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242 results for “distributed systems”
Distributed Multi-objective Optimization in Cyber-Physical Energy Systems
<p>The data includes results for a distributed multi-objective optimization in Cyber-Physical Energy Systems. The respective implementation for the scenarios can be found here: https://github.com/Digitalized-Energy-Systems/MOO-CPES/releases/tag/Distributed_Multi-objective_Optimization_in_Cyber-Physical_Energy_Systems<br>In this case, a multi-agent system exists for the optimization in which agents represent chp units or wind plants. For the optimization using the agents, the agents have to fulfill a target schedule, with contains of the sum of all unit schedules. Regarding the target schedule, three objectives are considered: minimizing the difference between the<br>produced power in sum and the given target schedule, minimizing the emissions and minimizing the uncertainties.</p>
DT-MAS architecture for smart maintenance of aircraft fuel distribution systems
<p><strong>Project Goal:</strong> Develop a digital twin architecture using a multi-agent system and AI for smart maintenance of aircraft distribution systems.</p> <p><strong>Objective:</strong> Build a reliable model that accurately represents the real system in an offline environment.</p> <p><strong>Methodology : </strong></p> <ul> <li>Developed a simulation based on an aircraft distribution system model, mimicking real system behavior.</li> <li>Created a dataset with four runs, five scenarios per run, and five operating points per scenario.</li> <li>Simulated healthy and faulty conditions using MATLAB-injected faults across various categories.</li> <li>Focused on four system components: hydraulic pump, tanks, engines, and pumps.</li> <li>Generated data for 11 healthy and faulty scenarios, including six fault types: <ul> <li>Noise on instruments</li> <li>Abnormal instrument readings</li> <li>Minor service problems</li> <li>External leakage</li> <li>Parameter deviation</li> <li>Structural deficiency</li> </ul> </li> <li>Features used for analysis: <ul> <li>Pump flow for pumps</li> <li>Pump motor speed for hydraulic pumps</li> <li>Driver power</li> <li>Tank volume and temperature</li> </ul> </li> </ul> <p><strong>Expected Results:</strong></p> <ul> <li>Compare performance of different asset health estimation models.</li> <li>Develop new predictive maintenance strategies.</li> <li>Predict and emulate complex aircraft behavior through multi-agent systems and AI.</li> </ul>
Distribution. Endemic to Trinidad I and Venezuela E of Lake Maracaibo, along the coast from Falcon State to Miranda State, the northern Mts (Cordillera Oriental, Cordillera Central, and Coro System), and extending S through the Llanos to the Rio Orinoco; it may extend into Arauca State, Colombia. in Atelidae
Distribution. Endemic to Trinidad I and Venezuela E of Lake Maracaibo, along the coast from Falcon State to Miranda State, the northern Mts (Cordillera Oriental, Cordillera Central, and Coro System), and extending S through the Llanos to the Rio Orinoco; it may extend into Arauca State, Colombia.
Subspecies and Distribution. S. I. labiatusE. Geoffroy Saint-Hilaire, 1812 — W Brazil, SE Peru, and N Bolivia, between the Rio Purus and Rio Madeira-Abuna system, S of the Rio Ipixuna, crossing the headwaters of the Rio Abuna in Bolivia, and S to the Rio Tahuamanu in N Bolivia, extending into SE Peru, but not W of the headwaters of the Rio Purus. S. L rufiventer Gray, 1843 — W Brazil (Amazonas State), between the rios Madeira and Purus, S from the Rio Solimoes to the Rio Ipixuna. S. I. thomasi Goeldi, 1907 — NW Brazil (Amazonas State), between the rios Japura and Solimoes, from the Auati-Parana to the Rio Tonantins. in Callitrichiade
Subspecies and Distribution. S. I. labiatusE. Geoffroy Saint-Hilaire, 1812 — W Brazil, SE Peru, and N Bolivia, between the Rio Purus and Rio Madeira-Abuna system, S of the Rio Ipixuna, crossing the headwaters of the Rio Abuna in Bolivia, and S to the Rio Tahuamanu in N Bolivia, extending into SE Peru, but not W of the headwaters of the Rio Purus. S. L rufiventer Gray, 1843 — W Brazil (Amazonas State), between the rios Madeira and Purus, S from the Rio Solimoes to the Rio Ipixuna. S. I. thomasi Goeldi, 1907 — NW Brazil (Amazonas State), between the rios Japura and Solimoes, from the Auati-Parana to the Rio Tonantins.
