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Fig. 12. Atergatopsis germaini A. Milne Edwards, 1865 in Atergatis Subdentatus (De Haan, 1835), Atergatopsis Germaini A. Milne Edwards, 1865 And Platypodia Eydouxi (A. Milne Edwards, 1865) (Crustacea: Decapoda: Xanthoidea: Xanthidae: Zosiminae) - First Stage Zoeal Descriptions With Implications For The Subfamily

Fig. 12. Atergatopsis germaini A. Milne Edwards, 1865 first stage zoea; a) dorsal view of abdomen; b) lateral view of abdomen.

Fig. 4 in Atergatis Subdentatus (De Haan, 1835), Atergatopsis Germaini A. Milne Edwards, 1865 And Platypodia Eydouxi (A. Milne Edwards, 1865) (Crustacea: Decapoda: Xanthoidea: Xanthidae: Zosiminae) - First Stage Zoeal Descriptions With Implications For The Subfamily

Fig. 4. Atergatis floridus (Linnaeus, 1767) first stage zoea; a) dorsal view of abdomen; b) lateral view of abdomen.

Fig. 5 in Atergatis Subdentatus (De Haan, 1835), Atergatopsis Germaini A. Milne Edwards, 1865 And Platypodia Eydouxi (A. Milne Edwards, 1865) (Crustacea: Decapoda: Xanthoidea: Xanthidae: Zosiminae) - First Stage Zoeal Descriptions With Implications For The Subfamily

Fig. 5. Atergatis subdentatus (de Haan, 1835) first stage zoea; a) anterior view of carapace; b) antennule; c) antenna; d) rostral spine.

Fig. 1 in Atergatis Subdentatus (De Haan, 1835), Atergatopsis Germaini A. Milne Edwards, 1865 And Platypodia Eydouxi (A. Milne Edwards, 1865) (Crustacea: Decapoda: Xanthoidea: Xanthidae: Zosiminae) - First Stage Zoeal Descriptions With Implications For The Subfamily

Fig. 1. Atergatis floridus (Linnaeus, 1767) first stage zoea; a) anterior view of carapace; b) rostral spine; c) antennule; d) antenna.

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Figure 3. A in The emigration of peoples from the area of Western Bosnia and Herzegovina during the Balkans civil conflict and implications for the Avifauna (Case study Pašića polje at Bosansko Grahovo)

Figure 3. A) The settlements located between arable land and pastures. B) Pastures – landscapes in which livestock grazing co-occurs with scattered trees and shrubs

Fig. 5 in Host associations of gall-inducing Prodiplosis longifila (Diptera: Cecidomyiidae) from Bolivia: implications for its use as a biological control agent for Jatropha gossypiifolia (Euphorbiaceae)

Fig. 5. Susceptibility of Jatropha gossypiifolia to Prodiplosis longifila. Morphologically similar galls induced on control Jatropha clavuligera (A) and Jatropha gossypiifolia (B) plants under no-choice conditions in quarantine in Pretoria, South Africa. Galling on a transplanted Jatropha gossypiifolia plant under the natural field conditions in Bolivia (C).

Fig. 4 in Host associations of gall-inducing Prodiplosis longifila (Diptera: Cecidomyiidae) from Bolivia: implications for its use as a biological control agent for Jatropha gossypiifolia (Euphorbiaceae)

Fig. 4. Relationship between the number of branches per plant and number of shoot tips with Prodiplosis longifila galls (A) and percentage of shoots (± SE) with Prodiplosis longifila galls (B) across 3 sites in Bolivia in Feb 2016. Different letters above SE bars indicate significant differences (Tukey's test, P <0.001).

Fig. 3 in Host associations of gall-inducing Prodiplosis longifila (Diptera: Cecidomyiidae) from Bolivia: implications for its use as a biological control agent for Jatropha gossypiifolia (Euphorbiaceae)

Fig. 3. Incidence of Prodiplosis longifila galls on Jatropha clavuligera (percentage of plants with galls) in relation to (A) sites and (B) sampling yr and season (± SE). Different letters above SE bars indicate significant differences (Tukey's test, P <0.001).

Fig. 1 in Host associations of gall-inducing Prodiplosis longifila (Diptera: Cecidomyiidae) from Bolivia: implications for its use as a biological control agent for Jatropha gossypiifolia (Euphorbiaceae)

Fig. 1. Rosette galls induced by Prodiplosis longifila in the growing shoot tip of Jatropha clavuligera. (A) Rosette gall in the terminal and axillary buds of Jatropha clavuligera with swollen petiole and rachis and malformed leaves. (B) Young gall in Jatropha clavuligera showing early stage larvae feeding on the nutritive tissue of the gall with no evidence of cell necrosis and fungal growth.

