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1,133 results for “Copepods”
Fig. 7 in A new cyclopoid copepod from Korean subterranean waters reveals an interesting connection with the Central Asian fauna (Crustacea: Copepoda: Cyclopoida)
Fig. 7. Monchenkocyclops changi gen. et sp. nov., allotype male. A. habitus, dorsal view. B. urosome, ventral view. C. right caudal ramus, dorsal view. D. right caudal ramus, lateral view. E. second endopodal segment of fourth swimming leg, anterior view. F. sixth leg, ventrolateral view. Arabic numerals indicating sensilla and pores consecutively from anterior to posterior end of body, and from dorsal to ventral side (excluding appendages). Scale bars 100 µm.
Fig. 1 in A new cyclopoid copepod from Korean subterranean waters reveals an interesting connection with the Central Asian fauna (Crustacea: Copepoda: Cyclopoida)
Fig. 1. Monchenkocyclops changi gen. et sp. nov., holotype female: A. habitus, dorsal view. B. antennula, dorsal view. Arabic numerals indicating sensilla and pores consecutively from anterior to posterior end of body, and from dorsal to ventral side (excluding appendages; those on cephalothorax not presented). Scale bars 100 µm.
Fig. 6 in A new cyclopoid copepod from Korean subterranean waters reveals an interesting connection with the Central Asian fauna (Crustacea: Copepoda: Cyclopoida)
Fig. 6. Monchenkocyclops changi gen. et sp. nov., A-E. holotype female. F. allotype male. A. second endopodal segment of third swimming leg, anterior view. B. left fourth swimming leg, anterior view. C. second endopodal segment of right fourth swimming leg, anterior view. D. fifth leg, anterior view. E. sixth leg, lateral view. Scale bar 100 µm.
Fig. 4 in A new cyclopoid copepod from Korean subterranean waters reveals an interesting connection with the Central Asian fauna (Crustacea: Copepoda: Cyclopoida)
Fig. 4. Monchenkocyclops changi gen. et sp. nov., A-E. holotype female. F. paratype female. A. urosome, dorsal view. B. antenna, dorsal view. C. labrum, anterior view. D. maxillula, posterior view. E. mandibula, anterior view. F. cutting edge of labrum, anterior view. Arabic numerals indicating sensilla and pores consecutively from anterior to posterior end of body, and from dorsal to ventral side (excluding appendages). Scale bars 100 µm.
Fig. 5 in A new cyclopoid copepod from Korean subterranean waters reveals an interesting connection with the Central Asian fauna (Crustacea: Copepoda: Cyclopoida)
Fig. 5. Monchenkocyclops changi gen. et sp. nov., holotype female: A. maxilla, anterior view. B. maxilliped, posterior view. C. first swimming leg, anterior view. D. second swimming leg, anterior view. Scale bar 100 µm.
Fig. 3 in A new cyclopoid copepod from Korean subterranean waters reveals an interesting connection with the Central Asian fauna (Crustacea: Copepoda: Cyclopoida)
Fig. 3. Monchenkocyclops changi gen. et sp. nov., holotype female: A. urosome, ventral view. B. urosome, lateral view. Arabic numerals indicating sensilla and pores consecutively from anterior to posterior end of body, and from dorsal to ventral side (excluding appendages). Scale bars 100 µm.
Fig. 2 in A new cyclopoid copepod from Korean subterranean waters reveals an interesting connection with the Central Asian fauna (Crustacea: Copepoda: Cyclopoida)
Fig. 2. Monchenkocyclops changi gen. et sp. nov., holotype female: A. cephalothoracic shield, lateral view. B. cephalothorax, dorsal view. C. pleurons of free prosomites, lateral view. D. rostrum, dissected and flattened, original anterior view. E. pleuron of second free prosomite (third pedigerous somite), dissected and flattened. Arabic numerals indicating sensilla and pores consecutively from anterior to posterior end of body, and from dorsal to ventral side (excluding appendages). Scale bars 100 µm.
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.
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.
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.
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.
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.
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.
