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opennotspecifiedJun 2015View details →

Distribution. SE Australia: confined to two subpopulations in NE Victoria (East Gippsland and the Barry Mts) and another in far SE New South Wales (South East Forests National Park and Yambulla State Forest). in Potoroidae

Distribution. SE Australia: confined to two subpopulations in NE Victoria (East Gippsland and the Barry Mts) and another in far SE New South Wales (South East Forests National Park and Yambulla State Forest).

Distribution. Malay Peninsula in S Thailand (only in a small area on the border with Malaysia), NW & C Peninsular Malaysia (largely restricted to mountainous areas in the W of the country, S of the Perak River and N of the Muar River, and Tasek Bera across to the Pahang River), and W Sumatra where confined to the Barisan Mts; it may have formerly occurred on Bangka I. in Hylobatidae

Distribution. Malay Peninsula in S Thailand (only in a small area on the border with Malaysia), NW & C Peninsular Malaysia (largely restricted to mountainous areas in the W of the country, S of the Perak River and N of the Muar River, and Tasek Bera across to the Pahang River), and W Sumatra where confined to the Barisan Mts; it may have formerly occurred on Bangka I.

opennotspecifiedJul 2018View details →

Distribution. Restricted to the Kahuzi Mts in E DR Congo; confined to a small montane region W of Lake Kivu between Lwiro and Mt Kahuzi (1700-3300 m). Probably widely distributed in undisturbed areas above 2000 m. in Soricidae

Distribution. Restricted to the Kahuzi Mts in E DR Congo; confined to a small montane region W of Lake Kivu between Lwiro and Mt Kahuzi (1700-3300 m). Probably widely distributed in undisturbed areas above 2000 m.

opennotspecifiedJul 2018View details →

Distribution. Confined to the upper slopes of Mt Kinabalu, although one damaged skull from Sarawak could represent this species. This would extend its range further S to other high mountains of Borneo, butit is unlikely, given the currently negative results in other high mountains of Sabah that have been sampled. in Soricidae

Distribution. Confined to the upper slopes of Mt Kinabalu, although one damaged skull from Sarawak could represent this species. This would extend its range further S to other high mountains of Borneo, butit is unlikely, given the currently negative results in other high mountains of Sabah that have been sampled.

Distribution. NW India, confined to the Chamba Valley of Himachal Pradesh State; it may also occur in the Kishtwar Valley ofJammu and Kashmir State. in Cercopithecidae

Distribution. NW India, confined to the Chamba Valley of Himachal Pradesh State; it may also occur in the Kishtwar Valley ofJammu and Kashmir State.

Distribution. Borneo, confined to an area of E Kalimantan, from the Kayan and Sembakung (= Sebuku) rivers in the N, S, and SW to the Mahakam River, the W boundary is not well known but certainly E of the Apau Kayan and the Kayan Mentarang National Park. in Cercopithecidae

Distribution. Borneo, confined to an area of E Kalimantan, from the Kayan and Sembakung (= Sebuku) rivers in the N, S, and SW to the Mahakam River, the W boundary is not well known but certainly E of the Apau Kayan and the Kayan Mentarang National Park.

Distribution. SE coastal Kenya, confined to a narrow stretch of forest along the lower Tana River, mainly from Garsen N nearly as far as Wenje; recently also found in the forests of the Tana River Delta. in Cercopithecidae

Distribution. SE coastal Kenya, confined to a narrow stretch of forest along the lower Tana River, mainly from Garsen N nearly as far as Wenje; recently also found in the forests of the Tana River Delta.

opennotspecifiedNov 2017View details →

Distribution. Uncertain but believed to have scattered distribution in E Africa; some authorities confine range to Imoteng Mts in South Sudan, Kakamega Forest in Kenya, and Mbete and Mufindi in Tanzania. in Muridae

Distribution. Uncertain but believed to have scattered distribution in E Africa; some authorities confine range to Imoteng Mts in South Sudan, Kakamega Forest in Kenya, and Mbete and Mufindi in Tanzania.

opennotspecifiedNov 2017View details →

Distribution. Formerly widespread across NW Australia, but now confined to rugged areas of the N Kimberley region, Western Australia, and the islands of Augustus, Carlia, Chambers, Cockatoo, Conilurus, Hidden, Jar, Lachlan, Uwins, Wargul Wargul, and Wollaston, off the Kimberley mainland. in Muridae

