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275 results for “Form 1”
Рис. 1. Устье р. Туманной (Λевый берег). ВиΑны постоянно Αействующий (А) и формирую- щийся (Б) воΑотоки, сбрасывающие воΑу из озера Αебяжьего Fig. 1. The mouth of the Tumannaya river (left bank). Visible permanent (A) and forming (B) watercourses that discharge water from lake Lebyazhye in Transboundary Migration And The Local Constraints In The Dynamic Of Fish Fauna In The Lower Reaches Of Tumannaya River
Рис. 1. Устье р. Туманной (Λевый берег). ВиΑны постоянно Αействующий (А) и формирую- щийся (Б) воΑотоки, сбрасывающие воΑу из озера Αебяжьего Fig. 1. The mouth of the Tumannaya river (left bank). Visible permanent (A) and forming (B) watercourses that discharge water from lake Lebyazhye
FIGURE 6. The handle form 1. A in The challenge of hard-to-reach spaces in mechanical fossil preparation: Development of the Wada air scribe, a novel short-bodied air scribe with an adjustable handle
FIGURE 6. The handle form 1. A, production process. The component numbers correspond to those in Figure 2; B, the handle in right lateral view; C, the handle in top view; D, the handle with the socket head screw (M4) in bottom view; E, the handle in left lateral view.
FIGURE 9. The Wada air scribe with handle forms 1 in The challenge of hard-to-reach spaces in mechanical fossil preparation: Development of the Wada air scribe, a novel short-bodied air scribe with an adjustable handle
FIGURE 9. The Wada air scribe with handle forms 1 (A-C) and 2 (D-F) at a straight angle (0 degrees) (A and D) and a right angle (90 degrees) (B and D), respectively. Using a closed-cell polyurethane foam sleeve cover to encase the handles can effectively reduce the impact on the hand (C and F).
FIGURE 1. Translucent 3D in Calcite precipitation forms crystal clusters and muscle mineralization during the decomposition of Cambarellus diminutus (Decapoda: Cambaridae) in freshwater
FIGURE 1. Translucent 3D-models of Cambarellus diminutus sample C7tank in combination with 3D-models of calcite clusters, which precipitated inside the carcass during its decomposition in freshwater. 1.1 3D-model without calcite clusters on day 1. 1.2 3D-model on day 2 showing a small amount of calcite clusters inside the cephalothorax and the first tergite. 1.3 3D-model on day 4 showing a lot of calcite clusters inside the antennules, the left major propodus, the rostrum, the cephalothorax, the tergites, the uropods, and the telson. 1.4 3D-model on day 7, showing widespread calcite clusters at the inner side of the carapace of the carcass except the dorsal side of the cephalothorax and the tergites (see also Figure.4.1). 3D-models were reconstructed based on µ-CT data.
Figure 1 in Ionic homeostasis, biochemical components and yield of Italian zucchini under nitrogen forms and salt stress
Figure 1. Accumulation of nitrogen - N (A), phosphorus - P (B), potassium - K (C), calcium - Ca (D) and magnesium - Mg (E) in Italian zucchini plants fertilized with different forms of nitrogen and irrigated with saline water. Means followed by different letters indicate significant difference by Tukey test at 0.05 probability level.
Fig. 1 in The local forms of Zootecus (Gastropoda: Pulmonata: Subulinidae) of Pakistan: an archaeomalacological case study
Fig. 1 - Left: map of Pakistan with the areas of the studied sites. A) Balochistan, sites WP16, WP 31, Uthal. B) Upper Sindh, Rohri Hills, site 59, site 480. Right: satellite view of the area of Balochistan, South of Uthal with location of the Lake Siranda and the lagoon of Miani Hor.
Fig. 1 in Revision of (Coutière, 1897) and Allied Forms (Decapoda: Caridea: Alpheidae).
Fig. 1. Bayesian and Maximum Likelihood concatenated tree (based on 16S and COI) of selected species of Salmoneus with focus on the S. cristatus species group, showing two different clades morphologically allied to S. cristatus. Numbers above or under each branch are bootstrap supports and Bayesian posterior probabilities, respectively (supports and probabilities under 60/0.6 are not shown). Insert photographs show S. franseni sp. nov. (yellow clade) and S. cristatus (red clade). Abbreviations used: FA, French Antilles; FP, French Polynesia; PG, Persian Gulf; PH, Philippines; PNG, Papua New Guinea; RS, Red Sea; HT, holotype; NT, neotype; PT, paratype. Sequences for S. aduncus, S. auroculatus, S. chadwickae, and S. shojaei were obtained from GenBank (see Ďuriš and Horká 2016; Komai 2022; Ashrafi et al. 2022).
