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FIGS. 91–94 Penthetria aestimata FIG. 91 in A Revision of fossil Bibionidae (Insecta: Diptera) from the Oligocene of Germany
FIGS. 91–94 Penthetria aestimata FIG. 91. Female, wing. Syntype of Penthetria aestimata Statz. LACMIP 2533.249 / LACMIP Type 3379. FIG. 92. Male, wing. LACMIP 2533.250. FIG. 93. Female, head and thorax. LACMIP 2533.249 / LACMIP Type 3379. FIG. 94. Female, terminalia. LACMIP 2533.249 / LACMIP Type 3379.
FIGS. 85–90 Hesperinus heeri FIG. 85 in A Revision of fossil Bibionidae (Insecta: Diptera) from the Oligocene of Germany
FIGS. 85–90 Hesperinus heeri FIG. 85. Female, wing. Holotype of Penthetria rottensis Statz. LACMIP 2533.233 / LACMIP Type 3383. FIG. 86. Female, wing. Holotype of Penthetria scita Statz. LACMIP 2533.234 / LACMIP Type 3384.
FIG. 74 in A Revision of fossil Bibionidae (Insecta: Diptera) from the Oligocene of Germany
FIG. 74. Bibio giganteus, female. Holotype of Plecia heroica Heyden & Heyden, 1865. NMHUK In 58802. Image reproduced with permission from NHMUK. FIG. 75. Bibio lignarius, female. Holotype of Bibio lignarius Germar, 1837. STIPB A 601. FIG. 76. Bibio mimas, female (tentatively associated). LACMIP 2533.1066. FIG. 77. Bibio pannosus, female. Holotype of Bibio pannosus Heyden & Heyden, 1865. NMHUK In 58815. Image reproduced with permission from NHMUK. FIG. 78. Bibio rohli, female. Holotype of Bibio rohli Heyden & Heyden, 1865. LACMIP 2533.237 / LACMIP Type 3367. FIG. 79. Bibio rottensis, female. Syntype of Bibio rottensis Heyden & Heyden, 1865. LACMIP 2533.238 / LACMIP Type 3368.
FIG. 23 in A Revision of fossil Bibionidae (Insecta: Diptera) from the Oligocene of Germany
FIG. 23. Plecia dubia, female. Syntype of Protomyia abava Heyden & Heyden, 1865. NHMUK In 58799. Image reproduced with permission from NHMUK. FIG. 24. Plecia dubia, female. Holotype of Helophilus primarius Germar, 1837. STIPB A-603. FIG. 25. Plecia dubia, female. Syntype of Plecia satyrus Statz, 1943. LACMIP 2533.287 / LACMIP Type 3419. FIG. 26. Plecia dubia, female from Enspel. GDKE PE 2008 5005. FIG. 27. Plecia exigua, female. Syntype of Plecia exigua Statz, 1943. LACMIP 2533.269 / LACMIP Type 3401. FIG. 28. Plecia exigua, male. Illustrated specimen of Plecia sp. 13 Statz, 1943. LACMIP 2533.256.
FIG. 47 in A Revision of fossil Bibionidae (Insecta: Diptera) from the Oligocene of Germany
FIG. 47. Plecia pennata, female. Holotype of Plecia pennata Statz, 1943. LACMIP 2533.282 / LACMIP Type 3414. FIG. 48. Plecia pinguis, female. Syntype of Protomyia pinguis Heyden & Heyden, 1865. NHMUK In 58811. Image reproduced with permission from NHMUK. FIG. 49. Plecia pinguis, female. Holotype of Protomyia lapidaria Heyden & Heyden, 1865. NHMUK In 58813. Image reproduced with permission from NHMUK. FIG. 50. Plecia pinguis, female. Holotype of Bibio brachypteroides Meunier, 1915. Siegburg Rott-28. FIG. 51. Plecia pinguis, female. Syntype of Plecia vulpina Statz, 1943. LACMIP 2533.296 / LACMIP Type 3428. FIG. 52. Plecia pinguis, male. Illustrated specimen of Plecia sp. 5 Statz, 1943. LACMIP 2533.261.
