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Figure 7 in Diversity and life-history traits of wild bees (Insecta: Hymenoptera) in intensive agricultural landscapes in the Rolling Pampa, Argentina

Figure 7. Mean number of (a) above-ground nesting bee individuals, (b) floral specialist bee individuals, (c) oligolectic bee individuals and (d) oil-collecting bee individuals in cropped area (n = 28 points) and semi-natural area (n = 11 points). ns indicates a non-significant result. Asterisks indicate that means are significantly different (Wilcoxon rank sum test, ** = P <0.01). Bars show SEs.

Figure 3 in New records of Nuuanuidae (Crustacea: Amphipoda: Senticaudata) from Korean waters, with descriptions of one new genus and two new species

Figure 3. Parvipalpus holocaudatus sp. nov., holotype, male. (A) Pereopod 3; (B) right pereopod 4; (C) left pereopod 4; (D) pereopod 5; (E) pereopod 6; (F) pereopod 7.

Figure 2 in Diversity and life-history traits of wild bees (Insecta: Hymenoptera) in intensive agricultural landscapes in the Rolling Pampa, Argentina

Figure 2. Semi-natural area of the study site: (a) semi-natural grassland; (b) the stream 'Arroyo Dulce' and its banks (Photos: Violette Le Féon).

Figure 5 in A gall mite, Aceria rhodiolae (Acari: Eriophyidae), altering the phytochemistry of a medicinal plant, Rhodiola rosea (Crassulaceae), in the Canadian Arctic

Figure 5. Coxigenital region of Aceria rhodiolae females from (A) Russia, and (B,C,E) Nunavik, Canada. (A,B) Differential interference contrast light microscopy, (C,E) scanning electron micrograph, (D) line drawing. Scale on (B) also applies to (A). Notations on (D) indicate palp, leg and idiosomal setae, and coxal apodemes (ap1, ap2, ap; pra, prosternal apodeme). Other arrows elsewhere indicate characteristic ridges on coxal plates (a,b,c); genital flange (fl), and underlying postgenital plate (pp), which bears setae 3a and extends anterolaterally into lateral flaps (f) that flank the genital coverflap; and ventral ridges on femur, genu, and coxal fields (E).

Figure 8 in A gall mite, Aceria rhodiolae (Acari: Eriophyidae), altering the phytochemistry of a medicinal plant, Rhodiola rosea (Crassulaceae), in the Canadian Arctic

Figure 8. (A) Healthy infructescence of a Rhodiola rosea plant from Nunavik (Canada) versus (B) a mite-infested inflorescence (mostly pale green or yellowish) that partly (centrally) developed into fruits (yellow to red). (C) Dried inflorescences from Labrador (Canada) with a few (upper right) to most (lower left) flowers galled, and a galled leaf (isolated, in the middle). (D) Dried inflorescences from western Russia that were preserved in an herbarium for over 100 years. (E,F) Enlargement of a galled flower and galled leaf from Labrador (same scale). Arrows point at some of the galled flowers (B‒D) or leaves (C). The scale on (C) also applies to (D), and is approximate for (A,B).

Figure 1 in A gall mite, Aceria rhodiolae (Acari: Eriophyidae), altering the phytochemistry of a medicinal plant, Rhodiola rosea (Crassulaceae), in the Canadian Arctic

Figure 1. (A) Map of Canada, showing the area surveyed for Rhodiola rosea in Nunavik, Québec (in white). The small arrow indicates a site where additional samples were taken in Labrador, Newfoundland. (B) Region along the coast of Ungava Bay where populations of R. rosea were surveyed (geographic extremes of study sites: northwest 61.078°N, 69.632°W; northeast 60.422°N, 64.839°W; south 58.023°N). Open circles indicate sites with at least a few galled plants, whereas solid circles indicate sites with no galled plants.

Figure 3 in Biotic components of dung beetles (Insecta: Coleoptera: Scarabaeidae: Scarabaeinae) from Pantanal - Cerrado Border and its implications for Chaco regionalization

Figure 3. Generalized tracks (GT A–L) of dung beetles, different biotic components observed in the Pantanal–Cerrado Border.

Figure 4 in Aquatic Diptera (Insecta) assemblages in four sympatric Eryngium (Apiaceae) phytotelmata in flowering and senescent times

Figure 4. Median number of Metriocnemus eryngiotelmatus larvae per plant in four Eryngium phytotelmata. The box indicates the 25th and 75th centiles, the line within the box indicates the median and the whiskers indicate the 90th and 10th centiles. Different letters indicate significant differences detected by Dunn's test (p <0.05).

Figure 2 in Necrophagous or predators? The role of Pheidole radoszkowskii Mayr (Hymenoptera: Formicidae) on Rattus norvegicus (Berkenhout) carcasses (Rodentia: Muridae)

Figure 2. Average number of Pheidole radoszkowskii that exhibited necrophagous feeding behaviour – NFB – (fed on exudates and on pieces of flesh from the carcass) and predatory feeding behaviour – PFB – (predated on fly larvae).

