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Fig. 7 in Comparative Analysis of Complete Mitogenomes of Two Gobies and Their Phylogenetic Implication.

Fig. 7. Phylogenetic trees of goby derived from Bayesian Inference (BI) method based on 13 PCGs + 2 rRNAs. The numbers at nodes are posterior probability values. GenBank accession numbers are placed in front of species names.

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Fig. 5 in Comparative Analysis of Complete Mitogenomes of Two Gobies and Their Phylogenetic Implication.

Fig. 5. The putative origin of L-strand replication (OL) of Oxyurichthys ophthalmonema (a) and Oxyurichthys microlepis (b).

Fig. 3 in Enigmatic decline of a common fish parasite (Diplostomum spp.) in the St. Lawrence River: Evidence for a dilution effect induced by the invasive round goby

Fig. 3. Mean abundance of Diplostomum spp. in two-year old yellow perch (Perca flavescens) at sites from the three fluvial lakes of the St. Lawrence River between years before and after the establishment of the invasive round goby. Data are expressed as mean number of metacercariae of the genus Diplostomum per fish including uninfected ones ± SEM. Significant differences among years within each locality are indicated by different letters beside histograms. Fish silhouettes within graph panels highlight the presence of the invasive round goby at that given site/year(s), the icon being gray if the species was only occasionally recorded. Main ring-billed gull colonies are illustrated on the map by bird silhouettes: 1 = Cornwall; 2 = Beauharnois; 3 = ̂ILe Deslauriers; 4 = ̂Ile Lefebvre.

Fig. 5 in Enigmatic decline of a common fish parasite (Diplostomum spp.) in the St. Lawrence River: Evidence for a dilution effect induced by the invasive round goby

Fig. 5. Trends in ring-billed gull (Larus delawarensis) populations (A) and in water levels in the St. Lawrence River (B) during the study period (1998‾2016). A: The solid black curve shows the variation over time of the total number of ring-billed gulls recorded along the St. Lawrence River from Cornwall to Trois-Rivìeres whereas dotted curves depict the change in gull counts in each of the main colonies within this area. The numbered bird icons match those shown in Figs. 1 and 3: Bird 1 = Cornwall; bird 2 = Beauharnois; bird 3 = ̂ILe Deslauriers; bird 4 = ̂Ile Lefebvre. B: Monthly mean water levels in April (green) and September (gray) at the Montreal Jetty no 1 station (solid lines) and at the Summerstown station (dashed lines). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Fig. 2 in Enigmatic decline of a common fish parasite (Diplostomum spp.) in the St. Lawrence River: Evidence for a dilution effect induced by the invasive round goby

Fig. 2. Variation in Diplostomum spp. mean abundance over years in Lake St. Francis (LSF-1) in (A) one-year old yellow perch (Perca flavescens) and (B) one-year old golden shiner. Data are expressed as mean number of metacercariae of the genus Diplostomum per fish including uninfected ones ± SEM. Significant differences among years within each locality are indicated by different letters above histograms. Black fish silhouettes within graph panels illustrate the occurrence of the invasive round goby among the fish captured at that site. See Fig. 3 for site location.

Fig. 1 in Enigmatic decline of a common fish parasite (Diplostomum spp.) in the St. Lawrence River: Evidence for a dilution effect induced by the invasive round goby

Fig. 1. Temporal changes in the mean abundance of Diplostomum spp. in spottail shiners (Notropis hudsonius) (green circle) and round gobies (Neogobius melanostomus) (black square) at two sites in the St. Lawrence River. Data are expressed as mean numbers of metacercariae of Diplostomum spp. per fish including uninfected ones ± SEM. Significant differences among years within each locality are indicated by different lower-case letters (round gobies) and upper-case letters (spottail shiners). Arrows within graph panels point to year of first sighting of the invasive round goby at each site. On the background map, sampling sites (̂Ilet Vert = IVT, ̂Iles de la Paix = IPA) are identified and the host species examined are represented by different fish silhouettes (green = spottail shiners, black = round gobies). Bird silhouettes indicate where main colonies of ring-billed gulls are localized: 2 = Beauharnois; 3 = ̂ILe Deslauriers. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Fig. 6 in Enigmatic decline of a common fish parasite (Diplostomum spp.) in the St. Lawrence River: Evidence for a dilution effect induced by the invasive round goby

