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18 results for “rst”
Fig.ç24.A mblyops sp. 3, male (NSMT-Cr 21369). A, anterior part of body (dorsal); B, eyeplate (right, dorsal); C, antennal scale (le, ventral); D, pair of genital organs; E, sternal process and proximal parts of genital organs; F, rst pleopod (le); G, proximal part of uropodal endopod (le, ventral). in The Genus Amblyops (Crustacea: Mysida: Mysidae: Erythropinae) from East Asia and Australia, with Descriptions of Ten New Species
Fig.ç24.A mblyops sp. 3, male (NSMT-Cr 21369). A, anterior part of body (dorsal); B, eyeplate (right, dorsal); C, antennal scale (le, ventral); D, pair of genital organs; E, sternal process and proximal parts of genital organs; F, rst pleopod (le); G, proximal part of uropodal endopod (le, ventral).
Fig.ç18.A mblyops surugensis sp. nov., holotype, female (NSMT-Cr 21364). A, rst thoracopodal endopod (le); B, second thoracopod (le); C, third thoracopod (le); D, distal part of endopod of the same limb (le); E, sixth thoracopod with rudimentary oostegite; F, eighth thoracopod with developed oostegite. in The Genus Amblyops (Crustacea: Mysida: Mysidae: Erythropinae) from East Asia and Australia, with Descriptions of Ten New Species
Fig.ç18.A mblyops surugensis sp. nov., holotype, female (NSMT-Cr 21364). A, rst thoracopodal endopod (le); B, second thoracopod (le); C, third thoracopod (le); D, distal part of endopod of the same limb (le); E, sixth thoracopod with rudimentary oostegite; F, eighth thoracopod with developed oostegite.
Fig.ç13.A mblyops paci cus sp. nov., holotype, male (NSMT-Cr 21355). A, rst thoracopodal endopod (le); B, second thoracopod (right); C, third thoracopod (right); D, eighth thoracopodal exopod (right); E, pair of genital organs and sternal process; F, endopod of fourth pleopod (right); G, distal part of endopod of fourth pleopod (right); H, exopod of h pleopod (right), I, uropod and telson (dorsal); J, posterior part of telson (dorsal). in The Genus Amblyops (Crustacea: Mysida: Mysidae: Erythropinae) from East Asia and Australia, with Descriptions of Ten New Species
Fig.ç13.A mblyops paci cus sp. nov., holotype, male (NSMT-Cr 21355). A, rst thoracopodal endopod (le); B, second thoracopod (right); C, third thoracopod (right); D, eighth thoracopodal exopod (right); E, pair of genital organs and sternal process; F, endopod of fourth pleopod (right); G, distal part of endopod of fourth pleopod (right); H, exopod of h pleopod (right), I, uropod and telson (dorsal); J, posterior part of telson (dorsal).
Fig.ç10.A mblyops okinawensis sp. nov., holotype, female (NSMT-Cr 21353). A–D, rst to fourth thoracopods (right); E, eighth thoracopo- dal endopod (le); F, eighth thoracopodal exopod with oostegite (right). in The Genus Amblyops (Crustacea: Mysida: Mysidae: Erythropinae) from East Asia and Australia, with Descriptions of Ten New Species
Fig.ç10.A mblyops okinawensis sp. nov., holotype, female (NSMT-Cr 21353). A–D, rst to fourth thoracopods (right); E, eighth thoracopo- dal endopod (le); F, eighth thoracopodal exopod with oostegite (right).
Fig.ç5.A mblyops izuensis sp. nov., holotype, male (NSMT-Cr 21348). A, eyeplate (le); B, antennular peduncle (le, dorsal); C, antenna (le, dorsal); D, antennal peduncle (le, dorsal); E, mandible and mandibular palp (le); F, maxillule (le); G, maxilla (le); H, rst thoracopod (le); I, second thoracopodal endopod (right); J, K, genital organ and sternal process. in The Genus Amblyops (Crustacea: Mysida: Mysidae: Erythropinae) from East Asia and Australia, with Descriptions of Ten New Species
Fig.ç5.A mblyops izuensis sp. nov., holotype, male (NSMT-Cr 21348). A, eyeplate (le); B, antennular peduncle (le, dorsal); C, antenna (le, dorsal); D, antennal peduncle (le, dorsal); E, mandible and mandibular palp (le); F, maxillule (le); G, maxilla (le); H, rst thoracopod (le); I, second thoracopodal endopod (right); J, K, genital organ and sternal process.
Fig.ç4.A mblyops australiensis sp. nov., holotype, male (NSMT-Cr 21346). A, rst thoracopodal endopod (right); B, second thoracopod (right); C, rst thoracopodal exopod (right); D, rst pleopod (right); E, fourth pleopod (le); F, uropod and telson (dorsal); G, uropodal endopod (right, ventral); H, telson (dorsal). in The Genus Amblyops (Crustacea: Mysida: Mysidae: Erythropinae) from East Asia and Australia, with Descriptions of Ten New Species
Fig.ç4.A mblyops australiensis sp. nov., holotype, male (NSMT-Cr 21346). A, rst thoracopodal endopod (right); B, second thoracopod (right); C, rst thoracopodal exopod (right); D, rst pleopod (right); E, fourth pleopod (le); F, uropod and telson (dorsal); G, uropodal endopod (right, ventral); H, telson (dorsal).