Figure 1 in Euryglossina (Euryglossina) perpusilla (Hymenoptera: Colletidae: Euryglossinae) nesting in pre-formed cavities in Bankisa atenuata (Proteaceae)
Figure 1. Nesting holes (preformed) in a branch of a live, yet partially burnt tree of Banksia attenuata Brown located at Star Swamp Reserve, Western Australia. A number of individuals of Euryglossina (Euryglossina) perpusilla Cockerell (Colletidae: Euryglossinae) were observed entering and exiting the holes, and two specimens, both females, were collected on 9 January 2017.
Diffraction images of a crystal of the complex formed by fragments of the integrin beta4 and the bullous pemphigoid antigen 1 (BP230, BPAG1e). PDB entry 6GVL.
<p>Data were collected on a single crystal at the beamline i03 of the Diamond synchrotron facility (Didcot, UK) using radiation of 0.97625 Å wavelength and a PILATUS3 6M detector. The dataset consists of 2400 images (0.15 degree oscillation per image).</p>
Diffraction images of a crystal of the complex formed by fragments of the integrin beta4 and the bullous pemphigoid antigen 1 (BP230, BPAG1e). Integrin high affinity point mutant. PDB entry 6GVK.
<p>Data were collected on a single crystal at the beamline XALOC of the ALBA-CELLS synchrotron facility (Cerdanyola del Vallés, Barcelona, Spain) using radiation of 0.97915 Å wavelength and a PILATUS 6M detector. The complete dataset is build up of three sub-sets measured at three different positions of a single crystal. Each sub-set consists of 1800 images (0.2 degree oscillation per image).</p>
Figure 1. Pseudomops septentrionalis. A-F. Color variation. A-C. Light form. D-F. Melanic form. G in First records of Pseudomops septentrionalis Hebard, 1917 (Blattodea: Blattellidae) in Nuevo León, Mexico
Figure 1. Pseudomops septentrionalis. A-F. Color variation. A-C. Light form. D-F. Melanic form. G. Abdomen in dorsal view, showing tufts of piliform bristles in T-3 and T-4. H-J. Specimens in their natural habitat. / A-F. Variación de color. A-C. Forma clara. D-F. Forma melánica. G. Abdomen en vista dorsal, mostrando mechones de cerdas piliformes en T-3 y T-4. H-J. Espécimenes en su hábitat natural.
Fig. 1 in A new species of Lycodon (Serpentes: Colubridae) from the Deccan Plateau of India, with notes on the range of Lycodon travancoricus (Beddome, 1870) and a revised key to peninsular Indian forms
Fig. 1. Lycodon deccanensis sp. nov. in life: (a) entire, dorsolateral view; (b–d) head profiles of a live uncollected specimen from Devarayana Durga; (e–f) live uncollected adult and juvenile from Melagiri, showing ontogenic color shift. Photos by K.G. Punith, M.V. Shreeram, and S.R.Ganesh.
Fig. 1 in First record of an infection by tissue cyst-forming coccidia in wild vizcachas (Lagostomus maximus, Rodentia) of Argentina
Fig. 1. Tissue cysts in various organs of plains vizcachas. Representative photomicrographs of histological sections of ovary (A–B), uterus (C), mammary gland (D), adrenal (E), spleen (F), and suspension of cysts recovered from the superficial fascia (G), all of them collected from infected adult vizcachas. Suspension of cysts recovered from amniotic sac of an infected embryo (H). Note that while the ovaries, mammary glands, superficial fascia and fluid from amniotic sac show a high density of cysts, the rest of the organs tend to show only one or very few cysts per section. White arrowheads indicate corpora lutea and black arrowheads indicate tissue cysts. A, B, C, E and F: hematoxilin-eosin staining. D: Masson's trichrome staining.
Fig. 1. A in A novel form of postcranial skeletal pneumaticity in a sauropod dinosaur: Implications for the paleobiology of Rebbachisauridae
Fig. 1. A. Simplified phylogeny of Diapsida showing position of Rebbachisauridae and both components of the rebbachisaurid Extant Phylogenetic Bracket sensu Witmer 1995 (Crocodylia and Aves). Rectangle indicates absence of postcranial pneumaticity; triangles indicate presence of postcranial pneumaticity. B. Hypothesized osteological correlates of pneumatic and other soft tissue structures in archosaurian vertebrae (based on O'Connor 2006).
Fig. 1 in Oviraptorosaur tail forms and functions
Fig. 1. Simplified theropod phylogenies, illustrating two competing hypotheses on the relationship between oviraptorosaurs and birds. A. Oviraptorosauria is the sister group to Aves and is positioned within Avialae phylogeny modified from Maryańska et al. 2002). B. Oviraptorosauria is the sister group to Paraves, which includes Aves and Deinonychusauria phylogeny modified from Senter 2007).
