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A new genus and species of nicothoid copepod (Crustacea: Copepoda: Siphonostomatoida) parasitic on the mysid Siriella okadai Ii from off Japan.

Neomysidion rahotsu, a new genus and species of the siphonostomatoid family Nicothoidae Dana, 1849, is described from the marsupium of the mysid Siriella okadai Ii in the shallow waters of the Seto Inland Sea of Japan. This is the first record of nicothoids parasitic on mysids in Asian waters. The new genus is closely related to the three other mysid-infesting nicothoid genera, Aspidoecia Giard & Bonnier, 1889, Mysidion Hansen, 1897 and Hansenulus Heron & Damkaer, 1986, but is distinguishable by: the trunk of adult females being remarkably transformed at maturity; the male cephalosome covered with numerous rounded knobs posterodorsally; the absence of caudal rami in the female; three-segmented antennules in both sexes; two-segmented antenna in the male; remarkable sexual dimorphism in the maxillae; the presence of a pair of spinulate sclerites between the maxillae in both sexes; three- segmented maxillipeds in both sexes; the absence of legs 1 to 5 in the female; the presence of two pairs of legs in the male; and egg-sacs laid free.

Anatomy, Comparative↗

An examination of the ability of inositol 1,4,5-trisphosphate to induce calcium release and tension development in skinned skeletal muscle fibres of frog and crustacea.

We have examined the ability of inositol 1,4,5-trisphosphate (InsP3) to cause contractions of mechanically skinned muscle fibres of frog and barnacle. InsP3 (10-500 microM) did not cause any tension development in 25 frog skinned fibres and 26 barnacle myofibrillar bundles, although contractions could be readily evoked by caffeine and by replacement of an impermeant anion by Cl-, treatments known to release calcium from the sarcoplasmic reticulum (SR). Four barnacle bundles did give responses to InsP3. InsP3 did not modify responses to caffeine or calcium-induced calcium release. Free Mg2+ was lowered to 40 microM and 15 mM D-2,3-diphosphoglycerate was added in order to inhibit the possible breakdown of InsP3 by inositol trisphosphatase. Neither measure revealed a response to InsP3. Arsenazo III absorbance measurements failed to detect any binding of Mg2+ (0-0.5 mM) by 0.35 mM InsP3 in our solutions. Inhibitors of SR calcium uptake (cadium, quercetin, furosemide), omission of EGTA from the solution and varying the temperature from 4 degrees to 22 degrees C also failed to reveal a response of frog skinned fibres to InsP3. The nucleotide GTP, which has been reported to enhance InsP3-induced calcium release from rat liver microsomes, had no effect at 50 microM on the response of frog fibres to InsP3. It is concluded that under conditions in which other calcium release mechanisms operate well, InsP3 is relatively ineffective at releasing calcium from the SR in amounts sufficient to induce contraction. Although we have been unable to find evidence to support the proposed role of InsP3 as an essential link in excitation-contraction coupling of skeletal muscle, we cannot entirely reject its role if essential cofactors are lost in the skinned preparations.

2,3-Diphosphoglycerate↗