Ecology of juvenile hawksbills (Eretmochelys imbricata) at Buck Island Reef National Monument, US Virgin Islands

Surveys of juvenile hawksbills around Buck Island Reef National Monument, US Virgin Islands from 1994 to 1999 revealed distributional patterns and resulted in a total of 75 individual hawksbill captures from all years; turtles ranged from 23.2 to 77.7 cm curved carapace length (CCL; mean 42.1 ± 12.3 cm SD). Juveniles concentrated where Zoanthid cover was highest. Length of time between recaptures, or presumed minimum site residency, ranged from 59 to 1,396 days (mean 620.8 ± 402.4 days SD). Growth rates for 23 juveniles ranged from 0.0 to 9.5 cm year^?1 (mean 4.1 ± 2.4 cm year^?1SD). Annual mean growth rates were non-monotonic, with the largest mean growth rate occurring in the 30–39 cm CCL size class. Gastric lavages indicated that Zoanthids were the primary food source for hawksbills. These results contribute to our understanding of juvenile hawksbill ecology and serve as a baseline for future studies or inventories of hawksbills in the Caribbean.     

Spatial and temporal variability in somatic growth of green sea turtles (<Emphasis Type="Italic">Chelonia mydas</Emphasis>) resident in the Hawaiian Archipelago

The somatic growth dynamics of green turtles (Chelonia mydas) resident in five separate foraging grounds within the Hawaiian Archipelago were assessed using a robust non-parametric regression modelling approach. The foraging grounds range from coral reef habitats at the north-western end of the archipelago, to coastal habitats around the main islands at the south-eastern end of the archipelago. Pelagic juveniles recruit to these neritic foraging grounds from ca. 35 cm SCL or 5 kg (~6 years of age), but grow at foraging-ground-specific rates, which results in quite different size- and age-specific growth rate functions. Growth rates were estimated for the five populations as change in straight carapace length (cm SCL year^–1) and, for two of the populations, also as change in body mass (kg year^–1). Expected growth rates varied from ca. 0–2.5 cm SCL year^–1, depending on the foraging-ground population, which is indicative of slow growth and decades to sexual maturity, since expected size of first-time nesters is 80 cm SCL. The expected size-specific growth rate functions for four populations sampled in the south-eastern archipelago displayed a non-monotonic function, with an immature growth spurt at ca. 50–53 cm SCL (~18–23 kg) or ca. 13–19 years of age. The growth spurt for the Midway atoll population in the north-western archipelago occurs at a much larger size (ca. 65 cm SCL or 36 kg), because of slower immature growth rates that might be due to a limited food stock and cooler sea surface temperature. Expected age-at-maturity was estimated to be ca. 35–40 years for the four populations sampled at the south-eastern end of the archipelago, but it might well be >50 years for the Midway population. The Hawaiian stock comprises mainly the same mtDNA haplotype, with no differences in mtDNA stock composition between foraging-ground populations, so that the geographic variability in somatic growth rates within the archipelago is more likely due to local environmental factors rather than genetic factors. Significant temporal variability was also evident, with expected growth rates declining over the last 10–20 years, while green turtle abundance within the archipelago has increased significantly since the mid-1970s. This inverse relationship between somatic growth rates and population abundance suggests a density-dependent effect on somatic growth dynamics that has also been reported recently for a Caribbean green turtle stock. The Hawaiian green turtle stock is characterised by slow growth rates displaying significant spatial and temporal variation and an immature growth spurt. This is consistent with similar findings for a Great Barrier Reef green turtle stock that also comprises many foraging-ground populations spanning a wide geographic range.Communicated by P.W. Sammarco, Chauvin     

Population ecology of the green/black turtle (<Emphasis Type="Italic">Chelonia mydas</Emphasis>) in Bahía Magdalena,Mexico

