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Figure 30 from: Marek P, Shear W, Bond J (2012) A redescription of the leggiest animal, the millipede Illacme plenipes, with notes on its natural history and biogeography (Diplopoda, Siphonophorida, Siphonorhinidae). ZooKeys 241: 77-112. https://doi.org/10.3897/zookeys.241.3831
Figure 30 - Sandstone microhabitat of Illacme plenipes.Top left, 50 kg sandstone from 29.xi.2005 rediscovery locality of Illacme plenipes; one ♀ with 666 legs was discovered from beneath the stone (scale bar = 5 cm, hand shovel shown for scale). Bottom left, 30 kg sandstone from the 16.xii.2007 locality, two ♀ (specimen #s: SPC001187, MIL0020) were discovered below the stone (scale bar = 5 cm, 15 cm ruler shown for scale). Top right, surface close up of sandstone from 16.xii.2007 locality with ♂ Illacme plenipes, not collected (scale bar = 5 mm). Bottom right, surface close up of sandstone from 29.xi.2005 locality with ♂ Illacme plenipes (specimen #: SPC000924, scale bar = 5 mm). Millipedes shown in right two pictures were found clinging to the surface of the stone.
Figure 7 from: Marek P, Shear W, Bond J (2012) A redescription of the leggiest animal, the millipede Illacme plenipes, with notes on its natural history and biogeography (Diplopoda, Siphonophorida, Siphonorhinidae). ZooKeys 241: 77-112. https://doi.org/10.3897/zookeys.241.3831
Figure 7 - Dorsal view of anterior region of head and labrum (♂). a Scanning electron micrograph: arrow, labrum with triangular tooth-lined orifice b Line drawing: shaded area, triangular tooth-line orifice; arrow, gnathochilarium. Scale bar 0.02 mm.
Figure 2-5 from: Marek P, Shear W, Bond J (2012) A redescription of the leggiest animal, the millipede Illacme plenipes, with notes on its natural history and biogeography (Diplopoda, Siphonophorida, Siphonorhinidae). ZooKeys 241: 77-112. https://doi.org/10.3897/zookeys.241.3831
Figure 2-5 - 2 Lateral (right) view of head and segments 1–5 (♂). a Lateral opening apparent between gnathochilarium and head capsule; gnathochilarium, mandible and head capsule noticeably separate at base, 1/3 head length distally from mandibular joint b Collum not covering head, with straight cephalic edge, gradually tapering laterally. Scale bar 0.5 mm. 3 Ventral view of head, antennae and segments 1 – 5 (♂).Scale bar 0.3 mm. 4 Lateral (right) view of antennomeres 5, 6 (♂).Arrow, small basiconic sensilla (Bs2) in cluster of 7 or 8 oriented apical dorsally (retrolaterally) in slight depression on antennomeres 5, 6. Scale bar 0.05 mm. 5 Oblique (right) view of right posterior gonopod (♂).Posterior gonopodal podomere 6 divided, comprising a bundle of 3 stylus-shaped articles. Scale bar 0.05 mm.
Figure 6 from: Marek P, Shear W, Bond J (2012) A redescription of the leggiest animal, the millipede Illacme plenipes, with notes on its natural history and biogeography (Diplopoda, Siphonophorida, Siphonorhinidae). ZooKeys 241: 77-112. https://doi.org/10.3897/zookeys.241.3831
Figure 6 - Illustration of anterior and posterior gonopods (♂). a Posterior gonopod with podomeres labeled P1-6 b Anterior gonopod with podomeres labeled A1-6 c 3 stylus-shaped articles. Scale bar 0.05 mm.
Figure 31 from: Marek P, Shear W, Bond J (2012) A redescription of the leggiest animal, the millipede Illacme plenipes, with notes on its natural history and biogeography (Diplopoda, Siphonophorida, Siphonorhinidae). ZooKeys 241: 77-112. https://doi.org/10.3897/zookeys.241.3831
Figure 31 - Subterranean soil microhabitat of Illacme plenipes. Left, sandstone crater; dotted line indicates crater's edges, arrows indicate two ♀ Illacme plenipes shown in situ upon removal of stone (specimen #s: SPC001187, MIL0020—lower individual with anterior trunk segments embedded in soil, upper individual with middle segments embedded in soil). Bottom middle, close up of lower individual from left image. Top right, dark sandy soil from microhabitat. Bottom right, close up of soil showing sandy grain structure.
Figure 28 from: Marek P, Shear W, Bond J (2012) A redescription of the leggiest animal, the millipede Illacme plenipes, with notes on its natural history and biogeography (Diplopoda, Siphonophorida, Siphonorhinidae). ZooKeys 241: 77-112. https://doi.org/10.3897/zookeys.241.3831
Figure 28 - Habitat of Illacme plenipes. Top left, view of oak forest where Illacme plenipes were encountered. Top right, close up of oak forest and sandstone pinnacle where Illacme plenipes occur. Bottom, landscape view of oak forest, cattle trails evident (composite stitched image of three photos, image sides slightly distorted).
