Orientation and ingestion rates of larval Anopheles albimanus in response to floating particles

Response of fourth-instar larvae of Anopheles albimanus Wiedemann (Diptera: Culicidae) to food and inert particles floating at the water surface was studied. In a choice test, larvae aggregated at powdered organic materials (blood meal, liver powder alfalfa flour and wheat flour) but not at inert materials (kaolin, chalk or charcoal). Larvae responded positively to proteins as well as some carbohydrates, but not to cellulose. Retention of larvae at food sources found by random locomotion was found to be responsible for larval aggregation. Larvae ingested food particles 6–9 times faster than insert particles. The significance of Anopheline feeding behavior in the development of formulations of stomach toxins (bacterial agents) used in larval control is discussed.

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Zusammenfassung Die vorliegende Studie befasst sich mit Verhaltensreaktionen von Anopheles albimanus Viertlarven auf an der Wasseroberfläche schwimmende Partikel. Verteilung und Orientierung der Larven wurde in einer Wahlapparatur quantifiziert. Nach Auftrag von Alfalfamehl, Weizenmehl, Stärke, Blutmehl, Leberpulver und Fischmehl wurde Aggregation der Larven in den beköderten Fächern der Apparatur beobachtet. Sowohl Proteine (Casein) als auch einige Kohlehydrate (Amylose, Amylopectin) lösten Aggregationen der Larven aus. Im Unterschied dazu führte Auftrag von Kreide, Kaolin, Polyaethylenpulver, Talcum oder Cellulose nicht zu Aggregationen. Zur Beschreibung der Entstehung larvaler Aggregationen bei Futterstoffen wurden die Schwimmbewegungen der Larven in Anwesenheit von Weizenmehl als Ködersubstanz quantifiziert. Da keine Attraktion der Larven im Sinne einer gerichteten Schwimmbewegung beobachtet werden konnte, wird geschlussfolgert, dass sofortige Beendung der Suchaktivität der Larven bei zufällig gefundenen Futterquellen für die beobachteten Aggregationen bei organischen Substanzen verantwortlich ist.Die Fressraten der Larven bei Angebot verschiedener Substanzen im Überschuss wurde bestimmt. Larven fülten drei von insgesamt sechs Darmabschnitten innerhalb von 15–30 min bei Angebot von Futtersubstanzen, während die Füllung von nur zwei Darmabschnitten mit inerten Materialien erst nach 90–120 min zu beobachten war. Die Resultate werden in Bezug auf wasseroberflächengebundene Formulierungen von Frassgiften diskutiert. Inerte Trägersubstanzen werden wahrscheinlich wesentlich langsamer aufgenommen als Futtersubstanzen. Da An. albimanus Larven nicht von Futterquellen angezogen werden, ist eine rasche und wirksame Giftaufnahme besonders dann zu erwarten, wenn die gesamte Oberfläche der Brutgewässer mit toxinhaltigen Trägerpartikeln bedeckt werden kann.

     

Influence of prey species and stages on predatory efficiency and development of two phytoseiid mites

The effect of prey species and the different stages of prey on the predatory efficiency and biology of the phytoseiid mites,Amblyseius gossipi Elbadry andTyphlodromus mangiferus sp. n. was studied. It was found that feeding either predator onTetranychus cucurbitacearum (Sayed) promoted faster development and a higher rate of oviposition than rearing on the twospotted spider mite,T. urticae (Koch). Different stages of both prey species also produced different responses in the biological activities of these predaceous mites.

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Résumé On a étudié l'effet de l'espèce de la proie et de ses différents stades sur l'efficacité et la biologie des acariens phytoseiides,Amblyseius gossipi Elbadry etTyphlodromus mangiferus sp. n. Il a été constaté que l'alimentation des 2 prédateurs avecTetranychus cucurbitacearus (Sayed) assure un dévelopment plus rapide et une fécondité plus élevée que leur élevage surT. urticae (Koch). Les différents stades de ces 2 proies produisent des réponses différentes dans les activités biologiques des 2 acariens prédateurs.

