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44 results for “Auricularia”

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zenodo32/100

FIGURE 15 in Redefinition of the genus Luciaphorus Mahunka, 1981 (Acari: Pygmephoridae) with redescription of L. perNiciosus Rack, 1983 and L. auriculariae Gao, Zou and Jiang, 1990

FIGURE 15. Luciaphorus auriculariae Gao, Zou and Jiang, 1990, male: A—left leg I in dorsal view, B—left leg II in dorsal view.

opennotspecifiedJan 2018View details →
zenodo32/100

FIGURE 4. Luciaphorus perniciosus Rack, 1983 in Redefinition of the genus Luciaphorus Mahunka, 1981 (Acari: Pygmephoridae) with redescription of L. perNiciosus Rack, 1983 and L. auriculariae Gao, Zou and Jiang, 1990

FIGURE 4. Luciaphorus perniciosus Rack, 1983, male: A—dorsum of the body, B—venter of the body. Legs omitted.

opennotspecifiedJan 2018View details →
zenodo32/100

FIGURE 3. Luciaphorus perniciosus Rack, 1983 in Redefinition of the genus Luciaphorus Mahunka, 1981 (Acari: Pygmephoridae) with redescription of L. perNiciosus Rack, 1983 and L. auriculariae Gao, Zou and Jiang, 1990

FIGURE 3. Luciaphorus perniciosus Rack, 1983, female: A–B—right legs III and IV in dorsal view, respectively.

opennotspecifiedJan 2018View details →
zenodo32/100

FIGURE 12 in Redefinition of the genus Luciaphorus Mahunka, 1981 (Acari: Pygmephoridae) with redescription of L. perNiciosus Rack, 1983 and L. auriculariae Gao, Zou and Jiang, 1990

FIGURE 12. Luciaphorus auriculariae Gao, Zou and Jiang, 1990, female: A—left leg I in dorsal view, B—left leg II in dorsal view.

opennotspecifiedJan 2018View details →
zenodo32/100

FIGURE 11 in Redefinition of the genus Luciaphorus Mahunka, 1981 (Acari: Pygmephoridae) with redescription of L. perNiciosus Rack, 1983 and L. auriculariae Gao, Zou and Jiang, 1990

FIGURE 11. Luciaphorus auriculariae Gao, Zou and Jiang, 1990, female: A—dorsum of the body, B—venter of the body. Legs omitted.

opennotspecifiedJan 2018View details →
zenodo32/100

FIGURE 8 in Redefinition of the genus Luciaphorus Mahunka, 1981 (Acari: Pygmephoridae) with redescription of L. perNiciosus Rack, 1983 and L. auriculariae Gao, Zou and Jiang, 1990

FIGURE 8. SEM micrograph of Luciaphorus perniciosus Rack, 1983, female: A—dorsal view, B—ventral view, Cprodorsum, D—anterior part of propodosomal plate, E—tergites D, EF and H, F—pseudanal setae.

opennotspecifiedJan 2018View details →
zenodo32/100

FIGURE 7 in Redefinition of the genus Luciaphorus Mahunka, 1981 (Acari: Pygmephoridae) with redescription of L. perNiciosus Rack, 1983 and L. auriculariae Gao, Zou and Jiang, 1990

FIGURE 7. DIC micrograph of Luciaphorus perniciosus Rack, 1983, female: leg II in dorsal view. Arrow points to subcuticular invagination.

opennotspecifiedJan 2018View details →
zenodo32/100

FIGURE 1. The phylogram inferred from a in Auricularia thailandica sp. nov. (Auriculariaceae, Auriculariales) a widely distributed species from Southeastern Asia

FIGURE 1. The phylogram inferred from a Maximum Likelihood analysis of ITS sequences of Auricularia. Species names are followed by the herbarium code or collection code or GenBank accession number. RAxML/ Bayesian posterior probabilities / MP bootstrap values ≥70 % are displayed above or below each node. The tree is rooted with Exidia recisa (MW315) and Exidiopsis sp. (FO46291).

opennotspecifiedMay 2015View details →
zenodo32/100

FIGURE 2 in Auricularia thailandica sp. nov. (Auriculariaceae, Auriculariales) a widely distributed species from Southeastern Asia

FIGURE 2. Auricularia thailandica (MFLU 130410, holotype). a. Basidiocarps. b. Cross-section of the fruitbody. c. Abhymenial hairs. d. Close-up of hymenial layer. e–k. Basidiospores. l. Clamp-connection of a hypha. Scale bars: b=500 μm, c=50 μm, d=25 μm, e–l =5 μm. (Photos by Asanka R. Bandara).

opennotspecifiedMay 2015View details →
zenodo32/100

FIGURE 3 in Diversity of Auricularia (Auriculariaceae, Auriculariales) in Thailand

FIGURE 3. Field photographs of Auricularia. a. A. asiatica (ST05). b,c. A. cornea (MRC8, AB51). d,e. A. delicata (DSK3, MRC7). f. A. thailandica (AB34). g. A. villosula (AB38). Diameter of coins: c=24 mm, g=20 mm.