The mangrove channels of Bahía Magdalena, Mexico, are important developmental areas for juvenile green, or black turtles (Chelonia mydas), but incidental bycatch and illegal hunting threaten population persistence. We studied size distribution, condition index (CI), growth rates, and mortality of black turtles in Estero Banderitas, the largest mangrove channel in Bahía Magdalena, to supply information for the development of effective conservation strategies. A total of 213 black turtles (including 88 recaptures) were caught in entanglement nets between July 2000 and July 2003. Average yearly catch per unit of effort (CPUE, 1 unit: 100 m of net fishing for 12 h) dropped during the study from 2.19 to 0.76. About 97% of all turtles were considered juveniles, average size was 54.6 ± 9.5 cm. Turtles were significantly smaller at the head of Estero Banderitas than in the central part of the Estero and in the open bay, indicating size-based habitat segregation. Average growth rate was 1.62 cm/year and declined with increasing size. Growth was seasonal and three times higher in summer (0.28 cm/month) than in winter (0.09 cm/month), body CI was also significantly higher during the summer months. A seasonalized von Bertalanffy growth function (VBGF) was used to model growth for the size range studied (43–73 cm SCL), with the parameters: L _∞ = 101 cm SCL; K = 0.04 year⁻¹; t ₀ = 0; C = 0.4 and t _s = 0.75. Growth data indicate that black turtles may spend up to 20 years in Bahía Magdalena before they reach maturity at about 77 cm SCL. The total mortality estimate (Z) from the length converted catch curve was 0.16, corresponding to a yearly survival probability of 0.85.     

Ecology of loggerhead marine turtles Caretta caretta in a neritic foraging habitat: movements, sex ratios and growth rates

Much is still to be learned about the spatial ecology of foraging marine turtles, especially for juveniles and adult males which have received comparatively little attention. Additionally, there is a paucity of ecological information on growth rates, size and age at maturity, and sex ratios at different life stages; data vital for successful population modelling. Here, we present results of a long-term (2002–2011) study on the movements, residency, growth and sex ratio of loggerhead turtles (Caretta caretta) in Amvrakikos Gulf (39°0′N 21°0′E), Greece, using satellite telemetry (N = 8) and ongoing capture–mark–recapture (CMR; N = 300 individuals). Individuals encountered at sea ranged from large juvenile to adult (46.2–91.5 cm straight carapace length) and demonstrated growth rates within published norms (<2.7 cm yr^?1) that slowed with increasing body size. We revealed that an unexpectedly high proportion of animals were male (>44 % of captures above 65 cm straight carapace length), compared to region-wide female-biased hatchling production, indicating sex-biased survival or possible behavioural drivers for likelihood of capture in the region. Satellite tracking confirmed that some turtles establish discrete, protracted periods of residency spanning more than 1 year, whilst others migrated away from the site. These findings are underlined by CMR results with individual capture histories spanning up to 7 years, and only 18 % of individuals being recaptured.     

A new method for high-resolution bivalve growth rate studies in hydrothermal environments

The age and shell growth rate of deep-sea hydrothermal bivalves were investigated for the first time using in situ chemical staining combined with high-resolution micro-increment analysis. A staining chamber developed for this purpose was applied to a patch of Bathymodiolus thermophilus mussels at 2,500 m depth at the 9°47′N vent field on the East Pacific Rise (EPR) in May 2010. This approach minimizes disturbance of the mussels in their habitat. Bathymodiolus thermophilus grows according to a circalunidian rhythm, with one increment formed each day, and displays tide-related growth rate variability. Based on the von Bertalanffy growth rate model, the largest shell collected (SL = 20.5 cm) would be 10.0 year old, with a growth rate of 4.2–1.1 cm year^?1 as the shell ages. This fast growth rate is consistent with the instability of the environment in this section of the EPR and observed recolonization rates and could reflect a specific adaptation of this species.     