FIGURE 6 in Redescription of Nanomysis siamensis W.M. Tattersall, 1921 (Crustacea: Mysida) after 100 years, with an update of its distribution in the Songkhla Lagoon System southern Thailand
FIGURE 6. The abundance (ind./m2) of Nanomysis siamensis W.M. Tattersall, 1921 at the Thale Luang, Thale Sap and Thale Sap Songkhla, Songkhla lagoon System, southern Thailand, during this study in 2019-2020.
FIGURE 5. Nanomysis siamensis W.M. Tattersall, 1921 in Redescription of Nanomysis siamensis W.M. Tattersall, 1921 (Crustacea: Mysida) after 100 years, with an update of its distribution in the Songkhla Lagoon System southern Thailand
FIGURE 5. Nanomysis siamensis W.M. Tattersall, 1921. Adult male (BL 3.8 mm, L; PSUZC-20190519-04.02), adult male (BL 3.7 mm, A–E, K; PSUZC-20190520-02.01), adult male (BL 4.3 mm, N; PSUZC-20190519-02.01), ovigerous female contain egg (BL 4.0 mm, M; PSUZC-20190519-04.02) and adult female with empty marsupium (BL 3.8 mm, F–J, O; PSUZC-20190519- 05.01). A–E, Right first to fifth male pleopods; F–J, Right first to fifth female pleopods; K, Dorsal view of tail fan; L–O, Dorsal view of telson. Scale bar equal 0.2 mm for A–N.
FIGURE 4. Nanomysis siamensis W.M. Tattersall, 1921 in Redescription of Nanomysis siamensis W.M. Tattersall, 1921 (Crustacea: Mysida) after 100 years, with an update of its distribution in the Songkhla Lagoon System southern Thailand
FIGURE 4. Nanomysis siamensis W.M. Tattersall, 1921. Adult male (BL 3.7 mm, A–F; PSUZC-20190520-02.01). A, Right fifth thoracopod; B, Right sixth thoracopod; C, Right seventh thoracopod; D, Right eighth thoracopod; E, Right penis. Scale bar equal 0.2 mm for A–E.
FIGURE 3. Nanomysis siamensis W.M. Tattersall, 1921 in Redescription of Nanomysis siamensis W.M. Tattersall, 1921 (Crustacea: Mysida) after 100 years, with an update of its distribution in the Songkhla Lagoon System southern Thailand
FIGURE 3. Nanomysis siamensis W.M. Tattersall, 1921. Adult male (BL 3.7 mm, A–F; PSUZC-20190520-02.01). A, Right first thoracopod; B, Right first thoracopodal endopod enlarged; C, Right second thoracopod; D, Right second thoracopodal endopod enlarged; E, Right third thoracopod; F, Right fourth thoracopod. Scale bar equal 0.2 mm for A–F.
FIGURE 1 in Redescription of Nanomysis siamensis W.M. Tattersall, 1921 (Crustacea: Mysida) after 100 years, with an update of its distribution in the Songkhla Lagoon System southern Thailand
FIGURE 1. Map showing the sampling stations of Nanomysis siamensis W.M. Tattersall, 1921 in the Songkhla Lagoon System, southern Thailand. The black stars and red star indicate the four stations of W.M. Tattersall (1921). The red one indicates the type locality of the species and numbered 22 black dots are for the present study.
