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FIGURE A11 A–B in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia

FIGURE A11 A–B. Diodora sp. (L = 13.5 mm, H = 7.3 mm), C–D. Euchelus atratus (L = 13 mm, W = 10 mm) E–F. Neocollonia pilula (L = 5 mm, W = 4.5 mm), G. Rochia nilotica, with young on the adult, H. Tectus fenestratus (H = 17.5 mm, W = 16 mm), I–J. Trochus maculatus (L = 27.8 mm, W = 28.7 mm), K–L. Astralium calcar (L = 18.5 mm, W = 38.4 mm) with operculum, M. Acanthopleura spinosa. Scale bars: 5 mm.

FIGURE A10 A. Pteraeolidia semperi, B. Chromodoris lineolata, C in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia

FIGURE A10 A. Pteraeolidia semperi, B. Chromodoris lineolata, C. Hypselodoris cf. placida, D. Phyllidiella nigra, E. Elysia marginata, F. Elysia sp., G. Thuridilla gracilis, H. Siphonaria sp., I–J. Nerita undata (L = 21 mm, W = 14.4 mm), K–L. Nerita striata (L = 15 mm, W = 11.1 mm), M–N. Nerita winteri (L = 12.1 mm, W = 8.7 mm), O–P. Neritodryas dubia (L = 14.9 mm, W = 9.8 mm), Q. Eoacmaea sp. (L = 9.3 mm, W = 4 mm), R–S. Diodora mus (L = 13.4 mm, W = 5.8 mm). Scale bars: 5 mm.

FIGURE A9 A–B in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia

FIGURE A9 A–B. Chicoreus strigatus (L = 25.2 mm, W = 12.1 mm), C–D. Drupella margariticola (L = 26.4 mm, W = 13 mm) from Papua 11 and Papua 15, E–F. Drupella margariticola (L = 21.8 mm, W = 12.3 mm) from Papua 21, form living in a marine lake without coral growth, G. Stylocheilus striatus, H. Diniatys monodonta (L = 5.2 mm, W = 3.2 mm), I–J. Auriculastra semiplicata (L = 16.9 mm, W = 5.3 mm), K. Melampus adamsianus (L = 9.7 mm, W = 5.2 mm), L–M. Melampus Downloadedfasciatus from (BrillL. = com 7.4 mm 06/, 21W / = 2024 06:27:04PM 5.2 mm), N. Melampus sculptus (via L =Open 11.3mm, AccessW. = 5.4 Thismm is), anO.open Melampus accesssp. (L article= 7.2 mm, distributedW = 4.5under mm), the terms of the CC BY 4.0 license. P–Q. Pythia pantherina (L = 11.3 mm, W = 7.1 mm). Scale bars: 5 mm https.://creativecommons.org/licenses/by/4.0/

FIGURE A4 A–B in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia

FIGURE A4 A–B. Alectryonella plicatula (L = 58.2 mm, H = 56.6 mm), C. Lopha cristagalli, D. Saccostrea sp., E. Saccostrea cucullata, F–G. Isognomon ephippium (L = 65 mm, H = 64 mm), H. Isognomon isognomum. Scale bars: 10 mm.

FIGURE A8 A–B in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia

FIGURE A8 A–B. Monetaria moneta (L = 28.9 mm, W = 19.8 mm), C–D. Naria miliaris, E–F. Littoraria scabra (L = 13 mm, W = 7.4 mm), G. Thylacodes sp., H. Nassarius graphiterus, I. Nassarius olivaceus, J–K. Reticunassa cf. paupera (L = 7.1 mm, W = 3.8 mm), L–M. Pollia undosa (L = 23.9 mm, W = 12.8 mm), N–O. Pollia fumosa (L = 19.1 mm, W = 11 mm). Scale bars: 5 mm. Downloaded from Brill.com 06/21/2024 06:27:04PM via Open Access. This is an open access article distributed under the terms of the CC BY 4.0 license. https://creativecommons.org/licenses/by/4.0/

FIGURE A3 A–C in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia

FIGURE A3 A–C. Brachidontes sp. (L = 35.3 mm; H = 17.7 mm) from Papua 21, D–F. Brachidontes sp. (L = 10.6 mm; H = 6.6 mm) from Papua 22, G–I. Brachidontes ustulatus (L= 40 mm; H = 17.3 mm) from Papua6, J–L. Brachidontes ustulatus (L = 28.4 mm; H = 12.5 mm) from Papua 18, M. Septifer bilocularis (L = 31.9 mm; H = 18.9 mm) from Papua11, N–O. Septifer bilocularis (L = 26.6 mm, W = 23.2 mm) from Papua15. Scale bars: 5 mm.

