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Main article: Trichoplax
Trichoplax is a small, flattened, animal around 1 millimetre across. Like an Amoeba, it has no regular outline, although the lower surface is somewhat concave, and the upper surface is always flattened. The body consists of an outer layer of simple epithelium enclosing a loose sheet of stellate cells resembling the mesenchyme of some more complex animals. The epithelial cells bear flagella, which the animal uses to help it creep along the seafloor.
The lower surface engulfs small particles of organic detritus, on which the animal feeds. It reproduces asexually, budding off smaller individuals, and the lower surface may also bud off eggs into the mesenchyme.
Phylogenetic position of the Placozoa
There is no convincing fossil record of the placozoa, although the Ediacaran biota (Precambrian, 550 million years ago) organism Dickinsonia may be allied with this phylum.
Traditionally, classification has been based on their level of organization: i.e. they possess no tissues or organs. However this may be as a result of secondary loss, so is inadequate to demark a clade. More recent work has attempted to classify them based on the DNA sequences in their genome; this has placed the phylum between the sponges and the eumetazoa. In such a feature-poor phylum, molecular data are considered to provide the most reliable approximation of the placozoans' phylogeny.
The Placozoa descending side by side with the sponges, cnidarians and ctenophores from a gallertoid by processes of differentiation
On the basis of their simple structure, the Placozoa were frequently viewed as a model organism for the transition from unicellular organisms to the multicellular animals (Metazoa) and are thus considered a sister taxon to all other metazoans:
Animals with tissues (Eumetazoa)
According to a functional-morphology model, all or most animals are descended from a gallertoid, a free-living (pelagic) sphere in seawater, consisting of a single ciliated layer of cells supported by a thin, noncellular separating layer, the basal lamina. The interior of the sphere is filled with contractile fibrous cells and a gelatinous extracellular matrix. Both the modern Placozoa and all other animals then descended from this multicellular beginning stage via two different processes:
Infolding of the epithelium led to the formation of an internal system of ducts and thus to the development of a modified gallertoid from which the sponges (Porifera), Cnidaria and Ctenophora subsequently developed.
Other gallertoids, according to this model, made the transition over time to a benthic mode of life; that is, their habitat has shifted from the open ocean to the floor (benthic zone). While the probability of encountering food, potential sexual partners, or predators is the same in all directions for animals floating freely in the water, there is a clear difference on the seafloor between the sides facing toward and away from the substrate, and between their orientation and the vertical direction perpendicular to the substrate. This results naturally in a selective advantage for flattening of the body, as of course can be seen in many benthic species. In the proposed functional-morphology model, the Placozoa, and possibly also several organisms known only from the fossil state, are descended from such a life form, which is now termed placuloid. Three different life strategies have accordingly led to three different lines of development:
Animals that live interstitially in the sand of the ocean floor were responsible for the fossil crawling traces that are considered the earliest evidence of animals and are detectable even prior to the dawn of the Ediacaran Period in geology. These are usually attributed to bilaterally symmetrical worms, but the hypothesis presented here views animals derived from placuloids, and thus close relatives of Trichoplax adhaerens, to be the producers of the traces.
Animals that incorporated algae as photosynthetically active endosymbionts, i.e. primarily obtaining their nutrients from their partners in symbiosis, were accordingly responsible for the mysterious creatures of the Ediacara fauna that are not assigned to any modern animal taxon and lived during the Ediacaran Period, before the start of the Paleozoic. Recent work has shown that some of the Ediacaran assemblages (e.g. Mistaken Point) were in deep water, below the photic zone, and that the organisms were not dependent on endosymbiotic photosynthesisers.
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Since 2011, Duisenberg school of finance has organised a prestigious, invitation-only annual event - the Tripartite Seminar - in cooperation with Cambridge, Tinbergen Institute and the Wharton School/University of Pennsylvania. The most recent Tripartite Seminar occurred 17-18 May 2013. See the programme descriptions of each year's Seminar below.
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