190 research outputs found

    Analyse de la distribution spatiale des Acanthaceae en Afrique Centrale et comparaison avec les théories phytogéographiques de Robyns, White et Ndjele.

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    Cette étude a pour but d\'analyser les modèles de distribution spatiale des Acanthaceae, récoltées en République Démocratique du Congo, au Rwanda et au Burundi et de comparer leur répartition spatiale avec les systèmes phytogéographiques qui couvrent cette zone. Elle porte sur 9181 échantillons regroupés en 48 genres et 310 espèces. Un système d\'information géographique a été utilisé pour réaliser des cartes de distribution de chaque espèce. La méthode multi variée de classification, appuyée par deux indices de structure spatiale (équitabilité et fragmentation) a permis de stratifier la zone d\'étude afin de permettre une comparaison visuelle avec les systèmes phytogéographiques définis par Robyns, White et Ndjele. On note une large distribution spatiale pour certaines espèces sur l\'ensemble du territoire, alors que d\'autres sont inféodées à certains territoires phytogéographiques bien déterminés. Les savanes situées au Sud de l\'équateur contiennent des sites plus riches en Acanthaceae que celles situées au Nord. Les centres d\'endémisme Guinéo-Congolais, Zambézien et Afromontagnard pourraient être les sources de migration des taxons. Les Acanthaceae suivent relativement bien le système phytogéographique de White et sont utilisables en tant que bioindicatrices afin de rapprocher la distribution spatiale des communautés végétales décrites par ce système.By means of 9181 samples representing 48 genus and 310 species, the spatial distribution models of the Acanthaceae family in Central Africa (Democratic Republic of Congo, Rwanda and Burundi) were analysed. Consequently, a comparison to existing phytogeographic systems for the study region was executed. Spatial distribution maps for each species were created using a geographic information system. Subdivision of the study area was realised using a multivariate classification analysis. Using two indices of spatial pattern (fragmentation, class size evenness), the classification result was compared to the phytogeographic zones defined by Robyns, White and Ndjele. While certain species showed a distribution throughout the study area, the presence of other species was found to be bound to one single phytogeographic territory in particular, or to a restricted number of them. The savannas situated in the southern part of the study area contained more Acanthaceae species than the zones situated north of the equator. The Guineo-Congolian, the Zambezian and the Afromontane centre of endemism are suggested to be the origins of taxon migration. Since it was observed that the spatial pattern of the Acanthaceae species corresponded up a certain extent to the phytogeographic system proposed by White, it can be concluded that the Acanthaceae could be used as bio-indicators to proxy the spatial distribution of plant communities as described by this system. Keywords: phytogeography, spatial analysis, Acanthaceae, Central Africa, district, sector.Sciences & Nature Vol. 5 (2) 2008: pp. 101-11

    Floristic and structural changes in secondary forests following agricultural disturbances: the case of Lama forest reserve in Southern Benin

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    Structural changes in secondary forests are less known in West Africa, and this precludes their management. This study aims at providing quantitative information on floristic composition and structure of the Lama secondary forests (Benin), so as to contribute to their restoration, and fill part of knowledge gaps on West African secondary forests. Data of 77 permanent plots each of 0.5 ha were used to analyze the floristic composition, the trajectory of the recovery and the recovery of stocking in these forests, compared to nearby old-growth forests. The results showed that the forests were less diversified with few species very common in the forest stands; the most dominant were Lonchocarpus sericeus and Anogeissus leiocarpa in the secondary forests, and Dialium guineense, Diospyros mespiliformis and Afzelia africana in the old-growth forests. The secondary forests hold more species than the mature ones. Their compositions will recover that of the original forest because species of the original forest were actively regenerating in the secondary forests. About 28 years after recovery, large trees were insufficient and basal area was about 60% of those of the mature forests. Further studies are needed to elucidate barriers to tree regeneration and dynamics of tree population.© 2016 International Formulae Group. All rights reserved.Keywords: Secondary forest, recovery, diversity, species composition, timber stock, Beni

