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Figure 5 from: Peris-Felipo FJ, Yari Z, van Achterberg C, Rakhshani E, Belokobylskij SA (2016) Review of species of the genus Adelurola Strand, 1928, with a key to species (Hymenoptera, Braconidae, Alysiinae). ZooKeys 566: 13-30. https://doi.org/10.3897/zookeys.566.6684
Figure 5 - Adelurola kamtshatica Belokobylskij (female, paratype). A Habitus, lateral view B Head (lateral view) and mandible C Face in front view D Mesosoma, lateral view E Metasoma and ovipositor, lateral view F First metasomal tergite G Fore and hind wings.
Supplementary material 4 from: Rusch JC, Strand DA, Laurendz C, Andersen T, Johnsen SI, Edsman L, Vrålstad T (2022) Exploring the eDNA dynamics of the host-pathogen pair Pacifastacus leniusculus (Decapoda) and Aphanomyces astaci (Saprolegniales) under experimental conditions. NeoBiota 79: 1-29. https://doi.org/10.3897/neobiota.79.82793
R-script of MCOCC occupancy analysis
Supplementary material 3 from: Rusch JC, Strand DA, Laurendz C, Andersen T, Johnsen SI, Edsman L, Vrålstad T (2022) Exploring the eDNA dynamics of the host-pathogen pair Pacifastacus leniusculus (Decapoda) and Aphanomyces astaci (Saprolegniales) under experimental conditions. NeoBiota 79: 1-29. https://doi.org/10.3897/neobiota.79.82793
R-Script of GLM analysis
Supplementary material 2 from: Rusch JC, Strand DA, Laurendz C, Andersen T, Johnsen SI, Edsman L, Vrålstad T (2022) Exploring the eDNA dynamics of the host-pathogen pair Pacifastacus leniusculus (Decapoda) and Aphanomyces astaci (Saprolegniales) under experimental conditions. NeoBiota 79: 1-29. https://doi.org/10.3897/neobiota.79.82793
ddPCR and qPCR data from the mesocosm experiments
Supplementary material 1 from: Rusch JC, Strand DA, Laurendz C, Andersen T, Johnsen SI, Edsman L, Vrålstad T (2022) Exploring the eDNA dynamics of the host-pathogen pair Pacifastacus leniusculus (Decapoda) and Aphanomyces astaci (Saprolegniales) under experimental conditions. NeoBiota 79: 1-29. https://doi.org/10.3897/neobiota.79.82793
Primers and probes used in the present study
Supplementary material 5 from: Rusch JC, Strand DA, Laurendz C, Andersen T, Johnsen SI, Edsman L, Vrålstad T (2022) Exploring the eDNA dynamics of the host-pathogen pair Pacifastacus leniusculus (Decapoda) and Aphanomyces astaci (Saprolegniales) under experimental conditions. NeoBiota 79: 1-29. https://doi.org/10.3897/neobiota.79.82793
Results of the GLMM model
Fig. 20 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 20. Lacronia tenuis (Roewer, 1917) comb. nov., ♂ (MNRJ 5533ꜝ), penis, distal part. A. Dorsal view. B. Left lateral view. C. Ventral view. D. Detail of stylus and ventral process, dorso-lateral view. Scale bars: A–C = 100 μm; D = 20 μm.
Fig. 4 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 4. Lacronia spp., schematic illustrations of the ♂ DS, showing the background variation and tubercles patterns of the specimens in vivo (except for L. boraceae (B. Soares, 1942) comb. nov., which information was only available in alcohol). A. L. ceci Kury & Orrico, 2006. B. L. camboriu Kury, 2003. C. L. ricardoi Kury, 2003. D. L. serripes (Mello-Leitão, 1923). E. L. boraceae comb. nov. F. L. nigra (B. Soares, 1942) comb. nov. G. L. tenuis (Roewer, 1917) comb. nov. Scale bars = 1 mm.
Fig. 1 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 1. The most frequent tree (k-values = 3, 4, 5, 6, 10, 15 and 20) retrieved using the Mendes (2011) protocol. Clade support values are indicated above the branches (Bremer index / SFq values). Clade stability is indicated below the branches by the sensitivity plots ('Navajo rugs'), which denotes the tested k-values (black squares indicate monophyly; white squares indicate non-monophyly). The k-values (= 2 and 3) retrieved two different trees, represented here as 2.1, 2.2, 3.1 and 3.2. in the Navajo rugs. Colored backgrounds indicate the following groups: Discocyrtus Holmberg, 1878 s. str. (grey), Lacronia Strand, 1942 (salmon), Mitobatinae Simon, 1879 (green), Neopachylinae Carvalho & Kury, 2020 (yellow), Pachylinae Sørensen, 1884 s. str. (purple) and Roeweriinae Carvalho & Kury, 2018 (blue). A red circle marks the DRMN-group. The unmarked groups are not members of either DRMN or Pachylinae s. str.
FIGURE 1. A–B in A new species of Dieida Strand, 1911 from Turkey (Lepidoptera: Cossidae)
FIGURE 1. A–B. Dieida versicolor sp. nov. copula Okurcalar, Turkey, 7 May 2005
Repair of Flexor Tendon Injuries With Eight Strand Core Stitch Without Postoperative Splinting
ClinicalTrials.gov study NCT03938935. IPD Sharing: Not stated. Countries: 0. Publications: 1.
Data from: Algal toxin impairs sea lion memory and hippocampal connectivity, with implications for strandings
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Data from: A new plant virus discovered by immunocapture of double stranded RNA; assessment of a novel approach for viral metagenomics studies
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Data from: Chimeric viruses blur the borders between the major groups of eukaryotic single-stranded DNA viruses
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Data from: The telomere bouquet is a hub where meiotic double-strand breaks, synapsis, and stable homolog juxtaposition are coordinated in the zebrafish, Danio rerio
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Data from: Rev7 and 53BP1/Crb2 prevent RecQ helicase-dependent hyper-resection of DNA double-strand breaks
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Data from: Down-regulation of Rad51 activity during meiosis in yeast prevents competition with Dmc1 for repair of double-strand breaks
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Data from: BrAD-seq: Breath Adapter Directional sequencing: a streamlined, ultra-simple and fast library preparation protocol for strand specific mRNA library construction
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Data from: Advanced characterization of DNA molecules in rAAV vector preparations by single-stranded virus next-generation sequencing
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Data from: SNP discovery in non-model organisms: strand-bias and base-substitution errors reduce conversion rates
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