FIGURE 2. Nanomysis siamensis W.M. Tattersall, 1921 in Redescription of Nanomysis siamensis W.M. Tattersall, 1921 (Crustacea: Mysida) after 100 years, with an update of its distribution in the Songkhla Lagoon System southern Thailand
FIGURE 2. Nanomysis siamensis W.M. Tattersall, 1921. Adult male (BL 3.8 mm, A, C, E, G; PSUZC-20190519-04.02), adult male (BL 3.7 mm, J–M; PSUZC-20190520-02.01), ovigerous female contain egg (BL 4.0 mm, B, D, F, H; PSUZC-20190519- 04.02) and adult female with empty marsupium (BL 3.8 mm, I; PSUZC-20190519-05.01). A, B, Habitus lateral view; C, D, Dorsal view of anterior body; E, F, Dorsal view of right antennule; G, H, Ventral view of right antenna; I, Ventral view of labrum; J, Ventral view of mandibles with palps; K, External view of mandibles enlarged; L, Right maxillule; M, Right maxilla. Scale bar equal 0.5 mm for A–B; 0.3 for C–H; 0.2 mm for I–J; 0.1 mm for K–M.
Distribution. NE Uzbekistan, N Kyrgyzstan, SE Kazakhstan, and NW China. Occurs in the W of Tianshan Mt System (except W Karatau), just E of the cities ofJambul and Shimkent in Kazakhstan and the city of Tashkent in Uzbekistan, and extends E through Tianshan Mts (excluding inner Tianshan) surrounding Issyk-Kul Lake and Jungarian Alatau, and in China at the edge of the distribution of the Gobi Argali (O. darwini) on the Chinese-Mongolian border. in Bovidae
Distribution. NE Uzbekistan, N Kyrgyzstan, SE Kazakhstan, and NW China. Occurs in the W of Tianshan Mt System (except W Karatau), just E of the cities ofJambul and Shimkent in Kazakhstan and the city of Tashkent in Uzbekistan, and extends E through Tianshan Mts (excluding inner Tianshan) surrounding Issyk-Kul Lake and Jungarian Alatau, and in China at the edge of the distribution of the Gobi Argali (O. darwini) on the Chinese-Mongolian border.
Distribution. Endemic to N Pacific Ocean, the majority ofrecords come from W North America from 32° 42° N to 54° 18' N, also recorded on the Pacific coast ofJapan from 35% to 41° 42° N. This suggests that distribution of this species spans the N Pacific Ocean, but with no records from the C Pacific Ocean, it remains possible that there are separate E and W populations. It has been suggested that distribution of this species is related to the deep current system of the subarctic. in Ziphiidae
Distribution. Endemic to N Pacific Ocean, the majority ofrecords come from W North America from 32° 42° N to 54° 18' N, also recorded on the Pacific coast ofJapan from 35% to 41° 42° N. This suggests that distribution of this species spans the N Pacific Ocean, but with no records from the C Pacific Ocean, it remains possible that there are separate E and W populations. It has been suggested that distribution of this species is related to the deep current system of the subarctic.
Subspecies and Distribution. P.g.gangeticaLebeck,1801—Ganges-Brahmaputra-MeghnaandKarnaphuli-SanguriversystemsofSNepal,N&NEIndia,andBangladesh. P. g. minor Owen, 1853 — Indus River system of SC Pakistan and NW India (Beas River). in Platanistidae
Subspecies and Distribution. P.g.gangeticaLebeck,1801—Ganges-Brahmaputra-MeghnaandKarnaphuli-SanguriversystemsofSNepal,N&NEIndia,andBangladesh. P. g. minor Owen, 1853 — Indus River system of SC Pakistan and NW India (Beas River).
Distribution. Coasts of E Central America and NE South America from c.16° N in Honduras to ¢.27° S in S Brazil. Range into the Orinoco River system in Venezuela is mapped for this species, but it is uncertain if this population belongs to the Guiana Dolphin or the Tucuxi (S. fluviatilis). in Delphinidae
Distribution. Coasts of E Central America and NE South America from c.16° N in Honduras to ¢.27° S in S Brazil. Range into the Orinoco River system in Venezuela is mapped for this species, but it is uncertain if this population belongs to the Guiana Dolphin or the Tucuxi (S. fluviatilis).
