First gut contents in a Cretaceous sea turtle

Modern sea turtles utilize a variety of feeding strategies ranging from herbivory to omnivory. In contrast, the diets of fossil sea turtles are poorly known. This study reports the first direct evidence: inoceramid bivalve shell pieces (encased in phosphatic material) preserved within the body cavities of several small protostegid turtles (cf. Notochelone) from the Lower Cretaceous of Australia. The shell fragments are densely packed and approximately 5-20 mm across. Identical shell accumulations have been found within coprolite masses from the same deposits; these are of a correct size to have originated from Notochelone, and indicate that benthic molluscs were regular food items. The thin, flexible inoceramid shells (composed of organic material integrated into a prismatic calcite framework) appear to have been bitten into segments and ingested, presumably in conjunction with visceral/mantle tissues and encrusting organisms. Although protostegids have been elsewhere interpreted as potential molluscivores, their primitive limb morphology is thought to have limited them to surface feeding. However, the evidence here that at least some forms were able to utilize benthic invertebrate prey indicates that, like modern sea turtles, protostegids probably exhibited a much broader range of feeding habits.     

First satellite tracks of neonate sea turtles redefine the ‘lost years’ oceanic niche

Few at-sea behavioural data exist for oceanic-stage neonate sea turtles, a life-stage commonly referred to as the sea turtle ‘lost years’. Historically, the long-term tracking of small, fast-growing organisms in the open ocean was logistically or technologically impossible. Here, we provide the first long-term satellite tracks of neonate sea turtles. Loggerheads (Caretta caretta) were remotely tracked in the Atlantic Ocean using small solar-powered satellite transmitters. We show that oceanic-stage turtles (i) rarely travel in Continental Shelf waters, (ii) frequently depart the currents associated with the North Atlantic Subtropical Gyre, (iii) travel quickly when in Gyre currents, and (iv) select sea surface habitats that are likely to provide a thermal benefit or refuge to young sea turtles, supporting growth, foraging and survival. Our satellite tracks help define Atlantic loggerhead nursery grounds and early loggerhead habitat use, allowing us to re-examine sea turtle ‘lost years’ paradigms.     

First records of dive durations for a hibernating sea turtle

The first published record, from the early 1970s, of hibernation in sea turtles is based on the reports of the indigenous Indians and fishermen from Mexico, who hunted dormant green turtles (Chelonia mydas) in the Gulf of California. However, there were no successful attempts to investigate the biology of this particular behaviour further. Hence, data such as the exact duration and energetic requirements of dormant winter submergences are lacking. We used new satellite relay data loggers to obtain the first records of up to 7h long dives of a loggerhead turtle (Caretta caretta) overwintering in Greek waters. These represent the longest dives ever reported for a diving marine vertebrate. There is strong evidence that the dives were aerobic, because the turtle surfaced only for short intervals and before the calculated oxygen stores were depleted. This evidence suggests that the common belief that sea turtles hibernate underwater, as some freshwater turtles do, is incorrect.     

Temperature-Dependent Sex Determination in Sea Turtles in the Context of Climate Change: Uncovering the Adaptive Significance

The adaptive significance of temperature-dependent sex determination (TSD) in reptiles remains unknown decades after TSD was first identified in this group. Concurrently, there is growing concern about the effect that rising temperatures may have on species with TSD, potentially producing extremely biased sex ratios or offspring of only one sex. The current state-of the-art in TSD research on sea turtles is reviewed here and, against current paradigm, it is proposed that TSD provides an advantage under warming climates. By means of coadaptation between early survival and sex ratios, sea turtles are able to maintain populations. When offspring survival declines at high temperatures, the sex that increases future fecundity (females) is produced, increasing resilience to climate warming. TSD could have helped reptiles to survive mass extinctions in the past via this model. Flaws in research on sex determination in sea turtles are also identified and it is suggested that the development of new techniques will revolutionize the field.     