FIGURE A1 A–B in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia

FIGURE A1 A–B. Acar plicata (L = 16.1 mm; H = 8.4 mm), C–D. Barbatia amygdalumtostum (L = 48.8 mm, H = 26.6 mm), E–F. Barbatia trapezina (L = 35.1 mm; H = 21.9 mm), G–H. Lamarcka ventricosa (L = 39.6 mm, H = 17.6 mm), I–J. Striarca symmetrica (L = 15 mm; H Downloaded= 11 mm from). Scale Brill.com bars: 5 06/ mm 21/. 2024 06:27:04PM via Open Access. This is an open access article distributed under the terms of the CC BY 4.0 license. https://creativecommons.org/licenses/by/4.0/

FIGURE A2 A–B. Tridacna squamosa, C–D in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia

FIGURE A2 A–B. Tridacna squamosa, C–D. Cardita pica (L = 25 mm, H = 8.1 mm), E–G. Cardita variegata (L = 33.4 mm, H = 14.5 mm), H-J. Ctena bella (L = 13.4 mm, H = 12 mm), K–M. Brachidontes striatulus. Scale bars: 5 mm. Downloaded from Brill.com 06/21/2024 06:27:04PM via Open Access. This is an open access article distributed under the terms of the CC BY 4.0 license. https://creativecommons.org/licenses/by/4.0/

FIGURE 3 in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia

FIGURE 3 Pearson correlations among species richness of molluscs and (A) connectivity of marine lakes to the adjacent sea, and (B) surface area of marine lakes.

FIGURE A6 A–B in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia

FIGURE A6 A–B. Cerithium coralium (L = 18.5 mm, W = 6.64 mm) from medium connected lake Papua 3, C–D. Cerithium coralium dwarf form (L = 9.5 mm, W = 4.4 mm) from low connected lake Papua 7, E. Cerithium coralium (L = 27 mm, W = 11.3 mm) from high connected lake Papua 11, F. Clypeomorus batillariaeformis, G–H. Cerithium zonatum (L = 23.5 mm, W = 9.5 mm). Scale bars: 5 mm.

FIGURE 2 in The diversity of molluscan faunas in marine lakes of Raja Ampat, West Papua, Indonesia

FIGURE 2 The percentage of feeding types of mollusc species from 11 lakes with the total number of species at the top of the graph. Lakes are ordered by degree of connection to the surrounding sea, ranging from low connection (left) to high connection (right).

FIGURE 8 in The Sea Slug Phanerophthalmus luteus (Gastropoda: Opisthobranchia) and its Habitat and Ecology at the Marine Jellyfish Lake (Ongeim'l Tketau), Palau, Western Pacific Ocean

FIGURE 8. Central and Western Pacific showing the distribution of Phanerophthalmus luteus (black stars) and the location of Jellyfish Lake, Palau (large gray star). Modified from distribution map for P. luteus in Austin, Gosliner, and Malaquias (2018, fig. 23).

FIGURE 5 in The Sea Slug Phanerophthalmus luteus (Gastropoda: Opisthobranchia) and its Habitat and Ecology at the Marine Jellyfish Lake (Ongeim'l Tketau), Palau, Western Pacific Ocean

FIGURE 5. Hydrography of Jellyfish Lake. The water column is divided into an oxic and an anoxic zone by a bacterial plate that creates a chemo- and thermocline. The bacteria absorb all the light and digest most of the vegetation (except larger branches). No foraminifera or animals are known to live below the bacterial plate due to the absence of oxygen in the water column. Phanerophthalmus luteus is restricted to the upper 3 to 10 m in the oxygenated part of the water column; they are most abundant between 4.5 and 7.6 m. Figure modified from Venkateswaran et al. (1993) by adding the depth distribution of P. luteus.

FIGURE 4 in The Sea Slug Phanerophthalmus luteus (Gastropoda: Opisthobranchia) and its Habitat and Ecology at the Marine Jellyfish Lake (Ongeim'l Tketau), Palau, Western Pacific Ocean

FIGURE 4. Bathymetry of Jellyfish Lake, Mecherchar Island. The gray line with arrows indicates the area in the lake of our marine survey to 10 m deep for sea slugs along the north and east sides of the lake. Black circles indicate the transect and collecting stations for foraminifera used to estimate the depth distribution of Phanerophthalmus luteus. Map and transect from Lipps and Langer 1999.