FIG. 7 in A Revision of fossil Bibionidae (Insecta: Diptera) from the Oligocene of Germany
FIG. 7. Penthetria aestimata, male. Syntype of Penthetria aestimata Statz, 1943. LACMIP 2533.250 / LACMIP Type 3380. FIG. 8. Penthetria claripennis, female. Holotype of Plecia claripennis Théobald, 1937. NHMB F 1382. FIG. 9. Penthetria gigantea, female. Holotype of Plecia gigantea Théobald, 1937. NHMB F 1380. FIG. 10. Penthetria lugens, female (non-type specimen). NHMB F 2410. FIG. 11. Penthetria nigra, female. Holotype of Penthetria nigra Statz, 1943. LACMIP 2533.232 / LACMIP Type 3382.
FIG. 17 in A Revision of fossil Bibionidae (Insecta: Diptera) from the Oligocene of Germany
FIG. 17. Plecia collossea, female. Holotype of Plecia collossea Heyden & Heyden, 1865. NHMUK In 58789. Image reproduced with permission from NHMUK. FIG. 18. Plecia collossea, male. Illustrated specimen of Plecia sp. 1 Statz, 1943. LACMIP 2533.257. FIG. 19. Plecia collossea, male. Illustrated specimen of Plecia sp. 2 Statz, 1943. LACMIP 2533.258. FIG. 20. Plecia conica, male. Holotype of Plecia conica Théobald, 1937. NHMB F 1398. FIG. 21. Plecia dubia, female. Holotype of Phthiria dubia Germar, 1837. STIPB A-595. FIG. 22. Plecia dubia, male. Syntype of Protomyia abava Heyden & Heyden, 1865. NHMUK In 58788. Image reproduced with permission from NHMUK.
FIG. 1 in A Revision of fossil Bibionidae (Insecta: Diptera) from the Oligocene of Germany
FIG. 1. Hesperinus heeri, female. Holotype of Penthetria rottensis Statz, 1943. LACMIP 2533.233 / LACMIP Type 3383. FIG. 2. Hesperinus heeri, female. Holotype of Penthetria scita Statz, 1943. LACMIP 2533.234 / LACMIP Type 3384. FIG. 3. Hesperinus heeri, male. Holotype of Protomyia heeri Heyden & Heyden, 1865. NHMUK In 58817. Image reproduced with permission from NHMUK. FIG. 4. Hesperinus heeri, male. STIPB A-544. FIG. 5. Hesperinus heeri, male. Siegburg Rott- 594. FIG. 6. Penthetria aestimata, female. Syntype of Penthetria aestimata Statz, 1943. LACMIP 2533.249 / LACMIP Type 3379.
River Erpe (Berlin, Germany) groundwater levels, temperature and 222-radon data set, June 2019
<p>Time series of groundwater levels and temperature, chloride concentrations as well as 222-radon activities in piezometers P0 to P9 and P11 located close to Heidemühle at the River Erpe, Berlin, Germany, collected between June and November 2019. In "Rn_eql_incubations.csv", "mea" denotes the mean activity and "sdd" the associated standard deviation.</p>
Data from: Impact of caesarean section on mode of delivery, pregnancy-induced and pregnancy-associated disorders, and complications in the subsequent pregnancy in Germany
Objectives: To analyze the impact of caesarean section (CS) on mode of delivery, pregnancy-induced and pregnancy-associated disorders, as well as complications in the subsequent pregnancy within German gynecological practices. Methods: 1,801 women with CS and 1,801 matched women with vaginal delivery (VD) from the IMS Disease Analyzer database were included. The impact of previous CS on the mode of delivery and pregnancy-associated disorders as well as complications prior to or during birth in the subsequent pregnancy were analyzed. Cox regressions were used to determine the influence of CS with regard to these outcomes. Results: Medical abortion and single spontaneous delivery were significantly less frequent in women with a history of CS compared to VD (OR equal to 0.52 and 0.04 respectively), whereas CS after CS was the significantly more common mode of delivery (79.0% versus 9.3%, OR=36.47). Gestational hypertension without significant proteinuria, gestational hypertension with significant proteinuria, and polyhydramnios were more frequent in women with CS than in women with VD (OR equal to 6.80, 1.71, and 2.29). Hemorrhage and maternal care for known or suspected disproportion were more common in the CS group than in the VD group (OR equal to 1.34 and 3.75). Prolonged pregnancy, preterm labor, abnormalities arising from forces of labor, and perineal laceration during delivery were significantly less frequent in women with CS than in women with VD (OR between 0.32 and 0.75), whereas long labor was more common (OR=2.09). Conclusion: Women with CS were more likely to undergo further CS and to develop major pregnancy-associated diseases in the following pregnancy compared to women with VD.
