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Fig. 19 in Systematic Review of Endemic Sulawesi Squirrels (Rodentia, Sciuridae), with Descriptions of New Species of Associated Sucking Lice (Insecta, Anoplura), and Phylogenetic and Zoogeographic Assessments of Sciurid Lice

Fig. 19. Specimen scores representing population samples of Prosciurillus alstoni and P. weberi (8- pointed star; N 5 5) projected onto the first and second principal components extracted from principalcomponents analysis. Symbols identifying samples of P. alstoni are: filled circle 5 Pinedapa, N 5 19; filled triangle 5 Kuala Navusu and Sungai Tolewonu, N 5 32; cross 5 southeastern peninsula, N 5 11; star 5 Usu, lectotype of sarasinorum. Heavy arrow identifies score for the holotype of weberi; delicate arrows point to lectotype (top) and paralectotype (bottom) of mowewensis. See table 21 for correlations and percent variance.

Fig. 11 in Systematic Review of Endemic Sulawesi Squirrels (Rodentia, Sciuridae), with Descriptions of New Species of Associated Sucking Lice (Insecta, Anoplura), and Phylogenetic and Zoogeographic Assessments of Sciurid Lice

Fig. 11. Collection localities for samples of four species in the Prosciurillus leucomus group: P. leucomus, P. alstoni, P. weberi, and P. topapuensis. The collection site for Prosciurillus sp., which is represented by a subfossil fragment, is also indicated. Distribution of the fifth member, P. rosenbergii, in Kepulauan Sangihe is portrayed on the map in figure 28. Numbers key to localities described in the gazetteer where specimens are also identified by museum initials and catalog numbers. The inset map, right (rectangle in larger map, above), contains collection sites (1–12) for P. topapuensis scattered along Musser's transect from the Sungai Miu to Gunung Nokilalaki. The dashed contour line at 1300 m marks the approximate boundary between tropical lowland evergreen rain forest and tropical lower montane forest.

Fig. 15 in Systematic Review of Endemic Sulawesi Squirrels (Rodentia, Sciuridae), with Descriptions of New Species of Associated Sucking Lice (Insecta, Anoplura), and Phylogenetic and Zoogeographic Assessments of Sciurid Lice

Fig. 15. Specimen scores representing two population samples of Prosciurillus leucomus projected onto the first and second principal components extracted from principal-components analysis. Symbols identifying samples are: filled circle 5 northeastern peninsula (Likupang, Teteamoet, Rurukan, Temboan; N 5 18); X 5 western segment of northern peninsula (Bumbulan, Sungai Paleleh, Gunung Ile-Ile, Labuan Sore, Bumbarujaba; N 5 8). Ellipses outline 95% confidence limits for the specimen scores representing each population sample. See table 18 for correlations and percent variance.

Fig. 12 in Systematic Review of Endemic Sulawesi Squirrels (Rodentia, Sciuridae), with Descriptions of New Species of Associated Sucking Lice (Insecta, Anoplura), and Phylogenetic and Zoogeographic Assessments of Sciurid Lice

Fig. 12. Dorsal views of skulls representing species of Prosciurillus. Top row, left to right: P. alstoni (AMNH 226076; Kuala Navusu; ONL 5 46.6 mm) and P. topapuensis (AMNH 225504; Gunung Kanino; ONL 5 45.0 mm); we employ these two as exemplars of species in the P. leucomus group. Bottom row, left to right: P. abstrusus (AMNH 101378, holotype; Pegunungan Mekongga; ONL 5 38.2 mm) and P. murinus (AMNH 225496; Gunung Kanino; ONL 5 34.4 mm); these are the only species comprising the P. murinus group.

Fig. 16 in Systematic Review of Endemic Sulawesi Squirrels (Rodentia, Sciuridae), with Descriptions of New Species of Associated Sucking Lice (Insecta, Anoplura), and Phylogenetic and Zoogeographic Assessments of Sciurid Lice

Fig. 16. Reproduction of Anderson's (1879) color plate of ''Sciurus alstoni'' (5 Prosciurillus alstoni).

