Shaping of colony elements in Laomedea flexuosa Hinks (Hydrozoa, Thecaphora) includes a temporal and spatial control of skeleton hardening.

The colonies of thecate hydroids are covered with a chitinous tubelike outer skeleton, the perisarc. The perisarc shows a species-specific pattern of annuli, curvatures, and smooth parts. This pattern is exclusively formed at the growing tips at which the soft perisarc material is expelled by the underlying epithelium. Just behind the apex of the tip, this material hardens. We treated growing cultures of Laomedea flexuosa with substances we suspected would interfere with the hardening of the perisarc (L-cysteine, phenylthiourea) and those we expected would stimulate it (dopamine, N-acetyldopamine). We found that the former caused a widening of and the latter a reduction in the diameter of the perisarc tube. At the same time, the length of the structure elements changed so that the volume remained almost constant. We propose that normal development involves a spatial and temporal regulation of the hardening process. When the hardening occurs close to the apex, the diameter of the tube decreases. When it takes place farther from the apex, the innate tendency of the tip tissue to expand causes a widening of the skeleton tube. An oscillation of the position at which hardening takes place causes the formation of annuli.     

Sclerotization of the perisarc of the calyptoblastic hydroid, Laomedea flexuosa 2. Histochemical demonstration of phenol oxidase and attempted demonstration of peroxidase

Histoehemical evidence is presented that cells, described as 'tanning cells', in the hydroid Laomedea flexuosa contain an orthodihydroxyphenol oxidase and transfer this enzyme to the perisarc. The detection of copper in the tanning cells provides further evidence for the presence of phenol oxidase, a copper-containing enzyme. Evidence is presented that this enzyme and the orthodihydroxyphenol, dopamine, are stored together in the same 1mu diameter spherical inclusions. The enzyme and orthodihydroxyphenolic substrate appear to be transferred together to the perisarc where it is thought that the dopamine is oxidized by the phenol oxidase to produce a quinone. The quinone is thought to cross-link the structural proteins to form a strong, inert exoskeleton, the perisarc. Attempts to demonstrate peroxidase using benzidine methods are also described. Both the spherical inclusions of the tanning cells and the perisarc of the hydrothecae give a reaction with benzidine in the absence of hydrogen peroxide. This suggests the presence of an oxidizing agent which is not a peroxidase but is possibly a quinone.     

Effect of histamine on duration of phases of the respiration cycle

Histamine produced either a bronchodilation or a bronchoconstriction in rats. In a 0.01-1.0 mcg/ml concentration histamine augmented the contractions amplitude in electrical stimulation of the trachea, in a 10-100 mcg/ml concentration histamine enhances the muscle tone thus decreasing the induced contractions. The histamine effects seems to be connected with its prevailing influence on different structures of the airways depending on the concentration. Its high concentrations act directly on the smooth muscle whereas its lower concentration affects receptors signaling the functional modules of the metasympathetic nervous system within the intramural ganglia of the trachea.     

Effect of isoprenaline on cells in different phases of the mitotic cycle

The effects of isoprenaline on parotid acinar cells in different phases of the mitotic cycle have been investigated. Cells in mitosis at the time of drug administration are not depleted of secretory granules whilst those in other phases are. The drug causes temporary blocks both in metaphase and in the G2 phase. The blocks are prolonged by repeated injections of the drug. Cells continue to undergo DNA synthesis during the period of secretion following the drug. The mitotic delay appears to be specific for the parotid and submaxillary glands.     

Distribution and reproduction of the temperate-specific morphotype of the coral Favites flexuosa in the subtropical region,Lyudao, Taiwan

Favites flexuosa is one of the abundant coral species in the temperate regions of Japan. Although the species ranges widely, from tropical to temperate regions of the Indo-Pacific, colonies of this species living in temperate areas exhibit specific morphological features (in terms of color and skeletal attributes). In addition, the temperate-specific morphotype is limited in distribution to the temperate regions of Japan and has not been recorded in subtropical Okinawa. In the present study, we recorded the temperate morphotype in subtropical Lyudao (Green Island), Taiwan, suggesting that the morphotype is more widely distributed than previously thought and may have colonized temperate Japan directly from Lyudao. We describe the first records of spawning at Lyudao, Taiwan, and also at Wakayama in temperate Japan. In laboratories located in either region, spawning was observed between 30?min and 1?h after sunset. Intraspecific crossing of morphotype samples from either region revealed that the fertilization rates were high (>90%). In addition, we crossed F. flexuosa with Diploastrea favus at Lyudao. The two species hybridized successfully although the fertilization rate was relatively low.     

