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Fig. 7 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 7. CVA of EFA coefficients and mean shape outline from seven species under same group. Within each species, the specimen is enclosed by a convex hull polygon. Separation on the first two canonical analysis axes.

opencc-by-4.0Mar 2023View details →

Fig. 2 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 2. Comparisons of relative expression levels of six genes possibly higher expressed in the pectoral fins of female silver eels between the "S-Female" (n = 7, four repeats) and "S-Male" (n = 5, four repeats) groups. (A) LOC108249696, (B) LOC110515957, (C) egr3, (D) cipc, (E) LOC111853410, (F) cttn. The arp was a housekeeping gene, and two female samples (F1 and F2) were used as the internal control for calculating relative expression levels. The y-axis was in log2 scale. The "S-Female" meant the female silver eels, and the "S-Male" meant the male silver eels. The solid black line represented the median value, and the solid black circle represented the outliers. Asterisks indicated significant differences (**P <0.01, ***P <0.001) in relative expression levels between two groups.

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Fig. 1 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 1. Scheme of the MOLAS database for the Japanese eel. Annotated information of the assembled transcripts, including DNA sequence, amino acids sequence, open reading frames, signal peptides, transmembrane domains, gene ontology, hit KEGG pathway, and FPKM values, can be searched by the names of genes or the transcript ID in the Full-text search. A sequence of DNA can also be used to find the transcript with high similarity through the Sequence Search/BLAST. Moreover, the Pairwise Comparison can compare the differences in expression levels of the transcripts between two different libraries or two library groups, and then the differentially expressed genes can be summarized to a gene list. Furthermore, the Import Genelist can analyze the protein function, gene ontology enrichment, heatmap of expression, and hit terms on a KEGG pathway for a gene list. Additionally, the Clustering can be used to categorize the expressional patterns of transcripts between two different libraries or two library groups. Finally, the KEGG GlobalView and Gene List Analysis can see the hit terms of transcripts on the map of KEGG pathway and compare the different gene lists by Venn diagrams, respectively.

Fig. 5 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 5. Plot graph of PCA scores of EF coefficient, circle represent 95 percent confidence ellipses.

Fig. 3 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 3. Box-plot Mean and SE of Size Frequency, Kruskal-Wallis test, non-parametric ANOVA, of eight Donacid valid species. 1: Donax (Latona) cuneatus; 2: D. (Latona) solidus; 3: D. (Latona) faba; 4: D. (Dentilatona) incarnatus; 5: D. (Deltachion) spinosus; 6: D. (Deltachion) bruneirufi; 7: D. (Deltachion) semisulcatus semisulcatus; 8: D. (Hecuba) scortum. Double asterisks (**) highly significant at p ≤ 0.01. In square box means centroid size in group is not significantly different at p> 0.05 under Mann-Whitney pairwise comparisons.

Fig. 4. Mean outline shape constructed from 10 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 4. Mean outline shape constructed from 10 harmonics of elliptic Fourier analysis of eight Donax species from Thai waters: Donax (Latona) cuneatus (A), D. (Latona) solidus (B), D. (Latona) faba (C), D. (Deltachion) spinosus (D), D. (Dentilatona) incarnatus (E), D. (Deltachion) bruneirufi (F), D. (Deltachion) semisulcatus semisulcatus (G) and D. (Hecuba) scortum (H).

Fig. 1 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 1. The relative distribution (%) of eight Donax species along the coastline show the sampling location and the distribution pattern.

Fig. 2 in Molecular Identification, Fatty Acid Profile and Trace Elements in a Stranded Fin Whale in Sabah (Borneo, Malaysia): Implications on Migration Routes and Trophic Ecology of Southern Fin Whales.

Fig. 2. (a) The phylogenetic tree showing the stranded baleen whale (Baleen whale KP/Sabah/02082012) clustered together with the fin whale Balaenoptera physalus (U13103, Z18633 and X61145). (b) The phylogenetic analysis of the cytochrome b gene sequence indicating that the stranded fin whale (Baleen whale KP/Sabah/02082012) is closely related to the specimen of fin whales from the southern hemisphere with accession number KC572845, which represents Balaenoptera physalus quoi.

