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35 results for “Peloponnese”
Wind and SOLAR RES predicted production data for Crete and Peloponnese - ONENET WP8
<p>WP8 aimed at the development and implementation of a web based app that enhances Active Power Management necessary for coordination of a TSOs and DSOs, using AI methods and cloud calculation engines that was tested in Peloponnese and Crete regions. Full description of the scope and results of WP8 Greek demo can be found in the relative deliverable <em>D8.2: Development and implementation of the “F-Channel” platform</em> (https://www.onenet-project.eu//wp-content/uploads/2023/10/OneNet_D8.2_V1.0.pdf). For purpose of this project similar, historical weather data in 1 hour resolution have been used in order to obtain behavior patterns of climatic parameters (daily, monthly, season) throughout region of interest. For this purpose various ERA5 climatic datasets has been used and AI algorithms applied in combination with terrain orography data. Modeled results was <strong>compared </strong>with <strong>operational data </strong>from TSO/DSO and appropriate model calibration has been provided based on deep learning AI algorithms.</p> <p>The data for Wind power plant modelled production is given in file <<a href="../api/records/10848817/draft/files/wind_res_onenet_wp8.csv/content" target="_blank" rel="noopener noreferrer">wind_res_onenet_wp8.csv</a>> in the following columns <time> ; <aa> ; <pw> ; <ws> ; <wp_name> . Columns are related to: Hourly time, wind park code, power [MWh], wind speed [m/s] and wind park name, respectively.</p> <p>The data for Solar power plant modelled production is given in file <<a href="../api/records/10848817/draft/files/solar_onenet_wp8.csv/content" target="_blank" rel="noopener noreferrer">solar_onenet_wp8.csv</a>> in the following columns <time> ; <name> ; <pw> ; <ta> ; <ghi> . Columns are related to: Hourly time, solar park name, power in MWh, ambient temperature and Global Horizontal irradiance [W/m2], respectively.</p>
Figure 1 in New localities of Iurus dufoureius dufoureius (Brullé, 1832) in the Peloponnese, Greece (Scorpiones: Iuridae)
Figure 1: Distribution of Iurus dufoureius dufoureius. White squares, new localities; black circles, localities known from literature.
Fig. 1-2 in Cryptophagus peloponnesicus nov.sp. (Cryptophagidae) from Peloponnese, Greece
Fig. 1-2: (1) Cryptophagus peloponnesicus nov.sp., holotype, habitus; (2) parameres. Fig. 3-4: (3) Cryptophagus axillaris REITTER, 1875, Romania, habitus; (4) Cryptophagus brisouti REITTER, 1874.
Western Peloponnese Seismological Data Acquisition - July 2016 to May 2017
<p><strong>2016_Data_Temporary_Network:</strong><br> Station Type: <em>3-Components Short Period</em><br> Format: <em>MSEED </em><br> Location: <em>Western Peloponnese</em><br> Deployment Time: <em>July to December 2016</em></p> <p><strong>2017_Data_Temporary_Network:</strong><br> Station Type: <em>3-Components Short Period</em><br> Format: <em>MSEED </em><br> Location: <em>Western Peloponnese</em><br> Deployment Time: <em>January to May 2017</em></p> <p><strong>Stations_Positions_DDMM: </strong>Stations Locations in Degree Minute format.<br> <br> <strong>Resp_Files_Temporary_Network:</strong> Response files for all stations 3 Components</p>
Compendium of R code and data for Mycenaean roads in the Peloponnese, Greece: least-cost path modelling using R and Movecost
<p><strong>Abstract</strong></p> <p><em>This study evaluates multiple methodologies and their variants for Least Cost Path (LCP) modelling, applied in combination with different Digital Elevation Models (DEMs), to explore the broader applicability of the Movecost package, using the Mycenaean road networks of the Peloponnese (Greece) as case studies. Using a geographic information system (GIS) and the R programming environment, this paper employs the Movecost package for the R statistical package to simulate ancient routes based on existing road segments. By integrating a variety of functions and parameters, this study evaluates their effectiveness across different DEMs, including both Shuttle Radar Topography Mission DEM (SRTM-DEM) and Copernicus DEM (COP-DEM) at 30 m spatial resolution. The study also examines how varying these parameters can lead to different modelling outcomes, underscoring the necessity of calibrating least-cost analysis to specific regional contexts. The road segments around Nichoria (Messenia), Ayios Ioannis Kazarma (Argolis), and in the Berbati Valley (Argolis), provide a historical canvas against which these methodological innovations are tested with the ultimate aim of exploring the capabilities of the Movecost package and how different combinations of DEM, function, parameter, and path points can effectively model the route through the existing road remains, highlighting the variability and context-specific nature of LCP modelling. The results suggest that the 'Wheeled-vehicle critical cost function' (WCS) was effective in modelling the roads through the extant remains based on start and endpoints suggested by previous research and posited by this paper. These results further suggest that Mycenaean roads likely served as key infrastructure links between major centres and ports or harbours, underscoring their role in facilitating regional trade and communication. However, this outcome represents one of several possible results, as the appropriateness of functions and the parameters tested depend on the specific landscape and archaeological context. This underscores the importance of careful parameter selection, providing insights into the economic and social landscapes of Mycenaean Greece, while also highlighting the potential of integrating spatial data with robust computational tools to enhance our understanding of ancient infrastructure.</em></p>
Subspecies and Distribution. T:s.stankoviciV.Martino&E.Martino,1931—WMacedoniaandadjacentNWGreeceMts. T. s. montenegrina Krystufek, 1994 — restricted to coastal lowlands of S Montenegro and adjacent Albania. Also present in C & S Albania and W Greece as far S as N Peloponnese, also on Corfu I in the Ionian Sea, but subspecies involved not known. in Talpidae
Subspecies and Distribution. T:s.stankoviciV.Martino&E.Martino,1931—WMacedoniaandadjacentNWGreeceMts. T. s. montenegrina Krystufek, 1994 — restricted to coastal lowlands of S Montenegro and adjacent Albania. Also present in C & S Albania and W Greece as far S as N Peloponnese, also on Corfu I in the Ionian Sea, but subspecies involved not known.
