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435 results for “sterilizing”
Complex basis of hybrid female sterility and Haldane's rule in Heliconius butterflies: Z-linkage and epistasis - RADseq and RNAseq reads, sterility phenotypes and pedigree
<p>RADseq and RNAseq reads (.fastq files), and sterility phenotypes and pedigree (.xlsx) using for QTL mapping of Heliconius pardalinus sterility crosses in Rosser, N., Edelman, N.B., Queste, L.M., Nelson, M., Seixas, F., Dasmahapatra, K.K. and Mallet, J., 2021. Complex basis of hybrid female sterility and Haldane’s rule in Heliconius butterflies: Z-linkage and epistasis, accepted for publication in Molecular Ecology. Queries to Neil Rosser (neil.rosser@york.ac.uk). </p> <p> </p>
Supporting data and codes for: A new biological species in the Mercurialis annua polyploid complex: functional divergence in inflorescence morphology, hybrid sterility and possible introgression
<p>This GitHub repository includes R codes and datasets for the paper: A new biological species in the Mercurialis annua polyploid complex: functional divergence in inflorescence morphology, hybrid sterility and possible introgression</p>
Operating diagram of hatching module, this module consists of two clearly separated sections, each consisting of two long tanks (2 × 0.2 × 0.2 m) designed to accommodate hatching boxes, a filtration tank and an independent water circulation pump with a cooling unit and UV sterilizer. This allows simultaneous monitoring of 16 batches of eggs. in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Operating diagram of hatching module, this module consists of two clearly separated sections, each consisting of two long tanks (2 × 0.2 × 0.2 m) designed to accommodate hatching boxes, a filtration tank and an independent water circulation pump with a cooling unit and UV sterilizer. This allows simultaneous monitoring of 16 batches of eggs.
Operating diagram of hatching module in Zoug jars, this system consists of a 300-litre temperature-controlled isothermal enclosure containing 10 one-litre Zoug jars, each able to accommodate several hundred eggs. An ascending current holds the eggs in suspension and carries the larvae to the surface. Another bottle connected to this device collects the larvae. The water circulating in the jars is independent of that used in the filtration circuit. A cooling unit and UV sterilizer complete the installation. in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Operating diagram of hatching module in Zoug jars, this system consists of a 300-litre temperature-controlled isothermal enclosure containing 10 one-litre Zoug jars, each able to accommodate several hundred eggs. An ascending current holds the eggs in suspension and carries the larvae to the surface. Another bottle connected to this device collects the larvae. The water circulating in the jars is independent of that used in the filtration circuit. A cooling unit and UV sterilizer complete the installation.
Operating diagram of DR1/DR2 double riffle; it consists of two independent sections (DR1 and DR2), each containing 630 litres of water and measuring 2.5 x 0.6 m. Each section contains a filtration system separate from the fish, a cooling unit and an ultraviolet sterilizer. An 80 W UQL lamp completes the lighting of the module lit during the day. in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Operating diagram of DR1/DR2 double riffle; it consists of two independent sections (DR1 and DR2), each containing 630 litres of water and measuring 2.5 x 0.6 m. Each section contains a filtration system separate from the fish, a cooling unit and an ultraviolet sterilizer. An 80 W UQL lamp completes the lighting of the module lit during the day.
