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Figure 25 in Systematic revision of the living species of Bullidae (Mollusca: Gastropoda: Cephalaspidea), with a molecular phylogenetic analysis
Figure 25. Images of living Indo-West Pacific Bulla species. A, Bulla ampulla, Tuticorin, India (H = 43 mm; photo by Malaquias). B, B. arabica sp. nov., Gulf of Aqaba, Red Sea (size unknown; adult specimen). C, B. quoyii, Edithburgh Jetty, South Australia (H = 30 mm; photo: J. Chuk). D, B. vernicosa, Panglao, Philippines (H = 30 mm; photo: M. Poddubetskaia). E, B. orientalis, Kerama Island, Japan (H = 15 mm; photo: A. Ono). F, B. vernicosa, Panglao, Philippines (H = 8 mm; photo: M. Poddubetskaia). G, B. peasiana, Hawaii (H = 15 mm; photo: S. Johnson).
Figure 19 in Systematic revision of the living species of Bullidae (Mollusca: Gastropoda: Cephalaspidea), with a molecular phylogenetic analysis
Figure 19. Outer lateral teeth of radula of Bulla mabillei (A, B), B. solida (C, D), B. gouldiana (E, F), and B. punctulata (G, H). A, Tenerife Island, Canary Islands (BMNH 20020457; H = 26.9 mm). B, Tenerife Island, Canary Islands (BMNH 20030774; H = 48.4 mm). C, off Florida (HBOM 62–281; H = 38.4 mm). D, off Florida (HBOM 62–281; H = 38.4 mm). E–F, Baja California, Mexico (CAS 101586; H = 28.4 mm). G–H, Santa Cruz Island, Galapagos (CAS 067270; H = 18.1, 17.6 mm). Scale bars: A–H = 100 Mm.
Figure 38 in Systematic revision of the living species of Bullidae (Mollusca: Gastropoda: Cephalaspidea), with a molecular phylogenetic analysis
Figure 38. Geographical distributions of Bulla ampulla, B. arabica sp. nov. and B. peasiana based on examined material and quoted literature records (A – Vayssière, 1906; B – Green, 1994).
Figure 11 in Systematic revision of the living species of Bullidae (Mollusca: Gastropoda: Cephalaspidea), with a molecular phylogenetic analysis
Figure 11. Gizzard plates and spines of Bulla striata (A–G) and B. occidentalis (H). A, E, Naples, Italy (BMNH 20030775; H = 24.6 mm). B, C, Ria Formosa, Portugal (BMNH 20050338; H = 25.0, 30.1 mm). D, Siné-Saloum, Senegal (BMNH 20030781; H = 15.7 mm). F–G, Ria Formosa, Portugal (BMNH 20050338; H = 31.3 mm). H, Cape of Santo António, Cuba (BMNH 20050351; H = 10.2 mm). Scale bars: A–E = 1 mm; F, H = 200 Mm; G = 500 Mm.
Figure 1. A, Bulla shell. B in Systematic revision of the living species of Bullidae (Mollusca: Gastropoda: Cephalaspidea), with a molecular phylogenetic analysis
Figure 1. A, Bulla shell. B, central nervous system of B. striata (Ria Formosa, Portugal, BMNH20050338; H = 29.40 mm). C, Bulla spp., external morphology of animal. c, columella; celo, cephalic lobe; ces, cephalic shield; cg, cerebral ganglion; bg, buccal ganglion; e, eye; g, genital ganglion; H, height; is, position of the involute spire; pa, parietal ganglion; palo, parapodial lobe; pc, parietal callus; pd, pedal ganglion; pl, pleural ganglion; poa, periocular area; sb, suboesophageal ganglion; sh, shell; sp., supraoesophageal ganglion; t, tentacle; v, visceral ganglion. Scale bar = 1 mm.
Divergent contributions of living roots to turnover of different soil organic carbon pools and their links to plant traits
<p>1. Rhizodeposits and root litter contribute critically to soil organic carbon (SOC) formation and decomposition. This root-induced SOC turnover shows great interspecific variations. Bulk SOC consists of diverse functional pools differing in formation and stabilization. Yet, it remains unclear which plant traits regulate the effects of living roots on the turnover of different SOC pools across species.</p> <p>2. By performing <sup>13</sup>CO<sub>2 </sub>continuous<sub> </sub>labelling of six grassland species for a growing season in a climate-controlled chamber, we quantified the contributions of living roots to the dynamics of the fast-cycling particulate organic C and the slow-cycling mineral-associated organic C, and explored their relations to plant traits.</p> <p>3. The results showed that new root-derived SOC varied more than threefold among the six species. The variation in new root-derived SOC was best explained by the ratio of shoot to root biomass. Plant species with higher shoot:root ratio formed more new root-derived SOC. Most of the root-derived C (72%) was incorporated into the particulate organic C pool. All species caused positive rhizosphere priming effects (RPE), which varied sevenfold across species. Among plant traits, specific root length was the best predictor of interspecific variations in the RPE, with greater RPE associated with higher specific root length. Most of the RPE (70%) occurred in the mineral-associated organic C pool. Our results also showed that most plant species caused more old SOC decomposition via the RPE than new SOC formation, leading to net SOC losses, especially for the mineral-associated organic C pool.</p> <p>4. Overall, we provide novel insights into the effects of plant traits on root-induced turnover of particulate and mineral-associated organic C. Our findings should be valuable for understanding how specific plant traits regulate SOC accumulation and stabilization.</p>
Figures 3-4 from: Fikácek M, Angus R (2011) A long-living species of the hydrophiloid beetles: Helophorus sibiricus from the early Miocene deposits of Kartashevo (Siberia, Russia). ZooKeys 130: 239-254. https://doi.org/10.3897/zookeys.130.1378
Figures 3-4 - Helophorus sibiricus (Motschulsky, 1860), drawings of the early Miocene fossil No. PIN 3285/5 from Kartashevo 3 piece 4 counterpiece. Abbreviations: mp4 maxillary palpomere 4, clyp clypeus, fr frons, ics intercalary stria, mt mentum, scut mesoscutellum, aps anapleural sutures of mesothorax, mtv metaventrite, av1 abdominal ventrite 1.
