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Fig. 5 in Small Free-Living Heterotrophic Flagellates from Marine Intertidal Sediments of the Sydney Region, Australia

Fig. 5. (a) Protaspa verrucosa, note ventral groove. (b) Thaumatomastix sp., general appearance of cell and showing a layer of body scales. (c)–(d) Clautriavia cavus, general appearance of different cells, (c) cell from Lee and Patterson (2000). (e) Gweamonas unicus, note coiled flagellum and flagellar insertion. (f)–(h) Eoramonas jungensis sp. nov., showing general appearance of different cells, note flagellar insertion and beating pattern of anterior flagellum. (i)–(j) Glissandra similis, showing general appearance of different cells, note the ventral groove. (k) Phyllomitus undulans, note two flagella adhering each other, from Lee (2002a). (l)–(m) Protist 1, showing general appearance, note flagellar insertion. (n) Protist 2, showing general appearance, note collar and two emergent flagella. All micrographs are DIC images. Scale bar in (h) = 5 μm for (e)–(h) and in (n) = 10 μm for other figures.

Fig. 4 in Small Free-Living Heterotrophic Flagellates from Marine Intertidal Sediments of the Sydney Region, Australia

Fig. 4. (a)–(b) Rhynchobodo longiciliatus, (a) general appearance of cell, (b) flagellar insertion into pocket. (c)–(d) Cercomonas sp.1, general appearance, note slender anterior part and hyaline cell body. (e)–(f) Cercomonas parva, (e) genera appearance showing a posterior flagellum attached to the body, (f) flexible body. (g)–(h) Cercomonas sp.2, general appearance, note both short flagella and cytoplasms drawn from the posterior part. (i) Cyranomonas australis, showing general appearance of different cells, note flagellar insertion. (j)–(k) Protaspa flexibilis sp. nov., general appearance of different cells, (j) nuclear caps around nucleus. All micrographs are DIC images. Scale bar in (k) = 10 μm for all figures with the exception of (b). Scale bar in (b) = 5 μm.

Fig. 2 in Gamma Radiation Tolerance and Protein Carbonylation Caused by Irradiation of Resting Cysts in the Free-living Ciliated Protist Colpoda cucullus

Fig. 2. Analysis of proteins (Left panel) and protein carbonylation by ECL (Right panel) from non-irradiated and 4000 Gy irradiated cells. The samples in the lanes were from non-irradiated cells (NonIR), 4000 Gy irradiated cells (IR), and cells incubated for 12 h after 4000 Gy irradiation (IR incubated). The protein bands and ECL signals were measured and are shown in parentheses for each lane relative to the Non-IR sample.

Fig. 4 in Gamma Radiation Tolerance and Protein Carbonylation Caused by Irradiation of Resting Cysts in the Free-living Ciliated Protist Colpoda cucullus

Fig. 4. Relative viability of Colpoda vegetative cells, wet cysts, and dry cysts after gamma radiation doses of 0 (non-irradiated), 500, 1000, 2000, 3000, and 4000 Gy. The column heights and attached bars are the means and standard errors, respectively, of six measurements at each dose. Double asterisks indicate a significant difference at p <0.01 (Mann-Whitney U test).

Fig. 3 in Gamma Radiation Tolerance and Protein Carbonylation Caused by Irradiation of Resting Cysts in the Free-living Ciliated Protist Colpoda cucullus

Fig. 3. Excystment of Colpoda dry cysts, after gamma irradiation at 0 (non-irradiated), 500, 1000, 2000, 3000, and 4000 Gy, as a function of time after induction of excystment. The points and bars mark the means and standard errors, respectively, of six measurements at each dose. The excystment mean ± SE at 3, 6, 24, and 96 h after the induction of excystment is shown in (a), (b), (c), and (d), respectively. The column heights and attached bars in (a) to (d) are the means and standard errors, respectively, of six measurements at each dose. Asterisks and double asterisks indicate a significant difference at p <0.05 and p <0.01, respectively (Mann-Whitney U test).

Fig. 3 in Small Free-Living Heterotrophic Flagellates from Marine Intertidal Sediments of the Sydney Region, Australia

Fig. 3. Apusomonadida, Cercomonadida, Protaspidae, Thaumatomonadidae and Protista incertae sedis. (a) Apusomonas proboscidea, (b) Cercomonas parva, (c) Cercomonas sp.1, (d) Cercomonas sp.2, (e) Protaspa flexibilis sp. nov., (f) Thaumatomastix sp., (g) Eoramonas jungensis sp. nov., (h) Gweamonas unicus, (i) Phyllomitus undulans (from Lee 2002a), (j) Protist 1, (k) Protist 2. Scale bar = 10 μm for all figures.

