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712 results for “towns”
FIGURES 48–52 in Review of the New World genus Acrotaphus Townes, 1960 (Hymenoptera: Ichneumonidae: Pimplinae), with descriptions of fifteen new species
FIGURES 48–52. Acrotaphus cuzconus sp. n., ♀ (holotype): 48, habitus; 49, head, dorsal view; 50, face, frontal view; 51, tarsal claw, scale bar =0.2 mm. 52. Distribution of Acrotaphus cuzconus sp. n. in the Neotropical region.
FIGURES 137–146 in Review of the New World genus Acrotaphus Townes, 1960 (Hymenoptera: Ichneumonidae: Pimplinae), with descriptions of fifteen new species
FIGURES 137–146. Acrotaphus latifasciatus (Cameron): 137, habitus, ♀ (holotype); 138, head, dorsal view, ♀ (holotype); 139, face, frontal view, ♀ (holotype); 140, habitus, ♂; 141, head, frontal view, ♂; 142, tarsal claw, ♀ (holotype); 143, sternite IX, ♂; 144, genital capsule, lateral view, ♂; 145, genital capsule, ventral view, ♂. Scale bars =0.2 mm. 146. Distribution of Acrotaphus latifasciatus (Cameron) in the Neotropical region.
FIGURES 1–7 in Review of the New World genus Acrotaphus Townes, 1960 (Hymenoptera: Ichneumonidae: Pimplinae), with descriptions of fifteen new species
FIGURES 1–7. Acrotaphus structures showing the points used to measure the proportions. 1. Head, in dorsal view: A/a =The distance of posterior ocelli from eyes / its own maximum diameter; B/b =margin of gena / length of eye. 2. Lower face, frontal view: C/c =the width / the height (from supraclypeal suture to base of antenna). 3. Fore wing: D/d =width of the vein 2rs-m / width of the abscissa of M between 2rs-m and 2m-cu. 4. Hind wing: E/e =abscissa of Cu1 between M and cu-a / length of cu-a. 5. Mesosoma and metasoma, lateral view: F/f =distance from tegula to head / distance from tegula to hind margin of propodeum; G/g =length of the ovipositor / length of the hind tibia. 6. Metasoma, dorsal view: H/h =height of the tergite I / its posterior width; I/i =height of the tergite II / its posterior width; J/j =height of the tergite III / its posterior width; K/k =height of the tergite IV / its posterior width; L/l =height of the tergite V / its posterior width. 7. Nomenclature of sternite IX and male genitalia of the Acrotaphus species.
FIGURES 127–136 in Review of the New World genus Acrotaphus Townes, 1960 (Hymenoptera: Ichneumonidae: Pimplinae), with descriptions of fifteen new species
FIGURES 127–136. Acrotaphus kourou sp. n.: 127, habitus ♀ (holotype); 128, head, dorsal view ♀ (holotype); 129, face, frontal view ♀ (holotype); 130, habitus ♂; 131, head, dorsal view ♂; 132, tarsal claw, scale bar =0.2 mm; 133, sternite IX ♂, scale bar =0.005 mm; 134, genital capsule, lateral view ♂, scale bar =0.005 mm; 135, genital capsule, ventral view ♂, scale bar =0.005 mm. 136. Distribution of Acrotaphus kourou sp. n. in the Neotropical region.
FIGURES 53–57 in Review of the New World genus Acrotaphus Townes, 1960 (Hymenoptera: Ichneumonidae: Pimplinae), with descriptions of fifteen new species
FIGURES 53–57. Acrotaphus dolichopus sp. n., ♀ (holotype): 53, habitus; 54, head, dorsal view; 55, face, frontal view; 56, tarsal claw, scale bar =0.2 mm. 57. Distribution of Acrotaphus dolichopus sp. n. in the Neotropical region.
FIGURES 117–126 in Review of the New World genus Acrotaphus Townes, 1960 (Hymenoptera: Ichneumonidae: Pimplinae), with descriptions of fifteen new species
FIGURES 117–126. Acrotaphus japi Higa & Penteado-Dias: 117, habitus, ♀; 118, head, dorsal view, ♀; 119, face, frontal view, ♀; 120, habitus, ♂; 121, head, frontal view, ♂; 122, tarsal claw, ♀, scale bar =0.2 mm; 123, sternite IX, ♂, scale bar =0.5 mm; 124, genital capsule, lateral view, ♂, scale bar =0.5 mm; 125, genital capsule, ventral view, ♂, scale bar =0.5 mm. 126. Distribu- tion of Acrotaphus japi Higa & Penteado-Dias in the Neotropical region.
