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46 results for “Ligiidae”
Figure 8 in Distribution, habitat and food preferences of sympatric high intertidal isopod species Ligia occidentalis and Ligia pallasii (Ligiidae: Oniscidea)
Figure 8. Differences in food preference for the two Ligia species [Ligia occidentalis (LO): F (4,53.45) = 15.918, p = 0.0001; Ligia pallasii (LP): F (4,53,45) = 15.928, p = 0.0004] as shown for mean dry weight consumed for each food type (error bars are ± 1 SE). Changes in weight of the different food types without isopods (none: F (4,22.15) = 0.699, p = 0.601) show minimal changes in weight possibly because of microbial activity. Values of p are based on analysis of variance. Letters above bars indicate significant differences among means (Post hoc Tukey tests).
Figure 6 in Distribution, habitat and food preferences of sympatric high intertidal isopod species Ligia occidentalis and Ligia pallasii (Ligiidae: Oniscidea)
Figure 6. Results of mesocosm experiments show that all treatments containing Ligia showed a significant decrease in dry weight of algal biomass compared with a control (none). The reduction in algal biofilm caused by Ligia pallasii (LP) treatment was significantly lower than that by either the Ligia occidentalis (LO) treatment or the combination of the two species (LO+LP). Letters above bars indicate significant differences among means (Post hoc Tukey tests).
Figure 5 in Distribution, habitat and food preferences of sympatric high intertidal isopod species Ligia occidentalis and Ligia pallasii (Ligiidae: Oniscidea)
Figure 5. Temperature records at Mussel Point cave (A) and Bodega Harbor (B) represented as mean temperature per month (average) and the monthly average of the daily maximum (max) and minimum (min) temperatures.
Figure 4 in Distribution, habitat and food preferences of sympatric high intertidal isopod species Ligia occidentalis and Ligia pallasii (Ligiidae: Oniscidea)
Figure 4. Monthly survey of Ligia pallasii at Mussel Point from March 2007 to December 2010. Overall abundance is represented as mean number of individuals per square metre and is composed of numbers from five different size classes (see key).
Figure 3 in Distribution, habitat and food preferences of sympatric high intertidal isopod species Ligia occidentalis and Ligia pallasii (Ligiidae: Oniscidea)
Figure 3. Monthly survey of Ligia occidentalis at Bodega Harbor from March 2007 to December 2010. Overall abundance is represented as mean number of individuals per square metre and is composed of numbers from four different size classes (see key).
Figure 2 in Distribution, habitat and food preferences of sympatric high intertidal isopod species Ligia occidentalis and Ligia pallasii (Ligiidae: Oniscidea)
Figure 2. Relative abundance of Ligia occidentalis (LO) and Ligia pallasii (LP) along the surveyed coastline (x axis left to right represents latitudinal coordinates of sampling sites from south to north). LO showed slight but not significant decline in abundance towards the northern range of the distribution Spearman's ρ – 0.0863, p <|ρ| = 0.3680. LP showed a small but significant decline towards the southern range limit (positive correlation with increasing latitude Spearman's ρ 0.5499, p <|ρ| = 0.0001. Lines within sites mark area of range overlap (solid line range limit of species in plot, dashed line range limit of other Ligia species).
Figure 1 in Distribution, habitat and food preferences of sympatric high intertidal isopod species Ligia occidentalis and Ligia pallasii (Ligiidae: Oniscidea)
Figure 1. Ligia occidentalis (A) and Ligia pallasii (B, C) can be distinguished by the distance between the eyes and the shape of the caudal peduncle of the uropod. Sexual dimorphism is only present in L. pallasii (B, female; C, male). All scale bars represent 10 mm. Photos: J. Sones.
Figure 7 in Distribution, habitat and food preferences of sympatric high intertidal isopod species Ligia occidentalis and Ligia pallasii (Ligiidae: Oniscidea)
Figure 7. Feeding preferences (mean rank ± 1 SE) of Ligia pallasii and Ligia occidentalis for different species of algal wrack (Nereocystis, Costaria, Ulva, Mazaella and Fucus); n = 20 (L. pallasii), 19 (L. occidentalis). Different letters indicate significant differences in rank of pairwise comparisons after Bonferoni corrections.
Figure 2 in Morphological and molecular data confirm species assignment and dispersal of the genus Ligia (Crustacea: Isopoda: Ligiidae) along northeastern coastal China and East Asia
Figure 2. Morphological characters of Ligia cinerascens and Ligia exotica. (I–III) Morphological traits of eyes (I), second antenna (II) and second antenna flagellum segments (III) of L. cinerascens in dorsal view. (IV, V) Morphological traits of the telson of L. cinerascens (IV) and L. exotica (V) in dorsal view and scanning electron microscopy images of partial enlarged spines on the pad of appendix masculina, showing terms used in the Results section: IAP, inner accessory processes; MDP, median process; PLP, posterolateral processes. (VI, VII) Morphological traits of appendix masculina of left second pleopod of L. cinerascens (VI) and L. exotica (VII) in ventral view, showing terms used in the Results section: IL, inner lateral; P, pad; PMP, posterior margin of pad; T, tip.
