The animal kingdom began with the evolution of stationary frond like organisms in the sea. There were several different types of organisms and thousands of fossils on the Avalon Peninsula in Canada (575-560 Ma); thus, scientists call this period the Avalon Explosion. Sea anemones evolved within this group by 560 Ma.
Figure 8‑2. Fossil cast of rangomorph Charnia masoni. Credit: Smith609. Used here per CC BY 2.5
There were several supposed animal ancestors dated prior to the Avalon Explosion, but they there are other more likely interpretations. Supposed animal embryos and remains of simple animals are more likely multicellular microorganisms and residues of chemical processes in rock, respectively. Scientists interpreted a chemical signature in ancient rocks (635 Ma) as evidence of sponges, but a microorganism produces the same chemical. Lack of sponge spicules (hard parts of sponges) for the next 100 million years of the fossil record indicates that the chemical is from a microorganism. This causes a significant change in animal evolution models, many of which had sponges at the base. Another proposed animal ancestor is the ctenophore; however, genetics indicates that ctenophores are more distant than sea anemones from triploblastic bilaterian animals such as mollusks, worms, and crustaceans.
Avalon fossils are part of the Ediacaran biota. The interpretation of Ediacaran biota is difficult because this entire group of animal ancestors no longer exists. They look like bags or fronds. One group is the rangomorphs, such as Charnia masoni (566 Ma) (Figure 8‑2).
Oxygen, algae (food for animals), and nutrients increased in seawater just prior to the Avalon Explosion, which provided animals (heterotrophs) a food source and oxygen for respiration. One theory is that Avalon animals might have fed by absorbing nutrients from the water by osmosis, but Nicholas Butterfield determined that osmosis of nutrients from sea water could not provide sufficient food. [1] He identified the 3-dimensional structure in Charnia as compartments filled with water that served as an exoskeleton and as digestion chambers that processed recalcitrant (digest slowly) substrates (food). A microbiome (a set of microorganisms such as in the stomach and intestines of animals) inside the chambers might have processed the food. If there were internal cavities that processed food, then this would be a link to the eventual evolution of sea anemones and moving animals since they have internal cavities with microbiomes that process food; however, the difference between sea anemones and moving animals and these early Avalon organisms is that sea anemones and moving animals use muscles to actively trap and push food into their internal cavity. Charnia might have had two parts: an upper frondlike section (Charnia masoni) that was suspended above the sea floor and a lower holdfast (Charniodiscus) that anchored it to the sea floor.
Muscles evolved within the Avalon organisms. The first fossil evidence of muscles is in Haootia from 560 Ma in Canada (Figure 8‑3). Haootia had a holdfast that held it to the sea floor, and an upper section that trapped food. It is now interpreted as a cnidarian (sea anemone) polyp. Nematostella vectensis is a modern sea anemone that buries itself in the sea floor and extends it tentacles to capture food in the water.
Figure 8-3a. Haootia (560 Ma), a probable cnidarian polyp (sea anemone) . Credit: (Left) Apokryltaros, Used here per CC BY-SA 4.0.
Figure 8-3b. Nematostella vectensis (starlet sea anemone). Credit: Smithsonian environmental research center. Used here per CC BY 2.0.
Sea anemones have a digestive cavity with a single opening that serves as a mouth and anus (Figure 8-4 and Figure 8‑5). They have two germ layers, the endoderm and the ectoderm. As with some of the early moving animals, they have a nerve net (nerves) and muscles but no centralized brain.
Figure 8‑4. Tentacles of Aulactinia veratra catch passing prey and thrust it into the mouth in the middle of the oral disc. Credit. James Dana. (1890) Corals and Coral Islands. Dodd, Mead, and Company.
Figure 8‑5. Sea anemone anatomy. 1. Tentacles 2. Mouth 3. Retracting muscles 4. Gonads 5. Acontial filaments 6. Pedal disk 7. Ostium 8. Coelenteron 9. Sphincter muscle 10. Mesentery 11. Column 12. Pharynx. Credit: Wikipedia. Lydia Kurkoski. Used here per CC BY-SA 4.0.
Figure 8‑6. “Reconstruction of the Ediacaran cnidarian Inaria karli, and the trilobozoan Albumares.” Credit: Apokryltaros. Used here per CC BY 2.5.
The frondose Ediacaran organism (560 Ma), Inaria Karli (Figure 8‑6), may have been a stem sea anemone without tentacles. [2] The word stem refers to the fact that an organism may be ancestral to a classification (phylum) of animals, such as cnidarians, but it is not within it.
Sea anemones, jellyfish, and other cnidarians are radially symmetric whereas moving animals have symmetric right and left sides (bilaterian). Even though they have different body plans, body patterning genes are expressed in the same order in anemones and bilaterians. This fact and many other genetic similarities link sea anemones with the subsequent evolution of moving animals between 560 and 520 Ma.
[1] Butterfield, N. Constructional and functional morphology of Ediacaran rangeomorphs. Geological Magazine. https://doi.org/10.17863/CAM.54216.
[2] Gehling, J.G., 1988, A cnidarian of actinian-grade from the Ediacaran Pound Subgroup, South Australia: Australasian Journal of Palaeontology, v. 12, p. 299–314,doi: 10.1080/03115518808619129.
Banner: Ediacaran frond like organism Dickinsonia. Credit: Vensimilus. Used here per CC BY 2.4