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234 results for “molecular characterisation”

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zenodo28/100

Figure 1 from: Hlebec D, Sivec I, Podnar M, Skejo J, Kučinić M (2021) Morphological and molecular characterisation of the Popijač's Yellow Sally, Isoperla popijaci sp. nov., a new stenoendemic stonefly species from Croatia (Plecoptera, Perlodidae). ZooKeys 1078: 85-106. https://doi.org/10.3897/zookeys.1078.66382

Figure 1 Morphology of Isoperla popijaci sp. nov. A head and pronotum in dorsal view (adult male HT) B habitus (larval PT) C habitus (adult male PT) D female terminalia in ventral view (PT) E everted male copulatory organ (HT). Scale bar: 0.5 mm A–E.

opencc-by-4.0Dec 2021View details →
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Figure 4 from: Hlebec D, Sivec I, Podnar M, Skejo J, Kučinić M (2021) Morphological and molecular characterisation of the Popijač's Yellow Sally, Isoperla popijaci sp. nov., a new stenoendemic stonefly species from Croatia (Plecoptera, Perlodidae). ZooKeys 1078: 85-106. https://doi.org/10.3897/zookeys.1078.66382

Figure 4 Extruded penis of Isoperla popijaci sp. nov. A male abdomen with extruded penis, ventral view B detail of penial armature on the lateral lobe, dorsal view C scales of the upper medial penial armature, dorsal view D pair of the scales spike-like on the ventral lobe, dorsal view.

opencc-by-4.0Dec 2021View details →
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Fig. 1 in Molecular and morphological characterisation of Pharyngostrongylus kappa Mawson, 1965 (Nematoda: Strongylida) from Australian macropodid marsupials with the description of a new species, P. patriciae n. sp.

Fig. 1 Distribution of Pharyngostrongylus kappa ex Macropus giganteus (open circles) and P. patriciae n. sp. ex Osphranter robustus (closed squares), O. antilopinus (closed triangles) and O. bernardus (inverted triangle). Tce symbol 'm' indicates localities from wcicc material included in molecular studies was collected

opencc-by-4.0Apr 2018View details →
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Figure 1 from: Hjalmarsson AE, Graf W, Jähnig SC, Vitecek S, Pauls SU (2018) Molecular association and morphological characterisation of Himalopsyche larval types (Trichoptera, Rhyacophilidae). ZooKeys 773: 79-108. https://doi.org/10.3897/zookeys.773.24319

Figure 1 Map showing sampling localities in A North America, and B East Asia. Colours/symbols indicate larval types of the OTUs. Elevation data from Jarvis et al. (2008), stream data from Andreadis et al. (2013).

opencc-by-4.0Jul 2018View details →
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Figure 2 from: Hjalmarsson AE, Graf W, Jähnig SC, Vitecek S, Pauls SU (2018) Molecular association and morphological characterisation of Himalopsyche larval types (Trichoptera, Rhyacophilidae). ZooKeys 773: 79-108. https://doi.org/10.3897/zookeys.773.24319

Figure 2 Summary of GMYC results from the CAD and COI, indicating the overlap in results from the two genes. Colours indicate larval types, inferred from this study and the literature.

opencc-by-4.0Jul 2018View details →
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Figures 23-28 from: Hjalmarsson AE, Graf W, Jähnig SC, Vitecek S, Pauls SU (2018) Molecular association and morphological characterisation of Himalopsyche larval types (Trichoptera, Rhyacophilidae). ZooKeys 773: 79-108. https://doi.org/10.3897/zookeys.773.24319

Figures 23-28 Thorax ventral, abdomen dorsal. 23 H. gregoryi 24 H. japonica, arrows indicate ventral gills 25 H. phryganea 26 H. gregoryi, 27 H. acharai 28 H. sylvicola. Arrows A points to anterior.

