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155 results for “South Florida”
Data from: Homing of invasive Burmese pythons in South Florida: evidence for map and compass senses in snakes
Navigational ability is a critical component of an animal's spatial ecology and may influence the invasive potential of species. Burmese pythons (Python molurus bivittatus) are apex predators invasive to South Florida. We tracked the movements of 12 adult Burmese pythons in Everglades National Park, six of which were translocated 21–36 km from their capture locations. Translocated snakes oriented movement homeward relative to the capture location, and five of six snakes returned to within 5 km of the original capture location. Translocated snakes moved straighter and faster than control snakes and displayed movement path structure indicative of oriented movement. This study provides evidence that Burmese pythons have navigational map and compass senses and has implications for predictions of spatial spread and impacts as well as our understanding of reptile cognitive abilities.
Figs. 1– 4. Strongylium spp., dorsal view. 1 in An Asian Species ofStrongyliumKirby (Coleoptera: Tenebrionidae) Newly Established in South Florida, U.S.A.
Figs. 1– 4. Strongylium spp., dorsal view. 1) S. cultellatum; 2) S. terminatum; 3) S. tenuicolle; 4) S. anthrax.
Subspecies and Distribution. S. p. putorius Linnaeus, 1758 — E & SE USA (Mississippi, Alabama & N Florida, through Georgia, N to SC Pennsylvania). S. p. ambarvalis Bangs, 1898 — SE USA (Peninsular Florida). S. p. interrupta Rafinesque, 1820 — USA (Canadian border in Minnesota, C North Dakota, E Wyoming, E Colorado, W Oklahoma, NW Texas, south to C Texas, and east to the Mississippi River along Louisiana, Arkansas, Missouri & Iowa, up to Wisconsin. in Mephitidae
Subspecies and Distribution. S. p. putorius Linnaeus, 1758 — E & SE USA (Mississippi, Alabama & N Florida, through Georgia, N to SC Pennsylvania). S. p. ambarvalis Bangs, 1898 — SE USA (Peninsular Florida). S. p. interrupta Rafinesque, 1820 — USA (Canadian border in Minnesota, C North Dakota, E Wyoming, E Colorado, W Oklahoma, NW Texas, south to C Texas, and east to the Mississippi River along Louisiana, Arkansas, Missouri & Iowa, up to Wisconsin.
Subspecies and Distribution. S. p. putorius Linnaeus, 1758 — E & SE USA (Mississippi, Alabama & N Florida, through Georgia, N to SC Pennsylvania). S. p. ambarvalis Bangs, 1898 — SE USA (Peninsular Florida). S. p. interrupta Rafinesque, 1820 — USA (Canadian border in Minnesota, C North Dakota, E Wyoming, E Colorado, W Oklahoma, NW Texas, south to C Texas, and east to the Mississippi River along Louisiana, Arkansas, Missouri & Iowa, up to Wisconsin. in Mephitidae
Subspecies and Distribution. S. p. putorius Linnaeus, 1758 — E & SE USA (Mississippi, Alabama & N Florida, through Georgia, N to SC Pennsylvania). S. p. ambarvalis Bangs, 1898 — SE USA (Peninsular Florida). S. p. interrupta Rafinesque, 1820 — USA (Canadian border in Minnesota, C North Dakota, E Wyoming, E Colorado, W Oklahoma, NW Texas, south to C Texas, and east to the Mississippi River along Louisiana, Arkansas, Missouri & Iowa, up to Wisconsin.
Distribution. SE USA, in S Illinois and S Indiana S to E Texas, and Florida, and E to North Carolina and South Carolina through W Kentucky, W Tennessee, Alabama, and Georgia. in Vespertilionidae
Distribution. SE USA, in S Illinois and S Indiana S to E Texas, and Florida, and E to North Carolina and South Carolina through W Kentucky, W Tennessee, Alabama, and Georgia.
Subspecies and Distribution. C.r.rafinesquiiLesson,1827—E&SIllinois,W&SIndiana,SOhio,SEMissouri,Ken-tucky,Tennessee,WNorthCarolina,andEArkansas(EUSA). C. r. macrotis Le Conte, 1831 — E North Carolina, South Carolina, Georgia, Florida, Alabama, Mississippi, Louisiana, E Texas, and extreme SW Arkansas. in Vespertilionidae
Subspecies and Distribution. C.r.rafinesquiiLesson,1827—E&SIllinois,W&SIndiana,SOhio,SEMissouri,Ken-tucky,Tennessee,WNorthCarolina,andEArkansas(EUSA). C. r. macrotis Le Conte, 1831 — E North Carolina, South Carolina, Georgia, Florida, Alabama, Mississippi, Louisiana, E Texas, and extreme SW Arkansas.