Fig.ç6.A mblyops izuensis sp. nov., holotype, male (NSMT-Cr 21348). A–D, rst to fourth male pleopods (A, B, right; C, D le); E, distal part of endopod of fourth male pleopod (le); F, distal part of exopod of fourth male pleopod (le); G, h male pleopod (right); H, uropod and telson (dorsal); I, proximal part of uropodal endopod (le, ventral); J, posterior part of telson (dorsal). in The Genus Amblyops (Crustacea: Mysida: Mysidae: Erythropinae) from East Asia and Australia, with Descriptions of Ten New Species
Fig.ç6.A mblyops izuensis sp. nov., holotype, male (NSMT-Cr 21348). A–D, rst to fourth male pleopods (A, B, right; C, D le); E, distal part of endopod of fourth male pleopod (le); F, distal part of exopod of fourth male pleopod (le); G, h male pleopod (right); H, uropod and telson (dorsal); I, proximal part of uropodal endopod (le, ventral); J, posterior part of telson (dorsal).
Fig.ç2.A mblyops amamiensis sp. nov., A–F, H, holotype, female (NSMT-Cr 21344); G, paratype, female (NSMT-Cr 21345). A, rst thoracopod (right); B, second thoracopod (right); C, fourth thoracopodal endopod (right); D, h thoracopod (right); E, uropod and telson (dorsal); F, uropodal endopod (right, ventral); G, uropodal endopod (le, ventral); H, posterior part of telson (dorsal). in The Genus Amblyops (Crustacea: Mysida: Mysidae: Erythropinae) from East Asia and Australia, with Descriptions of Ten New Species
Fig.ç2.A mblyops amamiensis sp. nov., A–F, H, holotype, female (NSMT-Cr 21344); G, paratype, female (NSMT-Cr 21345). A, rst thoracopod (right); B, second thoracopod (right); C, fourth thoracopodal endopod (right); D, h thoracopod (right); E, uropod and telson (dorsal); F, uropodal endopod (right, ventral); G, uropodal endopod (le, ventral); H, posterior part of telson (dorsal).
Fig.ç21.A mblyops timorensis sp. nov., holotype, male (NSMT-Cr 21366). A, rst thoracopodal endopod (right); B, second thoracopodal endopod (le); C, seventh thoracopodal exopod (le); D, genital organ (le, lateral); E, second pleopod (right); F, fourth pleopod (right); G, uropod and telson (dorsal); H, uropodal endopod (right, ventral); I, telson (dorsal). in The Genus Amblyops (Crustacea: Mysida: Mysidae: Erythropinae) from East Asia and Australia, with Descriptions of Ten New Species
Fig.ç21.A mblyops timorensis sp. nov., holotype, male (NSMT-Cr 21366). A, rst thoracopodal endopod (right); B, second thoracopodal endopod (le); C, seventh thoracopodal exopod (le); D, genital organ (le, lateral); E, second pleopod (right); F, fourth pleopod (right); G, uropod and telson (dorsal); H, uropodal endopod (right, ventral); I, telson (dorsal).
Fig.ç14.A mblyops sagamiensis sp. nov., holotype, female (NSMT-Cr 21361). A, anterior part of body (dorsal); B, eyeplate (le, dorsal); C, eyeplate (le, lateral); D, antenna (le, dorsal); E, antennal peduncle (le, lateral); F, mandible and mandibular palp (le); G, maxillule (le); H, maxilla (right); I, labrum (ventral); J, rst thoracopodal endopod (le). in The Genus Amblyops (Crustacea: Mysida: Mysidae: Erythropinae) from East Asia and Australia, with Descriptions of Ten New Species
Fig.ç14.A mblyops sagamiensis sp. nov., holotype, female (NSMT-Cr 21361). A, anterior part of body (dorsal); B, eyeplate (le, dorsal); C, eyeplate (le, lateral); D, antenna (le, dorsal); E, antennal peduncle (le, lateral); F, mandible and mandibular palp (le); G, maxillule (le); H, maxilla (right); I, labrum (ventral); J, rst thoracopodal endopod (le).
