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24 results for “Lophius”
Fig. 4 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract
Fig. 4: Length-weight relationship of L. budegassa for males (black dots), females (dark grey triangle) and undetermined (light grey square) specimens.
Fig. 7 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract
Fig. 7: Von Bertalanffy growth curves (dashed lines) for females (black) and males (grey) of L. budegassa in the study area. Dots and triangles represent observations for females and males, respectively.
Fig. 3 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract
Fig. 3: Heatmap representing the spatial distribution of blackbellied angler in terms of biomass per spatial unit, obtained from MEDITS survey data (1994-2021).
Fig. 6 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract
Fig. 6: Sections of illicia of L. budegassa (magnification 100x). Left: Female, 28.0 cm TL; Right: Female, 42.5 cm TL.
Fig. 2 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract
Fig. 2: Temporal evolution of biomass and density indices from MEDITS survey data (1994 2021). Shaded areas are standard deviations.
Fig. 8 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract
Fig. 8: Age bias plots between two readers with the mean age recorded (black points) and 95% confidence intervals (bars). Red points represent mean age estimates that differ significantly between readers.
Fig. 9. Lophius indicus Alock, 1889. A–D in Integrative taxonomy reveals unanticipated hidden diversity in the monotypic goosefish genus Lophiomus (Teleostei, Lophiidae), with description of three new species and resurrection of Chirolophius laticeps Ogilby, 1910
Fig. 9. Lophius indicus Alock, 1889. A–D. Large syntype (BMNH 1890.11.28.45). E–H. Small syntype (BMNH 1890.11.28.45.46). A. Preserved specimen, dorsal view. B. Ditto, ventral view. C. Ditto, floor of mouth. D. Ditto, X-ray radiograph. E. Preserved specimen, dorsal view. F. Ditto, ventral view. G. Ditto, floor of mouth. H. Ditto, X-ray radiograph. Photographed by L. Goodayle. © Trustees of the Natural History Museum, London (available under CC-BY 4.0).
Figure 3 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 3. - Monthly percentage of each maturity stage for males (A) and females (B) black-bellied anglerfish. Maturity stages: I, Immature; II, Maturing; III, Mature; IV, Spawning; V, Post-Spawning.
Figure 2 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 2. - Length-number distribution of Lophius budegassa sampled in the Saros Bay by commercial vessel between September 2006 and September 2008.
Figure 4 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 4. - Monthly variation of gonadosomatic index for males (A) Figure 5. - Percentage of sexually mature males (A) and females and females (B) Lophius budegassa between September 2006 and (B) Lophius budegassa according to total length. September 2008. Vertical bars represent standard error with sample size values indicated between brackets. and GSI values in females and males. Therefore, the results suggest a main spawning period from December to March decreases with increasing depth that may reflect a seasonal for blackbellied anglerfish. In females, spawning and postsegregation (García-Rodríguez et al., 2005). Laurenson et spawning stages have been seen from December to March al. (2008) found that the proportion of L. piscatorius varies and in males from January to March (Fig. 3A, B). At the same with both depth and season in Scottish waters. Several state- time, GSI values in males were high except in August and ments can explain this difference. Differentiation in growth November, while female GSI values were the highest in Janrate between sexes can cause an unbalanced proportion, uary (Fig. 4A, B). The spawning males can be seen almost all since the sex presenting faster growth rate will go through year around (Duarte et al., 2001; Landa et al., 2014), and this the most vulnerable smaller size phase quickly and, there- could increase the chances for a mature female to encounter fore decrease the predation proportion. Conversely, the sex with slower growth rate will be more likely to pass predation, with its abundance decreased disproportion- Table I. - Length at 50% maturity (L50) of Lophius budegassa obtained by other authors. ately in next development phases (Vicentini and Araújo,
Fig. 5 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract
Fig. 5: Maturity ogives for females (dark grey) and males (light grey) of L. budegassa.
Fig. 1 in On the biology of blackbellied angler, Lophius budegassa Spinola, 1807, in the north-western Mediterranean Abstract
Fig. 1: Study area. The black area showed in the frame at the top-right is GSA9.