FIGURES 38–47 in Review of the New World genus Acrotaphus Townes, 1960 (Hymenoptera: Ichneumonidae: Pimplinae), with descriptions of fifteen new species
FIGURES 38–47. Acrotaphus chedelae Gauld: 38, habitus ♀ (holotype), by Ronald Zuñiga; 39, head, dorsal view ♀; 40, face, frontal view ♀; 41; habitus ♂; 42 head, dorsal view ♂; 43, tarsal claw ♀; 44, sternite IX ♂; 45, genital capsule, lateral view ♂; 46, genital capsule, ventral view ♂. Scale bars =0.2 mm. 47. Distribution of Acrotaphus chedelae Gauld in the Neotropical region.
FIGURES 28–37 in Review of the New World genus Acrotaphus Townes, 1960 (Hymenoptera: Ichneumonidae: Pimplinae), with descriptions of fifteen new species
FIGURES 28–37. Acrotaphus bodoquenaensis sp. n.: 28, habitus ♀ (holotype); 29, head, dorsal view ♀ (holotype); 30, face, frontal view ♀ (holotype); 31; habitus ♂ (paratype); 32 head, dorsal view ♂ (paratype); 33, tarsal claw ♀ (holotype), scale bar =0.2 mm; 34, sternite IX ♂, scale bar =0.005 mm; 35, genital capsule, lateral view ♂, scale bar =0.005 mm; 36, genital capsule, ventral view ♂, scale bar =0.005 mm.37. Distribution of Acrotaphus bodoquenaensis sp. n. in the Neotropical region.
FIGURES 82–91 in Review of the New World genus Acrotaphus Townes, 1960 (Hymenoptera: Ichneumonidae: Pimplinae), with descriptions of fifteen new species
FIGURES 82–91. Acrotaphus franklini Gauld: 82, habitus, ♀ (holotype), by Ronald Zuñiga; 83, head, dorsal view, ♀ (para- type); 84, face, frontal view, ♀ (paratype); 85, habitus, ♂; 86, head, dorsal view, ♂; 87, tarsal claw, ♀, paratype; 88, sternite IX, ♂; 89, genital capsule, lateral view, ♂; 90, genital capsule, ventral view, ♂. Scale bars =0.2 mm. 91. Distribution of Acrotaphus franklini Gauld in the Neotropical region.
FIGURES 92–101 in Review of the New World genus Acrotaphus Townes, 1960 (Hymenoptera: Ichneumonidae: Pimplinae), with descriptions of fifteen new species
FIGURES 92–101. Acrotaphus fuscipennis (Cresson): 92, habitus, ♀; 93, head, dorsal view, ♀; 94, face, frontal view, ♀; 95, habitus, ♂; 96, head, dorsal view, ♂; 97, tarsal claw, ♀; 98, sternite IX, ♂; 99, genital capsule, lateral view, ♂; 100, genital cap- sule, ventral view, ♂. Scale bars =0.2 mm. 101. Distribution of Acrotaphus fuscipennis (Cresson) in the Neotropical region.
FIGURES 102–106 in Review of the New World genus Acrotaphus Townes, 1960 (Hymenoptera: Ichneumonidae: Pimplinae), with descriptions of fifteen new species
FIGURES 102–106. Acrotaphus homeofranklini sp. n., ♀ (holotype): 102, habitus; 103, head, dorsal view; 104, face, frontal view; 105, tarsal claw, scale bar =0.2 mm. 106. Distribution of Acrotaphus homeofranklini sp. n. in the Neotropical region.
Mandhal मांढळ (Maharashtra). View of one of a pair of tanks to the south of the town
<p>Mandhal मांढळ (Maharashtra). View of one of a pair of tanks to the south of the town, looking south toward Hudki Tekri, the hillock where a number of Vākāṭaka sculptures were found. At the ends of the tank proper, a brick temple and Śiva liṅgas of the Vākāṭaka period were discovered during excavations conducted by Nagpur University.</p>
FIGURE 8 in Ten new species of parasitoid wasps Mnioes Townes, 1946 (Hymenoptera: Ichneumonidae: Banchinae) described from Peru
FIGURE 8. Details of Mnioes tawa sp. nov. A. Habitus in lateral view of female (holotype) B. Habitus in lateral view of male (paratype) (scale bars = 1 mm).
FIGURE 3 in Ten new species of parasitoid wasps Mnioes Townes, 1946 (Hymenoptera: Ichneumonidae: Banchinae) described from Peru
FIGURE 3. Details of Mnioes iskay sp. nov. (holotype). A. Lateral habitus of female (scale bar = 1 mm) B. Dorsal view of propodeum C. Dorsal view of metasomal tergites I–II.
FIGURE 1 in Ten new species of parasitoid wasps Mnioes Townes, 1946 (Hymenoptera: Ichneumonidae: Banchinae) described from Peru
FIGURE 1. Details of Mnioes attenboroughi sp. nov. (paratype) A. Lateral habitus of female (scale bar = 1 mm), B. Lateral habitus of male (scale bar = 1 mm) C. Facial view of female D. Propodeum and first two metasomal tergites of female.