Historical Burden In Systematics And The Interrelationships Of 'Parareptiles'

The interrelationships within the clade comprised of turtles, pareiasaurs, and procolophonid-like taxa are investigated via a cladistic analysis incorporating 56 characters. A single most parsimonious tree was found (80 steps, c. i. = 0·8) in which the successive outgroups to turtles are: pareiasaurs, Sclerosaurus, lanthanosuchids, procolophonoids (=Owenetta, Barasaurus and procolophonids), and nyctiphruretians (= nycteroleterids). Thus, as suggested recently by other workers (Reisz, in Fischman, 1993) turtles are the highly modified survivors of a radiation of poorly-known reptiles commonly called ‘parareptiles’. Pareiasaurs are united with turtles on the basis of twenty unambiguous derived features which are absent in other basal amniotes (=‘primitive reptiles’) and reptiliomorph amphibians: for example, the medially located choana, enlarged foramina palatinum posterius, blunt cultriform process, fully ossified medial wall of the prootic, opisthotic-squamosal suture, lateral flange of exoccipital, loss of ventral cranial fissure, thickened braincase floor, ‘pleurosphenoid’ ossification, reduced presacral count, acromion process, trochanter major, reduced fifth pedal digit, and presence of transverse processes on most caudals. Recent phylogenetic proposals linking turtles with captorhinids, with dicynodonts, and with procolophonoids are evaluated. None of the proposed traits supporting the first two hypotheses is compelling. The procolophonoid hypotheses is supported by only one synapomorphy (the slender stapes). All other synapomorphies proposed in favour of the above groupings either occur in many other primitive amniotes, or are not primitive for turtles, or are not primitive for the proposed chelonian sister-group. Nyctiphruretus and Lanthanosuchids and nycteroleterids, often considered to be seymouriamorph amphibians, are demonstrated unequivocally to be amniotes. The ‘rhipaeosaurs’, currently considered to be pareiasaur relatives, are shown to be a heterogenous assemblage of seymouriamorphs, therapsids and nycteroleterids. The phylogeny proposed here indicates that many of the traits of the earliest known turtle, Proganochelys, previously interpreted as unique specialisations, also occur in pareiasaurs and other near outgroups of turtles, and must instead represent the primitive chelonian condition: for example, the wide parietals and the short quadrate flange of the pterygoid. The sequence of acquisition of chelonian traits is discussed: many features once thought to be diagnostic of turtles actually characterize larger groupings of procolophonomorphs, and must have evolved long before the chelonian shell appeared. These traits include most of the chelonian-pareiasaur synapomorphies listed above, and many others which characterize more inclusive groupings found in this analysis. In putting Proganochelys much closer to the main line of chelonian evolution, in elucidating the sequence of acquisition of chelonian traits, and in reducing greatly the number of differences between turtles and their nearest relatives, this study helps bridge one of the major gaps in the fossil record. The failure of previous cladistic analyses to identify correctly the nearest relatives of turtles is attributed to biased character selection, caused by an over-reliance on cranial characters deemed ‘important’ by earlier workers, and by a tendency to shoehorn ‘parareptile’ taxa into phylogenies derived from analyses restricted to ‘mainstream’ groups such as synapsids, diapsids, turtles, and ‘captorhinomorphs’. Many of the synapomorphies that resolve turtle origins are postcranial, and the three nearest outgroups to turtles are all highly bizarre groups which were dismissed as ‘too specialized’ by early workers and continued to be inadequately assessed even by workers using a cladistic framework.     