Fig. 6. Potential mechanisms to explain the observed sharp decline of Diplostomum spp. infection in fish in the St. Lawrence River. Those involving a dilution effect induced by the exotic round goby (Neogobius melanostomus) appears in pale red rectangles with rounded corners. Other biotic or abiotic factors are displayed in blue rectangles. Gastropod illustration, representing lymnaeid snails, is a graphic art by Tracey Saxby, provided by the Integration and Application Network (IAN), University of Maryland Center for Environmental Science (www.ian.umces.edu/imagelibrary). The bird image, used to illustrate a ring-billed gull (Larus delawarensis), is a public domain clipart downloaded from www. openclipart.org. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

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Figure 2. A photo and a in First record of the burrowing goby, Trypauchen vagina (Actinopterygii: Gobiidae), from the Iranian coast of the Persian Gulf

Figure 2. A photo and a radiograph of Trypauchen vagina, 140 mm TL from north of Qeshm Island in the Persian Gulf.

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Figure 1 in First record of the burrowing goby, Trypauchen vagina (Actinopterygii: Gobiidae), from the Iranian coast of the Persian Gulf

Figure 1. Distribution map of T. vagina recorded from the Persian Gulf. The solid square is the previously known locality (in 1985) and the open square corresponds to the new record locality at 26°56ʹN, 55°54ʹE, north of Qeshm Island.

Figure 2 in An alien species or another perspective to the freshwater gobies puzzle: a new finding in Lake Prespa

Figure 2. Economidichthys pygmaeus from Lake Prespa (a), and the perianal organ of one of the specimens (b).

Figure 1 in An alien species or another perspective to the freshwater gobies puzzle: a new finding in Lake Prespa

Figure 1. Distribution of Economidichthys sp. in western Greece (a) the location of Lake Prespa, and the sampling sites (b).

Figure 2. A in First record of the Western Greece goby - Economidichthys pygmaeus (Holly, 1929), in Greater Prespa Lake (Albania)

Figure 2. A: Photograph of a specimen of Economidichthys pygmaeus and B: Greater Prespa Lake littoral habitat (Albanian part) where the species has been captured.

Figure 1. A in First record of the Western Greece goby - Economidichthys pygmaeus (Holly, 1929), in Greater Prespa Lake (Albania)

Figure 1. A: Map of Albania and boundaries with the neighboring countries. B: Location of the sighting and capture of the specimens of Economidichthys pygmaeus.

opencc-by-4.0Dec 2015View details →

Figure 1 in First record of the chocolate shrimp-goby (Gobiidae: Cryptocentrus malindiensis) from Réunion Island with a brief description of its natural habitat

Figure 1. - Association between Cryptocentrus malindiensis and the shrimp Alpheus rubromaculatus near a lava flow of the Piton de la Fournaise, Réunion Island. A: General view; B: Close-up.

Figure 6 in What can goby otolith morphology tell us?

Figure 6. – Box plots of eight otolith variables that were useful in the separation of the recent species of the Pomatoschistus lineage and †Pomatoschistus sp. A: Ratio of otolith length and otolith height; B: ratio of sulcus length and otolith perimeter; C: Ratio of sulcus length and otolith height; D: Ratio of sulcus length and distance from sulcus end to the ventral margin; E: Ratio of sulcus height and sulcus perimeter; F: Ratio of sulcus perimeter and distance from sulcus tip to the ventral margin; G: Ratio of sulcus perimeter and distance from sulcus end to the ventral margin; H: Ratio of sulcus area and otolith area. Abbreviations: B.a., Buenia affinis; G.f., Gobiusculus flavescens; D.q., Deltentosteus quadrimaculatus; K.c., Knipowitschia croatica; P.m., Pomatoschistus marmoratus; P.q., Pomatoschistus quagga; †P. sp., †Pomatoschistus sp.

Figure 5 in What can goby otolith morphology tell us?

Figure 5. – PCA of the oxudercid lineages and †Pomatoschistus sp. based on all 23 otolith variables.