Figure 1: Asymmetric representation for the ¯rst four generations, in its elec- trical equivalent-THE RESPIRATORY IMPEDANCE IN AN ASYMMETRIC MODEL OF THE LUNG STRUCTURE
<p>For example, the average of the radius ratio<br> changes from 2¡0:1713 = 0:8881 to 0:8923 when only the ¯rst 16 generations are<br> taken into account, respectively to 0:8783 for the alveoli (generations 17-24)<br> [5]. This implies that the homothety factor changes, depending on the spatial<br> location within the tree. On the other hand, if we analyze the radius ratio from<br> generations 1 to 24 in steps of 4, we obtain an average of 0:8535, whereas if we<br> use steps of 2, we obtain an average homothety factor of 0:8623. These changes<br> might not seem signi¯cant, but one should recall that they are originated by<br> the symmetric geometry of the respiratory tree. However, when asymmetry<br> is considered, one deals with several homothety factors, i.e. as schematically<br> drawn in figure 1.</p>
Figure 1: Asymmetric representation for the ¯rst four generations, in its elec- trical equivalent-THE RESPIRATORY IMPEDANCE IN AN ASYMMETRIC MODEL OF THE LUNG STRUCTURE
<p>These changes<br> might not seem signi¯cant, but one should recall that they are originated by<br> the symmetric geometry of the respiratory tree. However, when asymmetry<br> is considered, one deals with several homothety factors, i.e. as schematically<br> drawn in ¯gure 1.</p>
Probing Patchy Reionization with the Void Probability Function in the era of RST
<p>Neutral hydrogen attenuates the Lyman-alpha emission of galaxies, dimming and increasing the apparent clustering of Lyman-Alpha Emitters (LAEs). LAEs are more likely to be observed in the regions that have already been ionized, so LAEs within more neutral intergalactic medium appear more clustered. Using the Jensen et al 2014 simulations of LAEs at various ionization fractions, we show how the Void Probability Function (VPF) measures the clustering signals caused by an increasingly neutral intergalactic medium. The VPF is sensitive to voids and can be easily compared for samples of the same number density, and therefore might be the best option for teasing out the particular clustering caused by 'inside-out' patchy reionization. We simulate what ionization fractions constraints the Lyman Alpha Galaxies in the Epoch of Reionization (LAGER) survey can give with the VPF, and motivate the use of the VPF for reionization surveys with WFIRST.</p>
Kobalt_RST (RST German Learner Treebank): Die Annotation von rhetorischen Strukturen im Kobalt-DaF-Korpus
<p>Das <a href="https://www.linguistik.hu-berlin.de/de/institut/professuren/korpuslinguistik/forschung/kobalt-daf">Kobalt-DaF-Korpus</a> ist ein systematisch erhobenes und tief annotiertes Deutschlernerkorpus, welches 80 deutschsprachige argumentative Texte von deutschen L1-Sprecher:innen und Deutschlerner:innen unterschiedlicher L1 enthält. Dieses Repositorium stellt eine zusätzliche Annotation des Kobalt-DaF-Korpus bzgl. rhetorischer Strukturen frei zur Verfügung. Folgende Informationen sind hier zu finden: (1) Die Darstellung des Annotationsprozesses (Annotationsframework, -richtlinie, und -verfahren). (2) Die annotierten rs3-Dateien.</p> <p>*Versionshinweise: Bislang sind ausschließlich die Texte der chinesischen Deutschlerner:innen und der deutschen L1-Sprecher:innen (insgesamt 40 Texte) verfügbar. Die Annotation der übrigen Texte folgt demnächst. </p> <p>*Die Annotationsarbeit wurde gefördert durch das Chinese Scholarship Council und die Deutsche Forschungsgemeinschaft (DFG) – SFB 1412, 416591334.</p>
AGN-151597 (Formerly RST-001) Phase I/II Trial for Advanced Retinitis Pigmentosa
ClinicalTrials.gov study NCT02556736. IPD Sharing: YES. Countries: 1. Publications: 1.
Mapping the Redshift Evolution of Hα Equivalent Width Distributions & RST Grism Surveys
<p>The Hα Equivalent Width (EW) is an observational proxy for the specific star formation rate (sSFR) and can give us valuable insight in regards to bursty star formation histories. Studies find Hα EW anti-correlates with stellar mass and increases in redshift similar to the `main sequence’ and sSFR redshift evolution. However, selection effects may bias the underlying results, such that measurements of the intrinsic correlations are needed. In this talk, I will be presenting a new methodology of constraining EW distributions by simulating emission line galaxies assuming an intrinsic EW distribution and applying selection criteria to match observations drawn from Hα narrowband surveys between z ~ 0.4 and 2. This nicely overlaps with the expected redshift coverage of RST planned surveys. We find EW intrinsically correlates with Hα luminosity and stellar mass, while ignoring selection effect corrections causes a steeper correlation. We also observe an increasing redshift evolution between EW and stellar mass. The correlation between EW and stellar mass is found to reproduce the EW distribution, LF, and SMF at all redshifts probed, which suggests it is shaped by physical processes associated with star formation. I will finish by discussing the implication of our results for RST survey planning by taking into account the effective EW threshold in slitless grism surveys set by the limiting resolving power using the redshift evolution of the EW — stellar mass correlation.</p>
RNA-seq of Arabidopsis thaliana roots exposed to the MAMP flg22 in the presence of a community of commensal bacteria [RST]
GEO Series GSE156425. Arabidopsis thaliana. 100 samples. Type: Expression profiling by high throughput sequencing.
A PCB Alignment System Using RST Template Matching with CUDA on Embedded GPU Board
<p>Datasets were used for testing for the embedded PCB alignment system project . The project was implemented in Robotics Lab, Department of Computer Science and Information Engineering, National Cheng Kung University, Taiwan.</p>
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