Fig. 5 in Taxonomic Study of the Genera Förster, 1850, and Cameron, 1903 (Hymenoptera, Ichneumonidae, Cryptinae) associated with (Hymenoptera, Tenthredinidae), with Description of a New Species

Fig. 5. Javra coreensis (Uchida, 1930), female (KPM-NK 5004375). A, head and antenna, lateral view; B, areolet of right fore wing; C, T1, lateral view; D, propodeum and T1, dorsal view, surface sculptures omitted except for left half of area basalis, area superomedia, area externa, area dentipara, and area postero; E, apical part of ovipositor, lateral view.

Fig. 4 in Taxonomic Study of the Genera Förster, 1850, and Cameron, 1903 (Hymenoptera, Ichneumonidae, Cryptinae) associated with (Hymenoptera, Tenthredinidae), with Description of a New Species

Fig. 4. Javra coreensis (Uchida, 1930), female (KPM-NK 5004375). A, lateral habitus; B, mesonotum, dorsal view; C, T2 and T3, dorsolateral view.

Fig. 1 in Taxonomic Study of the Genera Förster, 1850, and Cameron, 1903 (Hymenoptera, Ichneumonidae, Cryptinae) associated with (Hymenoptera, Tenthredinidae), with Description of a New Species

Fig. 1. Aptesis flavitrochanterus sp. nov., female (A―D, F, holotype, KPM-NK 5006655; E, paratype, KPM-NK 5006674). A, lateral habitus; B, head, frontal view; C, mesonotum, dorsal view; D, E, left hind tibia, anterior view; F, metasoma, dorsal view.

Fig. 2 in Taxonomic Study of the Genera Förster, 1850, and Cameron, 1903 (Hymenoptera, Ichneumonidae, Cryptinae) associated with (Hymenoptera, Tenthredinidae), with Description of a New Species

Fig. 2. Aptesis flavitrochanterus sp. nov., male (paratype, KPM-NK 5006658). A, lateral habitus; B, head, frontal view; C, outer surface of right flagellum.

Fig. 11 in Description Of Crinotonia Anastasiae, New Genus, New Species, A New Crinoid Associated Pontoniine Shrimp (Crustacea: Caridea) From Nha Trang Bay, Vietnam, With Inclusion Of Periclimenes Attenuatus Bruce, 1971, In The New Genus

Fig. 11. Pontoniopsis comanthi Borradaile, ovigerous female (PCL 1.5 mm), Mun Island, Nha Trang Bay: a, general view; b, front of carapace, dorsal view; c, antennule; d, antenna. Scale bar: a = 2 mm; b = 3 mm; c, d = 4 mm.

Fig. 6 in Description Of Crinotonia Anastasiae, New Genus, New Species, A New Crinoid Associated Pontoniine Shrimp (Crustacea: Caridea) From Nha Trang Bay, Vietnam, With Inclusion Of Periclimenes Attenuatus Bruce, 1971, In The New Genus

Fig. 6. Crinotonia anastasiae, new genus, new species, holotype (e), allotype (a-d, f): a, distal margin of sixth segment and telson, lateral view; b, telson, dorsal; c, uropods; d, e, distal part of telson; f, appendix interna of second male pleopods. Scale bar: a-c = 2 mm; d, e = 0.7 mm; f = 0.3 mm.

Fig. 3 in Description Of Crinotonia Anastasiae, New Genus, New Species, A New Crinoid Associated Pontoniine Shrimp (Crustacea: Caridea) From Nha Trang Bay, Vietnam, With Inclusion Of Periclimenes Attenuatus Bruce, 1971, In The New Genus

Fig. 3. Mouthparts of Crinotonia anastasiae, new genus, new species, allotype: a, mandibule; b, maxillula; c, maxilla; d, first maxilliped; e, second maxilliped; f, third maxilliped. Scale bar = 1 mm.