Distribution. Anti-tropical distribution: N Atlantic Ocean, in a poorly defined region ranging from Ireland to the Canary Is in the E, and from Nova Scotia to Florida in the W, Southern Hemisphere, recorded in S Brazil, South Africa, Madagascar, and S Australia. Nevertheless, due to the small number of records, the full extent of its distribution in the Southern Hemisphere is unclear. in Ziphiidae
Distribution. Anti-tropical distribution: N Atlantic Ocean, in a poorly defined region ranging from Ireland to the Canary Is in the E, and from Nova Scotia to Florida in the W, Southern Hemisphere, recorded in S Brazil, South Africa, Madagascar, and S Australia. Nevertheless, due to the small number of records, the full extent of its distribution in the Southern Hemisphere is unclear.
Subspecies and Distribution. T. m. manatus Linnaeus, 1758 — Greater Antilles and Gulf and Caribbean coasts of Mexico, Central America, and N South America (S to Alagoas and Sergipe states, Brazil). 1. m. latirostris Harlan, 1824 — SE USA, primarily Florida and Georgia, with seasonal movements to other states bordering the Gulf of Mexico and the Atlantic Ocean. in Trichechidae
Subspecies and Distribution. T. m. manatus Linnaeus, 1758 — Greater Antilles and Gulf and Caribbean coasts of Mexico, Central America, and N South America (S to Alagoas and Sergipe states, Brazil). 1. m. latirostris Harlan, 1824 — SE USA, primarily Florida and Georgia, with seasonal movements to other states bordering the Gulf of Mexico and the Atlantic Ocean.
Subspecies and Distribution. L. c. californicus Gray, 1837 — SW Oregon, and NW California (W USA). L. c. altamirae Nelson, 1904 — SE Tamaulipas (NE Mexico). L. c. asellus Miller, 1899 — SE Coahuila, NE, S Nuevo Leon, E & SE Zacatecas, San Luis Potosi, Aguascalientes, NE tip ofJalisco, N Guanajuato, and NW Querétaro (NC Mexico). L. c. bennettiz Gray, 1843 — SW California (SW USA), and NW Baja California (NW Mexico). L. c. curts Hall, 1951 — Is along the coast of Tamaulipas (NE Mexico). L. c. deserticola Mearns, 1896 — SE Oregon, S Idaho, SW Montana, NE & E California, Nevada, Utah except SE, and NW, W & SW Arizona (W & SW USA), and NW Sonora and NE Baja California (NW Mexico). The population in SW Montanais isolated. L. c. eremicus J. A. Allen, 1894 — S Arizona (SW USA), N Sonora except extreme NW, NW Chihuahua (N Mexico). L. c. festinus Nelson, 1904 — S Querétaro, Hidalgo, and N State of Mexico (C Mexico). L. c. magdalenae Nelson, 1907 — Magdalena I, Baja California Sur (NW Mexico). L. c. martirensis Stowell, 1895 —Baja California except NW & NE and NE Baja California Sur (NW Mexico). L. c. melanotis Mearns, 1890 — S South Dakota, SE Wyoming, Nebraska, E Colorado, Kansas, W Missouri, NE New Mexico, Oklahoma, W Arkansas, and N Texas (C USA). An isolated population exists in E Oklahoma. L. c. merriami Mearns, 1896 — S Texas (S USA), and NE Coahuila, N Tamaulipas, and N Nuevo Leon (NE Mexico). L. c. richardsonii Bachman, 1839 — C California (SW USA). L. c. sheldoni Burt, 1933 — Isla del Carmen, Baja California Sur (NW Mexico). L. c. texianus Waterhouse, 1848 — SE Utah, SW Colorado, NE Arizona, New Mexico except the NE, and W Texas (C USA), Chihuahua except the NW, W, & SW extremes, W Coahuila, E Durango, and NW Zacatecas (NC Mexico). L. c. wallawalla Merriam, 1904 — S Washington, C & W Oregon, NE California, and NW Nevada (NW USA). L. ¢. xanti Thomas, 1898 — Baja California Sur except the NE (NW Mexico). The Black-tailed Jackrabbit has been introduced into Massachusetts, NewJersey, Maryland, Virginia, and S Florida. in Leporidae
Subspecies and Distribution. L. c. californicus Gray, 1837 — SW Oregon, and NW California (W USA). L. c. altamirae Nelson, 1904 — SE Tamaulipas (NE Mexico). L. c. asellus Miller, 1899 — SE Coahuila, NE, S Nuevo Leon, E & SE Zacatecas, San Luis Potosi, Aguascalientes, NE tip ofJalisco, N Guanajuato, and NW Querétaro (NC Mexico). L. c. bennettiz Gray, 1843 — SW California (SW USA), and NW Baja California (NW Mexico). L. c. curts Hall, 1951 — Is along the coast of Tamaulipas (NE Mexico). L. c. deserticola Mearns, 1896 — SE Oregon, S Idaho, SW Montana, NE & E California, Nevada, Utah except SE, and NW, W & SW Arizona (W & SW USA), and NW Sonora and NE Baja California (NW Mexico). The population in SW Montanais isolated. L. c. eremicus J. A. Allen, 1894 — S Arizona (SW USA), N Sonora except extreme NW, NW Chihuahua (N Mexico). L. c. festinus Nelson, 1904 — S Querétaro, Hidalgo, and N State of Mexico (C Mexico). L. c. magdalenae Nelson, 1907 — Magdalena I, Baja California Sur (NW Mexico). L. c. martirensis Stowell, 1895 —Baja California except NW & NE and NE Baja California Sur (NW