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Figure 5 from: Fujiwara Y, Jimi N, Sumida PYG, Kawato M, Kitazato H (2019) New species of bone-eating worm Osedax from the abyssal South Atlantic Ocean (Annelida, Siboglinidae). ZooKeys 814: 53-69. https://doi.org/10.3897/zookeys.814.28869
Figure 5 Phylogenetic placement of Osedaxbraziliensis sp. n. based on nucleotide sequences on the concatenated COI, 16S, and 18S markers, using maximum likelihood. Scale bar represents 0.1 nucleotide substitutions per sequence position. Only bootstrap values greater than 50 are shown for each branch. Osedaxbraziliensis sp. n. is boxed.
Figure 4 from: Jeon D, Lee W, Soh HY (2019) New species of Caromiobenella Jeon, Lee & Soh, 2018 (Crustacea, Copepoda, Monstrilloida) from Chuja Island, Korea. ZooKeys 814: 33-51. https://doi.org/10.3897/zookeys.814.29126
Figure 4 Caromiobenellaohtsukai sp. n., male holotype (MABIK CR00244260), swimming legs with intercoxal sclerites A Right leg 1 with inset of outermost seta of third exopodal segment (arrow), anterior B Right leg 2, anterior C Right leg 3, anterior D Right leg 4, anterior. Scale bar in micrometers.
Figure 1 from: Fujiwara Y, Jimi N, Sumida PYG, Kawato M, Kitazato H (2019) New species of bone-eating worm Osedax from the abyssal South Atlantic Ocean (Annelida, Siboglinidae). ZooKeys 814: 53-69. https://doi.org/10.3897/zookeys.814.28869
Figure 1 Sampling location of Osedaxbraziliensis sp. n. Solid star indicates the sampling location where a whale carcass was discovered at a depth of 4,204 m.
Figure 3 from: Fujiwara Y, Jimi N, Sumida PYG, Kawato M, Kitazato H (2019) New species of bone-eating worm Osedax from the abyssal South Atlantic Ocean (Annelida, Siboglinidae). ZooKeys 814: 53-69. https://doi.org/10.3897/zookeys.814.28869
Figure 3 Photographs of unfixed Osedaxbraziliensis sp. n. A Palps (pa), trunk (tr) and a gelatinous hemispherical tube (tu)B lateral view of palps (pa), trunk (tr), ovary (o), and root (r)C ventral view of palps (pa) with pinnules (pi) and trunk (tr). Dwarf males (m) inhabit a gelatinous tube (tu), and D ventro-lateral view of an individual possessing a yellow bump (b) present behind prostomium E Ventral view of holotype (NMST-Pol H-685) possessing a yellow patch (pt)F Ventral view of an individual without yellow bump.
Figure 2 from: Jeon D, Lee W, Soh HY (2019) New species of Caromiobenella Jeon, Lee & Soh, 2018 (Crustacea, Copepoda, Monstrilloida) from Chuja Island, Korea. ZooKeys 814: 33-51. https://doi.org/10.3897/zookeys.814.29126
Figure 2 Caromiobenellaohtsukai sp. n., male holotype (MABIK CR00244260) A Cephalothorax, ventral B Two anterior scars on right side, each followed by rounded depression (asterisks) C Urosome, ventral, showing small, knob-like fifth legs (black arrows), medial protrusion on genital apparatus (white arrow), and caudal setae (II–VII) D Urosome, lateral, showing small knob-like fifth legs (black arrow) and medial protrusion on genital apparatus (white arrow). Scale bars in micrometers.
Figure 6 from: Srinui K, Ohtsuka S, Metillo EB, Nishibori M (2019) A new species of Acartia (Copepoda, Calanoida) from the Philippines, based on morphological and molecular analyses. ZooKeys 814: 71-94. https://doi.org/10.3897/zookeys.814.24601
Figure 6 Neighbor-joining phylogenetic tree based on the mitochondrial 16S (A) and COI (B) genes of Acartia (Odontacartia) edentata sp. n., and A. (O.) pacifica from Ariake Bay in the Seto Inland Sea and Korean waters. A. (O.) erythraea, A. (O.) ohtsukai and A. (O.) tseuensis sequences from GenBank were used as outgroups. Bootstrap values (percentage) are shown for nodes with support > 50%. Supporting valves of each node obtained from 1,000 bootstrap replications.
