988 resultados para Proteus vulgaris


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O presente trabalho teve como objetivo estudar os efeitos da aplicação de zinco em duas unidades de solos originalmente cobertas com vegetação de cerrado, classificadas como Latossolo Vermelho Amarelo-fase arenosa e Areias Quartzosas, que ocorrem no Município de São Simão no Estado de São Paulo Foram feitas determinações químicas do zinco solúvel em HCl 0,1 N, em amostras de solos antes e depois de terem recebido a calagem. As determinações de zinco foram complementadas com o teste microbiológico do Aspergilus niger Simultaneamente, foram conduzidos ensaios de campo com milho (Zea mays L.) e feijão Phaseolus vulgaris L.) para estudar os efeitos da aplicação de zinco nas duas unidades de solo. Outros experimentos com milho foram desenvolvidos sob condições controladas, em casa de vegetação, para estudos de aplicação de zinco. As conclusões do trabalho foram as seguintes: 1. Os resultados dos ensaios microbiológicos mostraram boa concordância com os testes químicos e com a resposta do milho a aplicação de zinco em condições de campo. 2. A cultura do milho deu boas respostas a aplicação de zinco quando cultido nos solos Areias Quartzosas, correspondendo a uma dose econômica de 2,4 kg/ha de zinco. 3. Não houve efeito do zinco para o milho quando este foi cultivado no Latossolo Vermelho Amarelo-fase arenosa. 4. Não houve efeitos do zinco na produção do feijoeiro nas duas unidades de solos. 5. O ensaio de vasos usando o milho como planta teste não foi eficiente na resposta dos solos as aplicações de zinco.

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Com o objetivo de realizar o sensoriamento climático, no perfil da copa de Hevea bvasiliensis cv. RRIM 600, utilizaram-se fitômetros com Beta vulgaris cv, Asgrow Wonder em 3 níveis de um seringal com 4 anos de idade, em Rio Claro (SP). Os fitômetros foram alocados na copa das árvores distribuídas ao acaso, nas alturas de 1,50m, 2,20m e 3,00m, do solo; sendo que 30 fitômetros foram colocados em cada nível. A exposição dos fitômetros foi realizada em três épocas: de 04 a 17 de maio, junho e setembro. Os valores médios da RAF e AFE mostraram-se mais altos no nível superior da copa e da VPS, VAF, TCR, TAL e RPF nos níveis inferiores. A radiação líquida revelou-se mais alta: na região inferior da copa pela manhã, na região mediana em torno do meio-dia e na região superior do perfil da copa da seringueira no período da tarde. O coeficiente de absorção aumentou pela manhã, tendendo a atingir um patamar ótimo da assíntota perto das 11:00 horas, estendendo-se pela tarde; sendo que o valor médio do coeficiente de absorção em seu patamar foi da ordem de 0,588.

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Oviposition of Zabrotes subfasciatus (Boheman, 1833) on Phaseolus vulgaris (Linnaeus, 1753) was studied immediately after emergence of the adults throughout the females life and in situations of host deprivation lasting for 1 to 10 days. The number of eggs laid daily, longevity, duration of oviposition and distribution of eggs per grain were studied. The number of eggs laid per day varied significantly, with the oviposition peak in the presence of the host (control group) occurring between day 2 and day 5 of oviposition. In the absence of the host, a shift in the oviposition peak to the first day after deprivation was observed, except for the group deprived for one day which showed a peak between days 1 and 4 after introduction of the host. The distribution of the eggs per grain in the control group and in the groups deprived of the host for 2, 5, 8 and 10 days, a larger egg aggregation was observed for all deprived groups compared to the control group.

