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22 results for “scree slopes”

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Figure 1 in Terrestrial isopods and myriapods in a forested scree slope: subterranean biodiversity, depth gradient and annual dynamics

Figure 1. Distribution of Isopoda, Diplopoda and Chilopoda along the depth gradient of the scree slope expressed as the total number of individuals trapped in two sampling periods (November 2008–November 2009; November 2009–July 2010).

opencc-by-4.0May 2016View details →
zenodo32/100

Figure 3 in Periglacial microclimate in low-altitude scree slopes supports relict biodiversity

Figure 3. Temperature variations (◦C) in the Kamenec scree slope from the beginning of December 2003 to the end of November 2004. ET, external ambient air temperature; IT, internal air temperature on lower margin of the scree slope near trap No. 2.

opennotspecifiedSep 2012View details →
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Figure 2 in Periglacial microclimate in low-altitude scree slopes supports relict biodiversity

Figure 2. Relation of average annual temperature (A), and the annual number of black frost days (B) for three meteorological stations: Strakonice (423 m a.s.l.), Kašperské Hory (737 m a.s.l.) and Churáňov (1118 m a.s.l.). From 1976 to 2005. F = 487.49, P <10−16; and F = 1,29 1,29 65.6, P ≤ 10−8, respectively.

opennotspecifiedSep 2012View details →
zenodo32/100

Figure 1 in Periglacial microclimate in low-altitude scree slopes supports relict biodiversity

Figure 1. Aerial photograph of Kamenec hill, autumnal aspect. The locations of pitfall traps are marked by full circles. Dashed line indicates the area with periglacial microclimate. Photo: L. Jenka.

opennotspecifiedSep 2012View details →
zenodo32/100

Figure 5 in Periglacial microclimate in low-altitude scree slopes supports relict biodiversity

Figure 5. Ordination diagram of the Redundancy Analysis method on the dataset with all arthropods. The first (horizontal) axis defined by the proximity to ice formation places explains 22.7% of the total variation in species data, while the second (vertical) axis explains another 18.5% of the variation, unrelated to the tested factor. NI, near ice, plots <5 m from the places with underground ice formation; Outside, all remaining plots. Ten species best fitted by the proximity of ice-formation places are shown: Acari: RhagGeli, Rhagidia gelida Thorell, 1872; Araneae: AcanNorv, Acantholycosa norvegica (Thorell, 1872); AnguTrip, Anguliphantes tripartitus (Miller and Svatoň, 1978); DiplBide, Diplocentria bidentata (Emerton, 1882); TenuAlac, Tenuiphantes alacris (Blackwall, 1853); WalcAtro, Walckenaeria atrotibialis (O. P.-Cambridge, 1878); Coleoptera: CoryAngu, Coryphium angusticolle Stephens, 1834; OmalCaes, Omalium caesum Gravenhost, 1806; PhylUndu, Phyllotreta undulata Kutschera, 1860; Diplopoda: GlomHexa, Glomeris hexasticha Brandt, 1833.

opennotspecifiedSep 2012View details →
zenodo32/100

Figure 4 in Periglacial microclimate in low-altitude scree slopes supports relict biodiversity

Figure 4. Ordination diagram of Canonical Correspondence Analysis, displaying first two axes constrained by the sample location category (3.4% of total variation explained, P = 0.002). NI, near ice, plots <5 m from the places with underground ice formation; MP, middle part; SP, side part; and UM, upper margin. Sixteen bryophyte species best explained by the location are shown: AnasSaxi, Anastrophyllum saxicola (Schrad.) R. M. Schust.; AndrRupe, Andreaea rupestris Hedw.; CephDiva, Cephaloziella divaricata (Sm.) Schiffn.; CephRube, Cephaloziella rubella (Nees) Warnst.; DicrScop, Dicranum scoparium Hedw.; DiplTaxi, Diplophyllum taxifolium (Wahlenb.) Dumort.; LophSude, Lophozia sudetica (Nees ex Hueneber) Grolle; LophVent, Lophozia ventricosa (Dicks.) Dumort.; PohlCrud, Pohlia cruda (Hedw.) Lindb.; PolyAlpi, Polytrichum alpinum Hedw.; PolyForm, Polytrichum formosum Hedw.; PtilCili, Ptilidium ciliare (L.) Hampe; RacoFasc, Racomitrium fasciculare (Hedw.) Brid.; RacoLanu, Racomitrium lanuginosum (Hedw.) Brid.; ScapNemo, Scapania nemorea (L.) Grolle; TetrPell, Tetraphis pellucida Hedw.