Figures 1-2 from: Fikácek M, Angus R (2011) A long-living species of the hydrophiloid beetles: Helophorus sibiricus from the early Miocene deposits of Kartashevo (Siberia, Russia). ZooKeys 130: 239-254. https://doi.org/10.3897/zookeys.130.1378
Figures 1-2 - Helophorus sibiricus (Motschulsky, 1860), photo of the early Miocene fossil No. PIN 3285/5 from Kartashevo 1 piece 2 counterpiece.
Figures 5-9 from: Fikácek M, Angus R (2011) A long-living species of the hydrophiloid beetles: Helophorus sibiricus from the early Miocene deposits of Kartashevo (Siberia, Russia). ZooKeys 130: 239-254. https://doi.org/10.3897/zookeys.130.1378
Figures 5-9 - Helophorus sibiricus (Motschulsky, 1860) 5 habitus of a recent specimen (Mongolia, Baga-Tenger, coll. National Museum, Prague) 6–7 detail of mentum, the arrow indicates a characteristic emargination on the anterior margin of mentum (6 fossil specimen, SEM micrograph 7 recent specimen, view from inside) 8–9 detailgranulation of head and pronotum, SEM micrographs (8 recent specimen 9 fossil specimen).
Figure 10 from: Fikácek M, Angus R (2011) A long-living species of the hydrophiloid beetles: Helophorus sibiricus from the early Miocene deposits of Kartashevo (Siberia, Russia). ZooKeys 130: 239-254. https://doi.org/10.3897/zookeys.130.1378
Figure 10 - Fossil and recent distribution of Helophorus sibiricus (Motschulsky, 1860). Subfossil Holocene records omitted.
Figure 3 from: Winterton S, Gillung J (2011) New genera of philopotine spider flies (Diptera, Acroceridae) with a key to living and fossil genera. ZooKeys 127: 15-27. https://doi.org/10.3897/zookeys.127.1824
Figure 3 - Quasi fisheri gen. et sp. n., male, anterolateral view [Morphbank: 693076]. Body length = 6.0 mm.
Figure 5 from: Winterton S, Gillung J (2011) New genera of philopotine spider flies (Diptera, Acroceridae) with a key to living and fossil genera. ZooKeys 127: 15-27. https://doi.org/10.3897/zookeys.127.1824
Figure 5 - Quasi fisheri gen. et sp. n., male, anterior view [Morphbank: 693078]. Body length = 6.0 mm.
Figure 1 from: Winterton S, Gillung J (2011) New genera of philopotine spider flies (Diptera, Acroceridae) with a key to living and fossil genera. ZooKeys 127: 15-27. https://doi.org/10.3897/zookeys.127.1824
Figure 1 - Quasi fisheri gen. et sp. n. A head and postpronotal lobes, anterior B wing C head, lateral. Schlingeriella irwini gen. et sp. n. D wing. Eulonchiella eocenica Meunier E head and postpronotal lobes, anterior F habitus in situ, lateral. Scale line = 0.2 mm.
Figure 7 from: Winterton S, Gillung J (2011) New genera of philopotine spider flies (Diptera, Acroceridae) with a key to living and fossil genera. ZooKeys 127: 15-27. https://doi.org/10.3897/zookeys.127.1824
Figure 7 - Schlingeriella irwini gen. et sp. n., female, lateral view [Morphbank: 693080]. Body length = 4.4 mm.
Figure 6 from: Winterton S, Gillung J (2011) New genera of philopotine spider flies (Diptera, Acroceridae) with a key to living and fossil genera. ZooKeys 127: 15-27. https://doi.org/10.3897/zookeys.127.1824
Figure 6 - Schlingeriella irwini gen. et sp. n., male, lateral view [Morphbank: 693079]. Body length = 2.4 mm.
Figure 4 from: Winterton S, Gillung J (2011) New genera of philopotine spider flies (Diptera, Acroceridae) with a key to living and fossil genera. ZooKeys 127: 15-27. https://doi.org/10.3897/zookeys.127.1824
Figure 4 - Quasi fisheri gen. et sp. n., male, dorsal view [Morphbank: 693077]. Body length = 6.0 mm.
