Find research datasets worth reusing

opencc-by-4.0Dec 2023View details →

Figure 1 in Perceptions of the Andean condor in the urban population of Ecuador

Figure 1. Study site, highlights the sierra region of Ecuador and the Antisana National Park (Antisana N. P.).

opencc-by-4.0Dec 2023View details →

Figura 2 in Perceptions of the Andean condor in the urban population of Ecuador

Figura 2. Modelo logístico que explica la probabilidad de identificación del cóndor andino por parte de la población urbana del Ecuador. P = probabilidad; línea gris = mujeres; línea negra = hombres.

opencc-by-4.0Dec 2015View details →

Fig. 2 in Occurrence of pathogens in populations of Ips typographus, Ips sexdentatus (Coleoptera, Curculionidae, Scolytinae) and Hylobius spp. (Coleoptera, Curculionidae, Curculioninae) from Austria, Poland and France

Fig. 2. Pathogens in I. typographus from different bio-geographic regions in Europe: n Northern continental – Baltic, o North-eastern Alps (transitional Atlantic – continental), p South-eastern Alps (transitional Alpine – Illyric), Q Western Alps and R Atlantic.

Fig. 1 in Distribution and Occurrence of the Neogregarine Pathogen, Ophryocystis anatoliensis (Apicomplexa) in Populations of Chrysomela populi L. (Coleoptera: Chrysomelidae)

Fig. 1. Infected (bold) and non-infected localities where Crysomela populi adults and larvae were collected in Turkey.

Fig. 2 in Distribution and Occurrence of the Neogregarine Pathogen, Ophryocystis anatoliensis (Apicomplexa) in Populations of Chrysomela populi L. (Coleoptera: Chrysomelidae)

Fig. 2. Ophryocystis anatoliensis infection levels in C. populi populations in Turkey during the three years.

Fig. 2 in Morphology and Sequence Data of Mexican Populations of the Ciliate Parasite of Marine Fishes Trichodina rectuncinata (Ciliophora: Trichodinidae)

Fig. 2. Photomicrographs of silver-impregnated adhesive discs and diagrammatic drawings of the denticles of respective morphotypes studied in the present paper; a and a'. From Enneanectes reticulatus, San Carlos, Sonora. b and b'. From Enneanectes reticulatus, San Carlos, Sonora. c and c'. From Tomicodon zebra, Zihuatanejo, Guerrero. d and d'. From Tomicodon zebra, Cuatunalco, Oaxaca.

Fig. 3 in Morphology and Sequence Data of Mexican Populations of the Ciliate Parasite of Marine Fishes Trichodina rectuncinata (Ciliophora: Trichodinidae)

Fig. 3. Bayesian inference tree of sequences of the 18S gene of trichodinid species of the genus Trichodina and Trichodinella, emphasizing on Trichodina rectuncinata. Numbers near internal nodes show the support value. Codes: ♦ Cuatunalco; * Zihuatanejo; ● San Carlos.

Fig. 1 in Morphology and Sequence Data of Mexican Populations of the Ciliate Parasite of Marine Fishes Trichodina rectuncinata (Ciliophora: Trichodinidae)

Fig. 1. Map showing the location of Mexico, and localities where populations of Trichodina rectuncinata were obtained.

Figure 4 in Population Dynamics of Amoeboid Protists in a Tropical Desert: Seasonal Changes and Effects of Vegetation and Soil Conditions

Figure 4. Relationship between amoeboid protist richness and soil parameters during the wet season in three microhabitats by CCA: PL: Pr. laevigata, PP: Pa. praecox, and BS: bare soil. The names and abbreviations of the amoeboid protist species can be found in table 3.

Figure 2 in Population Dynamics of Amoeboid Protists in a Tropical Desert: Seasonal Changes and Effects of Vegetation and Soil Conditions

Figure 2. Cumulative richness plots of amoeboid protists present under Pr. laevigata (PL), Pa. praecox (PP) and bare soil (BS) during dry and wet seasons at 0–30 cm. a) eruptive pseudopods, and b) acanthopodial pseudopods. ND: not determined.