Fig. 5 in Description Of Crinotonia Anastasiae, New Genus, New Species, A New Crinoid Associated Pontoniine Shrimp (Crustacea: Caridea) From Nha Trang Bay, Vietnam, With Inclusion Of Periclimenes Attenuatus Bruce, 1971, In The New Genus

Fig. 5. Crinotonia anastasiae, new genus, new species, allotype: a-d, dactylus of major second pereiopod. Scale bar = 2 mm.

Fig. 4 in Description Of Crinotonia Anastasiae, New Genus, New Species, A New Crinoid Associated Pontoniine Shrimp (Crustacea: Caridea) From Nha Trang Bay, Vietnam, With Inclusion Of Periclimenes Attenuatus Bruce, 1971, In The New Genus

Fig. 4. Crinotonia anastasiae, new genus, new species, allotype: a, first pereiopod; b, c, chela of first pereiopod; d, major second pereiopod; e, minor second pereiopod; f, chela of minor second pereiopod; g, third pereiopod; h, same, ventral margin of propodus; i, dactylus of third pereiopod; j, same, distal part. Scale bar: a, e, g = 1 mm; b, c, f, i = 0.5 mm; d = 2 mm; j =no scale bar.

Fig. 1 in Description Of Crinotonia Anastasiae, New Genus, New Species, A New Crinoid Associated Pontoniine Shrimp (Crustacea: Caridea) From Nha Trang Bay, Vietnam, With Inclusion Of Periclimenes Attenuatus Bruce, 1971, In The New Genus

Fig. 1. Crinotonia anastasiae, new genus, new species: a, holotype female; b, allotype male. Scale bar = 5 mm.

Fig. 7 in Description Of Crinotonia Anastasiae, New Genus, New Species, A New Crinoid Associated Pontoniine Shrimp (Crustacea: Caridea) From Nha Trang Bay, Vietnam, With Inclusion Of Periclimenes Attenuatus Bruce, 1971, In The New Genus

Fig. 7. Crinotonia attenuatus (Bruce), new combination: a, ovigerous female (PCL 3.8 mm); b, male (PCL 2.3 mm). Scale bar = 5 mm.

Fig. 2 in Temporal dynamics of species associations in the parasite community of European eels, Anguilla anguilla, from a coastal lagoon

Fig. 2. Intensity of infection (mean ± SE number of parasites per host, including infected hosts only) of the six most common helminth parasites of eels, Anguilla anguilla, in Comacchio Lagoons, during three sampling periods. Graphs on the right-hand side do not include the 2015–2017 period, as these species were not found during that period. See Table 1 for full species names.

Fig. 4 in Temporal dynamics of species associations in the parasite community of European eels, Anguilla anguilla, from a coastal lagoon

Fig. 4. Pairwise relationships between numbers of parasites per host for the three most common digenean parasites of eels, Anguilla anguilla, in Comacchio Lagoons, across all three sampling periods combined. The line represents the relationship (with 95% confidence intervals) predicted by the generalized linear model; see text. Tick marks indicate partial residuals with either positive (top) or negative values (bottom). See Table 1 for full species names.

Fig. 3 in Temporal dynamics of species associations in the parasite community of European eels, Anguilla anguilla, from a coastal lagoon

Fig. 3. Scatterplots of pairwise relationships between numbers of parasites per host for the three most common digenean parasites of eels, Anguilla anguilla, in Comacchio Lagoons, across all three sampling periods combined. See Table 1 for full species names.

Fig. 1 in Temporal dynamics of species associations in the parasite community of European eels, Anguilla anguilla, from a coastal lagoon

Fig. 1. Abundance (mean number of parasites per host, including non-infected hosts) of the six most common helminth parasites of eels, Anguilla anguilla, in Comacchio Lagoons, during three sampling periods: 2005–2006 (N = 140 eels), 2010–2013 (N = 131), and 2015–2017 (N = 30). Note that some values for the time period 2015–2017 are based on very few fish; see Table 1 for actual numbers and for full species names.