Loggerhead (Caretta caretta) and green (Chelonia mydas) turtles recruit to nearshore environments as juveniles. These often degraded habitats are associated with emerging diseases such as green turtle fibropapillomatosis (GTFP), however there are few studies on immune function in sea turtles. The objective of this research was to quantify phagocytosis of the innate immune system by flow cytometry and compare levels between animals from a degraded habitat (the Indian River Lagoon, FL) to a more pristine environment (the Trident Basin, Port Canaveral, FL), and across a range of temperatures. While in vitro temperatures did not alter rates of phagocytosis, it was higher in samples obtained in the summer than winter. Rates of phagocytosis in sea turtles with GTFP and from degraded environments with increased prevalence of GTFP were low compared to animals from the more pristine environment, suggesting that the environment can alter innate immunological function and thus contribute to the development of disease. / Includes bibliography. / Thesis (M.S.)--Florida Atlantic University, 2014. / FAU Electronic Theses and Dissertations Collection

Sea turtle hatchlings emerge from their nest and quickly crawl to the surf. During the crawl, hatchlings may encounter threats, biotic and abiotic, which can affect their ability to successfully reach the surf. The impact of these threats on hatchling survival during that crawl is largely undocumented. Current methods used to estimate cohort recruitment rely heavily on nest inventory data. This method, however, does not account for post-emergent hatchling mortality that occurs during the crawl. During the 2017-2018 nesting seasons, I quantified the fates of 1,379 loggerhead (Caretta caretta) hatchlings from 26 nest emergences during their crawl from the nest to the surf on the east and west coasts of Florida. I documented hatchling fates at 5 Florida nesting beaches: Wabasso, Boca Raton, Keewaydin Island, Naples, and Anna Maria Island. Overall, 6.5% of all emergent hatchlings died during the crawl from the nests to the surf. Ghost crabs, night herons, foxes, and coyotes killed hatchlings and photopollution and barriers on the beach (both abiotic threats) caused hatchling mortality. Anthropogenic (abiotic) threats accounted for more mortality than did predators. In order to assess how beach urbanization impacts hatchling mortality, I categorized each study site as urban (Wabasso and Naples), intermediate (Anna Maria Island and Boca Raton), or natural (Keewaydin Island) based on the relative levels of shoreline development and human activity at each beach. Sites with intermediate levels of urbanization accounted for greater levels of hatchling mortality than at other beaches due to the absolutely larger numbers of hatchlings lost to a disorientation event and to a beach barrier. Given the small numbers of emergences, at all sites, only a small proportion of the hatchlings mortalities (e.g., between 3 and 12 percent), site type could not be rigorously used as a discriminator. My results provide a better understanding of how specific environmental threats contribute to hatchling mortality. While nest-to-surf mortality is relatively low, its cumulative costs add up to several hundreds of thousands of hatchlings. Armed with this information, nesting beach managers can assess risks and focus their efforts to implement the most effective management practices to minimize losses of this imperiled species. / Includes bibliography. / Thesis (M.S.)--Florida Atlantic University, 2019. / FAU Electronic Theses and Dissertations Collection

Climate change will expose sea turtle nests to higher temperatures and more storms; both may negatively impact sea turtle nest success. In this study, unhatched eggs were collected from the Boca Raton, Florida beach and developmental stage at embryonic death determined. Elevated nest temperatures increased embryonic mortality, and the most significant relationship was between mortality and the percent of time embryos were exposed to temperatures above 34°C. Loggerhead turtles exhibited higher rates of mortality compared to green turtles at temperatures above 34°C. Only loggerhead nests were exposed to inundation, but embryonic mortality did not differ from noninundated nests. Beach profiles across the nesting season were also determined. A major storm altered the beach more in areas of coastal development; however, this was impacted by a nourishment project and the presence of a structured inlet. Future management strategies may need to protect sea turtle nests from extended periods at elevated temperatures. / Includes bibliography. / Thesis (M.S.)--Florida Atlantic University, 2017. / FAU Electronic Theses and Dissertations Collection