Temporal, spatial, and body size effects on growth rates of loggerhead sea turtles (Caretta caretta) in the Northwest Atlantic

In response to a call from the US National Research Council for research programs to combine their data to improve sea turtle population assessments, we analyzed somatic growth data for Northwest Atlantic (NWA) loggerhead sea turtles (Caretta caretta) from 10 research programs. We assessed growth dynamics over wide ranges of geography (9–33°N latitude), time (1978–2012), and body size (35.4–103.3 cm carapace length). Generalized additive models revealed significant spatial and temporal variation in growth rates and a significant decline in growth rates with increasing body size. Growth was more rapid in waters south of the USA (<24°N) than in USA waters. Growth dynamics in southern waters in the NWA need more study because sample size was small. Within USA waters, the significant spatial effect in growth rates of immature loggerheads did not exhibit a consistent latitudinal trend. Growth rates declined significantly from 1997 through 2007 and then leveled off or increased. During this same interval, annual nest counts in Florida declined by 43 % (Witherington et al. in Ecol Appl 19:30–54, 2009) before rebounding. Whether these simultaneous declines reflect responses in productivity to a common environmental change should be explored to determine whether somatic growth rates can help interpret population trends based on annual counts of nests or nesting females. Because of the significant spatial and temporal variation in growth rates, population models of NWA loggerheads should avoid employing growth data from restricted spatial or temporal coverage to calculate demographic metrics such as age at sexual maturity.     

Seasonal and diel variation in movement rhythms of sand dollar, Peronella lesueuri (Valenciennes 1841), in Cockburn Sound, Western Australia

Rates and direction of movement in the sand dollar Peronella lesueuri were measured in summer and winter in Cockburn Sound, a large coastal embayment in south-western Australia. P. lesueuri was found to have a diurnal activity pattern throughout the year and had a greater movement rate in the summer (mean of 5.3 cm h^?1, day; 3.9 cm h^?1, night) than in the winter (mean of 2.7 cm h^?1, day; 2.0 cm h^?1, night). Seasonal change in temperature and physiological requirements by the sand dollar are the most likely reason for the seasonal differences. Reasons for diurnal variation were not clear. Direction of movement was found to be random at both times of the year. Based on these movement rates, one sand dollar can bioturbate an approximate area of 0.1 m² day^?1 and 36.4 m² year^?1. At a conservative density estimate of 0.5 sand dollars per m² it takes approximately 20 days for the sand dollars to rework the entire area of the sediments in the habitats they occupy.     

Comparative skeletochronological analysis of Kemp’s ridley (<Emphasis Type="Italic">Lepidochelys kempii</Emphasis>) and loggerhead (<Emphasis Type="Italic">Caretta caretta</Emphasis>) humeri and scleral ossicles

Skeletochronological analysis of Kemp’s ridley (Lepidochelys kempii) and loggerhead (Caretta caretta) sea turtle humeri and scleral ossicles was conducted to (1) describe the characteristics of scleral ossicles in these species, (2) determine whether the scleral ossicles contain annually deposited skeletal growth marks and (3) evaluate the potential for skeletochronological analysis of ossicles to obtain age data for size classes and species of sea turtles whose humeri exhibit prohibitive amounts of growth mark resorption. Humeri, entire eyes, and/or individual scleral ossicles were collected from stranded, dead sea turtles that were found along the coasts of Florida, North Carolina, Virginia, and Texas, USA. Samples were taken from a total of 77 neritic, juvenile Kemp’s ridleys ranging from 21.1 to 56.8 cm straightline carapace length (SCL), as well as two Kemp’s ridley hatchlings. For loggerheads, samples were obtained from 65 neritic juvenile and adult turtles ranging from 44.7 to 103.6 cm SCL and ten hatchlings. Examination of the ossicles revealed the presence of marks similar in appearance to those found in humeri. The number of marks in the ossicles and humeri of individual juvenile Kemp’s ridleys for which both structures were collected (n = 55) was equivalent, strongly indicating that the marks are annual. However, in large juvenile and adult loggerhead turtles (n = 65), some significant resorption of early growth marks was observed, suggesting that although ossicles might be useful for skeletochronological analysis of small juveniles, they may not provide a reasonable alternative to humeri for obtaining age estimates for older loggerhead sea turtles.     

