Swimming performance of hatchling green turtles is affected by incubation temperature

In an experiment repeated for two separate years, incubation temperature was found to affect the body size and swimming performance of hatchling green turtles (Chelonia mydas). In the first year, hatchlings from eggs incubated at 26°C were larger in size than hatchlings from 28 and 30°C, whilst in the second year hatchlings from 25.5°C were similar in size to hatchings from 30°C. Clutch of origin influenced the size of hatchlings at all incubation temperatures even when differences in egg size were taken into account. In laboratory measurements of swimming performance, in seawater at 28°C, hatchlings from eggs incubated at 25.5 and 26°C had a lower stroke rate frequency and lower force output than hatchlings from 28 and 30°C. These differences appeared to be caused by the muscles of hatchlings from cooler temperatures fatiguing at a faster rate. Clutch of origin did not influence swimming performance. This finding that hatchling males incubated at lower temperature had reduced swimming ability may affect their survival whilst running the gauntlet of predators in shallow near-shore waters, prior to reaching the relative safety of the open sea.     

Nano-tags for neonates and ocean-mediated swimming behaviours linked to rapid dispersal of hatchling sea turtles

Dispersal during juvenile life stages drives the life-history evolution and dynamics of many marine vertebrate populations. However, the movements of juvenile organisms, too small to track using conventional satellite telemetry devices, remain enigmatic. For sea turtles, this led to the paradigm of the ‘lost years'' since hatchlings disperse widely with ocean currents. Recently, advances in the miniaturization of tracking technology have permitted the application of nano-tags to track cryptic organisms. Here, the novel use of acoustic nano-tags on neonate loggerhead turtle hatchlings enabled us to witness first-hand their dispersal and behaviour during their first day at sea. We tracked hatchlings distances of up to 15 km and documented their rapid transport (up to 60 m min⁻¹) with surface current flows passing their natal areas. Tracking was complemented with laboratory observations to monitor swimming behaviours over longer periods which highlighted (i) a positive correlation between swimming activity levels and body size and (ii) population-specific swimming behaviours (e.g. nocturnal inactivity) suggesting local oceanic conditions drive the evolution of innate swimming behaviours. Knowledge of the swimming behaviours of small organisms is crucial to improve the accuracy of ocean model simulations used to predict the fate of these organisms and determine resultant population-level implications into adulthood.     

Foraging ranges and movements of jackass penguins (Spheniscus demersus) established through radio telemetry

In order to study the movements and activities at sea of jackass penguins rearing chicks, a radio telemetry study was undertaken. Twenty five transmitters were attached to breeding adult penguins at their nest sites. These penguins were tracked for a total of 414 hours using a system of antennae on a motor–boat, the island and land–based stations. The foraging paths, foraging duration, foraging distances and swimming speeds were studied. The penguins' foraging patterns were similar; they generally left the island at night and travelled towards their foraging area, actively foraging from first light until they swam back to the island. The foraging durations and distances varied, as did the swimming speeds, according to availability of food.     

Orientation and swimming behavior of hatchling loggerhead turtles Caretta caretta L. during their offshore migration

Loggerhead turtle Caretta caretta L. hatchlings emerging from nests on the eastern coast of Florida swim offshore toward the Florida Current. Part of the trip is accomplished during an initial 20-h period of swimming (the “frenzy”); the remainder may take a day or more of oriented swimming. Swimming speeds are slower than those of green turtles Chelonia mydas L. Hatchlings are well oriented in an offshore direction when released into the ocean during the day or night. Completion of a crawl down the beach or a plunge into the surf are unnecessary for proper orientation. Immediately after entering the ocean at night, responses to light appear essential for oriented swimming. However, present hypotheses based upon phototropotaxis may not account for orientation later in the migration.     

An assessment of initial body size in loggerhead sea turtle (Caretta caretta) hatchlings in Turkey

Eggs, hatchlings, and adult loggerhead turtles, and incubation durations of clutches, were measured on three Turkish beaches (Dalyan, Fethiye and G?ksu Delta), and some physical features of nests were compared. These features were not statistically different among the beaches, except for nest depth and distance to the high water mark. There was a positive relationship between hatchling mass and egg size. The carapace length of hatchlings was correlated with both egg diameter and incubation duration. The duration of asynchronous emergence of hatchlings on Fethiye beach was slightly longer than on the other two beaches, and the size of hatchlings decreased as asynchronous emergence proceeded. Of the hatchlings that emerged first, those that died were significantly smaller in SCL and mass than those that lived. These results suggest that smaller hatchlings may not be vigorous enough to emerge earlier from nests, and that they may be less fit.     

