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1,342 results for “lichens”
Figure 2 in Epiphytic Bryophyte And Lichen Communities In Relation To Tree And Forest Stand Variables In Populus Tremula Forests Of South-East Latvia
Figure 2. Epiphytic bryophyte and lichen species in the studied territories. Tade Micr – Microreserve in Tadenava, Augs land – Augšzeme Protected Landscape Area, Star Rese – Starinas mežs Nature Reserve. Signal species include all WKH indicator species and red-listed species.
Figure 1. Studied territories. 1 in Epiphytic Bryophyte And Lichen Communities In Relation To Tree And Forest Stand Variables In Populus Tremula Forests Of South-East Latvia
Figure 1. Studied territories. 1 – Microreserve in Tadenava, 2– Augšzeme Protected Landscape Area, 3 – Starinas mežs Nature Reserve.
Figure 1 in Epiphytic Lichens In Latvian Manor Parks
Figure 1. Studied manor parks: 1 – Kr'slava manor park; 2 – Balvi manor park; 3 – VarakÔ'ni manor park; 4 – PreiÔi manor park; 5 – Litene manor park; 6 – Lizums manor park; 7 – JercÁnmui˛a manor park; 8 – Ungurmui˛a manor park; 9 – Krimulda manor park; 10 – StaÔÏene manor park; 11 – Lielvircava manor park; 12 – Mazme˛otne manor park; 13 – ZaÔenieki manor park; 14 – Apgunste manor park; 15 – Vadakste manor park; 16 – Smuku manor park; 17 – KalnsÁtas manor park; 18 – La˛asPadures manor park; 19 – DzÁrves manor park; 20 – L˚znava manor park.
Fig. 3 in Testate Amoeba Communities of Epilithic Mosses and Lichens: New Data from Russia, Switzerland and Italy
Fig. 3. Taxon richness (A) and test concentration (B) against moisture content expressed as a proportion.
Fig. 2 in Testate Amoeba Communities of Epilithic Mosses and Lichens: New Data from Russia, Switzerland and Italy
Fig. 2. Taxon richness (A), Simpson diversity (B) and test concentration (C) by region. Bars show mean and error bars the standard deviation. Letters denote significant differences (P <0.05) where the global test is significant, see text for details.
Fig. 5 in Testate Amoeba Communities of Epilithic Mosses and Lichens: New Data from Russia, Switzerland and Italy
Fig. 5. Taxon richness (A), Simpson diversity (B) and test concentration (C) for epilithic and epiphytic samples from the Karelia regions. Bars show mean and error bars the standard deviation. Letters denote significant differences (P <0.05), see text for details.
Fig. 4 in Testate Amoeba Communities of Epilithic Mosses and Lichens: New Data from Russia, Switzerland and Italy
Fig. 4. NMDS ordination of testate amoeba relative abundance data from epilithic and epiphytic vegetation of the Karelia region (BrayCurtis dissimilarity).
Fig. 1 in Testate Amoeba Communities of Epilithic Mosses and Lichens: New Data from Russia, Switzerland and Italy
Fig. 1. NMDS ordination of testate amoeba relative abundance data from epilithic mosses and lichens (Bray-Curtis dissimilarity).
Figure 1 in A first ecological description of the lichen-clad larva of Eublemmistis chlorozonea Hampson, 1902 (Lepidoptera: Erebidae) from a southern Afrotemperate forest
Figure 1 – Adult records of Eublemmistis in the southern African region. Red squares: E. chlorozonea. Blue squares: E. aberfoylea.
Figure 5 in A first ecological description of the lichen-clad larva of Eublemmistis chlorozonea Hampson, 1902 (Lepidoptera: Erebidae) from a southern Afrotemperate forest
Figure 5 – Cocoons found dangling from the bark of trees, attached by a silky, lichen covered thread.
Figure 4 in A first ecological description of the lichen-clad larva of Eublemmistis chlorozonea Hampson, 1902 (Lepidoptera: Erebidae) from a southern Afrotemperate forest
Figure 4 – Examples of a larva partially covered by lichen fragments (left), and one completely covered (right).
Figure 3 in A first ecological description of the lichen-clad larva of Eublemmistis chlorozonea Hampson, 1902 (Lepidoptera: Erebidae) from a southern Afrotemperate forest
Figure 3 – Larvae typically restrict themselves to the lichen-clad parts of various tree species: Podocarpus latifolius (left) and Curtisia dentata (right).