Loggerhead sea turtles (Caretta caretta) can be found worldwide, inhabiting tropical and subtropical coastal waters. The loggerhead was classified as an endangered species and placed on the International Union for Conservation of Nature and Natural Resources (IUCN) Red List in 1996 (IUCN 2006).The problem of sea turtle mortality as a result of collisions with vessels is of increasing concern, especially in the southeastern United States, where increased development along the coasts results in increased recreational boat traffic. In the United States, the percentage of strandings that were attributed to vessel strikes has increased from approximately 10% in the 1980's to a record high of 20.5% in 2004 (NMFS 2007). This report presents results from field experiments designed to investigate the ways in which loggerhead sea turtles are injured in boat collisions, and the effectiveness of several mitigation options for reducing the risk of fatal interactions. In order to conduct these field experiments, a synthetic sea turtle carapace was designed and built that approximated the structural behavior of a biological sea turtle carapace. Hodges (2008) quantified the material strength properties of loggerhead sea turtle carapaces. From these results, it was determined that the target parameter for simulating tensile strength in a synthetic carapace should be force per unit width of sample. Hodges designed and constructed an artificial carapace made of composite material for use in controlled experiments. Modifications were made to the design proposed by Hodges (2008) to facilitate rapid construction. Several designs were tested using the force per unit width as the target strength parameter and compared to the strength of the biological carapace. Tests on the design ultimately adopted showed a force per unit width 17.6% stronger than the biological carapace. The composite material being stronger than the biological carapace means the testing will result in conservative reports of damage. Once the design and construction methods were finalized, approximately 60 artificial carapaces were fabricated for field testing. A frame, weighting scheme and buoyancy unit were designed and fabricated so that each test carapace floated at proper draft and had realistic specific gravity and weight. Field testing procedures were designed to investigate the influence of a) boat speed, b) animal position in the water column, and c) vessel propulsion system on the severity of vessel collisions on turtles. All experiments were done with small (<6 m in length) vessels. Boat/sea turtle collisions were simulated by placing a test specimen (a synthetic carapace attached to a test frame) in the water column and striking it with the vessel. The speeds considered were idle (7 km/h), sub-planing (14 km/h), and planing (40 km/hr). The two animal positions in the water column were 1) at the water surface and 2) at "prop depth" (depth to the center of the propeller hub on the standard outboard motor). Five propulsion options were tested: 1) a standard outboard motor, 2) a standard outboard motor with Hydroshield® propeller guard 3) a standard outboard motor with Prop Buddy® propeller guard, 4) a jet outboard motor and 5) a jet-propelled personal watercraft, often referred to generically as a "jet ski". The experiments typically included five trials per test configuration. Catastrophic (presumably fatal) damage was defined to occur when any damage penetrated the carapace. Small wounds (< 4 cm in length) along the sides or rear of the artificial carapace, where the shell and bone extend beyond the edge of the body cavity, were not classified as catastrophic This definition was used to classify the effectiveness of the various mitigation options. Results indicate that reducing the speed of the vessel reduces the odds of severe damage to the animals. Of all of the tests performed with the standard outboard motor (including tests with propeller guards installed), 25% of those performed at idle speed resulted in catastrophic damage, compared to 100% for planing speed tests. The two tested propeller guards both modified the type of damage to the animal when compared to similar tests with the standard motor configuration, but they only slightly reduced the risk of catastrophic damage. At idle speed, with propeller guard installed, 10% of the tests resulted in catastrophic damage. The corresponding number for the standard motor was 40%. At planing speed, 100% of the tests resulted in catastrophic damage, with or without the propeller guard. No catastrophic injuries were observed during testing of both jet propulsion systems (jet outboard and jet ski) at any speed or depth in the water column. Both feature a much smaller draft than the standard outboard, which results in little chance of striking an animal below the surface. And both the jet outboard and the jet-powered watercraft feature water intakes that are relatively smooth and appeared to slide across the animal with minimal damage to the carapace when the model animal was floating on the surface. The experiments described here involved a limited range of hull configurations; results may be different for hulls or propulsion systems drastically different than those tested here. But the results obtained indicate that equipment, in the form of the boat's propulsion system, and the mode in which it is used both play a role in defining the risk of boats to turtles in the field.

