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412 results for “temperate forests”

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zenodo28/100

Tree and mycorrhizal fungal diversity drive intraspecific and intraindividual trait variation in temperate forests: evidence from a tree diversity experiment

<p>Scripts and dataset for Castro S&aacute;nchez-Bermejo et al., 2024 "Tree and mycorrhizal fungal diversity drive intraspecific and intraindividual trait variation in temperate forests: evidence from a tree diversity experiment"</p>

opencc-by-4.0Mar 2024View details →
zenodo28/100

Figure 10 in Application Of Lichen Functional Traits In Identification Of Temperate Old-Growth Broad-Leaved Forests

Figure 10. Lichen spore type in old (old­growth), middle (middle­aged) and young broad­leaved forest stands.

opencc-by-4.0Dec 2022View details →
zenodo28/100

Figure 6 in Composition and structure of plant communities in the Moist Temperate Forest Ecosystem of the Hindukush Mountains, Pakistan

Figure 6. Analysis of CCA plot illustrating correlation between calciumcarbonate and plant communities along axis-1 and 2.

opencc-by-4.0Dec 2022View details →
zenodo28/100

Supplementary material 2 from: Naseer A, Khalid AN, Healy R, Smith ME (2019) Two new species of Hygrophorus from temperate Himalayan Oak forests of Pakistan. MycoKeys 56: 33-47. https://doi.org/10.3897/mycokeys.56.30280

: Data type: media

opencc-zeroJul 2019View details →
zenodo28/100

Supplementary material 1 from: Naseer A, Khalid AN, Healy R, Smith ME (2019) Two new species of Hygrophorus from temperate Himalayan Oak forests of Pakistan. MycoKeys 56: 33-47. https://doi.org/10.3897/mycokeys.56.30280

: Data type: media

opencc-zeroJul 2019View details →
zenodo28/100

Figure 6 from: Naseer A, Khalid AN, Healy R, Smith ME (2019) Two new species of Hygrophorus from temperate Himalayan Oak forests of Pakistan. MycoKeys 56: 33-47. https://doi.org/10.3897/mycokeys.56.30280

Figure 6 Molecular phylogenetic analysis of Hygrophorus spp. based on LSU sequences. Maximum likelihood phylogram of Hygrophorus based on nrDNA LSU as generated with RAxML with 1000 bootstrap iterations. Bolded lettering refers to sequences generated in this study.

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

Figure 5 from: Naseer A, Khalid AN, Healy R, Smith ME (2019) Two new species of Hygrophorus from temperate Himalayan Oak forests of Pakistan. MycoKeys 56: 33-47. https://doi.org/10.3897/mycokeys.56.30280

Figure 5 Phylogenetic relationship of Hygrophorus spp. and its ECM roots from Pakistan and their allied Hygrophorus species based on nrDNA ITS sequences using the Maximum Likelihood method. Sequences generated during this study are in bold letters. Sequences from root tips were labelled as ECM.

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

Figure 4 from: Naseer A, Khalid AN, Healy R, Smith ME (2019) Two new species of Hygrophorus from temperate Himalayan Oak forests of Pakistan. MycoKeys 56: 33-47. https://doi.org/10.3897/mycokeys.56.30280

Figure 4 Anatomy of Hygrophorusscabrellus. A–HLAH35245 (holotype) A Basidia B Basidia with basidioles C Basidiospores D Cheilocystidia E Pleurocystidia F Stipitipellis G Tramal Hyphae H Pileipellis. Scale bars: 5.83 μm (A, B, D, E); 3.55 μm (C); 0.12 μm (F–H).

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

Figure 3 from: Naseer A, Khalid AN, Healy R, Smith ME (2019) Two new species of Hygrophorus from temperate Himalayan Oak forests of Pakistan. MycoKeys 56: 33-47. https://doi.org/10.3897/mycokeys.56.30280

Figure 3 Morphology of Hygrophorusscabrellus. A, B Basidiomata. LAH35245 (holotype). Scale bars: 0.88 cm (A); 0.48 cm (B).

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

Figure 2 from: Naseer A, Khalid AN, Healy R, Smith ME (2019) Two new species of Hygrophorus from temperate Himalayan Oak forests of Pakistan. MycoKeys 56: 33-47. https://doi.org/10.3897/mycokeys.56.30280

Figure 2 Anatomy of Hygrophorusalboflavescens. A–DLAH35243 (holotype) A Basida B Basidiospores C Pileipellis D Stipitipellis. Scale bars: 2.0 μm (A); 4.5 μm (B); 13.7 μm (C); 7.8 μm (D).

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

Figure 1 from: Naseer A, Khalid AN, Healy R, Smith ME (2019) Two new species of Hygrophorus from temperate Himalayan Oak forests of Pakistan. MycoKeys 56: 33-47. https://doi.org/10.3897/mycokeys.56.30280

Figure 1 Morphology of Hygrophorusalboflavescens (Holotype). A–D Basidiomata A, BLAH35244; FLAS-F-59457 C, DLAH35243. Scale bar: 1.5 cm.

