106 research outputs found

    The use of microencapsulated feeds to replace live food organisms in shrimp hatcheries

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    Abstract only.An adequate supply of hatchery produced shrimp fry is the major constraint to the intensification and growth of shrimp culture practices. If even 20% of the more than 500,000 ha of the world's existing tropical and sub-tropical brackishwater ponds were to stock at the relatively low density of 50,000 fry/ha/year, it would take thousands of new hatcheries to produce the 25 billion fry required. The availability of artificially produced diets to replace cultured live food organisms would alleviate many of the problems currently limiting shrimp hatchery production by: (i) reducing the level of technical skill required to operate a hatchery; (ii) assuring a reliable supply of a nutritionally balanced larval feed; (iii) reducing sources of contamination and larval disease; and (iv) simplifying hatchery design and capital cost requirements, thereby facilitating small scale hatchery development. Aquatic farms has been working with the Mars Microencapsulation Research Group (MMRG) to develop techniques for adapting current shrimp hatchery technology and design so that MMRG feeds can be used in existing hatcheries as a live feed replacement. Feeding trials have been conducted in commercial hatcheries in Hawaii, Malaysia and Thailand. The results of these trials and the techniques employed are discussed. Growth and survival of larvae fed microencapsulated diets as total or partial replacement of live foods was comparable to larvae cultured in control tanks using the standard operating procedures of the hatchery in which the trials were conducted. In trials to date, larval survival from nauplii to postlarvae has been as high as 70%

    Slate Pencils?: Education of Free and Enslaved African American Children at The Bray School, Williamsburg, Virginia, 1760-1774

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    There is a dearth of literature on the archaeology of childhood. Historical archaeology, by its unique nature as a discipline, can use a combination of written documents, the archaeological record, and oral histories to interpret past lives. Historical documents and correspondence of the Associates of the Late Reverend Dr. Thomas Bray attest to the establishment of The Bray School, a school created for free and enslaved African American children in eighteenth-century Williamsburg, Virginia. Appointed schoolmistress Mrs. Ann Wager played a significant role in what the children were being taught. An abundance of slate pencil fragments found on the Bray School site and oral histories contradict what is found in the written record

    Design and preliminary test of a fluidised bed photoreactor for ethylene oxidation on mesoporous mixed SiO2/TiO2 nanocomposites under UV-A illumination

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    Ethylene (C2H4) is a plant hormone that has numerous effects on many horticultural and ornamental crops. It accelerates senescence, stimulates chlorophyll loss, enhances excessive softening, promotes discoloration and browning during storage of fresh produce. Among the techniques used to remove or inhibit ethylene action during postharvest handling of fresh products (potassium-based system, high temperature catalytic oxidation, inhibition of ethylene receptors), the use of titanium oxide (TiO2)-based materials with photocatalytic activity under ultraviolet (UV) light is one of the most promising. A fluidised-bed photoreactor (FBP) was designed to decompose ethylene in the storage room atmosphere, and the relative prototype was manufactured. Since TiO2 powder alone is not suitable for use within a fluidised bed, preliminary tests to select the best support were performed. Alumina microspheres showed a good fluidisation behavior; its functionality was tested with different kind of support material and actual photocatalytic activity was tested using SiO2/TiO2-coated alumina microspheres. A reduction of approximately 72% of ethylene concentration in the tested 40 ppm ethylene gas mixture was observed after 4.5 h of 36W UV light exposure. FBP resulted to be suitable to avoid the detrimental presence of C2H4 in the atmosphere surrounding fresh products within cold storage rooms

    Human iPS cell-derived astrocyte transplants preserve respiratory function after spinal cord injury.

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    Transplantation-based replacement of lost and/or dysfunctional astrocytes is a promising therapy for spinal cord injury (SCI) that has not been extensively explored, despite the integral roles played by astrocytes in the central nervous system (CNS). Induced pluripotent stem (iPS) cells are a clinically-relevant source of pluripotent cells that both avoid ethical issues of embryonic stem cells and allow for homogeneous derivation of mature cell types in large quantities, potentially in an autologous fashion. Despite their promise, the iPS cell field is in its infancy with respect to evaluating in vivo graft integration and therapeutic efficacy in SCI models. Astrocytes express the major glutamate transporter, GLT1, which is responsible for the vast majority of glutamate uptake in spinal cord. Following SCI, compromised GLT1 expression/function can increase susceptibility to excitotoxicity. We therefore evaluated intraspinal transplantation of human iPS cell-derived astrocytes (hIPSAs) following cervical contusion SCI as a novel strategy for reconstituting GLT1 expression and for protecting diaphragmatic respiratory neural circuitry. Transplant-derived cells showed robust long-term survival post-injection and efficiently differentiated into astrocytes in injured spinal cord of both immunesuppressed mice and rats. However, the majority of transplant-derived astrocytes did not express high levels of GLT1, particularly at early times post-injection. To enhance their ability to modulate extracellular glutamate levels, we engineered hIPSAs with lentivirus to constitutively express GLT1. Overexpression significantly increased GLT1 protein and functional GLT1-mediated glutamate uptake levels in hIPSAs both in vitro and in vivo post-transplantation. Compared to human fibroblast control and unmodified hIPSA transplantation, GLT1-overexpressing hIPSAs reduced (1) lesion size within the injured cervical spinal cord, (2) morphological denervation by respiratory phrenic motor neurons at the diaphragm neuromuscular junction, and (3) functional diaphragm denervation as measured by recording of spontaneous EMGs and evoked compound muscle action potentials. Our findings demonstrate that hiPSA transplantation is a therapeutically-powerful approach for SCI
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