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opencc-by-4.0Aug 2017View details →

Allocation of rhodamine-loaded nanocapsules from blood circulatory system to adjacent tissues assessed in vivo by fluorescence spectroscopy

<p>Modern fluorescent modalities play an important role in the functional diagnostic of various physiological processes in living tissues. Utilizing the fluorescence spectroscopy approach we observe the circulation of fluorescent-labelled nanocapsules with rhodamine tetramethylrhodamine in a microcirculatory blood system. The measurements were conducted transcutaneously on the surface of healthy Wistar rat thighs in vivo. The administration of the preparation capsule suspension with a rhodamine concentration of 5 mg kg−1 of the animal weight resulted in a two-fold increase of fluorescence intensity relative to the baseline level. The dissemination of nanocapsules in the adjacent tissues via the circulatory system was observed and assessed quantitatively. The approach can be used for the transdermal assessment of rhodamine-loaded capsules in vivo.</p>

opencc-by-4.0Jun 2018View details →

Figure 3 in Fish Fauna of D'ering Memorial Wildlife Sanctuary and adjacent areas, Arunachal Pradesh, India

Figure 3. Photograph is showing the general topography and aquatic habitat near Sigar Village, located north to sanctuary.

opencc-by-4.0Dec 2014View details →

Text-fig. 4. Platanaceae 1–3. Macginitiea gracilis (LESQUEREUX) J. WOLFE et WEHR leaves and associated reproductive structures 1. Holotype of Aralia gracilis LESQUEREUX from Bridger Pass, Wyoming, USNM 330. 2. Specimen showing the typical configuration of five lobes, Killpecker Creek flora, Wyoming. UF 18126-13242. 3. Silicified M. gracilis leaf from Almont, North Dakota; arrow indicates adjacent Macginicarpa infructescence, UF 15722-29202a. 4. Macginicarpa infructescence from Almont, UF15722-35493. 5. Platananthus sp., Almont, UF 15722-62019. 6. Macginicarpa glabra MANCHESTER infructescence, enlarged from fig. 3, UF 15722-29202b. Specimens in figs 3-6 collected and donated by John Curtis. Scales = 1 cm. Images 3–6 light-dark inverted. in Revisions To Roland Brown'S North American Paleocene Flora

Text-fig. 4. Platanaceae 1–3. Macginitiea gracilis (LESQUEREUX) J. WOLFE et WEHR leaves and associated reproductive structures 1. Holotype of Aralia gracilis LESQUEREUX from Bridger Pass, Wyoming, USNM 330. 2. Specimen showing the typical configuration of five lobes, Killpecker Creek flora, Wyoming. UF 18126-13242. 3. Silicified M. gracilis leaf from Almont, North Dakota; arrow indicates adjacent Macginicarpa infructescence, UF 15722-29202a. 4. Macginicarpa infructescence from Almont, UF15722-35493. 5. Platananthus sp., Almont, UF 15722-62019. 6. Macginicarpa glabra MANCHESTER infructescence, enlarged from fig. 3, UF 15722-29202b. Specimens in figs 3-6 collected and donated by John Curtis. Scales = 1 cm. Images 3–6 light-dark inverted.

opencc-by-4.0Dec 2010View details →

Figs. 6-12 in Contribution to the knowledge of the fauna of the tribe Omaliini McLeay, 1825 (Coleoptera: Staphylinidae: Omaliinae) of the Baikal region and adjacent territories

Figs. 6-12. Pycnoglypta cornuta Shavrin, sp.n. 6-9 – male (6 – aedeagus, ventral view; 7 – aedeagus, lateral view, 8 - tergite VIII, 9 – sternite VIII), 10-12 – female (10 – tergite VIII, 11 – dternite VIII, 12 – female accessory sclerite). Scale bar 0.1 mm.

opencc-by-4.0Sep 2021View details →

Fig. 2. The 2019 in Wild bee pollinators foraging in peanut and cotton adjacent to native wildflower strips

Fig. 2. The 2019 mean (± SE) of bees per bee bowl captured in cotton and those with cotton pollen and unidentified pollen (= other) (a), and the mean (± SE) of bees per bee bowl captured in cotton with G. pulchella (IB), Monarda citriodora (mint), and Rudbeckia hirta (susan) (b).

opencc-by-4.0Sep 2021View details →

Fig. 1. The 2018 in Wild bee pollinators foraging in peanut and cotton adjacent to native wildflower strips

Fig. 1. The 2018 mean (± SE) of bees per bee bowl captured in peanut and those with peanut pollen (a), and the mean (± SE) of bees per bee bowl captured in peanut with Gaillardia pulchella (IB), and both G. pulchella and peanut pollen (b).

Fig. 6 in Diversity and spatial distribution of predacious Dolichopodidae (Insecta: Diptera) on organic vegetable fields and adjacent habitats in Brazil

Fig. 6. Grouping of assemblies Dolichopodidae flies in different habitats: vegetables, fallow, agroforestry, and native vegetation based on coefficient similarity (Bray-Curtis) on organic farms cultivating vegetables in the Federal District, Brazil.

Fig. 5 in Diversity and spatial distribution of predacious Dolichopodidae (Insecta: Diptera) on organic vegetable fields and adjacent habitats in Brazil

Fig. 5. Number of exclusive and shared (intersections) Dolichopodidae species in vegetable crops and fallow habitats, agroforestry, and native vegetation.