opencc-by-4.0Jul 2018View details →
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Figures 29-36 from: Hjalmarsson AE, Graf W, Jähnig SC, Vitecek S, Pauls SU (2018) Molecular association and morphological characterisation of Himalopsyche larval types (Trichoptera, Rhyacophilidae). ZooKeys 773: 79-108. https://doi.org/10.3897/zookeys.773.24319

Figures 29-36 Abdomen lateral, ventral. 29, 30 H. phryganea, arrow points to ventral medial sclerite 31, 32 H. gregoryi, arrow points to ventral medial sclerite 33, 34 H. japonica, arrow points to ventral protuberance 35, 36 H. sylvicola, arrow a indicates small rounded protuberance on lateral process, while arrow b indicates the ventral medial sclerite. Roman numbers indicate abdominal segments. Arrow A points to anterior.

opencc-by-4.0Jul 2018View details →
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Figures 37-44 from: Hjalmarsson AE, Graf W, Jähnig SC, Vitecek S, Pauls SU (2018) Molecular association and morphological characterisation of Himalopsyche larval types (Trichoptera, Rhyacophilidae). ZooKeys 773: 79-108. https://doi.org/10.3897/zookeys.773.24319

Figures 37-44 Anal prolegs, lateral, caudal. 37, 38 H. phryganea 39 H. gregoryi 40 H. tibetana 41, 42 H. japonica 43, 44 H. sylvicola. Key: arrows a distolateral accessory hook. arrows b protuberance/hook on dorsal plate. arrows c dorsal spine on basal anal claw. arrows d proximal accessory hooks fused with lateral sclerites. Arrow A points to anterior.

opencc-by-4.0Jul 2018View details →
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Figures 3-6 from: Hjalmarsson AE, Graf W, Jähnig SC, Vitecek S, Pauls SU (2018) Molecular association and morphological characterisation of Himalopsyche larval types (Trichoptera, Rhyacophilidae). ZooKeys 773: 79-108. https://doi.org/10.3897/zookeys.773.24319

Figures 3-6 Habitus of Himalopsyche larvae. 3 H. phryganea 4 H. gregoryi 5 H. japonica 6 H. sylvicola. Arrow A points to anterior.

opencc-by-4.0Jul 2018View details →
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Figures 15-22 from: Hjalmarsson AE, Graf W, Jähnig SC, Vitecek S, Pauls SU (2018) Molecular association and morphological characterisation of Himalopsyche larval types (Trichoptera, Rhyacophilidae). ZooKeys 773: 79-108. https://doi.org/10.3897/zookeys.773.24319

Figures 15-22 Thorax of Himalopsyche larvae in dorsal and lateral view. 15, 16 H. phryganea 17, 18 H. gregoryi, arrow a points to anterodorsal single coxal gill 19, 20 H. japonica, arrow a indicates anterodorsal single coxal gill; arrow b indicates the ventral gills 21, 22 H. sylvicola. Arrows A points to anterior.

opencc-by-4.0Jul 2018View details →
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Figures 7-10 from: Hjalmarsson AE, Graf W, Jähnig SC, Vitecek S, Pauls SU (2018) Molecular association and morphological characterisation of Himalopsyche larval types (Trichoptera, Rhyacophilidae). ZooKeys 773: 79-108. https://doi.org/10.3897/zookeys.773.24319

Figures 7-10 Pronotum of Himalopsyche larvae. 7 H. phryganea 8 H. anomala 9 H. japonica 10 H. sylvicola. Arrow A points to anterior.

opencc-by-4.0Jul 2018View details →
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Figures 11-14 from: Hjalmarsson AE, Graf W, Jähnig SC, Vitecek S, Pauls SU (2018) Molecular association and morphological characterisation of Himalopsyche larval types (Trichoptera, Rhyacophilidae). ZooKeys 773: 79-108. https://doi.org/10.3897/zookeys.773.24319