Warm water and cool nests are best. How global warming might influence hatchling green turtle swimming performance

For sea turtles nesting on beaches surrounded by coral reefs, the most important element of hatchling recruitment is escaping predation by fish as they swim across the fringing reef, and as a consequence hatchlings that minimize their exposure to fish predation by minimizing the time spent crossing the fringing reef have a greater chance of surviving the reef crossing. One way to decrease the time required to cross the fringing reef is to maximize swimming speed. We found that both water temperature and nest temperature influence swimming performance of hatchling green turtles, but in opposite directions. Warm water increases swimming ability, with hatchling turtles swimming in warm water having a faster stroke rate, while an increase in nest temperature decreases swimming ability with hatchlings from warm nests producing less thrust per stroke.     

Some Problems of Sea Turtle Ecology

Tagging programs have revealed parts of the patterns of reproductivemigration of some sea turtle populations, but much of the ecologicgeography of the species remains unknown. The present papertakes stock of the advances and gaps in our knowledge of thegroup. Kemp's ridley and the Tortuguero green turtle populationare used as sources of examples of these strong and weak areas.Possible causes of one-season nesting and its bearing on seaturtle demography are discussed. An apparent dichotomy in the"lost-year" ecology of the Tortuguero green turtles and Kemp'sridley is suggested. Some hatchlings of both evidently driftaway in major currents, while others pass this stage circlingin local eddies—Chelonia in the West Caribbean Gyre andLepidochelys kempi within the Gulf of Mexico.     

Orientation Cues Used by Hatchling Loggerhead Sea Turtles (Caretta caretta L.) During their Offshore Migration

Sea turtle hatchlings ernerge from underground nests, crawl to the ocean and swim out to sea. The orientation cues used to maintain offshore headings are unknown. Our field experiments suggest loggerhead hatchlings on the Atlantic coast of Florida continue on offshore headings by swimming into oceanic swells and wind-generated waves. Dependence on these cues appears complete when hatchlings are 3.0 km from shore. Because waves and swells usually approach from seaward directions, they are generally reliable guideposts.     

The Effects of Artificial Beach Nourishment on Marine Turtles: Differences between Loggerhead and Green Turtles

Marine turtle reproductive success is correlated with the stability and quality of the nesting environment. Female marine turtles show fidelity to nesting beaches, making artificial beach nourishment practices directly relevant to their recovery. We evaluated the impacts of artificial beach nourishment on Loggerhead ( Caretta caretta ) and Green turtles ( Chelonia mydas ) between artificially nourished and nonnourished beaches. We observed reduced nesting success (ratio of nesting emergences to emergences not resulting in nest deposition) for both species. This negative effect lasted for one season in Loggerheads and for at least one season in Green turtles. Physical attributes of the fill sand did not impede nesting attempts. We argue that the decrease in nesting success resulted from an altered beach profile not favorable for nest deposition, which subsequently improved in later seasons as the beach equilibrated to a more natural slope. We observed a 52.2% decrease in reproductive output (hatchlings km⁻¹ yr⁻¹) for Loggerheads one year postnourishment, with a 44.1% increase observed the two seasons postnourishment. In Green turtles, a 0.8% reduction was observed the first season postnourishment, despite a 13% increase in the nonnourished area. The reduction in reproductive output in both cases was primarily a consequence of decreased nesting success, lowering nest numbers. These results reveal stronger negative effects of beach nourishment on Loggerheads compared to Green turtles and the importance of minimizing excessive nonnesting emergences associated with artificial beach nourishment. Nourished areas also experienced more than 600% increase in the number of Loggerhead hatchlings disoriented by artificial lighting over two years postnourishment.     

Effect of waterfowl (Anas platyrhynchos) on indicator bacteria populations in a recreational lake Madison, Wisconsin.

A public swimming beach in Madison, wis., experienced intermittent high fecal coliform counts during the late summer and early fall of 1978. Public health officials closed the beach on a number of occasions. A public health survey identified a combination of waterfowl wastes and meteorological events as the explanation for the high bacteria counts. Fecal coliform bacteria were deposited by mallard ducks and multiplied in the beach sands. The bacteria were subsequently transported into the lake and resulted in high fecal coliform counts in the swimming area.     

Effect of waterfowl (Anas platyrhynchos) on indicator bacteria populations in a recreational lake Madison, Wisconsin.

A public swimming beach in Madison, wis., experienced intermittent high fecal coliform counts during the late summer and early fall of 1978. Public health officials closed the beach on a number of occasions. A public health survey identified a combination of waterfowl wastes and meteorological events as the explanation for the high bacteria counts. Fecal coliform bacteria were deposited by mallard ducks and multiplied in the beach sands. The bacteria were subsequently transported into the lake and resulted in high fecal coliform counts in the swimming area.     