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A variação espacial e temporal de rotíferos foi analisada em um reservatório pequeno, raso e eutrófico, com intensas florações de algas Cyanobacteria, em sete pontos de amostragem durante 17 meses (março/2002 a julho/2003). Foram identificados 52 táxons em 16 famílias, sendo Brachionidade, Conochilidae, Synchaetidae, Lecanidae, Collothecidae, Trichocercidae e Gastropodidae as mais frequentes. Collotheca sp. foi abundante no inverno (período seco), enquanto Conochilus coenobasis Skorikov, 1914 e Keratella cochlearis Gosse, 1851 apresentaram baixas abundâncias. Brachionus mirus var. reductus (Koste, 1972), Filinia longiseta (Ehrenberg, 1834) e Keratella lenzi (Hauer, 1953) apresentaram picos de abundância no verão (período chuvoso), e Kellicottia bostonensis (Rousselet, 1908), Ploesoma truncatum (Levander, 1894), Polyarthra remata (Skorikov, 1896), Polyarthra vulgaris Carlin, 1943 e Ptygura sp. no inverno, entretanto, relacionados a chuvas atípicas. Diferenças significativas do número de táxons e da abundância total dos rotíferos ocorreram entre os meses amostrados. A análise de correspondência canônica explicou 46% da relação da abundância dos rotíferos e variáveis ambientais, correlacionados com a pluviosidade, nitrito, temperatura da água, nitrogênio orgânico, nitrato e temperatura do ar. Houve flutuações na abundância dos rotíferos um mês após oscilações na abundância do fitoplâncton. A maior parte das correlações entre as abundâncias de espécies de rotíferos e do fitoplâncton foi positiva. Alguns táxons como Filinia longiseta, Keratella lenzi e K. cochlearis apresentaram variação temporal definida e semelhante a outros reservatórios eutróficos. A ausência de padrões claros de distribuição em algumas espécies foi atribuída a hidrodinâmica do reservatório, o qual foi construído recentemente, e as condições climáticas adversas durante o período de estudo, como as chuvas intensas no inverno.

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This paper deals about the nematocysts like a source of biometric information for comparison between the species Hydra vulgaris Pallas, 1766, Hydra vulgaris pedunculata Deserti et al., 2011 and Hydra pseudoligactis (Hyman, 1931). This biometric tool lets us carry out statistical comparisons and adding these results to the identification of specimens from different classificatory groups. In this particular study, we obtained significant differences between species, individuals of each species and nematocysts type when compared the biometry of its nematocysts. Another result was the variation in of particular nematocysts, like atrichous isorhiza and holotrichous isorhiza for the species H. vulgaris in relation to the column size.

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Revisão da literatura médica sôbre higiene de crustáceos e moluscos marinhos. Intoxicações por elementos extranhos às carnes de crustáceos e moluscos: por sais de cobre, vegetais tóxicos; estranho e chumbo nas conservas de crustáceos; botulismo. Putrefação de ostras e doenças de ostras provocadas por cogumelos; crustáceos e moluscos guardados em geladeiras bolorentas. Lista das espécies de moluscos comestíveis da Bahia de Guanabara. Lista das espécies de crustáceos comestíveis da Bahia de Guanabara. Veiculação de micro-organismos patogênicos ao homem por intermédio das carnes de crustáceos e de moluscos: veiculação do vibrião colérico, dos bacilos tíficos e paratíficos e de germes do grupo coli e do gênero Proteus. Vitalidade dos bacilos tíficos nas ostras. Listas dos moluscos veiculadores dos agentes causadores das febres tíficas e paratíficas. Conceitos antigos e modernos sõbre intoxicações por crustáceos; partidas de crustáceos salubres ou não conforme o local de venda. Estudos experimentais sôbre a "talassina" princípio tóxico existente em alguns crustáceos. "Mitilotoxina", intoxicações por mexilhões e outros acidentes incriminados aos moluscos. Enterotoxina estavfilocócica em ostras. Métodos de determinação da salubridade dos moluscos; verificações nas ostras brasileiras. Depuração dos crustáceos pelas soluções cloradas. Estabulação de caranguejos denominados vulgarmente de "guaiamus" e "ussás".

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Os autores mostraram a necessidade de estudar minuciosamente os fócos da doença para o melhor conhecimento das questões epidemiológicas e clínicas da mesma. Mostraram que os Veados e Cabritos pódem desempenhar papel importante na difusão do virus. Os autores dão gráficos sôbre a reação de Weil-Felix com nove Proteus em homens e animais.

