scholarly journals TomoSAR Mapping of 3D Forest Structure: Contributions of L-Band Configurations

2021 ◽  
Vol 13 (12) ◽  
pp. 2255
Author(s):  
Matteo Pardini ◽  
Victor Cazcarra-Bes ◽  
Konstantinos Papathanassiou

Synthetic Aperture Radar (SAR) measurements are unique for mapping forest 3D structure and its changes in time. Tomographic SAR (TomoSAR) configurations exploit this potential by reconstructing the 3D radar reflectivity. The frequency of the SAR measurements is one of the main parameters determining the information content of the reconstructed reflectivity in terms of penetration and sensitivity to the individual vegetation elements. This paper attempts to review and characterize the structural information content of L-band TomoSAR reflectivity reconstructions, and their potential to forest structure mapping. First, the challenges in the accurate TomoSAR reflectivity reconstruction of volume scatterers (which are expected to dominate at L-band) and to extract physical structure information from the reconstructed reflectivity is addressed. Then, the L-band penetration capability is directly evaluated by means of the estimation performance of the sub-canopy ground topography. The information content of the reconstructed reflectivity is then evaluated in terms of complementary structure indices. Finally, the dependency of the TomoSAR reconstruction and of its structural information to both the TomoSAR acquisition geometry and the temporal change of the reflectivity that may occur in the time between the TomoSAR measurements in repeat-pass or bistatic configurations is evaluated. The analysis is supported by experimental results obtained by processing airborne acquisitions performed over temperate forest sites close to the city of Traunstein in the south of Germany.

2019 ◽  
Author(s):  
Javier Cabau-Laporta ◽  
Alex M. Ascensión ◽  
Mikel Arrospide-Elgarresta ◽  
Daniela Gerovska ◽  
Marcos J. Araúzo-Bravo

AbstractHigh-throughput cell-data technologies such as single-cell RNA-Seq create a demand for algorithms for automatic cell classification and characterization. There exist several classification ontologies of cells with complementary information. However, one needs to merge them in order to combine synergistically their information. The main difficulty in merging is to match the ontologies since they use different naming conventions. To overcome this obstacle we developed an algorithm that merges ontologies by integrating the name-matching search between class label names with the structure mapping between the ontology elements. To implement our algorithms, we developed FOntCell, a software module in Python for efficient automatic parallel-computed fusion of ontologies in the same or similar knowledge domains. It processes the ontology attributes to extract relations and class synonyms. FOntCell integrates the semantic, name with synonyms, mapping with a structure mapping based on graph convolution. Since the structure mapping assessment is time consuming process, we designed two methods to perform the graph convolution: vectorial structure matching and constraint-based structure matching. To perform the vectorial structure matching we designed a general method to calculate the similarities between vectors of different lengths for different metrics. Additionally, we adapted the slower Blondel method to work for structure matching. These functionalities of FOntCell allow the unification of dispersed knowledge in one domain into a unique ontology. FOntCell produces the results of the merged ontology in OBO format that can be iteratively reused by FOntCell to adapt continuously the ontologies with the new data, such of the Human Cell Atlas, endlessly produced by data-driven classification methods. To navigate easily across the fused ontologies, it generates HTML files with tabulated and graphic summaries, and an interactive circular Directed Acyclic Graphs of the merged results. We used FOntCell to fuse CELDA, LifeMap and LungMAP Human Anatomy cell ontologies to produce comprehensive cell ontology.Author SummaryThere is a strong belief in the research community that there exist more cell types than the described in the literature, therefore new technologies were developed to produce a high volume of data to discover new cells. One issue that arises once the cells are discovered is how to classify them. One way to perform such classification is to use already existing cell classifications from different ontology sources but it is difficult to merge them. An ontology has semantic information providing the meaning of each term and structural information providing the relationship between terms as a graph. We developed a new Python module, FOntCell that merges efficiently cell ontologies and integrates semantic and structure information with our own graph convolution technique. Since the structure mapping assessment is time-consuming process we designed two methods to optimize the graph convolution: vectorial and constraint-based structure matching. To perform the vectorial structure matching we designed a method that calculates the similarities between vectors describing the graphs of different sizes. The functionalities of FOntCell allow the unification of dispersed knowledge into a unique ontology, to adapt continuously from new data, and to navigate across the fused ontologies by a graphic use interface.


1998 ◽  
Vol 38 (2) ◽  
pp. 9-15 ◽  
Author(s):  
J. Guan ◽  
T. D. Waite ◽  
R. Amal ◽  
H. Bustamante ◽  
R. Wukasch

A rapid method of determining the structure of aggregated particles using small angle laser light scattering is applied here to assemblages of bacteria from wastewater treatment systems. The structure information so obtained is suggestive of fractal behaviour as found by other methods. Strong dependencies are shown to exist between the fractal structure of the bacterial aggregates and the behaviour of the biosolids in zone settling and dewatering by both pressure filtration and centrifugation methods. More rapid settling and significantly higher solids contents are achievable for “looser” flocs characterised by lower fractal dimensions. The rapidity of determination of structural information and the strong dependencies of the effectiveness of a number of wastewater treatment processes on aggregate structure suggests that this method may be particularly useful as an on-line control tool.


2021 ◽  
Vol 22 (2) ◽  
pp. 880
Author(s):  
Thomas Schmitz ◽  
Ajay Abisheck Paul George ◽  
Britta Nubbemeyer ◽  
Charlotte A. Bäuml ◽  
Torsten Steinmetzer ◽  
...  

