Butterfly response to severe ENSO-induced forest fires in Borneo

Abstract.  1. Little is known about animal community response to severe El Niño Southern Oscillation (ENSO)-induced fire events. Here the response of butterflies to the 1997/98 ENSO-induced fire event in East Kalimantan (Indonesian Borneo) is assessed. In addition to the community-wide study, a detailed assessment of the lycaenid Jamides celeno is made.
2. Species richness declined significantly from 211 species pre-ENSO to 39 species post-ENSO and community composition changed significantly. Along with the decline in species richness there was a marked increase in dominance. Jamides celeno , for example, increased from 3% of the pre-ENSO assemblage to 58% of the post-ENSO assemblage. Like J. celeno , most of the species in the post-ENSO assemblage were generalists; most of the specialist species having disappeared from pre- to post-ENSO.
3. The major host plant used by J. celeno was the abundant resprouting Fordia splendidissima . Furthermore, significantly more eggs were laid on plants with the crazy ant, Anoplolepis gracilipes , present than on plants with other ants or no ant attendance. Caterpillar presence was significantly higher on plants tended by ants than on untended plants.
4. The median distance moved by J. celeno was 30 m with a maximum recorded distance of 290 m.
5. The abundance of J. celeno and other generalists in the post-ENSO assemblage at Wanariset was probably related to their ability to utilise the few available resources after the fire (e.g. F. splendidissima resprouts), their presence in degraded habitats surrounding the Wanariset forest, and their ability to disperse successfully by either being strong fliers (e.g. Euploea spp.) or being able to attain very high population sizes and thereby produce a surplus of dispersers (e.g. J. celeno ).     

Isolated plant mitochondria import chloroplast precursor proteins in vitro with the same efficiency as chloroplasts.

Most chloroplast and mitochondrial proteins are synthesized with N-terminal presequences that direct their import into the appropriate organelle. In this report we have analyzed the specificity of standard in vitro assays for import into isolated pea chloroplasts and mitochondria. We find that chloroplast protein import is highly specific because mitochondrial proteins are not imported to any detectable levels. Surprisingly, however, pea mitochondria import a range of chloroplast protein precursors with the same efficiency as chloroplasts, including those of plastocyanin, the 33-kDa photosystem II protein, Hcf136, and coproporphyrinogen III oxidase. These import reactions are dependent on the Deltaphi across the inner mitochondrial membrane, and furthermore, marker enzyme assays and Western blotting studies exclude any import by contaminating chloroplasts in the preparation. The pea mitochondria specifically recognize information in the chloroplast-targeting presequences, because they also import a fusion comprising the presequence of coproporphyrinogen III oxidase linked to green fluorescent protein. However, the same construct is targeted exclusively into chloroplasts in vivo indicating that the in vitro mitochondrial import reactions are unphysiological, possibly because essential specificity factors are absent in these assays. Finally, we show that disruption of potential amphipathic helices in one presequence does not block import into pea mitochondria, indicating that other features are recognized.     

The in vivo effects of 2.45 GHz microwave radiation on rabbit serum components and sleeping times

Summary An investigation was conducted to determine the effects of relatively low power density microwave exposures on various serum components of the Dutch rabbit. Both continuous wave and pulsed mode exposures at 2.45 GHz were used at power densities of 25, 10 and 5 mW/cm². Studies of 10 serum components were performed. Additional studies were conducted on changes in sleeping times of pentobarbital-sedated rabbits at various power densities. Gross and histopathological examinations were performed on representative samples of animals.Changes in the blood chemistry of irradiated animals were consistent with a dose-dependent response to a non-specific thermal stress at all power densities used. Observed physiological response, as well as rectal temperature measurements, indicated that the thermoregulatory capability of the rabbits was sufficient to compensate for the thermal burden at 5 and 10 mW/cm², but could be overridden by a 2 h exposure at 25 mW/cm². Pathology findings included a mild, repairable nephrosis in animals exposed at a power density of 25 mW/cm².A further investigation of analeptic effects at power densities varying from 5 mW/cm² to 50 mW/cm² resulted in a statistically significant decrease in sleeping times, apparently proportional to power density below 15 mW/cm².This research was partially supported by the US Army Medical Research and Development Command, Contract No. DADA17-72-C-2144. (The views expressed are those of the authors and do not necessarily reflect those of the Department of the Army)     

In vitro fertilization of mouse ova by spermatozoa exposed isothermally to radio-frequency radiation

Mouse spermatozoa were exposed in vitro for 1 h to 27- or 2,450-MHz CW RF radiation at SARs of 0 to 90 W/kg under isothermal (37 +/- 0.2 degrees C) conditions. Exposure at either frequency to RF radiation at SARs of 50 W/kg or greater resulted in a statistically significant reduction in the ability of irradiated sperm to fertilize mouse ova in vitro (P less than .05). Over the range of SARs there was no apparent difference in the effects of 27- vs. 2,450-MHz RF radiation. There were no readily detectable exposure effects on spermatozoan morphology, ultrastructure, or capacitation. The reduction of in vitro fertilization is attributed to a direct effect of RF radiation on spermatozoa rather than to heating.     

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.