A simultaneous treatment of lignocellulosic biomass (LCB) and low density oxodegradable polyethylene (LDPE oxo ) was carried-out using Pleurotus ostreatus at microcosm scale to obtain biotransformed plastic and oxidized lignocellulosic biomass. This product was used as raw matter (RM) to produce biochar enriched with phosphate solubilizing bacteria (PSB). Biochar potential as biofertilizer was evaluated in Allium cepa culture at greenhouse scale. Experiments including lignocellulosic mix and LDPE oxo were performed for 75 days in microcosm. Biotransformation progress was performed by monitoring total organic carbon (TOC), CO 2 production, laccase (Lac), manganese peroxidase (MnP), and lignin peroxidase (LiP) enzymatic activities. Physical LDPE oxo changes were assessed by atomic force microscopy (AFM), scanning electron microscopy (SEM) and static contact angle (SCA) and chemical changes by Fourier transform infrared spectroscopy (FTIR). Results revealed P . ostreatus was capable of LCB and LDPE oxo biotransformation, obtaining 41% total organic carbon (TOC) removal with CO 2 production of 2,323 mg Kg -1 and enzyme activities of 169,438 UKg -1 , 5,535 UKg -1 and 5,267 UKg -1 for LiP, MnP and Lac, respectively. Regarding LDPE oxo , SCA was decreased by 84%, with an increase in signals at 1,076 cm -1 and 3,271 cm -1, corresponding to C-O and CO-H bonds. A decrease in signals was observed related to material degradation at 2,928 cm -1 , 2,848 cm -1 , agreeing with CH 2 asymmetrical and symmetrical stretching, respectively. PSB enriched biochar favored A . cepa plant growth during the five-week evaluation period. To the best of our knowledge, this is the first report of an in vitro circular production model, where P . ostreatus was employed at a microcosmos level to bioconvert LCB and LDPE oxo residues from the agroindustrial sector, followed by thermoconversion to produce an enriched biochar with PSB to be used as a biofertilizer to grow A . cepa at greenhouse scale.

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<p><strong> </strong><strong>Objective.</strong> To describe a standardized flow cytometry protocol for the relative and absolute quantification of hematopoietic cell subpopulations from normal bone marrow, and to evaluate the expression of different lineage-specific cell markers with a reactivity associated to cell differentiation to be used as part of the routine quality control in cytometry laboratories. <strong>Materials and methods. </strong>The immunophenotypical analysis of different cell subpopulations was done with samples from normal bone marrow using a panel of monoclonal and polyclonal antibodies useful in the characterization of acute leukemias with four different fluorescences, by means of a protocol that combines cell labeling of membrane and cytoplasm antigens. Expression analysis was done in terms of mean fluorescence intensity (MFI). Fluorescent beads at a known concentration were added for calculating the absolute count of cells.  <strong>Results.</strong> The antibody panel used allowed the identification and quantification of different normal leukocyte subpopulations of lymphatic and myeloid origin, including CD34+ stem cells and more differentiated cell populations in the granulocytic, monocytic, and erythroid cell lines. We established reference values for cell populations and cell marker expression ranges as part of routine quality control of cytometry laboratories. <strong>Conclusion.</strong> Immunophenotypic patterns identified as well as absolute and relative reference values for the different normal leukocyte populations from bone marrow can be used by cytometry laboratories as a basis for establishing reference parameters in phenotypic analyses of hematologic neoplasia.<strong> </strong></p> <p><strong>Key words: </strong>multiparametric flow cytometry, immunophenotype, hematologic neoplasia, normal bone marrow, reference values, quality control.</p><br />