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In articles, already published, we have proved that the strain V. B. of Brazilian virus, goes through the placenta (Macacus rhesus) (1) and the apparently normal gastro-intestinal tube (1934-1937) (Canis familiaris) (2). Today we present the idea that the Brazilian virus can reach the milk of an animal even when the latter has only the unapparent disease. In former articles (**), we have shown that the goat (Capra hircus) can be an excellent reservoir of Brazilian virus, having the strain V. B. in its blood and presenting a Weil Felix reaction high and in “group”, with the disease unapparent. When the goats are bred in the laboratory, and even in some foci of the disease, they give a negative Weil Felix, being zero for all the nine strains of Proteus. In the interior of Brazil, in many localities, goats substitute cows, in supplying milk for children and adults, and in some districts goat’s milk is considered superior to cow’s milk, possessing marvellous qualities for men, women an children. Having proved, now, that goat’s milk can contain the virus even when the animal presents nothing clinically, and having also shown that this virus goes through the digestive tube apparently sound, it is easy to understand how infants-in-arms, that is, only a few months old, living in strictly domestic surroundings, can contract the disease; we have many such cases on record. Protocol of the experiments: Goat nº 2, white, January 1948. This animal had been inoculated with the V. B. strain of the Brazilian virus in June 1947, via intra-peritoneal, presenting nothing then, not even a feverish reaction. On that occasion it was not possible to isolate the virus of the blood, although the Weil Felix reaction was positive, high and in “group”. Now January 17, 1948, seven months later, the same animal was reinoculated with a semple of virus V. B. in the same manner (intra-peritoneal) two days after bringing forth two sturdy kids. The virus V. B. was obtained from guinea-pig n. 7170 whose thermic graph was as follows: Temperatura – 38,8 – 39,1 – 39,5 – 39,4 –39,8 – 40,4 – 40,2 – 40,1 - + Necropsy – Typical lesions. The spleen weighed 5 grammes. With 3c.c. of emulsion from the nervous system of this guinea-pig, we inoculated not only the goat, as also two guineapigs, number 14 and number 5. The following is the thermic graph of one: - Guinea-pig n. 14 – 38,9 – 39,1 – 39,2 – 39.2 – 40,7 – 41,0 – 40,5 – 40,4 – 40,1 - + Typical lesions. Guinea-pig n. 2 presented the following thermic graph after the infective inoculation: - 39,5 – 39,7 – 39,7 – 39,7 – 39,5 – 39,3 – 39,5 – 39,5 – 39,5 – etc. Clinically, this animal presented nothing unusual, feeding well and suckling the kids normally. The Weil Felix reaction was positive, in “group” high very similar to the reaction obtained in June 1947, with the first infective inoculation. On the third, fourth, fifth, sixth and seventh day after the infective inoculation, we took milk from the goat and inoculated male guinea-pigs via intra-celular and via intra-peritoneal, giving 5 c.c. to each animal. Guinea-pig n. 4663, inoculated with 5 c.c. of milk, via intra-muscular, taken on the third day of the infectaive inoculation, presented the following thermic graph: - 38.8 (*) – 39,1 – 39,0 – 39,1 – 40,1 – 40,1 – 40,8 (**) – 40,8 – Killed – Typical deisions (***). The virus V. B. of this goat, circulated naturally in the blood up to the third day, having passed into the milk, producing nothing in the kids, on account of the natural resistance of these animals to the disease. The Weil Felix reaction and that of Widal for the Burcellas suis, abortus and militensis were negative for the goat and the kids. It is remarkable that, even with inoculation of the living virus after a period of seven months we cannot get a real and absolute immunity of sensitive animals. We shall return to this subject later. The hart Mazama simplicicornis may be a carrier of the virus in Brasil. The experimental serum against the virus of Exanthematic neotropical typhus has not protected guinea-pigs.