Combination system of full-scale constructed wetlands and wetland paddy fields to remove nitrogen and phosphorus from rural unregulated non-point sources

Constructed wetlands (CWs) have been used effectively to remove nitrogen (N) and phosphorus (P) from non-point sources. Effluents of some CWs were, however, still with high N and P concentrations and remained to be pollution sources. Widely distributed paddy fields can be exploited to alleviate this concern. We were the first to investigate a combination system of three-level CWs with wetland paddy fields in a full scale to remove N and P from rural unregulated non-point sources. The removal efficiencies (REs) of CWs reached 57.3 % (37.4–75.1 %) for N and 76.3 % (62.0–98.4 %) for P. The CWs retained about 1,278 kg N ha^?1 year^?1 and 121 kg P ha^?1 year^?1. There was a notable seasonal change in REs of N and P, and the REs were different in different processing components of CWs. The removal rates of wetland paddy fields adopt “zero-drainage” water management according to local rainfall forecast and physiological water demand of crop growth reached 93.2 kg N ha^?1 year^?1 and 5.4 kg P ha^?1 year^?1. The rice season had higher potential in removing N and P than that in the wheat season. The whole combined system (0.56 ha CWs and 5.5 ha wetland paddy fields) removed 1,790 kg N year^?1 and 151 kg P year^?1, which were higher than those from CWs functioned alone. However, another 4.7-ha paddy fields were needed to fully remove the N and P in the effluents of CWs. The combination of CWs and paddy fields proved to be a more efficient nutrient removal system.     

Population age structure and rhizome growth of<Emphasis Type="Italic"> Cymodocea nodosa</Emphasis> in the Ria Formosa (southern Portugal)

The population age structure and derived population dynamics (recruitment, growth and mortality), rhizome growth and flowering effort of Cymodocea nodosa in the Ria Formosa (south of Portugal) were examined using reconstruction techniques. The horizontal rhizome elongation rates were low (13.8–30.7 cm year^–1), which is consistent with the low population growth rate (–2.35 to 0.29 year^–1). The vertical elongation rate was proportional to the horizontal growth except for one stand that was subjected to sand movements and had higher elongation rates. The mean leaf production varied from 11.8 to 14 leaves year^–1. The average shoot age varied from 0.70 to 1.04 years, and the oldest shoot found was 7.6 years. The mortality rates were the highest as yet reported for this species (0.99–3.70 year^–1). Observed low growth and high mortality are possibly associated with the development of eutrophic conditions in the Ria Formosa. The flowering probability found in Ria Formosa stands (<0.009–0.90 shoots^–1 year^–1) was comparable to that found in the Mediterranean and off the Canary Islands. Only two stands with flowering events were found inthe Ria Formosa population, which indicates that the stands are highly dependent on clonal growth to maintain themselves inthe Ria Formosa.Communicated by O. Kinne, Oldendorf/Luhe     

Hawksbill sea turtles in seagrass pastures: success in a peripheral habitat

Hawksbill sea turtles, Eretmochelys imbricata, are closely associated with coral reef and other hard-bottom habitats. Seagrass pastures are peripheral habitats for Caribbean hawksbills. With the decline in quality and quantity of coral reefs, seagrass habitats may become more important for hawksbills. We use data from a 30-year mark-recapture study of hawksbills and green turtles, Chelonia mydas, in the southern Bahamas to assess the quality of a seagrass habitat for hawksbills. Size distribution, residence times, and body condition index for the seagrass hawksbill aggregation are similar to those of hawksbill aggregations over Caribbean reefs. Somatic growth rates of seagrass hawksbills are in the upper range of those reported for reef hawksbills. Based on these parameters, peripheral seagrass habitats can support healthy, productive hawksbill aggregations. During the 30-year study, a sixfold variation in green turtle density in the study area did not affect the productivity or body condition of hawksbills.     

