Benthic resting eggs of calanoid copepods in Norwegian enclosures used in mariculture: abundance, species composition and hatching

Abundance, species composition and viability of benthic resting eggs of calanoid copepods were investigated in the sediments of seven Norwegian enclosed pond systems used in mariculture as well as in the sediments of the nearby open sea. The ponds represented different types of morphometry and zooplankton communities and were located from approximately 60 to 70 °N. Differences in environmental conditions in deep water also typical with anoxia and the presence of hydrogen sulphide at most of the localities. The lowest and highest egg densities in the enclosures were 7.5 ± 6.4 × 10⁴ and 5.5 ± 2.5 × 10⁶ m^-2, respectively, higher than in the sediments of the nearby open sea. Highest densities were found at larger or median depths. Altogether, egg densities higher than 10³ m^-2 were found of only four calanoid species; Eurytemora affinis, Acartia teclae, Acartia clausi, Temora longicornis. Hatching success was variable (0–92%), and no significant correlation to the presence of anoxia and hydrogen sulphide was found. This high hatching success was achieved with eggs exposed to hydrogen sulphide for several months. The recruitment potential to the plankton of nauplii was estimated from 4.8 to 1682 nauplii l^-1 for the different localities. The results showed that resting egg production is a common life history characteristic of some neritic calanoid species in Norwegian waters. In addition to copepod eggs, low densities (< 10³ m^-2) of eggs from rotifers and cladocerans were found in most of the localities.     

Differential distribution of ganglioside GM1 and sulfatide during the development of Xenopus embryos

A frozen section technique for frog oocytes was developed without using any organic solvent. It was applied to examine the distribution of acidic glycosphingolipids (ganglioside GM1 and sulfatide) in Xenopus oocytes, eggs and embryos by indirect immunofluorescence microscopy with specific monoclonal antibodies against the acidic glycolipids. Although glycolipids are generally present on the cell surface, GM1 and sulfatide were distributed in the cytoplasm of animal and vegetal hemispheres, respectively, of the fully grown oocytes and oviposited and fertilized eggs. In blastula, GM1 was present on the cell boundaries and in the Golgi of the blastomeres of animal hemisphere and marginal zone, whereas the staining of the outermost layer of animal blastomeres became faint or negligible at stage 9. Sulfatide in blastula was still observed in vegetal blastomeres. In gastrula, GM1 was distributed in the inner layer of ectoderm and the involuting mesoderm. In neurula, GM1 was concentrated in the dorsal midline including the closing neural tube, notochord and somites, while sulfatide was present in endoderm. The unique distribution of GM1 and sulfatide in oocytes, eggs and early embryos may help to elucidate one aspect of the biochemical bases laid on the animal–vegetal polarity.     

夜蛾科卵的分类(鳞翅目)(一)

本文记述了12种夜蛾的卵。 从不同方向的电镜像片显示出他们的形状和被用作分类的特征,包括精孔区的形态特征,纵脊和横道的状况,气孔的位置、形状和大小,小室的形状和表面结构,以及腹面的细微构造。     

Megagametophyte organization in diploid alfalfa meiotic mutants producing 4n pollen and 2n eggs

Megagametogenesis was studied in five diploid alfalfa mutants producing 4n pollen and 2n eggs, using a stain-clearing technique. All mutants produced embryo sacs with a variable number of supernumerary nuclei both at the early (bi- and tetra-nucleate) and at the late (eight-nucleate) stages of development. The presence of supernumerary nuclei is considered to be a consequence of the production of coenocytic megaspores. The production of 2n eggs was confirmed through cytological investigation by means of the diameter of the egg-cell nucleolus. The frequency of 2n eggs was lower than the frequency of binucleated macrospores as previously determined. This discrepancy may be due to environmental effects but also to the fact that binucleated macrospores may degenerate or may, after two mitotic divisions, give rise to eight-nucleated embryo sacs counted as normals.     

