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432 results for “nominalization”
Subspecies and Distribution. P. b. bougainville Quoy & Gaimard, 1824 — Bernier I and Dorre I, in Shark Bay, Western Australia. Nominate race reintroduced to Heirisson Prong and Faure I (Shark Bay) and to the Arid Recovery Project area in South Australia. in Peramelidae
Subspecies and Distribution. P. b. bougainville Quoy & Gaimard, 1824 — Bernier I and Dorre I, in Shark Bay, Western Australia. Nominate race reintroduced to Heirisson Prong and Faure I (Shark Bay) and to the Arid Recovery Project area in South Australia.
Subspecies and Distribution. O.c.cuniculusLinnaeus,1758—N,NE&EIberianPeninsula(Spain). O.c.algirusLoche,1858—S,SW&WIberianPeninsula(Spain,Portugal),NMorocco,NAlgeria(includingHabibasI). O.c.brachyotusTrouessart,1917—SFrance. O.c.cnossiusBate,1906—CreteI. O.c.habetensisCabrera,1923—Tanger-Tetouan-AlHoceimaRegion(NMorocco). O. c. huxleyi Haeckel, 1874 — Mediterranean Is (Balearic Is, Corsica, Sardinia, Sicily and Macaronesia (Azores, Madeira, and Canary Is). Original distribution after last Ice Age restricted to Iberian Peninsula, W France, and N Africa. Ancient introductions of the nominate subspecies probably during the Ro- man period have spread it throughout Europe, and now it is present in most of W, C & E Europe and the Mediterranean and Macaronesian Is (these mostly old introductions are also shaded on the map). During the 20" century it has been released into the steppes of the Black Sea in Ukraine and Russia (N Caucasus); introduced into Australia in 1788 and again in 1859 where it is now widespread; it is found on many Pacific Is, islands off the coast of South Africa and Namibia, and in New Zealand; successfully introduced only since 1936 into South America, nowadays with a limited range in Chile, Argentina, and Falkland Is, it is also present in the Caribbean Is (all these modern introductions not shaded in the map). Worldwide as domesticated forms. in Leporidae
Subspecies and Distribution. O.c.cuniculusLinnaeus,1758—N,NE&EIberianPeninsula(Spain). O.c.algirusLoche,1858—S,SW&WIberianPeninsula(Spain,Portugal),NMorocco,NAlgeria(includingHabibasI). O.c.brachyotusTrouessart,1917—SFrance. O.c.cnossiusBate,1906—CreteI. O.c.habetensisCabrera,1923—Tanger-Tetouan-AlHoceimaRegion(NMorocco). O. c. huxleyi Haeckel, 1874 — Mediterranean Is (Balearic Is, Corsica, Sardinia, Sicily and Macaronesia (Azores, Madeira, and Canary Is). Original distribution after last Ice Age restricted to Iberian Peninsula, W France, and N Africa. Ancient introductions of the nominate subspecies probably during the Ro- man period have spread it throughout Europe, and now it is present in most of W, C & E Europe and the Mediterranean and Macaronesian Is (these mostly old introductions are also shaded on the map). During the 20" century it has been released into the steppes of the Black Sea in Ukraine and Russia (N Caucasus); introduced into Australia in 1788 and again in 1859 where it is now widespread; it is found on many Pacific Is, islands off the coast of South Africa and Namibia, and in New Zealand; successfully introduced only since 1936 into South America, nowadays with a limited range in Chile, Argentina, and Falkland Is, it is also present in the Caribbean Is (all these modern introductions not shaded in the map). Worldwide as domesticated forms.
Subspecies and Distribution. M. m. marmota Linnaeus, 1758 — Alps in Germany, Austria, Switzerland, France, and Italy. M. m. latirostris Kratochvil, 1961 — High Tatra Mts of Slovakia and Poland. Nominate subspecies reintroduced to Romania (Carpathian Mts) and Slovenia (Julian Alps), and introduced into the Black Forest (Germany), the Massif Central, Jura, and Vosgues (France), the Pyrenees (France, Spain, and Andorra), E Austria, Apennine Mts (Italy), N Serbia, Montenegro. in Sciuridae
Subspecies and Distribution. M. m. marmota Linnaeus, 1758 — Alps in Germany, Austria, Switzerland, France, and Italy. M. m. latirostris Kratochvil, 1961 — High Tatra Mts of Slovakia and Poland. Nominate subspecies reintroduced to Romania (Carpathian Mts) and Slovenia (Julian Alps), and introduced into the Black Forest (Germany), the Massif Central, Jura, and Vosgues (France), the Pyrenees (France, Spain, and Andorra), E Austria, Apennine Mts (Italy), N Serbia, Montenegro.
