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Fig. 7 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 7. Habitus. Myrsidea ramoni sp.n. A-B, holotype female (A), paratype male (B). Myrsidea victoriae sp.n. C-D, holotype female (C), paratype male (D).

Fig. 6 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 6. Habitus. Myrsidea carmenae sp.n. A-B, holotype female (A), paratype male (B). Myrsidea franciscae sp.n. C-D, holotype female (C), paratype male (D).

Fig. 8 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 8. Bayesian phylogeny of Bornean Myrsidea studied based on analysis of the mitochondrial cytochrome c oxidase subunit I (COI) and elongation factor-1α (EF- 1α) genes. Outgroup taxon was removed from this figure for readability. Hosts belong to family Pycnonotydae are indicated on the right.

Fig. 4 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 4. Myrsidea ramoni sp.n. A, dorso-ventral view of female thorax and abdomen; B, head shape; C, dorsal view of male abdomen; D, male metasternal plate and sternites I–II; E, male genital sac sclerite.

Fig. 3 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 3. Myrsidea franciscae sp.n. A, dorso-ventral view of female thorax and abdomen; B, head shape; C, male metasternal plate and sternites I–II; D, male genital sac sclerite.

Fig. 2 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 2. Myrsidea carmenae sp.n. A, dorso-ventral view of female thorax and abdomen; B, head shape; C, male metasternal plate and sternites I–II; D, male genital sac sclerites.

Fig. 4 in Effects of latitude, host body size, and host trophic guild on patterns of diversity of helminths associated with humans, wild and domestic mammals of Mexico

Fig. 4. Parasite richness and average taxonomic distinctness by host trophic guild (the size of circle represents the number of hosts belonging to each trophic guild).

Fig. 1 in Effects of latitude, host body size, and host trophic guild on patterns of diversity of helminths associated with humans, wild and domestic mammals of Mexico

Fig. 1. Maps showing the geographic locations of the records, classified by phylum of the subsetted database.

Fig. 5 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 5. Myrsidea victoriae sp.n. A–D, dorso-ventral view of female thorax and abdomen (A), head shape (B), male metasternal plate and sternites I–II (C), male genital sac sclerite (D); Myrsidea macronoi E, male genital sac sclerite.

Fig. 1 in Diversity and host associations of Myrsidea chewing lice (Phthiraptera: Menoponidae) in the tropical rainforest of Malaysian Borneo

Fig. 1. Map of sampling localities (black dots) in the Yayasan Sabah Forest Management Area, Malaysian Borneo.

Fig. 7 in Arthropod parasites of Antarctic and Subantarctic birds and pinnipeds: A review of host-parasite associations

Fig. 7. Distribution of the records of parasitic arthropods in relation to host species and their distribution in the sub-regions of the Antarctic region. Legend: AAP = Antarctic Peninsula (including South Shetland Islands and Palmer Archipelago), AWS = Antarctica Weddell Sea sector, AAT = Antarctica Atlantic Ocean sector (including Bouvet Island), AIW = Antarctica Indian Ocean West sector, AIE = Antarctica Indian Ocean East sector, ARS = Antarctica Ross Sea sector (including Scott and Balleny Islands), APW = Antarctica Pacific Ocean West sector, APE = Antarctica Pacific Ocean East sector (including Peter I Island), SOI = South Orkney Island, SGI = South Georgia Island, SSI = South Sandwich Islands, PEI = Prince Edward Islands, CRI = Crozet Islands, KEI = Kerguelen Islands, HMI = Heard and McDonald Islands.

Fig. 6 in Arthropod parasites of Antarctic and Subantarctic birds and pinnipeds: A review of host-parasite associations

Fig. 6. Distribution of host species and host-parasite-location records in the Antarctic region, excluding stragglers and contaminants. Legend: (A) avian hosts, (B) pinniped hosts, (C) chewing lice, (D) sucking lice, (E) fleas, (F) ticks, (G) nasal mites, (H) feather mites.

