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Figure 9 from: Dostal A (2011) Taxonomic remarks about Semiclivina (Kult, 1947) new status, with description of Uroclivina subgen. n., and of two new species from South America (Coleoptera, Carabidae, Scaritinae, Clivinini). ZooKeys 132: 33-50. https://doi.org/10.3897/zookeys.132.1508

Figure 9 - Line drawings of genitalia of Semiclivina schmidi sp. n. a-c holotype, aedeagus a median lobe, left lateral view b and c left and right paramere, respectively, ventral view d-e paratype,ovipositor d left stylomere, lateral aspect e medial aspect. Scale bar = 1 mm.

Figure 6 from: Dostal A (2011) Taxonomic remarks about Semiclivina (Kult, 1947) new status, with description of Uroclivina subgen. n., and of two new species from South America (Coleoptera, Carabidae, Scaritinae, Clivinini). ZooKeys 132: 33-50. https://doi.org/10.3897/zookeys.132.1508

Figure 6 - Line drawings of genitalia of Semiclivina bergeri sp. n. a-d holotype- a median lobe, left lateral view b median lobe, apical portion, dorsal aspect c and d left and right paramere, respectively, ventral view e-f paratype, ovipositor left stylomere e lateral aspect f medial aspect. Scale bar = 1 mm.

Figure 3 from: Dostal A (2011) Taxonomic remarks about Semiclivina (Kult, 1947) new status, with description of Uroclivina subgen. n., and of two new species from South America (Coleoptera, Carabidae, Scaritinae, Clivinini). ZooKeys 132: 33-50. https://doi.org/10.3897/zookeys.132.1508

Figure 3 - Photograph of head and anterior portion of pronotum, dorsal view, of Semiclivina bergeri new species, Holotype, showing a tubercle at posterior margin of eye b incision of anterior margin of pronotum; Scale bar: 0,5 mm.

Figure 1 from: Dostal A (2011) Taxonomic remarks about Semiclivina (Kult, 1947) new status, with description of Uroclivina subgen. n., and of two new species from South America (Coleoptera, Carabidae, Scaritinae, Clivinini). ZooKeys 132: 33-50. https://doi.org/10.3897/zookeys.132.1508

Figure 1 - Photograph of prothorax and base of metathorax of Semiclivina species; right lateral view, showing the stridulation ridge (arrow); Scale bar: 0,5 mm.

Figure 4 from: Dostal A (2011) Taxonomic remarks about Semiclivina (Kult, 1947) new status, with description of Uroclivina subgen. n., and of two new species from South America (Coleoptera, Carabidae, Scaritinae, Clivinini). ZooKeys 132: 33-50. https://doi.org/10.3897/zookeys.132.1508

Figure 4 - Photograph of abdominal sterna IV-VII, ventral view, of a Semiclivina bergeri, sp. n., Holotype b Semiclivina schmidi sp. n., Holotype c Semiclivina oxyomma (Putzeys) d Semiclivina urophthalma(Putzeys); Scale bars: 0,5 mm.

Figure 5 from: Dostal A (2011) Taxonomic remarks about Semiclivina (Kult, 1947) new status, with description of Uroclivina subgen. n., and of two new species from South America (Coleoptera, Carabidae, Scaritinae, Clivinini). ZooKeys 132: 33-50. https://doi.org/10.3897/zookeys.132.1508

Figure 5 - Photograph of habitus of holotype of Semiclivina bergerisp. n., dorsal view; Scale bar: 2 mm.

Figure 8 from: Dostal A (2011) Taxonomic remarks about Semiclivina (Kult, 1947) new status, with description of Uroclivina subgen. n., and of two new species from South America (Coleoptera, Carabidae, Scaritinae, Clivinini). ZooKeys 132: 33-50. https://doi.org/10.3897/zookeys.132.1508

Figure 8 - Photograph of habitus of the holotype of Semiclivina schmidi sp. n., dorsal view; Scale bar: 2 mm.

Figure 6 from: Tu L, Sun N (2014) Acanoides gen. n., a new spider genus from China with a note on the taxonomic status of Acanthoneta Eskov & Marusik, 1992 (Araneae, Linyphiidae, Micronetinae). ZooKeys 375: 75-99. https://doi.org/10.3897/zookeys.375.6116

Figure 6 - Acanthoneta dokutchaevi (A–G) and Acanthoneta aggressa (H–J). A male, dorsal B male, lateral C male palp, prolateral D male palp, ventral E male palp, retrolateral F embolic division, ventral G embolic division, dorsal H epigynum, ventral I epigynum, posterior J epigynum, lateral (H–J photos provided by Don Buckle). EB epigynal basal part; EM embolic membrane; EP embolus proper; FiG Fickert's gland; LC lamella characteristica; P paracymbium; PCA proximal cymbial apophysis; PH pit hook; R radix; SC scape; ST stretcher; TA terminal apophysis; TH thumb of embolus. [Scale bars: mm].