FIGURE 10 in Redescriptions of the type specimens of synonymous nominal taxa of sea snakes (Serpentes: Elapidae: Hydrophis, Laticauda) at the Zoological Survey of India
FIGURE 10. Holotype of Platurus affinis ZSI 8289, dorsal (top), ventral (middle) and lateral (bottom) aspects. Photograph by Zoological Survey of India, Kolkata.
FIGURE 11 in Redescriptions of the type specimens of synonymous nominal taxa of sea snakes (Serpentes: Elapidae: Hydrophis, Laticauda) at the Zoological Survey of India
FIGURE 11. Modified reproduction of drawing of Hydrophis melanocinctus, H. alcocki and H. neglectus type specimens from Wall (1906).
FIGURE 9 in Redescriptions of the type specimens of synonymous nominal taxa of sea snakes (Serpentes: Elapidae: Hydrophis, Laticauda) at the Zoological Survey of India
FIGURE 9. Holotype of Hydrophis neglectus ZSI 8598, dorsal (top), ventral (middle) and lateral (bottom) aspects. Photograph by Zoological Survey of India, Kolkata.
FIGURE 1 in Redescriptions of the type specimens of synonymous nominal taxa of sea snakes (Serpentes: Elapidae: Hydrophis, Laticauda) at the Zoological Survey of India
FIGURE 1. Syntype of Hydrophis trachyceps ZSI 8266, dorsal (top), ventral (middle) and lateral (bottom) aspects. Photograph by Zoological Survey of India, Kolkata.
FIGURE 5 in Redescriptions of the type specimens of synonymous nominal taxa of sea snakes (Serpentes: Elapidae: Hydrophis, Laticauda) at the Zoological Survey of India
FIGURE 5. Holotype of Hydrophis dayanus ZSI 8278, dorsal (top), ventral (middle) and lateral (bottom) aspects. Photograph by Zoological Survey of India, Kolkata.
FIGURE 8 in Redescriptions of the type specimens of synonymous nominal taxa of sea snakes (Serpentes: Elapidae: Hydrophis, Laticauda) at the Zoological Survey of India
FIGURE 8. Holotype of Hydrophis melanocinctus ZSI 14470, dorsal (top), ventral (middle) and lateral (bottom) aspects. Photograph by Zoological Survey of India, Kolkata.
FIGURE 3 in Redescriptions of the type specimens of synonymous nominal taxa of sea snakes (Serpentes: Elapidae: Hydrophis, Laticauda) at the Zoological Survey of India
FIGURE 3. Holotype of Hydrophis fayrerianus ZSI 8270, dorsal (top), ventral (middle) and lateral (bottom) aspects. Photograph by Zoological Survey of India, Kolkata.
FIGURE 2 in Redescriptions of the type specimens of synonymous nominal taxa of sea snakes (Serpentes: Elapidae: Hydrophis, Laticauda) at the Zoological Survey of India
FIGURE 2. Holotype of Hydrophis crassicollis ZSI 8272, dorsal (top), ventral (middle) and lateral (bottom) aspects. Photograph by Zoological Survey of India, Kolkata.
FIGURE 4 in Redescriptions of the type specimens of synonymous nominal taxa of sea snakes (Serpentes: Elapidae: Hydrophis, Laticauda) at the Zoological Survey of India
FIGURE 4. Holotype of Hydrophis tuberculatus ZSI 8271, dorsal (top), ventral (middle) and lateral (bottom) aspects. Photograph by Zoological Survey of India, Kolkata.
FIGURE 7 in Redescriptions of the type specimens of synonymous nominal taxa of sea snakes (Serpentes: Elapidae: Hydrophis, Laticauda) at the Zoological Survey of India
FIGURE 7. Holotype of Hydrophis alcocki ZSI 8244, dorsal (top), ventral (middle) and lateral (bottom) aspects. Photograph by Zoological Survey of India, Kolkata.
FIGURE 6 in Redescriptions of the type specimens of synonymous nominal taxa of sea snakes (Serpentes: Elapidae: Hydrophis, Laticauda) at the Zoological Survey of India
FIGURE 6. Holotype of Distira andamanica ZSI 15238, dorsal (top), ventral (middle) and lateral (bottom) aspects. Photograph by Zoological Survey of India, Kolkata.