Data from: How traffic facilitates population expansion of invasive species along roads: the case of common ragweed in Germany
1. Because common ragweed (Ambrosia artemisiifolia L., henceforth Ambrosia) has negative effects on human health, it is a common focus for management, which would benefit from a better understanding of the underlying mechanisms by which the species spreads. Road systems are known to be invasion corridors, but the conduit function of vehicles for the rapid spread of Ambrosia along roads and for population extension along roadside verges has not yet been demonstrated convincingly. 2. To quantify the effect of different traffic volumes on the dispersal and population extension of Ambrosia we used two approaches: First, by combining field experiments along roads with records of the seed rain around single plants, we simulated a combined dispersal kernel that revealed the interactions between primary dispersal and traffic-mediated secondary dispersal. Second, we recorded seedling recruitment around isolated roadside populations over two years to determine how traffic-related parameters affect population extension. 3. The longest traffic-mediated dispersal distances exceeded those of primary dispersal by about one order of magnitude. Traffic volume had a significant positive effect on dispersal distances and on the lateral deposition of seeds on the road verge. 4. Seedling recruitment around isolated roadside populations was significantly higher in the driving direction than against, but only at the distance where the major seed rain of traffic-mediated dispersal is to be expected according to the combined dispersal kernel (3-15 m). 5. Synthesis and applications: This study isolates effects of road traffic from confounding mechanisms (e.g. mowing machinery, propagule pressure from infested fields) on common ragweed (Ambrosia artemsiifolia L.) invasions. Results demonstrate traffic-mediated dispersal in Ambrosia invasions as a routine and predictable process that facilitates population extension in the direction of traffic along roadsides, depending on traffic volume. This highlights the importance of prioritizing mowing along high use roads and mowing of isolated populations to prevent seed abscission and further spread of common ragweed Ambrosia.
Data from: Prevalence and treatment of sexually transmitted infections in men followed by urologists in Germany – a cross sectional study with 347,090 men
Aim: The goal of this retrospective analysis was to study the prevalence and treatment of the most common sexually transmitted infections (STI) in men followed by urologists in Germany. Methods: This study included a total of 347,090 men followed in 71 urology practices in Germany between 2013 and 2015. The first outcome was the prevalence of individuals diagnosed with STI between 2013 and 2015. The following eight types of STI infections were included in the analysis: chlamydial infection, gonococcal infection, anogenital warts, anogenital herpes infection, trichomoniasis, ulcus molle, phthiriasis, and syphilis. The second outcome was the prevalence of individuals with STI who received an appropriate therapy within 90 days of their initial STI diagnosis. Results: The most frequent STI was anogenital warts (0.64%), whereas the least frequent STI was syphilis (0.03%). The median age at diagnosis ranged from 30.3 years for chlamydia infection to 47.5 years for trichomoniasis. The proportion of individuals receiving treatment was the highest for trichomoniasis (90.6%) and the lowest for anogenital warts (49.9%). Conclusions: Overall, approximately 1.25% of men followed in urology practices in Germany between 2013 and 2015 were diagnosed with at least one STI. Further research is needed to gain a better understanding of the factors potentially associated with the risk of being diagnosed with STI in this setting in Germany. Moreover, there is a need for enabling higher rates of diagnosis and thus treatment of infected persons.