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It is well known that the culture media used in the presumptive diagnosis of suspiciuous colonies from plates inoculated with stools for isolation of enteric organisms do not always correctly indicate the major groups of enterobacteria. In an effort to obtain a medium affording more exact indications, several media (1-9) have been tested. Modifications of some of these media have also been tested with the result that a satisfactory modification of Monteverde's medium was finaly selected. This proved to be most satisfactory, affording, as a result of only one inoculation, a complete series of basic indications. The modification involves changes in the formula, in the method of preparation and in the manner of storage. The formulae are: A. Thymol blue indicator: NaOH 0.1/N .............. 34.4 ml; Thymol blue .............. 1.6 g; Water .................... 65.6 ml. B. Andrade's indicator. C. Urea and sugar solution: Urea ..................... 20 g; Lactose ................... 30 g; Sucrose ................... 30 g; Water .................... 100 ml. The mixture (C.) should be warmed slightly in order to dissolve the ingredients rapidly. Sterilise by filtration (Seitz). Keep stock in refrigeratior. The modification of Monteverde's medium is prepared in two parts. Semi-solid part - Peptone (Difco) 2.0 g; NaCl 0.5 g; Agar 0.5 g; Water 100.0 ml. Boil to dissolve the ingredients. Adjust pH with NaOH to 7.3-7.4. Boil again for precipitation. Filter through cotton. Ad indicators "A" 0.3 ml and "B" 1.0 ml. Sterilise in autoclave 115ºC, 15 minutes in amounts not higher than 200 ml. Just before using, add solution "C" asseptically in amounts of 10 ml to 200 ml of the melted semi-solid medium, maintained at 48-50ºC. Solid part - Peptone (Difco) 1.5 g; Trypticase (BBL) 0.5 g; Agar 2.0 g; Water 100,00 ml. Boil to dissolve the ingredients. Adjust pH with NaOH to 7.3-7.4. Boils again. Filter through cotton. Add indicators "A" 0.3 ml and "B" 1.0 ml; ferrous ammonium sulfate 0.02 g; sodiun thiosulfate 0.02 g. Sterilise in autoclave 115ºC, 15 minutes in amounts not higher than 200 ml. Just before using, add solution "C" asseptically in amounts of 10 ml to 200 ml of the melted solid medium, maintained at 48-50ºC. Final medium - The semi-solid part is dispensed first (tubes about 12 x 120 mm) in 2.5 ml amounts and left to harden at room temperature, in vertical position. The solid part is dispensed over the hardened semi-solid one in amounts from 2.0 ml to 2.5 ml and left to harden in slant position, affording a butt of 12 to 15 mm. The tubes of medium should be subjected to a sterility test in the incubator, overnight. Tubes showing spontaneous gas bubbles (air) should then be discarded. The medium should be stored in the incubator (37ºC), for not more than 2 to 4 days. Storage of the tubes in the ice-box produces the absorption of air which is released as bubbles when the tubes are incubated at 37ºC after inoculation. This fact confirmed the observation of ARCHAMBAULT & McCRADY (10) who worked with liquid media and the aplication of their observation was found to be essential to the proper working conditions of this double-layer medium. Inoculation - The inoculation is made by means of a long straight needle, as is usually done on the triple sugar, but the needel should penetrate only to about half of the height of the semi-solid column. Indol detection - After inoculation, a strip of sterelized filter papaer previously moistened with Ehrlich's reagent, is suspended above the surface of the medium, being held between the cotton plug and the tube. Indications given - In addition to providing a mass of organisms on the slant for serological invetigations, the medium gives the following indications: 1. Acid from lactose and/or sucrose (red, of yellowsh with strains which reduce the indicators). 2. Gas from lactose and/or sucrose (bubbles). 3. H[2]S production, observed on the solid part (black). 4. Motility observed on the semi-solid part (tubidity). 5. Urease production, observed on solid and semi-solid parts (blue). 6. Indol production, observed on the strip of filter paper (red or purplish). Indol production is not observed with indol positive strains which rapidly acidify the surface o the slant, and the use of oxalic acid has proved to give less sensitive reaction (11). Reading of results - In most cases overnight incubation is enough; sometimes the reactions appear within only a few hours of incubation, affording a definitive orientation of the diagnosis. With some cultures it is necessary to observe the medium during 48 hours of incubation. A description showing typical differential reaction follows: Salmonella: Color of the medium unchanged, with blackening of the solid part when H[2]S is positive. The slant tends to alkalinity (greenish of bluish). Gas always absent. Indol negative. Motility positive or negative. Shigella: Color of the medium unchanged at the beginning of incubation period, but acquiring a red color when the strain is late lactose/sucrose positive. Slant tending to alkalinity (greenish or purplish). Indol positive or negative. Motility, gas and H[2]S always negative. Proteus: Color of the medium generally changes entirely to blue or sometimes to green (urease positive delayed), with blackening of solid part when H[2]S is positive. Motility positive of negative. Indol positive. Gas positive or negative. The strains which attack rapidly sucrose may give a yellow-greenish color to the medium. Sometimes the intense blue color of the medium renders difficult the reading of the H[2]S production. Escherichiae and Klebsiellae: Color of the medium red or yellow (acid) with great and rapid production of gas. Motility positive or negative. Indol generally impossible to observe. Paracoli: Those lactose of sucrose positive give the same reaction as Esherichia. Those lactose or sucrose negatives give the same reactions as Salmonellae. Sometimes indol positive and H[2]S negative. Pseudomonas: Color of the medium unchanged. The slant tends to alkalinity. It is impossible to observe motility because there is no growth in the bottom. Alkaligenes: Color of the medium unchanged. The slant tends to alkalinity. The medium does not alter the antigenic properties of the strains and with the mass of organisms on the slant we can make the serologic diagnosis. It is admitted that this medium is somewhat more laborious to prepare than others used for similar purposes. Nevertheless it can give informations generally obtained by two or three other media. Its use represents much saving in time, labor and material, and we suggest it for routine laboratory work in which a quick presumptive preliminary grouping of enteric organisms is needed.