FIGURE 3 in The Sea Slug Phanerophthalmus luteus (Gastropoda: Opisthobranchia) and its Habitat and Ecology at the Marine Jellyfish Lake (Ongeim'l Tketau), Palau, Western Pacific Ocean

FIGURE 3. Vegetation of Jellyfish Lake, Mecherchar Island. A. The lake, slightly less than 400 m long, is in a hole at least 230 m deep (150 to 200 m from the top of the hole to the Lake's surface and 30 m to the bottom of the lake) in the Miocene limestone. North is at the top of the image. B. Dense terrestrial vegetation, including mangroves at the lake edges, hangs over the lake. The surrounding vegetation contributes organic debris to the lake. C. Bottom of the lake from 0 to 13 m is covered with plant debris and algal growth. Photograph is at 2 m deep looking down slope. D. One of many logs that have fallen into the lake and are now inhabited by a wide variety of algae and animals including P. luteus. View is down the log from a depth of about 0.5 m. Credits: A. Aerial photograph courtesy of Dr. Pat Colin. B.-D. Photographs by Jere H. Lipps, 2013.

FIGURE 7 in The Sea Slug Phanerophthalmus luteus (Gastropoda: Opisthobranchia) and its Habitat and Ecology at the Marine Jellyfish Lake (Ongeim'l Tketau), Palau, Western Pacific Ocean

FIGURE 7. Egg masses (more or less spherical to oblong white objects) of Phanerophthalmus luteus attached to filamentous and other algae on a slope in Jellyfish Lake. Photograph taken November 16, 2009, courtesy of Lori J. Bell.

Fig. 7 in Phylogeny, palaeoecology, and invasion of non-marine waters by the late Miocene hemicytherid ostracod Tyrrhenocythere from Lake Pannon

Fig. 7. Length (l) and height (h) ratio of early Tyrrhenocythere species from Pezinok (Danube Basin). The male valves are longer than the female ones.

Fig. 6 in Phylogeny, palaeoecology, and invasion of non-marine waters by the late Miocene hemicytherid ostracod Tyrrhenocythere from Lake Pannon

Fig. 6. Marginal pore canals on anterior margin and their transformation from straight Hemicytheria arrangement to brush−like Tyrrhenocythere one. A. Hemicytheria reniformis (Reuss, 1850), Hemicytheria folliculosa (Reuss, 1850), Hemicytheria omphalodes (Reuss, 1850), original by author. B. Hemicytheria biornata (Zalányi, 1944), original by author, Hemicytheria maeotica Olteanu 1989 after Olteanu and Vekua (1989). C. Hemicytheria major Sokač, 1972. D. Hemicytheria marginata Sokač, 1972 after Sokać (1972). E. Tyrrhenocythere transitivum sp. nov. F. Tyrrhenocythere pezinokensis (Jiříček, 1985). G. Tyrrhenocythere rastislavi sp. nov. original by author.

Fig. 2 in Phylogeny, palaeoecology, and invasion of non-marine waters by the late Miocene hemicytherid ostracod Tyrrhenocythere from Lake Pannon

Fig. 2. Geographical sketch (A) and lithological column (B) of Pezinok clay pit (Pipík 1998). C. Detail of the sequence with Tyrrhenocythere mirror swamps and shallow water sedimentation on the bord of freshwater−/miohaline lake (Baráth et al. 1999).

Fig. 5. Late Miocene hemicytherid ostracods from the layer 36 in Phylogeny, palaeoecology, and invasion of non-marine waters by the late Miocene hemicytherid ostracod Tyrrhenocythere from Lake Pannon

Fig. 5. Late Miocene hemicytherid ostracods from the layer 36+37A in Pezinok, Slovakia. A–C, I, L. Tyrrhenocythere transitivum sp. nov. A. RV♂, paratype, SNM RP27−21, external lateral view. B. LV♂, paratype, SNM RP27−18, external lateral view. C. LV♀, paratype, SNM RP26−4−4, external lateral view. I. LV♀, paratype, SNM RP27−19, internal lateral view; I1, central muscle scars; I2, detail of hinge. L. RV♀, paratype, SNM RP27−22, internal lateral view, detail of hinge. D. Tyrrhenocythere sp. 1, RV, SNM RP27−2, external lateral view; D1, SEM photo; D2, valve in transparent light. F. Tyrrhenocythere sp. 2, RV♀, SNM RP28−2, external lateral view. G, J. Tyrrhenocythere pezinokensis (Jiříček, 1985). G. LV♀, SNM RP27−8, internal lateral view, G1, central muscle scars; G2, detail of hinge. J. RV♀, paratype, SNM RP27−5, internal lateral view, detail of hinge. E, H, K. Tyrrhenocythere rastislavi sp. nov. E. RV♂, paratype, SNM RP26−16−1, external lateral view. H. RV♀, paratype, SNM RP27−15, internal lateral view; H1, central muscle scars; H2, detail of hinge. K. LV♀, paratype, SNM RP27−12, internal lateral view, detail of hinge.