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56 results for “southern Florida”
Physical Hydrologic Data for the National Audubon Society's 16 Research Sites in coastal mangrove transition zone of southern Florida, March 1986 - ongoing
Temperature, salinity and depth were continuously collected using Hydrolab/Hach sensors within the coastal mangrove transition zone at 16 sites from southern Biscayne Bay to Cape Sable. Data were collected at 12 sites within the coastal mangrove zone of Everglades National Park, incorporating the Cape Sable, Taylor River and Panhandle region. Data were collected at 4 sites within the coastal mangrove zone of southern Biscayne Bay, incorporating the Manatee Bay, Barnes Sound, and Card Sound regions. Rainfall, pH, and dissolved oxygen were collected at a number of these sites with varying periods of record.
Figs. 9–16. Genitalia. 9 in Banisia argutula (Lepidoptera: Thyrididae) is the dominant sapodilla borer in southern Florida
Figs. 9–16. Genitalia. 9, Banisia argutula male genitalia (Florida, Homestead, MGCL slide 3040); 10, B. argutula female genitalia (Florida, Homestead, MGCL slide 3074); 11, same, detail of ostium bursae and papillae anales; 12, B. myrsusalis male genitalia (Florida, Cutler Bay USDA Station, MGCL slide 3125); 13, B. myrsusalis female genitalia (same locality, MGCL slide 3124); 14, same, detail of ostium bursae and papillae anales; 15, B. argutula, detail of corpus bursae and accessory sac; 16, B. myrsusalis, detail of corpus bursae and accessory sac. ab, appendix bursae; as, accessory sac; AVIII, 8th abdominal segment; c, cornuti, cb, corpus bursae; db, ductus bursae; f, fibula; g, gnathos; la, lamella antevaginalis; msp, medial saccular process; ob, ostium bursae; p, phallus; pa, papillae anales; si, signum; sl, sacculus; u, uncus.
Figs. 1–8 in Banisia argutula (Lepidoptera: Thyrididae) is the dominant sapodilla borer in southern Florida
Figs. 1–8. Habitus of Banisia species. 1–4: Banisia argutula; 1, male, dorsal aspect (wings worn) (Florida, Homestead, TREC, 16-VI-2015, FSCA); 2, same, ventral; 3, female, dorsal aspect (Florida, Homestead,TREC, 11-VIII-2015,FSCA);4, same, ventral. 5–8: Banisia myrsusalis; 5, male, dorsal aspect (Florida, Homestead, Fuchs Hammock, 11-XII-1985, TSDC); 6, same, ventral; 7, small female, dorsal aspect (Florida, Miami, USDA ARS SHRS, 19–26-X-2015, FSCA); 8, same, ventral. Scale bars = 5 mm.
Fig. 1 in Diversity and prevalence of hemoparasites of wading birds in southern Florida, USA
Fig. 1. Plasmodium (Novyella) sp. stages observed in blood smear of a Glossy Ibis from Florida, USA that matched haplotype pMYCAME02. Representative trophozoites (*), erythrocytic meronts (arrow), macrogametocytes (double arrow), and microgametocytes (arrowhead) are marked. Some erythrocytes were infected with multiple parasites, e.g., (a) a cell with 4 trophozoites, (h) a cell with three early meronts, and (t) a cell with two early meronts. Scale bar = 10 Mm.
Fig. 2 in Description of Babesia coryicola sp. nov. from Florida pumas (Puma concolor coryi) from southern Florida, USA
Fig. 2. Genetic relationships of Babesia coryicola sp. nov. from Florida pumas (Puma concolor coryi) compared with other Babesia spp. based on near full length 18S rRNA gene sequences. The text in bold blue in the figure represents specimens analyzed in this study. Sequences in light blue are species that have been primarily associated with felid hosts. Green lineages are predominately associated with canid hosts but have been reported in felids. Several sequences derived from domestic cats (i.e., MW578972, PP151898, and PP151899) and wild felids (i.e., HQ187782 and HQ187782) were not included in the analysis because the sequences were short.
