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Fig. 1 in Appraisal of the impact of three insecticides on the principal rice pests and their predators in China

Fig. 1. Effects of Virtako on planthopper abundance (mean number ± SE). Means followed by the same lowercase letter are not significantly different (ANOVA and Tukey's HSD test, P> 0.05).

Fig. 3 in Appraisal of the impact of three insecticides on the principal rice pests and their predators in China

Fig. 3. Temporal dynamics of total numbers of predators per 50 hills where insecticide was applied (a) as a single application or (b) as 2 applications to rice plots.

Fig. 5 in Appraisal of the impact of three insecticides on the principal rice pests and their predators in China

Fig. 5. Temporal dynamics of predator insect diversity (a, diversity index; b, evenness index; c, dominance index; and d, species richness) in rice plots with various treatments (2 applications per season).

Fig. 2 in Appraisal of the impact of three insecticides on the principal rice pests and their predators in China

Fig. 2. Effects of Virtako on rice leaffolder abundance (mean number ± SE). Means followed by the same lowercase letter are not significantly different (ANOVA and Tukey's HSD test, P> 0.05).

Fig. 6 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct

Fig. 6. Four examples of the tissue expression profiling of unknown distinct unigenes (>500 bp) expressed highly in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis. Relative expression levels were determined as described in Fig. 5.

Fig. 4 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct

Fig. 4. Kyoto encyclopedia of gene and genomes (KEGG) analysis of unigenes expressed highly in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis. Each category contains more than 1 unigene sequences.

Fig. 2 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct

Fig. 2. Clusters of orthologous groups (COG) functional classification of unigenes expressed highly and specifically in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis.

Fig. 1 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct

Fig. 1. Statistics of sequences expressed specifically in each analyzed tissue of Bactrocera dorsalis.

Fig. 5 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct

Fig. 5. Six examples of the tissue expression profiling of predicted distinct unigenes (>500 bp) expressed highly in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis. Relative expression levels were determined by qRT-PCR in head (HE), thorax (TH), abdomen (AB), midgut (MG), fat body (FB), Malpighian tubules (MT), testes (TE), and male accessory glands and ejaculatory duct (MAG) samples from B. dorsalis males. Relative expression levels were calculated based on the value in head, which was ascribed an arbitrary value of 1. Different letters above the bars indicate significant differences based on Tukey's test (P ≤ 0.05).

Fig. 3 in Comparative transcriptome analysis of three Bactrocera dorsalis (Diptera: Tephritidae) organs to identify functional genes in the male accessory glands and ejaculatory duct

Fig. 3. Gene ontology (GO) classification of unigenes expressed highly in male accessory glands and ejaculatory duct tissue of Bactrocera dorsalis.

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Fig. 3 in Haemogregarine infections of three species of aquatic freshwater turtles from two sites in Costa Rica

Fig. 3. (A) Average haemogregarine parasitemias (±SD) between black river turtles, Rhinoclemmys funerea, collected from creek and pond sites. (B) Average haemogregarine parasitemias (±SD) of black river turtles, Rhinoclemmys funerea, and white-lipped mud turtles, Kinosternon leucostomum, were significantly different (p = 0.032).

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Fig. 1 in Haemogregarine infections of three species of aquatic freshwater turtles from two sites in Costa Rica

Fig. 1. Satellite image of Selva Verde and surrounding area showing the property of Selva Verde (outlined in yellow) with the creek site marked with narrow arrow and the pond marked with the thick arrow. White bar is 100 m. Inset: map of Costa Rica showing location of Selva Verde (black box) and La Pacifica (black star).

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Fig. 2 in Haemogregarine infections of three species of aquatic freshwater turtles from two sites in Costa Rica

Fig. 2. Haemogregarines from black river turtles, Rhinoclemmys funera (A–C) all parasites shown are premeronts except for a meront in B (arrow), white-lipped mud turtle, Kinosternon leucostomum (D–E) premeronts; (F) early meront (arrow), and scorpion mud turtle, K. scorpioides (G–I) all premeronts. Scale bar in panel I is 10 µm and applies to all micrographs.