Subspecies and Distribution. 1. t. truncatus Montagu, 1821 — worldwide in temperate and tropical waters as far S as New Zealand and generally as far as 45° N, but reaching the Faroe Is in the N Atlantic. 1: 1. ponticus Barabash-Nikiforov, 1940 — inhabits the Black Sea, Kerch Strait along with the connecting part of the Azov Sea, and the Turkish Straits system. in Delphinidae
Subspecies and Distribution. 1. t. truncatus Montagu, 1821 — worldwide in temperate and tropical waters as far S as New Zealand and generally as far as 45° N, but reaching the Faroe Is in the N Atlantic. 1: 1. ponticus Barabash-Nikiforov, 1940 — inhabits the Black Sea, Kerch Strait along with the connecting part of the Azov Sea, and the Turkish Straits system.
Subspecies and Distribution. C. o. obtusirostris Peters, 1851 — Save and Changane river systems of C & S Mozambique, with marginal intrusion into SE Zimbabwe and Limpopo Province of NE South Africa. C. o. chrysillus Thomas & Schwann, 1905 — from Maputo, S Mozambique, S to Maputaland, NE KwaZulu-Natal, E South Africa. C. o. limpopoensis Roberts, 1946 — from around mouth of Limpopo River S to coastal plains near Maputo, SE Mozambique. in Chrysochloridae
Subspecies and Distribution. C. o. obtusirostris Peters, 1851 — Save and Changane river systems of C & S Mozambique, with marginal intrusion into SE Zimbabwe and Limpopo Province of NE South Africa. C. o. chrysillus Thomas & Schwann, 1905 — from Maputo, S Mozambique, S to Maputaland, NE KwaZulu-Natal, E South Africa. C. o. limpopoensis Roberts, 1946 — from around mouth of Limpopo River S to coastal plains near Maputo, SE Mozambique.
Distribution. Amazonian lowlands of E Brazil S of the Amazon River, extending S to the cerrado biome in EC Brazil, primarily in the Rio Tapajos, Rio Xingu, and Rio Tocantins-Araguaia fluvial systems of Para, Maranhao, Tocantins, Minas Gerais, Goias, and Mato Grosso states. in Echimyidae
Distribution. Amazonian lowlands of E Brazil S of the Amazon River, extending S to the cerrado biome in EC Brazil, primarily in the Rio Tapajos, Rio Xingu, and Rio Tocantins-Araguaia fluvial systems of Para, Maranhao, Tocantins, Minas Gerais, Goias, and Mato Grosso states.
Distribution. Cameroon (S Sanaga River) S and E to the Congo/Ubangiriver system in Central African Republic, Equatorial Guinea (Rio Muni), Republic of the Congo, Gabon, and Angola; it may be present in W DR Congo. in Lorisidae
Distribution. Cameroon (S Sanaga River) S and E to the Congo/Ubangiriver system in Central African Republic, Equatorial Guinea (Rio Muni), Republic of the Congo, Gabon, and Angola; it may be present in W DR Congo.
Distribution. SE Brazil (W Rio de Janeiro, much of Sao Paulo, and S Minas Gerais states), from the Parana/Parnaiba river system E to Mantiqueira and Espinhaco ranges, N to the upper Rio Sao Francisco, and S to the Rio Tieteé. in Phitheciidae
Distribution. SE Brazil (W Rio de Janeiro, much of Sao Paulo, and S Minas Gerais states), from the Parana/Parnaiba river system E to Mantiqueira and Espinhaco ranges, N to the upper Rio Sao Francisco, and S to the Rio Tieteé.
Distribution. Amazonian Brazil (Amazonas State), S of the Rio Solimoes, E of the lower Rio Jurua, and W of the Purus/Tapaua river system; the S limit ofits geographic distribution remains unclear. in Phitheciidae
Distribution. Amazonian Brazil (Amazonas State), S of the Rio Solimoes, E of the lower Rio Jurua, and W of the Purus/Tapaua river system; the S limit ofits geographic distribution remains unclear.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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