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13 results for “Eucyclops serrulatus”
Figure 3 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)
Figure 3. Eucyclops serrulatus (Fischer) from the Dniester Liman (A, C, E) and Zakarpattia regions (B, D, F) of Ukraine. (A, B) P4, caudal side with feature abbreviations used; (C, D) antenna, caudal side; (E, F) caudal ramus with abbreviations.
Figure 3 in Congruent patterns of lineage diversity in two species complexes of planktonic crustaceans, Daphnia longispina (Cladocera) and Eucyclops serrulatus (Copepoda), in East European mountain lakes
Figure 3. Relationship of eight clades of the Eucyclops serrulatus complex, assessed by Bayesian inference of phylogeny, and haplotype variation of the 12S rRNA gene within clade I. The phylogenetic tree was based on the 1299-bp-long alignment consisting of fragments of mitochondrial genes for 12S rRNA and cytochrome b, and the nuclear gene for 18S rRNA. The scale bar represents genetic distance; numbers at nodes indicate branch support (as posterior probabilities). Haplotype network representing the variation within clade I is based on 43 sequences of the 383-bp-long 12S rDNA fragment. Individuals from the three main mountain regions are indicated by different shading (as in Figs 1, 2) in both tree and network: the Carpathians in dark grey (N = 24), Macedonian-Thracian massif in white (N = 9), and Dinaric Alps in light grey (N = 26). Mountain range abbreviations: Bje, Bjelasica; Dur, Durmitor; Pir, Pirin; Pro, Prokletije; Ret, Retezat; Ril, Rila; Sar, Šar Planina; Tat, Tatra Mountains; Tre, Treskavica; Zel, Zelengora. Countries are indicated by two-letter codes (see Table 1).
Figure 2 in Congruent patterns of lineage diversity in two species complexes of planktonic crustaceans, Daphnia longispina (Cladocera) and Eucyclops serrulatus (Copepoda), in East European mountain lakes
Figure 2. Sequence variation of the 528-bp-long fragment of the 12S rRNA gene within the Daphnia longispina complex from lakes of the studied East European mountain ranges. This is shown in a maximum likelihood tree (A) consisting only of sequences from the studied region (each haplotype represented once per lake), and in a parsimony network (B) of haplotypes of D. longispina s.s., amongst which 63 reference sequences from other European localities were also included. Three main mountain regions from this study are differentiated by shading: the Carpathians in dark grey, Macedonian-Thracian massif in white, and Dinaric Alps in light grey. Haplotypes from other localities, only included in the network, are enclosed by dashed lines. Mountain range abbreviations: Bje, Bjelasica; Dur, Durmitor; Pir, Pirin; Pro, Prokletije; Ret, Retezat; Ril, Rila; Tat, Tatra Mountains; Tre, Treskavica; Zel, Zelengora. Countries are indicated by two-letter codes (see Table 1).
Figure 1 in Congruent patterns of lineage diversity in two species complexes of planktonic crustaceans, Daphnia longispina (Cladocera) and Eucyclops serrulatus (Copepoda), in East European mountain lakes
Figure 1. Map of the sampled Eastern European mountain ranges (Bje, Bjelasica; Dur, Durmitor; Pir, Pirin; Pro, Prokletije; Ret, Retezat; Ril, Rila; Sar, Šar Planina; Tat, Tatra Mountains; Tre, Treskavica; Zel, Zelengora). The main mountain regions are differentiated by shading: the Carpathians in dark grey, Macedonian-Thracian massif in white, and Dinaric Alps in light grey. Countries are indicated by two-letter codes (see Table 1).
Figure 10 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)
Figure 10. Hyaline membrane of antennule; (A, C) 10th–11th segments, (E) 11th–12th segments and (B, D, F) coxopodite with coxal spine P4 of (A, B) Eucyclops taiwanensis sp. n.; (C, D) Eucyclops serrulatus (Fischer); and (E, F) Eucyclops macruroides (Lilljeborg) according to Monchenko (1974).
Figure 9 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)
Figure 9. Eucyclops taiwanensis sp. n., male, ZIN RN 55091 (paratype): (A) antenna; (B) P4, caudal side. Scale bar: 100 μm.
Figure 8 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)
Figure 8. Eucyclops taiwanensis sp. n., male, ZIN RN 55091 (paratype): (A) habitus, dorsal; (B) urosome with P5 and P6, ventral side; Scale bar: A = 67 μm, B = 100 μm.
Figure 7 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)
Figure 7. Eucyclops taiwanensis sp. n., female, ZIN RN 55090 (holotype): (A) P1; (B) P2; (C) P3; (D) P4; caudal side; Scale bar: 100 μm.
Figure 6 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)
Figure 6. Eucyclops taiwanensis sp. n., female, ZIN RN 55090 (holotype): (A) antenna; (B) mandible; (C) maxillula; (D) maxilla; (E) maxilliped. Scale bar: A = 67 μm, B–E = 50 μm.
Figure 5 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)
Figure 5. Eucyclops taiwanensis sp. n., female, ZIN RN 55090 (holotype): (A) habitus, dorsal; (B) urosome with P5, ventral side; (C) antennule with aesthetascs indicated by arrows; (D) hyaline membrane on segments 10–12 of antennule. Scale bar: A = 150 μm; B = 100 μm, C = 75 μm; D =37 μm.
Figure 4 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)
Figure 4. Distribution of Eucyclops serrulatus (Fischer) females from different localities on the base of caudal rami index INseta/OUTseta, and P4 exo Lseg/Sp1 (see Table 4 and text). Populations from Dniester Liman; Zakarpattia region; and from the type locality in Orlov Pond, Saint Petersburg: individuals from Orlov Pond resembling the Zakarpattia population ▲; individuals from Orlov Pond resembling Dniester Liman ♦ and individuals from Orlov Pond ○ looking like hybrids between the two Ukrainian populations.
Figure 1 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)
Figure 1. The localities of the Eucyclops serrulatus (Fischer) and Eucyclops taiwanensis sp. n., populations studied. Locality names are listed in Table 1.
Figure 2 in Genetic and morphological heterogeneity within Eucyclops serrulatus (Fischer, 1851) (Crustacea: Copepoda: Cyclopidae)
Figure 2. Phylogenetic tree constructed based on data from mitochondrial cytochrome c oxidase subunit I (CO1) region (651 bp) by the Bayesian method using the TPM1uf +G model. Numbers beside nodes indicate Bayesian posterior probabilities (BPP) and bootstrap values. Clade 1 includes sequences of Eucyclops serrulatus (Fischer) from the Zakarpattia region of Ukraine, Orlov Pond and Tavricheskii Pond in Saint Petersburg, Creteil Lake in Paris and the pond in Oslo; Clade 2: Eucyclops serrulatus sequences from the Dniester Liman in Ukraine, Orlov Pond in Saint Petersburg and Central Russia (Udmurtia). Clade 3: Eucyclops taiwanensis sp. n. sequences from ponds in Taiwan. Clade 4: Eucyclops cf. serrulatus sequences from the Xucar River in Spain.
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