What is Communicated in the Antipredator Calls of Lemurs: Evidence from Playback Experiments with Ringtailed and Ruffed Lemurs

Two hypotheses of signal specificity in antipredator calls (“referential signalling” and “response urgency”) are discussed in light of prior research on ground squirrels and vervet monkeys. These hypotheses then are examined with data on responses of semi-captive ringtailed and ruffed lemurs to antipredator call playbacks. Although the responses of ringtailed lemurs support a referential-signalling interpretation of their antipredator calls, those of ruffed lemurs do not conform well to either hypothesis. Rather, ruffed lemur antipredator calls seem best viewed as “affective” signals that may only reflect underlying emotional/motivational states.     

GTP-mediated Ca2+ release in rough endoplasmic reticulum. Correlation with a GTP-sensitive increase in membrane permeability.

Guanine nucleotides have been reported to stimulate reticular Ca2+ release. By using the structure-linked latency of microsomal mannose-6-phosphate phosphatase as an index of microsomal permeability [Arion, Ballas, Lange & Wallin (1976) J. Biol. Chem. 251, 4901-4907], the effects of GTP on Ca2+ release and membrane permeability were compared in liver microsomes. In a stripped rough-microsome preparation, GTP caused a dose-dependent increase in mannose 6-phosphate permeability. Half-maximal and maximal effects were observed at 3 microM- and 10 microM-GTP respectively. The time course of the change in membrane permeability coincided with the time course of GTP-dependent Ca2+ release. This increase in microsomal permeability displayed positive to-operativity with respect to GTP (Hill coefficient = 1.8). By analogy to the GTP-dependent Ca2+ release process, guanosine 5'-[gamma-thio]triphosphate and guanosine 5'-[beta gamma-imido]-triphosphate inhibited the ability of GTP to alter microsomal permeability, but were without effect when added alone. In the presence of 50 microM-GTP, complete inhibition of the GTP-dependent increase in microsomal permeability was achieved with 10 microM-guanosine 5'-[gamma-thio]triphosphate, whereas a 25% inhibition was observed with 10 microM-guanosine 5'-[beta gamma-imido]triphosphate. In contrast with previous observations in crude microsomal preparations, GTP-dependent Ca2+ release in the stripped rough-microsome preparation did not require the addition of poly(ethylene glycol), although the latter did stimulate the rate of Ca2+ release. The ability of GTP to alter microsomal permeability was blocked by prior treatment with the thiol reagent p-hydroxymercuribenzoate; complete inhibition was observed after a 10 min exposure to 50 microM. Inhibition was reversed by subsequent treatment with dithiothreitol. The marked similarities between the two GTP-sensitive processes indicate that they may function via the same mechanism.     

Impact d'une pollution urbaine sur la partie zooplanctonique d'un systeme neitique (Marseille - Cortiou)

Sewage of Marseilles' main outfall permanently pollutes a large coastal area centered around Cortiou, south of the city. In order to study the impact of that urban pollution on the zooplankton, more than 200 samples were collected between 1977 and 1981, according to several sampling strategies.Quantitatively, the study area showed a rather poor zooplankton. The more important populations were encountered near Cortiou, the non-perturbated reference point with lowest abundance of organisms. Sampling sites located near the outfall are sometimes azoic. Qualitatively, the observed communities are not characteristic of a heavily polluted environment, but correspond to an impoverished neritic community. In the more polluted area, the community is organized around the copepods Clausocalanus sp., Paracalanus sp. and Oithona helgolandica, and a group of less important species (Oithona nana and the cladoceran Evadne spinifera). Centropagidae, Coryceidae, Onceidae, but also Chaetognathians, Fritilliarins and the meroplanktonic larvae are more frequently encountered in clean water. Community structure is higher during the cold months than summer. The latter period frequently shows a disorganized zooplankton. In most situations, the copepod Acartia clausi plays a minor role in the structural definition of the communities.The variations observed seem largely independent of the parameters reflecting pollution intensity. Stress integration, in relation with the anterior community history (intensity of contact with polluted water, trophic potential of the area) seem to be the main regulator factors.

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Impact d'une pollution urbaine sur la partie zooplanctonique d'un systeme neitique (Marseille - Cortiou)