Figure 1 in Population Dynamics of Amoeboid Protists in a Tropical Desert: Seasonal Changes and Effects of Vegetation and Soil Conditions

Figure 1. Study area, showing vegetation patches in the desert of Tehuacán, Puebla, Mexico. In addition, the analyzed microhabitats are shown: Pr. laevigata, Pa. praecox and bare soil.

Fig. 4. A–P in Morphology and Morphogenesis of a Chinese Population of the Soil Urostylid Ciliate, Extraholosticha sylvatica (Foissner, 1982) Li et al., 2017 (Ciliophora, Hypotrichia)

Fig. 4. A–P Photomicrographs of Extraholosticha sylvatica, during morphogenesis after protargol staining. (A, B) Ventral views of oral primordium of the opisthe. Arrow indicates the parental midventral cirri. (C) Dorsal view of an early divider, arrow shows dorsal kinety anlage. (D, H) Ventral views of early dividers, arrows show the development of the frontoventral-transverse cirral anlagen. (E) Ventral view of an early divider, to show the left marginal anlagen. (F) Ventral view of an early divider, arrow indicates the undulating membranes anlage. (G) Ventral view, arrow demonstrates that old adoral zone of membranelles was renewed in the rear part. (I, J) Ventral (I) and dorsal (J) views of a middle divider, to show the frontoventral-transverse cirral anlagen (arrow in I) and the fusing macronuclear nodule (arrow in J). (K) Ventral view of a late divider, arrow showing the dorsal kinety anlage. (L, M) Ventral views of a late divider, to show the old midventral pairs (arrow in L), as well as newly formed transverse cirri (arrow in M), pretransverse cirri (arrowheads), and midventral pairs (doublearrowhead). (N) Dorsal view, to show the caudal cirri (arrow). (O, P) Dorsal views, showing the micronuclei (arrow) and macronuclear nodule (P). LMA, left marginal anlagen; Ma, macronuclear nodules; Mi, micronuclei; OP, oral primordium; RMA, right marginal anlagen.

Fig. 1. A–I in Morphology and Morphogenesis of a Chinese Population of the Soil Urostylid Ciliate, Extraholosticha sylvatica (Foissner, 1982) Li et al., 2017 (Ciliophora, Hypotrichia)

Fig. 1. A–I Illustrations of Extraholosticha sylvatica after protargol staining (A–C) and photomicrographs from life (D–G) and after protargol staining (H, I). (A–C) Ventral (A) and dorsal (B, C) view to show the general infraciliature (A, B) and the nuclear apparatus (C). Arrow in A shows the frontoventral cirri behind the leftmost frontal cirrus. (D, E) Ventral views of slightly squeezed specimens, arrows show two collecting canals (D) and the contractile vacuole (E). (F) Dorsal view, arrows point to the cortical granules. (G) Posterior portion of body, to show crystals (arrow) and lipid granules. (H) Ventral view of a representative individual, with an arrow showing the frontoventral cirri behind the leftmost frontal cirrus. (I) Dorsal view, to demonstrate dorsal kineties. AZM, adoral zone of membranelles; BC, buccal cirrus; CC, caudal cirri; E, endoral; FC, frontal cirri; FTC, frontoterminal cirri; LMR, left marginal row; Ma, macronuclear nodules; Mi, micronuclei; MP, midventral pairs; P, paroral; PTVC, pretransverse cirri; RMR, right marginal row; TC, transverse cirri; 1–5, dorsal kineties. Scale bars = 75 μm (A–E, H, I); 6 μm (F); 20 μm (G).

