Leukotriene C4 binding sites in the mouse forebrain: autoradiographic demonstration

The presence of binding sites for leukotriene C4 (LTC4) is demonstrated in the mouse forebrain, by using autoradiography of sections incubated with tritiated LTC4. The binding of LTC4 is inhibited by an excess of cold LTC4, but unaffected by the presence of a large excess of LTD4, which differs from LTC4 by the absence of a glutamic acid residue. The density of binding sites is minimal on fiber bundles and on choroid plexuses, maximal at the level of granule cell-rich structures such as the dentate gyrus and entorhinal area, and high in the cerebral cortex, thalamic relay nuclei and the caudoputamen. These data suggest that leukotrienes and their receptors might play a role as regulators of central neural activity, a hypothesis which was recently proposed by Lindgren et al.     

Immunochemical demonstration of the clonal organization of chimaeric mouse epidermis

The clonal organization of chimaeric mouse epidermis was demonstrated by in situ staining of whole-mount preparations using monoclonal antibodies directed against H-2k and H-2b antigens. A striking pattern of transversely oriented stripes or patches was found which extended from mid-dorsum to the flank region. The orientation of these patches indicates a preferred directional expansion of clones during the development of dorsal/lateral epidermis. The clonal pattern of the belly region differed in that stripes were not found, but a marked ventral midline boundary was observed. This demarcation line may be due to a physical effect, i.e. isolation of the left and right ventral halves of the epidermis during early embryogenesis with relatively little cell mingling following closure of the abdominal wall. The obvious nonhomogenous distribution of chimaeric components in dorsal/lateral and ventral epidermis contradicts assumptions of homogenous, fine-grained patchiness derived from electrophoretic analysis of tissue samples and used in studies of skin carcinogenesis. The observation that hair follicles may contain cells of both parental genotypes implies a polyclonal origin. Epidermal proliferative units as described by Potten (1974) were not revealed by the pattern of mosaicism at the cellular level in these chimaeric tissue sheets. This indicates that the proliferative compartment of each putative epidermal unit is polyclonal.     

Changes in the DNA labelling index after beta irradiation of the mouse epidermis

This study looked at the changes in the interfollicular DNA labelling index (LI) with time after strontium-90/yttrium-90 beta irradiation of approximately 100 mm2 of mouse flank skin, after a dose of 100 Gy which produces transitory moist desquamation. Within 24 hr of such a dose the LI of the irradiated area was essentially zero (0.07 +/- 0.03%), whilst those of the side area and of the control area were 15.0 +/- 2.6% and 21.4 +/- 2.7%, respectively. The LI of the side and the control areas then fell within 3-5 days to approximately 4% and approximately 2% respectively, whilst that of the irradiated area rose rapidly to a peak value of 30.2 +/- 1.7% at 10 days post-irradiation. There was a 20% reduction in the diameter of the area with detectable radiation damage within 5 days, and this is primarily due to cell proliferation and migration from the unirradiated margins of the field. In contrast, between days 10 and 20 the major source of repopulation is probably derived from local migration and proliferation of surviving hair follicle basal cells within the irradiated field.     

Circadian variation in the susceptibility of mouse epidermis to tumour induction by methylnitrosourea

To study possible circadian differences in the sensitivity of hairless mouse epidermis to a small dose of a short-acting alkylating carcinogen, groups of animals were painted once with 0.2 mg methylnitrosourea (MNU) at 08.00, 12.00, 20.00 and 24.00 h. Other animals were painted three times at weekly intervals at 08.00 and at 20.00 h, respectively. Significantly higher tumour yields were found in animals painted at 20.00 h (when the cell cycle progression and DNA synthesis rate are lowest, and when relatively large numbers of late G1 cells may accumulate) than at any other time point investigated. Hence a circadian variation in sensitivity to MNU in mouse epidermis is confirmed. This may be due to the variations in flux of cells through the S phase. The formation of DNA/carcinogen adducts may be facilitated at times of low flux with many cells in late G1, and fixation of these errors in DNA may take place by the subsequent increased flux through S, before repair is possible.     