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

Figure 5 in Two new species of Anaulacodesmus Attems, 1898 (Polydesmida: Dalodesmidae) from temperate forest fragments in southern Chile

Figure 5. Anaulacodesmus picassovallebuonai sp. nov., paratypes, lateral view, top: female, bottom: male. Scale: 4.0 mm. / Anaulacodesmus picassovallebuonai sp. nov., paratipos, vista lateral, arriba:

opencc-by-4.0Aug 2023View details →
zenodo28/100

Figure 4. A in Two new species of Anaulacodesmus Attems, 1898 (Polydesmida: Dalodesmidae) from temperate forest fragments in southern Chile

Figure 4. A. Hypoproct of Anaulacodesmus panterae sp. nov., ventrolateral view (not to scale). B. Left gonopod of Anaulacodesmus panterae sp. nov., lateral view. Scale: 0.2 mm. C. Left gonopod of Anaulacodesmus picassovallebuonai sp. nov., lateral view. Scale: 0.2 mm. Abbreviations: mb – middle branch; ab – anterior branch; sl – solenomere; me – medial branch. / A. Hipoprocto de Anaulacodesmus panterae sp. nov., vista ventrolateral (no tomado a escala). B. Gonópodo izquierdo de Anaulacodesmus panterae sp. nov., vista lateral. Escala: 0,2 mm. C. Gonópodo izquierdo de Anaulacodesmus picassovallebuonai sp. nov., vista lateral. Escala: 0,2 mm. Abreviaciones: mb – rama media; ab – rama anterior; sl – solenomero; me – rama medial.

opencc-by-4.0Aug 2023View details →
zenodo28/100

Fig. 1 in Seasonal Variations in the Assembly of Dung Beetles (Coleoptera: Geotrupidae and Scarabaeidae) Attracted to Macaque Feces in Temperate Forests in Japan

Fig. 1. Map of the study sites in Japan.

opennotspecifiedJun 2022View details →
dryad28/100

Data from: Roles of pathogens on replacement of tree seedlings in heterogeneous light environments in a temperate forest: a reciprocal seed sowing experiment

In forest communities, the Janzen–Connell (J-C) hypothesis proposes that species diversity is maintained by non-competitive distance- and/or density-dependent seedling mortality caused by host-specific natural enemies. However, the effects of pathogen associations from nearby conspecifics versus heterospecifics remain unknown in spatially heterogeneous light environments. Seeds of hardwood species Cornus controversa (Cornus) and Prunus grayana (Prunus) were sown beneath 6–7 Cornus and Prunus adults in both the forest understory (FU) and in gaps (Gap) created by felling all woody vegetation near the focal adults. Seedling growth, mortality, killing agents (e.g. pathogens that cause damping-off and leaf diseases), and root infection by arbuscular mycorrhizal fungi (AMF) were investigated. We found strong habitat effects on the expression of soil fungi beneath both tree species. Seedling mortality caused by soil-borne damping-off pathogens was greater in FU than in Gap, and AMF infection, which enhanced relative seedling growth rate, was greater in Gap than in FU. Seedling mortality caused by damping-off pathogens did not differ between Cornus and Prunus seedlings beneath the adults of conspecific or heterospecific adults in both FU and Gap, suggesting little distance-dependence or host preference in the fungus. Beneath the adults of Cornus and Prunus, the most prevalent leaf diseases were zonate leaf blight and angular leaf spot caused by the airborne pathogenic fungi Haradamyces foliicola and Phaeoisariopsis pruni-grayanae, respectively. Although these pathogens attacked the seedlings of both species, conspecific seedlings (i.e. home) showed more severe leaf damage, earlier leaf shedding and/or less defensive behaviour (cell wall defence) relative to heterospecific seedlings (i.e. away), suggesting negative distance-dependent attack (i.e. host preference) for these leaf diseases. As a result, greater seedling mortality was observed for conspecific seedlings under both FU and Gap treatments. Synthesis. In the temperate forest, the J-C hypothesis is largely mediated through the strong negative influence of airborne leaf diseases rather than through soil-borne damping-off pathogens. We found that airborne diseases demonstrated distance-dependent host preferences, which led to greater conspecific seedling damage regardless of environmental light conditions.

opencc-zeroDec 2015View details →
zenodo28/100

Figs. 6–13 in A New Click Beetle Genus from Chilean Temperate Forests, ALYMA (Coleoptera: Elateridae: Pomachiliini)

Figs. 6–13. Antenna of Alyma species. 6) A. pallipes; 7) A. ariasvillegasai; 8) A.

opennotspecifiedSep 2004View details →
zenodo28/100

Fig. 2 in A New Click Beetle Genus from Chilean Temperate Forests, ALYMA (Coleoptera: Elateridae: Pomachiliini)

Fig. 2. Dorsal habitus of Alyma lawlerae (Fig. 2) (Illustration Alexis Solodovnikov).

opennotspecifiedSep 2004View details →
zenodo28/100

Figs. 29–33 in A New Click Beetle Genus from Chilean Temperate Forests, ALYMA (Coleoptera: Elateridae: Pomachiliini)

Figs. 29–33. Male genitalia of Alyma species. 29) Alyma calafquenensis; 30) A.

opennotspecifiedSep 2004View details →
zenodo28/100

Fig. 3 in A New Click Beetle Genus from Chilean Temperate Forests, ALYMA (Coleoptera: Elateridae: Pomachiliini)

Fig. 3. Scanning electron micrograph of head of Alyma lawlerae.

opennotspecifiedSep 2004View details →
zenodo28/100

Fig. 1 in A New Click Beetle Genus from Chilean Temperate Forests, ALYMA (Coleoptera: Elateridae: Pomachiliini)

Fig. 1. Dorsal habitus of Alyma pallipes (Solier) (¼Cardiophorus pallipes Solier).

opennotspecifiedSep 2004View details →

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