Figure 2 from: Su S, Hirose E, Chen S, Mok M (2013) Photosymbiotic ascidians in Singapore: turbid waters may reduce living space. ZooKeys 305: 55-65. https://doi.org/10.3897/zookeys.305.4893
Figure 2 - Photosymbiotic ascidians collected. A Trididemnum cyclops, St. John's Island, Singapore (Depth = 0.5 m). Colonies are 2–6 mm on the long axis B Thorax of Trididemnum cyclops. Arrows indicatethe endostylarpigment cap. Scale bar = 100 mm. C Tunic spicules in the tunic of Trididemnum cyclops. Scale bar = 100 mm D Diplosoma simile, Pulau Semakau, Singapore (Depth = 0.5 m). Colonies are approximately 15 mm in diameter E Thorax of Diplosoma simile (left view). Scale bar = 100 mm F Lissoclinum bistratum, Pulau Semakau, Singapore (Depth = 0.5 m). Colonies are approximately 5 mm in diameter G Tunic spicules in the tunic of Lissoclinum bistratum. Scale bar = 100 mm H A testis with an uncoiled vas deferens of Lissoclinum bistratum. Scale bar = 100 mm I Lissoclinum punctatum, Pulau Semakau, Singapore (Depth = 0.5 m). Colonies are approximately 10 mm in diameter J Tunic spicules in the tunic of Lissoclinum punctatum. Scale bar = 100 mm K Tunic phycocytes of Lissoclinum punctatum. Scale bar = 100 mm L Lissoclinum timorense, Pulau Semakau, Singapore (Depth = 0.5 m). Colonies are approximately 10 mm in diameter M Thorax of Lissoclinum timorense (left view) N Tunic spicules in the tunic of Lissoclinum timorense. Scale bar = 100 mm. rt, retractor muscle; ts, testis; vd, vas deferens.
Figure 1 from: Su S, Hirose E, Chen S, Mok M (2013) Photosymbiotic ascidians in Singapore: turbid waters may reduce living space. ZooKeys 305: 55-65. https://doi.org/10.3897/zookeys.305.4893
Figure 1 - Collection sites of photosymbiotic ascidians in Singapore. A Pulau Semakau B Sentosa C St. John's Island and D Changi Beach.
Figure 1-6 from: Erwin T, M. Amundson L (2013) Beetles that live with ants (Carabidae, Pseudomorphini, Pseudomorpha Kirby, 1825): A revision of the santarita species group. ZooKeys 362: 29-54. https://doi.org/10.3897/zookeys.362.6300
Figure 1-6 - 1 Pseudomorpha huachinera sp. n., male holotype, ADP110112; Arroyo El Cocono, Sierra Huachinera, Sonora, México. Habitus, dorsal aspect, ABL = 5.88mm 2 Pseudomorpha patagonia sp. n., male holotype, ADP110694; Madera Canyon, Santa Rita Mountains, AZ. Habitus, dorsal aspect, ABL = 4.39mm 3 Pseudomorpha penablanca sp. n., female holotype, CAS8111005; Peña Blanca Lake, Arizona. Habitus, dorsal aspect, ABL = 6.37mm 4 Pseudomorpha pima sp. n., female holotype, CAS8111006; Madera Canyon (lower), Santa Rita Mountains, Arizona. Habitus, dorsal aspect, ABL = 6.76mm 5 Pseudomorpha santacruz sp. n., male holotype, ADP111870; Madera Canyon, Santa Rita Mountains, Arizona. Habitus, dorsal aspect, ABL = 5.78mm 6 Pseudomorpha santarita sp. n., male holotype, ADP110817; Pajarito Mountains, AZ. Habitus, dorsal aspect, ABL = 5.33mm.
Figure 13-17 from: Erwin T, M. Amundson L (2013) Beetles that live with ants (Carabidae, Pseudomorphini, Pseudomorpha Kirby, 1825): A revision of the santarita species group. ZooKeys 362: 29-54. https://doi.org/10.3897/zookeys.362.6300
Figure 13-17 - 13 Pseudomorpha huachinera sp. n., male paratype, ADP110961; Pajarito Mountains, AZ. Male genitalia, median lobe and parameres labeled as in repose in male, A right lateral aspect, B left lateral aspect, and C dorsal aspects. 14 Pseudomorpha patagonia sp. n., male paratype, ADP110694; Harshaw Creek, Patagonia Mountains, AZ 15 Pseudomorpha santacruz sp. n., male holotype, ADP111870; Madera Canyon, Santa Rita Mountains, AZ 16 Pseudomorpha santarita sp. n., male paratype, ADP110388; Santa Rita Ranch, Santa Rita Mountains, AZ 17 Pseudomorpha pima sp. n., female paratype, ADP109219; Bog Springs, Santa Rita Mountains, AZ. Ovipositor sclerites, Legend: gc1 gonocoxite 1; gc2 gonocoxite 2; lt laterotergite; b base of gonocoxite 2; bl blade of gonocoxite 2. Scale lines = 0.5 mm.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.