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58 results for “Fucales”
Figure 8 in Population and reproductive biology of two caprellid species (Crustacea: Amphipoda) associated to Sargassum cymosum (Phaeophyta: Fucales) on the southeast coast of Brazil
Figure 8. Frequency of females (F), males (M), ovigerous females (OF), mature females (MF) and juveniles (J) in size classes (total length in mm) of Pseudaeginella montoucheti over the studied period.
Figure 6 in Population and reproductive biology of two caprellid species (Crustacea: Amphipoda) associated to Sargassum cymosum (Phaeophyta: Fucales) on the southeast coast of Brazil
Figure 6. Monthly values of ovigerous female density (ind./g of algae) (mean ± standard error) of Paracaprella tenuis and Pseudaeginella montoucheti from October 2010 to September 2011.
Figure 7 in Population and reproductive biology of two caprellid species (Crustacea: Amphipoda) associated to Sargassum cymosum (Phaeophyta: Fucales) on the southeast coast of Brazil
Figure 7. Frequency of females (F), males (M), ovigerous females (OF), mature females (MF) and juveniles (J) in size classes (total length in mm) of Paracaprella tenuis over the studied period.
Figure 5 in Early development of Gongolaria montagnei (Fucales, Phaeophyta) germlings under laboratory conditions, with a view to enhancing restoration potential in the Eastern Mediterranean
Figure 5: Growth of Gongolaria montagnei embryos and germlings during incubation (31 days). Increase in relative growth rates (RGR) was observed in two phases (red lines), from days 8–15 (0.2 day−1) and days 21–31 (0.1 day−1).
Figure 4 in Early development of Gongolaria montagnei (Fucales, Phaeophyta) germlings under laboratory conditions, with a view to enhancing restoration potential in the Eastern Mediterranean
Figure 4: Divisions and developmental stages of Gongolaria montagnei. (A) Zygote after release from the conceptacle. (B) First division. (C) Second, most common, division. (D) Second, rare, division. (E) Development of the rhizoids (arrow). (F) Elongation of the rhizoids. (G) Fertilization membrane (arrow). (H) Hyaline apical hairs. (I) Germling after five weeks of culture. Scale bar = 100 μm.
Figure 2 in Early development of Gongolaria montagnei (Fucales, Phaeophyta) germlings under laboratory conditions, with a view to enhancing restoration potential in the Eastern Mediterranean
Figure 2: Thallus of Gongolaria montagnei during the reproductive period (A, scale bar = 3 cm), mature apical fronds (B, scale bar = 3 cm) and receptacles (C, scale bar = 2 mm).
Figure 1 in Early development of Gongolaria montagnei (Fucales, Phaeophyta) germlings under laboratory conditions, with a view to enhancing restoration potential in the Eastern Mediterranean
Figure 1: Map showing locations (marked with symbols and) where the reproductive phenology of Gongolaria montagnei was followed in sitU from February to May 2021. Mature receptacles were collected at Saronida ().
Figure 3 in Early development of Gongolaria montagnei (Fucales, Phaeophyta) germlings under laboratory conditions, with a view to enhancing restoration potential in the Eastern Mediterranean
Figure 3: Cross section of a receptacle of Gongolaria montagnei, showing antheridia (A) and oogonia (O). Scale bar = 100 μm.
Fig. 2 in Invertebrate Fauna Associated with Floating Sargassum horneri (Fucales: Sargassaceae) in the East China Sea
Fig. 2. Density of total taxa of epibionts on floating algae (A), abundance of total taxa (B), and Simpson's diversity index (C) presented as box plots. The number above each box indicates the number of examined algal rafts per station. The black line in each box shows the median and the whiskers show the range except for the outlier (black dot).
Fig. 3 in Invertebrate Fauna Associated with Floating Sargassum horneri (Fucales: Sargassaceae) in the East China Sea
Fig. 3. Correlations between number of total taxa and examined algal wet weight (A) (n=53, R2=0.21); abundance of total taxa and examined algal wet weight (B) (n=53, R2=0.41); and Simpson's diversity index and examined algal wet weight (C) (n=53, R2 = 0.10).
Figure 4 in Surveying seaweeds from the Ulvales and Fucales in the world's most frequently used artificial waterway, the Kiel Canal
Figure 4: Number of branches versus thallus height for Ulva intestinalis (A) and Ulva linza (B) collected in the Kiel Canal. Numbers indicate sampling sites and lines connect data in the sequence of sites along the canal (sites 1–16 for U. intestinalis and 9–16 for U. linza; compare Figure 1C).
