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Fig. 5a, b in Morphological, ecological and toxicological aspects of Raphidiopsis raciborskii (Cyanobacteria) in a eutrophic urban subtropical lake in southern Brazil
Fig. 5a, b. Bar graphs showing the percentage of Raphidiopsis raciborskii trichomes that are vegetative cells only, with akinetes, with heterocytes, or with both heterocytes and akinetes. Data represent samples taken from the lake inflow (a) and outflow (b), every month from November 2009 to November 2010.
Figure 3 in Culex quinquefasciatus predominance during integrated mosquito surveillance in an urban area of the Brazilian Amazon
Figure 3. Number of mosquitoes by species using two sampling techniques (A) collected indoors and outdoors (B) in nine neighborhoods from the city of Porto Velho, Rondônia, Brazilian Amazon.
Figure 7 in An assessment of the urban water footprint and blue water scarcity: A case study for Van (Turkey)
Figure 7. Comparison WF and WF green of WF crop of the Van province with the Upper Tigris River Basin (Muratoglu, 2019), the worldwide blue average (Mekonnen and Hoekstra, 2011b) and the Turkish average (Mekonnen and Hoekstra, 2011a).
Figure 5 in Small mammals in the diet of Barn Owls (Tyto furcata) in an urban area in Rio de Janeiro state, Brazil, with a new record of the dwarf mouse opossum (Cryptonanus)
Figure 5. Occlusal views fo the upper molar row of the rodents (A) Holochilus brasiliensis, (B) Mus musculus, and (C) Necromys lasiurus recorded in owl pellets at Campos dos Goytacazes, Rio de Janeiro state.
Figure 2 in Small mammals in the diet of Barn Owls (Tyto furcata) in an urban area in Rio de Janeiro state, Brazil, with a new record of the dwarf mouse opossum (Cryptonanus)
Figure 2. Installations for accommodation of the Tyto furcata pair outside a residence in an urban area of Campos dos Goytacazes, RJ. (A) Waterproofed wooden box, measuring 52 x 31.5 x 37 cm (length x width x height); (B) Box with perch; and (C) Camera positioned and focused on the artificial nest and its surroundings; (D) Immediate acceptance by the Tyto furcata pair of the artificial nest after its installation. Campos dos Goytacazes, RJ.
Fig. 10. A–K, M, O. Eurytreta minor Biernat. A in Urban and Peri-urban small and medium-size Enterprise Development for sustainable Vegetable Production and Marketing Systems
Fig. 10. A–K, M, O. Eurytreta minor Biernat. A. Dorsal valve RM Br133819, exterior, × 55. B, G, K. Dorsal valve RM Br133820, interior (B, × 40), oblique lateral view (G, × 40), detail of pseudointerarea (K, × 40). C, F, J, O. Ventral valve RM Br133821, exterior (C, × 75), oblique lateral view (F, × 80), detail of larval shell (J, × 60), detail of larval pitting (O, × 500). D, M. Dorsal valve RM Br133822, interior (D, × 50) and detail of pseudointerarea (M, × 135). E. Dorsal valve RM Br133823, oblique lateral view, × 90. H. Dorsal valve RM Br133824, interior, × 38. I. Dorsal valve RM Br133825, interior, × 53. L, N. Eoconulus sp. L. Dorsal valve RM Br133826, oblique lateral view, × 60. N. Dorsal valve RM Br133827, interior, × 50. All specimens from the Tremadoc chalcedonites, Wysoczki.
Fig. 1. A–L in Urban and Peri-urban small and medium-size Enterprise Development for sustainable Vegetable Production and Marketing Systems
Fig. 1. A–L. Leptembolon cf. lingulaeformis (Mickwitz). A, E. Ventral valve RM Br133755, interior (A, × 18) and oblique lateral view of interior (E, × 32). B. Ventral valve RM Br133756, exterior; × 23. C, G, J. Ventral valve RM Br133757, interior (C, × 15), oblique lateral view (G, × 23) and detail of pseudointerarea (J, × 54). D, I. Dorsal valve RM Br133758, oblique lateral view of interior (D, × 30) and detail of pseudointerarea (I, × 46). E. Ventral valve RM Br133759, oblique lateral view of exterior; × 30. H. Dorsal valve RM Br133760, oblique lateral view of interior; × 26. K. Ventral valve RM Br133761, interior; × 37. L. Ventral valve RM Br133762, oblique lateral view of umbo; × 92. M–O. Rowellella sp. M. Dorsal valve RM Br133763, oblique lateral view of juvenile dorsal valve; × 41. N, O. Indeterminate valve RM Br133764, oblique lateral view (N, × 84) and detail of ornamentation (O, × 110). P–R. Orbithele ceratopygarum (Brøgger). P, Q. Ventral valve RM Br133765, exterior (P, × 37) and detail of larval shell (Q, × 100). R. Ventral valve RM Br133766, oblique lateral view of ventral valve exterior; × 80. All specimens from the Tremadoc chalcedonites, Wysoczki.