Fig. 1 in Molecular Identification, Fatty Acid Profile and Trace Elements in a Stranded Fin Whale in Sabah (Borneo, Malaysia): Implications on Migration Routes and Trophic Ecology of Southern Fin Whales.

Fig. 1. Stranding site (red-filled triangle) of the fin whale at the Sitompok River (Lat. 05°34'672"N; Long.115°39'710"E) near Kuala Penyu (KP), a coastal town overlooking the South China Sea on the western shores of Sabah (Borneo, Malaysia) (inset map). The approximate location of the sighting of possible fin whales reported by De Boer (2000) is marked with a blue-filled circle. The distribution ranges of rorquals species, including fin whales, in the Philippine waters reported by Slijper et al. (1964) and Acebes (2014) are marked with green-filled circles. The locations of fin whales' migration ranges in Australian waters according to Aulich et al. (2019) are shown using red-filled circles. The stranding site of the unconfirmed fin whale species at Pulau Sugi (Junge 1950) is indicated by a yellow-filled circle.

Fig. 4 in Molecular Identification, Fatty Acid Profile and Trace Elements in a Stranded Fin Whale in Sabah (Borneo, Malaysia): Implications on Migration Routes and Trophic Ecology of Southern Fin Whales.

Fig. 4. (a) Concentrations of trace elements (Mean ± SD) in the skin and blubber of the southern fin whale recorded in the present study compared to (b) the concentrations of trace elements in the skin of southern right whales (Eubalaena australis) extracted from the results of Martino et al. (2013).

Fig. 3 in Molecular Identification, Fatty Acid Profile and Trace Elements in a Stranded Fin Whale in Sabah (Borneo, Malaysia): Implications on Migration Routes and Trophic Ecology of Southern Fin Whales.

Fig. 3. Comparison of the percentages of fatty acid profiles for (a) SFA, (b) MUFA and (c) PUFA in the tissues of adult male (M) and female (F) southern humpback whales during the early and late migrations extracted from the results of Waugh et al. (2012), epipelagic and mesopelagic (i.e., average) fish in the South China Sea (SCS) extracted from the supplementary data of Wang et al. (2019) and the southern fin whale in the present study.

Fig. 9 in Fig. 2. 60 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 9. Venn diagram showing the number of shared operational taxonomic units (OTUs) among adult, subadult, and juvenile Asian elephants at 97% similarity.

Fig. 8 in Fig. 2. 60 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 8. Venn diagram showing the number of shared operational taxonomic units (OTUs) between male and female Asian elephants at 97% similarity.

Fig. 5. Heatmap with a in Fig. 2. 60 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 5. Heatmap with a dendogram showing dietary plant abundance at the genus level for adult, subadult, and juvenile Asian elephants. Gradient heatmap shows the 20 most abundant genera.

Fig. 4. Heatmap with a in Fig. 2. 60 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 4. Heatmap with a dendogram showing dietary plant abundance at the genus level for male and female Asian elephants. Gradient heatmap shows the 20 most abundant genera.

Fig. 3 in Fig. 2. 60 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 3. Distribution (%) of plants consumed by adult, subadult, and juvenile Asian elephants in Taman Negara National Park (TNNP) at the genus level (20 most abundant genera).

Fig. 2 in Fig. 2. 60 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 2. Distribution (%) of plants consumed by male and female Asian elephants in Taman Negara National Park (TNNP) at the genus level (20 most abundant genera).

Fig. 1 in Fig. 2. 60 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 1. Distribution (%) of plants consumed by wild Asian elephants in Taman Negara National Park (TNNP) at the genus level (> 1% abundance).

opencc-by-4.0Jun 2022View details →

Fig. 3 in Fig. 12 in Identification and Distribution of Wedge Clams (Donacidae: Bivalvia) in Thailand by Geometric Morphometric and Molecular Analysis.

Fig. 3. Ecological niche models (in gray) of the summer seasons and their projection into winter (which result as null projection); from winter with its projection to summer, we show the projected area from winter to summer in an enlarged box.