Data from: A juvenile turtle (Testudines, Eucryptodira) from the Upper Jurassic of the Langenberg Quarry, Oker, Northern Germany
Turtles are frequently found in fluviatile to lagoonal and shallow marine sediments in the Upper Jurassic of Western Europe. These turtles usually show a mixture of basal and derived characters, but phylogenetic relationships are still largely unresolved. This is mainly due to the incompleteness of fossils and the lack of taxonomically unambiguous characters and is also related to the presence of different ontogenetic stages, which are not easy to compare. The morphological description of a new turtle from the Upper Jurassic of Langenberg Quarry (Oker, Lower Saxony, Germany) gives further insights into the ontogeny of basal eucryptodire turtles as well as into aquatic adaptation of Upper Jurassic turtles. The specimen is herein left in open nomenclature, due to the fact that it represents a juvenile individual. Several characters define the specimen as juvenile: its small size (7.28 cm carapace length); lateral carapacial fontanelles; enlarged vertebral scutes; a radial striation pattern covering the entire carapace; and the grade of ossification of preserved skull and limb elements. A clear aquatic adaptation of the individual is the elongated manus, a feature that is independent of ontogenetic age. The elongated manus may indicate a marine lifestyle and the individual possibly inhabited nearshore to offshore areas around the former Jurassic islands, which today form the Saxony Basin. The ossification pattern of the carapace of this eucryptodire turtle resembles that of known Jurassic paracryptodires and thus provides new insights to the ontogeny of Jurassic turtles.
Data from: Historical invasion records can be misleading: genetic evidence for multiple introductions of invasive raccoons (Procyon lotor) in Germany
Biological invasions provide excellent study systems to understand evolutionary, genetic and ecological processes during range expansions. There is strong evidence for positive effects of high propagule pressure and the associated higher genetic diversity on invasion success, but some species have become invasive despite small founder numbers. The raccoon (Procyon lotor) is often considered as a typical example for such a successful invasion resulting from a small number of founders. The species' largest non-native population in Germany is commonly assumed to stem from a small number of founders and two separate founding events in the 1930s and 1940s. In the present study we analyzed 407 raccoons at 20 microsatellite loci sampled from the invasive range in Western Europe to test if these assumptions are correct. Contrary to the expectations, different genetic clustering methods detected evidence for at least four independent introduction events that gave rise to genetically differentiated subpopulations. Further smaller clusters were either artifacts or resulted from founder events at the range margin and recent release of captive individuals. We also found genetic evidence for on-going introductions of individuals. Furthermore a novel randomization process was used to determine the potential range of founder population size that would suffice to capture all the alleles present in a cluster. Our results falsify the assumption that this species has become widespread and abundant despite being genetically depauperate and show that historical records of species introductions may be misleading.
Data from: Changes in Eocene plant diversity and composition of the vegetation: the lacustrine archive of Messel (Germany)
Based on high resolution palynological analysis of 680 samples from a core, short-term changes in plant diversity and floristic composition within the Paleogene greenhouse have been detected in the lacustrine succession of a Lower to Middle Eocene maar lake at Messel (Federal State of Hesse, Germany). The microfloristic data show that taxonomic diversity increased rapidly within some decades during recolonization of a volcanically devastated area around the lake. With the establishment of a climax vegetation at the end of recolonization the maximum in palynological diversity was reached in the crater area. During the following 640 Kyr the composition of the palynospectrum changed only gradually. However, different richness and evenness estimations show that alpha and gamma diversity decreased up to 35% which can be related to the establishment of an equilibrium stage within the climax vegetation that led to the dominance of an assemblage of self-replacing species. Nevertheless, time series analysis of alpha diversity changes within the climax vegetation reveals that orbitally controlled climate change of Milankovitch and Sub-Milanovitch order influenced the diversity of the vegetation resulting in a rise of beta diversity. Based on the composition of the vegetation and comparison to modern analogues our analysis now proves that Eocene paratropical plant diversity increased during periods of slightly higher temperature and precipitation. Therefore, both composition and diversity of the vegetation was highly susceptible to minor-scale short-term changes in climate even during equable greenhouse conditions.