Fig. 1 in Description of Babesia coryicola sp. nov. from Florida pumas (Puma concolor coryi) from southern Florida, USA
Fig. 1. Photomicrographs of Babesia coryicola sp. nov., type-material in blood smears from FP222 Florida puma (Puma concolor coryi) (A–C) showing ring and amoeboid trophozoites and FP93 (D) showing a compact ring form.
Fig. 4 in Description of Babesia coryicola sp. nov. from Florida pumas (Puma concolor coryi) from southern Florida, USA
Fig. 4. Genetic relationships of Babesia coryicola sp. nov. from Florida pumas (Puma concolor coryi) compared with other Babesia spp. based on partial cytb gene sequences. The text in bold in the figure represents specimens analyzed in this study.
Fig. 2 in A single Haemoproteus plataleae haplotype is widespread in white ibis (Eudocimus albus) from urban and rural sites in southern Florida
Fig. 2. Typical Haemoproteus plataleae stages from three infected white ibis (Eudocimus alba) from South Florida. All ibis were genetically confirmed to be infected with the EUDRUB01 lineage. A-E, an ibis from Juno Beach urban park; F, an ibis from Indian Creek urban park; and G-L, an ibis from the Solid Waste site. The latter bird had rare round forms (K-L), which were absent from other H. plataleae-infected ibis. Younger stages (C, H, I) had a an evident 'cleft' between the gametocyote and erythrocyte nucleus.
Fig. 3 in A single Haemoproteus plataleae haplotype is widespread in white ibis (Eudocimus albus) from urban and rural sites in southern Florida
Fig. 3. Phylogenetic relationship of Haemoproteus plataleae from white ibis (Eudocimus albus) with other Haemoproteus spp.
Fig. 1 in A single Haemoproteus plataleae haplotype is widespread in white ibis (Eudocimus albus) from urban and rural sites in southern Florida
Fig. 1. Box plots of parasitemia values of Haemoproteus plataleae in white ibis (Eudocimus albus) sampled from South Florida from 2010 to 2022 by year (A.), season (B.), and age (C. and D.). C. shows all ibis with general adult vs. juvenile age class designations and D. shows data for the subset of ibis that were aged to specific year for juveniles (1, 2, or 3 yrs old). Years 2015 and 2017 were significantly different from each other, but both were similar to other years. For remaining figures, factors that are differently colored are significantly different from each other. Note that the x-axis maximum varies between plots.
Fig. 6 in Description of Babesia coryicola sp. nov. from Florida pumas (Puma concolor coryi) from southern Florida, USA
Fig. 6. Genetic relationships of Babesia coryicola sp. nov. from Florida pumas (Puma concolor coryi) compared with other Babesia spp. based on partial COX3 gene sequences. The text in bold in the figure represents specimens analyzed in this study.
Fig. 5 in Description of Babesia coryicola sp. nov. from Florida pumas (Puma concolor coryi) from southern Florida, USA
Fig. 5. Genetic relationships of Babesia coryicola sp. nov. from Florida pumas (Puma concolor coryi) compared with other Babesia spp. based on partial COI gene sequences. The text in bold in the figure represents specimens analyzed in this study.
Fig. 3 in Description of Babesia coryicola sp. nov. from Florida pumas (Puma concolor coryi) from southern Florida, USA
Fig. 3. Genetic relationships of Babesia coryicola sp. nov. from Florida pumas (Puma concolor coryi) compared with other Babesia spp. based on partial β-tubulin gene sequences. The text in bold in the figure represents specimens analyzed in this study.
