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Figure 10 in An ornithological inventory in a reforested woodlot in western Paraná state, southern Brazil
Figure 10. Campylorhynchus turdinus photographed in the city of Santa Helena. Photo: Vagner Cavarzere.
Figure 1 in An ornithological inventory in a reforested woodlot in western Paraná state, southern Brazil
Figure 1. Santa Helena Relevant Ecological Interest Area in relation to the state of Paraná (A) and the counties of Diamante d'Oeste and Santa Helena (B). Green indicates remaining vegetation of over 50 ha.
Figure 3 in An ornithological inventory in a reforested woodlot in western Paraná state, southern Brazil
Figure 3. Accumulation curve of aquatic species recorded on the margins of the Santa Helena Relevant Ecological Interest Area, Santa Helena County.
Figure 4 in An ornithological inventory in a reforested woodlot in western Paraná state, southern Brazil
Figure 4. Individual of Busarellus nigricollis photographed at Santa Helena Relevant Ecological Interest Area, Santa Helena county. Photo: Vagner Cavarzere.
Figure 6 in Biological and ecological aspects of Bathygobius soporator (Valenciennes, 1837) (Perciformes, Gobiidae) from Santa Catarina, Southern Brazil
Figure 6. Gonadosomatic index (GSI) of males and females of the species B. soporator for the periods 1996-1997 (A) and 2005-2006 (B).
Figure 5 in Biological and ecological aspects of Bathygobius soporator (Valenciennes, 1837) (Perciformes, Gobiidae) from Santa Catarina, Southern Brazil
Figure 5. First maturation size (L₅₀) for males and females of B. soporator collected between the 1997-1998 and 2005-2006 periods.
Figure 2 in Biological and ecological aspects of Bathygobius soporator (Valenciennes, 1837) (Perciformes, Gobiidae) from Santa Catarina, Southern Brazil
Figure 2. Number of individuals (n) of the Bathygobius soporator species in the size classes. * significant for X² test with 1 degree of freedom.
Figure 1 in Biological and ecological aspects of Bathygobius soporator (Valenciennes, 1837) (Perciformes, Gobiidae) from Santa Catarina, Southern Brazil
Figure 1. Location of the sampling area (hatch area) at the Itajaí-açu river (Saco da Fazenda), the coast of Santa Catarina, Brazil.
Figure 4 in Biological and ecological aspects of Bathygobius soporator (Valenciennes, 1837) (Perciformes, Gobiidae) from Santa Catarina, Southern Brazil
Figure 4. Length – Weight relatioships for males (A, C) and females (B, D) of B. soporator in the 1997-1998 (A, B) and 2005-2006 (C, D) periods.
Figure 1 in Morphological description of Cyrtopleura costata (Bivalvia: Pholadidae) from southern Brazil
Figure 1. Shell and anatomic aspects of Cyrtopleura costata (MZSP 143461): (A) valves and accessory plates, external view; (B) left valve, internal view; (C) ventral whole view; (D) dorsal whole view; (E) left whole view; (F) left outer hemipalp cross section; (G) detail of location of accessory plates, anterior region, dorsal view; (H) left valve showing where flaps of mantle are inserted in region just posterior to umbo; (I) siphon in situ opening out of gallery; (J) incurrent siphon tip, opened longitudinally; (K) incurrent siphon margin detail. Scale bar: A-I = 1 cm; J, K = 1 mm.
Figure 2 in Morphological description of Cyrtopleura costata (Bivalvia: Pholadidae) from southern Brazil
Figure 2. Cyrtopleura costata general anatomy: (A) whole right view shell removed; (B) pallial cavity whole, fusion of both mantle lobes sectioned longitudinally, right mantle lobe removed; (C) digestive system in situ, right view, topologies of some adjacent structures also shown; (D) siphons, transverse section in their middle level; (E) pericardial region, dorsal view; (F) visceral ganglia lateral view; (G) cerebropleural ganglia lateral view; (H) labial palp profile in cross section; (I) flaps of mantle in region just posterior to umbo, right view; (J) transverse section of right mantle edge; (K) gill, cross section at mid-region. Scale bar: A-C, E, I = 1 cm; D, J, K = 2 mm; F, G = 1 mm; H = 200 µm.