Fig. 4 in Arthropod parasites of Antarctic and Subantarctic birds and pinnipeds: A review of host-parasite associations

Fig. 4. Genera of fleas (Ceratophyllidae – 1, Pygiopsyllidae – 2, Rhopalopsyllidae – 3), pentastomes (Reighardiidae – 4), hard ticks (Ixodidae – 5), parasitic mites (Laelapidae – 6, Halarachnidae – 7, Rhinonyssidae – 8) and feather mites (Alloptidae – 9, Avenzoariidae – 10, Freyanidae – 11, Xolalgidae – 12) recorded infesting Antarctic birds and mammals.

Fig. 5 in Arthropod parasites of Antarctic and Subantarctic birds and pinnipeds: A review of host-parasite associations

Fig. 5. Network representation and mean and standard deviation of degrees and betweenness centrality of the host-parasite associations by host families (A) and parasite families (B), excluding stragglers and contaminants. Degrees (number of connections of a given node) may be interpreted as a measure of the host breadth of a given parasite species or the parasite diversity of a given host species; node size is drawn proportional to the number of degrees. Betweenness centrality (proportion of shortest paths between nodes that pass through a given node) may be interpreted as a measure of the potential influence a species has over the spread of vectorborne pathogens through the network.

Fig. 3 in Arthropod parasites of Antarctic and Subantarctic birds and pinnipeds: A review of host-parasite associations

Fig. 3. Genera of sucking lice (Echinophthiriidae – 1) and chewing lice (Menoponidae – 2, Philopteridae – 3) recorded infesting Antarctic birds and mammals.

Fig. 2 in Arthropod parasites of Antarctic and Subantarctic birds and pinnipeds: A review of host-parasite associations

Fig. 2. Host-parasite associations at the family level between Antarctic birds and mammals and arthropods, excluding stragglers and contaminants. Phylogenetic trees are not drawn to scale (adapted from Dabert and Mironov, 1999; Whiting, 2002; Dowling and O'Connor, 2010; Zhang, 2011; Prum et al., 2015).

Fig. 1 in Arthropod parasites of Antarctic and Subantarctic birds and pinnipeds: A review of host-parasite associations

Fig. 1. Sub-areas of the Antarctic region. Legend: AAP = Antarctic Peninsula (including South Shetland Islands and Palmer Archipelago), AWS = Antarctica Weddell Sea sector, AAT = Antarctica Atlantic Ocean sector (including Bouvet Island), AIW = Antarctica Indian Ocean West sector, AIE = Antarctica Indian Ocean East sector, ARS = Antarctica Ross Sea sector (including Scott and Balleny Islands), APW = Antarctica Pacific Ocean West sector, APE = Antarctica Pacific Ocean East sector (including Peter I Island), SOI = South Orkney Island, SGI = South Georgia Island, SSI = South Sandwich Islands, PEI = Prince Edward Islands, CRI = Crozet Islands, KEI = Kerguelen Islands, HMI = Heard and McDonald Islands. The Antarctic Polar Front was drawn from Moore et al. (1999).

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Fig. 5 in Host associations of gall-inducing Prodiplosis longifila (Diptera: Cecidomyiidae) from Bolivia: implications for its use as a biological control agent for Jatropha gossypiifolia (Euphorbiaceae)

Fig. 5. Susceptibility of Jatropha gossypiifolia to Prodiplosis longifila. Morphologically similar galls induced on control Jatropha clavuligera (A) and Jatropha gossypiifolia (B) plants under no-choice conditions in quarantine in Pretoria, South Africa. Galling on a transplanted Jatropha gossypiifolia plant under the natural field conditions in Bolivia (C).

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Fig. 4 in Host associations of gall-inducing Prodiplosis longifila (Diptera: Cecidomyiidae) from Bolivia: implications for its use as a biological control agent for Jatropha gossypiifolia (Euphorbiaceae)

Fig. 4. Relationship between the number of branches per plant and number of shoot tips with Prodiplosis longifila galls (A) and percentage of shoots (± SE) with Prodiplosis longifila galls (B) across 3 sites in Bolivia in Feb 2016. Different letters above SE bars indicate significant differences (Tukey's test, P <0.001).