Pairwise FST values for Aedes aegypti populations in Florida and southern California
<p>In the affiliated paper we compare likely the oldest populations of <i>Aedes aegypti</i> in continental North America with some of the newest to illuminate the range of genetic diversity and structure that can be found within the invasive range of this important disease vector. <i>Aedes aegypti</i> populations in Florida have likely persisted since the 1600-1700s, while populations in southern California derive from new invasions that occurred in the last ten years. For this comparison, we genotyped 1,193 individuals from 29 sites at 12 highly variable microsatellites and a subset of these individuals at 23,961 single nucleotide polymorphisms (SNPs). This dataset contains the pairwise FST values generated with both genetic datasets.</p>
SNP Data for Aedes aegypti populations in Florida and southern California
<p>In the affiliated paper we compare likely the oldest populations of <i>Aedes aegypti</i> in continental North America with some of the newest to illuminate the range of genetic diversity and structure that can be found within the invasive range of this important disease vector. <i>Aedes aegypti</i> populations in Florida have likely persisted since the 1600-1700s, while populations in southern California derive from new invasions that occurred in the last ten years. For this comparison, we genotyped 1,193 individuals from 29 sites at 12 highly variable microsatellites and a subset of these individuals at 23,961 single nucleotide polymorphisms (SNPs). This dataset contains the SNP genetic information.</p>
Microsatellite data for Aedes aegypti populations in Florida and southern California
<p>In the affiliated paper we compare likely the oldest populations of <i>Aedes aegypti</i> in continental North America with some of the newest to illuminate the range of genetic diversity and structure that can be found within the invasive range of this important disease vector. <i>Aedes aegypti</i> populations in Florida have likely persisted since the 1600-1700s, while populations in southern California derive from new invasions that occurred in the last ten years. For this comparison, we genotyped 1,193 individuals from 29 sites at 12 highly variable microsatellites and a subset of these individuals at 23,961 single nucleotide polymorphisms (SNPs).</p>
Figure 6 in New North American records of Pyraloidea (Lepidoptera: Crambidae, Pyralidae) from southern Florida
Figure 6. Neoleucinodes torvis larvae on fruit of Solanum torvum, FL, Davie, April 2013. Scale in mm.
Figure 2 in New North American records of Pyraloidea (Lepidoptera: Crambidae, Pyralidae) from southern Florida
Figure 2. Habitus: A) Nomophila triticalis (FL, Vero Beach; FSCA). B) Microthyris lelex (FL, Key Largo Hammocks St. Bot. Site, 24 Feb. 1995; TSDC). C) Ancylosis bonhoti (FL, Fuchs Hammock, 28 Dec. 1986; TSDC). D) Ancylosis balconiensis (FL, Hollywood, Port Everglades, 20/21 July 2013; FSCA). Scale bars = 5 mm.
Figure 4 in New North American records of Pyraloidea (Lepidoptera: Crambidae, Pyralidae) from southern Florida
Figure 4. Male genitalia (not to scale): A) Ennomosia basalis (FL, Monroe Co. Key Largo Hammocks State Bot. Site, 2 Mar. 1995, JEH slide 1368; TSDC). B) Neoleucinodes torvis (FL, Broward Co. Davie, 24 Apr. 2013 ex S. torvum fruit, MGCL slide 1205; FSCA). C) Lineodes triangulalis (TX, Cameron Co. Brownsville, 3 Dec. 1975, NMNH slide 114956; NMNH). D) Cangetta micralis (FL, Monroe Co. Key Largo, 9 June 1975, MGCL slide 377; FSCA). E) Nomophila triticalis (FL, Vero Beach, MGCL slide 1290; FSCA).
Figure 1 in New North American records of Pyraloidea (Lepidoptera: Crambidae, Pyralidae) from southern Florida
Figure 1. Habitus: A) Ennomosia basalis male (FL, Key Largo, March 1995; TSDC). B) E. basalis female (FL, Key Largo, March 1995; TSDC). C) Neoleucinodes torvis male (raised ex larva, FL, Davie, April 2013; FSCA). D) N. torvis female (FL, Fuchs Hammock, 27 Dec. 1991; TSDC). E) Lineodes triangulalis (FL, Bahia Honda, 8 Nov. 1991; TSDC). F) Cangetta micralis (FL, Key Largo Hammocks St. Bot. Site, 2 Feb. 1995; TSDC). Scale bars = 5 mm.
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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