opennotspecifiedSep 2012View details →
zenodo28/100

Figure 3 in Terrestrial isopods and myriapods in a forested scree slope: subterranean biodiversity, depth gradient and annual dynamics

Figure 3. Activity dynamics of isopod Ligidium germanicum (LIGE); diplopods Mecogonopodium carpathicum (MECA), Polydesmus denticulatus (PODE), Trachysphaera acutula (TRAC); and centipedes Harpolithobius anodus (HAAN), Lithobius forficatus (LIFO), during the period November 2008– November 2009.

opencc-by-4.0May 2016View details →
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Figure 2 in Terrestrial isopods and myriapods in a forested scree slope: subterranean biodiversity, depth gradient and annual dynamics

Figure 2. The non-metric multidimensional scaling ordination analysis (NMS) diagram of Isopoda and Myriapoda collected during both sampling periods; variance explained by axes 1 and 2 as 87.0% and 8.7%, respectively (triangles – depths, dots – species). Abbreviations: i – Isopoda: LIGE – Ligidium germanicum, MEGR – Mesoniscus graniger, TRCA – Trichoniscus carpaticus; d – Diplopoda: JUCU – Julus curvicornis, LEMA – Leptoiulus mariae, LETR – L. trilobatus, MECA – Mecogonopodium carpathicum, POCO – Polydesmus complanatus, PODE – Polydesmus denticulatus, TRAC – Trachysphaera acutula, STST – Strongylosoma stigmatosum; c – Chilopoda: HAAN – Harpolithobius anodus, LI - Lithobius sp. juv., LIFO – Lithobius forficatus, LILU – Lithobius lucifugus; STAC – Strigamia acuminata, STTR – Strigamia transsilvanica.

opencc-by-4.0May 2016View details →
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Supplementary material 1 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914

Table S1

opencc-zeroMay 2020View details →
zenodo28/100

Figure 1 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914

Figure 1 Location of the study sites. 1 Doline next to Silická ľadnica Ice Cave 2 Vysoká Hill (both sites in Slovak Karst National Park) 3 Drienok Valley (Revúcka Highlands) 4 Belinské skaly (Cerová vrchovina Highlands) 5 Okopanec Hill (Malé Karpaty Mts.) 6–8 Three localities near the Zbrašov Aragonite Caves and Hůrka u Hranic (Moravian-Silesian Foothills) 9–11 Three localities in Chrudim region (Iron Mts.).

opencc-by-4.0May 2020View details →
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Supplementary material 2 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914

Table S2

opencc-zeroMay 2020View details →
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Figure 4 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914

Figure 4 Graphical presentation of myriapod community characteristics in different fixative solutions (N = number of individuals). A Formaldehyde to ethylene glycol ratio of sampled centipede species from all study sites, where both fixating solutions were used B formaldehyde to ethylene glycol ratio of sampled millipede species from all study sites, where both fixating solutions were used.

opencc-by-4.0May 2020View details →
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Figure 2 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914

Figure 2 A Overall depth distribution of centipede individuals and species B values of Shannon's diversity index and Pielou's evenness index, calculated for centipedes, at each of the study sites C mean values of Shannon's diversity index (±SD) calculated for centipedes, at each depth of the gradient (summarised data from all localities) D overall depth distribution of millipede individuals and species E values of Shannon's diversity index and Pielou's evenness index, calculated for millipedes, at each of the study sites F mean values of Shannon's diversity index (±SD) calculated for millipedes, at each depth of the gradient.

opencc-by-4.0May 2020View details →
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Figure 5 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914