Kings`s Gate | Henzendorf (Germany)
This stele depicts a Hittite warrior, based on a orthostat in Kings`s gate of the Hittite capital <a href="https://www.dainst.org/en/projekt/-/project-display/48178">Hattuša (Boğazköy)</a> a UNESCO World Heritage Site in Turkey. This copy / interpretation was made by a collaboration of polish and german artists (Ulrich Thiel, Kazimierz Krewniak and Adam Sobiraj). <br><br> <br> <i>Photo of the original orthostat| Bittel 1976: P. 231</i><br> <br> <b>Further reading:</b> <br> - <a href="http://hittitemonuments.com/bogazkoy/">hittitemonuments.com | Hattuša</a><br> - K. Bittel, Die Hethiter. (...), München: Verlag C.H. Beck, 1976<br> <b>Original at:</b> <br> Anatolian Civilizations Museum, Ankara<br> <br> Model by Felix Wolter, with permission of the landcare association, land owner and the Naturpark Schlaubetal, Germany. <br><br><a href="http://www.felixwolter.de/Henzendorf.html">HITTITES IN HENZENDORF | WEBSITE</a> Source: Objaverse 1.0 / Sketchfab
Teshub Cult Stele | Henzendorf (Germany)
A stele depicting the hittite God Teshub. The original model (Neo-Hittite, circa 1,180 BC - 700 BC) was found 1899 in Babylon (Iraq). This copy / interpretation was made by a collaboration of polish and german artists (Ulrich Thiel, Kazimierz Krewniak and Adam Sobiraj). <br> <i>Photo of original stele at the Istanbul Museum | <a href="http://www.hittitemonuments.com">hittitemonuments.com</a></i><br> <br> <b>Further reading:</b> <br> - R. Koldewey. Die Hettitische Inschrift (...), WVDOG, Heft 1; 1900.<br> - A. Muhibbe Darga. Hitit Sanatı. İstanbul: Akbank, 1992: Fig. 312; P. 329<br> <b>Original at:</b> <br> Eski Şark Eserleri Müzesi (Istanbul), GNT.S03.01.sld.01<br> <br> Model by Felix Wolter, with permission of the landcare association, land owner and the Naturpark Schlaubetal, Germany. <br><br><a href="http://www.felixwolter.de/Henzendorf.html">HITTITES IN HENZENDORF | WEBSITE</a> Source: Objaverse 1.0 / Sketchfab
Germany Telephone booth
Source: Objaverse 1.0 / Sketchfab
Heat Stress Exposure Maps - Base Scenario 1986 - 2005: Berlin, Germany (Map-1)
<p>Heat Stress Exposure Maps - Base Scenario 1986 - 2005: Berlin, Germany</p> <p>Map-1 (zip.file) ref. to DOI: 10.5281/zenodo.45015</p> <p> </p>
Could Google Trends be used to predict methamphetamine-related crime? An analysis of search volume data in Switzerland, Germany, and Austria
<p>Data for paper submitted to PLoS One on 2016-07-08. Title: Could Google Trends be used to predict methamphetamine-related crime? An analysis of search volume data in Switzerland, Germany, and Austria</p> <p>Authors: Alex Gamma, Roman Schleifer, Wolfgang Weinmann, Anna Buadze, Michael Liebrenz</p> <p>Format: ZIP-file</p> <p>Contains:<br /> - Two datafiles, each as .csv and .dta (Stata version 11) file.<br /> - README file with instructions</p> <p> </p> <p> </p>
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.