Predation byIridomyrmex humilis [Hym.: Formicidae] on eggs ofChrysoperla carnea [Neu.: Chrysopidae] released for inundative control ofIllinoia liriodendri [Hom.: Aphididae] infestingLiriodendron tulipifera

In an effort to suppress the tuliptree aphidIllinoia liriodendri (Monell), approximately 2,000 eggs ofChrysoperla carnea (Stephens) from a commercial insectary were released 4 times on each of 8 tuliptreesLiriodendron tulipifera L. in Berkeley, California, during the spring of 1984. On trees foraged by the Argentine antIridomyrmex humilis (Mayr), 98% of the eggs ofC. carnea were removed from the egg release tapes by the ants. A total of about 1,250 larvae per tree eclosed from the 8,000 eggs released on each tree without ants. Fifty percent of the larvae that did eclose died due to cannibalism or entrapment in the sticky egg release tapes and approximately 625 first instar larvae on each tree were free to forage for aphids. Inundative lacewing releases ofC. carnea did not suppress populations ofI. liriodendri due to ant predation, the low viability of commercial eggs (0–73% eclosion),

---

Résumé Dans le but de limiter les populations du puceron du tulipierIllinoia liriodendri (Monell), 4 lachers d'environ 2.000 œufs de provenance commerciale deChrysoperla carnea (Stephens) ont été réalisés au cours du printemps 1984 sur 8 tulipiersLiriodendron tulipifera L., à Berkeley en Californie. cannibalism by emerged larvae, and inadequate release technology. Sur les arbres visités par la fourmi d'ArgentineIridomyrmex humilis (Mayr), 98% des œufs deC. carnea ont été enlevés du support artificiel par les fourmis. Sur les arbres exempts de fourmis, la mortalité de 50% des larves est due au cannibalisme ou à leur engluement sur le support de lacher. A partir de 8.000 œufs déposés sur chaque arbre sans fourmi, on aboutit à environ 625 larves de 1^er stade susceptibles de rechercher des pucerons. Les lachers inondatifs deC. carnea n'ont pas limité les populations d'I. liriodendri. Les raisons en sont: la consommation par les fourmis, une faible viabilité de la plus grande partie des œufs commercialisés (0–73% d'éclosions), une technique inadaptée pour le lacher des œufs et le cannibalisme par les larves elles-mêmes deC. carnea.

     

Tandem repeats of a specific alternating purine-pyrimidine DNA sequence adjacent to protamine genes in the rainbow trout that can exist in the Z form

We have located an extensive (AC)n-rich but specific sequence downstream of three rainbow trout protamine genes. Although sharing considerable sequence homology, including a perfectly conserved 46 base pair repeat, the sequences exhibit a regular heterogeneity in the length of the (AC)n-rich tracts. Radioimmunoassay experiments, S1 nuclease sensitivity studies, two-dimensional electrophoretic analysis, and immunoelectron microscopy studies have been used to determine if the region could assume a Z DNA conformation. It was found that, in a supercoiled plasmid, the (AC)n-rich region has the ability to attain the Z DNA conformation under physiological conditions.     

A novel S = 3/2 EPR signal associated with native Fe-proteins of nitrogenase

In addition to their g = 1.94 EPR signal, nitrogenase Fe-proteins from Azotobacter vinelandii, Azotobacter chroococcum and Klebsiella pneumoniae exhibit a weak EPR signal with g approximately equal to 5. Temperature dependence of the signal was consistent with an S = 3/2 system with negative zero-field splitting, D = -5 +/- 0.7 cm-1. The ms = +/- 3/2 ground state doublet gives rise to a transition with geff = 5.90 and the transition within the excited ms = +/- 1/2 doublet has a split geff = 4.8, 3.4. Quantitation gave 0.6 to 0.8 spin . mol-1 which summed with the spin intensity of the S = 1/2 g = 1.94 line to roughly 1 spin/mol. MgATP and MgADP decreased the intensity of the S = 3/2 signal with no concomitant changes in intensity of the S = 1/2 signal.     

Two new species of Heterokrohnia (Chaetognatha) from Antarctic waters

Summary Two new species of the genus Heterokrohnia, H. longidentata and H. fragilis, are described and compared with the other three known Heterokrohnia species, H. mirabilis Ritter-Záhony 1911; H. bathybia Marumo and Kitou 1966 and H. involucrum Dawson 1968. The species have been found at great depths (1,000 m–2,000 m) near Elephant Island, north of the Antarctic Peninsula.     