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Animals (122 mice) were infected each with eighty cercariae of S. mansoni and subsequently challenged intravenously eight weeks later with the following gram-negative organisms. S. typhi, E. coli, Klebsiella-enterobacter species, Proteus mirabilis and Pseudomonas aeruginosa. Enumeration of bacteria in the liver, spleen and blood and S. mansoni from the portal sistem was performed from one to four weeks later in infected animals. A significant difference between infection produced by S. typhi and other gram negative organisms was observed: S. typhi persisted longer in the spleen and liver and could be recovered from S. mansoni worms up to three weeks following bacterial infection. Other gram negative bacteria disappeared from S. mansoni worms after two weeks of initial challenge. Additional animals (51 mice) infected with S. mansoni were given S. typhi, E. coli or sterile saline. After two weeks, animals were sacrificed and the recovery rate of worms from the portal system, and the mesenteric and hepatic oogram were determined. in animals infected with E. coli a significant decrease in the number of worms was observed compared to the saline control group; thirty worms were recovered in the control group compared to two worms in e. coli infected animals. In addition, the patterns of oviposition was significantly different in these latter animals suggesting complete inhibition of this process. Following S. typhi infection the difference in recovery of worms and pattern of oviposition was minimal. These findings suggest a difference in the interaction of various gram negative bacteria and S. mansoni and are consistent with the clinical observation of prolonged salmonella bacteremia in patients with schistosomiasis.

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The culture forms of L. mexicana pifanoi (LRC L-90), L. mexicana mexicana (LRC L-94, M-379); L. braziliensis braziliensis (LRC L-77, L-1, M-2903, H-LSS) and L. mexicana amazonensis (H-JMMO, M-JOF, H-21, H-PLL,M-1696) were tested with the following lectins: Canavalia ensiformis, Ricinus communis-120, Axinella polypoides, Phaseolus vulgaris, Evonymus europaeus, lotus tetragonolobus, Dolichos biflorus, Aaptos papillata II, Laburnum alpinum, Ulex europaeus, Arachis hypogaea and Soja hispida. All examined strains of Leishmania were agglutinated by C. ensiformis, R. communis-120 and A. popypoides. No agglutination reactions were observed with P. vulgaris, D.biflorus, A. papillata II, E. europaeus and L. tetragonolobus. Only L. m. pifanoi and the L. m. amazonensis strains H-JMMO and MJOF showed agglutination reactions with S. hispida, U. europaeus, L. alpinum and A. hypogaea, while L. m. mexicana (LRC L-94; M-379) strains, L. b. braziliensis H. LSS, LRC L-77; L-1; M-2903 and the L. m. amazonensis strains, H-PLL, H-21, M-1696 showed no agglutination reactions with these four lectins.

