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76 results for “814”
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.
Figure 44 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 44 Box plots for genitalia characters of the seven Monacha clades investigated. The lower and upper limits of the rectangular boxes indicate the 25th to 75th percentile range, and the horizontal line within the boxes is the median (50th percentile).
Figure 4 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 4 Acartia (Odontacartia) edentata sp. n., female (F) and male (A–E) (allotype) A Habitus, dorsal view B Habitus, lateral view C Antennule, Roman numerals denote segment numbers D Antennule, Roman numerals denote segment numbers E Rostrum of male F Rostrum of female.
Figure 3 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 3 Acartia (Odontacartia) edentata sp. n. female (A–G) and male (H) (holotype) A Mandible B Maxilla C Leg 1 D Leg 2 E Leg 3 F Leg 4 G Legs 5 H Legs 5.
Figure 2 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 2 Acartia (Odontacartia) edentata sp. n. female (holotype) A Habitus, dorsal view B Habitus, lateral view C Antennule, Roman numerals denote segment numbers D Antenna E Maxilla F Maxilliped.
Figure 7 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 7 Ranges of salinity and temperature of three Acartia species occurring in the tropical and subtropical zones of the Pacific and Indian oceans.
Figure 3 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 3 Bayesian 50% majority-rule consensus tree of the combined data set of COI and 16SrDNA haplotypes, and H3 and ITS2 common sequences (see Table 4). Posterior probabilities (left) and bootstrap support above 50% from ML analysis (right) are indicated next to the branches. Bootstrap analysis was run with 1000 replicates (Felsenstein 1985). The tree was rooted with M.cartusiana and M.parumcincta combined sequences obtained from GenBank (Table 4).
Figure 2 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 2 Maximum Likelihood (ML) tree of combined H3 and ITS2 common sequences of Monachacantiana s.l. (see Table 4). Numbers next to the branches indicate bootstrap support above 50% calculated for 1000 replicates (Felsenstein 1985). The tree was rooted with M.cartusiana and M.parumcincta combined sequences obtained from GenBank (Table 4).
Figure 18 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 18 Box plots for shell characters of the seven Monacha clades investigated. The lower and upper limits of the rectangular boxes indicate the 25th to 75th percentile range, and the horizontal line within the boxes is the median (50th percentile).
Figure 1 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 1 Maximum Likelihood (ML) tree of combined COI and 16SrDNA haplotypes of Monachacantiana s.l. (see Table 4). Numbers next to the branches indicate bootstrap support above 50% calculated for 1000 replicates (Felsenstein 1985). The tree was rooted with M.cartusiana and M.parumcincta combined sequences obtained from GenBank (Table 4).
Figure 2. CAD haplotype network. TCS Network based off 814 in Low Variation in Nuclear and Mitochondrial DNA Inhibits Resolution of Invasion Pathways across the Pacific for the Coconut Rhinoceros Beetle (Scarabeidae: Oryctes rhinoceros)
Figure 2. CAD haplotype network. TCS Network based off 814 base pairs of the CAD gene region from a total of 117 samples (8 to 39 from any given location) representing 234 total haplotypes. Hash marks represent a single base pair change. A PHASE algorithm was used to generate haplotypes from ambiguities present in the sequence data of a multi-copy nuclear gene, resulting in twice as many haplotypes as samples.
Figures 814-818 from: Lonsdale O (2021) Manual of North American Agromyzidae (Diptera, Schizophora), with revision of the fauna of the "Delmarva" states. ZooKeys 1051: 1-481. https://doi.org/10.3897/zookeys.1051.64603
Figures 814-818 Phytomyza plantaginis Robineau-Desvoidy, male genitalia 814 external genitalia, posterior 815 postgonite, lateral 816 hypandrium, ventral 817 phallus, ventral 818 phallus, left lateral.
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