Figure 1 from: Srinui K, Ohtsuka S, Metillo EB, Nishibori M (2019) A new species of Acartia (Copepoda, Calanoida) from the Philippines, based on morphological and molecular analyses. ZooKeys 814: 71-94. https://doi.org/10.3897/zookeys.814.24601
Figure 1 Distribution of Acartia (Odontacartia) pacifica and its sibling species based on data from this and previously published reports. In the present study, samples were obtained from three sites: Station 1, Acartia (Odontacartia) edentata sp. n., Leyte Island, the Philippines (black donut); Station 2, A. (O.) pacifica, Ariake Bay in the Seto Inland Sea, Japan (white donut); and Station 3, A. (O.) pacifica, South Korea Sea, Korea. Data from earlier studies indicate the distribution of A. (O.) pacifica in the Pacific Ocean (Steuer 1915; Tanaka 1965; Brodsky 1967; Ueda and Bucklin 2006); Korean waters (Kang 2011); the Yellow Sea, Chiekong River, Juilong Estuary, Changjiang Estuary, China (Shen and Lee 1963; Chen and Zhang 1965; Shang et al. 2007; Gao et al. 2008); eastern Indonesian waters of Java Sea, Bintulu coast, Indonesia (Früchtl 1923; Mulyadi 2004; Johan et al. 2013); the Gulf of Thailand (Pinkaew 2003); the Indian Ocean (Sewell 1933; Wellershaus 1969; Pillai 1971; Resai et al. 2004; Phukham 2008; Treeramaethee et al. 2013); water of the Great Barrier Reef, Moreton Bay, Australia (Farran 1936; Greenwood 1978); and type locality of A. (O.) pacifica (black square).
Figure 5 from: Srinui K, Ohtsuka S, Metillo EB, Nishibori M (2019) A new species of Acartia (Copepoda, Calanoida) from the Philippines, based on morphological and molecular analyses. ZooKeys 814: 71-94. https://doi.org/10.3897/zookeys.814.24601
Figure 5 SEM micrographs of Acartia (Odontacartia) edentata, sp. n., female (A–D) and male (E, F) A The genital double-somite lateral view B Urosomite, ventral view C Genital double-somite, ventral view D Rostrum, ventral view E Urosomite, dorsal view F Urosomite, ventral view.
Figure 1 from: Jeon D, Lee W, Soh HY (2019) New species of Caromiobenella Jeon, Lee & Soh, 2018 (Crustacea, Copepoda, Monstrilloida) from Chuja Island, Korea. ZooKeys 814: 33-51. https://doi.org/10.3897/zookeys.814.29126
Figure 1 Caromiobenellaohtsukai sp. n., male holotype (MABIK CR00244260) A Habitus in dorsal view with pit-setae 1–15 of right side indicated B Habitus in lateral view with poorly developed oral papilla indicated (arrow). Two lateral and one ventral eyes are indicated using dotted-lines (cf. Fig. 1A, B). Scale bar in micrometers.
Figure 4 from: Fujiwara Y, Jimi N, Sumida PYG, Kawato M, Kitazato H (2019) New species of bone-eating worm Osedax from the abyssal South Atlantic Ocean (Annelida, Siboglinidae). ZooKeys 814: 53-69. https://doi.org/10.3897/zookeys.814.28869
Figure 4 Scanning electron micrographs of Osedaxbraziliensis sp. n. A Ventro-lateral view of bump (b)B lateral view of palps (pa) with pinnules (pi), and C dorsal view of palps (pa) and oviduct (od)D Dwarf male taken from the tube of a female.
Figures 6-15 from: Pieńkowska JR, Manganelli G, Giusti F, Barbato D, Hallgass A, Lesicki A (2019) Exploration of phylogeography of Monacha cantiana s.l. continues: the populations of the Apuan Alps (NW Tuscany, Italy) (Eupulmonata, Stylommatophora, Hygromiidae). ZooKeys 814: 115-149. https://doi.org/10.3897/zookeys.814.31583
Figures 6-15 Shell variability in Monachacantiana s.l. CAN-5 from Piastra (FGC 41563) (6, 7), Foce di Pianza (FGC 41565) (8, 9) and Campo Cecina (FGC 41564) (10–12); CAN-6 from Campagrina (FGC 40322) (13–15).
Figures 42- 43 from: Pieńkowska JR, Manganelli G, Giusti F, Barbato D, Hallgass A, Lesicki A (2019) Exploration of phylogeography of Monacha cantiana s.l. continues: the populations of the Apuan Alps (NW Tuscany, Italy) (Eupulmonata, Stylommatophora, Hygromiidae). ZooKeys 814: 115-149. https://doi.org/10.3897/zookeys.814.31583
Figures 42- 43 Principal component analysis (PCA) and Redundancy analysis (RDA) with lineage applied to the original genitalia matrix (42) and Z-matrix (shape-related) (43).
Figures 35-41 from: Pieńkowska JR, Manganelli G, Giusti F, Barbato D, Hallgass A, Lesicki A (2019) Exploration of phylogeography of Monacha cantiana s.l. continues: the populations of the Apuan Alps (NW Tuscany, Italy) (Eupulmonata, Stylommatophora, Hygromiidae). ZooKeys 814: 115-149. https://doi.org/10.3897/zookeys.814.31583
Figures 35-41 Genitalia (proximal parts excluded) (35), internal structure of distal genitalia (36) and transverse sections of medial epiphallus (37, 39), basal and apical penial papilla (38, 40, 41) of Monachacantiana s.l. CAN-6 from Campagrina (FGC 40322).