Figure 2 in A first ecological description of the lichen-clad larva of Eublemmistis chlorozonea Hampson, 1902 (Lepidoptera: Erebidae) from a southern Afrotemperate forest
Figure 2 – Distribution of Eublemmistis chlorozonea observations over a 24-month period (August 2021–August 2023) in the southern Cape, South Africa (Google Earth 2023). George can be seen to the western part of the map and Knysna to the south-eastern part. Observation 20, near the Woodville big tree, was made by the last author (HSS) on the 26th of December 2013. On the insert are observations 1, 2, 3, 4, 5, 12, 14, 15, 16, 17, and 18 from Saasveld forest.
Data and Scripts for Schweiger et al. (2021) "Chemical properties of key metabolites determine the global distribution of lichens"
<p>Data and Scripts for Schweiger et al. (2021) "Chemical properties of key metabolites determine the global distribution of lichens".</p> <p>A detailed description of the individual files is provided in the "Schweiger-et-al-DataPublication-Index-Submissionfiles.txt" file.</p> <p>Summary of the study:</p> <p>In lichen symbioses, fungal secondary metabolites provide UV protection on which certain lichen algae such as trebouxioid green algae sensitively depend. These metabolites differ in their UV absorbance capability and solvability, and thus vary in their propensity of being leached from the lichen body by high precipitation and temperatures, with still unknown implications for the global distribution of lichens. In this global study, we show that the occurrence and chemical properties of fungal-derived metabolites are of eco-evolutionary significance for the global, latitudinal distribution of lichenized Trebouxiophyceae. This might represent an indirect environmental adaptation in which the mycobiont invests to protect the trebouxioid photobiont from harsh environmental conditions and, by doing this, secures its efficient source of photosynthetic carbon.</p>
Fig. 1 in New records of lichens and lichenicolous fungi from La Gomera (Canary Islands, Spain), including the new species: Usnea boomiana P. Clerc
Fig. 1. – Schematic map of the Canary Islands with the situation of Gomera (G). The other islands are: Gran Canaria (C), Fuerteventura (F), El Hierro (H), Lanzarote (L), La Palma (P) and Tenerife (T).
Presence data for vascular plant, bryophyte and lichen species in 100 vegetation plots (each 1 m2) from 32 shell-beds at Akerøya, Hvaler, SE Norway
<p><strong>We present a data set consisting of abundance data for 106 vascular plant species, 36 bryophyte species and 13 lichen species from 100 vegetation plots, each 1 m2, distributed on 32 shell-beds at Akerøya, Hvaler municipality, former Østfold (in 2022 Viken) county. The plots were analysed with respect to species composition in June 1979. These data formed the basis for the publication: Halvorsen, R. 1980. Numerical analysis and successional relationships of shell-bed vegetation at Akerøya, Hvaler, SE Norway. Norw. J. Bot. Vol. 27 pp. 71-95. Oslo. ISSN 0300-1156.</strong></p>
Fig. 1 in Lecaimmeria pakistanica, a new lichen from Azad Jammu and Kashmir, Pakistan
Fig. 1. Molecular phylogenetic analysis of Lecaimmeria pakistanica K.Habib, R.Zulfiqar & Khalid sp. nov. by the maximum likelihood method based on nrDNA sequences, including ITS1, 5.8S and ITS2. Numbers below branch node represent ML bootstrap (> 50%) based on 1000 replicates. Sequences generated from Pakistani collections are marked with black circle.
FIG. 4 in Two new crustose Cladonia species with strepsilin and other new lichens from the Serra de Maracaju, Mato Grosso do Sul, Brazil
FIG. 4. — Lecanora lichexanthoxylina Aptroot & M.F. Souza, sp. nov., holotype: A, habitus with UV; B, habitus. Width of pictures: A, 30 mm; B, 10 mm.
FIG. 3 in Two new crustose Cladonia species with strepsilin and other new lichens from the Serra de Maracaju, Mato Grosso do Sul, Brazil
FIG. 3. — Lecanora fluoroxylina Aptroot & M.F. Souza,sp. nov., isotype, habitus. Width of picture: 30 mm.
FIG. 2 in Two new crustose Cladonia species with strepsilin and other new lichens from the Serra de Maracaju, Mato Grosso do Sul, Brazil
FIG. 2. — Cladonia zebrathallina Aptroot & Spielmann, sp. nov., holotype: A, habitus; B, pycnidium; C, conidia. Width of pictures: A, 10 mm, B, 250 µm, C, 120 µm.
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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.