     

A simple system for plant cell microinjection and culture

Microinjection of plant protoplasts and cells has been recently reported, however a system that combines simplicity of design, harmless immobilization, high resolution visibility and ability to monitor individual target cells is lacking. This report describes a system which combines these features. It consists of a microinjection-microculture dish containing immobilized protoplasts and a simple chamber that maintains sterility and humidity during injection. Highly purified protoplast preparations are plated at low population density as a thin monolayer of widely separated cells embedded in agarose layered over a thicker (0.2 mm at center to 1 mm at edge) layer of agarose-solidified medium. This physical arrangement allows for rapid location, mapping and injection of the immobilized protoplasts and also their subsequent location for growth monitoring. The double layers of agarose provide adequate nutrition for culturing injected cells to the microcalli stage. In addition to protoplast injection, this system was also used to inject 3- to 4-day old nonspherical cells derived from protoplasts. Colony formation rates from injected protoplasts and cells with regenerated walls were equivalent to those of uninjected controls. Furthermore, tobacco protoplasts stored at 4°C in liquid medium for up to two weeks remained fully competent for plating and injection. These cold-stored protoplasts, when injected, formed colonies at rates similar to those from fresh preparations. The ability to store protoplasts without loss of viability considerably increases the ease and convenience of cell injection experiments.Mention of a trademark or proprietary product does not constitute a guarantee or warranty of the product by the USDA, and does not imply its approval to the exclusion of the other products that may also be suitable.     

Suitability of different mite prey for the development of the predatory mite,Phytoseiulus persimilis

Development of the phytoseiid mitePhytoseiulus persimilis Athias-Henriot was studied when fed on three mite species as prey. The tenuipalpid mite,Brevipalpus pulcher (Canestrini & Fanzago), is an unsuitable prey forP. persimilis as predatory larvae reared on any stages developed to the protonymphal stage only. WhenP. persimilis larvae were reared on the eriophyid mite,Eriophyes dioscoridis Soliman & Abou-Awad, only a few developed to adulthood, but failed to oviposit. On the contrary, predatory larvae fed on the tetranychid mite,Tetranychus urticae Koch, matured in a significantly shorter period and resulting females exhibited a high rate of reproduction.     

Levels of 7 alpha-hydroxy-4-cholesten-3-one in plasma reflect rates of bile acid synthesis in man

A method for analysis of 7 alpha-hydroxy-4-cholesten-3-one in plasma is described. Following solid-phase extraction/purification the compound is determined by high-performance liquid chromatography using a UV detector. The median concentration in healthy subjects was 12 ng/ml (range 3-40). The levels were lower in diseases associated with a low bile acid production: extrahepatic cholestasis, less than 1.5 ng/ml (range less than 0.9-3); liver cirrhosis less than 1.5 ng/ml (range less than 0.9-38), and higher in diseases associated with a high bile acid production: cholestyramine treatment, 188 ng/ml (range 54-477); ileal resection 397 ng/ml (range 128-750). The levels were essentially normal in patients with colon resection. The results are consistent with a strong positive correlation between the levels of 7 alpha-hydroxy-4-cholesten-3-one in plasma and the rate of bile acid synthesis.     

Filtration rates of mosquito larvae in suspensions of latex microspheres and yeast cells

Filtration rates of fourth instars of Aedes aegypti L., Anopheles albimanus Wiedemann, Anopheles quadrimaculatus Say and Culex quinquefasciatus Say (Diptera: Culicidae) were determined by quantifying removal rates of suspended latex microspheres or yeast cells. Average filtration rates were 33–34 l/larva/h (An. quadrimaculatus), 49–55 (An. albimanus), 490–590 (C. quinquefasciatus) or 590–690 l/larva/h (Ae. aegypti) for larvae exposed to latex beads suspended in phagostimulant yeast extract solutions. In suspensions of yeast cells, filtration rates of Ae. aegypti and C. quinquefasciatus were not significantly different from filtration rates in latex bead suspensions. Larval density, ranging from 0.3 to 2.4 individuals/ml in tests with Ae. aegypti and C. quinquefasciatus and up to 4.8 larvae/ml in tests with Anopheles, did not influence filtration rates.