Distribution. Formerly widespread across NW Australia, but now confined to rugged areas of the N Kimberley region, Western Australia, and the islands of Augustus, Carlia, Chambers, Cockatoo, Conilurus, Hidden, Jar, Lachlan, Uwins, Wargul Wargul, and Wollaston, off the Kimberley mainland.

opencc-by-4.0Jun 2022View details →

Scaling theory of wave confinement in classical and quantum periodic systems

Data repository to manuscript 'Scaling theory of wave confinement in classical and quantum periodic systems'. The upload contains the file "README.txt" explaining the content of the upload.

opencc-by-4.0Apr 2024View details →

Data for article "Non-Stokesian dynamics of magnetic helical nanoswimmers under confinement

<h4>Data for article "Non-Stokesian dynamics of magnetic helical nanoswimmers under confinement", A. Fazeli, V. Thakore, T. Ala-Nissila, M. Karttunen</h4> ● Published version: https://doi.org/10.1093/pnasnexus/pgae182 ● Preprint version: https://doi.org/10.48550/arXiv.2311.00839   The article studied the effect of the degree of confinement on the propulsion of electromagnetically propelled helical nanoswimmers. The helices were subjected to different degrees of confinement between two infinite parallel plates and driven using a rotating magnetic field at different frequencies. The degree of confinement (Gamma) is defined as the ratio of a helix’s outer diameter over the distance between the two boundary plates. At the highest level in the directory hierarchy, there are two folders, i.e., “Simulation_Production_Files”, and “Simulations_by_Nanoswimmers”. The first one consists of the source code of the Lattice-Boltzmann Method package implemented in LAMMPS used for running the simulations. It also includes a Matlab script used for calculating the required simulation variables to put in the LAMMPS input script for a given simulation. The other folder, i.e., “Simulations_by_Nanoswimmers”, has subfolders first broken down by the swimmer’s name (i.e., H0-8), then by Gamma, and finally by field driving frequency. Each simulation folder, i.e., at “Simulations_by_Nanoswimmers/H0*/Gamma_0.*/Field_Frequency_*/”, consists of seven types of file as described in the table below. <table> <tbody> <tr> <td> File </td> <td> Description </td> </tr> <tr> <td> script.in </td> <td> LAMMPS input script. LAMMPS executes calculations by reading commands from this file. </td> </tr> <tr> <td> H*.data </td> <td> Swimmer’s geometry data file. This lists the xyz coordinates of the constituent atoms of the helix’s surface area.   </td> </tr> <tr> <td> bodies-*.lammpstrj </td> <td> A simulation output file. This lists the xyz coordinates of all helix’s atoms per timestep. </td> </tr> <tr> <td> H1cm-*.lammpstrj </td> <td> A simulation output file. This lists the xyz coordinates and linear velocities of the helix’s center of mass per timestep. </td> </tr> <tr> <td> H1omega-*.lammpstrj </td> <td> A simulation output file. This lists the xyz coordinates and linear velocities of an outer atom (i.e., an atom with a distance of minor radius plus major radius from the helix’s centerline). The tangential velocities of this atom are used to calculate the helix’s angular velocity.     </td> </tr> <tr> <td> H1plane-*.lammpstrj </td> <td> A simulation output file. This lists the xyz coordinates of the three atoms used to construct a hypothetical plane fixed with respect to the helix body. This plane is used to keep track of orientation when calculating the helix’s angular velocity. </td> </tr> <tr> <td> torques-*.txt </td> <td> A simulation output file. These list the viscous drag torque experienced by the helix around the x-, y-, and z- axes. </td> </tr> </tbody> </table>   The asterisks refer to the Shell (bash) wildcard character.

opencc-by-4.0May 2024View details →

Data and code for paper: Design Optimization of Geometric-Confined Cardiac Organoids Enabled by Machine Learning Techniques

Collection of the code for the generation of figures, analysis and data for the paper: Design Optimization of Geometric-Confined Cardiac Organoids Enabled by Machine Learning Techniques. Ensemble learning classifiers, PACMAP & Trimap code in python file. All figures and additional analysis in R code.

opencc-by-4.0Mar 2024View details →

Data for critical fluctuations in a confined driven-dissipative quantum condensate

All the raw data sets collected for this project are included in this submission. 'Readme.text' files are included with the data sets explaining what the data sets are and how to read them.  We divided the real space data into 8 diifferent files for uploading purposes. We had trouble uploading it as a single file due to the large file size so we divided the data into 8 different files.  Files real_space_data_1,real_space_data_2, real_space_data_3, real_space_data_4, real_space_data_5, real_space_data_6,real_space_data_7 and real_space_data_8  are a SINGLE data set.