The FAIR is in Town: figshare, The Turing Way, and Open Science Quest at the OSFAIR2019
<p><strong>Episode Summary:</strong> </p> <p>In this episode we are highlighting some of the tools on show at the Open Science FAIR 2019 in Porto, Portugal. </p> <p><strong>Links: </strong></p> <ul> <li><a href="https://figshare.com/">figshare</a> <ul> <li><a href="https://figshare.com/authors/Alan_Hyndman/580840">Alan Hyndman</a></li> </ul> </li> <li><a href="https://the-turing-way.netlify.com/introduction/introduction">The Turing Way Book</a></li> <li><a href="https://github.com/alan-turing-institute/the-turing-way">The Turing Way GitHub </a> <ul> <li><a href="https://www.research.manchester.ac.uk/portal/rachael.ainsworth.html">Rachael Ainsworth</a></li> </ul> </li> <li><a href="https://zenodo.org/record/2646121#.XYJVASgzZPY">Open Science Quest</a> <ul> <li><a href="https://twitter.com/jonatortue">Jonathan England</a></li> </ul> </li> </ul> <p><strong>Quotes:</strong></p> <p>'So two reasons: because you have to and just because it is for the good of society'</p> <p>'Make reproducible research too easy not to do'</p> <p>'I wanted to change the way people became aware of Open Science best practices'</p>
Health profile of elderly users of a town public program of physical activity: a cross-sectional study
<p>This repository contains the full database generated in the study entitled "Health profile of elderly users of public physical activity programs in the city of Porto Alegre" (Hospital de Clínicas de Porto Alegre). This project was approved by the Institutional Review Board (IRB) in 2018 and carried out between 2018-2020.</p> <p> </p>
FIGURE 2 in A new species and southernmost record of Cestrus Townes (Hymenoptera Ichneumonidae, Cryptinae)
FIGURE 2. Cestrus itatiensis sp. nov., Holotype female. A. Head, frontal view. B. Propodeum, dorsal view. C. Apex of ovipositor, left side. D. Dorsal view.
Data from: Sleepless in town – drivers of the temporal shift in dawn song in urban European Blackbirds
Organisms living in urban environments are exposed to different environmental conditions compared to their rural conspecifics. Especially anthropogenic noise and artificial night light are closely linked to urbanization and pose new challenges to urban species. Songbirds are particularly affected by these factors, because they rely on the spread of acoustic information and adjust their behaviour to the rhythm of night and day, e.g. time their dawn song according to changing light intensities. Our aim was to clarify the specific contributions of artificial night light and traffic noise on the timing of dawn song of urban European Blackbirds (Turdus merula). We investigated the onset of blackbird dawn song along a steep urban gradient ranging from an urban forest to the city centre of Leipzig, Germany. This gradient of anthropogenic noise and artificial night light was reflected in the timing of dawn song. In the city centre, blackbirds started their dawn song up to 5 hours earlier compared to those in semi-natural habitats. We found traffic noise to be the driving factor of the shift of dawn song into true night, although it was not completely separable from the effects of ambient night light. We additionally included meteorological conditions into the analysis and found an effect on the song onset. Cloudy and cold weather delayed the onset, but cloud cover was assumed to reflect night light emissions, thus, amplified sky luminance and increased the effect of artificial night light. Beside these temporal effects, we also found differences in the spatial autocorrelation of dawn song onset showing a much higher variability in noisy city areas than in rural parks and forests. These findings indicate that urban hazards such as ambient noise and light pollution show a manifold interference with naturally evolved cycles and have significant effects on the activity patterns of urban blackbirds.
Data from: Social capital predicts corruption risk in towns
Corruption is a social plague: gains accrue to small groups, while its costs are borne by everyone. Significant variation in its level between and within countries suggests a relationship between social structure and the prevalence of corruption, yet, large-scale empirical studies thereof have been missing due to lack of data. In this paper, we relate the structural characteristics of social capital of settlements with corruption in their local governments. Using datasets from Hungary, we quantify corruption risk by suppressed competition and lack of transparency in the settlement's awarded public contracts. We characterize social capital using social network data from a popular online platform. Controlling for social, economic and political factors, we find that settlements with fragmented social networks, indicating an excess of bonding social capital has higher corruption risk, and settlements with more diverse external connectivity, suggesting a surplus of bridging social capital is less exposed to corruption. We interpret fragmentation as fostering in-group favouritism and conformity, which increase corruption, while diversity facilitates impartiality in public life and stifles corruption.
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Allen Brain Atlas
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International Brain Laboratory public data
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