Figure 2 from: Tu L, Sun N (2014) Acanoides gen. n., a new spider genus from China with a note on the taxonomic status of Acanthoneta Eskov & Marusik, 1992 (Araneae, Linyphiidae, Micronetinae). ZooKeys 375: 75-99. https://doi.org/10.3897/zookeys.375.6116

Figure 2 - Acanoides beijingensis sp. n. A male palp, prolateral B male palp, prolateral, with embolic division removed C male palp, retrolateral D embolic division, ventral E embolic division, dorsal F epigynum, ventral G epigynum, dorsal H epigynum, lateral. CG copulatory groove; CO copulatory opening; DP dorsal plate; EA extensible area of epigynal basal part; EM embolic membrane; EP embolus proper; FG fertilization groove; FiG Fickert's gland; LC lamella characteristica; MP median plate; P paracymbium; PCA proximal cymbial apophysis; R radix; S spermathecae; TA terminal apophysis; TH thumb of embolus; VP ventral plate. [Scale bars: mm].

Figure 1 from: Tu L, Sun N (2014) Acanoides gen. n., a new spider genus from China with a note on the taxonomic status of Acanthoneta Eskov & Marusik, 1992 (Araneae, Linyphiidae, Micronetinae). ZooKeys 375: 75-99. https://doi.org/10.3897/zookeys.375.6116

Figure 1 - Acanoides beijingensis sp. n. (A–C) and Acanoides hengshanensis (D–F). A male, dorsal B female, dorsal C male, lateral, rectangle indicates ventrolateral rows of bristles on Mt I D male, lateral, rectangle indicates ventrolateral rows of bristles on Mt I E male, dorsal F female, dorsal. [Scale bars: mm].

Figure S1 from: Tu L, Sun N (2014) Acanoides gen. n., a new spider genus from China with a note on the taxonomic status of Acanthoneta Eskov & Marusik, 1992 (Araneae, Linyphiidae, Micronetinae). ZooKeys 375: 75-99. https://doi.org/10.3897/zookeys.375.6116

Figure S1 - Linyphiid phylogeny resulting from Maximum Likelihood analysis based on molecular data. Numbers at the nodes are bootstrap value. Branches in color indicate the four robustly supported clades within linyphiids: S Stemonyphantes clade (blue) L1 "linyphiines"-1 clade (pale green) L2 "linyphiines-2" clade (dark blue) ME "micronetines-erigonines" clade (red, with "Distal erigonines" clade in green). Taxa in different colors sampled from different groups: grey, outgroup; blue, Stemonyphantinae; pale green, Linyphiinae; dark blue, Mynogleninae; pink, Dubiaraneinae; black, Micronetinae; red, Ipainae, Acanthoneta and Acanoides gen. n.; green, Erigoninae. Red stars indicate the two out-group taxa: cyatholipid Alaranea and theridiosomatid Theridiosoma embedded within Linyphiidae.

Figure 5 from: Tu L, Sun N (2014) Acanoides gen. n., a new spider genus from China with a note on the taxonomic status of Acanthoneta Eskov & Marusik, 1992 (Araneae, Linyphiidae, Micronetinae). ZooKeys 375: 75-99. https://doi.org/10.3897/zookeys.375.6116

Figure 5 - Acanoides hengshanensis. A palp (embolic division removed), prolateral B palp, retrolateral, arrow indicates pointed tooth on posterolateral margin C embolic division, ventral D embolic division, dorsal E detail of D F detail of C G epigynum, ventral H epigynum, dorsal. AX apex of embolus; CG copulatory groove; CO copulatory opening; DM distal membrane of terminal apophysis; EA extensible area of epigynal basal part; EM embolic membrane; EP embolus proper; FG fertilization groove; LC lamella characteristica; P paracymbium; PCA proximal cymbial apophysis; R radix; S spermatheca; SPT suprategulum; TA terminal apophysis; TH thumb of embolus; VP ventral plate. [Scale bars: mm].

Figure 7 from: Tu L, Sun N (2014) Acanoides gen. n., a new spider genus from China with a note on the taxonomic status of Acanthoneta Eskov & Marusik, 1992 (Araneae, Linyphiidae, Micronetinae). ZooKeys 375: 75-99. https://doi.org/10.3897/zookeys.375.6116

Figure 7 - Collecting localities of Acanoides species and Acanthoneta aggressa, Acanoides beijingensis sp. n. (Beijing, Hebei); Acanoides hengshanensis (Hunan, Beijing); Acanthoneta dokutchaevi (Jilin).

Figure 3 from: Tu L, Sun N (2014) Acanoides gen. n., a new spider genus from China with a note on the taxonomic status of Acanthoneta Eskov & Marusik, 1992 (Araneae, Linyphiidae, Micronetinae). ZooKeys 375: 75-99. https://doi.org/10.3897/zookeys.375.6116

Figure 3 - Acanoides hengshanensis. A male palp, prolateral B male palp, ventral C male palp, retrolateral, arrow indicates pointed tooth on posterolateral margin D embolic division, ventral E embolic division, dorsal F epigynum, ventral G epigynum, dorsal. CG copulatory groove; CO copulatory opening; DP dorsal plate; EA extensible area of epigynal basal part; EM embolic membrane; EP embolus proper; FG fertilization groove; FiG Fickert's gland; LC lamella characteristica; P paracymbium; PCA proximal cymbial apophysis; R radix; S spermatheca; TA terminal apophysis; TH thumb of embolus; VP ventral plate. [Scale bars: mm].

