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70 results for “harpacticoids”

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Figure 7 in A new subterranean Maraenobiotus (Crustacea: Copepoda) from Slovenia challenges the concept of polymorphic and widely distributed harpacticoids

Figure 7. Maraenobiotus slovenicus sp. nov., line drawings, (A–C) holotype female; (D, E) allotype male: (A) genital segment with attached spermatophore, ventral; (B) last urosomite, anal somite and furcal rami, ventral; (C) last urosomite, anal somite and furcal rami, dorsal; (D) last urosomite, anal somite and furcal rami, ventral; (E) anal somite and furcal rami, dorsal.

opencc-by-4.0Jun 2015View details →
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Figure 4 in A new subterranean Maraenobiotus (Crustacea: Copepoda) from Slovenia challenges the concept of polymorphic and widely distributed harpacticoids

Figure 4. Maraenobiotus slovenicus sp. nov., SEM micrographs, (A–D) damaged paratype male 1; (E–H) paratype male 2: (A) mouth appendages, ventral; (B) maxillule and maxilla, ventral; (C) central part of left antennule, ventral; (D) antenna, ventral; (E) left antennule, lateral; (F) first three urosomites, lateral; (G) anal somite and caudal rami, lateral; (H) detail of first urosomite, with cuticular window, large pore, and sensillum, lateral.

opencc-by-4.0Jun 2015View details →
zenodo40/100

Figure 3 in A new subterranean Maraenobiotus (Crustacea: Copepoda) from Slovenia challenges the concept of polymorphic and widely distributed harpacticoids

Figure 3. Maraenobiotus slovenicus sp. nov. (A, B) SEM micrographs, paratype female 3; (C–H) damaged paratype male 1: (A) first two urosomites and P5; (B) P1–P3, ventrolateral; (C) habitus with several large epibiotic ciliates, ventral; (D) P4–P6, ventral; (E) last two urosomites and caudal rami, ventral; (F) antennule, ventral; (G) distal part of right antennule, ventral; (H) central part of right antennule, ventral.

opencc-by-4.0Jun 2015View details →
zenodo40/100

Figure 1 in A new subterranean Maraenobiotus (Crustacea: Copepoda) from Slovenia challenges the concept of polymorphic and widely distributed harpacticoids

Figure 1. Maraenobiotus slovenicus sp. nov., SEM micrographs, paratype female 1: (A) habitus, dorsal; (B) cephalothorax, dorsal; (C) anterior part of cephalothorax, dorsal; (D) right antennule, dorsal; (E) free pedigerous somites, dorsal; (F) first three urosomites, dorsal; (G) last three urosomites and caudal rami, dorsal; (H) right caudal ramus, dorsal.

opencc-by-4.0Jun 2015View details →
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Fig. 7. Laophontella horrida dentata Mielke, 1992 in Three new harpacticoid copepods for Korea from marine interstitial habitats

Fig. 7. Laophontella horrida dentata Mielke, 1992, SEM photographs, adult male, lateral view; A, anterior part of cephalothorax and first segment of antennula; B, apical setae on first leg endopod; C, sixth leg and last two exopodal segments of fourth swimming leg; D, caudal ramus; E, detail of armature and ornamentation of proximal part of caudal ramus; F, detail of principal caudal seta.

opencc-by-4.0Dec 2019View details →
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Fig. 4. Laophontodes norvegicus George, 2018, male 1 in Three new harpacticoid copepods for Korea from marine interstitial habitats

Fig. 4. Laophontodes norvegicus George, 2018, male 1, ventral view; A, CLM photograph; B-H, SEM photographs; A, habitus; B, habitus; C, antennula; D, detail of armature and ornamentation of proximal part of antennula; E, detail of armature and ornamentation of central part of antennula; F, detail of armature and ornamentation of distal part of antennula; G, labrum and mouth appendages; H, first swimming leg.

opencc-by-4.0Dec 2019View details →
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Fig. 5. Laophontodes norvegicus George, 2018, male 1 in Three new harpacticoid copepods for Korea from marine interstitial habitats