Figure 2 in First record of invasive Stenochrus portoricensis Chamberlin, 1922 (Arachnida: Schizomida: Hubbardiidae) from the Southern region of Brazil
Figure 2. World distribution of Stenochrus portoricensis Chamberlin, 1922 (Schizomida: Hubbardiidae). (red star = new record). (Reddell & Cokendolpher, 1995), and Brignolizomus Florianópolis is a popular touristic destination in woodwardi (Harvey, 1992) and B. walteri Harvey, 2000, Brazil, currently attracting thousands of visitors from from Queensland, Australia, at around 27°34′S (Harvey, various parts of the country and around the world each 2000). In the Americas, the southernmost record of a year. Furthermore, over the past 33 years, the city′s popschizomid previously published was a single female of ulation has doubled (DATASUS, 2023). It is possible that Stenochrus portoricensis from Ubatuba, São Paulo State, S. portoricensis was inadvertently introduced by the re- Brazil, at 23°26′S (Santos et al., 2008). Our record herein is cent population growth, in addition to the intense tourfrom slightly further south in the Americas at 27°35′48″S istic activity, which might have contributed to the casual in Brazil. transportation of this species. First described in the West Indies, Stenochrus portori- The specific location where these specimens were censis has been reported worldwide (Fig. 2), including collected used to function as a composting center for several localities in Europe, e.g., Canary Islands (Martín the Federal University of Santa Catarina (UFSC). For many & Oromí, 1984; Oromí & Martín, 1992), Spain (Barranco years, this center collected organic waste from garden- et al., 2014), Czech Republic (Korenko et al., 2009), ing activities across the entire campus. Additionally, oth- Germany (Armas & Rehfeldt, 2015; Lauterbach et al., er factors like agricultural practices, the sale of ornamen- 2020), Slovakia (Christophoryová et al., 2013), England tal plants and soil materials, in addition with the parthe- (Cloudsley-Thompson, 1949), Switzerland (Krajcovicova nogenetic strategy of the species, might also have con- et al., 2021), and Poland (Zawierucha et al., 2013). Most tributed to the introduction of Stenochrus portoricensis of those records consisted of specimens collected from further south in the neotropics. greenhouses, suggesting that the specimens may have been transported along with soil or cultivated pot plants
Figure 1. Stenochrus portoricensis Chamberlin, 1922 in First record of invasive Stenochrus portoricensis Chamberlin, 1922 (Arachnida: Schizomida: Hubbardiidae) from the Southern region of Brazil
Figure 1. Stenochrus portoricensis Chamberlin, 1922 (Schizomida: Hubbardiidae), female. (A) habitus, dorsal view. (B) dorsal view of prosoma (arrows point to setal locations). (C) pedipalpal spur on trochanter (arrow points to spur). (D) spermatheca, dorsal view, rotated so anterior is to left side); (E) habitat where the specimens were collected from, Campus of the UFSC.
Figure 7 in Ecological and reproductive parameters of the seabob shrimp, Xiphopenaeus spp. (Heller, 1862) on the southern coast of the state of Espírito Santo, Brazil: potential use of less sampling effort
Figure 7. Cohen's power curve for evaluating the sample size of two samples.
Figure 4 in Population biology of the fiddler crab Uca maracoani (Crustacea, Ocypodidae) inhabiting an impacted mangrove area on the southern coast of São Paulo state, Brazil
Figure 4. Frequency of juveniles (%) of Uca maracoani by month.
Fig. 6 in Two new remarkable and endangered catfish species of the genus Cambeva (Siluriformes, Trichomycteridae) from southern Brazil
Fig. 6. Type locality of Cambeva betabelardense sp. nov.
Fig. 4 in Two new remarkable and endangered catfish species of the genus Cambeva (Siluriformes, Trichomycteridae) from southern Brazil
Fig. 4. Type locality of Cambeva alphabelardense sp. nov.
Figure 3 in Composition and dynamics of mixed flocks of birds in a remnant of Submontane Atlantic Rain Forest in southern Brazil
Figure 3. Distribution of the three sampling sectors (I, II, and III) in the study area, in Parque Nacional Aparados da Serra, municipality of Praia Grande, southern Santa Catarina state, Brazil.
Figure 1 in Composition and dynamics of mixed flocks of birds in a remnant of Submontane Atlantic Rain Forest in southern Brazil
Figure 1. Location of the study area in Parque Nacional Aparados da Serra, municipality of Praia Grande, southern Santa Catarina state, Brazil.
Figure 7 in Composition and dynamics of mixed flocks of birds in a remnant of Submontane Atlantic Rain Forest in southern Brazil
Figure 7. Monthly variation of the average size (in the number of individuals) of the mixed flocks of birds, in Parque Nacional Aparados da Serra, municipality of Praia Grande, southern Santa Catarina, Brazil, between October 2016 and September 2017.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.