Fig. 3. A–F in Morphology and Morphogenesis of a Chinese Population of the Soil Urostylid Ciliate, Extraholosticha sylvatica (Foissner, 1982) Li et al., 2017 (Ciliophora, Hypotrichia)

Fig. 3. A–F Morphogenesis of Extraholosticha sylvatica after protargol staining. (A, B) Ventral (A) and dorsal (B) view of a late divider. Arrowheads mark the dorsal kineties anlagen. (C, D) Ventral and dorsal view of a late divider. Note that two frontoterminal cirri (arrows in C), the pretransverse cirri (arrowheads in C), transverse cirri (double-arrowheads) and dorsal kineties anlagen (arrowheads in D) are formed in both the proter and the opisthe, as well as caudal cirri derived from the posterior end of dorsal kinety anlage 5 in both daughter cells (arrows in D). (E, F) Ventral (E) and dorsal (F) view of the same late specimen, to demonstrate that almost all the cirri have arrived their final place. Arrows denote the caudal cirri formed from dorsal kinety anlage 5 and arrowheads mark the dorsal kineties anlagen. DKA, dorsal kineties anlagen; LMA, left marginal anlagen; Ma, macronuclear nodules; Mi, micronuclei; RMA, right marginal anlagen. Scale bars = 75 μm (A–F).

Fig. 2. A–H in Morphology and Morphogenesis of a Chinese Population of the Soil Urostylid Ciliate, Extraholosticha sylvatica (Foissner, 1982) Li et al., 2017 (Ciliophora, Hypotrichia)

Fig. 2. A–H Morphogenesis in Extraholosticha sylvatica, after protargol staining. (A, B) Ventral views of an early divider, to show the newly formed oral primordium. Arrow shows that midventral pairs take part in the formation of oral primordium. (C, D) Ventral (C) and dorsal (D) view of an early divider. Arrow in (C) shows frontoventral-transverse cirral anlagen, arrowheads show the undulating membranes anlagen in the proter and the opisthe, while arrows in (D) note that the dorsal kineties anlagen are formed in old structure. (E) Ventral view of an early divider. Arrow shows the frontoventral-transverse cirral anlagen and arrowheads mark the undulating membranes anlagen in the proter and the opisthe. (F) Ventral view of an early divider. Note that the frontoventral-transverse cirral anlagen are developing (arrow), the posterior part of the old adoral zone of membranelles is renewed (arrowhead), the vertical split of the undulating membranes anlage (double-arrowhead) in the proter. (G, H) Ventral (G) and dorsal (H) view of a middle divider, arrow depicts newly formed frontoventral transverse cirri and arrowheads mark the leftmost frontal cirrus and the frontoventral cirri separated from the undulating membranes anlagen in both proter and opisthe. DKA, dorsal kineties anlagen; LMA, left marginal anlagen; Ma, macronuclear nodules; Mi, micronuclei; OP, oral primordium; RMA, right marginal anlagen. Scale bars = 75 μm (A–H).

Fig. 7 in Differences Of The Bog And Dry Site Scots Pine Population Seedlings Germination And Early Growth

Fig. 7. Comparison of development stage when the terminal bud is formed between seedlings from bog site and dry site (mean development stage and standard error).

Fig. 5 in Differences Of The Bog And Dry Site Scots Pine Population Seedlings Germination And Early Growth

Fig. 5. Dry site seedlings early growth stages change during the first season till terminal bud formation.

Fig. 6 in Differences Of The Bog And Dry Site Scots Pine Population Seedlings Germination And Early Growth

Fig. 6. Bog site seedlings early growth stages change during the first season till terminal bud formation.

Fig. 1 in Wood Properties Of Nine Pinus Sylvestris Open-Pollinated Families Originating From Different Lithuanian Populations

Fig. 1. Field trials with open-pollinated progeny of Lithuanian Pinus sylvestris L. populations, established in 1983.

Fig.1 in Population Dynamics And Characterization Of Clostridium Macerans On Host Plant Of Flax

Fig.1. The AUDPC of Clostridium macerans as pathogen on the genotypes of flax during ontogenesis. abcd - AUDPC followed by the same letters in each column are not statistically significant by LSD0.05 (1.69).