Figure 29 from: Marek P, Shear W, Bond J (2012) A redescription of the leggiest animal, the millipede Illacme plenipes, with notes on its natural history and biogeography (Diplopoda, Siphonophorida, Siphonorhinidae). ZooKeys 241: 77-112. https://doi.org/10.3897/zookeys.241.3831
Figure 29 - Oak forest understory habitat of Illacme plenipes. Top, base of sandstone pinnacle (from Fig. 28), where specimens were found. Bottom, mossy oak forest—close-up of habitat where Illacme plenipes individuals were encountered.
Figure 1 from: Marek P, Shear W, Bond J (2012) A redescription of the leggiest animal, the millipede Illacme plenipes, with notes on its natural history and biogeography (Diplopoda, Siphonophorida, Siphonorhinidae). ZooKeys 241: 77-112. https://doi.org/10.3897/zookeys.241.3831
Figure 1 - Niche-based distribution model inferred in Maxent. The model indicates predicted habitat suitability for Illacme plenipes based on climatic variables extracted from known geographical coordinates of the species. High levels of habitat suitability are denoted in blue and low levels in red (reverse heat map). Coordinates of recently collected specimens are indicated by a circle around the locations (northwest of the Gabilan Range) to preserve the confidentiality of sensitive habitat. Localities surveyed for additional populations of Illacme plenipes: 1 Frank Raines Park 2 Henry Coe State Park 3 Fremont Peak State Park 4 Pinnacles National Monument 5 Mount Madonna County Park 6 Alum Rock 7 Joseph D. Grant County Park 8 El Rancho Cienega del Gabilan.
Figure 1 from: Vinarski M (2015) Conceptual shifts in animal systematics as reflected in the taxonomic history of a common aquatic snail species (Lymnaea stagnalis). Zoosystematics and Evolution 91(2): 91-103. https://doi.org/10.3897/zse.91.4509
Figure 1 - A great pond snail in its natural environment. 12.08.2014. Russia, Western Siberia, "Malaya Sos'va" Nature Reserve, Kopanoye Lake (photo: M. Vinarski).
Figure 4 from: Vinarski M (2015) Conceptual shifts in animal systematics as reflected in the taxonomic history of a common aquatic snail species (Lymnaea stagnalis). Zoosystematics and Evolution 91(2): 91-103. https://doi.org/10.3897/zse.91.4509
Figure 4 - Varieties of Lymnaea stagnalis as they were identified by malacologists of the 19th century. A. Lymnaea stagnalis var. typica (det. S. Clessin; ZIN). B. Lymnaea stagnalis var. media (det. C.A. Westerlund; GNM). C. Lymnaea stagnalis var. producta (det. C.A. Westerlund; GNM). D. Lymnaea stagnalis var. rosea (identified by a unknown person; ZMUC). E. Lymnaea stagnalis var. colpodia (det. C.A. Westerlund; GNM). F. Lymnaea stagnalis var. variegata (det. C.A. Westerlund; GNM). G. Lymnaea stagnalis var. turgida (det. C.A. Westerlund; GNM). H. Lymnaea stagnalis var. raphidia (det. C.A. Westerlund; GNM). I. Lymnaea stagnalis var. palustriformis (det. A. Fuchs, NHMW). Scale bars 5 mm.
Figure 2 from: Vinarski M (2015) Conceptual shifts in animal systematics as reflected in the taxonomic history of a common aquatic snail species (Lymnaea stagnalis). Zoosystematics and Evolution 91(2): 91-103. https://doi.org/10.3897/zse.91.4509
Figure 2 - Evolution of accuracy in illustrations of Lymnaea stagnalis shell through two centuries. Sources of images: A. Aldrovandi 1606. B. Lister 1678. C. Bonanni 1681. D. Klein 1753. E. Seba 1758. F. Schröter 1779.
Figure 2 from: Caubet Y, Richard F-J (2015) NEIGHBOUR-IN: Image processing software for spatial analysis of animal grouping. In: Taiti S, Hornung E, Štrus J, Bouchon D (Eds) Trends in Terrestrial Isopod Biology. ZooKeys 515: 173–189. https://doi.org/10.3897/zookeys.515.9390
Figure 2 - Virtual configurations used for software validation. Virtual configurations used to compile the data presented in the Table 1. Part 2.8 is one of the 10 replicates obtained with a random distribution. All other configurations have been designed in order to reach the desired level of aggregation and affinity between groups. The filled and empty shapes represented two virtual groups in the population.
