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165 results for “Northern Europe”
FIGURES 5–9 in New and rarely found species of asynaptine Porricondylinae (Diptera: Cecidomyiidae) in northern Europe
FIGURES 5–9. Camptomyia hedmarki, male, holotype. 5: Genitalia, ventral. 6: Apex of gonostylus, ventral. 7: Zoom of central parts of genitalia, ventral. 8: Fourth flagellomere, lateral. 9: Aedeagus and parameres, ventral. Scales for 5, 0.1 mm, for 6, 0.025 mm, for 7–9, 0.05 mm. Arrows refer to characters described in the diagnosis. Abbreviations: dpm = dorsal parameres, vpm = ventral parameres.
FIGURES 1–4 in New and rarely found species of asynaptine Porricondylinae (Diptera: Cecidomyiidae) in northern Europe
FIGURES 1–4. Genitalic morphology of Asynapta spp. 1: Gonostylus of A. inflatoides, ventral, paratype. 2: Gonostylus of A. rickebasta, ventral, holotype. 3: Aedeagus and parameres of A. rickebasta, ventral, holotype. 4: Genitalia of A. taigensis, ventral, holotype. Scales for 1–3, 0.025 mm, for 4, 0.05 mm. Arrows refer to characters described in the diagnoses.
FIGURES 18–24 in New and rarely found species of asynaptine Porricondylinae (Diptera: Cecidomyiidae) in northern Europe
FIGURES 18–24. Morphology of Asynaptini spp. 18: Genitalia of Asynapta baltica, ventral, specimen from Sweden. 19: Aedeagus and parameres of A. baltica, ventral, specimen from Latvia. 20: Genitalia of Asynapta inflata, ventral, specimen from Sweden. 21–24: Camptomyia fulva, specimen from Sweden. 21: Fourth flagellomere, lateral. 22: Genitalia, ventral. 23: Ninth tergite, dorsal. 24: Aedeagus and parameres, ventral. Scales for 18, 20–22, 0.05 mm, for 19, 23–24, 0.025 mm. Arrows refer to characters described in the diagnoses.
FIGURES 6–11. 6 in Miscophus Jurine, 1807 (Hymenoptera, Crabronidae) in Central, Northern, and Eastern Europe
FIGURES 6–11. 6. Miscophus minutus ♀, propodeum. 7. Miscophus spurius ♀, propodeum. 8. Miscophus postumus ♀, propodeum. 9. Miscophus cappadocicus ♀, propodeum. 10. Miscophus johni ♀, propodeum. 11. Miscophus albufeirae ♀, foreleg.
FIGURES 18–22. 18 in Miscophus Jurine, 1807 (Hymenoptera, Crabronidae) in Central, Northern, and Eastern Europe
FIGURES 18–22. 18. Miscophus eatoni ♀, propodeum. 19. Miscophus concolor male, propodeum. 20. Miscophus johni ♀, foreleg. 21. Miscophus albufeirae ♀, propodeum. 22. Miscophus eatoni ♀, head.
FIGURES 29–30. 29 in Miscophus Jurine, 1807 (Hymenoptera, Crabronidae) in Central, Northern, and Eastern Europe
FIGURES 29–30. 29. Miscophus johni ♀, head lateral view. 30. Miscophus concolor male, last sternites lateral view.
FIGURE 3 in A new species of the soft scale insect genus Pulvinaria Targioni Tozzetti (Hemiptera: Coccomorpha: Coccidae) on Rhododendron spp. in Northern Europe
FIGURE 3. Leaves of Rhododendron x yakushimanum 'Percy Wiseman' covered in sooty mould and with some Pulvinaria rhododendri Kahrer & Hodgson, sp. nov. on the twigs. Photograph by Inger-Lise Fonneland.
