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275 results for “Form 1”
Figure 2 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 2 Map of Kuwait indicating known distribution of Talonostrea salpinx sp. nov. Blue circle for field records, red diamond for cited material, red square for type locality. Details of localities are given in Table 1.
Figure 5 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 5 Talonostrea salpinx sp. nov. Paratypes from Khor Al-Subiyah, NMW.Z.2021.009.005 A, B clump with and without upper valves C in situ photograph of a shell from a sheltered position D small upper valve with an array of trumpet-shaped projections along margin E Inner views of four shells showing variation in shape and internal colouration.
Figure 1 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 1 Oyster beds and reefs in northern Kuwait A, B Khor Al-Subiyah C, D Ashairij E, F Boubyan Island (North Khor Al-Subiyah).
Figure 4 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 4 Talonostrea salpinx sp. nov. from Ashairij A, B clump with and without upper valves, shell h is holotype C inner views of lower and upper valves of holotype, NMW.Z. 2021.009. 001 D inner views of upper valves of five paratypes showing variation in shape and colouration, NMW.Z.009.002 E upper valve with a trumpet shapes projection, arrowed F a small upper valve showing radial purple-black colour banding.
Figure 3 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 3 Bayesian phylogenetic tree based on cox1 and 16S DNA sequence data. Bayesian posterior probability higher than 0.9 are reported in correspondence of the nodes.
FIGURE 1 in Allopatric color forms of Scaphidium morimotoi Löbl, 1982 (Coleoptera, Staphylinidae, Scaphidiinae) endemic to the Amami Islands, the Ryukyus, Japan
FIGURE 1. Map of the Amami Islands.
Figure 1 from: Marino de Remes Lenicov AM, Faltlhauser AC, Foieri A, Salinas NA, Hernández MC, Sosa AJ (2024) New morphological and biological contributions to adults and immature forms of Pissonotus paraguayensis (Fulgoromorpha, Delphacidae) in wetlands of Argentina. ZooKeys 1188: 227-250. https://doi.org/10.3897/zookeys.1188.113350
Figure 1 Different rearing and test devices for Pissonotus paraguayensisA device for aquatic plants utilised for rearing and host range tests B device for rearing and tests with plants in water-pics C small petri dishes with L. g. susp. hexapetala utilised in life cycle study D hanging plastic cylinders utilised in host range test for terrestrial plants.
Figure 1 from: Usman M, Dyer PS, Brock M, Wade CM, Khalid AN (2024) Two novel species of arctic-alpine lichen-forming fungi (Ascomycota, Megasporaceae) from the Deosai Plains, Pakistan. MycoKeys 102: 285-299. https://doi.org/10.3897/mycokeys.102.113310
Figure 1 Oxneriaria crittendenii sp. nov. holotype (LAH37193) A thallus B margins C apothecia under stereomicroscope D ascospores in Lugol's solution E conidia F pycnidium. Photos by Muhammad Usman. Scale bars: 5 cm (A); 1 mm (B, C); 20 μm (D, E); 100 μm (F).
Supplementary material 1 from: Žikić V, Mitrović M, Stanković SS, Fernández-Triana JL, Lazarević M, van Achterberg K, Marczak D, Milošević MI, Shaw MR (2024) An integrative taxonomic study of north temperate Cotesia Cameron (Hymenoptera, Braconidae, Microgastrinae) that form silken cocoon balls, with the description of a new species. Journal of Hymenoptera Research 97: 255-276. https://doi.org/10.3897/jhr.97.116378
Supplementary information
Figure 1 from: Žikić V, Mitrović M, Stanković SS, Fernández-Triana JL, Lazarević M, van Achterberg K, Marczak D, Milošević MI, Shaw MR (2024) An integrative taxonomic study of north temperate Cotesia Cameron (Hymenoptera, Braconidae, Microgastrinae) that form silken cocoon balls, with the description of a new species. Journal of Hymenoptera Research 97: 255-276. https://doi.org/10.3897/jhr.97.116378
Figure 1 Aggregated ball-like cocoon A cooperative work of all parasitoid larvae in spinning the cocoon mass (C. vanessae ex Aglais urticae) B spun cocoon mass (C. tibialis ex Mythimna conigera).
Scheme 1 from: Peleshok K, Bondar B, Kryskiw L, Kucher T, Poliak O, Logoyda L (2021) Non-extractive spectrophotometric determination of valsartan in pure form and in pharmaceutical products by ion-pair complex formation with bromophenol blue and methyl red. Pharmacia 68(4): 851-858. https://doi.org/10.3897/pharmacia.68.e73559
Scheme 1 Proposal of the reaction pathway between valsartan and BPB with formation Valsartan-Bromphenol blue complex.
Text-fig. 8. Mhengere Hill fossiliferous localities (1–3). Silicified tree trunks and fragments of wood are abundant in the poorly indurated basal deposits (marly sand and conglomerate) as well as in the silicified lime-rich sandstones that form the hill, which is interpreted to be the remains of a palaeopan. Image modified from Google Earth. in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 8. Mhengere Hill fossiliferous localities (1–3). Silicified tree trunks and fragments of wood are abundant in the poorly indurated basal deposits (marly sand and conglomerate) as well as in the silicified lime-rich sandstones that form the hill, which is interpreted to be the remains of a palaeopan. Image modified from Google Earth.
