Age-specific Chaoborus predation on rotifer prey

SUMMARY. 1. This is the first study to examine predator-prey interactions between Chaoborm instars and rotifer prey. The predatory behaviour of instars I–III of Chaoborus pimctipennis and the diet selectivity of instars I—IV feeding on rotifers were examined in the laboratory. Prey used in direct observations of predatory behaviour included a variety of rotifers (Symhacta pectlnata, S. ohUmga, Polyarthra remata, Asplanchna girodi, Keratella crassa, spined and unspined forms of Keratella cochlearis) and two crustaceans (Bosmitia longirostris, Mesocyclops edax nauplii. 2. In general, strike efficiencies (percentage of strikes resulting in inges- tion) increased in successive instars I—III. Early instar (I and II) strike efficiencies were low when compared with other invertebrate predators. For a given instar. mean prey handling times varied among prey species more than strike efficiencies. Mean handling times for small, soft-bodied rotifers were lowest and those for wide, hard-bodied prey were highest. 3. Instar I exhibited significantly greater selectivity for the small, soft- bodied S. obUmga than for the larger S. pectinata, hard-bodied K. crassa, and spined and unspined forms of K. cochlearis. Instars II—IV positively selected both the large and small Symhaeta species over all Keratella species. The relationship between Chaobortts selectivity and prey value (weight of prey per unit handling time) can be described by a power function. Ingestion rates of rotifers by older instars (III and IV) are among the highest reported for invertebrate predators. 4. Rotifer vulnerability to Chaoborus predation probably depended on rotifer cuticle texture, body width, and hydrodynamic disturbances. Spined rotifers were not necessarily protected from Chaoborus predation because Chaohorus can manipulate and swallow them. Giguere et al.'s 1982) encounter rate model must be modified to predict encounter rates of slow-moving rotifer prey with Chaohorus.     

Short-term movements of chalk-stream invertebrates

SUMMARY 1. Trays of gravel were implanted for 24 h periods in several chalk streams. The trays were variously modified to monitor colonization from different sources, particularly drift (D), other downstream movements (DSM), upstream movements (USM), and all sources combined (ALL).
2. The abundance of invertebrates in the streams was high (maximum of 717 per 0.04 m²) and colonization of the trays was extensive, especially by Gammarus pulex , the predominant species in all but one of the streams (maximum number of individuals of G. pulex per tray: for D, 473; for DSM, 462; tor USM, 286; and tor ALL, 639). In some cases benthic densities were achieved in the trays in the 24 h exposure period, and in most cases any one source of colonization could provide benthic densities in a few days.
3. Patterns of movement differed between species, between size classes of G. pulex , and between sites for particular species. No one source of colonization could be regarded as generally predominant although downstream movements in total (D + DSM) usually far exceeded USM. DSM was usually an important source of colonization.
4. The extent and direction of movement appeared to be determined by local factors and were explained in terms of the high densities of invertebrates and the current and substratum characteristics of each site.
5. Estimates of the relative importance of different sources of colonization varied greatly according to the criteria used in determining proportions.     

Construction of DNA-probes and their immunochemical detection using nonradioactive hybridization tests

Simple and efficient chemical approaches to preparation of DNA probes carrying 2,4-dinitrophenyl, dansyl or biotin residues were developed. The residues were introduced using following DNA derivatization procedures: a) transamination of cytidine residues with O-(4-aminobutyl)hydroxylamine; b) mercuration of pyrimidine residues followed by beta-mercaptoethanol modification. It was shown that 2,4-dinitrophenyl-containing DNA probes can be used for nonradioactive hybridization detection of nucleic acids. DNP-DNA: DNA complexes were detected using mouse antibodies specific to 2,4-dinitrophenyl groups, which were developed with peroxidase-conjugated antimouse immunoglobulins. Peroxidase-catalyzed chemoluminescent reaction of luminol oxidation with hydrogen peroxide allowed to detect 10 picograms of the dinitrophenylated single-stranded DNA probe.     

Functionally important lysine residues in inorganic pyrophosphatase from E. coli. II. Isolation and characteristics of modified tryptic peptide and analysis of the functional role of lysine residues controlling enzyme activity

Inactivation of inorganic pyrophosphatase from E. coli by pyridoxal-5'-phosphate is due to the modification of a lysine residue located in the tryptic peptide with the Asp-Leu-Pro-Glu N-terminal sequence. In course of the enzymatic process this lysine-residue appears to be in the protonated state and either operators as the proton donor for the product of the enzymatic reaction or is involved in stabilization of the transition state.     