Fig. 3 in A report of 26 unrecorded bacterial species in Korea, isolated from urban streams of the Han River watershed in 2018
Fig. 3. Transmission electron micrographs of cells of the strains isolated in this study. Strains: 1, IMCC34901 (1.0 μm); 2, IMCC34902 (0.5 μm); 3, IMCC34903 (0.2 μm); 4, IMCC34905 (2.0 μm); 5, IMCC34906 (0.2 μm); 6, IMCC34908 (0.5 μm); 7, IMCC34909 (0.7 μm); 8, IMCC34910 (0.5 μm); 9, IMCC34912 (0.7 μm); 10, IMCC34913 (0.2 μm); 11, IMCC34914 (0.5 μm); 12, IMCC34916 (1.0 μm); 13, IMCC34917 (0.2 μm); 14, IMCC34925 (0.7 μm); 15, IMCC34926 (0.5 μm); 16, IMCC34927 (0.7 μm); 17, IMCC34928 (0.7 μm); 18, IMCC34930 (0.5 μm); 19, IMCC34933 (0.2 μm); 20, IMCC34934 (0.2 μm); 21, IMCC34935 (0.2 μm); 22, IMCC34941 (0.2 μm); 23, IMCC34942 (0.2 μm); 24, IMCC34944 (0.2 μm); 25, IMCC34946 (0.5 μm); 26, IMCC34948 (0.2 μm). Sizes of scale bars are indicated in pa- renthesis after the strain ID.
evolution of urban scaling BR
<p>This is the data used for the paper. Evolution if urban scaling: evidences for Brazil</p>
Supplementary datasets for Three years are worth 30 years of secondary succession in urban-industrial grassland restoration
<p>Data used for a manuscript sent to AVS in 2018.</p>
Figures 5-6 from: Gentile R, Cardoso TS, Costa-Neto SF, Teixeira BR, D'Andrea PS (2018) Community structure and population dynamics of small mammals in an urban-sylvatic interface area in Rio de Janeiro, Brazil. Zoologia 35: 1-12. https://doi.org/10.3897/zoologia.35.e13465
Figures 5-6 Small mammal community structure in CFMA and Pau da Fome, Rio de Janeiro, Brazil, for the (5) 2001 and (6) 2012–2015 samplings. (A, B, C, D, E, F, G, H, K, L) CFMA transects, (C1, D1, E1, F1, G1) Pau da Fome transects.
Figures 2-4 from: Gentile R, Cardoso TS, Costa-Neto SF, Teixeira BR, D'Andrea PS (2018) Community structure and population dynamics of small mammals in an urban-sylvatic interface area in Rio de Janeiro, Brazil. Zoologia 35: 1-12. https://doi.org/10.3897/zoologia.35.e13465
Figures 2-4 Plots of the Non-metric Multidimensional Scaling Analysis between the two periods and areas studied (● CFMA and Pau da Fome) for the small mammal species: (2) comparison between 2001 and 2012-2015 samplings including all transects pulled; (3) comparison among transects in 2001 (transects from A to D in disturbed forests and from E to H in peridomicile areas of CFMA; transects from C1 to G1 in disturbed forest of Pau da Fome); (4) comparison among transects for the 2012-2015 period (transects A, B, K, L in disturbed forest areas of CFMA; E1 in disturbed forest areas of Pau da Fome; C, D in peridomicile areas of CFMA; C1 and D1 in peridomicile areas of Pau da Fome; E and F in preserved forest areas of CFMA).