Immobilisation of manganese,cobalt and nickel by deep-sea-sediment microbial communities

Box core samples BC26 and BC36 from geologically different settings were examined to test the hypothesis that autochthonous microbial communities from polymetallic-nodule-rich Central Indian Basin sediments actively participate in immobilising metal ions. The bottom water dissolved oxygen concentration was reported to be 4.2–4.3 mL·L^?1 in the northern siliceous ooze (BC26) and 4.1–4.2 mL·L^?1 in the southern pelagic red clay (BC36); the sedimentation rates for these regions were 0.834 and 0.041 cm·kyr^?1, respectively. An onboard experiment, conducted under oxic and sub-oxic conditions with 100 μmol of Mn, Co and Ni, showed that microbial immobilisation under sub-oxic conditions was higher than in azide-treated controls in BC26 for Mn, Co and Ni at 30, 2 and 4 cm below sea floor (bsf), respectively, after 45 days. The trend in immobilisation was BC 26>BC 36, Co>Mn>Ni under oxic conditions and Mn>Co>Ni under sub-oxic conditions. The depth of maximum immobilisation for Co in BC26 under sub-oxic conditions coincided with the yield of cultured Co-tolerant bacteria and Ni only with organic carbon at 4 cm bsf. This study demonstrates that the organic carbon content and bioavailable metal concentrations in sediments regulate microbial participation in metal immobilisation.     

Analysis of a Fisheries Model for Harvest of Hawksbill Sea Turtles (Eretmochelys imbricata)

The hawksbill sea turtle ( Eretmochelys imbricata ) is valued for its mottled shell, called bekko in Japan. Populations of hawksbills have declined worldwide, and currently there is a ban on all international trade of hawksbill shell and products (Convention on International Trade of Endangered Species of Wild Fauna and Flora). In 1992 the Bekko Association of Japan introduced a fisheries model for hawksbill sea turtles in Cuba. The model estimated a sustainable yield of 5500 turtles from Cuban feeding grounds. We examined the model to determine whether this level of harvest was reasonable. Little biological information is available for hawksbills, so the model contained a number of simplifying assumptions, and several of its parameters were unsupported by data. The population was assumed to be at equilibrium, with a constant number of recruits (1-year-old turtles) and constant annual survival and growth rates. We analyzed the model to see how population size and sustainable yield results were affected by changes in various model parameters, and we found that the model was most sensitive to annual survival probability, which was assumed to be a constant 90% per year for all turtles greater than 1 year old. When we entered growth curves generated by mark-recapture data from other hawksbill populations, the model predicted a wide range of population sizes and sustainable yields. We determined that the assumptions of the current model make it unreliable for predicting sustainable yield of hawksbills, and that much research is needed to produce a more accurate model for management of this endangered species.     

Threshold to maturity in a long-lived reptile: interactions of age, size, and growth

Thresholds to sexual maturity—either age or size—are critical life history parameters. Usually investigated in short-lived organisms, these thresholds and interactions among age, size, and growth are poorly known for long-lived species. A 34-year study of captive green turtles (Chelonia mydas) that followed individuals from hatching to beyond maturity provided an opportunity to evaluate these parameters in a long-lived species with late maturity. Age and size at maturity are best predicted by linear growth rate and mass growth rate, respectively. At maturity, resource allocation shifts from growth to reproductive output, regardless of nutrient availability or size at maturity. Although captive turtles reach maturity at younger ages than wild turtles, the extensive variation in captive turtles under similar conditions provides important insights into the variation that would exist in wild populations experiencing stochastic conditions. Variation in age/size at maturity should be incorporated into population models for conservation and management planning.     

Lights and shadows: growth patterns in three sympatric and congeneric sponges (Ircinia spp.) with contrasting abundances of photosymbionts