Mexico). L. c. melanotis Mearns, 1890 — S South Dakota, SE Wyoming, Nebraska, E Colorado, Kansas, W Missouri, NE New Mexico, Oklahoma, W Arkansas, and N Texas (C USA). An isolated population exists in E Oklahoma. L. c. merriami Mearns, 1896 — S Texas (S USA), and NE Coahuila, N Tamaulipas, and N Nuevo Leon (NE Mexico). L. c. richardsonii Bachman, 1839 — C California (SW USA). L. c. sheldoni Burt, 1933 — Isla del Carmen, Baja California Sur (NW Mexico). L. c. texianus Waterhouse, 1848 — SE Utah, SW Colorado, NE Arizona, New Mexico except the NE, and W Texas (C USA), Chihuahua except the NW, W, & SW extremes, W Coahuila, E Durango, and NW Zacatecas (NC Mexico). L. c. wallawalla Merriam, 1904 — S Washington, C & W Oregon, NE California, and NW Nevada (NW USA). L. ¢. xanti Thomas, 1898 — Baja California Sur except the NE (NW Mexico). The Black-tailed Jackrabbit has been introduced into Massachusetts, NewJersey, Maryland, Virginia, and S Florida.
Distribution. SW USA (Florida), and from NE Mexico (Coahuila), S through Central America into South America to Argentina and Uruguay; also on Puerto Rico and Lesser Antilles. in Molossidae
Distribution. SW USA (Florida), and from NE Mexico (Coahuila), S through Central America into South America to Argentina and Uruguay; also on Puerto Rico and Lesser Antilles.
Fig. 1 in Bledius beattyi Blackwelder (Coleoptera: Staphylinidae: Oxytelinae), New to the United States, and Co-Occurrences of some Bledius Leach and Dyschiriodes Jeannel (Coleoptera: Carabidae: Scaritinae) Species in South Florida
Fig. 1. Distributions in Gulf of Mexico and Caribbean Sea. Bledius beattyi: •, published records; m, new records. Dyschiriodes sublaevis: s, published records; e, new record.
Development of microsatellite markers for colony delineation of the invasive Asian subterranean termite in South Florida and Taiwan
<p>Delineating the colony identity of <em>Coptotermes gestroi </em>(Wasmann) is a core issue of colony elimination in the implementation of subterranean termite baiting systems. Invasion history is believed the possible cause of genetic variabilities among colonies. Haplotype network analysis of mitochondrial cytochrome <em>c</em> oxidase subunit II revealed the multiple origins of American <em>C</em>.<em> gestroi</em> from<em> </em>the Philippines and Southeast Asia and the Taiwan population only from the Philippines. We further developed 21 new microsatellite markers for the comparison of genetic variabilities on colony delineation of <em>C</em>.<em> gestroi </em>colonies from South Florida (invaded ~30 years; 3–7 generations) and Taiwan (~110 years; 13–27 generations). The present microsatellite markers with 1–4 alleles per locus have validated the effectiveness of colony delineation for three incipient colonies reared in the laboratory and three field colonies from Taiwan. Genetic admixture of the Floridian <em>C</em>. <em>gestroi</em> probably caused by recent invasion history, multiple invasions, and anthropogenic activities among regions. A possible introduction event likely occurred through human-mediated activities between Fort Lauderdale and Miami. Overall, these new microsatellite markers provide suitable and efficient candidate genetic markers for colony delineation of <em>C</em>. <em>gestroi</em> to consolidate the effectiveness of the colony elimination system in termite management.</p>
Public attitudes toward Biscayne Bay in South Florida
<p>This data set was collected using Centiment survey panels, limited to English and Spanish speaking adults in the Miami-Dade metro area. Questions and scales covered a range of activities, values and attitudes associated with the marine estuary Biscayne Bay. </p>
The Miami Heart Study at Baptist Health South Florida
ClinicalTrials.gov study NCT02508454. IPD Sharing: UNDECIDED. Countries: 1. Publications: 1.
Public attitudes toward Biscayne Bay in South Florida
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Data from: The impact of salinity on mycorrhizal colonization of a rare legume in south Florida pine rocklands
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Development of microsatellite markers for colony delineation of the invasive Asian subterranean termite in South Florida and Taiwan
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American crocodile captures in South Florida
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Data from: Homing of invasive Burmese pythons in South Florida: evidence for map and compass senses in snakes
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Disparities of HIV risk and PrEP use among transgender women of color in South Florida.
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