Figure 7 from: Gentile R, Cardoso TS, Costa-Neto SF, Teixeira BR, D'Andrea PS (2018) Community structure and population dynamics of small mammals in an urban-sylvatic interface area in Rio de Janeiro, Brazil. Zoologia 35: 1-12. https://doi.org/10.3897/zoologia.35.e13465
Figure 7 Canonical correspondence analysis (CCA) and relationship among species, transects (A, B, C, D, E, F) and habitat variables (CANO – percentage of canopy cover; TREE – number of trees with diameter at breast height ≥ 5; VCS – percentage of vegetation cover on the soil; VVO – vertical vegetation obstruction) for the 2012–2015 period in CFMA, Rio de Janeiro, Brazil.
Figure 9 from: Gentile R, Cardoso TS, Costa-Neto SF, Teixeira BR, D'Andrea PS (2018) Community structure and population dynamics of small mammals in an urban-sylvatic interface area in Rio de Janeiro, Brazil. Zoologia 35: 1-12. https://doi.org/10.3897/zoologia.35.e13465
Figure 9 Age structure of the marsupial Didelphis aurita for the 2012–2015 period in CFMA and Pau da Fome, Rio de Janeiro, Brazil.
Figure 1 from: Gentile R, Cardoso TS, Costa-Neto SF, Teixeira BR, D'Andrea PS (2018) Community structure and population dynamics of small mammals in an urban-sylvatic interface area in Rio de Janeiro, Brazil. Zoologia 35: 1-12. https://doi.org/10.3897/zoologia.35.e13465
Figure 1 Map of the study area indicating the sampling localities in CFMA and Pau da Fome region, State of Rio de Janeiro, Brazil. 1) CFMA – Peridomicile, 2–3) CFMA – Disturbed Forest, 4) CFMA – Preserved Forest, 5) Pau da Fome – Peridomicile, 6) Pau da Fome – Disturbed Forest.
Figure 8 from: Gentile R, Cardoso TS, Costa-Neto SF, Teixeira BR, D'Andrea PS (2018) Community structure and population dynamics of small mammals in an urban-sylvatic interface area in Rio de Janeiro, Brazil. Zoologia 35: 1-12. https://doi.org/10.3897/zoologia.35.e13465
Figure 8 Proportion of reproductively active females of the marsupial Didelphis aurita for the 2012–2015 period in CFMA and Pau da Fome, Rio de Janeiro, Brazil.
Supplementary material 1 from: Balzan MV, Debono I (2018) Assessing urban recreation ecosystem services through the use of geocache visitation and preference data: a case-study from an urbanised island environment. One Ecosystem 3: e24490. https://doi.org/10.3897/oneeco.3.e24490
Supplementary Information
Urban-rural collective expectations
<p>Dataset for Urban-rural collective expectations</p>
Figures 2-7 from: Back JP, Suzin A, Aguiar LM (2019) Activity Budget and Social Behavior of Urban Capuchin Monkeys (Sapajus sp.) (Primates, Cebidae). Zoologia 36: 1-10. https://doi.org/10.3897/zoologia.36.e30845
Figures 2-7 Social webs expressing interactions (in percentage of the total observation records) for each sex-age dyad of urban capuchin monkeys in each social behavior: (2) social play, n = 1,476 events; (3) grooming, n = 547; (4) threat, n = 241; (5) aggression, n = 31; (6) allocarrying, n = 193; (7) food sharing, n = 39. Percentages of emissions and receptions are in decreasing order in all columns, except for social play. Line thickness is proportional to the percentages of interactions of each dyad. (AF) adult females, (JUV) juveniles, (AM) adult male, (SUB) subadults, (INF) infants.
Figure 1 from: Back JP, Suzin A, Aguiar LM (2019) Activity Budget and Social Behavior of Urban Capuchin Monkeys (Sapajus sp.) (Primates, Cebidae). Zoologia 36: 1-10. https://doi.org/10.3897/zoologia.36.e30845
Figure 1 Proportions of records (in percentage) of behavioral categories in the activity budget of sex-age classes of urban capuchin monkeys. Boxes represent the interquartile ranges; horizontal lines within the boxes represent the medians; whiskers indicate minimum and maximum values; circles indicate the proportions of records per hour of observation. Different letters indicate significant differences between sex-age classes. Kruskal-Wallis followed by Dunn's test; p ≤ 0.05. (AF) adult females, (AM) adult male, (SUB) subadults, (JUV) juveniles.
ScienceDex guides
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.