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FIGURE 9 in New data on cave spiders (Arachnida: Araneae) of Iran, with new species and records

FIGURE 9. Habitus of Troglohyphantes megagynus sp. n., female. A lateral view; B dorsal view; C prosoma, anterior view.

FIGURE 6 in New data on cave spiders (Arachnida: Araneae) of Iran, with new species and records

FIGURE 6. Male palp of Harpactea zagros sp. n. A prolateral view; B ventral view; C retrolateral view. Scale bars: 0.2 mm. Abbreviations: 'Cd'—'conductor', Em—embolus.

FIGURE 8 in New data on cave spiders (Arachnida: Araneae) of Iran, with new species and records

FIGURE 8. Copulatory organs of Odontodrassus mundulus (A–C) and Synaphosus syntheticus (D). A, B male palp, ventral and retrolateral views; C, D epigynes, ventral view. Scale bars: 0.2 mm.

FIGURE 5 in New data on cave spiders (Arachnida: Araneae) of Iran, with new species and records

FIGURE 5. Male palp of Dysdera elamana sp. n. A retrolateral view; B dorsal view; C ventral view. Scale bars: 0.2 mm. Abbreviation: Ac—anterior crest, Mc—median crest, Vc—ventral crest.

FIGURE 10 in New data on cave spiders (Arachnida: Araneae) of Iran, with new species and records

FIGURE 10. Female of Troglohyphantes megagynus sp. n. A epigyne, ventral view; B same, dorsal view; C same, caudal view; D same, lateral view; E, abdomen, ventral view. Scale bars: 0.2 mm. Abbreviations: Be—base of epigyne, DPS—distal part of scape, Eg—epigynal groove, Ll—lateral lobe, PMP—posterior median plate, PPS—proximal part of scape, Sr—stretcher.

opennotspecifiedDec 2007View details →

FIGURE 1. A in New data on morphology and natural history of Deltamys kempi Thomas, 1919 (Cricetidae, Sigmodontinae) from central-eastern Argentina

FIGURE 1. A, Gastric morphology (a composite drawing based on LER 483 and 486); B and C, dorsal and ventral views of the phallus; and D, ventral aspect of the baculum of Deltamys kempi (LER 539) from central-eastern Argentina. References: a, dorsal papilla; b, proximal baculum or bony shaft; c, lateral bacular process or lateral cartilaginous digit; d, distal baculum or middle cartilaginous digit (scale = 1 mm).

opennotspecifiedDec 2007View details →

FIGURE 2 in New data on morphology and natural history of Deltamys kempi Thomas, 1919 (Cricetidae, Sigmodontinae) from central-eastern Argentina

FIGURE 2. Seasonal variation in: A) Trapp success; and B) percentage of reproductive individuals for Deltamys kempi from central-eastern Argentina during the years 2004-2006.

FIGURE 4 in Morphological studies and molecular data on a new marine ciliate, Apokeronopsis sinica n. sp. (Ciliophora: Urostylida), from the South China Sea

FIGURE 4. Unmatched sites from SSrRNA gene sequences alignment. Numbers represent the positions of the nucleotides. Missing sites are compensated by gaps (-). Matched sites are marked with dots (.).

FIGURE 3 in Morphological studies and molecular data on a new marine ciliate, Apokeronopsis sinica n. sp. (Ciliophora: Urostylida), from the South China Sea

FIGURE 3. Comparison of Apokeronopsis species. A. crassa (A, B, from Song et al. 2004), A. wrighti (C, D, from Long et al. 2008), A. antarctica (E, F, from Petz 1995), A. ovalis (G, H, from Shao et al. 2009), A. bergeri (I, J, from Li et al. 2008), and A. sinica (K, L, original), to show the morphology of live cells (A, C, E, G, I, K), infraciliature (B, D, F, H, J, L). Scale bars in (A, B, I, J) =100 µm, in (C–H, K, L) = 60 µm.

FIGURE 2 in Morphological studies and molecular data on a new marine ciliate, Apokeronopsis sinica n. sp. (Ciliophora: Urostylida), from the South China Sea

FIGURE 2. Photomicrographs of Apokeronopsis sinica n. sp. from live cells (A–E, I, J) and after protargol impregnation (K–O), and ventral views of live cells of A. crassa (F), A. bergeri (G) and A. wrighti (H). (A) Ventral view of the typical specimen. (B) Ventral view, showing the contractile vacuole (arrow). (C) Lateral view. (D) Ventral view of the anterior portion, arrows indicate the cilia of adoral zone of membranelles, arrowheads mark the paroral membranes and double-arrowheads depict the buccal cirri. (E) Lateral view to show the large cortical granules distributed on dorsal side. (I) Ventral view, to show the cortical granules: vermeil large (arrows), colorless large (arrowheads) and colorless small ones (double-arrowheads). (J) Ventral view, showing the cortical granules between the cirri rows. (K) infraciliature of the ventral side of a typical specimen. (L) Ventral view of the anterior portion, arrow indicates the paroral membrane and arrowhead marks the endoral membrane. (M) Ventral view of the anterior-right portion, arrowheads refer to frontoterminal cirri, and arrows show the buccal cirri. (N) Macronuclear nodules. (O) Ventral view of the posterior portion, note the transverse cirri (arrows). Scale bars in (A, B, C, F, G, H) = 100 µm, in (K) = 80 µm.

