Hemichordate
Hemichordate Temporal range:
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Acorn worm, a hemichordate. | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Subkingdom: | Eumetazoa |
Clade: | ParaHoxozoa |
Clade: | Bilateria |
Clade: | Nephrozoa |
Superphylum: | Deuterostomia |
Clade: | Ambulacraria |
Phylum: | Hemichordata Bateson, 1885 |
Classes | |
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Hemichordata (
Acorn worms are solitary worm-shaped organisms. They generally live in burrows (the earliest secreted tubes)
Anatomy
The body plan of hemichordates is characterized by a muscular organization. The anteroposterior axis is divided into three parts: the anterior prosome, the intermediate mesosome, and the posterior metasome.
The body of acorn worms is worm-shaped and divided into an anterior proboscis, an intermediate collar, and a posterior trunk. The proboscis is a muscular and
The prosome of pterobranchs is specialized into a muscular and ciliated cephalic shield used in locomotion and in secreting the coenecium. The mesosome extends into one pair (in the genus Rhabdopleura) or several pairs (in the genus Cephalodiscus) of tentaculated arms used in filter feeding. The metasome, or trunk, contains a looped digestive tract, gonads, and extends into a contractile stalk that connects individuals to the other members of the colony, produced by asexual budding. In the genus Cephalodiscus, asexually produced individuals stay attached to the contractile stalk of the parent individual until completing their development. In the genus Rhabdopleura, zooids are permanently connected to the rest of the colony via a common stolon system.
They have a diverticulum of the foregut called a stomochord, previously thought to be related to the chordate notochord, but this is most likely the result of convergent evolution rather than a homology. A hollow neural tube exists among some species (at least in early life), probably a primitive trait that they share with the common ancestor of chordata and the rest of the deuterostomes.[7] Hemichordates have a nerve net and longitudinal nerves, but no brain.[8][9]
Some species biomineralize in calcium carbonate.[10]
Circulatory system
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Hemochordates have an
Development
Together with the
The enteropneusts have two developmental strategies: direct and indirect development. The indirect developmental strategy includes an extended pelagic plankotrophic tornaria larval stage, which means that this hemichordate exists in a larval stage that feeds on plankton before turning into an adult worm.[13] The Pterobranch genus most extensively studied is Rhabdopleura from Plymouth, England and from Bermuda.[14][15][16][17]
The following details the development of two popularly studied species of the hemichordata phylum Saccoglossus kowalevskii and Ptychodera flava. Saccoglossus kowalevskii is a direct developer and Ptychodera flava is an indirect developer. Most of what has been detailed in Hemichordate development has come from hemichordates that develop directly.
Ptychodera flava
P. flava’s early cleavage pattern is similar to that of S. kowalevskii. The first and second cleavages from the single cell zygote of P. flava are equal cleavages, are
Saccoglossus kowalevskii
Eggs of S. kowalevskii are oval in shape and become spherical in shape after fertilization. The first cleavage occurs from the animal to the vegetal pole and usually is equal though very often can also be unequal. The second cleavage to reach the embryos four cell stage also occurs from the animal to the vegetal pole in an approximately equal fashion though like the first cleavage it’s possible to have an unequal division. The eight cell stage cleavage is latitudinal; so that each cell from the four cell stage goes on to make two cells. The fourth division occurs first in the cells of the animal pole, which end up making eight blastomeres (mesomeres) that are not radially symmetric, then the four vegetal pole blastomeres divide to make a level of four large blastomeres (macromeres) and four very small blastomeres (micromeres). The fifth cleavage occurs first in the animal cells and then in the vegetal cells to give a 32 cell blastomere. The sixth cleavage occurs in a similar order and completes a 64 cell stage, finally the seventh cleavage marks the end of the cleavage stage with a blastula with 128 blastomeres. This structure goes on to go through gastrulation movements which will determine the body plan of the resulting gill slit larva, this larva will ultimately give rise to the marine acorn worm.[20][21]
Genetic control of dorsal-ventral hemichordate patterning
Much of the genetic work done on hemichordates has been done to make comparison with chordates, so many of the genetic markers identified in this group are also found in chordates or are homologous to chordates in some way. Studies of this nature have been done particularly on S. kowalevskii, and like chordates S. kowalevskii has dorsalizing bmp-like factors such as bmp 2/4, which is homologous to Drosophila’s decapentaplegic dpp. The expression of bmp2/4 begins at the onset of gastrulation on the ectodermal side of the embryo, and as gastrulation progresses its expression is narrowed down to the dorsal midline but is not expressed in the post anal tail. The bmp antagonist chordin is also expressed in the endoderm of gastrulating S. kowalevskii. Besides these well known dorsalizing factors, further molecules known to be involved in dorsal ventral patterning are also present in S. kowalevskii, such as a netrin that groups with netrin gene class 1 and 2.[6] Netrin is important in patterning of the neural system in chordates, as well as is the molecule Shh, but S. kowalevskii was only found to have one hh gene and it appears to be expressed in a region that is uncommon to where it is usually expressed in developing chordates along the ventral midline.
Classification
Hemichordata are divided into two classes: the
There are 130 described species of Hemichordata and many new species are being discovered, especially in the deep sea.[26]
Phylogeny
A phylogenetic tree showing the position of the hemichordates is:
Deuterostomia
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The internal relationships within the hemichordates are shown below. The tree is based on 16S +18S rRNA sequence data and phylogenomic studies from multiple sources.[27][28][29]
Hemichordata |
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References
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Other references
- Cameron, C.B. (2005). "A phylogeny of the hemichordates based on morphological characters". Canadian Journal of Zoology. 83 (1): 196–2. doi:10.1139/z04-190.