Fig. 5. Laophontodes norvegicus George, 2018, male 1, ventral view, SEM photographs; A, distal part of maxilliped and basis of first swimming leg; B, third exopodal segment of second swimming leg; C, tubular pore on second exopodal segment of second swimming leg; D, distal frill of fourth urosomite; E, caudal ramus; F, detail of ornamentation of proximal part of caudal ramus; G, lateral setae on caudal ramus; H, distal part of caudal ramus.

opencc-by-4.0Dec 2019View details →
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Fig. 3. Phyllopodopsyllus thiebaudi santacruzensis Mielke, 1989 in Three new harpacticoid copepods for Korea from marine interstitial habitats

Fig. 3. Phyllopodopsyllus thiebaudi santacruzensis Mielke, 1989; A-D, SEM photographs; E-H, CLM photographs; A, B, male 1, lateral view; C, D, male 2, ventral view; E-H, female 4, dissected and mounted on microscope slides, anterior view: A, habitus; B, anal somite and caudal rami; C, habitus; D, distal part of antennula; E, first swimming leg; F, second swimming leg; G, third swimming leg; H, fourth swimming leg.

opencc-by-4.0Dec 2019View details →
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Fig. 2. Phyllopodopsyllus thiebaudi santacruzensis Mielke, 1989 in Three new harpacticoid copepods for Korea from marine interstitial habitats

Fig. 2. Phyllopodopsyllus thiebaudi santacruzensis Mielke, 1989, SEM photographs; A-C, female 2, dorsal view; D-G, female 3, ventral view; H, male 1, lateral view: A, habitus; B, anterior part of cephalothorax with rostrum and first segment of antennula; C, anal somite and caudal rami; D, habitus; E, anal somite and caudal rami; F, endopod and first two exopodal segment of second swimming leg; G, distal part of third exopodal segment of fourth swimming leg; H, distal part of antennula.

opencc-by-4.0Dec 2019View details →
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Fig. 1. Phyllopodopsyllus thiebaudi santacruzensis Mielke, 1989 in Three new harpacticoid copepods for Korea from marine interstitial habitats

Fig. 1. Phyllopodopsyllus thiebaudi santacruzensis Mielke, 1989, SEM photographs, female 1, lateral view: A, habitus; B, cephalothoracic shield; C, tergites of free prosomites; D, genital somite with proximal part of fifth leg; E, distal part of fifth leg; F, anal somite and caudal ramus; G, second endopodal segment of first swimming leg; H, exopod of antenna.

opencc-by-4.0Dec 2019View details →
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Fig. 2 in The benthic harpacticoids (Crustacea, Copepoda) of Budakskyi (Shabolatskyi) Lagoon, North-West coast of the Black Sea, Ukraine

Fig. 2. Distribution of bottom substrate in Budagskyi lagооn. Legend: 1 – silt, 2 – sand.

opencc-by-4.0Nov 2018View details →
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Fig. 1 in The benthic harpacticoids (Crustacea, Copepoda) of Budakskyi (Shabolatskyi) Lagoon, North-West coast of the Black Sea, Ukraine

Fig. 1. Location of the lagoons along the North-Western Black Sea Coast.

opencc-by-4.0Nov 2018View details →
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FIGURE 2. Harpacticoid copepod with a in The tantulocarid genus Arcticotantalus removed from Basipodellidae into Deoterthridae (Crustacea: Maxillopoda) after the description of a new species from Greenland, with first live photographs and an overview of the class

FIGURE 2. Harpacticoid copepod with a tantulus larva (ZMUC CRU4884) of Arcticotantulus kristenseni sp. nov. attached to the posterior abdominal somite. This attachment site is typical, but attachment can occur everywhere on the host. Arrow points at larval head.

opennotspecifiedDec 2009View details →
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Figure 2 in Freshwater harpacticoids (Crustacea: Copepoda: Harpacticoida) in Norway – a comprehensive contribution from G.O. Sars, and a provisional checklist

Figure 2. Map of Norway. Division in main geographical regions used to show the distributions of freshwater harpacticoids in Norway (Table 2).