Figures 11-14 Mesolegs and head of Himalopsyche larvae. 11 Mesoleg of H. gregoryi 12 Mesoleg of H. sylvicola, arrows indicate dorsal fringe of setae on legs 13 Mesoleg of H. sylvicola. Arrows indicate pennate setae on coxa and femora 14 Head of H. phryganea, arrow points to lateral protuberances on mandible.

opencc-by-4.0Jul 2018View details →
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Figure 7 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188

Figure 7 Scatter plot of functional odontostyle (blue square) and replacement odontostyle (white square) against body length of Lonigidoruspolyae sp. n. juveniles (J1-J4) and females (blue), and male odontostyle (red).

opencc-by-4.0Mar 2019View details →
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Figure 6 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188

Figure 6 Longidoruspolyae sp. n. A–E anterior end of first- to fourth-stage juveniles and female F–J tail of first- to fourth- stage juvenile and female. Scale bar: 20 μm.

opencc-by-4.0Mar 2019View details →
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Figure 9 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188

Figure 9 Phylogenetic tree using D2-D3 expansion segments of the 28S rRNA gene inferred from a Bayesian analysis with GTR+I+G model. Numbers represent the Bayesian posterior probabilities.

opencc-by-4.0Mar 2019View details →
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Figure 4 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188

Figure 4 Longidoruspolyae sp. n., male A anterior region B amphidial fovea C labial region D junction of two testes E distal part of testis F sperm cells G nerve ring H, I posterior end, different magnifications J tail and spicules K supplements. Scale bars: 20 μm (A–C, F, G, J, K); 40 μm (D, E, H); 100 μm (I).

opencc-by-4.0Mar 2019View details →
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Figure 3 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188

Figure 3 Longidoruspolyae sp. n., holotype A anterior end B pharyngeal region, arrows point to at nerve ring, pharyngeal bulb and cardia C intestine, posterior part with inclusions D anterior genital branch E vagina and part of the posterior genital branch F sphincter G intestine inclusion at higher magnification H tail I vagina J posterior ovary. Scale bars: 20 μm (A, F–I); 40 μm (E, J); 100 μm (B–D).

opencc-by-4.0Mar 2019View details →
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Figure 5 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188

Figure 5 Longidoruspolyae sp. n. A–D anterior end of first- (J1) to fourth- (J4) stage juveniles E–H tail of first to fourth juvenile stages I variations in J1-J4 habitus shapes. Scale bars: 25 μm (A–H); 1 mm (I).

opencc-by-4.0Mar 2019View details →
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Figure 8 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188

Figure 8 Bulgarian populations of Longidoruspisi Edward, Misra & Singh, 1964, anterior end of female (A) and male (B) female C, D vagina and part of reproductive system (different populations) E–G pre-rectum inclusions H labial region I vagina J–M variations in tail shape, female (J, L, M) and male (K). Populations: A, L Petrich C, E–G, M Sandanski D, H, I, J Kromidovo B, K male specimens from a tobacco field, Petrich region. Scale bars: 20 μm (A–G, J–M); 12 μm (H, I).

opencc-by-4.0Mar 2019View details →
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Figure 2 from: Lazarova SS, Elshishka M, Radoslavov G, Lozanova L, Hristov P, Mladenov A, Zheng J, Fanelli E, De Luca F, Peneva VK (2019) Molecular and morphological characterisation of Longidorus polyae sp. n. and L. pisi Edward, Misra & Singh, 1964 (Dorylaimida, Longidoridae) from Bulgaria. ZooKeys 830: 75-98. https://doi.org/10.3897/zookeys.830.32188

Figure 2 Longidoruspolyae sp. n., female A anterior region B, C variations in vagina D, E variations in tail shape F–H intestine inclusions I posterior genital branch J part of reproductive system. Scale bars: 20 μm (A–H); 100 μm (I, J).

opencc-by-4.0Mar 2019View details →

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Last verified 2026-04-30Open record

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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.

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neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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