    Quantum Symmetries and Strong Haagerup Inequalities

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    In this paper, we consider families of operators {xr}rΛ\{x_r\}_{r \in \Lambda} in a tracial C^\ast-probability space (A,ϕ)(\mathcal A, \phi), whose joint \ast-distribution is invariant under free complexification and the action of the hyperoctahedral quantum groups {Hn+}nN\{H_n^+\}_{n \in \N}. We prove a strong form of Haagerup's inequality for the non-self-adjoint operator algebra B\mathcal B generated by {xr}rΛ\{x_r\}_{r \in \Lambda}, which generalizes the strong Haagerup inequalities for \ast-free R-diagonal families obtained by Kemp-Speicher \cite{KeSp}. As an application of our result, we show that B\mathcal B always has the metric approximation property (MAP). We also apply our techniques to study the reduced C^\ast-algebra of the free unitary quantum group Un+U_n^+. We show that the non-self-adjoint subalgebra Bn\mathcal B_n generated by the matrix elements of the fundamental corepresentation of Un+U_n^+ has the MAP. Additionally, we prove a strong Haagerup inequality for Bn\mathcal B_n, which improves on the estimates given by Vergnioux's property RD \cite{Ve}

    Is there an optimal minimally invasive technique for left anterior descending coronary artery bypass?

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    <p>Abstract</p> <p>Background</p> <p>The aim of this retrospective study was to evaluate the clinical outcome of three different minimally invasive surgical techniques for left anterior descending (LAD) coronary artery bypass grafting (CABG): Port-Access surgery (PA-CABG), minimally invasive direct CABG (MIDCAB) and off-pump totally endoscopic CABG (TECAB).</p> <p>Methods</p> <p>Over a decade, 160 eligible patients for elective LAD bypass were referred to one of the three techniques: 48 PA-CABG, 53 MIDCAB and 59 TECAB. In MIDCAB group, Euroscore was higher and target vessel quality was worse. In TECAB group, early patency was systematically evaluated using coronary CT scan. During follow-up (mean 2.7 ± 0.1 years, cumulated 438 years) symptom-based angiography was performed.</p> <p>Results</p> <p>There was no conversion from off-pump to on-pump procedure or to sternotomy approach. In TECAB group, there was one hospital cardiac death (1.7%), reoperation for bleeding was higher (8.5% vs 3.7% in MIDCAB and 2% in PA-CABG) and 3-month LAD reintervention was significantly higher (10% vs 1.8% in MIDCAB and 0% in PA-CABG). There was no difference between MIDCAB and PA-CABG groups. During follow-up, symptom-based angiography (n = 12) demonstrated a good patency of LAD bypass in all groups and 4 patients underwent a no LAD reintervention. At 3 years, there was no difference in survival; 3-year angina-free survival and reintervention-free survival were significantly lower in TECAB group (TECAB, 85 ± 12%, 88 ± 8%; MIDCAB, 100%, 98 ± 5%; PA-CABG, 94 ± 8%, 100%; respectively).</p> <p>Conclusions</p> <p>Our study confirmed that minimally invasive LAD grafting was safe and effective. TECAB is associated with a higher rate of early bypass failure and reintervention. MIDCAB is still the most reliable surgical technique for isolated LAD grafting and the least cost effective.</p

    Operative blood loss and use of blood products after full robotic and conventional low anterior resection with total mesorectal excision for treatment of rectal cancer

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    To date, no studies have investigated the estimated blood loss (EBL) after full robotic low anterior resection (R-LAR) in a case-matched model, comparing it with the conventional open approach (O-LAR). Forty-nine patients in the R-LAR and 105 in the O-LAR group were matched for age, gender, BMI (body mass index), ASA (American Society of Anesthesiology) class, tumor–node–metastasis (TNM) classification and UICC (Union for International Cancer Control) stage, distance of the lower edge of the tumor from the anal verge, presence of comorbidities, and preoperative hemoglobin (Hb). EBL was significantly higher in the O-LAR group (P < 0.001); twelve units of packed red blood cells were globally transfused in the O-LAR group, compared to one unit only in the R-LAR (P = 0.051). A significantly higher postoperative Hb drop (3.0 vs. 2.4 g/dL, P = 0.015) was registered in the O-LAR patients. The length of hospital stay was much lower for the R-LAR group (8.4 vs. 12.4 days, P < 0.001). The number of harvested lymph nodes (17.4 vs. 13.5, P = 0.006) and extent of distal margin (2.9 vs. 1.9 cm, P < 0.001) were significantly higher in the R-LAR group. Open surgery was confirmed as the sole variable significantly associated (P < 0.001) with blood loss (odds ratio = 4.41, 95% CI 2.06–9.43). It was a confirmed prognosticator of blood loss (P = 0.006) when a preoperative clinical predictive model was built, using multivariate analysis (odds ratio = 3.95, 95% CI 1.47–10.6). In conclusion, R-LAR produced less operative blood loss and less drop in postoperative hemoglobin when compared to O-LAR. Other clinically relevant outcomes were similar or superior to O-LAR