Thesis (M.S.)--Georgia Southern University, 2007. / Title from PDF title page (viewed on Feb. 19, 2008). Electronic version approved: December 2007. Includes bibliographical references (p. 35-37).

Thesis (M. S.)--Civil and Environmental Engineering, Georgia Institute of Technology, 2009. / Committee Chair: Scott, David; Committee Member: Kurtis, Kimberly; Committee Member: Work, Paul. Part of the SMARTech Electronic Thesis and Dissertation Collection.

Thesis (M.S.)--Georgia Southern University, 2009. / "A thesis submitted to the Graduate Faculty of Georgia Southern University in partial fulfillment of the requirements for the degree Master of Science." Directed by David C. Rostal. ETD. Includes bibliographical references (p. 47-49)

The greatest sea turtle nesting in the United States occurs in Florida, which accounts for more than 85% (Shoop et al, 1985). Five species of sea turtle have been documented nesting in Florida, including the loggerhead (Caretta caretta), green (Chelonia mydas), leatherback (Dermochelys coriacea), kemp’s ridley (Lepidochelys kempi), and hawksbill (Eretmochelys imbricata) sea turtles. In southeast Florida, the loggerhead is the most common nester. The distribution of loggerhead nest numbers laid in 85 survey zones stretching along Broward County beaches between the Palm Beach County line and the Port Everglades Inlet have been highly correlated for aver a decade (P<<0.001). This study attempted to understand the reasons for this distribution by evaluating the distributions of false crawls and nesting success rates from 2000 through 2010. The nest and false crawl patterns in the 85 beach zones were all highly correlated for all 11 years (P < 0.01). These strong positive correlations indicate that these turtles receive preemergence cues, such as visual or depth profile, to primarily determine their emergence locations. However, weaker correlations between yearly nesting and nesting success patterns indicate that on-beach (post-emergence) cues also play a less important role in nest site selection.

