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Figure 1 from: David J, Geoffroy J (2011) Additional moults into 'elongatus' males in laboratory-reared Polydesmus angustus Latzel, 1884 (Diplopoda, Polydesmida, Polydesmidae) – implications for taxonomy. ZooKeys 156: 41-48. https://doi.org/10.3897/zookeys.156.2045
Figure 1 - Dorsal view of a Polydesmus angustus male of stadium IX after its death at the age of 19 months. The trunk consists of 19 podous rings – bearing 32 pairs of legs plus regressed gonopods (8th leg-pair) – and one apodous ring anterior to the telson.
Figure 4 from: Espinasa L, D. Bartolo N, E. Newkirk C (2014) DNA sequences of troglobitic nicoletiid insects support Sierra de El Abra and the Sierra de Guatemala as a single biogeographical area: Implications for Astyanax. Subterranean Biology 13: 35-44. https://doi.org/10.3897/subtbiol.13.7256
Figure 4 - The Boquillas River has changed its course throughout time. The Boquillas River currently separates the karstic areas of Sierra de Guatemala from the Sierra the El Abra. In the upper part of the figure, the Boquillas River is seen crossing the sierras through the Servilleta canyon. On the bottom part of the figure, a fossil canyon indicates the river's ancient course. Caves that in the past connected the Sierra de El Abra in the south to the Sierra de Guatemala in the north were only recently geologically truncated by the erosion of the new river course. Limestone is restricted to the green forested hills.
Figure 3 from: Espinasa L, D. Bartolo N, E. Newkirk C (2014) DNA sequences of troglobitic nicoletiid insects support Sierra de El Abra and the Sierra de Guatemala as a single biogeographical area: Implications for Astyanax. Subterranean Biology 13: 35-44. https://doi.org/10.3897/subtbiol.13.7256
Figure 3 - Base pair differences versus estimates of divergence in nicoletiids. Base pair differences in the 16S rRNA fragment is plotted against estimates of divergence times millions of years ago (Mya). Molecular clock calibrating points were extracted from: a populations of Anelpistina musticensis that got separated into different islands when the sea level rose after glacial times 12,000 years ago (Espinasa et al. 2011) b and c species of Prosthecina and d species of Anelpistina from Baja California that got separated from the mainland species when the Gulf of Cortes formed 5 mya (Espinasa et al. 2009) e time when nicoletiids arose from a common ancestor with Lepismatids 302 mya (Regier et al. 2010), and f time when insects arose from a common ancestor with anostraca in the Silurian-Ordovician boundary 427 mya (Gaunt and Miles 2002). The lower arrow indicates the 11–12 bp differences between the Sierra de Guatemala and the Sierra de El Abra Anelpistina populations. Such sequence difference is consistent with a common origin very recently, less than 12,000 years ago, and therefore after the environmental disturbances of the ice age.
Figure 2 from: Espinasa L, D. Bartolo N, E. Newkirk C (2014) DNA sequences of troglobitic nicoletiid insects support Sierra de El Abra and the Sierra de Guatemala as a single biogeographical area: Implications for Astyanax. Subterranean Biology 13: 35-44. https://doi.org/10.3897/subtbiol.13.7256
Figure 2 - Anelpistina quinterensis is one of the most troglomorphic described species of nicoletiids. This relatively large eyeless insect is albino and has extremely elongated appendages. Its habitat is restricted to very humid portions of the caves such as mud banks. It is doubtful that it can survive in an epigean environment. Its habitat probably reflects connectivity within a karstic area throughout geologic times and during the evolutionary history of the species.
Figure 1 from: Espinasa L, D. Bartolo N, E. Newkirk C (2014) DNA sequences of troglobitic nicoletiid insects support Sierra de El Abra and the Sierra de Guatemala as a single biogeographical area: Implications for Astyanax. Subterranean Biology 13: 35-44. https://doi.org/10.3897/subtbiol.13.7256
Figure 1 - The Cañon de la Servilleta of the River Boquillas separates the contiguous Sierra de Guatemala, to the north, from the Sierra de El Abra, in the south. Limestone is restricted to the green forested hills. This study tested if this 100 m high, 100 m wide canyon was an effective biological barrier that prevented underground migration of troglobites between the two karstic areas.
Figure 3 from: Gomez-Zurita J (2011) Rhyparida foaensis (Jolivet, Verma & Mille, 2007), comb. n. (Coleoptera, Chrysomelidae) and implications for the colonization of New Caledonia. ZooKeys 157: 33-44. https://doi.org/10.3897/zookeys.157.1320
Figure 3 - Male (a dorsal b lateral) and female c, d genitalia of Rhyparida foaensis (Jolivet, Verma & Mille).