    Consistent patterns of common species across tropical tree communities

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    Trees structure the Earth’s most biodiverse ecosystem, tropical forests. The vast number of tree species presents a formidable challenge to understanding these forests, including their response to environmental change, as very little is known about most tropical tree species. A focus on the common species may circumvent this challenge. Here we investigate abundance patterns of common tree species using inventory data on 1,003,805 trees with trunk diameters of at least 10 cm across 1,568 locations1,2,3,4,5,6 in closed-canopy, structurally intact old-growth tropical forests in Africa, Amazonia and Southeast Asia. We estimate that 2.2%, 2.2% and 2.3% of species comprise 50% of the tropical trees in these regions, respectively. Extrapolating across all closed-canopy tropical forests, we estimate that just 1,053 species comprise half of Earth’s 800 billion tropical trees with trunk diameters of at least 10 cm. Despite differing biogeographic, climatic and anthropogenic histories7, we find notably consistent patterns of common species and species abundance distributions across the continents. This suggests that fundamental mechanisms of tree community assembly may apply to all tropical forests. Resampling analyses show that the most common species are likely to belong to a manageable list of known species, enabling targeted efforts to understand their ecology. Although they do not detract from the importance of rare species, our results open new opportunities to understand the world’s most diverse forests, including modelling their response to environmental change, by focusing on the common species that constitute the majority of their trees.Publisher PDFPeer reviewe

    Field methods for sampling tree height for tropical forest biomass estimation

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    1.Quantifying the relationship between tree diameter and height is a key component of efforts to estimate biomass and carbon stocks in tropical forests. Although substantial site-to-site variation in height-diameter allometries has been documented, the time consuming nature of measuring all tree heights in an inventory plot means that most studies do not include height, or else use generic pan-tropical or regional allometric equations to estimate height. 2. Using a pan-tropical dataset of 73 plots where at least 150 trees had in-field ground-based height measurements, we examined how the number of trees sampled affects the performance of locally-derived height-diameter allometries, and evaluated the performance of different methods for sampling trees for height measurement. 3. Using cross-validation, we found that allometries constructed with just 20 locally measured values could often predict tree height with lower error than regional or climate-based allometries (mean reduction in prediction error = 0.46 m). The predictive performance of locally-derived allometries improved with sample size, but with diminishing returns in performance gains when more than 40 trees were sampled. Estimates of stand-level biomass produced using local allometries to estimate tree height show no over- or under-estimation bias when compared with estimates using measured heights. We evaluated five strategies to sample trees for height measurement, and found that sampling strategies that included measuring the heights of the ten largest diameter trees in a plot outperformed (in terms of resulting in local height-diameter models with low height prediction error) entirely random or diameter size-class stratified approaches. 4. Our results indicate that even remarkably limited sampling of heights can be used to refine height-diameter allometries. We recommend aiming for a conservative threshold of sampling 50 trees per location for height measurement, and including the ten trees with the largest diameter in this sample

    Consistent patterns of common species across tropical tree communities

    Get PDF
    Trees structure the Earth’s most biodiverse ecosystem, tropical forests. The vast number of tree species presents a formidable challenge to understanding these forests, including their response to environmental change, as very little is known about most tropical tree species. A focus on the common species may circumvent this challenge. Here we investigate abundance patterns of common tree species using inventory data on 1,003,805 trees with trunk diameters of at least 10 cm across 1,568 locations1,2,3,4,5,6 in closed-canopy, structurally intact old-growth tropical forests in Africa, Amazonia and Southeast Asia. We estimate that 2.2%, 2.2% and 2.3% of species comprise 50% of the tropical trees in these regions, respectively. Extrapolating across all closed-canopy tropical forests, we estimate that just 1,053 species comprise half of Earth’s 800 billion tropical trees with trunk diameters of at least 10 cm. Despite differing biogeographic, climatic and anthropogenic histories7, we find notably consistent patterns of common species and species abundance distributions across the continents. This suggests that fundamental mechanisms of tree community assembly may apply to all tropical forests. Resampling analyses show that the most common species are likely to belong to a manageable list of known species, enabling targeted efforts to understand their ecology. Although they do not detract from the importance of rare species, our results open new opportunities to understand the world’s most diverse forests, including modelling their response to environmental change, by focusing on the common species that constitute the majority of their trees
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