opennotspecifiedJan 2017View details →
zenodo32/100

FIGURE 2 in Diversity of Auricularia (Auriculariaceae, Auriculariales) in Thailand

FIGURE 2. Auricularia asiatica (BBH 895). a. Basidiocarp. b. Cross-section. c. Abhymenial hairs. d. Basidia. e. Close-up of hymenial layer. f–l. Basidiospores. m. Clamp connection of hyphae. Scale bars: a=mm, b=500 μm, c=250 μm, d=100, e=25 μm, f–m=5 μm.

opennotspecifiedJan 2017View details →
zenodo32/100

FIGURE 1 in Diversity of Auricularia (Auriculariaceae, Auriculariales) in Thailand

FIGURE 1. Phylograms inferred from maximum likelihood analyses of ITS+rpb2 sequences of Auricularia. Species names are followed by the herbarium code or collection code or GenBank accession number. Newly produced sequences are in bold. Bootstrap support values of the ML analysis / Bayesian posterior probabilities ≥70 % are displayed above each node. The ITS tree is rooted with Eichleriella deglubens (FO12006), The tree is rooted with Tremella mesenterica (CBS6973) and Tremella globispora (CBS6972).

opennotspecifiedJan 2017View details →
zenodo32/100

FIGURE 3. Auricularia heimuer. A–D cultivated basidiomata. E in Species clarification of the most important and cultivated Auricularia mushroom "Heimuer": evidence from morphological and molecular data

FIGURE 3. Auricularia heimuer. A–D cultivated basidiomata. E wild basidiomata (holotype). Scale bars: B = 10 cm, D–E = 5 cm.

opennotspecifiedDec 2014View details →
zenodo32/100

FIGURE 2 in Species clarification of the most important and cultivated Auricularia mushroom "Heimuer": evidence from morphological and molecular data

FIGURE 2. Maximum parsimony strict consensus tree illustrating the phylogeny of Auricularia based on ITS+nLSU sequences. Branches are labeled with parsimony bootstrap proportions (before slanting line) higher than 50% and Bayesian posterior probabilities (after slanting line) more than 0.95.

opennotspecifiedDec 2014View details →
zenodo32/100

FIGURE 1 in Species clarification of the most important and cultivated Auricularia mushroom "Heimuer": evidence from morphological and molecular data

FIGURE 1. Maximum parsimony strict consensus tree illustrating the phylogeny of Auricularia based on ITS sequences. Branches are labeled with parsimony bootstrap proportions (before slanting line) higher than 50% and Bayesian posterior probabilities (after slanting line) more than 0.95.

opennotspecifiedDec 2014View details →
zenodo32/100

FIGURE 4 in Species clarification of the most important and cultivated Auricularia mushroom "Heimuer": evidence from morphological and molecular data

FIGURE 4. Microscopic structures of Auricularia heimuer (photographed from the holotype). A Cross-section displaying medulla. B abhymenial hairs. C–D Basidia (indicated by a). E–F Basidiospores. Bars: A = 100 μm; B = 10 µm; C = 20 µm; D–E = 10 μm; F = 5 µm.

opennotspecifiedDec 2014View details →
dryad32/100

Data from: Love them all: mothers provide care to foreign eggs in the European earwig Forficula auricularia

Open the record for dataset details and reuse information.

publicJan 2019View details →
zenodo28/100

DATA SET - Sublethal exposure to deltamethrin impairs maternal egg care in the European earwig Forficula auricularia

<p>Data set of the manuscript entitled &quot;Sublethal exposure to deltamethrin impairs maternal egg care in the European earwig&nbsp;Forficula auricularia&quot; and published in the journal Chemosphere.</p>

opencc-by-4.0Jun 2020View details →
dryad28/100

Data from: Maternal programming of offspring in relation to food availability in an insect (Forficula auricularia)

Maternal effects can induce adjustments in offspring phenotype to the environment experienced by the mother. Of particular interest is if mothers can program their offspring to cope best under matching environmental conditions, but the evidence for such anticipatory maternal effects (AME) is limited. In this study, we manipulated experimentally the food availability experienced by mothers and their offspring in the European earwig (Forficula auricularia). Offspring produced by females that had access to high- or low-food quantities were cross-fostered to foster mothers experiencing matched or mismatched environments. Offspring experiencing food availability matching the one of their mothers had an increased survival to adulthood compared to offspring experiencing mismatched conditions. Females experiencing high food laid larger clutches. This clutch-size adjustment statistically explained the matching effect when offspring experienced high food, but not when experiencing low food conditions. There were no effects of matching on offspring growth and developmental rate. Overall, our study demonstrates that AME occurs in relation to food availability enhancing offspring survival to adulthood under matching food conditions.

opencc-zeroDec 2015View details →
dryad28/100

Data from: Maternal programming of offspring in relation to food availability in an insect (Forficula auricularia)

Open the record for dataset details and reuse information.

publicMar 2016View details →

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