Figure 1 from: Gomez-Zurita J (2011) Rhyparida foaensis (Jolivet, Verma & Mille, 2007), comb. n. (Coleoptera, Chrysomelidae) and implications for the colonization of New Caledonia. ZooKeys 157: 33-44. https://doi.org/10.3897/zookeys.157.1320
Figure 1 - Habitus of three species of Dematochroma a Male holotype of Dematochroma piceum Baly from Lord Howe Island (N.H.M., London) b male of Dematochroma laboulbenei (Montrouzier) from Thio, New Caledonia (voucher no. IBE-JGZ-NC-0112; I.B.E., Barcelona), and c male of Dematochroma antipodum (Fauvel) from L'Aoupinié, New Caledonia (voucher no. IBE-JGZ-NC-0144; I.B.E., Barcelona). Scale bar = 5 mm.
Figure 5 from: Vilhelmsen L (2011) Head capsule characters in the Hymenoptera and their phylogenetic implications. ZooKeys 130: 343-361. https://doi.org/10.3897/zookeys.130.1438
Figure 5 - Posterior view of head capsule of A Macroxyela ferruginea (Xyeloidea, Xyelidae)¸ modified from MB 102885 B Onycholyda amplecta (Pamphilioidea, Pamphiliidae); modified from MB 102837 C Ceraphron sp. (Ceraphronoidea, Ceraphronidae); modified from MB 78643 D Pseudofoenus sp. (Evanioidea, Gasteruptiidae); modified from MB 103810. Numbers indicate character numbers:character states.
Figure 7 from: Vilhelmsen L (2011) Head capsule characters in the Hymenoptera and their phylogenetic implications. ZooKeys 130: 343-361. https://doi.org/10.3897/zookeys.130.1438
Figure 7 - Selected character state changes mapped onto a phylogeny of Hymenoptera. Tree modified from Vilhelmsen et al. 2010a, fig. 69. Outgroup taxa have been removed and terminals have been collapsed to the family or superfamily level; Aulacidae, Diapriidae, Chrysidoidea and Vespoidea are treated as monophyletic. Not all character state changes shown; changes marked with a * have equally parsimonious alternative optimisations.
Figure 6 from: Vilhelmsen L (2011) Head capsule characters in the Hymenoptera and their phylogenetic implications. ZooKeys 130: 343-361. https://doi.org/10.3897/zookeys.130.1438
Figure 6 - Posterior view of head capsule of A Taeniogonalos gundlachii (Trigonaloidea, Trigonalidae); modified from MB 103043 B Dusona egregia (Ichneumonoidea, Ichneumonidae); modified from MB 103363 C Megastigmus transvaalensis (Chalcidoidea, Torymidae); modified from MB 101672 D Isostasius sp. (Platygastroidea, Platygastridae); modified from MB 103503. Numbers indicate character numbers:characters states.
Figure 4 from: Vilhelmsen L (2011) Head capsule characters in the Hymenoptera and their phylogenetic implications. ZooKeys 130: 343-361. https://doi.org/10.3897/zookeys.130.1438
Figure 4 - Anterior view of head capsule of A Acanthochalcis sp. (Chalcidoidea, Chalcididae), modified from MB 134808 B Mymaromma anomalum (Mymarommatoidea, Mymarommatidae); modified from MB 101797 C Pelecinus polyturator (Pelecinidae); modified from MB 79061 D Sparasion formosum (Platygastridae); modified from MB 103049. Numbers indicate character numbers:character states.
Figure 3 from: Vilhelmsen L (2011) Head capsule characters in the Hymenoptera and their phylogenetic implications. ZooKeys 130: 343-361. https://doi.org/10.3897/zookeys.130.1438
Figure 3 - Anterior view of head capsule of A Cephalonomia stephanoderis (Chrysidoidea, Bethylidae); modified from MB 102531 B Pison chilense (Apoidea, Crabronidae); modified from MB 102586 C Dusona egregia (Ichneumonoidea, Ichneumonidae); modified from MB 134625 D Orgilus gracilis (Ichneumonoidea, Braconidae); modified from MB 103649. Numbers indicate character numbers:character states.
Figure 1 from: Vilhelmsen L (2011) Head capsule characters in the Hymenoptera and their phylogenetic implications. ZooKeys 130: 343-361. https://doi.org/10.3897/zookeys.130.1438
Figure 1 - Anterior view of head capsule of A Macroxyela ferruginea (Xyeloidea, Xyelidae); modified from MB 102882 B Athalia rosae (Tenthredinoidea, Tenthredinidae); modified from MB 102486 C Tremex columba (Siricoidea, Siricidae); modified from MB 134704 D Orussus abietinus (Orussoidea, Orussidae); modified from MB 134672. Numbers indicate character numbers:character states.