Resumé Le rejet permanent du grand émissaire de Marseille (5 m³, sec^–1) perturbe considérablement, par son importance, le système néritique du secteur de Cortiou. Afin d'approcher l'impact de cette pollution sur la partie zooplanctonique du système, plus de 200 prélèvements, concernant l'hydrologie et le plancton, ont of é\'t é réalises entre 1977 et 1981, selon différentes strategiés d'échantillonnage (suivi de masse d'eau, radiales, réseaux).Quantitativement on observe, sur l'ensemble de la zone étudiée, une abondance générale en zooplancton moyenne, voire faible. Les effectifs les plus importants se rencontrent cependant dans la cuvette de Cortiou, alors que le point de référence considéré comme non perturbé présente les effectifs les plus faibles. Les stations situées face à l'égout sont parfois azoïques.Qualitativement les peuplements ne paraissent pas trés caractéristiques d'un secteur pollué mais correspondent plutôt à un appauvrissement du peuplement néritique. Dans le secteur le plus pollué, la composition spécifique varie au cours du temps autour d'une communauté composée d'un groupe important avec Clausocalanus sp., Paracalanus sp., Oithona helgolandica et d'un groups de taxons moins fréquents représentés par des larves méroplanctoniques, Oithona nana et Evadne spinifera, tandis que les coryceidés, onceidés, Centropages typicus, chaetognathes et fritillaires se retrouvent plus fréquemment en eaux propres. La structure des populations est plus importante en période froide qu'en période chaude, période durant laquelle la communauté planctonique est fortement désorganisée. Paradoxalement Acartia clausi joue un rôle assez secondaire dans la définition structurelle de la communauté.Les fluctuations observées paraissent cependant peu liées à des paramètres reflétant l'intensité de la pollution. L'intégration du stress, en relation avec l'histoire antérieure de la communauté (intensité et durée du contact avec la nappe de dilution, potentialités trophiques) semblent ainsi prépondérantes.

     

Regulation of expression of glutamine synthetase in a symbiotic Nostoc strain associated with Anthoceros punctatus.

A characteristic of N2-fixing cyanobacteria in symbiotic associations appears to be release of N2-derived NH4+. The specific activity of the primary ammonium-assimilating enzyme, glutamine synthetase (GS), was found to be three- to fourfold lower in Nostoc sp. strain 7801 grown in symbiotic association with the bryophyte Anthoceros punctatus than in free-living Nostoc sp. strain 7801. Quantitative immunological assays with antisera against GS purified from Nostoc sp. strain 7801 and from Escherichia coli indicated that similar amounts of the GS protein were present in symbiotic (50 micrograms mg-1) and free-living (68 micrograms mg-1) cultures. The conclusion from these experiments is that GS is regulated by a posttranslational mechanism in Anthoceros-associated Nostoc sp. strain 7801. However, the results of comparative catalytic and immunological experiments between N2- and NH4+-grown free-living Nostoc sp. strain 7801 implied control of GS synthesis. A correlation was not observed between the level of GS expression and the extent of symbiotic heterocyst differentiation in Nostoc sp. strain 7801 associated with A. punctatus.     

Purification and characterization of trichosanthin. Homology to the ricin A chain and implications as to mechanism of abortifacient activity

Trichosanthin, a protein from the Chinese medicinal herb Trichosanthes kirilowii, was purified in two essentially quantitative steps involving CM-Sephadex chromatography and reverse-phase high performance liquid chromatography. The protein was found to have a molecular mass of 25-26 kDa, to contain no cysteine, and to contain no glycosidic linkages. Pure trichosanthin was found to have potent abortifacient activity in pregnant mice. In order to understand the molecular basis of this unique biological activity, we have examined the amino acid sequence of the protein. As purified, trichosanthin was found to contain two amino-terminal sequences which differed only in the absence or presence of a tyrosine at residue 1. Sequence analysis of trichosanthin has allowed for determination of the NH2-terminal 38-amino acid residues. Comparison of this sequence to those present in a data base revealed homology with the ricin A-chain. Consistent with this structural homology, we have found that trichosanthin is a potent inhibitor of protein synthesis in a reticulocyte lysate system.     

A Phorbol Ester-Sensitive Kinase Catalyzes the Phosphorylation of P0 Glycoprotein in Myelin

The proposed structural protein of peripheral nerve myelin, P0, has been shown to have several covalent modifications. In addition to being glycosylated, sulfated, and acylated, P0 is phosphorylated, with the intracellular site of this latter addition being in question. By employing nerve injury models that exhibit different levels of P0 biosynthesis in the absence and presence of myelin assembly, we have examined the cellular location of P0 phosphorylation. It is demonstrated that there is comparable P0 phosphorylation in both normal and crush-injured adult rat sciatic nerves, although the level of biosynthesis of P0 differs between these myelin maintaining and actively myelinating nerve models, respectively. The glycoprotein does not appear to be phosphorylated readily in the transected adult sciatic nerve, a preparation in which P0 biosynthesis is observed but that lacks myelin membrane. These observations suggest that the modification is not associated with the biosynthesis or maturation of P0 in the endoplasmic reticulum or Golgi, but that it instead occurs after myelin assembly. That P0 phosphorylation occurs in the normal nerve even when translation is inhibited by cycloheximide treatment lends further support to this conclusion. P0 is shown to be phosphorylated on one or more serine residues, with all or most of the phosphate group(s) being labile as evidenced by pulse-chase analysis. Addition of a biologically active phorbol ester, 12-O-tetradecanoylphorbol-13-acetate or 4 beta-phorbol 12,13-dibutyrate, substantially increases the extent of [32P]orthophosphate incorporation into the glycoprotein of normal and crushed nerve but not transected nerve. Biologically inactive 4 alpha-phorbol 12,13-didecanoate has no effect on P0 phosphorylation. Similarly, the addition of the cyclic AMP analog 8-bromo-cyclic AMP causes no appreciable changes in P0 labeling. These findings indicate that the phorbol ester-sensitive enzyme, protein kinase C, may be responsible for the phosphorylation of P0 within the myelin membrane.