FIGURE 6. The 50 in Spelaeonaias gen. nov., a new true-branched cyanobacterium from Cave Vlychada (Diros, Peloponnese, Greece)
FIGURE 6. The 50% majority rule consensus tree as inferred from MrBayes. Posterior probalities are provided on or below the nodes. The GenBank accession numbers of sequences are given on the right of the taxa names. The scale corresponds to substitutions/site. Characters in bold indicate the taxon from Vlychada Cave.
FIGURE 5 in Spelaeonaias gen. nov., a new true-branched cyanobacterium from Cave Vlychada (Diros, Peloponnese, Greece)
FIGURE 5. Fluorescence emission spectrum of cells obtained by the Lambda scan module of CLSM. Two-dimensional spectral characteristic of fluorescence is illuminated with the blue laser (488 nm) and recorded as arbitrary units. Note the first peak for phycoerythrin (PE) (582 nm) and the second for phycobiliproteins (PC: phycocyanin and APC: allophycocyanin) (669 nm) including the small shoulder for chlorophyll a.
FIGURE 4. A–C in Spelaeonaias gen. nov., a new true-branched cyanobacterium from Cave Vlychada (Diros, Peloponnese, Greece)
FIGURE 4. A–C. Confocal (CLSM) photomicrographs showing filaments of Spelaeonaias floccida covered by sheaths. A. 41 x-y optical sections (z step= 0.13 μm) showing the Y-type of true branching; note the central spaces devoid of fluorescence in the filaments, corresponding to the area of nucleoids. B. 30 x-y optical sections (z step= 0.13 μm) showing a degraded basal cell (dc) promoting a false branching. C. Main filament with secondary branches; division of initial cells (at arrows) implying further formation of secondary branches. Color allocation: DNA nucleic acids labelled with Hoechst 33258, cyan; reflection from minerals, white; autofluorescence of extracellular polymeric substances, green; colocalized autofluorescence of cyanobacteria in the red (phycobilins) and blue channels (chlorophylls), magenta. Scale bars = 10 μm.
FIGURE 3. A–D in Spelaeonaias gen. nov., a new true-branched cyanobacterium from Cave Vlychada (Diros, Peloponnese, Greece)
FIGURE 3. A–D. TEM micrographs of Spelaeonaias floccida showing cell division and mode of branching. A. Filament with short barrel cells showing a general view of dividing cells for branch formation; the oblique division of an initial cell at arrow. B. Oblique section at a particular part of a filament showing one heterocyte (h) with a polar plug of cyanophycin (cy) connected to the adjacent cell by a neck; note the extra wall layer (wl) surrounding the heterocyte. C. Cell division at a certain region of the filament and formation of a new septum (s); D–E. After the first division of the initial cell (ic) the resulting cell (arrow) changes polarity and is further dividing for the formation of a secondary branch. Scale bars = 2 μm (B) and 5 μm (A–D).
FIGURE 1. A–J in Spelaeonaias gen. nov., a new true-branched cyanobacterium from Cave Vlychada (Diros, Peloponnese, Greece)
FIGURE 1. A–J. LM and SEM micrographs of Spelaeonaias floccida. A. Filaments of Spelaeonaias floccida showing the main filament and the secondary branches. B. Division of an initial cell, giving rise to two cells that change division polarity for the formation of a secondary branch. C. Secondary filament with a necridic cell (nc). D–G. Main and secondary filaments with the characteristic Y-type of branching; heterocytes at arrows. H. Hormogonia with an intercalary heterocyte at arrow. I. A single hormogonium with a terminal heterocyte (arrow). J. Single hormogonium as seen under SEM; the heterocyte (arrow) in a secondary filament is also obvious. Figs A–B from fresh material. Figs C–J from cultures. Scale bars = 10 μm (A–D, F, H, I) and 20 μm (Ε, G, J).