FIGURE 1. Apokeronopsis sinica n in Morphological studies and molecular data on a new marine ciliate, Apokeronopsis sinica n. sp. (Ciliophora: Urostylida), from the South China Sea

FIGURE 1. Apokeronopsis sinica n. sp. from live cells (A–D) and after protargol impregnation (E–F). (A, B) Ventral views of two typical specimens. (C) Dorsal view; to show the sparsely distributed large granules. (D) Details of the cortex, double-arrowheads indicate the smaller cortical granules, arrows mark the vermeil larger ones and arrowheads mark the colorless larger ones. (E, F) Ventral and dorsal views of the infraciliature and nuclear apparatus. AZM = adoral zone of membranelles; BC = buccal cirri; BiC = bicoronal cirri; DK = dorsal kineties; EM = endoral membrane; FTC = frontoterminal cirri; LMR = left marginal row; Ma = macronuclei; MC = midventral complex; PM = paroral membrane; RMR = right marginal row; TC = transverse cirri. Scale bars = 80 µm.

Fig. 18 in New Data onCosmobaris Discolor(Boheman) andHypolixus pica(F.) (Coleoptera: Curculionidae) Associated withAmaranthus(L.) (Amaranthaceae)

Fig. 18. Relative abundance and stage distribution of Cosmobaris discolor in Amaranthus spinosus at Yeşilköy, Dörtyol District, Hatay Province, Turkey.

Figs. 13–17 in New Data onCosmobaris Discolor(Boheman) andHypolixus pica(F.) (Coleoptera: Curculionidae) Associated withAmaranthus(L.) (Amaranthaceae)

Figs. 13–17. Host plant and some biological stages of Hypolixus pica. 13) Amaranthus spinosus; 14) Pupa;

Fig. 8 in Efficient New Above-Ground Bucket Traps Produce Comparable Data to that of Standard Transects for the Endangered American Burying Beetle,Nicrophorus AmericanusOlivier (Coleoptera: Silphidae)

Fig. 8. Suggested improvements to above-ground bucket trap design using a wooden rain cover and landing pad to reduce disturbances from scavengers, reduce maintenance, and increase bait-life.

Fig. 5 in Efficient New Above-Ground Bucket Traps Produce Comparable Data to that of Standard Transects for the Endangered American Burying Beetle,Nicrophorus AmericanusOlivier (Coleoptera: Silphidae)

Fig. 5. Average differences in abundance estimates for Nicrophorus americanus between methods using various sample-effort conversion rates (n = 20). Normalized average differences are mean differences divided by their standard deviations to provide a standardized scale for comparisons because abundance estimates—and therefore differences between them—are inherently smaller when trap-nights are artificially increased.

Fig. 4 in Efficient New Above-Ground Bucket Traps Produce Comparable Data to that of Standard Transects for the Endangered American Burying Beetle,Nicrophorus AmericanusOlivier (Coleoptera: Silphidae)

Fig. 4. Sample site layout (n = 28) showing 800-m site buffers (open circles). The order in which trap methods were used during the two sample periods at each site included buckets then transects (circles), transects then buckets (squares), and transects during both sample periods at control sites (triangles).

Fig. 7 in Efficient New Above-Ground Bucket Traps Produce Comparable Data to that of Standard Transects for the Endangered American Burying Beetle,Nicrophorus AmericanusOlivier (Coleoptera: Silphidae)

Fig. 7. ANOVA group means showing the relationship between beetle captures and the numbers of disturbed traps. Beetle abundance values were ranked for the three sample nights at each site such that increasing rank represented increasing abundance. Precision was low in groups 4 and 5 due to small sample sizes (n = 6 and n = 4, respectively).

Fig. 1 in Efficient New Above-Ground Bucket Traps Produce Comparable Data to that of Standard Transects for the Endangered American Burying Beetle,Nicrophorus AmericanusOlivier (Coleoptera: Silphidae)

Fig. 1. Layout of a standard pitfall trap transect showing an 800-m trap sample range (USFWS estimate) and a 200-m trap sample range in comparison to 20-m trap spacing to illustrate the lack of independence among traps in a transect.

opennotspecifiedJan 2010View details →

Figure 9. A–D in A new genus of African Acrometopini (Tettigoniidae: Phaneropterinae) based on morphology, chromosomes, acoustics, distribution, and molecular data, and the description of a new species

Figure 9. A–D, left cercus of male Altihoratosphaga species. A, Altihoratosphaga hanangensis sp. nov. B, Altihoratosphaga nou. C, Altihoratosphaga montivaga. D, Altihoratosphaga nomima. All specimens were collected from Ruaha National Park. Scale bar: 2 mm. E–H, subgenital plates of male Altihoratosphaga species. E, A. hanangensis sp. nov. F, A. nou. G, A. montivaga. H, A. nomima. All specimens were collected from Ruaha National Park. Scale bar: 2 mm. I, right tegmen of male A. hanangensis sp. nov. Scale bar: 0.5 cm. J, subgenital plate of female A. hanangensis sp. nov. Scale bar: 1 mm. K, ovipositor of A. hanangensis sp. nov. Scale bar: 1 mm.