Fig. 2 in Small Free-Living Heterotrophic Flagellates from Marine Intertidal Sediments of the Sydney Region, Australia

Fig. 2. (a)–(b) Mastigamoeba psammobia, (a) general appearance of cell, note cytoplasms drawn from the posterior end, (b) general appearance of different cell and note pseudopodia. (c) Hexamita inflata, general appearance, note the nucleus. (d) Trepomonas agilis, general appearance of cell. (e) Chilomastix cuspidata, showing general appearance. (f) Stephanopogon sp., showing general appearance. (g) Saepicula pulchra, showing general appearance of cell. (h)–(j) Goniomonas amphinema. (h) Form I, (i) Form II, (j) Form III, note flagellar ar- rangement. (k) Roombia truncata, note attached cell to the substrate by the tip of the posterior flagellum, note extrusomes, surface striations and deep gullet. (l) Telonema subtilis, showing general appearance. (m) Harpagon descissus, general appearance of cell. (n)–(o) Spironema multiciliatum, (n) general appearance of cell, (o) note the kinetics. (p) Psammosa unguis, general appearance of cell. (q) Bicosoeca conica, general appearance of cell. (r) Apusomonas proboscidea, genera appearance of cell, note the V-shaped structure on dorsal face. All micrographs are DIC images except for (b), which is phase contrast images. Scale bar in (r) = 10 μm for all figures.

Fig. 1 in Gamma Radiation Tolerance and Protein Carbonylation Caused by Irradiation of Resting Cysts in the Free-living Ciliated Protist Colpoda cucullus

Fig. 1. Excystment of Colpoda wet cysts, after gamma irradiation at 0 (non-irradiated), 500, 1000, 2000, 3000, and 4000 Gy, as a function of time after the induction of excystment. The points and bars mark the means and standard errors, respectively, of six measurements at each dose. The excystment mean ± SE at 3, 6, 9, and 36 h after induction of excystment is shown in (a), (b), (c), and (d), respectively. The column heights and attached bars in (a) to (d) are the means and standard errors, respectively, of six measurements. Asterisks and double asterisks indicate a significant difference at p <0.05 and p <0.01, respectively (Mann-Whitney U test).

Fig.3. Relation between depression level expresed Fig.4 in Oxidative Stress Indicators, Depression And Qua Lity Of Live L Evel S In Co Rona Ry Heart Disease Patients

Fig.3. Relation between depression level expresed Fig.4. Box plot displaying the distribution of the in Geriatric depression score points and oxidative data showing differences in Geriatric depression stress parameter (GPx) score points in primary and recurrent SCHD patients according to gender.

Fig.1. Relation between depression level expresed Fig.2 in Oxidative Stress Indicators, Depression And Qua Lity Of Live L Evel S In Co Rona Ry Heart Disease Patients

Fig.1. Relation between depression level expresed Fig.2. Relation between depression level expresed in Geriatric depression score points andlevelof in Geriatric depression score points and oxidative life Quality. stress parameter (MDA).

opencc-by-4.0Dec 2009View details →

Fig.1. Funnel trap for gathering living RESULTS AND DISCUSSION D.latissimus a in Conceptual Application Of Dytiscus Latissimus Linnaeus, 1758 (Dytiscidae, Coleoptera) Gathering Methods In Natural Habitat

Fig.1. Funnel trap for gathering living RESULTS AND DISCUSSION D.latissimus a result of the individual (from Jan G.M. Cuppen and other): As many years application of the material gathering methods was 1 – float; 2- rubber; 3 – aeration net; a possibility to catch on regular and predictable 4 – entrance Ø 30 mm. basis a required number of animals for our laboratory research. itself. This can be identified from locating specific cuts on it. (Vahrusevs 2009) The key to a successful egg collection is a search of the plants used by beetles during their Below is an example from field notes of catching reproduction period, as well as the correct beetles during the autumn season: locating of clutches. Such plants in our reservoir "The research on the reservoir was done during under study are Carex acuta, Carex rostrata, 11.10.2009 - 28.10.2009. Caltha palustris. One has to identify suitable plants in the locations of beetles' clutches The weather conditions were favourable. It was (usually located on the sunny side along the quite warm and windless all this time in order to coast of a water reservoir). The person gathering work comfortably. Water temperature was +7-8 ŗ the material has to grasp with fingers the C. We worked as usual on the proven location. underwater part of the identified plant stem Coordinates in Google Earth (latitude 55 ° 52'33 reaching almost to its base, and slowly palpate it.95 "C; longitude 26 ° 35'18.78" H). by letting it through the fingers in the upwards direction. The upwards direction is imperative, We prepared the traps in advance (they had to as stems of many sedge plants have microscopic be repaired and mended, and modernized a little. thorns which are rooting upwards. If this method (Fig.2.). is not followed, an injury of a palm can occur. A stem of the plant which has protruding bumps We took along 21 trap to the water reservoir. The on it guarantees the presence of a clutch. A stem bait was pieces of beef heart. The traps were in its normal condition is usually smooth and placed along the coastline. The first "throw" was often flat. Such plants as Caltha palustris which kept in the water for almost a week with regular have fleshy stem are to be studied in addition check ups made every day or every second day. visually as eggs can be located inside the stem Traps were installed partly dipped under water.