Venous blood gases and lactates of wild loggerhead sea turtles (Caretta caretta) following two capture techniques

During summer of 2001, venous blood gases were determined in loggerhead sea turtles (Caretta caretta) captured by trawl (n = 16) in coastal waters of South Carolina and Georgia (USA) as part of a sea turtle census program and captured in pound nets (n = 6) in coastal North Carolina (USA) during a study of sea turtle population biology. Trawls were towed for 30 min, so turtles captured were forcibly submerged for < or = 30 min. Pound nets are passive gear in which fish and sea turtles are funneled into a concentrated area and removed periodically. Sea turtles in pound nets are free to surface and to feed at will. Blood was obtained from the dorsal cervical sinus as quickly as possible after landing on the boat (range 2-10 min trawl, 1-2 min pound net) and at 30 min after landing just prior to release. Blood gases including pH, partial pressures of O2 and CO2 (pO2, pCO2), and lactate were measured within 10 min. Instrument measurements for pH, pO2, and pCO2 made at 37 C were corrected to cloacal temperature and HCO3- was calculated from temperature-corrected pH and pCO2. Venous blood pH and bicarbonate were higher, and pO2 and lactate were lower from pound net-captured turtles compared to trawl captured turtles at the initial sampling time. In pound net turtles, pH and bicarbonate declined and lactate increased during 30 min on deck. In trawled sea turtles, venous blood pH increased and pCO2 and pO2 decreased during the 30 min on deck. Both capture systems caused perturbations in blood gas, acid-base, and lactate status, though alterations were greater in trawl captured turtles.     

Risk analysis reveals global hotspots for marine debris ingestion by sea turtles

Plastic marine debris pollution is rapidly becoming one of the critical environmental concerns facing wildlife in the 21st century. Here we present a risk analysis for plastic ingestion by sea turtles on a global scale. We combined global marine plastic distributions based on ocean drifter data with sea turtle habitat maps to predict exposure levels to plastic pollution. Empirical data from necropsies of deceased animals were then utilised to assess the consequence of exposure to plastics. We modelled the risk (probability of debris ingestion) by incorporating exposure to debris and consequence of exposure, and included life history stage, species of sea turtle and date of stranding observation as possible additional explanatory factors. Life history stage is the best predictor of debris ingestion, but the best‐fit model also incorporates encounter rates within a limited distance from stranding location, marine debris predictions specific to the date of the stranding study and turtle species. There is no difference in ingestion rates between stranded turtles vs. those caught as bycatch from fishing activity, suggesting that stranded animals are not a biased representation of debris ingestion rates in the background population. Oceanic life‐stage sea turtles are at the highest risk of debris ingestion, and olive ridley turtles are the most at‐risk species. The regions of highest risk to global sea turtle populations are off of the east coasts of the USA, Australia and South Africa; the east Indian Ocean, and Southeast Asia. Model results can be used to predict the number of sea turtles globally at risk of debris ingestion. Based on currently available data, initial calculations indicate that up to 52% of sea turtles may have ingested debris.     

Predicted distributions and abundances of the sea turtle ‘lost years’ in the western North Atlantic Ocean

Oceanic dispersal characterizes the early juvenile life-stages of numerous marine species of conservation concern. This early stage may be a ‘critical period’ for many species, playing an overriding role in population dynamics. Often, relatively little information is available on their distribution during this period, limiting the effectiveness of efforts to understand environmental and anthropogenic impacts on these species. Here we present a simple model to predict annual variation in the distribution and abundance of oceanic-stage juvenile sea turtles based on species’ reproductive output, movement and mortality. We simulated dispersal of 25 cohorts (1993–2017) of oceanic-stage juveniles by tracking the movements of virtual hatchling sea turtles released in a hindcast ocean circulation model. We then used estimates of annual hatchling production from Kemp's ridley Lepidochelys kempii (n = 3), green Chelonia mydas (n = 8) and loggerhead Caretta caretta (n = 5) nesting areas in the northwestern Atlantic (inclusive of the Gulf of Mexico, Caribbean Sea and eastern seaboard of the U.S.) and their stage-specific mortality rates to weight dispersal predictions. The model's predictions indicate spatial heterogeneity in turtle distribution across their marine range, identify locations of increasing turtle abundance (notably along the U.S. coast), and provide valuable context for temporal variation in the stranding of young sea turtles across the Gulf of Mexico. Further effort to collect demographic, distribution and behavioral data that refine, complement and extend the utility of this modeling approach for sea turtles and other dispersive marine taxa is warranted. Finally, generating these spatially-explicit predictions of turtle abundance required extensive international collaboration among scientists; our findings indicate that continued conservation of these sea turtle populations and the management of the numerous anthropogenic activities that operate in the northwestern Atlantic Ocean will require similar international coordination.     

