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Figure 4 in Breeding biology, diet and vocal repertoire of White-rumped Monjita Xolmis velatus

Figure 4. Seasonality in breeding records of White-rumped Monjita Xolmis velatus in Brazil based on citizen science data, the literature and this study.

Figure 3 in Breeding biology, diet and vocal repertoire of White-rumped Monjita Xolmis velatus

Figure 3. Food delivered to nestlings of White-rumped Monjita Xolmis velatus, Rio Claro, São Paulo, Brazil. A: larva, B: Oligochaeta, C: Erythemis vesiculosa, D: Zammara tympanum, E: Lepidoptera (moth), F: Blattodea, G: Myriapoda, H: Kentropyx aff. paulensis (Luiz Carlos Ramassotti)

Figure 2 in Breeding biology, diet and vocal repertoire of White-rumped Monjita Xolmis velatus

Figure 2. Food delivered to nestlings of White-rumped Monjita Xolmis velatus, Rio Claro, São Paulo, Brazil. A‒C = Scarabaeidae; D = Grylloidea; E = Ensifera; F = Tettigoniidae, Conocephalinae, Copiphorini; G‒H = Lycosidae (Luiz Carlos Ramassotti)

Figure 1 in Breeding biology, diet and vocal repertoire of White-rumped Monjita Xolmis velatus

Figure 1. Nests of White-rumped Monjita Xolmis velatus. A: nest 1 with nestlings, Analândia, São Paulo, Brazil, 15 November 2008 (Rogério Carlos Machado); B: nest 2 with eggs, Marília, São Paulo, Brazil, 23 October 2010 (Manuel Gonzales); C‒F: nest 3, Rio Claro, São Paulo, Brazil; C: adult at entrance to PVC pipe, 20 October 2021 (Luiz Ramassotti); D: nest, 29 October 2021 (Carlos Otávio Araujo Gussoni); E: nest with nestlings, 20 October 2021 (Carlos Otávio Araujo Gussoni); F: nestling, 22 October 2021 (Carlos Otávio Araujo Gussoni)

Figure 5 in Breeding biology, diet and vocal repertoire of White-rumped Monjita Xolmis velatus

Figure 5. Begging calls of a fledgling (A) and calls of an adult (B) White-rumped Monjita Xolmis velatus. Sonogram made using software Raven Pro 1.6.1 (Center for Conservation Bioacoustics 2019).

Figure 2 in Biology, pathotype, and virulence of Globodera rostochiensis populations from Kenya

Figure 2: Figure showing the mean number of different developmental stages of Globodera rostochiensis, of 'HAR1' and 'Ecosse' populations in resistant cv. 'Laura' and susceptible cv. 'Désirée' in the glasshouse in the second experiment.

Figure 1 in Biology, pathotype, and virulence of Globodera rostochiensis populations from Kenya

Figure 1: Figure showing the mean number of different developmental stages of Globodera rostochiensis, 'HAR1' and 'Ecosse' populations in resistant cv. 'Laura' and susceptible cv. 'Désirée' in the glasshouse during the first experiment.

Figure 4 in Biology, pathotype, and virulence of Globodera rostochiensis populations from Kenya

Figure 4: Percentage hatch of Globodera rostochiensis 'HAR1' population in PRD for three successive generations of cysts without diapause. Vertical bars are mean percentage ± standard error (n = 4).

Figure 3 in Biology, pathotype, and virulence of Globodera rostochiensis populations from Kenya

Figure 3: Mean reproduction factor (±SE) of six populations of Globodera rostochiensis from Kenya on the susceptible cultivar 'Désirée' for three successive generations without diapause. Vertical bars show the standard error of the mean (n = 6). Means within a population with the same small letter are not significantly different (p> 0.05).

