeba-like organism dividing in asexual cycles, first to produce two cells, then four, eight, 16, 32 and so on, ultimately resulting in hundreds of thousands of spore-like cells that were then released to start the cycle over again.

The pattern of cell division is so similar to the early stages of animal (including human) embryology that until now they were thought to represent the embryos of the earliest animals. Professor Stefan Bengtson said: "These fossils force us to rethink our ideas of how animals learned to make large bodies out of cells."

The research team studied the microscopic fossils using high energy X-rays at the Swiss Light Source in Switzerland, a particle accelerator called a synchrotron. The images revealed the organization of the cells within their protective cyst walls. "It allowed us to make a perfect computer model of the fossil that we could cut up in any way that we wanted, but without damaging the fossil in any way," said co-author Dr John Cunningham. "We would never have been able to study the fossils otherwise!"

The X-ray microscopy revealed that the fossils had features that multicellular embryos do not, and this led the researchers to the conclusion that the fossils were neither animals nor embryos but rather the reproductive spore bodies of single-celled ancestors of animals.

The organisms should not have been fossilized — they were just gooey clusters of cells — but they were buried in sediments rich in phosphate that impregnated the cell walls and turned them to stone. Lead author Therese Huldtgren says "The fossils are so amazing that even their nuclei have been preserved." Philip Donoghue admits "We were very surprised by our results — we've been convinced for so long that these fossils represented the embryos of the earliest animals — much of what has been written about the fossils for the last ten years is flat wrong. Our colleagues are not going to like the result."

FundingThe research was funded by the Natural Environment Research Council, the Swedish Research Council, the Paul Scherrer Institut, Ministry of Science and Technology of China, National Natural Science Foundation of China, and EU FP7.
ParticipationTherese Huldtgren is a doctoral student at the Department of Palaeozoology, Swedish Museum of Natural History, and Stockholm University (Stockholm, Sweden).

Dr John Cunningham is a Research Associate at the School of Earth Sciences, University of Bristol (UK).

Professor Chongyu Yin is a Researcher at the Institute of Geology, Chinese Academy of Geological Sciences (Beijing, China).

Professor Marco Stampanoni is Head of X-ray Tomography at the Paul Scherrer Institut (Villigen, Switzerland) and Assistant Professor for X-ray Microscopy at the Department for Information Technology and Electrical Engineering of ETH Zürich, and Institute of Biomedical Engineering of the University of Zürich and ETH Zürich.

Dr Federica Marone is a beamline scientist at the Paul Scherrer Institute (Villigen, Switzerland).

Professor Philip Donoghue is Professor of Palaeobiology in the School of Earth Sciences, University of Bristol (UK).

Professor Stefan Bengtson is Professor of Palaeozoology, Swedish Museum of Natural History (Stockholm, Sweden).
CitationFossilized Nuclei and Germination Structures Identify Ediacaran “Animal Embryos” as Encysting Protists. Therese Huldtgren, John A. Cunningham, Chongyu Yin, Marco Stampanoni, Federica Marone, Philip C. J. Donoghue, Stefan Bengtson. Science 2011; 334(6063): 1696-1699. doi:10.1126/science.1209537

Abstract

Globular fossils showing palintomic cell cleavage in the Ediacaran Doushantuo Formation, China, are widely regarded as embryos of early metazoans, although metazoan synapomorphies, tissue differentiation, and associated juveniles or adults are lacking. We demonstrate using synchrotron-based x-ray tomographic microscopy that the fossils have features incompatible with multicellular metazoan embryos. The developmental pattern is comparable with nonmetazoan holozoans, including germination stages that preclude postcleavage embryology characteristic of metazoans. We conclude that these fossils are neither animals nor embryos. They belong outside crown-group Metazoa, within total-group Holozoa (the sister clade to Fungi that includes Metazoa, Choanoflagellata, and Mesomycetozoea) or perhaps on even more distant branches in the eukaryote tree. They represent an evolutionary grade in which palintomic cleavage served the function of producing propagules for dispersion.

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Last Updated on Monday, 26 December 2011 23:37