FIGURES 29–38 in A review of Coelopoetinae (Lepidoptera, Gelechioidea, Pterolonchidae), a moth subfamily confined to western North America, with descriptions of seven new species

FIGURES 29–38. Male genitalia of Coelopoeta spp. Above lateral view with juxta and one valva excluded; below ventral view, with phallus excluded. Figure 29. C. glutinosi Walsingham. Figure 30: C. aprica sp. nov., holotype; Figure 31: C. phaceliae Kaila, California, Nevada Co.; Figure 32: C. aurora sp. nov., holotype; Figure 33: C. fulminea sp. nov., holotype; Figure 34: C. alboflava sp. nov., holotype; Figure 35: C. sariae sp. nov., holotype; Figure 36: C. maiadella sp. nov., holotype; Figure 37: C. fissurina sp. nov., holotype; 38: C. valalbui sp. nov., holotype.

FIGURES 2–4. 2 in A review of Coelopoetinae (Lepidoptera, Gelechioidea, Pterolonchidae), a moth subfamily confined to western North America, with descriptions of seven new species

FIGURES 2–4. 2. Head of Coelopoeta glutinosi Walsingham; 3. Head of Coelopoeta phaceliae Kaila; 4. Abdominal skin of Coelopoeta aurora (L. Kaila prep. 6374) showing the shape of sternum 2 and the spine bands of tergal segments.

FIGURE 1. A in A review of Coelopoetinae (Lepidoptera, Gelechioidea, Pterolonchidae), a moth subfamily confined to western North America, with descriptions of seven new species

FIGURE 1. A neighbor-joining tree, generated under the K2P nucleotide substitution model of 16 barcode sequences retrieved from Coelopoeta specimens.

FIGURE 44 in A review of Coelopoetinae (Lepidoptera, Gelechioidea, Pterolonchidae), a moth subfamily confined to western North America, with descriptions of seven new species

FIGURE 44. Gall made by the larva of C. glutinosi on Eriodictyon californicum. Photo, courtesy of Valeriu Albu with permission to use.

FIGURES 11–16 in A review of Coelopoetinae (Lepidoptera, Gelechioidea, Pterolonchidae), a moth subfamily confined to western North America, with descriptions of seven new species

FIGURES 11–16. Habitus of Coelopoeta spp. All images at the same scale as the first image. Figure 11: C. aprica sp. nov, ♂, holotype; Figure 12: C. aprica sp. nov., ♀, paratype, California, San Diego County; Figure 13: C. phaceliae Kaila, ♂, California, Plumas County; Figure 14: C. phaceliae, ♂, California, Solano County; Figure 15: C. phaceliae, ♂, paratype, California, San Mateo County; Figure 16: C. phaceliae, ♂, paratype, California, Siskiyou County.

FIGURES 23–28 in A review of Coelopoetinae (Lepidoptera, Gelechioidea, Pterolonchidae), a moth subfamily confined to western North America, with descriptions of seven new species

FIGURES 23–28. Habitus of Coelopoeta spp. All images at the same scale as the first image. Figure 23: C. fulminea sp. nov., ♀, paratype, Canada, British Columbia, Manning Park; Figure 24: C. alboflava sp. nov., ♂, holotype; Figure 25: C. sariae sp. nov. ♂, holotype; Figure 26: C. maiadella Kaila, ♂, holotype; Figure 27: C. fissurina sp. nov., ♂, holotype; Figure 28. C. valalbui, ♂, holotype.

FIGURES 5–10 in A review of Coelopoetinae (Lepidoptera, Gelechioidea, Pterolonchidae), a moth subfamily confined to western North America, with descriptions of seven new species

FIGURES 5–10. Habitus of Coelopoeta glutinosi Walsingham. All images at the same scale as the first image. Figure 5: ♂, California, Marin County; Figure 6: ♂, California, Los Angeles County; Figure 7: ♀, California, Solano County; Figure 8: ♂, California, Ventura County; Figure 9: ♀, California, Monterey County; Figure 10: ♀, California, Los Angeles County.