A small fishery with a high impact on sea turtle populations in the eastern Mediterranean

Sea turtles were targeted by fisheries in the Mediterranean from 1920 to 1970 and have undergone severe exploitation. At least 30,000 to 40,000 turtles were caught along the Palestinian coastline during the 1920s to 1930s. Although intentional cap- ture of marine turtles is now illegal, sea turtles are still incidentally caught by the fishing industry, making it a major cause of sea turtle mortality. The present study as- sesses the impact of the Israeli fishery fleet on the turtle population in the Levantine basin based on on-board observations and a fishermen survey. The results show that gillnets and trawlers are the main threats to sea turtles in this area. 21 turtles were caught during 1385.5 hours of trawling observations – a catch rate of 0.015 turtles per hour. We estimate that a total of 1,315 turtles are caught annually by Israeli trawlers. According to the fishermen survey, ～21 turtles are caught each year by a single gillnet vessel, yielding an annual estimate of 1,672 turtles for the whole gillnet fleet. We have also found that only a small fraction of the turtles injured by trawlers is represented in the strandings. The mortality rate through trawling and the stranding density is the highest in the region, emphasizing the urgent need to regulate the Israe- li fishery. This fishery poses a major threat to the whole Levantine sea turtle popula- tion, especially during the vulnerable reproduction stage.     

Relationship between tropical cyclones and the distribution of sea turtle nesting grounds

Aim This study examines the relationship between the distribution of existing sea turtle nesting sites and historical patterns of tropical cyclone events to investigate whether cyclones influence the current distribution of sea turtle nesting sites. The results, together with information on predicted cyclone activity and other key environmental variables, will help in the identification and prediction of future nesting sites for sea turtles as changes to the coastal environment continue. Location Queensland, Australia. Methods We used data on the nesting distribution of seven populations of four species of sea turtles [green (Chelonia mydas), flatback (Natator depressus), hawksbill (Eretmochelys imbricata) and loggerhead (Caretta caretta)] from the eastern Queensland coast, and tropical cyclone track data from 1969 to 2007 to explore the relationship between (1) sea turtle nesting phenology and cyclone season, and (2) sea turtle nesting sites and cyclone distribution. Furthermore, using two green turtle populations as a case study, we investigated the relationship between cyclone disturbance and sea turtle reproductive output, nesting site and season. Bootstrapping was used to explore if current sea turtle nesting sites are located in areas with lower or higher cyclone frequency than areas where turtles are currently not nesting. Results All populations of sea turtles studied here were disturbed by cyclone activity during the study period. The exposure (frequency) of tropical cyclones that crossed each nesting site varied greatly among and within the various sea turtle populations. This was mainly a result of the spatial distribution of each population’s nesting sites. Bootstrapping indicated that nesting sites generally have experienced lower cyclone activity than other areas that are available for nesting. Main conclusions Tropical cyclones might have been sufficiently detrimental to sea turtle hatching success on the eastern Queensland coast that through a natural selection process turtles in this region are now nesting in areas with lower cyclone activity. Therefore, it is important that future studies that predict climate or range shifts for sea turtle nesting distributions consider future cyclone activity as one of the variables in their model.     