Figure 3 in Aquatic Diptera (Insecta) assemblages in four sympatric Eryngium (Apiaceae) phytotelmata in flowering and senescent times

Figure 3. Median number of Polypedilum parthenogeneticum larvae per plant in four Eryngium phytotelmata. The box indicates the 25th and 75th centiles, the line within the box indicates the median and the whiskers indicate the 90th and 10th centiles. Different letters indicate significant differences detected by Dunn's test (p <0.05).

Figure 2 in Aquatic Diptera (Insecta) assemblages in four sympatric Eryngium (Apiaceae) phytotelmata in flowering and senescent times

Figure 2. Cumulative total of Diptera observed in successive plants (n = 40 plants for each species in autumn and in spring). (A) Eryngium horridum; (B) Eryngium stenophyllum; (C) Eryngium aff. serra; (D) Eryngium elegans. Logarithmic equations with R2 values; p <0.001 for all R2 except for E. stenophyllum in autumn (p = 0.09).

Figure 8 in Two new Geoplaninae species (Platyhelminthes: Continenticola) from Southern Brazil based on an integrative taxonomic approach

Figure 8. Obama maculipunctata sp. nov. in dorsal view. (A) Photograph of a live specimen (holotype MZUSP PL.1565). (B) Dorsal pattern of pigmentation of the holotype. (C) Eye pattern of a fixed specimen (paratype MZU PL.00197). (D) Photograph of monolobated eyes of a fixed specimen (paratype MZU PL.00197) in clove oil. (E) Photograph of trilobated eyes of a fixed specimen (paratype MZU PL.00197) in clove oil.

Figure 2 in Two new Geoplaninae species (Platyhelminthes: Continenticola) from Southern Brazil based on an integrative taxonomic approach

Figure 2. Cratera ochra sp. nov., holotype, in dorsal view. (A) Photograph of the live specimen. (B) Dorsal pattern of pigmentation of the preserved specimen.

Figure 1. Bayesian phylogenetic tree inferred from the 640 in Two new Geoplaninae species (Platyhelminthes: Continenticola) from Southern Brazil based on an integrative taxonomic approach

Figure 1. Bayesian phylogenetic tree inferred from the 640-bp of cytochrome c oxidase subunit I gene under GTR + I + G model of sequence evolution. The two new species are highlighted in light grey (Cratera ochra sp. nov.) and dark grey (Obama maculipunctata sp. nov.). Values indicate support for each node according to the maximum posterior probabilities>70% and bootstrap support values> 70%, respectively.

Figure 3 in Phytotelmata colonization in bamboo (Guadua sp.) culms in northeast Argentina

Figure 3. Hypothetic schema of a trophic web for stumps of bamboo community in Corrientes Province, Argentina. The circle represents the schematic stem wall, the arrows indicate energy flow.

Figure 3 in Aspects of natural history in a sand boa, Eryx muelleri (Erycidae) from arid savannahs in Burkina Faso, Togo, and Nigeria (West Africa)

Figure 3. Relationships between (a) Snout-Vent-Length (SLV) and Tail Length (TL), and between (b) SVL and Head Length (HL) in Eryx muelleri. Specimens from Togo, Burkina Faso and Nigeria were pooled.

Figure 4 in Phylogeography of the Eurasian red squirrel (Sciurus vulgaris orientis) on the boreal island of Hokkaido, Japan

Figure 4. Network of the 29 cytochrome b gene haplotypes of Sciurus vulgaris orientis in Hokkaido Island, Japan, using statistical parsimony. Haplotype names correspond to Appendix 1. Missing haplotypes are indicated by open circles. Lines connecting haplotypes indicate the relationship. Numbers in parentheses indicate the number of individuals. Haplotypes without parentheses are from just one individual.

Figure 3 in Temporal dynamics of invertebrate and aquatic plant communities at three intermittent ponds in livestock grazed Patagonian wetlands

Figure 3. Seasonal variation of total taxa richness (A), mean density (A), and relative contribution of biomass (B) of most abundant groups of aquatic invertebrates at three ponds in a Patagonian wetland (Mallín Crespo) during the study period (May 2008 to April 2009). Livestock stocking period is indicated by the black bar.

Figure 3. Diplecogaster tonstricula n in Diplecogaster tonstricula, a new species of cleaning clingfish (Teleostei: Gobiesocidae) from the Canary Islands and Senegal, eastern Atlantic Ocean, with a review of the Diplecogaster-ctenocrypta species-group

Figure 3. Diplecogaster tonstricula n. sp., CCML uncat., paratype, specimen 1, 22.9 mm SL. Head lateral line system. (A) Dorsal view of head; (B) ventral view of head. Bar 1 mm.

Figure 1 in New species of Australopericoma Vaillant (Diptera: Psychodidae) from the Brazilian semiarid region and key to males of the genus

Figure 1. Australopericoma paraibana Cordeiro & Bravo sp. nov. (A) anterior view of head, palpi and antenna; (B) head, posterior view; (C) antenna, apical flagellomeres; (D) flagellomeres showing ascoids; (E) wing; (F) ventral view of male terminalia, showing part of epandrium, cerci, epiproct and hypoproct; (G) dorsal view of male terminalia, showing hypandrium, gonopods and aedeagal complex.