Effect of aluminum and lead salts on lipid peroxidation and cell survival in human skin fibroblasts

The aim of this study was to see whether aluminum (Al) and lead (Pb) salts are toxic for cultured human fibroblasts under different experimental conditions, in the controllable situation offered by cell cultures. Cell survival and membrane lipid peroxidation served as markers of Al and Pb toxicity. Evaluation of the living cells was carried out using a colorimetric method, the mitochondrial reduction of 1-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT). Lipoperoxidation assay was performed on whole cell homogenates by measuring thiobarbituric acid-reactive substances (TBARS) produced after incubation with ascorbic acid-ferrous sulfate. Al(III) and Pb(II) salts (300 μM) produce a considerable decrease in cell survival after an exposure period of 4 d, evident with the three fetal calf serum concentrations in the culture media: 2, 5, and 10%. Taking into account in vitro cell aging, the cytotoxic effects of Al(III) and Pb(II) are greater in senescent fibroblasts than in young cells. Lead-induced cytotoxicity is higher than Al-induced cytotoxicity. A mechanism that contributes to cellular toxicity is membrane lipid peroxidation; our results demonstrate that Al(III) and Pb(II) ions, 400 μM, exert an antioxidant-like effect or a pro-oxidant action on cell membranes depending on exposure time. We describe significant increases in TBARS formation associated with the presence of 400 μM Al(III) or Pb(II) salts in the culture media. Our study also revealed that these heavy metals induce a cell age-dependent action on membrane lipoperoxidation that is greater in senescent fibroblasts and this could have severe consequences for maintenance of cellular integrity.     

A comparative analysis of the evolution of variation in appearance of eggs of European passerines in relation to brood parasitism

Host of brood parasites increase the ability of rejecting cuckooeggs by production of (1) a clutch with little variation amongeggs and (2) a clutch that differs the most from the modal phenotypeof the population. These hypotheses have been tested by Øienet at. (1995), although they did not control for common phylogeneticancestry. We analyze the evolution of egg color and markingpatterns in European passerines, which are potential hosts ofdie European cuckoo (Cuculus canorus), using Felsenstein's (1985)independent comparative method to control for the effect ofcommon phylogenetic descent We found a significant positiverelationship between interclutch variation in appearance ofhost eggs and parasitism rate, but this relationship disappearedwhen hole-nesting species were excluded from the analysis; andwe found a highly significant multiple regression between rejectionrate and intra- and interclutch variation in egg appearance,even when hole nesters were excluded from the analysis. Thepartial correlation coefficients were negative for intraclutchvariation and positive with interclutch variation in agreementwidi the hypotheses. Therefore, the use of the independent comparativemethod strengthens the hypothesis that the evolution of eggpatterns in hosts is associated with different stages of coevolutionwith the brood parasite.     

Effect of fertilized,unfertilized, and UV‐irradiated hosts on parasitism and suitability for Trichogramma parasitoids

Trichogramma spp. (Hymenoptera: Trichogrammatidae) parasitoids have been commonly used as biological control agents in insect pest management. Host quality is believed to influence parasitism, host preference, and suitability for parasitoids. To date, limited studies have compared the parasitism of Trichogramma parasitoids on fertilized, unfertilized, and sterilized host eggs. Hence, we studied the performance of three Trichogramma egg parasitoids, Trichogramma japonicum Ashmead, Trichogramma chilonis Ishii, and Trichogramma leucaniae Pang & Chen, on fertilized, unfertilized, and ultraviolet (UV)‐irradiated fertilized (UVF) eggs of rice moth, Corcyra cephalonica (Stainton) (Lepidoptera: Pyralidae). In a no‐choice test, T. japonicum and T. leucaniae parasitized significantly more fertilized or UVF than unfertilized hosts, and T. chilonis parasitized significantly more UVF than either fertilized or unfertilized hosts. In a choice test, all three Trichogramma parasitoids parasitized UVF hosts the most, and unfertilized hosts the least. There were similar percentages of adult emergence and female progeny among fertilized, unfertilized, and UVF hosts for all three Trichogramma parasitoids, except that T. japonicum had significantly lower adult emergence on fertilized hosts. We also found that all three Trichogramma parasitoids developed slower on unfertilized hosts. Regardless of host treatments, T. leucaniae had the longest developmental time and T. chilonis had the shortest. We conclude that Trichogramma parasitoids prefer parasitizing UVF eggs of C. cephalonica without negative effects on their emergence and sex allocation.     

