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Supplementary material 1 from: Guilder J, Copp GH, Thrush MA, Stinton N, Murphy D, Murray J, Tidbury HJ (2022) Threats to UK freshwaters under climate change: Commonly traded aquatic ornamental species and their potential pathogens and parasites. In: Giannetto D, Piria M, Tarkan AS, Zięba G (Eds) Recent advancements in the risk screening of freshwater and terrestrial non-native species. NeoBiota 76: 73-108. https://doi.org/10.3897/neobiota.76.80215

Threats to UK freshwaters under climate change: Commonly traded aquatic ornamental species and their potential pathogens and parasites

Supplementary material 1 from: Mumladze L, Kuljanishvili T, Japoshvili B, Epitashvili G, Kalous L, Vilizzi L, Piria M (2022) Risk of invasiveness of non-native fishes in the South Caucasus biodiversity and geopolitical hotspot. In: Giannetto D, Piria M, Tarkan AS, Zięba G (Eds) Recent advancements in the risk screening of freshwater and terrestrial non-native species. NeoBiota 76: 109-133. https://doi.org/10.3897/neobiota.76.82776

Combined AS-ISK report including the 96 screenings for the 32 fish species screened for the South Caucasus

Supplementary material 1 from: Marić A, Špelić I, Radočaj T, Vidović Z, Kanjuh T, Vilizzi L, Piria M, Nikolić V, Škraba Jurlina D, Mrdak D, Simonović P (2022) Changing climate may mitigate the invasiveness risk of non-native salmonids in the Danube and Adriatic basins of the Balkan Peninsula (south-eastern Europe). In: Giannetto D, Piria M, Tarkan AS, Zięba G (Eds) Recent advancements in the risk screening of freshwater and terrestrial non-native species. NeoBiota 76: 135-161. https://doi.org/10.3897/neobiota.76.82964

Combined AS-ISK report including the 68 screenings for the 17 salmonid species screened for the Danube and Adriatic basins of Bosnia and Herzegovina, Croatia, Montenegro and Serbia (including Kosovo)

Supplementary material 2 from: Piria M, Radočaj T, Vilizzi L, Britvec M (2022) Climate change may exacerbate the risk of invasiveness of non-native aquatic plants: the case of the Pannonian and Mediterranean regions of Croatia. In: Giannetto D, Piria M, Tarkan AS, Zięba G (Eds) Recent advancements in the risk screening of freshwater and terrestrial non-native species. NeoBiota 76: 25-52. https://doi.org/10.3897/neobiota.76.83320

Combined AS-ISK report for the 24 non-native aquatic plant species screened for their potential risk of invasiveness in the Pannonian and Mediterranean regions of Croatia.

Figure 11 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species

Figure 11. Illustration showing how marine incursion could drive sea–land transition and diversification of the M. japonica complex. A, marine incursion leads to large-scale sea–land transition. B, isolation caused by subsequent marine regression drives terrestrial species diversification. C, stepping-stone dispersal maintains gene flow between different regions. Arrows show the direction of dispersal.

Figure 10 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species

Figure 10. Morinoia aosen sp. nov. female paratype, from Beijing. A, antennae I–II. B, gnathopod I. C, gnathopod II. D, propodus of gnathopod II. E, pleopod. F, the tip of spine (on the propodus of gnathopod II).

Figure 9 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species

Figure 9. The telson in Morinoia species. A, B, telson of Morinoia aosen sp. nov. C, telson of M. paludosus. D, telson of M. japonica. White arrows show the interspecific difference. Images of M. paludosus and M. japonica modified from Cheng et al. (2011).

Figure 7 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species

Figure 7. Morinoia aosen sp. nov. male holotype, from Beijing. A, pereopod III. B, pereopod IV. C, pereopod V. D, pereopod VI. E, pereopod VII.

Figure 8 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species

Figure 8. The uropod III in Morinoia species. A, B, uropod III of Morinoia aosen sp. nov. C, D, uropod III of M. japonica. E–G, uropod III of M. paludosus. White arrows show the interspecific difference and black arrows show the intraspecific difference. Images of M. paludosus and M. japonica modified from Cheng et al. (2011).

Figure 3 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species

Figure 3. Population structure of Morinoia japonica species complex based on COI haplotypes. A, minimum spanning network. Each circle represents a unique mitochondrial COI haplotype, with size proportional to frequency. B, assignment of 89 COI haplotypes to K = 5 genetic clusters inferred from STRUCTURE simulations. Colours indicate posterior probability of assignment of each individual to a particular cluster based on the combination of ten replicate runs.

Figure 4 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species

Figure 4. Morinoia aosen sp. nov. from Beijing. A, male, holotype, IZCAS-I-A1700–1, 8.5 mm. B, female, paratype, IZCASI-A1700–2, 7.6 mm.