Energetics during hatchling dispersal of the olive ridley turtle Lepidochelys olivacea using doubly labeled water

Studies of metabolism are central to the understanding of the ecology, behavior, and evolution of reptiles. This study focuses on one phase of the sea turtle life cycle, hatchling dispersal, and gives insight into energetic constraints that dispersal imposes on hatchlings. Hatchling dispersal is an energetically expensive phase in the life cycle of the olive ridley turtle Lepidochelys olivacea. Field metabolic rates (FMRs), determined using the doubly labeled water (DLW) method, for L. olivacea hatchlings digging out of their nest chamber, crawling at the sand surface, and swimming were five, four, and seven times, respectively, the resting metabolic rate (RMR). The cost of swimming was 1.5 and 1.8 times the cost of the digging and crawling phases, respectively, and we estimated that if L. olivacea hatchlings swim at frenzy levels, they can rely on yolk reserves to supply energy for only 3-6 d once they reach the ocean. We compared our RMR and FMR values by establishing an interspecific RMR mass-scaling relationship for a wide range of species in the order Testudines and found a scaling exponent of 1.06. This study demonstrates the feasibility of using the DLW method to estimate energetic costs of free-living sea turtle hatchlings and emphasizes the need for metabolic studies in various life-history stages.     

Response of southern right whales to simulated swim‐with‐whale tourism at Península Valdés,Argentina

Guidelines for sustainable tourism involving swimming with large whales are not well‐developed compared to those focused on programs of swimming with delphinids. From September to November 2005 and August to September 2006, we collected behavioral and movement data for southern right whales (Eubalaena australis) exposed to interactions with boats and swimmers at Península Valdés, Argentina. Whales were tracked from shore using a theodolite before, during, and after a series of directed interactions with swimmers and a boat. Resting, socializing, and surface active behavior decreased, traveling increased, and whales swam faster and reoriented more often during interactions. Responses were variable by age/sex class, with mother/calf pairs showing strongest responses. Increased levels of tourism activity are a concern, as reduction in resting time and disruption of socialization among adults, juveniles, and mother/calf pairs have unknown long‐term consequences. Additional data should be collected for whale behavior in proposed tourism and nontourism areas to build a long‐term database which can be used to determine if reactions of whales change over time. Our data suggest that swimming with whales in Chubut Province should not be legalized until further investigations are completed, especially in light of the recent southern right whale die‐offs recorded in Península Valdés.     

Locomotion in hatchling leatherback turtles Dermochelys coriacea

Hatchling leatherback turtles can only swim forwards, and employ synchronized beating of the forelimbs whether swimming slowly or quickly. The hind limbs make no contribution to propulsion. Effectively, the hatchlings have two swimming speeds; subsurface and fast (30 cm s^-1) or surfaced and slow (8 cm s^-1). Intermediate velocities are transitory; the hatchlings were never seen to rest without movement, nor did they exhibit gliding of the type seen in green turtles. During fast ('vigorous') swimming, power is developed on both the upstroke and downstroke of the limb cycle. During slow swimming, power is only developed during the upstroke—a consequence of the orientation of the axis of limb beat which is opposite in direction to that of cheloniid sea turtles. Terrestrial locomotion is laboured and features an unstable gait which involves simultaneous movement of all four limbs and forward overbalancing during each limb cycle.     

Comparisons of egg incubation and hatchling traits among captive cohorts of the Chinese three-keeled pond turtle, Chinemys reevesii

Freshly-laid eggs of the Chinese three-keeled pond turtle (Chinemys reevesii) from captive cohorts in Hunan, Shanghai and Jiangxi were incubated at four constant temperatures of 24, 26, 28 and 30 °C to assess the effects of incubation temperature and cohort origin on incubation duration and hatchling phenotypes. Eggs from the three cohorts differed in size and shape. Egg mass and width were greatest in the Hunan cohort, smallest in the Jiangxi cohort, with the Shanghai cohort in between. Incubation duration decreased with increasing temperature and differed among the cohorts, with longer incubation duration for eggs from the Jiangxi cohort than those from the Hunan or Shanghai cohorts. Incubation temperatures significantly affected hatchling size and hatchlings from 30 °C were smaller than those from the lower temperatures in terms of carapace size and body mass. When incubated at a common temperature, hatchlings from the Hunan and Shanghai cohorts were larger than those from the Jiangxi cohort. The swimming capacity of hatchlings was affected by incubation temperature, but did not differ among the cohorts. The characteristics of eggs and hatchlings were similar among the Hunan and Shanghai cohorts, but they differed significantly from the Jiangxi cohort.     

Invertebrate infestation on eggs and hatchlings of the loggerhead turtle, Caretta caretta, in Dalaman, Turkey

The damage caused by some invertebrates to the eggs and hatchlings of loggerhead turtles, Caretta caretta, was investigated during the summer of 2002 on Dalaman beach, Turkey. The specimens, identified to family or genus levels, from nine families representing seven orders were recorded as infesting nests of loggerhead turtles. The heaviest impacts on loggerhead turtle nests was made by Pimelia sp. (Tenebrionidae, Coleoptera). Twenty-four (36.3%) out of 66 intact loggerhead hatched nests were affected by these larvae. Larval damage by Pimelia sp. was recorded in 188 (10.6%) out of 1773 eggs, but only in two (0.28%) hatchlings. The results show that fewer insects were in the nest the further from vegetation and therefore the relocation of nests from the water's edge to further inland close to vegetation may increase the infestation rate of the eggs.     