Ecotourism for the survival of sea turtles and other wildlife

This paper discusses generally why humans should bother to conservesea turtles. In doing so, it considers both economic and non-economic reasonsand outlines threats to the existence of sea turtles and ways in which tourismmay either contribute to the conservation or decline of their populations.Turtle-based ecotourism at Mon Repos in southern Queensland is described. As aresult of a survey conducted by the authors, it is shown that turtle-basedecotourism at Mon Repos has positive social (indirect) consequences for theconservation of sea turtles. Furthermore, it is argued that ecotourismoperations at Mon Repos have positive direct impacts on the sustainability ofpopulations of sea turtles. However, using a simple model, it is emphasised thatthis impact is limited because turtles are migratory. A model is also developedto capture the possible relationship between turtle populations and thesustainability of ecotourism dependent on turtle populations, and is extended toother wildlife species. Significant interdependence exists between thesustainability of these two variables. The theory is related toCiriacy-Wantrup's social safe minimum conservation standard forspecies' survival.     

Microhabitat selection by sea turtles in a dynamic thermal marine environment

1. Reproductive fitness is often compromised at the margins of a species' range due to sub-optimal conditions. 2. Set against this backdrop, the Mediterranean's largest loggerhead sea turtle (Caretta caretta) rookery at Zakynthos (Greece) presents a conundrum, being at a very high latitude for this species, yet hosting a high concentration of nesting. 3. We used visual surveys combined with global positioning system (GPS) tracking to show that at the start of the breeding season, individuals showed microhabitat selection, with females residing in transient patches of warm water. As the sea warmed in the summer, this selection was no longer evident. 4. As loggerhead turtles are ectothermic, this early season warm-water selection presumably speeds up egg maturation rates before oviposition, thereby allowing more clutches to be incubated when sand conditions are optimal during the summer. 5. Active selection of warm waters may allow turtles to initiate nesting at an earlier date.     

Development of a Summarized Health Index (SHI) for Use in Predicting Survival in Sea Turtles

Veterinary care plays an influential role in sea turtle rehabilitation, especially in endangered species. Physiological characteristics, hematological and plasma biochemistry profiles, are useful references for clinical management in animals, especially when animals are during the convalescence period. In this study, these factors associated with sea turtle surviving were analyzed. The blood samples were collected when sea turtles remained alive, and then animals were followed up for surviving status. The results indicated that significantly negative correlation was found between buoyancy disorders (BD) and sea turtle surviving (p < 0.05). Furthermore, non-surviving sea turtles had significantly higher levels of aspartate aminotranspherase (AST), creatinine kinase (CK), creatinine and uric acid (UA) than surviving sea turtles (all p < 0.05). After further analysis by multiple logistic regression model, only factors of BD, creatinine and UA were included in the equation for calculating summarized health index (SHI) for each individual. Through evaluation by receiver operating characteristic (ROC) curve, the result indicated that the area under curve was 0.920 ± 0.037, and a cut-off SHI value of 2.5244 showed 80.0% sensitivity and 86.7% specificity in predicting survival. Therefore, the developed SHI could be a useful index to evaluate health status of sea turtles and to improve veterinary care at rehabilitation facilities.     

绿海龟卫星追踪报道

自2001年来,惠东港口海龟国家级自然保护区已成功地利用卫星追踪了21只海龟的洄游路线。本文利用美国卫星信号发射器(Tag)和法国Argos系统追踪3只成年雌性绿海龟。跟踪海龟"西沙"和"南沙"26d,二者均在海口市附近海域消失;"东沙"从阳江市海陵岛出发,取东南向至菲律宾,然后沿菲律宾西海岸向南,最后在巴拉望岛西侧海域逗留,共追踪111d。该试验说明港口海龟具有不同的洄游线路,偏爱沿岸的浅海洄游;洄游路线与等温线之间无显著关系;海龟洄游具有明确的目的地。建议政府相关部门采取科学策略来保护海龟。     

