Comparaison de plusieurs indices de diversité dans l’étude d’un peuplement de Mantes

The biological diversity of praying Mantids has been analysed to illustrate some classical indices between stability and diversity on the one hand and the numbers of individuals and species on the other. A good description of the Mantid communities can be reached by using only two parameters : the « a », of Fischer for specific richness and the « E » of Margalef for interspecific relations

Beating of hemp bast fibres: an examination of a hydro-mechanical treatment on chemical, structural, and nanomechanical property evolutions

In this study, a gradually increased hydro-mechanical treatments duration were applied to native hemp bast fibres with a traditional pulp and paper beating device (laboratory Valley beater). There is often a trade-off between the treatment applied to the fibres and the effect on their integrity. The multimodal analysis provided an understanding of the beating impact on the fibres at multiple scales and the experimental design made it possible to distinguish the effects of hydro- and hydro-mechanical treatment. Porosity analyses showed that beating treatment doubled the macroporosity and possibly reduced nanoporosity between the cellulose microfibrils. The beating irregularly extracted the amorphous components known to be preferentially located in the middle lamellae and the primary cell walls rather than in the secondary walls, the overall increasing the crystallinity of cellulose from 49.3 % to 59.1 %, but a non-significant change in the indentation moduli of the cell wall was observed. In addition, beating treatments with two distinct mechanical severities showed a disorganization of the cellulose conformation, which significant dropped the indention moduli by 11.2 GPa and 8.4 GPa for 10 and 20 minutes of Valley beater hydro-mechanical treatment, respectively, compared to hydro-treated hemp fibres (16.6 GPa). Pearson’s correlation coefficients between physicochemical features and the final indentation moduli were calculated. Strong positive correlations were highlighted between the cellulose crystallinity and rhamnose, galactose and mannose as non-cellulosic polysaccharide components of the cell wall

Vermiculite with hydroxy-aluminium interlayer and kaolinite formation in a subtropical sandy soil from south Brazil

International audienceThe purpose of this study was to investigate the clay mineral phases in a Rhodic Acrisol soil and subsequently discuss their evolution in substropical conditions. Prairie and forest soil profiles were sampled and clay fractions of the parent material and soil horizons analyzed by X-ray diffraction (XRD) at the Federal University of Santa Maria, Rio Grande do Sul-Brazil. The XRD results show the presence of interstratified kaolinite-smectite as well as illite in the parent material. These minerals were also found in the soil samples but with two new phases: hydroxy-aluminium interlayered vermiculite (HIV), which showed incomplete collapse with treatment at 550°C, and a newly formed kaolinite (d = 7,17 A). Under a subtropical climate and a sandy lithology, HIV and kaolinite appear to be a result of a specific pedogenic clay formation, in relation with the natural vegetation. Originally under the prairie area, the intensity of the weathering processes were weak (within 2:1 clay minerals), as only small quantities of kaolinite and Fe oxides, and no evidence of gibbsite, were found

Presentation_1_Unravelling B cell heterogeneity: insights into flow cytometry-gated B cells from single-cell multi-omics data.pdf

IntroductionB cells play a pivotal role in adaptive immunity which has been extensively characterised primarily via flow cytometry-based gating strategies. This study addresses the discrepancies between flow cytometry-defined B cell subsets and their high-confidence molecular signatures using single-cell multi-omics approaches.MethodsBy analysing multi-omics single-cell data from healthy individuals and patients across diseases, we characterised the level and nature of cellular contamination within standard flow cytometric-based gating, resolved some of the ambiguities in the literature surrounding unconventional B cell subsets, and demonstrated the variable effects of flow cytometric-based gating cellular heterogeneity across diseases.ResultsWe showed that flow cytometric-defined B cell populations are heterogenous, and the composition varies significantly between disease states thus affecting the implications of functional studies performed on these populations. Importantly, this paper draws caution on findings about B cell selection and function of flow cytometric-sorted populations, and their roles in disease. As a solution, we developed a simple tool to identify additional markers that can be used to increase the purity of flow-cytometric gated immune cell populations based on multi-omics data (AlliGateR). Here, we demonstrate that additional non-linear CD20, CD21 and CD24 gating can increase the purity of both naïve and memory populations.DiscussionThese findings underscore the need to reconsider B cell subset definitions within the literature and propose leveraging single-cell multi-omics data for refined characterisation. We show that single-cell multi-omics technologies represent a powerful tool to bridge the gap between surface marker-based annotations and the intricate molecular characteristics of B cell subsets.</p

Table_1_Unravelling B cell heterogeneity: insights into flow cytometry-gated B cells from single-cell multi-omics data.xlsx

IntroductionB cells play a pivotal role in adaptive immunity which has been extensively characterised primarily via flow cytometry-based gating strategies. This study addresses the discrepancies between flow cytometry-defined B cell subsets and their high-confidence molecular signatures using single-cell multi-omics approaches.MethodsBy analysing multi-omics single-cell data from healthy individuals and patients across diseases, we characterised the level and nature of cellular contamination within standard flow cytometric-based gating, resolved some of the ambiguities in the literature surrounding unconventional B cell subsets, and demonstrated the variable effects of flow cytometric-based gating cellular heterogeneity across diseases.ResultsWe showed that flow cytometric-defined B cell populations are heterogenous, and the composition varies significantly between disease states thus affecting the implications of functional studies performed on these populations. Importantly, this paper draws caution on findings about B cell selection and function of flow cytometric-sorted populations, and their roles in disease. As a solution, we developed a simple tool to identify additional markers that can be used to increase the purity of flow-cytometric gated immune cell populations based on multi-omics data (AlliGateR). Here, we demonstrate that additional non-linear CD20, CD21 and CD24 gating can increase the purity of both naïve and memory populations.DiscussionThese findings underscore the need to reconsider B cell subset definitions within the literature and propose leveraging single-cell multi-omics data for refined characterisation. We show that single-cell multi-omics technologies represent a powerful tool to bridge the gap between surface marker-based annotations and the intricate molecular characteristics of B cell subsets.</p