FIGURE 2. A–F in Spelaeonaias gen. nov., a new true-branched cyanobacterium from Cave Vlychada (Diros, Peloponnese, Greece)
FIGURE 2. A–F. TEM micrographs of Spelaeonaias floccida. A. Longitudinal section showing a septum (s) without intercellular connection between vegetative cells, the outer membrane (om) and the plasma membrane (pm). Note the thick and compact sheath near the cell wall, becoming diffluent externally. the thylakoids are scattered throughout the cyatoplasm forming curled bundles of 2–4 parallel arranged membranes, with phycobilisomes (pb) on their surface. B. Grazing thin section providing a top view of phycobilisomes as stellate structures, associated with thylakoidal membranes; the plasma membrane is followed by a thin layer of peptidoglycan (pl) and an outer membrane (om). C. Carboxysomes (cb) seen as polyhedral bodies. D. Peptidoglycan layer crossed by pore structures (arrow). E–F. Nucleoid regions surrounded by thylakoids and scattered through the cytoplasm; cy = cyanophycin granule. Scale bars = 500 nm (A, C–F) and 100 nm (B).
FIGURE 4 in Hydraena lotti sp. nov., a new member of the " Haenydra " lineage from the Peloponnese (Greece), with additional records of Hydraena species in the region (Coleoptera, Hydraenidae)
FIGURE 4. Hydraena lotti sp. nov. A) – B) male metatibia; C) – D) female metatibia; E)– F) male mesotibia.
FIGURE 2 in Hydraena lotti sp. nov., a new member of the " Haenydra " lineage from the Peloponnese (Greece), with additional records of Hydraena species in the region (Coleoptera, Hydraenidae)
FIGURE 2. Hydraena lotti sp. nov. A) male elytral apex; B) female elytral apex; C) female tergite X; D) gonocoxite.
FIGURE 3 in Hydraena lotti sp. nov., a new member of the " Haenydra " lineage from the Peloponnese (Greece), with additional records of Hydraena species in the region (Coleoptera, Hydraenidae)
FIGURE 3. Hydraena lotti sp. nov. A) aedeagus, lateral view; B) aedeagus dorsal view; C) aedeagus dorsolateral view; D) spermatheca.
FIGURE 5 in Hydraena lotti sp. nov., a new member of the " Haenydra " lineage from the Peloponnese (Greece), with additional records of Hydraena species in the region (Coleoptera, Hydraenidae)
FIGURE 5. Type locality of Hydraena lotti sp. nov. Greece, Peloponnese, Taygetos Mountains, Lagadha stream above Lagadha pass, 1,100 m. Photo D.T. Bilton.
Figure 3. The hitherto known Bythinella spp. from Peloponnese Peninsula. 1 in Some new Bythinella spp. from southern Greece (Gastropoda: Bythinellidae)
Figure 3. The hitherto known Bythinella spp. from Peloponnese Peninsula. 1: Bythinella kwanti Glöer & Reuselaars, 2020, 2: B. atypicos Reischütz et al., 2008, 3: B. petrosensis Glöer & Reuselaars, 2020, 4: B. liandinaensis Glöer & Reuselaars, 2020, 5: B. beckmanni Reischütz et al., 2008.
Figure 24 from: Roháček J (2021) The Herniosina story continues in the Mediterranean: H. calabra sp. nov. from Calabria and H. erymantha Roháček, new female from the Peloponnese (Diptera, Sphaeroceridae). ZooKeys 1061: 165-190. https://doi.org/10.3897/zookeys.1061.72235
Figure 24 Herniosina erymantha Roháček, 2016, female laterally, with a mite on thoracic pleuron (Greece: Peloponnese). Body length ~ 2.2 mm.
Figures 21-22 from: Roháček J (2021) The Herniosina story continues in the Mediterranean: H. calabra sp. nov. from Calabria and H. erymantha Roháček, new female from the Peloponnese (Diptera, Sphaeroceridae). ZooKeys 1061: 165-190. https://doi.org/10.3897/zookeys.1061.72235
Figures 21-22 Habitat of Herniosina calabra sp. nov. 21 General view of the habitat in Serre Calabresi at Mongiana, alder trees and herbaceous undergrowth surrounding a small creek (25.v.2018) 22Juncus tuft, a microhabitat of the species.
Figures 15-20 from: Roháček J (2021) The Herniosina story continues in the Mediterranean: H. calabra sp. nov. from Calabria and H. erymantha Roháček, new female from the Peloponnese (Diptera, Sphaeroceridae). ZooKeys 1061: 165-190. https://doi.org/10.3897/zookeys.1061.72235
Figures 15-20 Herniosina calabra sp. nov., female paratypes. 15 Mid tibia, dorsally 16 ditto, anteriorly 17 postabdomen, dorsally 18 ditto, ventrally 19 ditto, laterally 20 spermathecae. Abbreviations: ce – cercus, S – sternum, T – tergum. Scale bars: 0.3 mm (15, 16); 0.1 mm (17–20).
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Allen Brain Atlas
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