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Zusammenfassung Die Filtrierraten von Viertlarven der Stechmückenarten Aedes aegypti, Anopheles albimanus, Anopheles quadrimaculatus und Culex quinquefasciatus wurden in Laborversuchen bestimmt. Dabei wurde die Filtrierrate definiert als ein Wasservolumen, welches pro Stunde von einer Larve von den Testpartikeln (Hefezellen oder Latexkugeln mit einem Durchmesser von 2 m) befreit wurde. Nach Exposition der Larven in Dichten zwischen 0.15 und 2.4 Larven/ml (Ae. aegypti und C. quinquefasciatus), oder zwischen 0.6 und 4.8 Larven/ml (Anopheles) wurde der Partikelgehalt der Suspensionen in einem elektronischen Partikelzähler bestimmt. Die Filtrierraten wurden über die Verringerung der Partikeldichte mit zunehmender Larvendichte entsprechend einer in der Literatur angegebenen Formel berechnet.Suspensionen von Hefezellen wurden von Ae. aegypti Larven mit einer Leistung von 680±220 l/Larve/h gefiltert. Bei Larven von C. quinquefasciatus wurden Filtrierraten von 600±120 l/Larve/h gemessen. Die Filtrierraten beider Arten waren unabhängig von der Larvendichte. In Suspensionen von Latexpartikeln (zur Phagostimulation der Larven wurden diese Partikel in Lösungen von Hefeextrakt angeboten) wurden die folgenden Filtrierraten festgestellt: An quadrimaculatus: 33–34, An. albimanus: 49–55, C. quinquefasciatus: 490–590, und Ae. aegypti: 560–690 l/Larve/h. Die Larvendichte hatte auch hier keinen Einfluss auf die Filtrierrate. Hefezellen und Latexpartikel wurden von Ae. aegypti und C. quinquefasciatus mit statistisch nicht signifikant verschiedenen Filtrierraten aufgenommen. Die Filtrierraten der Anopheles Larven waren um mehr als eine Zehnerpotenz kleiner als die Filtrierraten von Culex und Aedes, und auch untereinander signifikant verschieden. Der Einfluss der Filtrierraktivität von Stechmückenlarven auf das Seston der Brutgewässer wird diskutiert.

     

Ammonium-nitrogen metabolism and nitrogen fixation in azotobacter vinelandii

The probable effect of increasing levels of ammonium nitrogen on the growth, efficiency of nitrogen fixation, and main cellular constituents of Azotobacter vinelandii was studied under shaking and static culture conditions. The presence of NH₄⁺-N up to 50 mgl^-1 level has no harmful effect on the multiplication as well as the yield efficiency ratio of the tested organism. A. vinelandii was able to fix dinitrogen in the presence of NH₄⁺-N when both nitrogen sources were available in the culturing medium. The efficiency of nitrogen fixation was affected by the initial presence of NH₄⁺-N in the medium, it was quite low at the highest level. The crude protein efficiency ratio was correlated inversely with the initial NH₄⁺-N concentration, whereas the total carbohydrate efficiency ratio as well as the total lipid efficiency ratio were positively correlated with the NH₄⁺-N concentration. The presence of NH₄⁺-N in the culturing medium has no essential influence on the qualitative composition of the amino acids in the Azotobacter cells.     

Competitive adherence as a mechanism of bacterial interference

To determine whether competition among bacteria for specific attachment sites on host cells can explain bacterial interference, Staphylococcus aureus strain 502A was tested in turn against two different nasal coryneforms, a strain of Pseudomonas aeruginosa, and a virulent strain of S. aureus, all in the presence of nasal mucosal cells. Particularly examined was the influence of sequence in which bacteria were presented to the nasal cells in comparison with initial mixtures and individual suspensions. Results paralleled those observed in clinical prophylaxis: the bacterium first to adhere to the epithelial cells was able, under uniform conditions, to interfere with the colonization of subsequently added bacteria. Secondary adherence was not eliminated but substantially reduced, and was probably related to steric blockage by the initial colonizer and its particular ability to dissociate from the host cell.     

BIOSYSTEMATIC STUDIES IN THE BOUTELOUA CURTIPENDULA COMPLEX. V. MEGASPOROGENESIS AND EMBRYO SAC DEVELOPMENT

Megasporogenesis and embryo sac development in the sexually reproducing taxa Bouteloua warnockii (2n = 22), B. media (2n = 20), B. uniflora Vasey var. uniflora (2n = 20), B. uniflora var. coahuilensis Gould and Kapadia (2n = 20), and B. curtipendula var. curlipendula (2n = 40) all were found to be of the Adoxa type, in which all 4 megaspores persist and divide once to form an 8-nucleate embryo sac. On the other hand, evidence indicated that plants of B. curtipendula var. caespitosa with high ancuploid chromosome numbers reproduce by pseudogamous fertilization of an aposporous embryo sac. In this taxon the megaspore mother cell did not go beyond the first anaphase of meiosis and the functional embryo sac developed from a nucellar cell. Although the 8-nucleate embryo sac was typical, a 3-nucleate embryo sac was observed to develop in some cases.