Characterizing watercraft-related mortality of sea turtles in Florida

Mortality from being struck by a motorized watercraft is considerable for many aquatic vertebrates around the world, including sea turtles. We studied stranded (i.e., dead, sick, or injured) sea turtles found in Florida, USA, during 1986–2014 and identified those with sharp force or blunt force injuries indicative of a vessel strike. About a third of stranded loggerheads (Caretta caretta), green turtles (Chelonia mydas), and leatherbacks (Dermochelys coriacea) had a vessel-strike injury (VSI). The frequency of this injury was lower but still substantial for stranded Kemp's ridleys (Lepidochelys kempii; 26.1%) and hawksbills (Eretmochelys imbricata; 14.8%). Over the study period, the annual number of stranded loggerheads, green turtles, and Kemp's ridleys with a VSI increased as did the annual number of vessels registered in Florida. Eighty-one percent of the stranded turtles with a VSI were found in the southern half of Florida and 66% of those were found along the southeast coast. By coastal county, the proportion of stranded sea turtles with a VSI was positively related to the mean annual number of registered vessels. The percentage occurrence of a VSI was highest for adult loggerheads, green turtles, and leatherbacks, and reproductively active individuals appeared to be particularly vulnerable to these injuries. We conducted necropsies on 194 stranded sea turtles with a VSI and concluded that this injury was the cause of death or the probable cause of death in ≥92.8% of these cases. During 2000–2014, we estimate that the mean annual numbers of stranded sea turtles that died from a VSI were 142–229 loggerheads, 101–162 green turtles, 16–32 Kemp's ridleys, 4–6 leatherbacks, and 2–4 hawksbills. Considering that only about 10–20% of sea turtles that died likely washed ashore, the overall annual mortality may have been 5–10 times greater than that represented by strandings. Most of the significant clusters of stranded sea turtles with a VSI occurred at inlets or passes and the probability that a stranded sea turtle had a VSI decreased with increasing distance from inlets or passes, navigable waterways, and marinas. We suggest focusing initial management efforts on reducing watercraft-related mortality for all sea turtle species around 8 inlets in southeast Florida, reproductively active loggerheads and green turtles along the coast of southeast Florida, and Kemp's ridleys and adult male loggerheads at passes along the coast of southwest Florida. Published 2019. This article is a U.S. Government work and is in the public domain in the USA. The Journal of Wildlife Management published by Wiley Periodicals, Inc. on behalf of The Wildlife Society     

Temperature and the life-history strategies of sea turtles

1. 1. Sea turtles have a high fecundity, high mortality, great longevity life history strategy.

2. 2. With the exception of the leatherback, turtle distribution is constrained by the 20°C surface isotherm.

3. 3. All sea turtles exhibit temperature-dependent sex determination (TSD) with pivotal temperatures close to 29°C.

4. 4. It is suggested that hatchling sex ratio will vary chaotically because of TSD.

5. 5. Because of TSD and natal homing, sea turtles are likely to be adversely affected by global warming.

6. 6. TSD and global warming have implications for conservation/management of sea turtles.

     

To Eat or not to Eat an Endangered Species: Views of Local Residents and Physicians on the Safety of Sea Turtle Consumption in Northwestern Mexico

Sea turtles have historically been an important food resource for many coastal inhabitants of Mexico. Today, the consumption of sea turtle meat and eggs continues in northwestern Mexico despite well-documented legal protection and market conditions providing easier access to other more reliable protein sources. Although there is growing evidence that consuming sea turtles may be harmful to human health due to biotoxins, environmental contaminants, viruses, parasites, and bacteria, many at-risk individuals, trusted information sources, and risk communicators may be unaware of this information. Therefore, we interviewed 134 residents and 37 physicians in a region with high rates of sea turtle consumption to: (1) examine their knowledge and perceptions concerning these risks, as a function of sex, age, occupation, education and location; (2) document the occurrence of illness resulting from consumption; and (3) identify information needs for effective risk communication. We found that 32% of physicians reported having treated patients who were sickened from sea turtle consumption. Although physicians believed sea turtles were an unhealthy food source, they were largely unaware of specific health hazards found in regional sea turtles, regardless of location. By contrast, residents believed that sea turtles were a healthy food source, regardless of sex, age, occupation, and education, and they were largely unaware of specific health hazards found in regional sea turtles, regardless of age, occupation, and education. Although most residents indicated that they would cease consumption if their physician told them it was unhealthy, women were significantly more likely to do so than men. These results suggest that residents may lack the necessary knowledge to make informed dietary decisions and physicians do not have enough accurate information to effectively communicate risks with their patients.     