Temperature regulation in a burrow-nesting tropical seabird,the Wedge-tailed Shearwater (Puffinus pacificus)

Summary At low air temperatures (2.3–13.9°C), Wedge-tailed Shearwaters (Puffinus pacificus) shivered and their oxygen consumption increased to as much as 283% of the mean value (0.77 ml O₂/g·h) within the thermoneutral zone of air temperature (23–34°C). The minimal thermal conductance of the tissues and plumage was similar to the value predicted from the body mass (320.5 g). The oxygen consumption of the birds within their thermoneutral zone was lower than predictions based on body mass. At elevated air temperatures, the shearwaters panted at respiratory frequencies as high as 260 respirations/min; maximal respiratory frequencies were not invoked until the birds had become hyperthermic. During exposure to a hot environment, the oxygen consumption of the birds increased and in most instances the shearwaters were not able to lose heat equivalent to their concurrent metabolic heat production.Symbols and abbreviations BMR basal metabolic rate - C _total total thermal conductance - f respiratory frequency - TEWL total evaporative water loss - T _st stomach temperature - T _re rectal temperature     

Purification of acetylcholinesterase from horse erythrocytes using affinity chromatography

A commercial preparation of water-soluble acetylcholinesterase from horse red cells has been purified to a specific activity of 2380 U/mg of protein (a 1660-fold purification) by a twofold affinity chromatography on the known sorbent of Sepharose-p-[NH-(CH2)5-C(O)NH(CH2)5C(O)NH-]-C6H4-N+(CH3)3 X Br- at pH 7.5. A selective elution of the enzyme was carried out from 10 mM of the phosphate buffer solution which contains 0.2% of triton X-100. Subsequent desorption of the enzyme proceeded with 5 mM of phenyltrimethylammonium bromide introduced into the buffer. Such effective preparations of acetylcholinesterase have not been previously produced. Effectiveness of the affinity sorbents considerably depends on the nature of the ligand which is covalent-linked with a Sepharose matrix and on the length of the attachment spacer arm ("insert") between them. A reversible inhibitory effect of certain ligands (tetramethylammonium, phenyltrimethylammonium) and their derivatives on acetylcholinesterase is estimated in comparison.     

Endocrine function of the heart. Structure and biological properties of peptides secreted by the heart atrium

Apart from the generally known functions, the heart has also an endocrine function. Atrial cardiocytes, being typical secretory cells, release peptide hormones into the blood stream: atrial natriuretic peptide containing 28 amino acids and cardiodilatin. The structure of atrial peptides was determined. It was shown that both peptides were derived from their common precursor, a protein containing 151 amino acids. The presence of specific receptors is demonstrated on plasmatic membranes of cells of kidney epithelium, arterial smooth muscle, arterial endothelium, kidney cortex and hypophysis. The interaction of atrial peptides with these receptors activates the guanylate cyclase system. The biological action of atrial peptides manifests itself in the quick, massive and instantaneous increase of diuresis and electrolyte excretion, elevated clearance of creatinine, decrease of kidney vascular resistance, intensification of glomerular filtration, inhibition of stimulated secretion of aldosterone, relaxation of blood vessels, elimination of arterial and intestinal spasm induced by various endogenous and exogenous vasoconstrictors and in correction of kidney hypertension. Various radioimmunoassays for the presence of atrial peptides in human plasma were developed; it was shown that in patients with congestive heart failure the content of atrial peptides is increased.     

5-Amino-4-imidazolecarboxamide is a mutagen in E. coli

5-Amino-4-imidazolecarboxamide (5A4IC), the base moiety of a common intermediate in de novo purine biosynthesis, was found to be mutagenic in E. coli. Using a series of mutants in the tryptophan synthetase A gene, 5A4IC was observed to cause transition and transversion mutations at similar levels. At 400 micrograms/ml in the growth medium, it stimulates the base substitution GC----AT 4.8-fold; AT----GC 20-fold; AT----CG (2 sites) an average of 6.0-fold; AT----TA 7.8-fold; and GC----CG 6.1-fold. The transversion GC----TA was not tested. In contrast to the base, 5-amino-4-imidazolecarboxamide riboside is not mutagenic at a similar molar concentration.     

Dynamics of immunoglobulins and immunocompetent lymphocytes in guinea pigs with experimental ascariasis

The paper presents data on variations in the level of serous immunoglobulins (Ig M and Ig G classes), immunocompetent T- and B-lymphocytes in lymphoid organs (spleen, mesenteric, portal and mediastinal lymph nodes) and specific antiparasitic antibodies in guinea pigs during the dynamics of experimental ascariasis.     

Method for histological preparation of bone sections containing titanium implants

A thin sectioning technique involving hand grinding has been developed to produce 20-40-microns-thick sections of bone-titanium implant sites. Components include: 1) surface staining of sections prior to mounting on slides so bone labels (oxytetracycline-HCl and 2,4-bis(N,N-dicarbomethyl)aminomethylfluorescein (DCAF] can be seen in sections viewed with transmitted light, 2) a pneumatic sample press for bonding sections to slides with a thin, uniform glue line and without trapped air bubbles, and 3) bonding methyl methacrylate embedded sections to clear acrylic slides with methyl methacrylate monomer to provide enhanced bond strength and grinding properties compared to those obtainable with glass slides. Sample cracking and distortion is minimized and the tissue-implant interface can be kept intact. The expense of start-up equipment for this technique is minimal.