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opencc-by-4.0Oct 2009View details →

Figure 6 in Gliridae (Rodentia, Mammalia) with a simple dental pattern: a new genus and new species from the European Early and Middle Miocene

Figure 6. Simplomys aljaphi (Hugueney et al., 1978) from Montaigu-le-Blin (modified after Hugueney et al., 1978). A, P4-M3 AC. MB 191 holotype. B, p4-m3 P.O. C, P4 AC. MB 103. D, M1 F.S.L. 97 461. E, m3 AC. MB 706. F, m3 F.S.L. 97 464. Right side specimens underlined. Holotype in italics.

opencc-by-4.0Oct 2009View details →

Figure 10 in Gliridae (Rodentia, Mammalia) with a simple dental pattern: a new genus and new species from the European Early and Middle Miocene

Figure 10. Temporal distribution of average surface of the upper and lower cheek teeth in species of Simplomys gen. nov. from the Aragonian type area (Calatayud–Montalbán basin, Spain). Only localities with at least five measurable specimens of each element are included. Horizontal bars represent two times the standard deviation. Modified after García-Paredes, 2006.

opencc-by-4.0Jul 2006View details →

Fig. 12 in A new species of the European freshwater bryozoan fauna: Plumatella similirepens WOOD, 2001 (Bryozoa, Phylactolaemata)

Fig. 12: Scanning electron micrograph of the suture. a) Plumatella repens from the same hatchery. b) Typical Plumatella repens from an Italian natural site. Scale bars = 20 µm.

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Fig. 5 in A new species of the European freshwater bryozoan fauna: Plumatella similirepens WOOD, 2001 (Bryozoa, Phylactolaemata)

Fig. 5: Plumatella similirepens. Scanning electron micrograph of dorsal valve. a) Paved annulus with three series of regularly distributed tubercles. Scale bar = 100 µm. b) Detail of a) showing nodules on both annulus and fenestra and polar region. Scale bar = 50 µm.

opencc-by-4.0Jul 2006View details →

Fig. 1 in A new species of the European freshwater bryozoan fauna: Plumatella similirepens WOOD, 2001 (Bryozoa, Phylactolaemata)

Fig. 1: Plumatella similirepens. Longitudinal striations (arrow) of a fragment of the encrusted ectocyst. Scale bar = 100 µm

Influence of European beech (Fagus sylvatica) rot hole habitat characteristics on invertebrate community structure and diversity - Dataset

The data and R scripts pertinent to the Journal of Insect Science manuscript titled "Influence of European beech (Fagus sylvatica) rot hole habitat characteristics on invertebrate community structure and diversity". Environmental variables are given in "Rot Hole and Site Data", whilst community data are given as counts in "Rot Hole Community Data - counts" and as relative  abundance in "Rot Hole Community Data - relative abundances".

opencc-by-4.0Dec 2016View details →

PERCEIVE: WP1: Framework for comparative analysis of the perception of Cohesion Policy and identification with the European Union at citizen level in different European countries: Survey at citizen level and data relative to regional performance of the Cohesion Policy and institutional quality

1. Orignal PERCEIVE survey data (STATA file) 2. description of survey questions, descriptive results (word file) 3. EU Deliverable document with descriptive analysis of survey questions   ***please cite the following when using the microdata: Bauhr, M., & Charron, N. (2020). The EU as a savior and a saint? Corruption and public support for redistribution. Journal of European Public Policy, 27(4), 509-527. https://www.tandfonline.com/doi/full/10.1080/13501763.2019.1578816

Survey on Speech-and-Language Therapists' attitudes and approaches towards multilingualism across four European countries

The file contains all the responses of 300 Speech-and-Language Therapists (SLTs) from Germany, Austria, Italy and Switwerland to a series of questions concerning the provision of speech and language therapy to multilingual children with Developmental Language Disorders. Both the original responses and numerically coded versions are included. Two excel sheets are provided: in the first sheet all responses to the general questionnaire are reported, whereas in the second sheet a subset of the responses obtained from 154 German-speaking SLT respondents are included (more in-depth analyses will be performed on an extended dataset concerning German-speaking SLTs only). These responses have been analysed and presented in the paper titled "Speech and Language Therapy service for multilingual children: Attitudes and approaches across four European countries".

Fig. 7 in Atlas of European millipedes 3: Order Chordeumatida (Class Diplopoda)

Fig. 7. Percentage of species recorded from 1, 2–3, 4–7 …> 512-1023 50 km squares of European Chordeumatida C.L. Koch, 1847 (blue columns) and Julida Brandt, 1833 without Macaronesian endemics (red columns, data from Kime & Enghoff 2017).

Fig. 5 in Atlas of European millipedes 3: Order Chordeumatida (Class Diplopoda)

Fig. 5. Area codes as used in the atlas, from Fauna Europaea guidelines (de Jong et al. 2014: supplementary material 1), reproduced with permission. Note that MN (Montenegro) and SB (Serbia) are collectively shown as YU (Yugoslavia) on this map. Also note that CY (Cyprus) is not covered by the atlas.

Fig. 2. A in Atlas of European millipedes 3: Order Chordeumatida (Class Diplopoda)

Fig. 2. A selection of European species of Chordeumatida C.L. Koch, 1847, various families. A. Halleinosoma noricum Verhoeff, 1913 (Trachygonidae Cook, 1896). B. Syngonopodium aceris Verhoeff, 1913 (Attemsiidae Verhoeff, 1899). C. Xylophageuma zschokkei Bigler, 1912 (Haaseidae Attems, 1899), in copula. D. Haplogona oculodistincta (Verhoeff, 1893) (Verhoeffiidae Verhoeff, 1899), in copula. E. Haasea fonticulorum (Verhoeff, 1910) (Haaseidae), in copula. Jörg Spelda has pointed out that on Figs 2C and 2E, both showing copulation in species of Haaseidae, the female is seen to be partially covered in a fine web (most evident in Fig. 2E), probably produced by the male's spinning glands and perhaps serving to 'strap down' the female to the ground. Photo credits: Jörg Spelda.

