coResearchers have long appreciated the significant relationship between body size and an animal's overall adaptive strategy and life history. However, much more emphasis has been placed on interpreting body size than on the actual calculation of it. One measure of size that is especially important for human evolutionary studies is stature. Despite a long history of investigation, stature estimation remains plagued by two methodological problems: (1) the choice of the statistical estimator, and (2) the choice of the reference population from which to derive the parameters.This work addresses both of these problems in estimating stature for fossil hominids, with special reference to A.L. 288-1 (Australopithecus afarensis) and WT 15000 (Homo erectus). Three reference samples of known stature with maximum humerus and femur lengths are used in this study: a large (n=2209) human sample from North America, a smaller sample of modern human pygmies (n=19) from Africa, and a sample of wild-collected African great apes (n=85). Five regression techniques are used to estimate stature in the fossil hominids using both univariate and multivariate parameters derived from the reference samples: classical calibration, inverse calibration, major axis, reduced major axis and the zero-intercept ratio model. We also explore a new diagnostic to test extrapolation and allometric differences with multivariate data, and we calculate 95% confidence intervals to examine the range of variation in estimates for A.L. 288-1, WT 15000 and the new Bouri hominid (contemporary with [corrected] Australopithecus garhi). Results frequently vary depending on whether the data are univariate or multivariate. Unique limb proportions and fragmented remains complicate the choice of estimator. We are usually left in the end with the classical calibrator as the best choice. It is the maximum likelihood estimator that performs best overall, especially in scenarios where extrapolation occurs away from the mean of the reference sample. The new diagnostic appears to be a quick and efficient way to determine at the outset whether extrapolation exists in size and/or shape of the long bones between the reference sample and the target specimen. 相似文献
We studied stand structures and soil properties in an old-growth forest and two 30-yr-old second-growth stands. In the old-growth forest, the total density and basal area average 1566 trees > 1.25 m height ha-1 and 46.73 m2 ha-1. The dominant trees are Scutia buxifolia and Celtis tala. Using multivariate techniques we distinguished three stands: PS1, dominated by S. buxifolia, is 1000 m far from the river. Its soil is shallow and loamy. PS2 and PS3, co-dominated by S. buxifolia and C. tala, are over 1200 m distant from the river. There the soil is deeper and has thicker texture and higher phosphorus and calcium concentrations than the near-the-river forest soil. Scutia buxifolia shows reverse J-shaped size-distributions and has morphological features of stress-tolerant species. Celtis tala shows oscillating decay size-curves that suggest recruitment pulses related to small gaps and it has morphological features of competitive species. Celtis tala was selectively cut in the past in the second-growth stands SNRD and SRD. The stand SNRD, 1000 m far from the river, is dominated by S. buxifolia. The second species is Schinus polygamus which presents the bell-shaped size-structure of the pioneer species. SNRD does not differ from its old-growth counterpart PS1 in total tree density, basal area and tree branching. The stand SRD, over 1200 m distant from the river, is co-dominated by S. buxifolia and by C. tala trees regenerated from stumps. SRD does not differ from its old-growth counterparts PS2 and PS3 in total tree density and basal area. As to tree branching, it does not differ from PS3, but differs from PS2. All the stands are being invaded by the exotic tree Ligustrum lucidum.The differences between the old-growth stands seem to be related to the gradients of soil texture and nutrient concentrations raising edaphic stress towards the river. In SNRD, the stress, the stress-tolerance of S. buxifolia, and the aptitude of S. polygamus to recruit in disturbed habitats seem to have prevented the post-logging recruitment of C. tala. In SRD, C. tala regenerated possibly due to a better competitive performance in a more favorable site. Under protection the second-growth stands recovered the old-growth quantitative features. We recommend the restoration of the qualitative features and the control of L. lucidum. 相似文献