Figure 1 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species

Figure 1. Map of East Asia showing sampling sites. Different-coloured dots correspond to different species delimited by ABGD: Morinoia aosen sp. nov. (red), M. paludosus (green), M. japonica (blue), M. sp1 (green), M. sp2 (pink), M. sp3 (light purple), M. sp4 (purple) and M. sp5 (yellow). White dots represent the coastal Platorchestia pacifica species complex.

Figure 2. A in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species

Figure 2. A, time-calibrated tree obtained from BEAST 2 based on concatenated loci. The divergence times and 95% highest posterior density are showed at nodes of interest. The sea–land transition occurred about 15.63 Mya, corresponding with the divergence between coastal Platoechestia pacifica and terrestrial Morinoia japonica. The ancestral range reconstructions from the DEC+j model in BioGeoBEARS are indicated at the internal nodes. The bars and species at the right of the tree were inferred from species delimitation based on K2P distance. B, biogeographical reconstruction of stepping-stone dispersal in M. japonica from the Japanese islands to north-eastern continental China. C, sea-level fluctuations (blue line) modified from Miller et al. (2005). The light blue vertical shading indicates the Miocene marine incursion during a high sea-level period.

Figure 6 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species

Figure 6. Morinoia aosen sp. nov. male holotype, from Beijing. A, antennae I–II. B, uropods. C, gnathopod I. D, gnathopod II. E, uropod I. F, uropod II.

Figure 5 in Sea-land transition drove terrestrial amphipod diversification in East Asia, with a description of a new species

Figure 5. Morinoia aosen sp. nov. male holotype, from Beijing. A, upper lip. B, left mandible. C, right mandible. D–E, maxilla I. F, maxilla II. G, lower lip. H, maxilliped.

Figure 3 in Ants (Hymenoptera: Formicidae) from Miocene Ethiopian amber: filling gaps in the geological record of African terrestrial biota

Figure 3. Technomyrmex svojtkai sp. nov., photomicrographs of paratype workers and additional, partial worker, specimen MAIG 6020. A, paratype 1, ventral view. B, paratype 2, dorsal view. C, paratype 2, left lateral view, anterior-oblique orientation. D, non-type, partially preserved worker, right lateral view. Scale bars: 0.25 mm.

Figure 2 in Ants (Hymenoptera: Formicidae) from Miocene Ethiopian amber: filling gaps in the geological record of African terrestrial biota

Figure 2. Technomyrmex svojtkai sp. nov. Phase contrast X-ray synchrotron microtomography of holotype worker NHMW-N6976, with indication of measurements as reported in Material and methods. A, lateral view of body with legs and antennae virtually removed, and with petiole and gaster virtually uncurled to approximate the life position. The left lateral side of the head and mesosoma being crushed, the figure shows them from the horizontally flipped right side in standard left profile view. B, reconstruction in dorsal view, without legs and antennae, and with gaster largely concealing the petiole as in approximate life position. C, head in full-face view. D, head without antennae in full-face view. E, mandibles in dorsal view. F, petiole in dorsal view, with articulation with gaster as preserved. F, gaster in ventral view, with articulation with petiole as preserved, showing the first gastral tergite concavity for accommodation of petiole. Abbreviations: AIII–AVII, abdominal segments III to VII. Scale bars: 0.5 mm, except 0.2 mm for E.

Figure 1 in Ants (Hymenoptera: Formicidae) from Miocene Ethiopian amber: filling gaps in the geological record of African terrestrial biota

Figure 1. Technomyrmex svojtkai sp. nov., holotype worker NHMW-N6976. A, photomicrograph in right lateral view, with tip of gaster curled toward the mouthparts. B, 3D model in nearly the same position, imaged by synchrotron microtomography. C–E, 3D model of body with antennae and legs virtually removed: C, anterior (frontal) view; D, left lateral view; E, posterior (dorsal) view. Scale bar: 0.5 mm. Animated versions of this are available in Supporting Information online (Figs S1, S2).

Figure 5 in Ants (Hymenoptera: Formicidae) from Miocene Ethiopian amber: filling gaps in the geological record of African terrestrial biota

Figure 5. Ravavy goldmani sp. nov., photomicrographs. A–B, holotype male NIGP180512, C–F, paratype male IGR. ET2015/001a. A, right lateral view, slightly posterodorsal–oblique orientation. B, oral view, slightly right–lateral–oblique orientation. C, dorsal view, slightly right lateral, anterior oblique orientation. D, ventral view, slightly right–lateral, posterior oblique orientation. E, right lateral, slightly ventral, anterior oblique view. F, caudal view of genitalia, slightly right lateral oblique. Scale bars: 0.5 mm for A, B, F; 1.0 mm for C–E.

Figure 4 in Ants (Hymenoptera: Formicidae) from Miocene Ethiopian amber: filling gaps in the geological record of African terrestrial biota

Figure 4. Ravavy goldmani sp. nov., holotype male NIGP180512, photomicrographs. A, left lateral view, slightly anterioroblique orientation. B, ventral view, slightly left-lateral-oblique orientation. Scale bars: 0.5 mm.