Are salinas a suitable alternative breeding habitat for Little Terns Sterna albifrons?

This paper describes the breeding population, breeding habitats and reproductive variables of Little Terns Sterna albifrons in natural (sandy beaches) and alternative (salinas) habitats. Studies of nesting success conducted between 1998 and 2002 in these two types of habitat were combined with a literature review of census work from the past 30 years in order to assess whether salinas are suitable alternative breeding habitat for Little Terns. Most of the Portuguese Little Tern population now breeds in salinas. Census data from the last 30 years show that this is a recent breeding behaviour, because until the 1990s most colonies were located on sandy beaches. Destruction and disturbance of the natural habitat has caused this habitat shift. Despite this shift, the Portuguese Little Tern breeding population did not decline during this period and no significant differences were found in nesting success between natural and alternative habitats. This might indicate that salinas are a suitable alternative breeding habitat for Little Terns, but differences in laying period, clutch size and egg size were recorded between birds nesting on sandy beaches and in salinas in the same area. Birds nested earlier on sandy beaches and laid larger clutches and eggs than in salinas. These data suggest that, when both habitats are available, older and/or higher quality birds prefer sandy beaches for breeding, presumably trying to re-nest in salinas when first breeding attempts failed. We discuss conservation priorities and management actions for both habitats.     

Spatial and Temporal Variation of Macroinvertebrate Drift in Two Neotropical Streams1

The detection of spatial variation in macroinvertebrate drift depends on the spatial scale of investigation in streams of the La Selva Biological Station, Costa Rica. Drift samples were taken in a spatially nested design, with two streams, two reaches per stream, two riffles per reach, and four replicate samples per riffle. Drift showed little variation among streams, but varied significantly at the scales of reach and riffle, with variation among samples also high. In addition, sampling took place at two temporal scales: diel and at two different periods that differed in rainfall conditions. Drift diel periodicity was a clear pattern, while only density of individuals varied among sampling periods. This is the first study of macroinvertebrate drift at multiple spatial scales, despite the recognition that multi‐scale studies are essential for a more complete understanding of community patterns and processes.     

Non-polluting wood and pulp delignification: Biomimetic ligninase system

Summary We report the delignification ofPinus radiata D Don,Eucalyptus globulus andEucalyptus grandis woods (formic acid treated and untreated) by 2 h treatment with a hemin/hydrogen peroxide system. The untreated chips and sawdust ofE. globulus were 30% and 50% delignified respectively. No significant effects were found forP. radiata sawdust;P. radiata treated chips (organosolv pulp) did not show any further delignification upon hemin/peroxide action, 25% delignification was achieved in untreated chips. In the case ofE. grandis untreated wood the delignification was better in sawdust than in chips, but in smaller percentage than in the otherEucalyptus species. This relation is maintained in substrates, treated with formic acid or untreated. The delignification of chips in both species ofEucalyptus was improved when they were pre-treated with formic acid. The loss of lignin in theE. grandis andE. globulus sawdust (pre-treated with formic acid) was 79% and 75% respectively.     

Time course and subcellular distribution of the radioactivity in a synaptic terminal after supplying the perikaryon with labelled glutamic acid

Summary The cell bodies of the preganglionic neurons of the chick ciliary ganglion were supplied with ³H-glutamic acid by intracerebral injection. The ciliary ganglia were studied with light and E.M. radioautography at 3, 18, 24 hours, 2, 6 and 16 days after injection. The reaction in the ganglion was intense over the preganglionic structures but very weak over the ganglionic cell bodies. The reaction increased in intensity from the myelinated region toward the ending; within the axon, the radioactivity was rather peripheral during early stages and more evenly distributed from the second day onward. The ending showed two peaks of radioactivity, at 18 hours and at 6 days; these peaks are interpreted as the accumulation of material which arrived in two phases; the first with an average velocity greater than 80 mm/ day and the second with a velocity of 2–5 mm/day. Within the nerve ending, the material transported in the fast phase was associated preferentially with the axoplasm rich in synaptic vesicles, close to the synaptic region, whereas the material transported in the slow phase was associated rather with mitochondria and the axoplasm devoid of synaptic vesicles that lies away from the synaptic surface. In contrast to what is observed with lysine, the density of the reaction on the preterminal axons was much lower than that on the endings. It is suggested that a protein rich in glutamyl residues with a rather long mean-life is transported to the ending in the fast phase.On leave from the Catholic University, Santiago, Chile.Supported by Institut National de la Santé et de la Recherche Médicale, France and IBRO. Acknowledgement. I express my sincere thanks to Dr. B. Droz for his hospitality and for helpful discussions throughout the work.     

Assembly of microspheres from acidic proteinoids and histones or histone-like proteinoids

Basic polyamino acids, whether organismic or synthetic in origin, alter the morphology of proteinoid microspheres in which they are included. The particles obtained with histone are essentially indistirguishable under the light microscope from those obtained with proteinoids of histone-like composition (histonoids). In each instance, structures of morphological complexity similar to those of some microfossils are obtained.     