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A partir de 154 espécimens de alimentos, representados por hortaliças (alface), leite e merenda escolar, obteve-se o isolamento e identificação de 400 amostras de bacilos Gram negativos. Esta amostragem se distribuiu em 339 enterobactérias (Escherichia, Shigella, Citrobacter, Klebsiella, Enterobacter, Serratia e Proteus) e 61 de gêneros afins (Acinetobacter, Flavobacterium, Aeromonas e Pseudomonas). Submetendo-se as culturas aos antimicrobianos: sulfadiazina (Su), estreptomicina (Sm), tetraciclina (Tc), cloranfenicol (Cm), canamicina (Km), ampicilina (Ap), ácido nalidíxico (Nal) e gentamicina (Gm), observou-se apenas seis estirpes sensíveis a todas as drogas e sensibilidade absoluta à Gm. A predominância dos modelos Su (27,6%) e Su-Ap (39,6%) incidiu nas enterobactérias, enquanto que, 18,0% para Ap e 9,8% para Su-Ap foram detectados nos gêneros afins. Para caracterização da resistência foram realizados testes de conjugação e a totalidade das culturas não revelou transferência para o gene que confere resistência ao ácido nalidíxico. Relevantes são as taxas de amostras R+ observadas nos bacilos entéricos, oscilando em torno de 90% (leite e merenda escolar) e alface, em torno de 70%

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Memòria elaborada a partir d’una estada al projecte Proteus de la New York University entre abril i juny del 2007. Les tècniques de clustering poden ajudar a reduir la supervisió en processos d’obtenció de patrons per a Extracció d’Informació. Tanmateix, és necessari disposar d’algorismes adequats a documents, i aquests algorismes requereixen mesures adequades de similitud entre patrons. Els kernels poden oferir una solució a aquests problemes, però l’aprenentatge no supervisat requereix d’estrat`egies m´es astutes que l’aprenentatge supervisat per a incorporar major quantitat d’informació. En aquesta memòria, fruit de la meva estada de mes d’Abril al de Juny de 2007 al projecte. Proteus de la New York University, es proposen i avaluen diversos kernels sobre patrons. Ini- cialment s’estudien kernels amb una família de patrons restringits, i a continuació s’apliquen kernels ja usats en tasques supervisades d’Extracció d’Informació. Degut a la degradació del rendiment que experimenta el clustering a l’afegir informació irrellevant, els kernels se simpli- fiquen i es busquen estratègies per a incorporar-hi semàntica de forma selectiva. Finalment, s’estudia quin efecte té aplicar clustering sobre el coneixement semàntic com a pas previ al clustering de patrons. Les diverses estratègies s’avaluen en tasques de clustering de documents i patrons usant dades reals.

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Allometric growth variation was compared for Plagioporus idoneus, Lepocreadium pegorchis, Opecoeloides furcatus, Bacciger israelensis, Aphanurus stossichi and Parahurleytrema trachinoti collected from East Mediterranean fishes. The pharynx, the oral and the ventral sucker diameters always showed a negative allometry. The other parameters tested were variable with the species. We study the effects of some environmental factors: the influence of the host species is analysed in Plagioporus idoneous, wich parasitizes Oblada melanura, Diplodus sargus and D. vulgaris and in Lepocreadium pegorchis, wich parasitizes Pagellus erythrinus, Lithognathus mormyrus and Spicara smaris; the influence of the microhabitat and the intensity of infection is analysed in Bacciger israelensis and Aphanurus stossichi, both parasites of Boops boops. We report significant differences with the host species, for the allometric growth of the testes; the effect of the microhabitat was revealed by the hindbody allometric value; no significant difference was detected in relation with the intensity of infection.

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The fate of Bacillus sphaericus spores in the aquatic environment was investigated by suspending spores in dialysis bags in fresh and seawater. Spore viability was lost more rapidly in seawater. Neither B. sphaericus nor B. thuringiensis israelensis (B.t.i.) spores mixed with pond sediment appeared to attach to the sediment. However, rapid decrease in B.t.i. toxicity suggested attachment of parasporal bodies to sediment. B. sphaericus toxin settled more slowly and less completely. B. sphaericus spores fed to larvae of four aquatic invertebrates were mostly eliminated from the animal gut in less than one week. An exception was the cranefly (Tipula abdominalis) where spores persisted in the posterior gut for up to five weeks.