FIGURE 1 in A new species of the soft scale insect genus Pulvinaria Targioni Tozzetti (Hemiptera: Coccomorpha: Coccidae) on Rhododendron spp. in Northern Europe
FIGURE 1. Young adult females and late-stage nymphs of Pulvinaria rhododendri Kahrer & Hodgson, sp. nov. on Rhododendron repens 'Scarlet Wonder'. Photograph by Inger-Lise Fonneland.
FIGURE 6 in Key to Ptychopteridae (Diptera) larvae of Northern Europe, with notes on distribution and biology
FIGURE 6. Distribution of Ptychoptera species within the geographical area defined as Northern Europe, delineated by grey line. A. Ptychoptera contaminata; B. P. hugoi; C. P. minuta; D. P. scutellaris. Blue dots show specific records, blue raster indicates confirmed but unspecified presence and red raster indicates likely presence.
FIGURE 7 in Key to Ptychopteridae (Diptera) larvae of Northern Europe, with notes on distribution and biology
FIGURE 7. The COI distance tree of N-European Ptychopteridae based on data from Table S2, produced by MEGA X (Kumar et al. 2018), and inferred by using the Maximum Likelihood method and the Kimura 2-parameter model (Kimura 1980). The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. There were a total of 662 positions in the final dataset. Ptychoptera hugoi, BOLD SYSTEMS reference FIFLY093-12, is included for comparison. Notes: 1 One individual of P. minuta variety did not cluster with the main group of this species. 2 Main group of P. minuta. 3 Seven individuals fell into this P. lacustris cluster. 4 Two individuals fell into this aberrant P. lacustris cluster.
FIGURE 5 in Key to Ptychopteridae (Diptera) larvae of Northern Europe, with notes on distribution and biology
FIGURE 5. Distribution of Ptychoptera species within the geographical area defined as Northern Europe, delineated by grey line. A. Ptychoptera albimana; B. P. lacustris; C. P. longicauda; D. P. paludosa. Blue dots show specific records, blue raster indicates confirmed but unspecified presence and red raster indicates likely presence.
Data from: Observed and dark diversity dynamics over millennial time scales: Fast-life history traits linked to expansion lags of plants in northern Europe
<p>Global change drivers (e.g. climate and land use) affect the species and functional traits observed in a local site but also its dark diversity—the set of species and traits locally suitable but absent. Dark diversity links regional and local scales and, over time, reveals taxa under expansion lags by depicting the potential biodiversity that remains suitable but is absent locally. Since global change effects on biodiversity are both spatially and temporally scale dependent, examining long-term temporal dynamics in observed and dark diversity would be relevant to assessing and foreseeing biodiversity change. Here, we used sedimentary pollen data to examine how both taxonomic and functional observed and dark diversity changed over the past 14500 years in northern Europe. We found that taxonomic and functional observed and dark diversity increased over time, especially after the Late Glacial and during the Late Holocene. However, dark diversity dynamics revealed expansion lags related to species' functional characteristics (dispersal limitation and stress intolerance) and an extensive functional redundancy when compared to taxa in observed diversity. We highlight that assessing observed and dark diversity dynamics is a promising tool to examine biodiversity change across spatial scales, its possible causes, and functional consequences.</p>
Data from: Rapid genetic and ecological differentiation during the northern range expansion of the venomous yellow sac spider Cheiracanthium punctorium in Europe
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Data from: Effects of host species and environmental factors on the prevalence of Batrachochytrium dendrobatidis in northern Europe
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Data from: Lyme neuroborreliosis and bird populations in northern Europe
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Data from: Observed and dark diversity dynamics over millennial time scales: Fast-life history traits linked to expansion lags of plants in northern Europe
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Data from: Patterns of modern pollen and plant richness across northern Europe
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Data from: Forest snail faunas from Transylvania (Romania), and their relationship to the faunas of Central and Northern Europe
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Demographic history has shaped the strongly differentiated corkwing wrasse populations in Northern Europe
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Phenology of Lupinus polyphyllus from Central to Northern Europe
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