Supplementary material 1 from: Buru JC, Osunkoya OO, Dhileepan K, Firn J, Scharaschkin T (2019) Eco-physiological performance may contribute to differential success of two forms of an invasive vine, Dolichandra unguis-cati, in Australia. NeoBiota 46: 23-50. https://doi.org/10.3897/neobiota.46.33917
: Data type: occurrence
Supplementary material 1 from: Novoa A, Kumschick S, Richardson DM, Rouget M, Wilson JRU (2016) Native range size and growth form in Cactaceae predict invasiveness and impact. In: Daehler CC, van Kleunen M, Pyšek P, Richardson DM (Eds) Proceedings of 13th International EMAPi conference, Waikoloa, Hawaii. NeoBiota 30: 75–90. https://doi.org/10.3897/neobiota.30.7253
Selected species and traits : Explanation note: NA = No information available.
Fig. 1. A in Skull of a dromaeosaurid dinosaur Shri devi from the Upper Cretaceous of the Gobi Desert suggests convergence to the North American forms
Fig. 1. A. Map of Mongolia and Inner Mongolia of China with the Upper Cretaceous sites yielding remains of dromaeosaurid dinosaurs. B. Photograph of Khulsan locality, from where the specimen described in this paper was collected, photographed in the 1971 during the PolishMongolian Paleontological Expeditions (from the Collections of the Institute of Palaeobiology PAS). Geographic data from: Jerzykiewicz and Russell 1991; Jerzykiewicz et al. 1993; Norell and Makovicky 1999; Dingus et al. 2008; Godefroit et al. 2008; Watabe et al. 2010; Tsogtbaatar et al. 2019; Chen et al. 2022. Map modified from Czepiński 2020b. Transcriptions of the locality names follow Benton (2000).
Fig. 1. A – 18S in A Hotspot of Amoebae Diversity: 8 New Naked Amoebae Associated with the Planktonic Bloom-forming Cyanobacterium Microcystis
Fig. 1. A – 18S rDNA maximum likelihood phylogeny of Vannella, including Microcystis–associated strains (in bold). ML bootstrap values respectively posterior probabilities are shown at the nodes. GenBank accession numbers are given together with the species names. B – LM pictures of V. planctonica (strains A2FBB: 2, 4, 5, 9–13 and A4P4ZHB: 1, 3, 6–8) showing locomotive trophozoites (1–8), a grazing amoeba with a Microcystis cell inside a food vacuole (9), floating forms (10–11) and a cyst stage (12–13). C – LM pictures of V. simplex (strain A17WVB) showing the floating form (14), locomotive amoebae (15–18) with the presence of food vacuoles containing partly digested Microcystis cells (17), posteriorly adhered fecal pellets (15–16), a long flagellum-like pseudopodium encircling a Microcystis cell (17–18) and grazing amoebae on a colony of Microcystis aeruginosa with expanded (arrow) or contracted (arrowhead) flagellum-like pseudopodia visible in some of the trophozoites (19). The presence of a contracticle vacuole, a nucleus or a cyst opening is indicated by a black arrow, a black arrowhead or a white arrow respectively. Scale bars: 20 µm.
Figure 1 in Comparative anatomical studies on the cranial nerves of the fully formed embryos of the Nile tilapia Oreochromis niloticus (Ostiechthyes-Cichlidae). I. Nervus glossopharyngeus
Figure 1. Graphic reconstruction of nervus glossopharyngeus of Oreochromis niloticus in a lateral view. CE. Cerebellum. G.P. Petrosal ganglion. MO. Medulla Oblongata. N.AAB.1 Nerve to the 1st adductor arcus brachialis muscle. N.CSY. Cranial sympathetic nerve. N.EP.L. Nerve to the epithelial lining.N.ILAB.1 Nerve to the 1st internal levator arcus branchialis muscle. N.OV.1 Nerve to the 1st obliquus ventralis muscle.N.PSB. Nerve to pseudobranch.N.IX Nervus glossopharyngeus Nn.ELAB.1 Nerves to the first external levator arcus branchialis muscle.Nn.EP.L. Nerves to the epithelial lining. Nn.GFM. Nerves to the gill filament muscles. Nn.Gr.+EP.L. Nerves for gill rakers and the epithelial lining. Nn.PSB. Nerves to the pseudobranch. R.CM.IX+N.CSY. Ramus communicans of the glossopharyngeal nerve and the cranial sympathetic nerve. R.PH.IX Ramus pharyngeus of nervus glossopharyngeus. R.PR. IX Ramus pretrematicus of nervus glossopharyngeus. R.PT.IX Ramus posttrematicus of the glossopharyngeal nerve. R.SY.IX Ramus sympathetic connecting the glossopharyngeal nerve. RO.IX Glossopharyngeal root. Rr.PT.+PR.IX Rami posttrematicus and pretrematicus of the glossopharyngeal nerve.
Fig. 1 in So different but nonetheless the same species: multiple geographic clines explain the diverse forms of the anthidiine bee Rhodanthidium caturigense s.l. (Apoidea: Megachilidae: Anthidiini)
Fig. 1 Rhodanthidium caturigense. Male from Greece (ex coll. W. Arens)
SURVEY FORM (1): CHATGPT APPLICATION SUPPORTING LEARNING FRENCH GRAMMAR AT THE UNIVERSITY OF TRANSPORT AND COMMUNICATION
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FIGURE 1 in Rhodolith-forming species of the subfamilies Neogoniolithoideae and Hydrolithoideae (Rhodophyta, Corallinales) from Espírito Santo State, Brazil
FIGURE 1. Location of the sampling sites in Southern Espírito Santo (ES), Brazil.
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