Figure 1 in A new cyst-forming nematode, Cactodera tianzhuensis n. sp. (Nematoda:Heteroderinae) from Polygonum viviparum in China with a key to the Genus Cactodera
Figure 1: Line drawing of C. tianZhUenSiS n. sp. A: Anterior region of second-stage juvenile; B: Head of second-stage juvenile; C, H: Cyst and cysts. D: Lateral field; E: Fenestration in vulval cone; F, G: Tail of second-stage juvenile (Scale bar: H = 500 μm; C = 200 μm; A, F, E = 20 μm; B = 10 μm; D, G = 5 μm).
Fig. 1 in Genetic characterisation of Tanqua (von Linstow, 1879) (Nematoda: Gnathostomatidae) larval forms including new host and locality records
Fig. 1. Phylogenetic tree (of 18S sequences of nematodes) inferred using the Maximum Likelihood Method. The bootstrap values higher than 80 are indicated next to the branches. The new sequences generated from this study are indicated with asterisks.
Fig. 1 in Borings formed by Late Cretaceous endobiontic foraminifers within larger benthic foraminifers
Fig. 1. Outline of the foraminifer Talpinella cunicularia and its trace within the equatorial layer of Orbitoides. A. Cross−section parallel to the equatorial layer. The trace, which may have bifurcated ends, forms around the embryonic apparatus of Orbitoides. Resorption may have removed early chamber walls of T. cunicularia (stippled lines). After Baumfalk et al. (1982). B. Cross−section perpendicular to the equatorial layer of which the trace is confined to. The equatorial layer of chamberlets is flanked by layers of lateral chamberlets. Adapted from Görmüş and Sagular (1998). Not to scale.
Fig. 1 in Mat-forming coccoid cyanobacteria from early Silurian marine deposits of Sudetes, Poland
Fig. 1. Geological map of the northern part of the Bardzkie Mountains (Sudetes, southwestern Poland) and stratigraphic section of the Early Palaeozoic deposits at the Żdanów road−cut (after Porębska 1982, and Wyżga 1987; modified).
Tab. 1 in The local forms of Zootecus (Gastropoda: Pulmonata: Subulinidae) of Pakistan: an archaeomalacological case study
<p>Tab. 1 - Historical names, dimensions and whorl numbers of the Z <i>ootecus</i> described from Afghanistan and Pakistan. AMNH, American Museum of Natural History; NHMUK, National History Museum, London; PZS, Proceedings of the Zoological Society of London.</p><table><tbody><tr><th><b>Local taxa</b></th><th><b>Collecting areas</b></th><th><b>H mm</b></th><th><b>D mm</b></th><th><b>H/D</b></th><th><b>Whorls</b></th></tr></tbody><tbody><tr><th>1) <i>Zootecus pullus</i> Gray, 1834 - P.Z.S., 2: 66</th><td>Balochistan, Quetta; Kutch; Bank of Ganges; Delhi; Uttar Pradesh</td><td>10</td><td>4</td><td>2.5</td><td>9-10</td></tr><tr><th>2) <i>Zootecus chion</i> (smaller form) <i>gracilior minor</i> (Pfeiffer, 1856)</th><td>Not specified</td><td>11</td><td>4</td><td>2.75</td><td></td></tr><tr><th>3) <i>Zootecus insularis chion</i> (Solem, 1979, tab. IV: 30)</th><td>Afghanistan</td><td>11.8±0.15 (9.8-14.3)</td><td>5.66±0.071 (4.3-6.4)</td><td>2.279 2.234</td><td>7 3/4 + (7 1/8-9)</td></tr><tr><th>4) <i>Zootecus polygyratus</i> Reeve, 1849</th><td>Sindh (Rohri Hills); Baluchistan (Gwadar)</td><td>12</td><td>4</td><td>3</td><td>9</td></tr><tr><th>5) <i>Zootecus chion</i>, Pfeiffer, 1856</th><td>Afghanistan; Punjab; Sindh</td><td>12</td><td>0.5</td><td>2.4</td><td>7-8</td></tr><tr><th>6) <i>Zootecus chion</i> (#2), Pfeiffer, 1856</th><td>Samples from Hyderabad</td><td>14</td><td>6</td><td>2.333</td><td></td></tr><tr><th>7) <i>Zootecus agrensis</i> Kur. r 1856 - Malakozoologische Blätter, 2: 107</th><td>India: Agra</td><td>16</td><td>6</td><td>2.666</td><td>9</td></tr><tr><th>8) <i>Zootecus estellus</i> Benson, 1857 - A.M.N.H. ser. 2, 19: 327</th><td>Punjab; Sindh; Rajasthan; Andhra Pradesh</td><td>18</td><td>6</td><td>3</td><td>8</td></tr><tr><th>9) <i>Zootecus pertica</i> Benson, 1857 - A.M.N.H. ser. 2, 19: 328</th><td>Sindh</td><td>20</td><td>5</td><td>4</td><td>10</td></tr></tbody></table>
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