Limnology and performance of waste treatment lagoons

By arranging sewage ponds in series, some feedback relationships within the food web are disconnected, but stability may increase. This particularly applies to a persistent clearwater-state in the last cell caused by mass growths of Daphnia or other zooplankton in the absence of fish. Microbial pollution in this case is reduced to a level which may permit nearly unrestricted irrigation. The oxygen balance of lagoons is, apart from the diurnal cycle, subject to substantial temporal variations. This also applies to continuous-flow laboratory models with a constant (BOD-load, temperature) or a constant-cycle (light) chemical and physical environment. An example is given illustrating a high adjustment stability of a lagoon in consequence of a catastrophic perturbation.The strong tendency of lagoons towards an oligomictic behaviour is promoted by thermal stratification and by a vertical gradient in the metabolic activity (oxidation/reduction potential). The hydrodynamic conditions oscillate between plug flow in periods of convective overturn and short-circuiting if thermal stratification has developed. Nevertheless, the average performance (BOD removal) for a particular season could be calculated with a reasonable accuracy. As a basis for this calculation, nomographs were developed from which the rate coefficient K₁ of BOD removal for a given combination of residence time and BOD load can be read.     

Versuche zum angenommenen Kontrastverlust im Gesang der Blaumeise (Parus caeruleus) auf Teneriffa

Zusammenfassung Der Gesang von Blaumeisen-Populationen in Mitteleuropa, Spanien, Marokko und auf Teneriffa wurde miteinander verglichen (Abb. 1). In Süddeutschland und auf Teneriffa wurden Klang-Attrappen-Versuche durchgeführt.1. Der Blaumeisen-Gesang ist in Marokko und auf Teneriffa sehr ähnlich. Er unterscheidet sich vom Blaumeisengesang in Europa (Mitteleuropa und Spanien) in folgenden Eigenschaften (2.–4.):2. Ihm fehlen phrasierte Strophen (Abb. 2 a–c, e, 3, 4 a, b, f, g), also Strophen, in denen dasselbe Element mindestens viermal nacheinander wiederholt wird.3. Er enthält mehr verschiedene Elemente (Abb. 5, 7).4. Die interindividuelle Variation ist größer (Abb. 6, 7).5. Die Unterschiede zwischen dem Blaumeisen-Gesang in Europa und auf Teneriffa lassen sich nicht mit der Kontrast-Betonungs- und der Kontrast-Verlust-Hypothese nachLack &Southern (1949) undMarler (1960) erklären. Die Lernentzugs-Hypothese erklärt sie besser.6. Die Blaumeisen von Teneriffa und Marokko sind sehr nahe miteinander verwandt, aber vermutlich sind sie von den europäischen Blaumeisen artlich nicht getrennt.

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The song of the Blue Tit (Parus caeruleus) on Tenerife: Experiments on a presumed loss of contrast

Summary Songs of Blue Tit populations from Central Europe, Spain, Morocco and Tenerife (fig. 1) were compared. Playback experiments were made in South Germany and on Tenerife.1. Blue Tit songs from Morocco and Tenerife are very similar. They differ from songs of Blue Tits in Europe (Central Europe and Spain) in the following characteristics (2–4):2. Lack of phrased songs (fig. 2 a–c, e, 3, 4 a, b, f, g), i. e. songs with the same notes repeated successively at least four times.3. A greater number of different types of notes (fig. 5, 7).4. Greater interindividual variation (fig. 6, 7).5. Differences between Blue Tit song from Europe and from Tenerife cannot be explained by the hypothesis of contrast reinforcement and loss of contrast, according toLack &Southern (1949) andMarler (1960). The withdrawal of learning hypothesis is a better explanation.6. Blue Tits on Tenerife and Morocco are very closely related to each other but are probably not a different species from the Blue Tits of Europe.

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Für die Übersetzung danken wir FrauR. Jellis und HerrnP. Lundberg.     

Carbamyl phosphate synthetase A of Neurospora crassa.

Carbamyl phosphate synthetase A of Neurospora crassa was partially purified from mitochondrial extracts. It is an extremely unstable enzyme (t 1/2 = 45 min at 25 detrees C) made up of two unequal subunits. The native enzyme has a molecular weight of approximately 175,000, and the large subunit has a molecular weight of about 125,000. Both the native enzyme and its large subunit are quite asymmetric, as revealed by slow sedimentation in sucrose gradents (7.3S and 6.6S, respectively). The small subunit has not been identified physically as a separate entity. The denaturation of the native, glutamine-dependent activity is correlated with dissociation of subunits, the larger of which retains a more stable, ammonia-dependent activity. Neither substrates nor any other agents except glycerol or polyethylene glycol appreciably stabilized the glutamine-dependent activity. Kinetic studies showed the native enzyme to have a Km for glutamine of about 0.16 mM, and a Km for NH4Cl of about 16 mM, at the optimal pH, 8.0. The enzyme, using either N donor, has a K+ requirement for activity, for which NH4+ can substitute. The glutamine leads to glutamate reaction, which requires the small subunit, also requires the large subunit and all reaction substrates for optimal activity. Other evidences of subunit interaction are the greater activity of the native enzyme, as opposed to the large subunit, with low concentrations of adenosine 5'-triphosphate-Mg2+, and in the stimulation of the ammonia-dependent activity of the native enzyme by glycine. Curiously, although the enzyme's role in biosynthesis is confined to the arginine pathway, it is completely indifferent to arginine or its precursors as feedback effectors or activators. The enzyme is compared with carbamyl phosphate synthetases of other organisms.     