Figure 1 in Morphological and molecular data confirm species assignment and dispersal of the genus Ligia (Crustacea: Isopoda: Ligiidae) along northeastern coastal China and East Asia
Figure 1. Sample locations, phylogenetic relationships and evolutionary networks of Ligia spp. along northeastern coastal China. (I) Localities and sequencing sample size of Ligia cinerascens and Ligia exotica. The coloured pie chart in the map shows haplotypes and sequencing sample size. The coloured seashores indicate the distribution range of each species (or clade). The colours of the outer ring represent the species assignment and those of the inner pie chart show the different genetic clades. The abbreviations of each location and the sample size are detailed in Table 1. (II, III) Minimum spanning network (MSN) among haplotypes for 16S rDNA (II) and cytochrome c oxidase subunit I (cox1) (III) of L. cinerascens and L. exotica. Sampled haplotypes are indicated by circles. Numbers show the expected mutation steps between haplotypes. When the mutation step was equal to 1, it was omitted. (IV) Phylogenetic relationships recovered by neighbor-joining (NJ), maximum parsimony (MP) and Bayesian inference (BI) based on 16SA datasets. The outgroups are Ligia oceanica (Ligiidae) and Idotea baltica (Idoteidae). Values under the branches of the tree indicate bootstrap in NJ, MP and Bayesian posterior probability (BPP) from 16SA datasets. The '+' symbol denotes bootstrap or BPP values = 100%, whereas the '−' symbol presents bootstrap or BPP values <50%. Scale bar shows the number of substitutions per site.
FIGURE 7. Ligia exotica Roux, 1828. Female, 26 in A morphological and molecular study of Ligia exotica Roux, 1828 (Crustacea: Isopoda: Ligiidae) from Japan, with descriptions of two new species
FIGURE 7. Ligia exotica Roux, 1828. Female, 26 mm (OMNH-Ar-12588). Scales: 1 mm.
FIGURE 4. Ligia exotica Roux, 1828. Male, 32 in A morphological and molecular study of Ligia exotica Roux, 1828 (Crustacea: Isopoda: Ligiidae) from Japan, with descriptions of two new species
FIGURE 4. Ligia exotica Roux, 1828. Male, 32 mm (OMNH-Ar-12585). Scales: 0.3 mm.
FIGURE 9 in A morphological and molecular study of Ligia exotica Roux, 1828 (Crustacea: Isopoda: Ligiidae) from Japan, with descriptions of two new species
FIGURE 9. Ligia furcata sp. nov. Holotype, male, 36 mm (OMNH-Ar-12599). Scales: 0.5 mm.
FIGURE 12 in A morphological and molecular study of Ligia exotica Roux, 1828 (Crustacea: Isopoda: Ligiidae) from Japan, with descriptions of two new species
FIGURE 12. Ligia furcata sp. nov. Paratype, female, 32 mm (OMNH-Ar-12601). Scales: 1 mm.
FIGURE S2 in A morphological and molecular study of Ligia exotica Roux, 1828 (Crustacea: Isopoda: Ligiidae) from Japan, with descriptions of two new species
FIGURE S2. (Continued) B.
FIGURE S2 in A morphological and molecular study of Ligia exotica Roux, 1828 (Crustacea: Isopoda: Ligiidae) from Japan, with descriptions of two new species
FIGURE S2. (Continued) C.
Fig. 4 in Two new species of Ligia Fabricius, 1798 (Crustacea: Isopoda: Ligiidae) from coasts of the Persian and Aden gulfs
Fig. 4 Ligia persica sp. nov., male (holotype). a–d Pereiopods 1–4, respectively
Fig. 14 in Two new species of Ligia Fabricius, 1798 (Crustacea: Isopoda: Ligiidae) from coasts of the Persian and Aden gulfs
Fig. 14 Ligia yemenica sp. nov., male (holotype). a Pereiopod 5. b Pereiopod 6. c, d Pereiopod 7; d dactylus
Fig. 6 in Two new species of Ligia Fabricius, 1798 (Crustacea: Isopoda: Ligiidae) from coasts of the Persian and Aden gulfs
Fig. 6 Ligia persica sp. nov., male (holotype). a Pleopod 2. b, c Pleopod 2 endopod, distal part; b caudal surface; c rostral surface. d Penes
Fig. 3 in Two new species of Ligia Fabricius, 1798 (Crustacea: Isopoda: Ligiidae) from coasts of the Persian and Aden gulfs
Fig. 3 Ligia persica sp. nov., male (holotype). a Maxillule. b Right mandible. c Maxilla. d Maxilliped
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