Membrane Potential and Catecholamine Secretion by Bovine Adrenal Chromaffin Cells: Use of Tetraphenylphosphonium Distribution and Carbocyanine Dye Fluorescence

Changes in plasma membrane potential of isolated bovine adrenal chromaffin cells were measured independently by two chemical probe methods and related to corresponding effects on catecholamine secretion. The lipophilic cation tetraphenylphosphonium (TPP+) and the carbocyanine dye 3,3'-dipropylthiadicarbocyanine [DiS-C3-(5)] were used. The necessity of evaluating the subcellular distribution of TPP+ among cytoplasmic, mitochondrial, secretory granule, and bound compartments was demonstrated and the resting plasma membrane potential determined to be -55 mV. The relationship between membrane potential and catecholamine secretion was determined in response to variations in extracellular K+ and to the presence of several secretagogues including cholinergic receptor ligands, veratridine, and ionophores for Na+ and K+. The dependence of potential on K+ concentration fit the Goldman constant field equation with a Na/K permeability ratio of 0.1. The dependence of both K+- and veratridine-evoked catecholamine secretion on membrane potential exhibited a potential threshold of about -40 mV before a significant rise in secretion occurred. This is likely related to the threshold for opening of voltage-sensitive Ca2+ channels. Acetylcholine and nicotine evoked a large secretory response without a sufficiently sustained depolarization to be detectable by the relatively slow potential sensitive chemical probes. Decamethonium induced a detectable depolarization of the chromaffin cells. Veratridine and gramicidin evoked both membrane depolarization and catecholamine release. By contrast the K ionophore valinomycin evoked significant levels of secretion without any depolarization. This is consistent with its utilization of an intracellular source of Ca2+ and the independence of its measured secretory response on extracellular Ca2+.     

A new rodent (Caviomorpha: Dinomyidae) from the upper Miocene of southwestern Brazilian Amazonia

Recently, the fossil record of rodents from southwestern Brazilian Amazonia has been reviewed with regards to its diversity as well as its ecological relationships. In the reviews, the necessity to report new specimens collected with stratigraphic control was stated. Here, a new dinomyid specimen collected during a 2015 expedition to the Niterói locality, Acre River, is reported. The material is a fragment of skull with the right P4–M1 and the left P4–M2 preserved. The cheek teeth are protohypsodont, a characteristic employed to differentiate Potamarchinae dinomyids from the euhypsodont dinomyids Eumegamyinae and Tetrastylinae. The occlusal surface of the cheek teeth is composed of lophs with interruptions, showing little wear, which suggests that the specimen is not fully ontogenetically developed. The specimen has a unique combination of characters (protohypsodont and pentalophodont cheek teeth, with the leading edges of similar thickness to the trailing edges, and presence of a groove on the bottom of the infraorbital foramen) not present in other known dinomyids, which led us to erect a new taxon. The abundant and diverse fossil record of protohypsodont dinomyids suggests that an important radiative event may have occurred during the middle–late Miocene of northern South America.

http://zoobank.org/urn:lsid:zoobank.org:pub:E082C3C6-47B6-4D83-9009-A64879AAFC7A

http://www.zoobank.org/NomenclaturalActs/16235A7B-A261-445E-8DD4-940AB21DCB06     

Three dimensional typological studies using scanning electron microscopy for characterization of Termitomyces pellets obtained from submerged growth conditions

There are gaps in existing understanding of fungal pellet growth dynamics. We used scanning electron microscopy (SEM) for morphological characterization of the biomass organization of Termitomyces pellets for seven species: T. microcarpus (TMI1), T. albuminosus (TAL1, TAL2), T. striatus (TSTR), T. aurantiacus (TAUR), T. heimii (THE1, THE2), T. globulus (TGLO) and T. clypeatus (TCL1, TCL2, TCL3, TCL4, TCL5). We assessed the utility of SEM for morphological and structural characterization of Termitomyces spp. in three dimensional (3D) pellet form to identify ideal pellet morphology for industrial use. Typological classification of Termitomyces species was based on furrows, isotropy, total motifs and fractal dimensions. The pellets formed were entangled and exhibited highly compacted mycelial mass with microheterogeneity and microporosity. The mean density of furrows of Termitomyces species was between 10,000 and 11,300 cm/cm², percentage isotropy was 30?80 and total motifs varied from 300 to 2500. TGLO exhibited the highest furrow mean density, 11243 cm/cm², which indicated a compact, cerebroid structure with complex ridges and furrows, whereas TAL2 exhibited the lowest furrow density. TMI1a exhibited a high percentage isotropic value, 74.6, TSTR exhibited the lowest, 30.9. Total motif number also was used as a typological classification parameter. Fractal values were 2.64?2.78 for various submerged conditions of Termitomyces species. TAL1 exhibited the highest fractal dimension and TAL2 the lowest, which indicates the complexity of branching patterns. Three-dimensional SEM image analysis can provide insight into pellet micromorphology and is a powerful tool for exploring topographical details of pellets.     

Sea urchin Hox genes: insights into the ancestral Hox cluster

We describe the Hox cluster in the radially symmetric sea urchin and compare our findings to what is known from clusters in bilaterally symmetric animals. Several Hox genes from the direct-developing sea urchin Heliocidaris erythrogramma are described. CHEF gel analysis shows that the Hox genes are clustered on a < or = 300 kilobase (kb) fragment of DNA, and only a single cluster is present, as in lower chordates and other nonvertebrate metazoans. Phylogenetic analyses of sea urchin, amphioxus, Drosophila, and selected vertebrate Hox genes confirm that the H. erythrogramma genes, and others previously cloned from other sea urchins, belong to anterior, central, and posterior groups. Despite their radial body plan and lack of cephalization, echinoderms retain at least one of the anterior group Hox genes, an orthologue of Hox3. The structure of the echinoderm Hox cluster suggests that the ancestral deuterostome had a Hox cluster more similar to the current chordate cluster than was expected Sea urchins have at least three Abd-B type genes, suggesting that Abd-B expansion began before the radiation of deuterostomes.      

Late Quaternary caviomorph rodents (Rodentia: Hystricognathi) from the Serra da Capivara,northeastern Brazil,with description of a new taxon

In this paper, fossil rodents (Hystricognathi: Caviomorpha) from the late Quaternary of the southwestern State of Piauí, northeastern Brazil, are described. The material comes from archaeological/palaeontological sites located in the region of the Serra da Capivara. The late Quaternary taxa of this region include Galea Meyen, 1832, Kerodon rupestris Wied-Neuwied, 1820, Hydrochoeridae indet., Dasyprocta Illiger, 1811, cf. Myocastor Kerr, 1792, Thrichomys Trouessart, 1880, Phyllomys Lund, 1839, Coendou magnus Lund, 1839 and a new taxon with chinchilloid affinities. The Coendou magnus and cf. Myocastor material represents the northernmost records of these taxa. The unexpected presence of a new extinct taxon contributes to the understanding of the ancient rodent faunas from South America. Today, the studied area is located within the Caatinga Biome but some of the fossil taxa, such as Hydrochoeridae and cf. Myocastor, indicate wetter environments and permanent water bodies during the late Pleistocene–early Holocene.

http://www.zoobank.org/urn:lsid:zoobank.org:pub:92711BC3-8997-4474-A8AF-83DF4F91BB48     

Free radicals from plastic syringes.

We have found that disposable sterile plastic syringes can leach free radicals into the fluids they hold. The free radical we observe appears to be a nitroxide (aminoxyl radical) because in aqueous solution it produces a 1:1:1 three line spectrum with a hyperfine splitting constant of 16.9 G.