Figure 2 in Notes on the breeding biology of birds in riverine floodplains of western Amazonia

Figure 2. Plain-winged Antshrike Thamnophilus schistaceus fledgling, Rondônia, Brazil, June 2018 (Tomaz Nascimento de Melo)

Figure 6 in Notes on the breeding biology of birds in riverine floodplains of western Amazonia

Figure 6. Nest and eggs of Euler's Flycatcher Lathrotriccus euleri in a dried cocoa Theobroma cacao fruit (Malvaceae), Rondônia, Brazil, September 2017 (Tomaz Nascimento de Melo)

Figure 5 in Notes on the breeding biology of birds in riverine floodplains of western Amazonia

Figure 5. Nest of Spotted Tody-Flycatcher Todirostrum maculatum constructed on the root of a Capsiandra sp. (Fabaceae) near the Madeira River, Rondônia, Brazil, July 2018 (Tomaz Nascimento de Melo)

Figure 4 in Notes on the breeding biology of birds in riverine floodplains of western Amazonia

Figure 4. Nest of Specked Spinetail Cranioleuca gutturata in floodplain várzea forest, Rondônia, Brazil, June 2018 (Tomaz Nascimento de Melo)

Figure 1 in Notes on the breeding biology of birds in riverine floodplains of western Amazonia

Figure 1. White-bearded Hermit Phaethornis hispidus nest with two nestlings, Rondônia, Brazil, June 2018 (Tomaz Nascimento de Melo)

Fig. 13 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 13: The effect of hydrodynamics inside the Y-Cave, the location behind section B-B' (Fig. 2) at 5.5 m of depth, where the unusually coloured sediment sample was collected for analysis.

Fig. 12 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 12: Limestone tablets from the three representative sites after the 1-year exposure period: A) with bioaccumulation at site 1; B) corroded at site 3; C) abraded at site 6 (Fig. 3, Tab. 1).

Fig. 11 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 11: Cave features: A) stalactites in the chamber with the air pocket (section C-C'); B) submerged stalagmites and flowstones with a lack of marine cave biota (section C-C'); C) submerged scallops (asymmetrical, cuspate, oyster-shell-shaped dissolution depressions in the cave walls used as an indicator of flow direction; Murphy, 2012), (section D-D'); D) corroded cave walls (section F-F').

Fig. 5 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 5: The annual variation of temperature along the Y-Cave (from August 23–27, 2003 to July 4/October 8, 2004). Measurement positions are given in Fig. 3 and depths in Table 1.

Fig. 10 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 10: The mass (m.f.) and volume fractions (v.f.) of four sediment categories in the sediment sample collected behind section B-B' (Fig. 2), at 5.5 m of depth inside the Y-Cave; A) detrital terrigenous sediment>4 mm, B) mixed biogenic and terrigenous detritus, C) shells of gastropod Homalopoma sanguineum, D) other biogenic material – shells, tests and skeletons of other marine organisms.

Fig. 4 in Biological response to geochemical and hydrological processes in a shallow submarine cave

Fig. 4: Living communities inside the Y-Cave: A) the entrance part of the cave, vertical wall, depth 9 m, biocenosis of semi-dark caves (GSO, see text for explanation of acronym) dominated by numerous sponge species; B) the entrance part of the cave, ceiling, depth 6 m, GSO dominated by scleractinian coral Leptopsammia pruvoti; C) the entrance part of the cave, overhang, depth 7 m, GSO dominated by scleractinian coral Madracis pharensis; D) the entrance part of the cave, vertical wall (near the bottom), depth 9 m, GSO, a large specimen of the orange sponge Agelas oroides dominates the photo; E) the middle part of the cave, in front of the section C-C', bottom, depth 10 m, a massive white specimen of the sponge Chondrosia reniformis; F) the middle part of the cave, between sections C-C' and D-D', vertical wall and overhang, depth 5 m, the transition from GSO to biocenosis of caves and ducts in total darkness (GO, see text for explanation of acronym), the community is dominated by serpulids; G) the middle part of the cave, between sections C-C' and D-D', vertical wall, depth 5 m, transition from GSO to GO, a dense population of brachiopod Novocrania anomala, encrusting sponge Placospongia decorticans and serpulids; H) the end part of the cave, near the section G-G', vertical wall with overhang and horizontal shelf, depth 6 m, GO with scarce calcareous sponges and serpulids (see Fig. 2 for position of the sections).