Loggerhead (Caretta caretta) and leatherback (Dermochelys coriacea) sea turtles as well as their eggs and hatchlings have been protected on their nesting beach in South Africa (SA) since 1963. Both nesting populations were expected to show similar trends in recovery following the application of identical protection and conservation measures. The loggerhead nesting population has responded favourably to these protection efforts. In contrast, the leatherback nesting population showed an initial increase but is currently stable. The reason for this difference in response is thought to be due to differential offshore mortality of these two species. This prompted an investigation into the different sources of sea turtle mortality in the South Western Indian Ocean (SWIO). Specific aims were to identify and quantify sources of loggerhead and leatherback mortality on nesting beaches as well as in the oceans. Reasonable survivorship at all age classes is important to ensure recruitment of new nesting individuals into sea turtle populations. Mortality of nests, eggs per nest and hatchlings were quantified over two seasons for the loggerheads and leatherbacks nesting in SA. The beach was patrolled on foot to encounter and record females emerging from the ocean and later, hatchlings from their nests. The nests were then monitored during the incubation period and excavated once hatched. The fates of 925 nests were determined during these two nesting seasons (2009/2010 and 2010/2011). The main source of loggerhead and leatherback nest destruction was predation (8.6 percent and 15.7 percent respectively) followed by nest erosion (2.2 percent and 6.3 percent respectively). Overall nest success was high but higher for loggerheads (89 percent) than for leatherbacks (78 percent). The main cause of egg mortality for both species was early developmental arrest, followed by predation by ants and ghost crabs. Hatchlings en route to the sea were almost exclusively predated by ghost crabs (4.2 percent of emerged loggerhead hatchlings and 3.2 percent of emerged leatherback hatchlings). It appears that both species benefit from the coastal conservation efforts. When sea turtles leave the nesting beach, either as hatchlings or adults, conservation and monitoring becomes more difficult and sea turtles are exposed to a multitude of threats, including anthropogenic threats. Age classes tend to be spatially separated due to different habitat and dietary requirements. The type of threat sea turtles are exposed to thus depends on the current age class. Offshore sources of mortality in the SWIO were identified and where possible loggerhead and leatherback mortality was quantified and mapped spatially. Loggerheads were mostly exposed to and had the highest mortality in the artisanal fisheries in the SWIO (> 1000 per annum), inshore trawling (ca. 41 per annum), shark nets (protective gill nets) (21.6 ± 6.7 per annum) and the pelagic longline fishery (5.0 ± 4.4 per annum). In contrast, leatherbacks with a pelagic lifestyle, were mostly exposed to pelagic longline fisheries (7.8 ± 7.8 per annum). A spatial analysis of fishing activities indicated that leatherback home ranges overlapped 41percent with pelagic longline fishing activity in the SA EEZ, whereas the overlap between pelagic longliners and loggerhead home ranges was 29 percent. The quantified sources of mortality provide some explanation for the trend in the loggerhead nesting population but not the trend in the leatherback nesting population. Hatchling survivorship to adulthood was estimated to determine the viability of the two nesting populations as well as to determine whether offshore mortality was responsible for the difference in recovery of the two populations. Loggerhead hatchling survivorship to adulthood was estimated at between 2 and 10 per 1000 hatchlings, the minimum requirement for an increasing population. The adopted sophisticated model shows that leatherbacks have a survival rate of 5 to 10 per 1 000 hatchlings. However, this suggests that the population is increasing, but the leatherback population is stable. Perhaps the age to maturity of SA leatherbacks is greater than 12 years, or fisheries-related mortality affects younger age classes than initially thought. It is therefore recommended that the turtle monitoring area is extended to include other potential nesting grounds. In addition, observer or monitoring programs for commercial as well as artisanal fisheries needs to be extended throughout the SWIO to quantify sea turtle mortality. Ultimately a comprehensive multi-regional approach is required for the conservation of these highly migratory species.

<p>Colonization by bacteria and fungi has been shown to reduce hatching success of sea turtle nests. Presence of microbial pathogens is commonly associated with egg failure, and in some species, it has even been shown to cause up to 90% nest mortality. Developing sea turtle embryos can only rely on non-specific defenses, such as the eggshell and the proteins present in the egg albumen. For a long time, it has been suggested that the fluid in which the eggs are coated during oviposition may contain antimicrobial properties that might protect eggs against potential pathogens that are found in the egg chamber. This study aimed to evaluate the antimicrobial properties of the cloacal fluid of loggerhead sea turtles. Cloacal fluid samples were collected at the Wassaw National Wildlife Refuge, Georgia during the 2021 nesting season (June-July). Protein fractionation of the samples was carried out using commercially available ultracentrifugation devices of 3K, 10K and 30K molecular cut-off weights. A microplate-based turbidimetric growth inhibition assay recorded the antimicrobial activity of the peptide fractions and the crude extract. We found that the cloacal fluid of loggerheads has antimicrobial properties against <i>Serratia marcescens</i> and <i>Morganella morganii</i>, and some mild action against <i>Pseudomonas aeruginosa</i>. Results obtained from the microplate-based turbidimetric assay were confirmed by assessing viability of cells upon 24 hours of exposure to the fluid. Furthermore, this study found that the cloacal fluid contains proteins with molecular weight ranging from approximately 5 to 250 kDa, and that proteins with higher molecular weights (MW>30kDa) are found in greater abundance. Further studies are needed to understand the mechanism of action of the proteins and peptides present in the cloacal fluid to potentially develop antimicrobial compounds that can be used to increase hatching success globally.</p>