Copepod diapause duration estimation code for manuscript: Lipid load triggers migration to diapause in Arctic Calanus copepods - insights from underwater imaging
<p>This is a script and data upload by Frederic Maps (Université Laval) which creates figure 10 as well as other exploratory plots for publication Schmid, Maps, Fortier 2018: Lipid load triggers migration to diapause in Arctic Calanus copepods - insights from underwater imaging, to be published in the journal of plankton research (JPR).</p>
Figure 2 in TaXonomic Catalog of the Brazilian Fauna: the intriguing copepod order Monstrilloida (Crustacea: Copepoda), taXonomy and diversity
Figure 2. Distinctive morphological characters of the Monstrilloid copepods described from Brazil: (A) Cymbasoma rochai male genital complex showing spiniform processes; (B) C. rochai female fifth leg and ovigerous spines; (C) Monstrilla careli female fifth leg, ventral view; (D) M. pustulata female forehead with integumental field of pustules; (E) same, fifth leg, ventral view; (F) M. satchmoi, bilobed female oral papilla, lateral view; (G) same, left antennule, dorsal view; (H) C. brasiliensis female fifth legs, ventral view; (I) same, right antennule, dorsal view; (J) M. bahiana male genital complex, lateral view; (K) same, ventral view showing lappets; (L) same male right geniculate antennule, dorsal view; (M) M. fosshageni male genital complex, semi-lateral view; (N) same, lateral view; (O) M. fosshageni male left geniculate antennule, dorsal view.
Figure 3 in TaXonomic Catalog of the Brazilian Fauna: the intriguing copepod order Monstrilloida (Crustacea: Copepoda), taXonomy and diversity
Figure 3. Distribution of species of the copepod order Monstrilloida: (A) Brazilian map showing the number of Monstrilloida species recorded from each state; (B) Monstrilloida species number by Brazilian marine ecoregions. State abbreviations: (AC) Acre, (AL) Alagoas, (AM) Amazonas, (AP) Amapá, (BA) Bahia, (CE) Ceará, (DF) Federal District, (ES) Espírito Santo, (GO) Goiás, (MA) Maranhão, (MG) Minas Gerais, (MS) Mato Grosso do Sul, (MT) Mato Grosso, (PA) Pará, (PB) Paraíba, (PE) Pernambuco, (PI) Piauí, (PR) Paraná, (RJ) Rio de Janeiro, (RN) Rio Grande do Norte, (RO) Rondônia, (RR) Roraima, (RS) Rio Grande do Sul, (SC) Santa Catarina, (SE) Sergipe, (SP) São Paulo, (TO) Tocantins.
Figure 1 in TaXonomic Catalog of the Brazilian Fauna: the intriguing copepod order Monstrilloida (Crustacea: Copepoda), taXonomy and diversity
Figure 1. Monstrilloid copepod species described from Brazil: (A) Cymbasoma rochai adult female, dorsal view; (B) Monstrilla careli adult female, lateral view; (C) same, dorsal view; (D) M. pustulata adult female, lateral view; (E) same, dorsal view; (F) M. satchmoi adult female, lateral view; (G) Caromiobenella brasiliensis adult female, ventral view; (H) same, dorsal view; (I) C. brasiliensis adult male, lateral view; (J) same, dorsal view; (K) Monstrilla bahiana adult male, dorsal view; (L) same, ventral view; (M) Cymbasoma rochai adult male, ventral view; (N) Monstrillopsis fosshageni adult male, lateral view. Illustrations modified from Suárez-Morales and Dias (2000, 2001), Dias and Suárez-Morales (2023), Suárez-Morales et al. (2020). Scale bar: 0.5 mm.
Figure 3 in Seasonal variations in body length and fecundity of 2 copepod species: Thermocyclops crassus (Fischer, 1853) and Eudiaptomus drieschi (Poppe & Mrázek, 1895
Figure 3. Monthly variations in mean egg numbers and lengths of females and males of 2 copepod species in Lake Yenişehir during the study period (broken lines show that no E. drieschi was found in this period).
Figure 2 in Seasonal variations in body length and fecundity of 2 copepod species: Thermocyclops crassus (Fischer, 1853) and Eudiaptomus drieschi (Poppe & Mrázek, 1895
Figure 2. Monthly variations of temperature, phosphate, nitrate, dissolved oxygen, and chlorophyll-a during the study in Lake Yenişehir, from May 2003 to June 2004 (±SD).
Figure 6 in Seasonal variations of abundance and live/dead compositions of copepods in Mersin Bay, northeastern Levantine Sea (eastern Mediterranean)
Figure 6. Percentage of dead copepods at the coastal and open water stations (a), and the percentage of dead copepods at 0–100 and 100–195 m at the open water station (b).
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