Fig. 2 in Host associations of gall-inducing Prodiplosis longifila (Diptera: Cecidomyiidae) from Bolivia: implications for its use as a biological control agent for Jatropha gossypiifolia (Euphorbiaceae)

Fig. 2. Morphological and histological changes in the rosette galls induced by Prodiplosis longifila on Jatropha clavuligera. (A) Vertical sectional view of a portion of the galled shoot showing the inflamed axillary position (*) (bar = 1 mm). (B) Cross sectional view of a portion of the galled shoot showing the hyperplasied stems and leaves (bar = 0.33 mm); * indicates the location where the larvae congregate; le = leaf. (C) Cross sectional view of a galled leaf showing the intense hyperplasied upper mesophyll (bar = 0.18 mm); arrows point to the hypertrophied epidermis. (D) Cross sectional view of a leaf axil (bar = 0.33 mm); * indicates the location where the larvae congregate; note the vertically dividing epidermal cells towards the bottom, whereas the laterally occurring epidermal cells are hypertrophied. (E) Cross sectional view of the stem showing variously dividing cortical cells (bar = 30 μm); the arrow indicates cell proliferation. (F) Compactly arranged parenchymatous nutritive cells, each with a prominent nucleus (n) and dense cytoplasm (cyt) (bar = 10 μm). (G) Low magnification image of galled stem showing layers of nutritive cells (nc), where the larvae feed (lfs) (bar = 30 μm). In fact, the cells lying opposite, which appear to be empty, show signs of regeneration (rc). In the far interior of the stem cortex, numerous phenol-included cells (pic) occur. Far interior into the stem cortex numerous phenol including cells (pic) occur. (H) An enlarged view of a phenol-including cell (bar = 18 μm).

Fig. 9 in Modelling the distribution of the Ocellated Lizard in France: implications for conservation

Fig. 9. Areas within the potential niche of the Ocellated Lizard (in orange) for which there are no observation data (in red), based on Model 6 with its presence probability threshold of 0.70 combined with presence data from observations including a buffer zone with a 5-km radius.

Fig. 5 in Modelling the distribution of the Ocellated Lizard in France: implications for conservation

Fig. 5. Change in vegetation cover from 2000 to 2016: standard deviation of the yearly NDVI values relative to the NDVI mean value for the month of July.

Fig. 3 in Modelling the distribution of the Ocellated Lizard in France: implications for conservation

Fig. 3. Localization of the total presence data for the Ocellated Lizard Timon lepidus collected in France during the period 1970 to 2016.

Fig. 8 in Modelling the distribution of the Ocellated Lizard in France: implications for conservation

Fig. 8. Location of populations that have disappeared in relation to the predicted presence map generated by Model 6 (blue dots).

Fig. 7 in Modelling the distribution of the Ocellated Lizard in France: implications for conservation

Fig. 7. The predicted distribution map generated by Model 6 (in pink) with specific locations of presence data (from observations) from the dataset (black dots).

Fig. 6 in Modelling the distribution of the Ocellated Lizard in France: implications for conservation

Fig. 6. Predictive modelling maps showing presence probability of the Ocellated Lizard (Timon lepidus) in the study area.

Figure 10 in Modelling the distribution of the Ocellated Lizard in France: implications for conservation

Figure 10: Contribution of protected nature areas to the conservation of Timon lepidus. Predicted presence within protected areas (dark purple) and predicted distribution range (light purple).

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Figure 2. - K2P in Range extension of Gerres infasciatus (Perciformes: Gerreidae) from the Red Sea and the Arabian Gulf, with distributional implications for the G. filamentosus complex

Figure 2. - K2P distance neighbouring-joining tree of COI sequences (615 bp) of gerreid species in the Gerres filamentosus complex; G. oyena used as outgroup.

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Figure 1. - Gerres filamentosus complex. A in Range extension of Gerres infasciatus (Perciformes: Gerreidae) from the Red Sea and the Arabian Gulf, with distributional implications for the G. filamentosus complex

Figure 1. - Gerres filamentosus complex. A: Gerres infasciatus. SMF 35412, 99.5 mm SL, off Jizan, Saudi Arabia, Red Sea; B: G. microphthalmus, NSMT-P 45901, holotype, female, 189 mm SL, Kyushu, Japan; C: G. macracanthus, SMF 35037, 98 mm SL, off Jizan, Saudi Arabia, Red Sea; D: G. filamentosus, KAUMI 12250, 139 mm SL, off Sabah, Borneo Island, Malaysia. Photographs (A, C) were taken by S.V. Bogorodsky and (D) by M. Matsunuma.