Figure 1 from: Caubet Y, Richard F-J (2015) NEIGHBOUR-IN: Image processing software for spatial analysis of animal grouping. In: Taiti S, Hornung E, Štrus J, Bouchon D (Eds) Trends in Terrestrial Isopod Biology. ZooKeys 515: 173–189. https://doi.org/10.3897/zookeys.515.9390
Figure 1 - Flow chart of the creation of a new NEIGHBOUR-IN file. This figure presents the different steps in the creation of a new file, from the importation of the snapshot to the calculation of the statistics of dispersion.
Figure 4 from: Caubet Y, Richard F-J (2015) NEIGHBOUR-IN: Image processing software for spatial analysis of animal grouping. In: Taiti S, Hornung E, Štrus J, Bouchon D (Eds) Trends in Terrestrial Isopod Biology. ZooKeys 515: 173–189. https://doi.org/10.3897/zookeys.515.9390
Figure 4 - Spatial distribution in woodlice. Graphic outputs of spatial distribution patterns obtained in three configurations with monospecific or bispecific populations including two groups of eight individuals: a PD-PD: The two groups are Porcellio dilatatus (red and green) b PD-PS: Porcellio dilatatus (red) and Porcellio scaber (green) c PD-AV: Porcellio dilatatus (red) and Armadillidium vulgare (green). The outputs show 64 cells. Each cell is represented with a colour corresponding to the individual(s) in that cell. The colour is mixed using green and red proportional to the number of green and red individuals. If the cell is empty, the colour is black. The intensity of the colour reflects the number of individuals. The position of the individual is determined by its point G (centre-point).
Figure 3 from: Caubet Y, Richard F-J (2015) NEIGHBOUR-IN: Image processing software for spatial analysis of animal grouping. In: Taiti S, Hornung E, Štrus J, Bouchon D (Eds) Trends in Terrestrial Isopod Biology. ZooKeys 515: 173–189. https://doi.org/10.3897/zookeys.515.9390
Figure 3 - Aggregation heterogeneity in woodlice. Aggregation patterns of two groups of woodlice illustrating the Aggregation Heterogenity Index (AHI) and the Spatial Mixed Index (SMI). PD: Porcellio dilatatus, PS: Porcellio scaber, CC: Cylisticus convexus. Values of indexes: PD-PD: AHI=0.93 & SMI=0.80; PD-PS: AHI=0.67 & SMI=0.60; PD-CC: AHI=0.63 & SMI=0.33.
Figure 4 from: Krapp-Schickel T, Vader W (2015) Stenothoids living with or on other animals (Crustacea, Amphipoda). Zoosystematics and Evolution 91(2): 215-246. https://doi.org/10.3897/zse.91.5715
Figure 4 - Stenothoe bartholomea sp. n. female 3 mm holotype. P 3–4, P 6–7 peraeopod 3–4; peraeopod 6–7; P 4', P 4'' entire leg with coxa resp. distal end of propodus P 4 enlarged; P 7' distal end of propodus P 7 enlarged.
Figure 7 from: Krapp-Schickel T, Vader W (2015) Stenothoids living with or on other animals (Crustacea, Amphipoda). Zoosystematics and Evolution 91(2): 215-246. https://doi.org/10.3897/zse.91.5715
Figure 7 - Stenothoe miersii (Haswell, 1879) male 3 mm; P 5–7 peraeopod 5–7; U 1–3 uropod 1–3; U 3' third uropod enlarged; Ep 3 third epimeral plate; T telson.
Figure 3 from: Krapp-Schickel T, Vader W (2015) Stenothoids living with or on other animals (Crustacea, Amphipoda). Zoosystematics and Evolution 91(2): 215-246. https://doi.org/10.3897/zse.91.5715
Figure 3 - Stenothoe bartholomea sp. n. female 3 mm holotype. Gn 2, Gn 2', Gn 2'' gnathopod 2 from both sides and tip of carpus + merus resp. palmar corner enlarged.
Figure 19 from: Krapp-Schickel T, Vader W (2015) Stenothoids living with or on other animals (Crustacea, Amphipoda). Zoosystematics and Evolution 91(2): 215-246. https://doi.org/10.3897/zse.91.5715
Figure 19 - Stenula solsbergi (Schneider, 1884): Md mandible; Mx 1 maxilla 1; Gn 1 gnathopod 1; Gn 1', Gn 1 '' gnathopod 1 right and left distally enlarged.
Figure 18 from: Krapp-Schickel T, Vader W (2015) Stenothoids living with or on other animals (Crustacea, Amphipoda). Zoosystematics and Evolution 91(2): 215-246. https://doi.org/10.3897/zse.91.5715
Figure 18 - Stenula pugilla sp. n. male 3 mm: Gn 2 gnathopod 2; P 6, 7 peraeopod 6, 7; U 1–3 uropod 1–3; T telson.
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International Brain Laboratory public data
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OpenNeuro
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