Single and double isotope labeling of social insect colonies: Gamma-emitting radionuclides as individually identifiable markers

Gamma-emitting radionuclides were used in single and double-isotope combinations to label individual colonies of the subterranean termite Reticulitermes flavipes Kol. Each of these radionuclides produces a characteristic and identifiable energy spectrum upon decay, and using whole-body gamma spectroscopy, the characteristic spectral emission signatures of each isotope and their relative quantities were detected in workers, brachypterous nymphs, and alates.Radionuclides present in a food source were rapidly incorporated into workers, and reached detection limits within one to three days. Isotopic labels were transferable between colony members, and all individuals in laboratory colonies were labeled within 21 days of initial contact with foragers that had fed at a labeled food source.Single- and double-label nuclide markers were transferred to sexual forms (prealates and alates) by social food flow. Applications of radionuclide labeling and gamma spectroscopic analysis in insect behavioral ecology are discussed.

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Résumé Des radionucléides ont été utilisés seuls ou en combinaison par 2 pour marquer des individus de colonies de Reticulitermes flavipes. Chaque radionucléide possède ses caractères spectraux. Avec un spectroscope très sensible, pouvant contenir l'insecte entier, il est possible d'identifier les signatures spectrales de chaque isotope et les quantités relatives de chacun d'eux chez les ouvriers, les larves brachyptères et les ailés.Les radionucléides présents dans le papier consommé sont rapidement incorporés chez les ouvriers, et atteignent le seuil de détection en 1 à 3 jours. Le marquage isotopique se transmet entre les membres de la colonie; tous les habitants de colonies de laboratorie ont été contaminés en 21 jours, après des contacts avec des individus alimentés sur une source marquée.Les marqueurs isotopiques avec 1 ou 2 radionucléides sont transférés aux sexués par les échanges trophallaxiques. La discussion porte sur les applications du marquage aux radionucléides et l'analyse au spectroscope en écologie éthologique des insectes.

     

Diurnal variation in the stable isotope composition of water and dry matter in fruiting Lupinus angustifolius under field conditions

In this paper, we present an integrated account of the diurnal variation in the stable isotopes of water (δD and δ¹⁸O) and dry matter (δ¹⁵N, δ¹³C, and δ¹⁸O) in the long‐distance transport fluids (xylem sap and phloem sap), leaves, pod walls, and seeds of Lupinus angustifolius under field conditions in Western Australia. The δD and δ¹⁸O of leaf water showed a pronounced diurnal variation, ranging from early morning minima near 0‰ for both δD and δ¹⁸O to early afternoon maxima of 62 and 23‰, respectively. Xylem sap water showed no diurnal variation in isotopic composition and had mean values of ?13·2 and ?2·3‰ for δD and δ¹⁸O. Phloem sap water collected from pod tips was intermediate in isotopic composition between xylem sap and leaf water and exhibited only a moderate diurnal fluctuation. Isotopic compositions of pod wall and seed water were intermediate between those of phloem and xylem sap water. A model of average leaf water enrichment in the steady state (Craig & Gordon, pp. 9–130 in Proceedings of a Conference on Stable Isotopes in Oceanographic Studies and Palaeotemperatures, Lischi and Figli, Pisa, Italy, 1965; Dongmann et al., Radiation and Environmental Biophysics 11, 41–52, 1974; Farquhar & Lloyd, pp. 47–70 in Stable Isotopes and Plant Carbon–Water Relations, Academic Press, San Diego, CA, USA, 1993) agreed closely with observed leaf water enrichment in the morning and early afternoon, but poorly during the night. A modified model taking into account non‐steady‐state effects (Farquhar and Cernusak, unpublished) gave better predictions of observed leaf water enrichments over a full diurnal cycle. The δ¹⁵N, δ¹³C, and δ¹⁸O of dry matter varied appreciably among components. Dry matter δ¹⁵N was highest in xylem sap and lowest in leaves, whereas dry matter δ¹³C was lowest in leaves and highest in phloem sap and seeds, and dry matter δ¹⁸O was lowest in leaves and highest in pod walls. Phloem sap, leaf, and fruit dry matter δ¹⁸O varied diurnally, as did phloem sap dry matter δ¹³C. These results demonstrate the importance of considering the non‐steady‐state when modelling biological fractionation of stable isotopes in the natural environment.     

