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A WESTERN Australian first trial to return oysters to an Albany estuary is exceeding scientists' expectations, a year into the ambitious project.

Coral reefs off Tanzania's coast are being destroyed, most beyond repair.

As well as being a beautiful species capable of changing its colour, shape and even gender, new research published today shows that parrotfish, commonly found on healthy coral reefs, can also play a pivotal role in providing the sands necessary to build and maintain coral reef islands.

As well as being a beautiful species capable of changing its colour, shape and even gender, new research published today shows that parrotfish, commonly found on healthy coral reefs, can also play a pivotal role in providing the sands necessary to build and maintain coral reef islands.

As well as being a beautiful species capable of changing its colour, shape and even gender, new research published today shows that parrotfish, commonly found on healthy coral reefs, can also play a pivotal role in providing the sands necessary to build and maintain coral reef islands.

UM Rosenstiel School-led team reveals new details on modern-day stromatolites.

UM Rosenstiel School-led team reveals new details on modern-day stromatolites.

They once inhabited the seafloor and have been steadily buried: Microorganisms in the sub-surface sediments at the bottom of the Arabian Sea reveal details of fluctuations in climate and environmental conditions over the past 52,000 years.

When reefs decline, parrotfish thrive.

Age and growth data are central to management or conservation strategies for any species. Circumstantial evidence suggests that male whale sharks (Rhincodon typus) grow to asymptotic sizes much smaller than those predicted by age and growth studies and consequently, there may be sex-specific size and growth patterns in the species. We tested this hypothesis by using stereo-video and photo-identification studies to estimate the growth rates of 54 whale sharks that were resighted over a period of up to a decade at Ningaloo Reef. We found that male growth patterns were consistent with an average asymptotic total length (TL) of approximately 8-9 m, a size similar to direct observations of size at maturity at aggregation sites world-wide and much smaller than the sizes predicted by earlier modeling studies. Females were predicted to grow to an average asymptotic length of around 14.5 m. Males had growth coefficients of K = 0.088 year-1, whereas limited resighting data suggested a growth coefficient of K = 0.035 year-1 for females. Other data including re-sightings of an individual male over two decades, records of sex-specific maximum sizes of individuals captured in fisheries and data from juveniles growing in aquaria were also consistent with the suggestion of sex-specific growth profiles for the species. We argue that selection for sex-specific growth patterns could explain many of the otherwise enigmatic patterns in the ecology of this species including the tendency of the species to form aggregations of juvenile males in coastal waters.

Tropical shallow-water habitats represent the marine environments with the greatest biodiversity; however, these habitats are the most vulnerable to climate warming. Corals, seagrasses, and macroalgae play a crucial role in the structure, functions, and processes of the coastal ecosystems. Understanding their growth and physiological responses to elevated temperature and interspecific sensitivity is a necessary step to predict the fate of future coastal community. Six species representatives, including Pocillopora acuta, Porites lutea, Halophila ovalis, Thalassia hemprichii, Padina boryana, and Ulva intestinalis, collected from Phuket, Thailand, were subjected to stress manipulation for 5 days. Corals were tested at 27, 29.5, 32, and 34.5°C, while seagrasses and macroalgae were tested at 27, 32, 37, and 42°C. After the stress period, the species were allowed to recover for 5 days at 27°C for corals and 32°C for seagrasses and macroalgae. Non-destructive evaluation of photosynthetic parameters (Fv/Fm, Fv/F0, ϕPSII and rapid light curves) was carried out on days 0, 3, 5, 6, 8, and 10. Chlorophyll contents and growth rates were quantified at the end of stress, and recovery periods. An integrated biomarker response (IBR) approach was adopted to integrate the candidate responses (Fv/Fm, chlorophyll content, and growth rate) and quantify the overall temperature effects. Elevated temperatures were found to affect photosynthesis, chlorophyll content, and growth rates of all species. Lethal effects were detected at 34.5°C in corals, whereas adverse but recoverable effects were detected at 32°C. Seagrasses and macroalgae displayed a rapid decline in photosynthesis and lethal effects at 42°C. In some species, sublethal stress manifested as slower growth and lower chlorophyll content at 37°C, while photosynthesis remained unaffected. Among all, T. hemprichii displayed the highest thermotolerance. IBR provided evidence that elevated temperature affected the overall perf

Changes in marine ecosystems from human stressors, and concerns over how species will respond to these changes have emphasized the importance of understanding and monitoring crucial demographic parameters for population models. Long-lived, migratory, marine vertebrates such as sea turtles are particularly vulnerable to changes. Life-history parameters like growth-in-body size can be largely influenced by environmental processes which can impact population growth. We analyzed a 40-year (1981-2021) capture-mark-recapture dataset from the protected UNESCO World Heritage Site, Aldabra Atoll, Seychelles, to estimate key population parameters, including body growth, for immature green turtles (Chelonia mydas) and hawksbill turtles (Eretmochelys imbricata). Curved carapace length (CCL) range was 34.3-110.9 cm (mean ± SD: 51.0 ± 11.4 cm, n = 1191) for green turtles and 28.7-89.4 cm (47.7 ± 14.4 cm, n = 538) for hawksbill turtles. Recapture events, with an 11-month minimum period, revealed a mean annual growth rate of 3.2 ± 1.5 cm year−1 for green turtles (n = 75) and 2.8 ± 1.4 cm year−1 for hawksbill turtles (n = 110). Hawksbill turtles exhibited a non-monotonic growth rate while no significant growth-size relationship was detected for green turtles. Green turtle mean annual growth per 10-cm size class was highest in the larger size classes (50‒69.9 cm). Hawksbill turtle growth rate was highest in the larger size classes (50‒69.9 cm) then declined in the largest size class (70‒79.9 cm). Green turtles and hawksbill turtles may spend > 8 and 18 years, respectively, using Aldabra, Seychelles, as a foraging ground.