Although the theoretical capacity of silicon is ten times higher than that of graphite, the overall electrode capacity of Si anodes is still low due to the low Si loading and heavy metal current collector. Here, a novel flexible 3D Si/C fiber paper electrode synthesized by simultaneously electrospraying nano‐Si‐PAN (polyacrylonitrile) clusters and electrospinning PAN fibers followed by carbonization is reported. The combined technology allows uniform incorporation of Si nanoparticles into a carbon textile matrix to form a nano‐Si/carbon composite fiber paper. The flexible 3D Si/C fiber paper electrode demonstrate a very high overall capacity of ≈1600 mAh g‐1 with capacity loss less than 0.079% per cycle for 600 cycles and excellent rate capability. The exceptional performance is attributed to the unique architecture of the flexible 3D Si/C fiber paper, i.e., the resilient and conductive carbon fiber network matrix, carbon‐coated Si nanoparticle clusters, strong adhesion between carbon fibers and Si nanoparticle clusters, and uniform distribution of Si/C clusters in the carbon fiber frame. The scalable and facile synthesis method, good mechanical properties, and excellent electrochemical performance at a high Si loading make the flexible 3D Si/C fiber paper batteries extremely attractive for plug‐in electric vehicles, flexible electronics, space exploration, and military applications. 相似文献
Optoacoustic (photoacoustic) imaging is often performed with one‐dimensional transducer arrays, in analogy to ultrasound imaging. Optoacoustic imaging using linear arrays offers ease of implementation but comes with several performance drawbacks, in particular poor elevation resolution, i.e. the resolution along the axis perpendicular to the focal plane. Herein, we introduce and investigate a bi‐directional scanning approach using linear arrays that can improve the imaging performance to quasi‐isotropic transverse resolution. We study the approach theoretically and perform numerical simulations and phantom measurements to evaluate its performance under defined conditions. Finally, we discuss the features and the limitations of the proposed method.
The poor elevation resolution in a linear scan (left image) is overcome by the proposed bi‐directional scanning approach that yields isotropic transverse resolution (right). 相似文献
Three kinds of enzymes, agarase, β-1,4-mannanase, and β-1,3-xylanase, required for isolation of protoplasts from the red alga Bangia atropurpurea (Roth) C. Ag. were prepared from bacterial culture fluids of Vibrio sp. PO-303, Vibrio sp. MA-138, and Alcaligenes sp. XY-234, respectively, isolated from the sea environment. The optimal pH of all enzymes was around 7.5. Suitable conditions for protoplast isolation from B. atropurpurea were examined. The pretreatment of the fronds with pa-pain solution (20 mM Mes buffer, pH 7.5, containing 2% papain and 0.5 M mannitol) contributed to successful protoplast isolation. When razor-cut fragments of the fronds (about 200 mg in fresh weight) immersed in 20 mM Mes buffer, 7.5, containing 0.5 M mannitol and one unit each of agarase, β-1,4-mannanase, and β-1,3-xylanase were incubated at 22°C for 90 min with gentle agitation, 5.7 × 106 protoplasts were released from them. Many protoplasts regenerated into fronds of regular or irregular shape. 相似文献
A review is presented of the techniques currently used in the collection and separation of isolated teeth and bones of fossil vertebrates. These involve the collection and disaggregation of the sediment, its sieving, concentration and sorting of the residue, and curation of the fossils obtained. 相似文献
Much of the effort in any genomics programme arises from the need to generate and purify large numbers of identical molecules, since most analytical tools rely on the analysis of bulk DNA. Biological steps such as bacterial cloning--commonly used to prepare bulk samples of defined DNA fragments--are capricious and introduce their own restrictions and distortions. The analysis of single molecules, either directly or by in vitro enzymatic amplification, makes possible the examination of native genomic DNA without the complications and restrictions of biological propagation. Techniques already exist for the in vitro propagation of genomic fragments and for genome mapping, and offer the advantages of speed, flexibility and predictable behaviour. Single molecule sequencing, for which many approaches are being developed, is more challenging, but offers even greater rewards in terms of throughput and read length. 相似文献