Invertebrate Histology. Группа авторов

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Invertebrate Histology - Группа авторов


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cells, fusiform cells, vibrate cells, and lymphocytes. By light microscopy, however, only two coelomocyte types, hyalinocytes (agranulocytes) and granulocytes, are discernible (Xing et al. 2008). Hyalinocytes are characterized by a central nucleus and scant cytoplasm lacking granules. Granulocytes share similar features but have fine granular cytoplasm.

      1.3.7 Respiratory System

Photo depicts tiedmann's body in a mottled star. Photo depicts the histology of gill in a white urchin showing epidermal surface (E), supported by connective tissue (Ct), and a central lumen lined by coelomic epithelium (C).

      In asteroids these evaginations of the body wall are called papulae. They can be branched and in species with paxillae, the papulae typically sit in the water‐filled branchial space beneath this umbrella‐shaped specialized surface structure. In regular echinoids there are five pairs of peristomial gills on the peristomial membrane, at the margin of each interambulacral plate, that likely provide gas exchange for the muscular apparatus of the lantern. These originate as evaginations from the peripharyngeal (lantern) coelom and have similar histologic features to asteroid papulae. Coelomic fluid is pumped to and from the peristomial gill lumen by the muscles and ossicles of Aristotle's lantern. In irregular echinoids, modified tube feet of the petaloids act as gills.

      Holothuroids have specialized podia near the oral cavity (buccal podia) and tube feet which, similar to other species, function as gills. The primary respiratory organ, which provides gas exchange to the coelomic viscera, is paired internal respiratory trees, which arise as diverticula from the wall of the cloaca. These diverticula form a highly branched system of blind‐ended tubes that contain sea water. Histologically, the structure of the respiratory tree is similar to papulae and peristomial gills. The internal surface is covered by a simple low cuboidal epithelium separated from the external coelomic epithelium by a very thin connective tissue dermis. Gas exchange occurs across the surface from sea water that is actively pumped into the respiratory tree from the cloaca.

      1.3.8 Nervous System

      The nervous system in echinoderms lacks ganglia, which are present in most other invertebrate species. The central nervous system in asteroids consists of a central circumoral ring and five radial nerves that extend within the center of the ambulacral groove to the tip of each ray. Each have a sensory and a motor component. The peripheral nervous system consists of the intraepithelial nerve nets previously described in the body wall. The sensory ectoneural nerve net extends along the epidermis and the motor hyponeural nerve net extends along the coelomic epithelial lining. These nerve nets are connected by neurons that cross the dermis. In Echinoidea, the ectoneural nerve system is the main component and consists of a circumoral nerve ring, radial nerves, podial nerves, and subepidermal nerve plexus. The radial nerves arise from the circumoral nerve ring and extend through the lantern and along the ambulacral plates, coursing between the radial canal and test. Radial nerves give rise to podial nerves that supply the tube feet. The hyponeural nerve system is a series of five radially positioned plaques of nervous tissue below the circumoral nerve ring. Some regular sea urchins have an entoneural nerve system consisting of a nerve ring around the periproct which gives rise to innervation of the gonads.

      1.3.9 Reproductive System

Photo depicts the histology of the ventral nerve cord (N) in a mottled star. Photos depict the histology of the ovary (a) in a Caribbean thorny star, and testicle (b) in a mottled star.
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