Fig. 4. A in Atlas of European millipedes 3: Order Chordeumatida (Class Diplopoda)

Fig. 4. A selection of European subterranean species of Chordeumatida C.L. Koch, 1847, various families. A. Schizmohetera curcici Makarov, 2001, topotype (Neoatractosomatidae Verhoeff, 1901). B. Serbosoma kucajense (Ćurčić & Makarov, 1998), topotype (Anthroleucosomatidae Verhoeff, 1899). C. Egonpretneria vudutschaljdi Antić & Dražina, 2015 (Anthogonidae Ribaut, 1913). D. Cornogonopus pavicevici Antić, 2020, the latest addition to the European chordeumatidan fauna, holotype (Anthroleucosomatidae) E. Haasia likana (Strasser, 1966) (Anthogonidae). F. Dyocerasoma intermedium Makarov, Lučić, Mitić & Rađa, 2003 (Craspedosomatidae Gray, 1843). Photo credits: Marjan Komnenov (A), Dragan Antić (B, D), Tamara Čuković-Malenica (C), Tvrtko Dražina (E), Kazimir Muculinić (F).

Fig. 8 in Atlas of European millipedes 3: Order Chordeumatida (Class Diplopoda)

Fig. 8. Year (decade) of publication of valid names of European Chordeumatida C.L. Koch, 1847 (blue columns) and Julida Brandt, 1833 without Macaronesian endemics (red columns, data from Kime & Enghoff 2017 and from Table 5 of the present work).

Fig. 26 in An unexpected discovery of a new subgenus and a species of Plusiocampa (Campodeidae, Diplura) alongside an overview of Central European subterranean campodeids

Fig. 26. Distribution of Plusiocampinae (Plusiocampa Silvestri, 1912 and Hystrichocampa Condé, 1962) in Central Europe; blue indicates karst regions.

Figs 24–25 in An unexpected discovery of a new subgenus and a species of Plusiocampa (Campodeidae, Diplura) alongside an overview of Central European subterranean campodeids

Figs 24–25. Plusiocampa (Plusiocampa) dobati Condé in Dobat, 1975. Urosternite I. 24. Male. 25. Female. a1 = a1-glandular setae. Scale bars = 0.1 mm.

Figs 18–23 in An unexpected discovery of a new subgenus and a species of Plusiocampa (Campodeidae, Diplura) alongside an overview of Central European subterranean campodeids

Figs 18–23. Plusiocampa (Plusiocampa) dobati Condé in Dobat, 1975. 18. Cupuliform organ of the last antennomere. 19. Central cylindrical structure of an olfatory chemoreceptor sensillum of the cupuliform organ. 20. Gouge sensilla. 21. Frontal process. 22. Telotarsal end of metathoracic leg. 23. Detail of telotarsal claw. Scale bars in µm.

Figs 13–17 in An unexpected discovery of a new subgenus and a species of Plusiocampa (Campodeidae, Diplura) alongside an overview of Central European subterranean campodeids

Figs 13–17. Plusiocampa (Pentachaetocampa) inopinata subgen. et sp. nov. 13. Tarsal end of metathoracic leg. 14. Detail of telotarsal claw. 15. Urosternites I-II of a female. 16. g1-glandular setae of urosternite I of a female. 17. Stylus of urosternite VII. Scale bars in µm.

Figs 5–6 in An unexpected discovery of a new subgenus and a species of Plusiocampa (Campodeidae, Diplura) alongside an overview of Central European subterranean campodeids

Figs 5–6. Plusiocampa (Pentachaetocampa) inopinata subgen. et sp. nov. Urosternite I. 5. Male. 6. Female. a1 = a1-glandular setae, g1 = g1-glandular setae. Scale bars: = 0.1 mm.

Figs 3–4 in An unexpected discovery of a new subgenus and a species of Plusiocampa (Campodeidae, Diplura) alongside an overview of Central European subterranean campodeids

Figs 3–4. Plusiocampa (Pentachaetocampa) inopinata subgen. et sp. nov., holotype, ♀. 3. Pro-, meso- and metanotum, left side. 4. Urotergites I–IX, left side. Scale bars = 0.2 mm.

Data from: Cryogenic land surface processes shape vegetation biomass patterns in northern European tundra

Tundra ecosystems have experienced changes in vegetation composition, distribution, and productivity over the past century due to climate warming. However, the increase in above-ground biomass (AGB) may be constrained by cryogenic land surface processes (LSP) that cause topsoil disturbance and variable microsite conditions. These effects have remained unaccounted for in tundra biomass models, although they can impact multiple opposing feedbacks between the biosphere and atmosphere, ecosystem functioning and biodiversity. Here, by using field-quantified data from northern Europe, remote sensing, and machine learning, we show that LSP substantially constrain AGB in tundra. The three surveyed LSP (cryoturbation, solifluction and nivation) collectively reduced AGB by an average of 123.0 g m-2 (-30.0%). This effect was significant over landscape positions and was especially pronounced in snowbed environments, where the mean reduction in AGB was 57.3%. Our results imply that LSP are pivotal in shaping future patterns of tundra biomass, as long as cryogenic ground activity is retained by climate warming. These are the key data and codes related from Aalto et al., (2021).