Nematocysts and Taxonomy in Laomedea, Gonothyraea and Obelia (Hydrozoa, Campanulariidae)

The cnidoms of Laomedea flexuosa, Gonothyraea loveni, Obelia geniculata, O. longissima and O. dichotoma were studied by light and scanning electron microscopy to find out whether the nematocysts could be used as taxonomic characters. Three b-rhabdoid heteroneme nematocysts (microbasic b-mastigophore) and three isorhizous haploneme nematocysts (atrichous isorhiza) were distinguished. A small b-rhabdoid nematocyst with spindle-shaped capsule occurred in all the species examined. In the polyp and planula of G. loveni , and the planula of L. flexuosa it was the only nematocyst present. Specific for L. flexuosa was a b-rhabdoid with curved capsule. In the polyp and newly-liberated medusa of O. longissima another b-rhabdoid appeared with bean-shaped capsule and markedly long spines at the distal tube. The polyp and newly-liberated medusa of O. dichotoma were characterized by two different isorhizas. A special type of isorhiza occurred in the polyp of O. geniculata . The curved capsules of the different isorhizas varied somewhat in shape and size. Differences in nematocyst structure and occurrence are presumed to provide characters for taxonomy. Thus, O. dichotoma and O. Iongissima are regarded as separate species due to their distinctly different nematocysts, in conjunction with other morphological and ecological differences.     

Cell reproduction cycle of mycoplasma

The cell reproduction cycle of parasitic wall-free bacteria, mycoplasma, is reviewed. DNA replication of Mycoplasma capricolum starts at a fixed site neighboring the dnaA gene and proceeds to both directions after a short arrest in one direction. The initiation frequency fits to the slow speed of replication fork and DNA content is set constant. The replicated chromosomes migrate to one and three quarters of cell length before cell division to ensure delivery of the replicated DNA to daughter cells. The cell reproduction is based on binary fission but a branch is formed when DNA replication is inhibited. Mycoplasma pneumoniae has a terminal structure, designated as an attachment organelle, responsible for both host cell adhesion and gliding motility. Behavior of the organelle in a cell implies coupling of organelle formation to the cell reproduction cycle. Several proteins coded in three operons are delivered sequentially to a position neighboring the previous organelle and a nascent one is formed. One of the duplicated attachment organelles migrates to the opposite pole of the cell before cell division. It is becoming clear that mycoplasmas have specialized cell reproduction cycles adapted to the limited genome information and parasitic life.     

Redescription of Laomedea exigua M. Sars, a hydroid new to Scandinavia, with comments on its nematocysts, life cycle and feeding movements

The little-known hydroid Laomedea exigua M. Sars, 1857, is recorded for the first time from Scandinavian waters. The species is redescribed and the life cycle, lacking a medusa stage, is confirmed by rearing. The nematocysts are diagnostic of the species. Tentacles and hypostome co-operate in capturing prey.     

Life cycle,physiology, ecology and red tide occurrences of the fish-killing raphidophyte Chattonella