Figure 4 from: Tu L, Sun N (2014) Acanoides gen. n., a new spider genus from China with a note on the taxonomic status of Acanthoneta Eskov & Marusik, 1992 (Araneae, Linyphiidae, Micronetinae). ZooKeys 375: 75-99. https://doi.org/10.3897/zookeys.375.6116

Figure 4 - Acanoides beijingensis sp. n. A palp (embolic division removed), prolateral B palp, retrolateral, arrow indicates half rounded lateral tooth on paracymbium C embolic division, ventral D embolic division, dorsal E detail of D F detail of C G epigynum, ventral H epigynum, dorsal. AX apex of embolus; CG copulatory groove; CO copulatory opening; DM distal membrane of terminal apophysis; DSA distal suprategular apophysis; EA extensible area of epigynal basal part; EM embolic membrane; EP embolus proper; FG fertilization groove; LC lamella characteristica; MP median plate; P paracymbium; PCA proximal cymbial apophysis; R radix; S spermatheca; SE serrated area on embolus; SPT suprategulum; TA terminal apophysis; TH thumb of embolus; VP ventral plate. [Scale bars: mm].

Figure 10 from: Kavanaugh D, Archambeault S, Roopnarine P, Ledford J (2011) A re-consideration of the taxonomic status of Nebria lacustris Casey (Coleoptera, Carabidae, Nebriini) based on multiple datasets – a single species or a species complex? ZooKeys 147: 199-228. https://doi.org/10.3897/zookeys.147.2082

Figure 10 - A Principal components analysis of distance measurements on Nebria lacustris (blue open circles) and Nebria bellorum (filled red squares). PC I (x axis) is a measure of allometric size, while PC II is a shape contrast between the DS measure and all others B Upper figure repeated to highlight dissimilarity between geographically proximate specimens of Nebria bellorum and specimens of Nebria lacustris from North Carolina, Tennessee, Kentucky, and Virginia (filled blue triangles). Geographically distant specimens from Iowa are indicated by filled green circles, and fall within the central area of Nebria lacustris's morphometric distribution (see text for further discussion). All other specimens of Nebria lacustris are shown as grey dots.

Figure 8 from: Kavanaugh D, Archambeault S, Roopnarine P, Ledford J (2011) A re-consideration of the taxonomic status of Nebria lacustris Casey (Coleoptera, Carabidae, Nebriini) based on multiple datasets – a single species or a species complex? ZooKeys 147: 199-228. https://doi.org/10.3897/zookeys.147.2082

Figure 8 - Illustration of measurements; LH = length head; LP = length pronotum; LE = length elytra; DS = longitudinal distance from anterior margin of pronotum to position of left midlateral seta

Figure 9 from: Kavanaugh D, Archambeault S, Roopnarine P, Ledford J (2011) A re-consideration of the taxonomic status of Nebria lacustris Casey (Coleoptera, Carabidae, Nebriini) based on multiple datasets – a single species or a species complex? ZooKeys 147: 199-228. https://doi.org/10.3897/zookeys.147.2082

Figure 9 - Box plots of body size (measured as the first principal component, PC I) segregated by species and gender. 1 = Nebria lacustris, 2 = Nebria bellorum. Mid-lines in boxes represent sub-sample distribution median PC I scores (median body size), lower and upper limits of boxes represent 25% and 75% limits of distributions respectively, and upper and lower whiskers represent 5% and 95% limits respectively. Nebria lacustris adults are significantly larger than those of Nebria bellorum, and females of both species are significantly larger than males.

Figure 11 from: Kavanaugh D, Archambeault S, Roopnarine P, Ledford J (2011) A re-consideration of the taxonomic status of Nebria lacustris Casey (Coleoptera, Carabidae, Nebriini) based on multiple datasets – a single species or a species complex? ZooKeys 147: 199-228. https://doi.org/10.3897/zookeys.147.2082

Figure 11 - Principal components analysis scores of Nebria lacustris versus location and elevation. Body size (PC I) varies significantly with the three factors, while the independent shape variable, PC II, varies significantly with location. Individual regression lines drawn on plots represent individual relationships within multiple regression models (see text for explanation). A quadratic model is selected for the relationship between PC I and longitude because a first order linear model results in non-normally distributed residuals (linear model is shown as light blue straight line). "N" on plots indicates cardinal direction north.

Figures 6-7 from: Kavanaugh D, Archambeault S, Roopnarine P, Ledford J (2011) A re-consideration of the taxonomic status of Nebria lacustris Casey (Coleoptera, Carabidae, Nebriini) based on multiple datasets – a single species or a species complex? ZooKeys 147: 199-228. https://doi.org/10.3897/zookeys.147.2082

Figures 6-7 - Dorsal habitus; scale line = 1.0 mm 6 Nebria bellorum Kavanaugh, male, Smokemont, Swain County, North Carolina 7 Nebria lacustris Casey, female, Harpers Ferry, Jefferson County, West Virginia.