The saliva of blood-sucking leeches contains a plethora of anticoagulant substances. One of these compounds derived from Haementeria ghilianii, the 66mer three-disulfide-bonded peptide tridegin, specifically inhibits the blood coagulation factor FXIIIa. Tridegin represents a potential tool for antithrombotic and thrombolytic therapy. We recently synthesized two-disulfide-bonded tridegin variants, which retained their inhibitory potential. For further lead optimization, however, structure information is required. We thus analyzed the structure of a two-disulfide-bonded tridegin isomer by solution 2D NMR spectroscopy in a combinatory approach with subsequent MD simulations. The isomer was studied using two fragments, i.e., the disulfide-bonded N-terminal (Lys1–Cys37) and the flexible C-terminal part (Arg38–Glu66), which allowed for a simplified, label-free NMR-structure elucidation of the 66mer peptide. The structural information was subsequently used in molecular modeling and docking studies to provide insights into the structure–activity relationships. The present study will prospectively support the development of anticoagulant-therapy-relevant compounds targeting FXIIIa.


1984 ◽  
Vol 41 ◽  
Author(s):  
W. Krakow ◽  
J. T. Wetzel ◽  
D. A. Smith ◽  
G. Trafas

AbstractA high resolution electron microscope study of grain boundary structures in Au thin films has been undertaken from both a theoretical and experimental point of view. The criteria necessary to interpret images of tilt boundaries at the atomic level, which include electron optical and specimen effects, have been considered for both 200kV and the newer 400kV medium voltage microscopes. So far, the theoretical work has concentrated on two different [001] tilt bounda-ries where a resolution of 2.03Å is required to visualize bulk lattice structures on either side of the interface. Both a high angle boundary, (210) σ=5, and a low angle boundary, (910) σ=41, have been considered. Computational results using multislice dynamical diffraction and image simulations of relaxed bounda-ries viewed edge-on and with small amounts of beam and/or specimen inclina-tion have been obtained. It will be shown that some structural information concerning grain boundary dislocations can be observed at 200kV. However, many difficulties occur in the exact identification of the interface structure viewed experimentally for both [001] and [011] boundaries since the resolution required is near the performance limit of a 200kV microscope. The simulated results at 400kV indicate a considerable improvement will be realized in obtain-ing atomic structure information at the interface.


2017 ◽  
Vol 9 (12) ◽  
pp. 1229 ◽  
Author(s):  
Victor Cazcarra-Bes ◽  
Maria Tello-Alonso ◽  
Rico Fischer ◽  
Michael Heym ◽  
Konstantinos Papathanassiou

1982 ◽  
Vol 2 (12) ◽  
pp. 1501-1513
Author(s):  
Janet Kurjan ◽  
Benjamin D. Hall

The SUP4 tRNA Tyr locus in Saccharomyces cerevisiae has been studied by the isolation and characterization of mutations at the SUP4 gene which result in the loss of suppressor function. Most of the mutations act as single-site mutations, whereas about a third of the mutations are deletions of the entire gene. Two meiotic fine-structure maps of the gene were made. The first mapping technique placed 10 mutations plus the sup4 + anticodon on a map by a measurement of levels of recombination between pairs of mutations. The second map utilized a more qualitative estimate of recombination frequency, allowing 69 mutations and the sup4 + anticodon to be mapped. The maps were compared with the physical structure of the gene for the 34 mutations whose nucleotide alteration has been determined by DNA sequencing (Koski et al., Cell 22 :415-425, 1980; Kurjan et al., Cell 20 :701-709, 1980). Both maps show a good correlation with the physical structure of the gene, even though certain properties of genetic fine-structure maps, such as marker effects and “map expansion,” were seen.


Author(s):  
J. Doblas ◽  
A. Carneiro ◽  
Y. Shimabukuro ◽  
S. Sant’Anna ◽  
L. Aragão ◽  
...  

Abstract. In this study we analyse the factors of variability of Sentinel-1 C-band radar backscattering over tropical rainforests, and propose a method to reduce the effects of this variability on deforestation detection algorithms. To do so, we developed a random forest regression model that relates Sentinel-1 gamma nought values with local climatological data and forest structure information. The model was trained using long time-series of 26 relevant variables, sampled over 6 undisturbed tropical forests areas. The resulting model explained 71.64% and 73.28% of the SAR signal variability for VV and VH polarizations, respectively. Once the best model for every polarization was selected, it was used to stabilize extracted pixel-level data of forested and non-deforested areas, which resulted on a 10 to 14% reduction of time-series variability, in terms of standard deviation. Then a statistically robust deforestation detection algorithm was applied to the stabilized time-series. The results show that the proposed method reduced the rate of false positives on both polarizations, especially on VV (from 21% to 2%, α=0.01). Meanwhile, the omission errors increased on both polarizations (from 27% to 37% in VV and from 27% to 33% on VV, α=0.01). The proposed method yielded slightly better results when compared with an alternative state-of-the-art approach (spatial normalization).


RNA ◽  
2010 ◽  
Vol 16 (6) ◽  
pp. 1108-1117 ◽  
Author(s):  
S. Quarrier ◽  
J. S. Martin ◽  
L. Davis-Neulander ◽  
A. Beauregard ◽  
A. Laederach

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