Figure 1 in Reproductive biology of Lophius budegassa (Lophiidae) in the North Aegean Sea
Figure 1. - Map of the study area; Saros Bay, in the North Aegean Sea. ● Sampling stations.
FIGURES 10–15. Pseudalataspora lophii n in Three new species of Myxosporea (Bivalvulida: Ceratomyxidae: Alatasporidae) from the gall bladders of anglerfishes Lophius spp. (Teleostei: Lophiidae) in the Northeast Atlantic Ocean
FIGURES 10–15. Pseudalataspora lophii n. sp. 10. Young trophozoite with non-bifurcated tip, unstained fixed specimen. 11. Trophozoite with developing spores and bifurcated tip, unstained fixed specimen. 12. Spore, sutural view, stained with Giemsa. 13. Spore, sutural view, unstained fixed specimen. 14. Spore, polar view, stained with Giemsa. Scale-bars: 10μm.
FIGURE 15. Pseudalataspora lophii n in Three new species of Myxosporea (Bivalvulida: Ceratomyxidae: Alatasporidae) from the gall bladders of anglerfishes Lophius spp. (Teleostei: Lophiidae) in the Northeast Atlantic Ocean
FIGURE 15. Pseudalataspora lophii n. sp. Micrograph of sutural view of fresh spore, unstained. Scale-bar: 10μm.
FIGURES 8–9. Alataspora budegassai n in Three new species of Myxosporea (Bivalvulida: Ceratomyxidae: Alatasporidae) from the gall bladders of anglerfishes Lophius spp. (Teleostei: Lophiidae) in the Northeast Atlantic Ocean
FIGURES 8–9. Alataspora budegassai n. sp. 8. SEM of sporoblast, showing hooked free end (arrowed). 9. TEM of section of sporoblast, showing tendrils attached to wall of gall bladder (arrowed). Scale-bars: 10μm
FIGURES 1–3. Ceratomyxa lophii n in Three new species of Myxosporea (Bivalvulida: Ceratomyxidae: Alatasporidae) from the gall bladders of anglerfishes Lophius spp. (Teleostei: Lophiidae) in the Northeast Atlantic Ocean
FIGURES 1–3. Ceratomyxa lophii n. sp. 1. Trophozoite, stained with Giemsa. 2. Spore, sutural view, stained with Giemsa. 3. Spore, sutural view, unstained fixed specimen. Scale-bars: 10μm.
Data from: Complete loss of the MHC II pathway in an anglerfish, Lophius piscatorius
Genome studies in fish provide evidence for the adaptability of the vertebrate immune system, revealing alternative immune strategies. The reported absence of the major compatibility complex (MHC) class II pathway components in certain species of pipefish (genus <i>Syngnathus</i>) and cod-like fishes (order Gadiformes) is of particular interest. The MHC II pathway is responsible for immunization and defence against extracellular threats through the presentation of exogenous peptides to T helper cells. Here we demonstrate the absence of all genes encoding MHC II components (CD4, CD74 A/B, and both classical and non-classical MHC II α/β) in the genome of an anglerfish, <i>Lophius piscatorius</i>, indicating loss of the MHC II pathway. In contrast, it has previously been reported that another anglerfish, <i>Antennarius striatus</i>, retains all MHC II genes, placing the loss of MHC II in the <i>Lophius</i> clade to their most recent common ancestor. In the three taxa where MHC II loss has occurred, the gene loss has been restricted to four or five core MHC II components, suggesting that, in teleosts, only these genes have functions that are restricted to the MHC II pathway.
Clinical Validation of Lophius Biosciences Kit T-Track® CMV in Allo-HSCT Recipients
ClinicalTrials.gov study NCT02156479. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Clinical Validation of Lophius Biosciences Kit T-Track® CMV in Kidney Transplant Recipients
ClinicalTrials.gov study NCT02083042. IPD Sharing: Not stated. Countries: 1. Publications: 1.
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