Figs. 9–15 in The Newly Recorded Fern-spore Feeding Moths in the Genus , Meyrick 1889 (Lepidoptera: Stathmopodidae) from Taiwan, with Notes on Life History of Three Species.

Figs. 9–15. Adult specimens and genitalia of Calicotis rotundinidus. 9–10, Male specimen, TAIWAN: Hulian, Shioulin, Gekou; 11–12, Female specimen, TAIWAN: New Taipei City, Wulai, Bauching temple; 13–14, Male genitalia; 15, Female genitalia. Scale bars: 9–12 = 5 mm; 13–14 = 1 mm; 15 = 1 mm.

Figs. 2–8 in The Newly Recorded Fern-spore Feeding Moths in the Genus , Meyrick 1889 (Lepidoptera: Stathmopodidae) from Taiwan, with Notes on Life History of Three Species.

Figs. 2–8. Adult specimens and genitalia of Calicotis attiei. 2–3, Male specimen, TAIWAN: Hualian, Shioulin, Gekou; 4–5, Female specimen, TAIWAN: Hualian, Shioulin, Gekou; 6–7, Male genitalia; 8, Female genitalia. Scale bars: 2–5 = 5 mm; 6–7 = 1 mm; 8 = 1 mm.

Fig. 35 in The Newly Recorded Fern-spore Feeding Moths in the Genus , Meyrick 1889 (Lepidoptera: Stathmopodidae) from Taiwan, with Notes on Life History of Three Species.

Fig. 35. Eggs of Calicotis attiei (blue arrows) on the sporangiospores of Microsorum scolopendria. Image by Masahiko Tanahashi. Scale bar = 1 mm

Figs. 23–34 in The Newly Recorded Fern-spore Feeding Moths in the Genus , Meyrick 1889 (Lepidoptera: Stathmopodidae) from Taiwan, with Notes on Life History of Three Species.

Figs. 23–34. Immatures and adults of Calicotis species from Taiwan. 23, Immature artifacts of C. attiei on Nephrolepis biserrata. 24, Larva of C. attiei. 25, Cocoon of C. attiei. 26, Adult resting, photo of C. attiei. 27, Immature artifacts of C. rotundinidus on Asplenium austalasicum. 28, Larva of C. rotundinidus. 29, Cocoon of C. rotundinidus. 30, Adult resting, photo of C. rotundinidus. 31, Immature artifacts of C. exclamationis on Neolepisorus fortune. 32, Larva of C. exclamationis. 33, Cocoon of C. excalamationis. 34, Adult resting, photo of C. excalamationis.

Figs. 16–22 in The Newly Recorded Fern-spore Feeding Moths in the Genus , Meyrick 1889 (Lepidoptera: Stathmopodidae) from Taiwan, with Notes on Life History of Three Species.

Figs. 16–22. Adult specimens and genitalia of Calicotis exclamationis. 16–17, Male specimen, TAIWAN: New Taipei City, Pinglin, Jianshanhu; 18–19, Female specimen, TAIWAN: Taoyuan, Fuxing, Shiuanyuan; 20–21, Male genitalia; 22, Female genitalia. Scale bars: 16–19 = 5 mm; 20–21 = 1 mm; 22 = 1 mm.

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Fig. 1. A in Figs. 23-34 in The Newly Recorded Fern-spore Feeding Moths in the Genus , Meyrick 1889 (Lepidoptera: Stathmopodidae) from Taiwan, with Notes on Life History of Three Species.

Fig. 1. A map of Taiwan showing the occurrence records of Pteropus dasymallus. Full circles, empty circles and empty triangles represent resident populations and sporadic and dubious records, respectively. Approximate locations are presented for numbers 1–6, 9 and 21, where precise coordinates are unavailable (please refer to Table 1 for the details of localities).