Ovulation does not constrain egg parcel size in the simultaneous hermaphrodite Serranus subligarius

Among egg trading hermaphrodites, any factor which limits the number of eggs released by a female role hermaphrodite can potentially limit the mating success of the male role hermaphrodite fertilizing those eggs. This work examines the hypothesis that the timing of ovulation constrains the size of egg parcels and thereby limits male mating success in the egg parceling hermaphroditic fish Serranus subligarius. Two alternatives were evaluated: (1) Ovulation is a discrete event preceding spawning. It does not constrain the size of egg parcels and therefore does not limit mating success of male role partners. (2) Ovulation is an incremental process occurring throughout the spawning period. It limits the number of eggs available for release in each parcel and thereby limits mating success of the male role partner. Assessment of ovulation was conducted in a field stock of S. subligarius. Fish from size matched pairs were manually stripped at the onset of the spawning period or quarantined and sampled at the end of the spawning period. Fish sampled at either time point had the same number of eggs, suggesting that ovulation was a discrete event occurring at the onset of the spawning period. The diurnal cycle of ovulation was observed in naturally spawning hermaphrodites captured at intervals throughout the day. Ovulation began 2–4 h before spawning began. Some fish appeared to ovulate the entire day's clutch of eggs before spawning, while other fish released egg parcels before completing ovulation. I conclude that the pattern of ovulation is not uniform throughout the spawning stock. Because of the variability in timing of ovulation relative to parcel release, ovulation does not consistently limit the size of egg parcels and therefore is unlikely to be a physiological limit to male role mating success in S. subligarius hermaphrodites.     

Role of F Pili in the Penetration of Bacteriophage fl

Early stages of infection of Escherichia coli with the filamentous bacteriophage f1 were examined in the electron microscope. Purified phage-bacteria complexes were prepared at various time intervals after the initiation of synchronous infection. Cells were scored for the total number of F pili, the number of F pili with f1 attached, the number of intact phage particles which occurred at the surface of the cell, and F pilus length. Electron microscope autoradiographs were also prepared at each time interval. The results showed that the average number of F pili with f1 attached decreased with time as phage deoxyribonucleic acid (DNA) entered the cell. Concomitant with this loss, the remaining F pili became shorter. The rate of entry of phage DNA into the cell followed, with a short lag, the rate of loss of F pili with f1 attached. During the lag period, intact phage particles accumulated at the surface of the cell. The results from radioautographs showed that no phage DNA could be located within the F pilus. These results suggest that F pili are resorbed by the cell during infection with the bacteriophage f1. Parallel experiments with noninfected cultures further suggest that pilus resorption may be a normal cellular phenomenon.     

Streptococcus bovis endocarditis

A case is described of bacterial endocarditis caused by Lancefield group D Streptococcus bovis. Because of its sensitivity to the less toxic antibiotics such as penicillin, the importance of laboratory differentiation from the more resistant enterococci is emphasized. Treatment in this case was complicated by penicillin allergy and cardiac failure. The condition finally responded to clindamycin therapy and aortic valve replacement.     

Similarity in Several Properties of Psychrophilic Bacteria Grown at Low and Moderate Temperatures

Several properties of psychrophilic pseudomonads were studied with cells grown in batch culture in nutrient broth at 2 and 30 C. No differences were observed in the size, catalase activity, deoxyribonucleic acid, ribonucleic acid, or protein content of cells grown at either temperature. The importance of comparing physiologically similar cells is discussed.     

Relatedness Among Rhizobium and Agrobacterium Species Determined by Three Methods of Nucleic Acid Hybridization

Deoxyribonucleic acid (DNA) was isolated from 20 strains of Rhizobium and Agrobacterium and from one strain of Serratia marcescens; the guanine plus cytosine content of each DNA sample was determined by thermal denaturation. Radioactive DNA was isolated from three reference strains following the uptake of [2-(14)C]thymidine in the presence of deoxyadenosine. Ribonucleic acid (RNA) polymerase was used to synthesize radioactive RNA on DNA templates from the three reference strains. Radioactive DNA and RNA from the three reference strains were each hybridized with filter-bound DNA from all of the 21 test strains in 6 x SSC (standard saline citrate) and 50% formamide at 43 C for 40 hr. DNA/DNA relatedness was also determined by spectrophotometric measurement of the rates of association of single-stranded DNA. The order of relatedness between strains was similar by each method. Overall standard deviations for the DNA/DNA and DNA/RNA membrane filter techniques were +/-0.87 and +/-1.03%, respectively; that for the spectrophotometric technique was +/-4.11%. The DNA/DNA membrane technique gave higher absolute values of hybridization than did the DNA/RNA technique. R. leguminosarum and R. trifolii could not be distinguished from each other by these techniques. These results also indicated close relationships between R. lupini and R. japonicum, and (with less certainty) between R. meliloti and R. phaseoli. Of all the rhizobia tested against the A. tumefaciens 371 reference strain, the R. japonicum strains were the most unrelated. The three Agrobacterium strains used were as related to the R. lupini and R. leguminosarum references as were several rhizobium strains.     

Spontaneous Periodic Hypothermia: Diencephalic Epilepsy

The case of a patient with episodic hypothermia and profuse sweating believed to be due to diencephalic epilepsy is reported. Despite intensive investigations no other manifestations of hypothalamic dysfunction were found. Conventional antiepileptic drugs were without effect but the patient was successfully treated by total sympathectomy.     

A MORPHOLOGICAL AND HISTOLOGICAL STUDY OF THE TOMATO MUTANT ‘CURL’

The dominant tomato mutant ‘Curl’ differs from normal plants in several striking respects including the following: misshapen laminar structures such as leaves, sepals, and petals; stunted petiole and rachis; and persistent growth of blade and stem tissue from the adaxial surface of the rachis. These tissues as well as others which appear morphologically normal show gross histological abnormalities. Also evident in sections of mutant tissue is the appearance of areas containing numerous crystalline inclusions and a lack of bodies showing a stainable starch reaction in palisade and mesophyll of leaves and in endodermis and pith cells of the stem.     

Two New Serological Groups of Actinomyces

Actinomyces odontolyticus and A. viscosus are designated as group E and group F in the serological grouping of the Actinomyces.     

Histidine-Mediated Control of Tryptophan Biosynthetic Enzymes in Neurospora crassa

The formation of the five tryptophan biosynthetic enzymes of Neurospora crassa was shown to be derepressed in histidine-starved cells. This histidine-mediated derepression was not due to a lowered intracellular concentration of tryptophan in these cells. Furthermore, histidine-mediated derepression of tryptophan enzymes was found to be coordinate and not subject to reversal by tryptophan of either exogenous or biosynthetic origin. The synthesis of tryptophan enzymes also was found to be coordinate in cells which were not histidine-starved. Although histidine is clearly involved in regulating the synthesis of tryptophan enzymes, it did not prevent either tryptophan-mediated derepression of tryptophan enzymes or indole-3-glycerol phosphate-mediated derepression of tryptophan synthetase.