Effective seed sterilization methods require optimization across maize genotypes
<p>Studies of plant-microbe interactions using synthetic microbial communities (SynComs) often require the removal of seed-associated microbes by seed sterilization before inoculation to provide gnotobiotic growth conditions. A diversity of seed sterilization protocols have been developed in the past and have been used on different plant species with various amounts of validation. From these studies, it has become clear that each plant species requires its own optimized sterilization protocol. It has, however, so far not been tested if the same protocol works equally well for different varieties and seed sources of one plant species. We evaluated six seed sterilization protocols on two different varieties (Sugar Bun & B73) of maize. All unsterilized maize seeds showed fungal growth upon germination on filter paper, highlighting the need for a sterilization protocol. A short sterilization protocol with hypochlorite and ethanol was sufficient to prevent fungal growth on Sugar Bun germinants, however, a longer protocol with heat treatment and germination in fungicide was needed to obtain clean B73 germinants. This difference may have arisen from the effect of either genotype or seed source. We then tested the protocol that performed best for B73 on three additional maize genotypes from four sources. Seed germination rates and fungal contamination levels varied widely by genotype and geographic source of seeds. Our study shows that consideration of both variety and seed source is important when optimizing sterilization protocols and highlights the importance of including seed source information in plant-microbe interaction studies that use sterilized seeds.</p>
Specific report on sterilized baby food packaging
<p>This data was used for the redaction of the project deliverable "D2.3: Specific report on sterilized baby food ". It is a Specific report on barriers and opportunities for European consumers concerning innovative packaging of sterilized baby food.</p> <p>Moreover, this data is from the scientific publications "<a href="https://www.sciencedirect.com/science/article/pii/S0166497221001723#gs1"><strong>Misalignments between users and designers as source of inspiration: A novel hybrid method for physical new product development</strong></a>" and“<a href="https://www.sciencedirect.com/science/article/pii/S0272494421001778?via%3Dihub%22%20l%20%22ack001"><strong>A meaningful reminder on sustainability: When explicit and implicit packaging cues meet</strong></a>”.</p>
Quality control traceability during the packing and release process of Ceratitis capitata for Sterile Insect Technique
<p><strong>Abstract</strong></p> <p>In programs applying the Sterile Insect Technique (SIT), the quality of insects deployed in the field determines the success in preventing, suppressing, containing, or eradicating the pest population. In the fruit fly emergence and release facility (ERF) of the Moscamed Program in Mexico, irradiated pupae of <em>Ceratitis capitata</em> are packed in Mexico-type towers, and key adult quality parameters, such as emergence, fliers, and survival, are determined throughout the packing, handling and release process. However, different methodologies are used to estimate the percentage of fliers in the different stages of the process, raising doubts of whether observed differences are due to the effect of each stage or to the methodology used. With this in mind, we developed an alternative called “Adult Flier device” (= AF-device) to evaluate the adult flier parameter following a critical evaluation path of five steps: 1) upon arrival at ERF, 2) post-packing, 3) post-holding, 4) post-chilling, and 5) post-release, where adult fliers and survival under stress were evaluated. We also compared the current methodologies for the estimation of "absolute fliers" available in different operating manuals. Our results suggest that the AF-device allows reliable traceability of sterile insect quality parameters throughout the packing and release process, since no significant differences were observed with the control treatments. In the chilling stage, the five methodologies tested were equivalent, but the AF-device was less time-consuming and required less manpower and biological material than the other methodological options. Our results demonstrate that the use of the AF-device can be a feasible, versatile, innovative, and efficient alternative to evaluate quality control parameters throughout the process of packing and releasing sterile insects, providing reliable results in a timely manner with less hand labor using minimal biological material.</p>
Nasturtium x sterile (Airy Shaw) Oefel. (BR0000010504314)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Nasturtium x sterile (Airy Shaw) Oefel. (BR0000010503584)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Nasturtium x sterile (Airy Shaw) Oefel. (BR0000010504802)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Nasturtium x sterile (Airy Shaw) Oefel. (BR0000010503959)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Nasturtium x sterile (Airy Shaw) Oefel. (BR0000010504673)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Nasturtium x sterile (Airy Shaw) Oefel. (BR0000010504345)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Nasturtium x sterile (Airy Shaw) Oefel. (BR0000010504352)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Nasturtium x sterile (Airy Shaw) Oefel. (BR0000010504642)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Nasturtium x sterile (Airy Shaw) Oefel. (BR0000010503553)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Nasturtium x sterile (Airy Shaw) Oefel. (BR0000012195091)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Figure 1 in Ability of Sterile Males to Inhibit Female Remating in the Oriental Fruit Fly, Bactrocera dorsalis (Hendel) (Diptera: Tephritidae)
Figure 1. Numbers of rematings observed per cage for females first mated to fertile wild or sterile DTWP males at 3 intervals after the initial mating. Each cage held 10 test females. Symbols represent mean values + 1 SE; N = 8 in all cases.
Figure 1 in Effect of Pupal Holding Density on Emergence Rate, Flight Ability, and Yield of Sterile Male Mediterranean Fruit Flies (Diptera: Tephritidae)
Figure 1. Emergence rate (top) and flight ability (bottom) for Hawaii- and Guatemaladerived flies when held at loadings of 250, 350, or 450 ml per eclosion tower tray. Bar heights represent mean values over all trays for a given density (15 dates X 6 trays per loading amount per date = 90 trays total), and error bars represent 1 SE.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.