Figure 5 Vertical distribution of myriapods along the depth gradient in different fixative solutions (data recalculated for the same number of traps). Trend line: dashed = formaldehyde, dotted = ethylene glycol. A Vertical distribution of Chilopoda specimens along the depth gradient (5–95 cm) at five scree slopes in different fixative solutions B vertical distribution of centipede species along the depth gradient at five scree slopes in different fixative solutions C vertical distribution of Diplopoda specimens along the depth gradient (5–95 cm) at five scree slopes in different fixative solutions D vertical distribution of millipede species along the depth gradient at five scree slopes in different fixative solutions.

opencc-by-4.0May 2020View details →
zenodo28/100

Figure 3 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914

Figure 3 Generalised Additive Models of depth distribution pattern of A centipedes and B millipedes. Only species with significant pattern are illustrated. (F-values, * p < 0.05, ** p < 0.01): ALamyctes emarginatus (13.1**), Lithobius forficatus (17.2**), Lithobius lucifugus (5.0*), Lithobius nodulipes (9.7**) BArchiboreoiulus pallidus (22.7**), Cylindroiulus nitidus (5.4*), Glomeris connexa (5.4*), Hylebainosoma tatranum (5.4*), Leptoiulus proximus (7.3*), Mastigona bosniensis (10.5**), Megaphyllum projectum (5.4*), Melogona transsylvanica (15.2**), Polydesmus complanatus (13.1**), Trachysphaera acutula (5.4*), Unciger foetidus (4.9*).

opencc-by-4.0May 2020View details →
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Figure 3 from: Jakšová P, Ľuptáčik P, Miklisová D (2019) Distribution of Oribatida (Acari) along a depth gradient in forested scree slopes. Subterranean Biology 31: 29-48. https://doi.org/10.3897/subtbiol.31.36241

Figure 3 Monthly temperature fluctuations along the depth gradient of the investigated screes. Abbreviations: AJ – Ardovská jaskyňa Cave, BS – Belinské skaly Rocks, DK – Drienčanský kras Karst, MR – Malý Ružínok Valley, SL – Silická ľadnica Cave.

opencc-by-4.0Oct 2019View details →
zenodo28/100

Figure 4 from: Jakšová P, Ľuptáčik P, Miklisová D (2019) Distribution of Oribatida (Acari) along a depth gradient in forested scree slopes. Subterranean Biology 31: 29-48. https://doi.org/10.3897/subtbiol.31.36241

Figure 4 Distribution of Oribatida along the vertical profile of the screes expressed as a total number of trapped individuals and species richness. Abbreviations: AJ – Ardovská jaskyňa Cave, BS – Belinské skaly Rocks, DK – Drienčanský kras Karst, MR – Malý Ružínok Valley, SL – Silická ľadnica Cave, *Number of individuals = 661.

opencc-by-4.0Oct 2019View details →
zenodo28/100

Figure 1 from: Jakšová P, Ľuptáčik P, Miklisová D (2019) Distribution of Oribatida (Acari) along a depth gradient in forested scree slopes. Subterranean Biology 31: 29-48. https://doi.org/10.3897/subtbiol.31.36241

Figure 1 Localities of samplings. 1 – Ardovská jaskyňa Cave, 2 – Belinské skaly Rocks, 3 – Drienčanský kras Karst, 4 – Malý Ružínok Valley, 5 – Silická ľadnica Cave.

opencc-by-4.0Oct 2019View details →
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Figure 3 from: Rudy J, Rendoš M, Ľuptáčik P, Mock A (2018) Terrestrial isopods associated with shallow underground of forested scree slopes in the Western Carpathians (Slovakia). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. Title. ZooKeys 801: 323-335. https://doi.org/10.3897/zookeys.801.24113

Figure 3 Depth distribution of Mesoniscusgraniger. Site 1 is out of the species range. Study sites 4 and 5 were not depicted, because whole depth gradient was not represented (see locality description).

opencc-by-4.0Dec 2018View details →
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Figure 2 from: Rudy J, Rendoš M, Ľuptáčik P, Mock A (2018) Terrestrial isopods associated with shallow underground of forested scree slopes in the Western Carpathians (Slovakia). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. Title. ZooKeys 801: 323-335. https://doi.org/10.3897/zookeys.801.24113

Figure 2 Ethylene glycol to formaldehyde ratio of sampled specimens from all study sites, where both fixating solutions were used.

opencc-by-4.0Dec 2018View details →

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