Stimulation of DNA synthesis and myo-inositol incorporation in mammalian cells

Phosphatidylinositol (PI) synthesis and its role in controlling the cell cycle has been investigated using fibroblasts and liver cells in culture. PI synthesis as measured by incorporation of [³H]-myo-inositol into trichloroacetic acid precipitable material during 0–60 min after serum or growth factor stimulation of serum-starved cells is increased in primary fetal rat liver cells, rat embryo fibroblasts, and 3T3 mouse cells. In contrast, growth stimulation of 3T3 cells and hepatocytes rendered quiescent in G₁ by amino acid starvation is not accompanied by increased incorporation of [³H]-myo-inositol into trichloroacetic acid precipitable material. This suggests that those cells might be arrested at a different point in G₁ than cells arrested by serum depletion. Inhibition of PI synthesis by δ-hexachlorocyclohexane (HCH), a steric analog of myo-inositol, during early times (e.g., 0–4 hr) after growth stimulation, reversibly blocks initiation of DNA synthesis in 3T3 cells. The results support the idea that increased PI synthesis in response to growth stimulation in the cell types studied here is a prerequisite for progression through G₁ and subsequent entry into S phase.     

Site-specific substituted cobalt(II) horse liver alcohol dehydrogenases. Preparation and characterization in solution, crystalline and immobilized state.

The specific substitution, using highly selective techniques, of catalytic and/or noncatalytic zinc ions by cobaltous ions in horse liver alcohol dehydrogenase (EC 1.1.1.1) has been studied with dissolved, crystalline and agarose-immobilised enzyme, in order to examine the effect of protein structure on the specificity of the metal exchange. The different binding sites can be clearly distinguished by the absorption spectra of their cobalt derivatives. In solution an anaerobic column chromatographic method made it possible to exchange half of the zinc in the enzyme by cobalt ions in a much shorter time than previous procedures. By raising the temperature in the exchange step, even the slowly exchanging zinc ions were substituted by cobalt, yielding products similar to cobalt alcohol dehydrogenases described earlier. Treatment of crystal suspensions of the enzyme with chelating agents (preferentially dipicolinic acid) gave an inactive protein with two zinc ions remaining bound. The enzyme could be reactivated by treatment of the crystalline protein with 5 mM zinc or cobaltous ions or by dialysis of dissolved inactive protein against 20 microM zinc or 1 mM cobaltous ions. Higher metal concentrations led to denaturation but the inactive protein could be crystallized from solution and then reactivated completely at higher metal concentrations. The preparation and absorption spectrum show that cobalt is bound specifically at the catalytic sites. Since metal substitution at these sites critically depends on the maintenance of the correct tertiary and quaternary structure, these must be preserved in the crystal lattice and partially altered in solution when the catalytic zinc ions are removed (or when excess of metal ions is applied), thus demonstrating the structure-stabilizing role of the catalytic metal ions. The enzyme immobilised on agarose, with unchanged content of active sites [Schneider-Bernl?hr et al. (1978) Eur. J. Biochem. 41, 475--484], was treated like the crystal suspensions. Although half of the zinc was removed, some activity remained. After reactivation with cobaltous ions, a loss of about 30% active sites was measured. Thus the apparently homogenous bound enzyme was rather heterogeneous in the properties of its catalytic metal binding sites. These results are taken as further proof for the dependence of the metal substitution on the proper tertiary and quaternary structure which is strained by multiple interactions in the covalently immobilised enzyme.     

Trypanosoma theileri: In vitro cultivation in tsetse fly and vertebrate cell culture systems

Epimastigote forms of Trypanosoma theileri were grown at 25°C in insect cell culture media and in Glossina tissue cultures for more than 6 months. Doubling times of 10–14 h during exponential growth were observed. In cell cultures which had been derived from pupal tsetse flies growth rates were higher than in cell free media; in a larval cell line, however, growth of T. theileri was inhibited. Ecdysteroids and juvenile hormone I reduced multiplication of T. theileri in cell free media. When T. theileri was incubated in different sera only fetal calf serum (FCS) supported growth. Epimastigote forms transformed into trypomastigote bloodforms when cultured at 37°C in FCS, vertebrate cell cultures, and Eagle's medium, but not in insect media or Glossina cell cultures. Oxygen uptake of epimastigotes could be inhibited by rotenone antimycin A and cyanide; trypomastigotes were not affected by these inhibitors.     

Mesurement of longitudinal ion profiles in single roots of Hordeum and Atriplex by use of flameless atomic absorption spectroscopy

Summary A method is described by which the Na⁺ and K⁺ content in 0.5 mm sections of single roots of Hordeum distichon L. and Atriplex hortensis L. can be determined by use of flameless atomic absorption spectroscopy. By this method the longitudinal profiles of K⁺ and Na⁺ along low salt roots and roots which had been equilibrated with or grown in K⁺-free 1 mM Na⁺-solution were determined. The profiles reveal that high K⁺/Na⁺ ratios in the cytoplasm are maintained also in K⁺-free solutions. In solutions containing 1 mM Na⁺ a high K⁺/Na⁺ selectivity was found to be dependent on sufficient aeration. From the ion profiles the cytoplasmic (110 mM) and vacuolar (20 mM) K⁺ concentration in low salt barley roots—values which are unobtainable by compartmental analysis—could be estimated.     

Blood parasites of some birds from Ghana

A total of 135 birds of 26 species in 13 families was examined for blood parasites; 43 birds (31.9%) of 13 species were infected; species of the Ploceidae were the most heavily infected. Species of Haemoproteus occurred most commonly 29 birds) while Leucocytozoon and Plasmodium species were virtually absent. There was no significant difference in the prevalence of hematozoa in birds from the mature rainforest and those in a savannah-urban setting.     

Viererbruten des Kaiseradlers(Aquila heliaca)

Ohne Zusammenfassung