Fig. 2 in Diversity and spatial distribution of predacious Dolichopodidae (Insecta: Diptera) on organic vegetable fields and adjacent habitats in Brazil

Fig. 2. Mean abundance (± SE) of Dolichopodidae flies collected in different rural properties with vegetable crops, fallow, agroforestry, and native vegetation in the Federal District, Brazil.

Fig. 1 in Diversity and spatial distribution of predacious Dolichopodidae (Insecta: Diptera) on organic vegetable fields and adjacent habitats in Brazil

Fig. 1. Organic vegetable farms sampled in Ceilândia (I), Taguatinga (II), Paranoá (III), and Lamarão (IV), Federal District, Brazil.

Fig. 4 in Diversity and spatial distribution of predacious Dolichopodidae (Insecta: Diptera) on organic vegetable fields and adjacent habitats in Brazil

Fig. 4. Adjustment to the log normal distribution model of the Dolichopodidae assembly per habitat on organic farms producing vegetable in the Federal District, Brazil.

Fig. 3 in Diversity and spatial distribution of predacious Dolichopodidae (Insecta: Diptera) on organic vegetable fields and adjacent habitats in Brazil

Fig. 3. Distribution of relative abundance by species of Dolichopodidae flies collected on organic farms producing vegetables in the Federal District, Brazil.

opencc-by-4.0Jul 2018View details →

Fig. 1 in Revision of the genus Thinophilus Wahlberg (Diptera: Dolichopodidae) from Singapore and adjacent regions: A long term study with a prudent reconciliation of a genetic to a classic morphological approach

Fig. 1. Present extension of Singapore's mangroves (in green). The numbers indicate the sites that were sampled during the 1-month Singapore Mangrove Insect Project (SMIP 2009); and the 2-year Mangrove Insect Project (MIP 2012-2014). 1, Mandai mangroves; 2, Kranji Nature Trail; 3, Sungei Buloh Wetland Reserve; 4, Lim Chu Kang; 5, Sarimbun mangroves; 6, Berlayer Creek; 7, Pulau Semakau original or old mangrove (SMO); 8, Pulau Semakau, replanted or new mangrove (SMN); 9, Changi creek; 10, Pulau Tekong; 11, Pulau Ubin, Chek Jawa; 12, Pasir Ris; 13, Pulau Seletar; 14, Sungei Cina.

opencc-by-4.0Jul 2018View details →

Fig. 4 in Revision of the genus Thinophilus Wahlberg (Diptera: Dolichopodidae) from Singapore and adjacent regions: A long term study with a prudent reconciliation of a genetic to a classic morphological approach

Fig. 4. Thinophilus apicatus sp. nov., male. A, Detail of surstyli ventrally; B, Tips cerci dorsally; C, Ventral view of epandrium; D, Lateral view of epandrium.

opencc-by-4.0Jul 2018View details →

Fig. 3 in Revision of the genus Thinophilus Wahlberg (Diptera: Dolichopodidae) from Singapore and adjacent regions: A long term study with a prudent reconciliation of a genetic to a classic morphological approach

Fig. 3. Thinophilus apicatus sp. nov., male. A, Mid femur; B, Hind femur; C, Posterior view of fore leg; D, Anterior view of fore coxa.

FIGURE 1 in A new species of Knodus (Characiformes: Characidae), with deep genetic divergence, from the Mearim and Munim river basins, Northeastern Brazil, and evidence for hidden diversity in adjacent river basins

FIGURE 1 | Knodus guajajara, holotype, CICCAA 4883, 31.4 mm SL, Alto Alegre do Pindaré municipality, Igarapé Arapapá, Pindaré River drainage, Mearim River basin.

FIGURE 4 in A new species of Knodus (Characiformes: Characidae), with deep genetic divergence, from the Mearim and Munim river basins, Northeastern Brazil, and evidence for hidden diversity in adjacent river basins

FIGURE 4 | Knodus guajajara, CICCAA 4861, paratype, male, 31.9 mm SL Maranhão, Mearim River basin. A. Hooks on pelvic fin. B. Hooks on anal fin. (Photographed by F. P. Ottoni).

FIGURE 2 in A new species of Knodus (Characiformes: Characidae), with deep genetic divergence, from the Mearim and Munim river basins, Northeastern Brazil, and evidence for hidden diversity in adjacent river basins

FIGURE 2 | Knodus guajajara, paratypes. A. CICCAA 1518, 22.8 mm SL, Brazil, Maranhão, Alto Alegre do Pindaré municipality, igarapé Jenipapo, Pindaré River drainage, Mearim River basin. B. CICCAA 2696, 40.2 mm SL, Brazil, Maranhão, Chapadinha municipality, stream in riparian forest on the road BR–222, Munim River basin.

FIGURE 3 in A new species of Knodus (Characiformes: Characidae), with deep genetic divergence, from the Mearim and Munim river basins, Northeastern Brazil, and evidence for hidden diversity in adjacent river basins

FIGURE 3 | Knodus guajajara, CICCAA 4861, paratype, 31.9 mm SL, jaw suspensorium. A. Premaxillary. B. Maxilla. C. Dentary. Scale bar = 1 mm.