Respiration in neonate sea turtles

The pattern and control of respiration is virtually unknown in hatchling sea turtles. Using incubator-raised turtles, we measured oxygen consumption, frequency, tidal volume, and minute volume for leatherback (Dermochelys coriacea) and olive ridley (Lepidochelys olivacea) turtle hatchlings for the first six days after pipping. In addition, we tested the hatchlings' response to hypercapnic, hyperoxic, and hypoxic challenges over this time period. Hatchling sea turtles generally showed resting ventilation characteristics that are similar to those of adults: a single breath followed by a long respiratory pause, slow frequency, and high metabolic rate. With hypercapnic challenge, both species responded primarily by elevating respiratory frequency via a decrease in the non-ventilatory period. Leatherback resting tidal volume increased with age but otherwise, neither species' resting respiratory pattern nor response to gas challenge changed significantly over the first few days after hatching. At the time of nest emergence, sea turtles have achieved a respiratory pattern that is similar to that of actively diving adults.     

Metabolic scaling in turtles

Bennett and Dawson (1976) presented an analysis of the relationship of metabolic rate (MR) and body mass among turtles, based on 10 studies, but unlike most of other groups of ectotherms, there has been no update to include the many later reports on turtles. Here I present a review of the data on turtle metabolic rates at 20, 25, and 30 °C, along with regression equations and graphical analyses from a large number of studies. Two generalities emerge: (1) reported metabolic rates for sea turtles are higher than for other chelonians, although it is not certain whether this is an intrinsic characteristic of sea turtles or an artifact related to experimental conditions (such as greater activity of sea turtles in metabolic chambers and the fact that a number of studies were done with the turtles out of water), and (2) the slopes of the log–log plots of metabolic rate (MR) vs. body mass [b in the allometric equation MR = a(mass)^b] are mostly lower than previously reported in smaller studies.     

Long-term trends in abundance of green sea turtles (Chelonia mydas) assessed by non-lethal capture rates in a coastal fishery

Sea turtle populations underwent severe decline in historical times, mainly through harvesting eggs and adults on nesting beaches. With the reduction of this threat in many areas, coupled with other conservation actions, some populations have demonstrated encouraging recovery, although remaining below their previous levels and undergone additional modern threats such as incidental capture in fisheries and pollution. Trends in sea turtle populations have usually been assessed through monitoring of females or nests on nesting beaches. Here we present data from a 22-year monitoring period for a juvenile green sea turtle Chelonia mydas mixed-stock in southeastern Brazil that were incidentally captured in passive non-lethal pound nets. A total of 3639 green turtles were captured in 5323 fishing days.pound⁻¹ with mortality rate of 2%. Captures occurred in all months, but bycatch rates, excluding recapture events, were higher in September and October, probably due to the recruitment of turtles migrating from southern areas, as well as recruits from the oceanic zone. Capture rates increased by 9.2% per year in the period from 1995 to 2016, in line with increasing source populations, particularly the main source contributor at Ascension Island, but also Trindade Island (Brazil) and Aves Island (Venezuela). Mean Curved Carapace Length of green turtles was higher during austral summer/early autumn and decreased markedly in May, probably due to the small-sized individuals that recruited to the study site. We show that the incidental capture of sea turtles in non-lethal fisheries, such as Brazilian pound nets, could also provide data on trends of populations nesting in distant places, and can contribute to the assessment of population status of sea turtles within Regional Management Units throughout the Atlantic Ocean.