opennotspecifiedApr 2016View details →
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Figure 1 in Freshwater harpacticoids (Crustacea: Copepoda: Harpacticoida) in Norway – a comprehensive contribution from G.O. Sars, and a provisional checklist

Figure 1. Drawings by G. O. Sars. Cut-outs from original plates (see Table 1, Supplementary material 1 for archive item Ms. Fol. 1109: 492) accompanying the unpublished manuscript "Om de i Christiania's Omegn forekommende Ferskvandskrebsdyr" from 1862 (see Table 1, Supplementary material 1 for archive item Ms. Fol. 1109: 613). A - Canthocamptus (Canthocamptus) staphylinus, B - Bryocamptus (Rheocamptus) pygmaeus, C - Elaphoidella gracilis, D - Attheyella (Attheyella) crassa. The original plates with all drawings are included in Supplementary material 2.

opennotspecifiedApr 2016View details →
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Fig. 2 Harpacticoid families collected from Stations 325 and 346 in Community structure and species diversity of Harpacticoida (Crustacea: Copepoda) at two sites in the deep sea of the Angola Basin (Southeast Atlantic)

Fig. 2 Harpacticoid families collected from Stations 325 and 346 (Angola Basin). Families are sorted according to the total number of collected individuals N (columns) and dominance (pie charts). "Others" refer to the following families (in decreasing order from left to right): Station 325 = Paramesochridae, Huntemanniidae, Ancorabolidae, Cletodidae, Aegisthidae, Miraciidae, Rhizotrichidae, Canuellidae; Station 346 = Neobradyidae, Paramesochridae, Zosimeidae, Canthocamptidae, Idyanthidae, Miraciidae, Huntemanniidae, Cletodidae, Aegisthidae, Ancorabolidae, Tisbidae, Canuellidae, Rometidae, Dactylopusiidae

opennotspecifiedSep 2013View details →
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Figure 4 in Benthic harpacticoid copepods of the Yenisei Gulf and the adjacent shallow waters of the Kara Sea

Figure 4. Multi-dimensional scaling (MDS-ordination) plot of stations based on Gamma+ taxonomic similarity and factored by the species assemblages.

opennotspecifiedAug 2016View details →
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Figure 2 in Benthic harpacticoid copepods of the Yenisei Gulf and the adjacent shallow waters of the Kara Sea

Figure 2. Total harpacticoid abundance (a), number of species (b) and Margalef's diversity index (c, d) plotted against the distance from the river mouth (a–c) and chlorophyll a content in water (d). Lines show the second-order polynomial approximations, squared multiple correlation values (R2) are given.

opennotspecifiedAug 2016View details →
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Figure 3 in Benthic harpacticoid copepods of the Yenisei Gulf and the adjacent shallow waters of the Kara Sea

Figure 3. Canonical correspondence analysis (CCA-ordination) (axis 1 versus axis 2) based on squareroot transformed harpacticoid abundances. Plot of stations versus environmental variables is shown. Environmental variables are: surface water salinity (SALSURF), near-bottom salinity (SALBOT), depth (DEPTH), distance from the river mouth (DISTANCE), mean particle size (MPS), silt-clay content (SILT/ CLAY), sediment sorting (SORTING), turbidity (TURBID), chlorophyll a (Chl a) content in water column (CHLa) and near-bottom temperature (TEMP). Assemblage labelling: (a) (squares), (b) (triangles), (c) (circles), (d) (diamonds).

opennotspecifiedAug 2016View details →
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FIGURE 4 in Three new ameirid harpacticoids from Korea and first record of Proameira simplex (Crustacea: Copepoda: Ameiridae) *

FIGURE 4. Ameira zahaae sp. nov., allotype male: A, urosome, ventral view; B, rostrum and first two segments of antennula, dorsal view; C, basis of first swimming leg, anterior view; D, abnormal third exopodal segment of second swimming leg, anterior view; E, fifth leg, ventro-lateral view (undissected); F, sixth leg, ventro-lateral view (undissected). Arabic numerals on urosome numbering sensilla and pores as in female. Arrows pointing most prominent specific features.

opennotspecifiedDec 2012View details →

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