Brote epidemico de tinea corporis por Microsporum gypseum

Summary A small epidemic of tinea corporis due to M. gypseum is reported. There were 13 children affected, ages 1–15 years. These children belonged to 6 neighbouring families and all used a common playground, an empty lot located nearby. Cultures were positive for M. gypseum in the 13 children and the agent was also isolated from 2 soils collected in the playing-ground. Soil isolates were classified as N. gypsea. Clinically, the lesions were circinated and had active borders, they were preferentially located in the trunk. Most children (8/13) had multiple lesions. These and other pertinent aspects are discussed in the text.     

Susceptibility to mercurials of clinical Pseudomonas aeruginosa isolated in México

Susceptibility to inorganic mercuric ions and to organomercurials of 237 Pseudomonas aeruginosa clinical strains isolated in Mexico was determined by agar dilution tests. Resistant strains fell into two classes: i) narrow-spectrum resistant strains (27% of total isolates) resistant only to mercuric ions and to merbromin, and most grouped in pyocin type 1; and ii) broad-spectrum resistant strains (5%) with additional resistances to thimerosal, phenylmercury, methylmercury and p-hydroxymercuribenzoate, that belonged mostly to pyocin type 10. Mercurial resistant isolates showed a higher proportion of resistance to antibiotics and metals than did mercurial sensitive isolates, and broad-spectrum resistant strains had the highest frequency of resistance to antibiotics and to tellurite and arsenate.     

The effects of felodipine and bepridil on calcium-stimulated calmodulin binding and calcium pumping ATPase of cardiac sarcolemma before and after removal of endogenous calmodulin

Summary The Ca²⁺ channel blockers felodipine and bepridil are known to affect selectively functions of calmodulin. We studied their effects on calmodulin binding and ATPase activities of calmodulin-containing and calmodulin-depleted rabbit heart sarcolemma. Both drugs as well as the specific anti-calmodulin drug calmidazolium at a concentration of 50 µM, inhibited the Ca²⁺-stimulated calmodulin binding to calmodulin-depleted sarcolemma. Within the concentration range of 3 to 100 µM all three drugs also progressively inhibited Ca²⁺ pumping ATPase in calmodulin containing sarcolemma, although the enzyme was assayed at saturating Ca²⁺ (100 µM). The inhibitory potency of calmidazolium and bepridil, but not that of felodipine, increased when the membrane protein concentration in the ATPase assay was lowered. At low membrane protein concentration 30 µM calmidazolium completely blocked calmodulin-dependent Ca²⁺ pumping ATPase, whereas the inhibition caused by 30 µM felodipine or bepridil remained partially. A similar inhibition pattern of the drugs was found in the calmodulin binding experiments. Within a concentration range of 3 to 30 µM, all three drugs had negligible effects on the basal Ca²⁺ pumping ATPase which was measured in calmodulin-depleted sarcolemma. In conclusion, the characteristics of the anti-calmodulin action of felodipine on the rabbit heart sarcolemmal Ca²⁺ pumping ATPase are not different from those of bepridil. Both drugs may inhibit the enzyme by interference with the Ca²⁺-stimulated binding of calmodulin.Abbreviations Ca²⁺ pumping ATPase Ca²⁺ stimulated Mg²⁺-dependent ATP hydrolyzing activity - Na⁺ pumping ATPase Na⁺-stimulated K⁺- and Mg²⁺-dependent ATP hydrolyzing activity - Tris-maleate tris (hydroxymethyl) aminomethane hydrogen maleate - Hepes N-2-hydroxyethylpiperazine-N-2-ethanesulfonic acid - Mes 2-(N-morpholino) ethane sulfonic acid and Egta, ethylene glycol bis (p-amino ethylether)-N,N,N,N tetraacetic acid     

Immunological relationships between Artemia RNA polymerases and between RNA polymerases II from different eukaryotic organisms

Summary Rabbit antibodies against Artemia RNA polymerase II have been raised and utilized to study the immunological relationships between the subunits from RNA polymerases I, II and III from this organism and RNA polymerase II from other eukaryotes. We describe here for the first time the subunit structure of Artemia RNA polymerases I and III. These enzymes have 9 and 13 subunits respectively. The anti-RNA polymerase II antibodies recognize two subunits of 19.4 and 18 kDa common to the three enzymes, and another subunit of 25.6 kDa common to RNA polymerases II and III. The antibodies against Artemia RNA polymerase II also react with the subunits of high molecular weight and with subunits of around 25 and 33 kDa of RNA polymerase II from other eukaryotes (Drosophila melanogaster, Chironomus thummi, triticum (wheat) and Rattus (rat)). This interspecies relatedness is a common feature of eukaryotic RNA polymerases.Abbreviations RNAp RNA polymerase - DPT diazophenylthioether - SDS sodium dodecylsulfate