opencc-by-4.0Dec 2022View details →

FIGURE 4. Alligatorid fossils from the Live Oak fossil site. A in Oldest record of Alligator in southeastern North America

FIGURE 4. Alligatorid fossils from the Live Oak fossil site. A: Isolated tooth, likely mid-rostral position (UF 424640) in lingual view. B: Isolated tooth, likely anterior position (UF 424639) in lingual view. C: Caudal vertebra exhibiting a fully fused neurocentral suture (UF 424637) in left lateral view. D: Caudal vertebra exhibiting a fully fused neurocentral suture (UF 424638) in left lateral view. E: Osteoderm (UF 424633) in dorsal view. F: Osteoderm (UF 424635) in dorsal view.

Figure 3. CCA showing the relationship between 16 in Assessments of environmental variables affecting the spatiotemporal distribution and habitat preferences of living Ostracoda (Crustacea) species in the Enez Lagoon Complex (Enez-Evros Delta, Turkey)

Figure 3. CCA showing the relationship between 16 species (red triangles) and 9 environmental variables (red arrows). See Tables 2 and 4 for an explanation of abbreviations and variables.

Figure 2 in Assessments of environmental variables affecting the spatiotemporal distribution and habitat preferences of living Ostracoda (Crustacea) species in the Enez Lagoon Complex (Enez-Evros Delta, Turkey)

Figure 2. Jaccard's coefficient similarity dendrograms showing the faunal similarity among the 12 sampling sites (based on presence/absence of species) and clustering relationships among the 16 ostracod species. (Species codes are given in Table 3.)

Fig. 1 in Assessments of environmental variables affecting the spatiotemporal distribution and habitat preferences of living Ostracoda (Crustacea) species in the Enez Lagoon Complex (Enez-Evros Delta, Turkey)

Fig. 1. Map of the eight studied coastal lagoons. Selected sampling sites at Tuzla Lake 1 (St-1), Tuzla Lake 2 (St-2), Tuzla Lake 3 (St-3), Taz (St-4), Işık (St-5), Dalyan (St-7, 8, and 9), Kuvalak (St-10), and Taşaltı (St-11 and 12) were used for comparisons of the lagoons. The sampling sites are indicated by red circles; the red arrows show the direction of water currents.

opencc-by-4.0Dec 2022View details →

Figure 1 in First report of Epibiont ciliates (Ciliophora: Peritrichia) living in Brinkhurstia americanus (Oligochaeta: Alluroididae) in a Neotropical river

Figure 1. Brinkhurstia americanus. (A) Anterior ventral chaetae; (B) epibiont ciliates associated in the posterior region; and (C) epibiont ciliates. Scale bars: (A) and (B) 100 μm; (C) 10 μm.

opencc-by-4.0Mar 2022View details →

Fig. 1 in Living with the enemy: activity rhythms of the red fox Vulpes vulpes (Carnivora, Canidae) and some potential preys in an urban environment

Fig. 1 - Satellite view of the municipal area of Padua and location of the camera traps. / Immagine satellitare del territorio comunale di Padova e posizione delle trappole fotografiche (Image/Immagine: Google Satellite).

opencc-by-4.0Mar 2022View details →

Fig. 2 in Living with the enemy: activity rhythms of the red fox Vulpes vulpes (Carnivora, Canidae) and some potential preys in an urban environment

Fig. 2 - Temporal activity overlap between the red fox and its potential preys. The shaded area under the two density estimates represents the overlap coefficient. / Sovrapposizione dell'attività temporale tra la volpe rossa e le sue potenziali prede. L'area ombreggiata sotto le due stime di densità rappresenta il coefficiente di sovrapposizione.

opencc-by-4.0Feb 2013View details →

Fig. 1. Pyllidia ocellata Cuvier, 1804. A. rhinophores. B. anus. C. dorsal view. D. ventral view. E. oral tentacles. A-C. living animal. D, E in A report on species of phyllidiid and polycerid nudibranch including two species new to Korea

Fig. 1. Pyllidia ocellata Cuvier, 1804. A. rhinophores. B. anus. C. dorsal view. D. ventral view. E. oral tentacles. A-C. living animal. D, E. preserved specimen. An arrow indicates anus. Scales=5 mm.