Supplementary material 3 from: Karasawa S (2016) Eleven nominal species of Burmoniscus are junior synonyms of B. kathmandius (Schmalfuss, 1983) (Crustacea, Isopoda, Oniscidea). ZooKeys 607: 1-24. https://doi.org/10.3897/zookeys.607.8253
Summary of diagnostic features of each nominal species of Burmoniscus in Japan according to the respective original descriptions :
Stalization of the Furuta pendulum: Linear, nonlinear and AI based controllers (nominal case)
<p><br>Stabilization control of the Furuta pendulum in Matlab/Simulink Simscape environmet in nominla case.</p> <p><br>Linear controllers</p> <ul> <li>LQR</li> <li>PID</li> </ul> <p>Nonlinear controllers</p> <ul> <li>Feedback Linearization</li> <li>SMC</li> </ul> <p>AI-based controllers</p> <ul> <li>Feedback Linearization with adaptive nerual networks</li> <li>Reiforcement Learning</li> <li>Feedback Linearization with Reinforcement Learning compensation</li> </ul> <p> </p>
Nominal FAST5/FASTQ Evaluation Data Set
<p>FAST5/FASTQ data used for accuracy characterization of decoding techniques applied to the HEDGEs DNA-information storage code. FASTQ data is used to evaluate the hard-decoding algorithm as explained by Press et al. in (<a href="https://doi.org/10.1073/pnas.2004821117">https://doi.org/10.1073/pnas.2004821117</a>). FAST5 data is used in evaluation for both our novel Alignment Matrix soft decoder (<a href="https://doi.org/10.5281/zenodo.11454877">https://doi.org/10.5281/zenodo.11454877</a>), and the soft decoder developed by Chandak et al. in the publication (<a href="https://doi-org.prox.lib.ncsu.edu/10.1109/ICASSP40776.2020.9053441">10.1109/ICASSP40776.2020.9053441</a>). Our code repository at <a href="https://doi.org/10.5281/zenodo.11454877">https://doi.org/10.5281/zenodo.11454877</a> includes a GPU accelerated adaptation of Chandak et al.’s algorithm in order to scale analysis on the submitted FAST5 data, and this is the version of code used to evaluate the algorithm’s accuracy and runtime overhead.</p> <p> </p> <p>Within the archive there are several sub-archives. Explanations for each sub-archive can be found for the corresponding archive name within the README.md file.</p> <p> </p>
FIGURES 9–12 in An integrative redescription of Hypsibius dujardini (Doyère, 1840), the nominal taxon for Hypsibioidea (Tardigrada: Eutardigrada)
FIGURES 9–12. Hypsibius exemplaris sp. nov.: 9—adult habitus (ventrolateral view, PCM, holotype); 10—adult habitus (lateral view, SEM, paratype); 11 —bucco-pharyngeal apparatus, the arrowhead indicates large pharyngeal apophyses (PCM, paratype); 12—bucco-pharyngeal apparatus (SEM, paratype). All scale bars in µm.
FIGURES 25–29 in An integrative redescription of Hypsibius dujardini (Doyère, 1840), the nominal taxon for Hypsibioidea (Tardigrada: Eutardigrada)
FIGURES 25–29. Hypsibius cf. convergens (Urbanowicz, 1925) from Poland, seen in PCM: 25—habitus, ventral view; 26— bucco-pharyngeal apparatus; 27—claws I; 28—claws IV; Hypsibius pallidus Thulin, 1911 from Poland, seen in PCM: 29— claws IV. All scale bars in µm.
FIGURES 5–8 in An integrative redescription of Hypsibius dujardini (Doyère, 1840), the nominal taxon for Hypsibioidea (Tardigrada: Eutardigrada)
FIGURES 5–8. Hypsibius dujardini (Doyère, 1840), claws: 5—claws I (PCM, neoparatype); 6—claws IV, the arrowhead indicates the longitudinal bar at the posterior claw base, and the empty arrowhead indicates the pseudolunula at the anterior claw base (PCM, neoparatype); 7—claws II (SEM, neoparatype); 8—claws IV, the empty arrowhead indicates the pseudolunula at the anterior claw base (SEM, neoparatype). All scale bars in µm.
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Allen Brain Atlas
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OpenNeuro
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