Parthenogenetic activation of mouse and rabbit eggs by electric stimulation in vitro

The present study was undertaken to determine conditions for parthenogenetic activation of mouse and rabbit eggs by electric stimulation in vitro. The cumulus-free eggs were submitted to square direct current pulses at output voltage of 1.0 to 2.5 kV/cm for 25 to 200 μsec. The best conditions for the activation of mouse eggs were 1.5 kV/cm for 100 μsec, in which 78% of eggs were activated, 32% of which developed to blastocysts in vitro. When the nonelectric solution (0.3M mannitol) was used for electric stimulation, the activation rate was quite low (16%). Optimal conditions for activation of rabbit eggs were 1.5 kV/cm for 200 μsec, in which 77% of eggs were activated, 25% of which developed to blastocysts. Unlike mouse eggs, rabbit eggs frequently had three pronuclei after electric stimulation. It is clearly shown that electric stimulus can induce parthenogenetic activation of the mouse and rabbit eggs in vitro.     

Boophilus microplus: digestion of hemoglobins by the engorged female tick

When the cattle tick Boophilus microplus, after dropping from its host, was maintained at 27 C, the digestion of hemoglobins in the gut proceeded at a steady rate and was virtually complete by the 13th day. The rate was essentially the same whether the ticks were strains susceptible (Yeerongpilly) or resistant (Biarra) to organophosphorous compounds or whether the hosts were British breed, Brahman or banteng cattle, or buffalo. Ferrihemoglobin appeared in the gut contents and hematin was deposited. About 10% of the hematin released from the hemoglobin was transferred to the eggs and from them to the larvae. Translucent ticks, sometimes found on heavily infested hosts and referred to as “serum” ticks, had about half the normal hemoglobin content.     

A method for hatching the eggs of the aphid Schizaphis graminum

Techniques are described for the collection of fertile eggs of Schizaphis graminum (Rond.) on filter paper, and for the subsequent sterilization and incubation of the eggs under various temperature and photoperiodic conditions.19% of the eggs incubated continuously at 16°C in complete darkness hatched in 81 days after deposition. 45% of the eggs chilled at 6°C for 40 days (starting 10 days after deposition) hatched in 71 days if the postchilling incubation at 16°C was completed in darkness. The results indicate a further enhancement in the percentage egg hatch and a reduction in developmental time when the eggs were subjected to a light-dark regime during the post-chilling incubation.

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Zusammenfassung Es wird eine einfache und effektive Methode beschrieben, die Eier von Schizaphis graminum auf Filterpapier zu sammeln, sie nachfolgend zu sterilisieren und unter verschiedenen Temperatur- und Photoperiodebedingungen bis zum Schlüpfen zu inkubieren.Hierbei wurden folgende Resulate erzielt: (a) Inkubation der Eier in vollkommener Dunkelheit bei 16°C führte zu einem Schlupferfolg von 19% nach einer Entwicklungszeit von im Mittel 81 Tagen; (b) Kühlung der Eier bei 6°C während 40 Tagen (vom 10. Tag nach der Eiablage an) erhöhte die Schlupfrate unter ansonsten gleichen Bedingungen auf 45% und reduzierte die Entwicklungszeit auf 71 Tage; (c) durch einen Licht/Dunkel-Rhythmus, dem die Eier nach der 40-tägigen Kühlung ausgesetzt wurden, konnte eine weitere Steigerung der Schlupfrate und eine Verkürzung der Entwicklungszeit erreicht werden.