Figure 4 in What can goby otolith morphology tell us?

Figure 4. – Box plots of eight otolith variables that were useful in the separation of the five oxudercid lineages. A: Ratio of sulcus area and otolith area. B: Ratio of sulcus perimeter and otolith perimeter. C: Ratio of sulcus perimeter and distance from sulcus end to the ventral margin. D: Ratio of sulcus length and otolith length. E: Ratio of sulcus length and distance from sulcus end to the ventral margin. F: Ratio of sulcus length to otolith perimeter. G: Ratio of distance from sulcus tip to the ventral margin and distance from sulcus end to the ventral margin. H: Ratio of distance from sulcus end to the ventral margin and otolith perimeter. Abbreviations: Ac, Acanthogobius lineage; Mu, Mugilogobius lineage; Pe, Periophthalmus lineage; Po, Pomatoschistus lineage; St, Stenogobius lineage; †Po, †Pomatoschistus sp. from Brzobohatý (1994).

Figure 2 in What can goby otolith morphology tell us?

Figure 2. – Otolith morphology of the studied oxudercid species (left sagittae, inner face). Mugilogobius lineage: A: Chlamydogobius eremius ZSM-PIS-43854 (P-GO-1052). B: Stigmatogobius sadanundio ZSM-PIS-43856 (P-GO-1056). C: Brachygobius xanthozonus ZSM- PIS-43865 (P-GO-1075). D: Schismatogobius roxasi ZSM-PIS-43866 (P-GO-1077). Stenogobius lineage: E: Gobioides broussonnetii ZSM-PIS-43852 (P-GO-1048). F, G: Awaous flavus ZSM-PIS-43853 (P-GO-1051, -1050). H: Stiphodon atropurpureus ZSM-PIS-43862 (P-GO-1070). Acanthogobius lineage: I: Rhinogobius rubromaculatus ZSM-PIS-43860 (P-GO-1064). J: R. zhoui ZSM-PIS-43859 (P-GO- 1062/63-2). K: R. candidianus ZSM-PIS-43858 (P-GO-1060). L: R. formosanus ZSM-PIS-43864 (P-GO-1073). Pomatoschistus lineage: M: Pomatoschistus marmoratus NMP P6d 32/2017-7. N: Buenia affinis NMP P6d 30/2017-6. O: Gobiusculus flavescens NMP P6V 142775. P: Deltentosteus quadrimaculatus NMP P6d 34/2017-9. Periophthalmus lineage: Q: Boleophthalmus dussumieri ZM-CBSU Khamirr 38. R: Scartelaos tenuis ZM-CBSU Helleh 86. S, T: Periophthalmus waltoni ZM-CBSU Gowater 1745 (male), ZM-CBSU Gowater 1736 (female).

Figure 1 in What can goby otolith morphology tell us?

Figure 1. – Left otolith of Rhinogobius candidianus (ZSM-PIS-43858 (P-GO-1060 L)): nomenclature (A) and measurements (B). Abbreviations: OA, otolith area; OH, otolith height; OL, otolith length; OP, otolith perimeter; SuA, sulcus area; SuH, sulcus height; SuL, sulcus length; SuP, sulcus perimeter; SuEndV, distance from sulcus end to the ventral margin; SuTipV, distance from sulcus tip to the ventral margin.

Figure 3 in What can goby otolith morphology tell us?

Figure 3. – Otolith morphology of †Pomatoschistus sp. (A-C: NHM 1993/140/4, NHM 1993/140/6, NHM 1993/140/8, all three mirrored) and the studied recent species of the sand-gobies, i.e. Pomatoschistus marmoratus (D-F: NMP P6d 32/2017-4, NMP P6d 32/2017-7, NMP P6d 32/2017-1), P. quagga (G-I: NMP P6d 33/2017-4, NMP P6d 33/2017-5, NMP P6d 33/2017-7), Gobiusculus flavescens (J-L: NMP P6V 142777, NMP P6V 142778, NMP P6V 142776) and Knipowitschia croatica (M-O: NMP P6d 31/2017-7, NMP P6d 31/2017-2, NMP P6d 31/2017-3). All images show the left sagitta from the inner face.