Figure 2 from: Vilhelmsen L (2011) Head capsule characters in the Hymenoptera and their phylogenetic implications. ZooKeys 130: 343-361. https://doi.org/10.3897/zookeys.130.1438
Figure 2 - Anterior view of head capsule of A Megischus sp. (Stephanoidea, Stephanidae), modified from MB 103607 B Taeniogonalos gundlachii (Trigonaloidea, Trigonalidae); modified from MB 103032 C Megalyra fasciipennis (Megalyroidea, Megalyridae); modified from MB 103568 D Pseudofoenus sp. (Evanioidea, Gasteruptiidae); modified from MB 103788. Numbers indicate character numbers:character states.
Figure 4 from: A. Hopkins W, Moser B, Garst D, J. Richardson D, I. Hammond C, A. Lazo-Wasem E (2014) Morphological and molecular characterization of a new species of leech (Glossiphoniidae, Hirudinida): Implications for the health of its imperiled amphibian host (Cryptobranchus alleganiensis). ZooKeys 378: 83-101. https://doi.org/10.3897/zookeys.378.6545
Figure 4 - Internal anatomy of Placobdella appalachiensis sp. n., Paratype USNM 1232939 collected from an adult eastern hellbender (Cryptobranchus alleganiensis) from stream reach A3 in southwest Virginia, USA. Ventral view, atrial cornuae (AC), ejaculatory duct (ED), intestinal ceca (IC), proboscis (Pr), testisac (T). Scale bar equals 2 mm.
Figure 3 from: A. Hopkins W, Moser B, Garst D, J. Richardson D, I. Hammond C, A. Lazo-Wasem E (2014) Morphological and molecular characterization of a new species of leech (Glossiphoniidae, Hirudinida): Implications for the health of its imperiled amphibian host (Cryptobranchus alleganiensis). ZooKeys 378: 83-101. https://doi.org/10.3897/zookeys.378.6545
Figure 3 - Ventral surface of Placobdella appalachiensis sp. n., Holotype USNM 1232924 collected from an adult eastern hellbender (Cryptobranchus alleganiensis) from stream reach A3 in southwest Virginia, USA. Scale bar equals 1 mm.
Figure 1 from: A. Hopkins W, Moser B, Garst D, J. Richardson D, I. Hammond C, A. Lazo-Wasem E (2014) Morphological and molecular characterization of a new species of leech (Glossiphoniidae, Hirudinida): Implications for the health of its imperiled amphibian host (Cryptobranchus alleganiensis). ZooKeys 378: 83-101. https://doi.org/10.3897/zookeys.378.6545
Figure 1 - Map of two streams in southwest Virginia, USA where hellbenders were collected from 8 stream reaches over 3 consecutive years. Leeches were only detected in stream reach A3.
Figure 2 from: A. Hopkins W, Moser B, Garst D, J. Richardson D, I. Hammond C, A. Lazo-Wasem E (2014) Morphological and molecular characterization of a new species of leech (Glossiphoniidae, Hirudinida): Implications for the health of its imperiled amphibian host (Cryptobranchus alleganiensis). ZooKeys 378: 83-101. https://doi.org/10.3897/zookeys.378.6545
Figure 2 - Dorsal surface of Placobdella appalachiensis sp. n., Holotype USNM 1232924 collected from an adult eastern hellbender (Cryptobranchus alleganiensis) from stream reach A3 in southwest Virginia, USA. Scale bar equals 1 mm.
Figure 5 from: A. Hopkins W, Moser B, Garst D, J. Richardson D, I. Hammond C, A. Lazo-Wasem E (2014) Morphological and molecular characterization of a new species of leech (Glossiphoniidae, Hirudinida): Implications for the health of its imperiled amphibian host (Cryptobranchus alleganiensis). ZooKeys 378: 83-101. https://doi.org/10.3897/zookeys.378.6545
Figure 5 - Relationship between total body length (cm) of eastern hellbenders (Cryptobranchus alleganiensis) and the number of leeches (Placobdella appalachiensis sp. n.) they harbored. All hellbenders were collected from stream reach A3 in southwest Virginia, USA.
Figure 5 from: Hua B, Jiang L, Yue C (2014) Larval morphology of Panorpodes kuandianensis (Insecta, Mecoptera, Panorpodidae) and its evolutionary implications. ZooKeys 398: 69-82. https://doi.org/10.3897/zookeys.398.6675
Figure 5 - Chaetotaxy of the larval trunk of Panorpodes kuandianensis. Abbreviations: CS = cervical sclerite, D = dorsal seta, L = lateral seta, M = mid-dorsal seta, MD = minute dorsal seta, MSD = minute subdorsal seta, MSV = minute subventral seta, MV = minute ventral seta, PP = proleg-like process, SD = subdorsal seta, Sp = spiracle, SV = subventral seta, V = ventral seta, XD = prothoracic seta.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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