Diurnal variation in vascular function: role of sleep

Although vascular function is lower in the morning than afternoon, previous studies have not assessed the influence of prior sleep on this diurnal variation. The authors employed a semiconstant routine protocol to study the contribution of prior nocturnal sleep to the previously observed impairment in vascular function in the morning. Brachial artery vascular function was assessed using the flow-mediated dilation technique (FMD) in 9 healthy, physically active males (mean ± SD: 27 ± 9 yrs of age), at 08:00 and 16:00 h following, respectively, 3.29 ± .37 and 3.24 ± .57 h prior sleep estimated using actimetry. Heart rate and systolic and diastolic blood pressures were also measured. The data of the experimental sleep condition were compared with the data of the "normal" diurnal sleep condition, in which FMD measurements were obtained from 21 healthy individuals who slept only during the night, as usual, before the morning test session. The morning-afternoon difference in FMD was 1 ± 4% in the experimental sleep condition compared with 3 ± 4% in the normal sleep condition (p =?.04). This difference was explained by FMD being 3 ± 3% lower in afternoon following the prior experimental sleep (p =?.01). These data suggest that FMD is more dependent on the influence of supine sleep than the endogenous circadian timekeeper, in agreement with our previous finding that diurnal variation in FMD is influenced by exercise. These findings also raise the possibility of a lower homeostatic "set point" for vascular function following a period of sleep and in the absence of perturbing hemodynamic fluctuation.     

Diurnal variation in the feeding pattern of rabbits

Laboratory rabbits maintained under controlled lighting and fed $\text{ad libitum}$ exhibit a weak but consistent diurnal fluctuation in feed intake. There are two major periods of eating; at the beginning and the end of the light period. This results in similar feed consumption for the light and dark periods. Water intake shows a similar diurnal variation to that of feed intake. If the normal lighting cycle is retarded by 6 hours, the animals adjust their diurnal rhythm of feeding behaviour to the new lighting cycle within 8 to 15 days. Comparative studies on rats are included.     

Diurnal variation in the functioning of cowpea nodules

Nitrogenase (EC 1.7.99.2) activity of nodules of cowpea (Vigna unguiculata [L.] Walp), maintained under conditions of a 12-hour day at 30°C and 800 to 1,000 microeinsteins per square meter per second (photosynthetically active radiation) and a 12-hour night at 20°C, showed a marked diurnal variation with the total electron flux through the enzyme at night being 60% of that in the photoperiod. This diurnal pattern was, however, due to changes in hydrogen evolution. The rate of nitrogen fixation, measured by short-term ¹⁵N₂ assimilation or estimated from the difference in hydrogen evolution in air or Ar:O₂ (80:20; v/v), showed no diurnal variation. Carbon dioxide released from nodules showed a diurnal variation synchronized with that of nitrogenase functioning and, as a consequence, the apparent `respiratory cost' of nitrogen fixation in the photoperiod was almost double that at night (9.74 ± 0.38 versus 5.70 ± 0.90 moles CO₂ evolved per mole N₂ fixed). Separate carbon and nitrogen balances constructed for nodules during the photoperiod and dark period showed that, at night, nodule functioning required up to 40% less carbohydrate to achieve the same level of nitrogen fixation as during the photoperiod (2.4 versus 1.4 moles hexose per mole N₂ fixed).