The marine fish-killing raphidophytes of the genus Chattonella currently consist of five species, i.e. C. antiqua, C. marina, C. minima, C. ovata and C. subsalasa. The distribution of Chattonella species was confirmed in tropical, subtropical and temperate regions in the world accompanying mass mortalities of fishes in nature and in aquaculture. The fish-killing mechanisms are still unclear, but suffocation is the ultimate cause of fish death. Increasing evidence is pointing towards the generation of reactive oxygen species (ROS, e.g. superoxide), which are responsible for the gill tissue injury and mucus production that leads to death of fishes. A taxonomic revision was proposed based on morphology and genetic diversity that Chattonella antiqua and Chattonella ovata should be varieties of Chattonella marina possessing nomenclatural priority. Optimum temperatures for growth are 25 °C for C. antiqua and C. marina, 25–30 °C for C. ovata and 20–30 °C for Chattonella subsalsa. Adequate ranges of salinity for growth were about 20–30 for Chattonella species. Chattonella cells generally divide once a day. Laboratory culture experiments with artificial synthetic medium demonstrated that C. antiqua, C. marina and C. ovata used only Fe chelated with EDTA for growth, although tested diatoms and dinoflagellates used rather many kinds of chelated Fe. A suitable concentration of humic acid supplied with iron also had enhancing effects on the growth of C. antiqua. Diel vertical migration was observed in Chattonella, and the cells reached 7.5 m deep at night in the case of C. antiqua demonstrated by a mesocosm experiment in the Seto Inland Sea. Chattonella species have diplontic life history and have haploid cyst stage in their life cycle. Encystment was observed through formation of pre-encystment small cells after the depletion of nitrogen, and the small cells sink to the sea bottom to complete cyst formation by attachment to the solid surface such as diatom frustules and sand grains. Newly formed cysts are in the state of spontaneous dormancy and they need cold temperature period of four months or longer for maturation (acquisition of germination ability). Cysts germinate in early summer and resultant vegetative cells play an important role as seed populations in blooming in the summer season. However, relatively small part of cyst populations actually germinate from bottom sediments, and success of red tide formation is dependent on the growth in water columns. Since red tides of Chattonella were observed when diatoms were scarce in seawater, diatoms appear to have a key for the predominance of Chattonella in water columns. Diatom resting stages in sediments need light for germination/rejuvenation, whereas Chattonella cysts can germinate even in the dark, implying the selective germination of Chattonella cysts at the sea bottom under calm oceanographic conditions which contribute to bloom formation of Chattonella. As a mechanism of red tide occurrences of Chattonella in coastal sea, “diatom resting hypothesis” was presented. Biological control using diatoms is proposed through the germination/rejuvenation of resting stages suspending from bottom sediments to euphotic layer by sediment perturbation with submarine tractors or fishing trawling gears. Since diatoms have much higher growth rates, and newly joined diatom vegetative cells grow faster and prevent occurrence of Chattonella red tides as a result. As another prevention strategy for Chattonella red tides, algicidal bacteria inhabiting in seaweed beds and seagrass beds are presented. Co-culture of fish and seaweeds in aquaculture areas, and the developments of seaweed- and seagrass-beds would be practical and ultimately environment-friendly strategies for the prevention of harmful red tides of Chattonella by virtue of natural algicidal bacteria supplied from seaweeds and leaves of seagrass.     

Observations on the anatomy,behaviour, reproduction and life cycle of the cubozoan Carybdea sivickisi

Substantial numbers of the very small carybdeid jellyfish, Carybdea sivickisi, have been observed feeding actively by divers in the vicinity of fringing coral reefs. During the day specimens were seen in close association with the substrate and with sessile macroalgae. They appeared able to adhere to substrates by contact with an area on the aboral surface of the bell. Individuals maintained in the laboratory showed the same adhering ability. The adhesive organs correspond to 4 areas of raised secretory epithelium on the aboral surface.Following capture, one isolated specimen extruded a long gelatinous strand containing several thousand developing embryos and numerous functional nematocysts. The embryos developed into characteristic cubozoan planulae, which were able to attach themselves temporarily to substrates by means of nematocysts. After 4 days of free swimming, planulae began to attach permanently and to develop into sessile polyps with 3 or 4 tentacles, each armed with a single stenotele.The species displays sexual dimorphism and evidence for spermatophore formation and transfer which parallel that reported for Tripedalia cystophora. The presence of sperm-storage sacs in both sexes, the production of an embryo mass, the adhering behaviour and an apparent association with algal substrates are among features apparently unique to the species.     

Effect of the tumor promoter TPA on the distribution of PHA-stimulated human lymphocytes by cell cycle phases

Patterns of the cell cycle distribution in human peripheral blood lymphocytes, stimulated by PHA alone and PHA plus 12-o-tetradecanoylphorbol-13-acetate (TPA), were studied using DNA cytometry in different times after PHA stimulation. In the first period (nearly 3 days after PHA stimulation) TPA induces no significant differences in the characters under consideration, but in the later period, when the proliferation of the cultures stimulated by PHA alone is reducing, in other cultures stimulated by PHA plus TPA the percentage of cells in S-phase does not reduce, whereas the percentage of cells in G2-phase is rising, which may suggest that this phase is blocked. Concurrently the tetraploid cells are appearing. Accumulation of cells in G2-phase can be overcome by the application of chlorpromazine, which is known to inhibit the membrane-associated protein kinase C.