OBSERVATIONS ON LEAF AND BUD FORMATION IN HYDROCHARIS MORSUS-RANAE

Regular sequences of leaf and bud formation occur in several members of the Hydrocharitaceae, including Hydrocharis, in which buds are normally formed in the axil of every second leaf of the phyllotactic spiral. Leaf inception begins by periclinal divisions of the inner cells of the 2-layered tunica. Bud formation, which occurs in the apical meristem itself, immediately following the inception of the subtending leaf primordium, begins by divisions in various planes in the corpus, the 2 tunica layers remaining continuous throughout. The young bud meristem soon gives rise to a lateral bud, before leaf formation begins upon it. Because of these and other features, this species is one of considerable morphogenetic interest. Morphogenesis of the whole plant, and in particular the factors controlling the regular sequence of leaf and bud formation, have been and are being investigated experimentally.     

A Persistent Daily Rhythm in Photosynthesis

The luminescent marine dinoflagellate, Gonyaulax polyedra, exhibits a diurnal rhythm in the rate of photosynthesis and photosynthetic capacity measured by incorporation of C¹⁴O₂, at different times of day. With cultures grown on alternating light and dark periods of 12 hours each, the maximum rate is at the 8th hour of the light period. Cultures transferred from day-night conditions to continuous dim light continue to show the rhythm of photosynthetic capacity (activity measured in bright light) but not of photosynthesis (activity measured in existing dim light). Cultures transferred to continuous bright light, however, do not show any rhythm. Several other properties of the photosynthetic rhythm are similar to those of previously reported rhythms of luminescence and cell division. This similarity suggests that a single mechanism regulates the various rhythms.     

An Electron Microscope Study of Intranuclear Inclusions in Mouse Liver and Hepatoma

An electron microscope study of intranuclear inclusions which occur in giant cells in a transplantable mouse hepatoma and in enlarged liver cells in mice fed a diet containing bentonite demonstrates that these inclusions are formed by invaginations of the nuclear envelope, and corroborates a previous histochemical study which revealed that the contents of the inclusions are of cytoplasmic origin. In the hepatoma cells the intranuclear inclusions are abundant, small, and situated close to the border of the nucleus, and there are wide openings from the cytoplasm into the invaginations whose contents include lipid droplets, ergastoplasm, and structurally normal mitochondria. In the enlarged liver cells the inclusions are fewer in number, generally much larger than those in the hepatoma, hence they extend deeper into the nucleus, and the interior is continuous with the cytoplasm through only a small opening. Some normal ergastoplasm is present within the inclusions but all other constituents are abnormal. Both normal and degenerating mitochondria occur in the cytoplasm but only degenerating ones are found within the inclusions. Both types of inclusions arise in greatly enlarged cells in which an attempt is made to maintain the normal nuclear surface/nuclear volume ratio by the development of the invaginations of the nuclear envelope.     

Action Spectra for Two Effects of Light on Luminescence in Gonyaulax polyedra

The luminescence of the marine dinoflagellate Gonyaulax polyedra shows an endogenous diurnal rhythm. The effect of light during the phase of low luminescence capacity may be observed as an enhancement of luminescence during the subsequent bright phase. During the bright phase, however, illumination diminishes the capacity for luminescence. The action spectra for these two effects of light have been determined, and the major pigments of Gonyaulax have been examined. A consideration of the action spectrum and the pigment complement of Gonyaulax suggests that photosynthesis during the day is responsible, directly or indirectly, for the enhancement of luminescence during the following night. Photoinhibition of luminescence is in part attributable to light absorbed by the photosynthetic pigments. However, activity observed in the far red region of the spectrum beyond the absorption maximum of chlorophyll a suggests that an additional pigment, present in small amounts, may also act as sensitizer for photoinhibition.     

Effect of Phenolic Acids and Esters on Respiration and Reproduction of Bacteria in Urine

Vanillic, syringic, gallic, and protocatechuic acids, methyl-p-hydroxybenzoate, and propyl-p-hydroxybenzoate generally inhibited respiration in vitro of Escherichia coli, Proteus vulgaris, Pseudomonas aeruginosa, and Aerobacter aerogenes in human urine. In the absence of any other available carbon source, certain of the phenolic compounds were utilized. Reproduction was generally suppressed in urine buffered to pH 7, 5.6, 4.5, and 4.0. The phenolic compounds were used in the range of 0.11 to 0.99 μmole/ml.     

Characterization of Certain Gram-Negative Bacteria from Surface Waters

Cultures of gram-negative bacteria with oxidative glucose metabolism were isolated from surface waters by a highly selective technique, and were classified into 11 types. The predominant type, making up about 50% of the isolated cultures, was cytochrome oxidase-positive, produced fluorescent pigment, and failed to grow at 37 C. A similar type, which differed in being cytochrome oxidase-negative, constituted about 10% of the isolates. Both types of bacteria probably were composed of more than one species. A third type, composed of purple-pigmented pseudomonads, made up approximately 30% of the isolated cultures, and probably represented the predominant species. Other bacterial types isolated constituted less than 10% of the cultures examined.     

The linkage between the polysaccharide and mucopeptide components of the cell wall of Lactobacillus casei

1. The linkage between the polysaccharide and mucopeptide components of the cell wall of Lactobacillus casei is rapidly hydrolysed under mild acid-hydrolysis conditions. 2. The release of the polysaccharide is accompanied by the hydrolysis of an N-acetylhexosaminide linkage. The N-acetylhexosamine residue readily forms chromogen and it is concluded that it is substituted on C₍₃₎ by the adjacent sugar. 3. Continued heating of the polysaccharide in acid results in a slower release of reactive N-acetylhexosamine due to the hydrolysis of glycosidic linkages within the polysaccharide. 4. After the linkage between the polysaccharide and mucopeptide has been hydrolysed, acid phosphatase will release approx. 40% of the total phosphorus as inorganic phosphate. 5. It is concluded that the polysaccharide component of the cell wall is joined through its reducing end group to a phosphate grouping in the mucopeptide.     

In vitro differentiation of rabbit blastocyst cells

Summary Six- and seven-day post-coitus (p.c.) rabbit embryos have been cultured in an attempt to establish a trophectodermal cell line. Results indicate that cells with epithelial characteristics (i.e. positive staining for cytokeratin) will survive in culture until Passage 3. At that time a fibroblastlike cell becomes predominant. In addition, we have found that the presence of the inner cell mass is required for embryo explants often results in the development of cells that spontaneously contract. These cells stain positively for myosin, which indicates that they may be precardiac cells. Maximum diastolic potential was −59±1.2 mV and the threshold potential was −53±2.3 mV. Spontaneously contracting cells did not respond to atropine, acetylcholine, epinephrine, isoproterenol, or propranolol. Action potential seems to be a result of an inward calcium current, because the beating rate is decreased in a dose-related manner with the calcium channel blocker verapamil, whereas the voltage-sensitive sodium channel blocker tetrodotoxin was without effect. This work was supported by grants HD21302, HD07069, DK31091, and HL37320 from the National Institutes of Health, Bethesda, MD, with additional support from a University of Alabama at Birmingham Cardviovascular Research and Training Center Award.