Stored reserves of nonstructural carbohydrate of the nodule only partly satisfied the requirement for carbon at night, and fixation was dependent on continued import of translocated assimilates at all times. Measurements of the soluble nitrogen pools of the nodule together with ¹⁵N studies indicated that, both during the day and night, nitrogenous products of fixation were effectively translocated to all organs of the host plant despite low rates of transpiration at night. Reduced fluxes of water through the plant at night were apparently counteracted by increased concentration of nitrogen, especially as ureides, in the xylem stream.

     

Electron microscopical demonstration of thiols and disulphides in the porcine epidermis

Summary This study describes the electron microscopical distribution of free thiols and disulphides in the epidermis of the domestic pig and the wild boar, as compared to light microscopical histochemistry. With the silver methenamine method, silver labelling of thiols was clearly achieved on the keratohyalin and cytofilament accumulations in the cells of the living epidermis and the plasma membrane of granular cells. To a certain extent, the envelope and cytoplasm of young corneocytes reacted equally intensively. Disulphides were very abundant in the filaments, keratohyalin granules, and cell envelope of granular cells, and, particularly, in the envelope (marginal band) of corneal cells; the latter structure being distinctly delineated from the background. As a specific feature, the viable epidermis of the wild boar stained strongly for disulphides. The results obtained are discussed in view of actual concepts of epidermal keratinization and corneal cell function.     

Diurnal variations in photosynthetic rates: comparisons of ultraphytoplankton with a larger phytoplankton size fraction

We compared the composition and photosynthetic activity of twosize fractions of phytoplankton during a cruise from the Gulfof Maine to the Sargasso Sea in August 1983. At every station,and at every depth, ultraplankton (defined here as cells passingthrough 3 µm pores in filters) made a major contributionto both the standing crop of chlorophyll and the rate of primaryproduction. Ultraphytoplankton assemblages were dominated byphycoerythrin-rich cyanobacteria. Overall, the ultraplanktoncontribution to total primary production was greatest at lowphoton fluxes: (i) at the beginning and end of the photoperiod;(ii) with increasing depth in the euphotic zone; and (iii) whendaily irradiance was low. The composition of ultraphytoplanktonvaried with depth. Surface (2 m) ultraphytoplankton assemblageswere almost exclusively composed of phycoerythrin-rich cyanobacteriawith smaller (0.2–0.8 µm) cyanobacteria predominating.Below the surface mixed-layer, the proportion of larger (0.8–30 µm) to smaller cyanobacteria increased and the eukaryoticcomponent of the ultraphytoplankton often became important.At two Sargasso Sea stations, the greatest numbers of cyanobacteriawere below the mixed layer at the 1% light level, while themaximum numbers of eukaryotic ultraphytoplankters occurred deeperstill, at the 0.5% light level, coincident with the chlorophyllmaximum. At the bottom of the euphotic layer in the SargassoSea. eukaryotes numerically dominated the ultraphytoplanktonand made a major contribution to the chlorophyll maximum.     

Measurement of the erythrocyte orientation in a flow by spin labeling

When a suspension of erythrocytes labeled in their membrane with a fatty acid paramagnetic molecule is allowed to flow in a flat quartz sample cell, the recorded electron paramagnetic spectra change as a function of the orientation of the cell in the magnetic field. This indicates that the red cells are themselves oriented in the flow. Such spectral variations have been reproduced by a numerical simulation procedure, which allowed us to quantify the proportion of oriented red blood cells by measuring the amplitude of some characteristic lines on the experimental spectra. Orientation rates were then measured as a function of various rheological parameters, such as shear rate, hematocrit and viscosity of the suspending medium. The kinetics of the disorientation process was determined by stopping the flow.     

Diurnal variation in the numbers of birds feeding at a sewage works in summer

Diurnal variation in the abundance of different species on a sewage works wasfound to be related to their respective roosting behaviour as well as their feeding pattern.