Figure 3 in Surveying seaweeds from the Ulvales and Fucales in the world's most frequently used artificial waterway, the Kiel Canal
Figure 3: Morphology of material genetically identified as Ulva intestinalis collected from the Kiel Canal. Sampling sites with salinity recorded during collection are indicated. (A–B) Display the typical unbranched morphotype of U. intestinalis, whereas some specimens only exhibited branches at the thallus base (C–D); i is a close-up of thallus base of D. (E–F) Display branched forms of U. intestinalis with reduced thallus size encountered at low salinity sampling sites.
Figure 1 in Surveying seaweeds from the Ulvales and Fucales in the world's most frequently used artificial waterway, the Kiel Canal
Figure 1: Map of the study area and distribution of chemical parameters and detected species. (A) Map of the Kiel Canal (black line) in Northern Germany with location of sampling sites (arrowheads). (B) Salinity, dissolved inorganic nitrogen (DIN) and phosphate at the sampling sites 1–16 and the reference sites C1–C3 outside the canal, where only water parameters were measured. (C) Spatial distribution of Ulvales and Fucus species within the Kiel Canal. Arrows indicate major inflows of freshwater, names refer to larger towns or regions to facilitate orientation.
Figure 2 in Surveying seaweeds from the Ulvales and Fucales in the world's most frequently used artificial waterway, the Kiel Canal
Figure 2: Maximum likelihood tree inferred from tufA sequences, representing Ulvales species and their respective morphotypes, present in the Kiel Canal. Numbers at nodes refer to bootstrap values>70. Branch lengths are drawn proportionally to the amount of sequence change and GenBank accession numbers are given for all included samples. Clades containing specimens investigated within this study are highlighted in gray. Sample sites and their recorded salinity within the Kiel Canal are indicated. Samples marked with a solid circle are of unbranched morphology, those labeled with an asterisk are branched.
Figure 5 in Surveying seaweeds from the Ulvales and Fucales in the world's most frequently used artificial waterway, the Kiel Canal
Figure 5: Morphology of material genetically identified as Ulva linza collected from the Kiel Canal. Sampling sites with salinity recorded during collection are indicated. Branched and unbranched morphotypes of U. linza observed at two sampling sites with relatively high (A–B) and low (C–D) salinity are shown.
FIG. 3 in The canopy-forming alga Ericaria brachycarpa (J.Agardh) Molinari-Novoa & Guiry (Fucales, Phaeophyceae) shows seasonal and depth adaptation to the incoming light levels
FIG. 3. — Lineal fitting of the photosynthesis/PFD data at the lineal part of the P/PFD curve for the algal specimens collected at different depths.
FIG. 4 in The canopy-forming alga Ericaria brachycarpa (J.Agardh) Molinari-Novoa & Guiry (Fucales, Phaeophyceae) shows seasonal and depth adaptation to the incoming light levels
FIG. 4. — Photosynthesis at saturation (Psat), photosynthesis at low light levels (Pb) and dark respiration (Rd) for specimens thriving at 3 and 20 m (not transplanted: nt3 and nt20) and for those transplanted at the same depth (3to3 and 20to20) and at different depths (3to20 and 20to3) after 11 and 90 days after transplantation.
FIG. 1 in The canopy-forming alga Ericaria brachycarpa (J.Agardh) Molinari-Novoa & Guiry (Fucales, Phaeophyceae) shows seasonal and depth adaptation to the incoming light levels
FIG. 1. — Percentage abundance of Ericaria brachycarpa (J. Agardh) MolinariNovoa & Guiry at the sampling station estimated from 50 reticulated quadrats of 625 cm2 per depth.
FIG. 2. — C in Homogeneity of photosynthetic features in canopy-forming macroalgae of the order Fucales from shallow and sheltered environments
FIG. 2. — C:N, C:P, N:P ratios in tissues for each of the studied species. Names are abbreviations from those in Figure 1.
FIG. 1. — A in Homogeneity of photosynthetic features in canopy-forming macroalgae of the order Fucales from shallow and sheltered environments
FIG. 1. — A, photosynthesis/PFD curves for the tested algae, error bars refer to SE; B, lineal fitting of the Photosynthesis/PFD data for the tested algae at the lineal part of the curve. Cystoseira compressa stands for Cystoseira compressa subsp. pustulata (Ercegovic) Verlaque and Cystoseira foeniculacea for Cystoseira foeniculacea f. tenuiramosa (Ercegovic) A.Gómez Garreta, M.C.Barceló, M.A.Ribera & J.Rull Lluch.
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