The Conservation of Sea Turtles: Practices and Problems

The various techniques in common use for conservation and restorationof depleted sea turtle populations are reviewed, namely: banninginternational commerce; operating artificial hatcheries, bothin the natural beach environment and in styrofoam and othertypes of incubators; "head-starting" of hatchlings in captivity;protection of nesting females by means of beach patrols; andtranslocation of eggs or hatchlings to distant areas from whichturtles have been extirpated or to which it is desired to introducenew colonies. The difficulties of monitoring the results ofall of these techniques are discussed, and potential dangersor disadvantages of each approach are reviewed. It is concludedthat, until unequivocal data become available, turtle conservationistsshould continue to pursue common sense or logically sound restorationprograms, but should constantly re-evaluate their actions inthe light of the latest available knowledge and modify or desistfrom current approaches as necessary.     

Effect of position-fixing interval on estimated swimming speed and movement pattern of fish tracked with a stationary positioning system

Ultrasonic telemetry using stationary positioning systems allows several fish to be tracked simultaneously, but systems that are incapable of sampling multiple frequencies simultaneously can record data from only one transmitter (individual) at a time. Tracking several individuals simultaneously thus results in longer intervals between successive position fixes for each fish. This deficiency leads to loss of detail in the tracking data collected, and may be expected to cause loss of accuracy in estimates of the swimming speeds and movement patterns of the fish tracked. Even systems that track fish on multiple frequencies are not capable of continuous tracking due to technical issues. We determined the swimming speed, area occupied, activity rhythm and movement pattern of cod (Gadus morhua) using a stationary single-channel positioning system, and analysed how estimates of these behavioural parameters were affected by the interval between successive position fixes. Single fish were tracked at a time, and position fixes were eliminated at regular intervals in the original data to generate new data sets, as if they had been collected in the course of tracking several fish (2–16). In comparison with the complete set, these data sets gave 30–70% decreases in estimates of swimming speed depending on the number of fish supposedly being tracked. These results were similar for two individuals of different size and activity level, indicating that they can be employed as correction factors to partly compensate for underestimates of swimming speed when several fish are tracked simultaneously. Tracking `several' fish only slightly affected the estimates of area occupied (1–15%). The diurnal activity rhythm was also similar between the data sets, whereas details in search pattern were not seen when several fish were tracked simultaneously.     

Comparisons of egg incubation and hatchling traits among captive cohorts of the Chinese three-keeled pond turtle, Chinemys reevesii

Freshly-laid eggs of the Chinese three-keeled pond turtle (Chinemys reevesii) from captive cohorts in Hunan, Shanghai and Jiangxi were incubated at four constant temperatures of 24, 26, 28 and 30 °C to assess the effects of incubation temperature and cohort origin on incubation duration and hatchling phenotypes. Eggs from the three cohorts differed in size and shape. Egg mass and width were greatest in the Hunan cohort, smallest in the Jiangxi cohort, with the Shanghai cohort in between. Incubation duration decreased with increasing temperature and differed among the cohorts, with longer incubation duration for eggs from the Jiangxi cohort than those from the Hunan or Shanghai cohorts. Incubation temperatures significantly affected hatchling size and hatchlings from 30 °C were smaller than those from the lower temperatures in terms of carapace size and body mass. When incubated at a common temperature, hatchlings from the Hunan and Shanghai cohorts were larger than those from the Jiangxi cohort. The swimming capacity of hatchlings was affected by incubation temperature, but did not differ among the cohorts. The characteristics of eggs and hatchlings were similar among the Hunan and Shanghai cohorts, but they differed significantly from the Jiangxi cohort.     

Length‐weight relationship of fish species from the Bijagós Archipelago,Guinea‐Bissau

Length–weight relationships were estimated for six teleost fish species occurring in Bijagós Archipelago, Guinea‐Bissau. Samples were collected seasonally during three dry seasons (2013/2014, 2014/2015, 2015/2016) and two rainy seasons (2015 and 2016). Fishes were captured by three methods: angled from the beach or a boat; using beach seine with a mesh size ranging 0.5–1 cm; drift netting from a boat (mesh size 2 cm). This work provides the length‐weight relationship for three fish species that are not reported in FishBase (Citharichthys stampflii, Gerres nigri and Psettodes belcheri) as well as for three species from which we present a wider size range (Eucinostomus melanopterus, Scomberomorus tritor and Sphyraena afra).