Über den bau der eischale von bulimus (Helicidae)

Zusammenfassung Der kohlensaure Kalk der untersuchten Helicideneischalen — Bulimus maximus (Durchmesser der Schale 23,6 x 25,1 mm, Dicke 0,25 mm), nicht näher bestimmte Schneckeneischale aus Sta. Catharina Brazil (Durchmesser 22,5 x 16,3 mm, Dicke 0,15 mm) — ist Calcit gemäß Optik (negativ einachsiges Konoskopbild) and Meigenscher Reaktion (in Übereinstimmung mit Kellys Beobachtungen bei Bulimus oblongus). Der Phosphatgehalt der Schale ist äuBerst gering trotz reichlichen Vorkommens der KELLyschen Phosphatkörnehen; diese sind in Wirklichkeit Gaseinschüisse. Erhitzen von Schalenstiicken braunt den Kalk bei Verkohlung der organischen Substanz durch and durch ; these durchsetzt also die Calcitkristalle, in Übereinstimmung mit Kellys Erfahrungen beim Entkalken. Erhitzen his zum Verbrennen der organischen Substanz (Wiederweißwerden der Schalenstücke) hebt die Doppelbrechung auf (Umwandlung des Calciumcarbonats in -oxyd); zugleich erscheint bräunliche Trübung im durchfallenden Licht wohl infolge des Austretens der Kohlensäure.Die Mammillenschicht auf der Innenseite der Schale besteht aus einzelnen Calcitindividuen oder Gruppen von solchen; diese Kristallkörnchen wachsen (zum Teil) zu den annähernd senkrecht stehenden Prismen aus, deren optische Achse rneist gegen die Schalenfläche geneigt ist. Vor allem bei Bulimus maximus lassen die Prismen eine innere grobgeschichtete and eine äußere feinstreifige Lage unterscheiden; die erste enthält die Gaseinschliisse, die sich bei der Schneckeneischale aus Sta. Catharina Brazil bis in die Mammillen hinein finden, and von rundlicher Form sind, während she bei Bulimus maximus zum Teil spaltenartig erscheinen. An manchen Stellen der Eischale aus Sta. Catharina Brazil tragen die Mamillen an ihrem freien Ende Scheiben aus radial gestellten Kalknadeln oder Rosetten aus größeren Kristallen, die bis zur Berührung benachbarter auswachsen können.     

Rapid development of cleaning behaviour by Torresian crows Corvus orru on non-native banteng Bos javanicus in northern Australia

In this paper we report the observation of a rapidly developed vertebrate symbiosis involving ectoparasite cleaning by a native corvid of northern Australia, the Torresian crow Corvus orru , on a recently introduced bovid ungulate, the banteng Bos javanicus . Facultative symbioses benefiting both participants (mutualisms) between birds and mammals appear to be rare, despite the apparent advantages obtained by the participants (ecto-parasite removal from the host and food provision to the cleaner). On three separate dates we observed a total of four C. orru individuals eliciting facilitation behaviours by a total of ten female banteng to assist in the removal of ectoparasites. Our observations document the first-known incidence of facultative cleaning behaviour by a native bird species on a non-native, wild vertebrate that has developed in approximately 150 years since the banteng's introduction to Australia.     

Homeostatic control of presynaptic release is triggered by postsynaptic membrane depolarization.

Homeostatic mechanisms regulate synaptic function to maintain nerve and muscle excitation within reasonable physiological limits. The mechanisms that initiate homeostasic changes to synaptic function are not known. We specifically impaired cellular depolarization by expressing the Kir2.1 potassium channel in Drosophila muscle. In Kir2.1-expressing muscle there is a persistent outward potassium current ( approximately 10 nA), decreased muscle input resistance (50-fold), and a hyperpolarized resting potential. Despite impaired muscle excitability, synaptic depolarization of muscle achieves wild-type levels. A quantal analysis demonstrates that increased presynaptic release (quantal content), without a change in quantal size (mEPSC amplitude), compensates for altered muscle excitation. Because morphological synaptic growth is normal, we conclude that a homeostatic increase in presynaptic release compensates for impaired muscle excitability. These data demonstrate that a monitor of muscle membrane depolarization is sufficient to initiate synaptic homeostatic compensation.     

The lactose transport protein is a cooperative dimer with two sugar translocation pathways.

The Major Facilitator Superfamily lactose transport protein (LacS) undergoes reversible self-association in the detergent-solubilized state, and is present in the membrane as a dimer. We determined the functional unit for proton motive force (Deltap)-driven lactose uptake and lactose/methyl-beta-D-galactopyranoside equilibrium exchange in a proteoliposomal system in which a single cysteine mutant, LacS-C67, defective in Deltap-driven uptake, was co-reconstituted with fully functional cysteine-less protein, LacS-cl. From the quadratic relationship between the uptake activity and the ratio of LacS-C67/LacS-cl, we conclude that the dimeric state of LacS is required for Deltap-driven uptake. N-ethylmaleimide (NEM) treatment of proteoliposomes abolished the LacS-C67 exchange activity but left the LacS-cl unaffected. After NEM treatment, the exchange activity decreased linearly with increasing ratios of LacS-C67/LacS-cl, suggesting that the monomeric state of LacS is sufficient for this mode of transport. We propose that the two subunits of LacS are functionally coupled in the step associated with conformational reorientation of the empty binding site, a step unique for Deltap-driven uptake.     

Exploitation of Arabidopsis-tomato synteny to construct a high-resolution map of the ovatecontaining region in tomato chromosome 2.

High-resolution genetic and physical maps were constructed for the region of chromosome 2 containing the major fruit-shape locus ovate. A total of 3,000 NIL F2 and F3 NILs derived from Lycopersicon esculentum cv. Yellow Pear (TA503) x L. pennellii (a wild tomato) were used to position ovate adjacent to the marker TG645 and flanked by markers TX700 and BA10R (a 0.03-cM interval). BAC libraries and a BIBAC library were screened with the closest marker, TG645. Genetic mapping with the ends of isolated BAC clones revealed that two BAC clones (100 and 140 kb) both contained the ovate locus. Screening of sequences from these BAC clones revealed synteny between this segment of tomato chromosome 2 and the chromosome-4 region of Arabidopsis containing the BAC clone ATAP22. Microsynteny between the two genomes was exploited to find additional markers near the ovate locus. The placement of ovate on a BAC clone will now allow cloning of this locus and, hence, may open the door to understanding the molecular basis of fruit development and also facilitate the genetic engineering of fruit-shape characteristics. This also represents the first time that microsynteny with Arabidopsis has been exploited for positional cloning purposes in a different plant family.     

PYCNOGENOL chewing gum minimizes gingival bleeding and plaque formation.

PYCNOGENOL is an antioxidant phytochemical shown to have antiinflammatory activity in both the in vitro and in vivo models. This study compared the effects of chewing gums with and without PYCNOGENOL on gingival bleeding and plaque formation in 40 human subjects. In this double-blind study, subjects were assigned randomly to receive either control gums without PYCNOGENOL or experimental gums containng 5 mg PYCNOGENOL. Subjects used chewing gums for 14 days. Gingival bleeding and plaque scores were taken before and after the experiment. PYCNOGENOL chewing gums significantly reduced gingival bleeding, while no changes were noted in bleeding indexes in control subjects who used regular chewing gums. Subjects using regular control gums had significant increases of dental plaque accumulation during the two-week period. No increases in plaque accumulation were noted in subjects using PYCNOGENOL chewing gums. The data of this study suggest that the use of Pycnogenol chewing gums can minimize gingival bleeding and plaque accumulation.