Figures 30-34 from: Pieńkowska JR, Manganelli G, Giusti F, Barbato D, Hallgass A, Lesicki A (2019) Exploration of phylogeography of Monacha cantiana s.l. continues: the populations of the Apuan Alps (NW Tuscany, Italy) (Eupulmonata, Stylommatophora, Hygromiidae). ZooKeys 814: 115-149. https://doi.org/10.3897/zookeys.814.31583
Figures 30-34 Genitalia (proximal parts excluded) (30), transverse sections of medial epiphallus (31, 32) and basal and apical penial papilla (33, 34) of Monachacantiana s.l. CAN-5 Campo Cecina (FGC 41564).
Figures 25-29 from: Pieńkowska JR, Manganelli G, Giusti F, Barbato D, Hallgass A, Lesicki A (2019) Exploration of phylogeography of Monacha cantiana s.l. continues: the populations of the Apuan Alps (NW Tuscany, Italy) (Eupulmonata, Stylommatophora, Hygromiidae). ZooKeys 814: 115-149. https://doi.org/10.3897/zookeys.814.31583
Figures 25-29 Genitalia (proximal parts excluded) (25), internal structure of distal genitalia (26), transverse sections of medial epiphallus (27) and basal and apical penial papilla (28, 29) of Monachacantiana s.l. CAN-5 from Foce di Pianza (FGC 41565).
Figures 19-24 from: Pieńkowska JR, Manganelli G, Giusti F, Barbato D, Hallgass A, Lesicki A (2019) Exploration of phylogeography of Monacha cantiana s.l. continues: the populations of the Apuan Alps (NW Tuscany, Italy) (Eupulmonata, Stylommatophora, Hygromiidae). ZooKeys 814: 115-149. https://doi.org/10.3897/zookeys.814.31583
Figures 19-24 Genitalia (proximal parts excluded) (19), internal structure of distal genitalia (20), transverse sections of medial epiphallus (21, 22) and basal and apical penial papilla (23, 24) of Monachacantiana s.l. CAN-5 from Piastra (FGC 41563).
Figures 16- 17 from: Pieńkowska JR, Manganelli G, Giusti F, Barbato D, Hallgass A, Lesicki A (2019) Exploration of phylogeography of Monacha cantiana s.l. continues: the populations of the Apuan Alps (NW Tuscany, Italy) (Eupulmonata, Stylommatophora, Hygromiidae). ZooKeys 814: 115-149. https://doi.org/10.3897/zookeys.814.31583
Figures 16- 17 Principal component analysis (PCA) and Redundancy analysis (RDA) with lineage constraint applied to the original shell matrix (16) and Z-matrix (shape-related) (17).
Figures 45-47 from: Pieńkowska JR, Manganelli G, Giusti F, Barbato D, Hallgass A, Lesicki A (2019) Exploration of phylogeography of Monacha cantiana s.l. continues: the populations of the Apuan Alps (NW Tuscany, Italy) (Eupulmonata, Stylommatophora, Hygromiidae). ZooKeys 814: 115-149. https://doi.org/10.3897/zookeys.814.31583
Figures 45-47 Syntypes and original labels of Monacha species from Apuan Alps established by Mabille (1881). Helixapuanica (45) (MHNG-MOLL-115981), Helixardesa (46) (MHNG-MOLL-115982), Helixsobara (47) (MHNG-MOLL-116022) (by courtesy of E. Tardy, Muséum d'histoire naturelle, Genève, Switzerland).
Figure 2 from: Fujiwara Y, Jimi N, Sumida PYG, Kawato M, Kitazato H (2019) New species of bone-eating worm Osedax from the abyssal South Atlantic Ocean (Annelida, Siboglinidae). ZooKeys 814: 53-69. https://doi.org/10.3897/zookeys.814.28869
Figure 2 Whale skeleton discovered at a depth of 4,204 m in the South Atlantic Ocean. A Sunken whale skeleton of the Atlantic minke whale (Balaenopterabonaerensis). Seven vertebrae are visible in this field of view. Osedaxbraziliensis sp. n. had colonised the first two bones on the right B Close-up view of a vertebra colonized by O.braziliensis sp. n. Galatheid crabs (Munidopsis spp.), amphipods (Stephonyx sp.), and gastropods (Rubyspira sp.) were also seen on and around the bones.
Figure 4 from: Pieńkowska JR, Manganelli G, Giusti F, Barbato D, Hallgass A, Lesicki A (2019) Exploration of phylogeography of Monacha cantiana s.l. continues: the populations of the Apuan Alps (NW Tuscany, Italy) (Eupulmonata, Stylommatophora, Hygromiidae). ZooKeys 814: 115-149. https://doi.org/10.3897/zookeys.814.31583
Figure 4 The median-joining haplotype network for COI haplotypes of Monachacantiana s.l. The colours of the circles indicate Monacha species, and their size is proportional to haplotype frequencies. Small black circles are hypothetical missing intermediates. The numbers next to the branches indicate distance between taxa expressed in numbers of mutant positions. Only numbers above 10 are indicated.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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