Photoaffinity labeling of mammalian alpha 1-adrenergic receptors. Identification of the ligand binding subunit with a high affinity radioiodinated probe

We have synthesized and characterized a novel high affinity radioiodinated alpha 1-adrenergic receptor photoaffinity probe, 4-amino-6,7-dimethoxy-2-[4-[5-(4-azido - 3 - [125I]iodophenyl) pentanoyl] - 1 - piperazinyl] quinazoline. In the absence of light, this ligand binds with high affinity (KD = 130 pM) in a reversible and saturable manner to sites in rat hepatic plasma membranes. The binding is stereoselective and competitively inhibited by adrenergic agonists and antagonists with an alpha 1-adrenergic specificity. Upon photolysis, this ligand incorporates irreversibly into plasma membranes prepared from several mammalian tissues including rat liver, rat, guinea pig, and rabbit spleen, rabbit lung, and rabbit aorta vascular smooth muscle cells, also with typical alpha 1-adrenergic specificity. Autoradiograms of such membrane samples subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis reveal a major specifically labeled polypeptide at Mr = 78,000-85,000, depending on the tissue used, in addition to some lower molecular weight peptides. Protease inhibitors, in particular EDTA, a metalloprotease inhibitor, dramatically increases the predominance of the Mr = 78,000-85,000 polypeptide while attenuating the labeling of the lower molecular weight bands. This new high affinity radioiodinated photoaffinity probe should be of great value for the molecular characterization of the alpha 1-adrenergic receptor.     

Size heterogeneity of the largest subunit of nuclear RNA polymerase II. An immunological analysis

Antibodies raised against the 180-kDa subunit of cauliflower RNA polymerase II bind selectively to the largest subunit of RNA polymerase II purified from a variety of plant species. The selective binding of this antibody to the largest RNA polymerase II subunit has allowed us to probe for the size of this subunit in crude cell extracts, in fractions containing partially purified RNA polymerase II, and in isolated nuclei. Fractions containing RNA polymerase II were subjected to electrophoresis in the presence of sodium dodecyl sulfate, blotted onto nitrocellulose, and blots were probed with antibody. Immunoglobulin complexes were revealed with 125I-Protein A. Published purification procedures result in rapid conversion of a 220-kDa subunit to a 180-kDa polypeptide, but purification at high pH (pH 9.0) retards this proteolysis. RNA polymerase II associated with isolated nuclei is largely protected from proteolytic degradation, and a 240-kDa polypeptide as well as a 220-kDa polypeptide can be detected. These results suggest that the 180-kDa subunit of RNA polymerase II arises artificially during cell lysis and enzyme purification, and that even the 220-kDa polypeptide may be a degradation product of a 240-kDa polypeptide in plants.     

Effect of pinealectomy on seasonal changes in antler growth and concentrations of testosterone and prolactin in white-tailed deer

A 2-year study was conducted to determine under controlled conditions the role of the pineal gland in regulating the seasonal changes in antler growth and reproduction of male white-tailed deer. Blood samples were drawn from 6 pinealectomized (PX) and 18 control (C) deer at intervals of 2 weeks and analyzed for testosterone (T) and prolactin (Prl). Relative scrotal circumference and main beam antler length were recorded. Relative scrotal circumference was similar in PX and C groups, but the normal pattern was delayed 1 to 3 months in the PX deer relative to the C deer. The mean dates of beginning antler growth, velvet shedding, antler casting and pelage changes were significantly later in both years for PX deer than in C deer. Testosterone concentrations peaked 1 month later in the PX deer than in the C deer for both yearling and 2-year-old deer. Prl concentrations in C deer, but not in PX deer, were correlated highly with day length, and the PX deer were delayed relative to the C deer in showing the normal Prl pattern. Increasing levels of Prl in both groups coincided with beginning antler growth in both years. These results indicate that the pineal gland does not originate the seasonal cycles of male white-tailed deer but may synchronize cycles among individual deer, and regulate the circannual rhythm of Prl concentrations which may in turn influence other hormonal cycles.     

Ligation of highly modified bacteriophage DNA

After digestion by TaqI or nicking by DNAase I, five highly modified bacteriophage DNAs were tested as substrates for T4 DNA ligase. The DNAs used were from phages T4, XP12, PBS1, SP82, and SP15, which contain as a major base either glucosylated 5-hydroxymethylcytosine, 5-methylcytosine, uracil, 5-hydroxymethyluracil, or phosphoglucuronated, glucosylated 5-(4′,5′-dihydroxypentyl)uracil, respectively. The relative ability of cohesive-ended TaqI fragments of these DNAs and of normal, λ DNA to be ligated was as follows: $\text{λ}\text{DNA}\text{=}\text{XP}\text{12}\text{DNA}\text{>}\text{SP}\text{82}\text{DNA}\text{?}\text{nonglucosylated}\text{T}\text{4}\text{DNA}\text{>}\text{T}\text{4}\text{DNA}\text{=}\text{PBS}\text{1}\text{DNA}\text{?}\text{SP}\text{15}\text{DNA}$. TaqI-T4 DNA fragments were also inefficiently ligated by Escherichia coli DNA ligase. However, annealing-independent ligation of DNAase I-nicked T4, PBS1, and λ DNAs was equally efficient. We conclude that the poor ligation of TaqI fragments of T4 and PBS1 DNAs was due to the hydroxymethylation (and glucosylation) of cytosine residues at T4's cohesive ends and the substitution of uracil residues for thymine residues adjacent to PBS1's cohesive ends destabilizing the annealing of the restriction fragments. Only SP15 DNA with its negatively charged, modified base was unable to serve as a substrate for T4 DNA ligase in an annealing-independent reaction; therefore, its modification directly interfered with enzyme binding or catalysis.