The life-history traits of long-lived benthic littoral invertebrates remain poorly understood. In this study, we analysed patterns of growth in three abundant sublittoral sponges from the western Mediterranean Sea, chosen for their close phylogenetic relatedness, sympatric distribution, and contrasting amounts of photosymbionts: high in Ircinia fasciculata, lower in I. variabilis, and absent in I. oros. Sponge area, perimeter, number of oscula, and epibiont abundance were quantified from in situ digital images taken monthly for 1.5 years and volumetric growth rates were calculated from empirical area–volume relationships. Volumetric growth rates were different among species and coherent with the photosymbiont abundance: high in I. fasciculata (40.03 ± 4.81 % year^?1, mean ± SE), low in I. variabilis (5.65 ± 6.11 % year^?1), and almost nil in I. oros (?0.04 ± 3.02 % year^?1). Furthermore, a marked seasonality was observed in the first two species, with greater growth during the warm season. The high growth rates of I. fasciculata were likely fuelled by symbiont-derived photosynthates and required to compete in the well-lit, algal-dominated habitats this species prefers. In contrast, I. variabilis and I. oros tended to dwell in shaded habitats, where competition from slow-growing invertebrates is intense, and featured lower growth rates. The flattened morphology and lower circularity of I. variabilis indicates a capacity for adaptation to any space that is freed, while I. oros had less oscula and was more massive and circular, suggesting a strategy of passive occupation and minimisation of biological interactions. The results show that even congeneric species living sympatrically can achieve important biomass using different growth and substrate occupation strategies.     

Predicting the spatial distribution of mangroves in a South African estuary in response to sea level rise,substrate elevation change and a sea storm event

The spatial distribution of mangroves in the Mngazana Estuary under sea level rise induced by climate change, together with different substrate elevation change scenarios was predicted for 2020, 2050 and 2100. The present inundation frequency tolerance range was from 0.8 to 31.2 %, equivalent to substrate elevation thresholds of 1.1 and 1.7 m amsl. These thresholds were measured by field surveys and analysis of a gauge station situated near the mouth of the estuary. The predictions were based on the assumption that the inundation frequency tolerance range of mangrove stands remains constant in the future. Through the use of a digital elevation model an initial increase of 2.10 ha year^?1 was found in mangrove area between present and 2020 (from 122.6 to 143.6 ha). This was due to habitat becoming available that is currently too compacted for seedling establishment to occur. This compaction resulted from human and cattle traffic for grazing. Thereafter there would be a mean loss of 0.66 ha year^?1 from 2020 through 2100. Landward migration of mangroves would not take place due to the elevation limit of adjacent non-mangrove areas. In addition, the loss rate would increase to 1.01 ha year^?1 under insufficient sediment accretion, but would decrease to 0.18 ha year^?1 under thriving mangroves condition. The analysis of sea storm event in September 2008 showed that local water level increased by 28 cm and maximum affected area was 87.0 ha (about 71 % of mangrove stands). The inundation continued over 5 days. The results indicated that the combination impact of sea level rise, substrate elevation change and sea storm would possibly be a threat to tropical African estuaries with large flat intertidal areas and mangroves.     

Growth dynamics of Saccharina latissima (Laminariales,Phaeophyceae) in Aarhus Bay,Denmark, and along the species’ distribution range

Growth dynamics of Saccharina latissima in a Danish embayment (56°03.793N, 10°16.148E) were investigated through an annual cycle (March 1999–March 2000) and related to patterns found in previous studies covering the distribution range of the species. The kelps exhibited meristematic growth as well as distal tissue loss all year around. Elongation rate peaked in spring (March–May, 0.75 cm day^?1), whereas maximum biomass growth occurred in May–July at higher insolation. S. latissima accumulated nitrogen (N) in November–March, when ambient N levels were high and the fast growth in March–July was followed by a depletion of these reserves. Light regimes and seasonal fluctuations of nutrients were, thus, major factors explaining the seasonal growth pattern of S. latissima in this temperate bay. Differences in light and exposure along depth gradients affected the growth, loss and storage product dynamics. High losses of N and carbon (C) through summer abscission of distal tissue question the efficiency of translocation, especially at shallower depths, where losses are accelerated by, e.g., high temperature. A large-scale comparison further highlighted that warming advanced the timing, increased the level of peak growth and also seemed to expand the growth period. Growth rates of the studied Danish population fell in the low end of the range for similar latitudes and temperatures, probably due to sub-optimal salinities (avg. 23.3 psu) in combination with periodically high summer temperatures (max. 21.1 °C).     

Mesocosm and in situ observations of the burrowing shrimp Calocaris templemani (Decapoda: Thalassinidea) and its bioturbation activities in soft sediments of the Laurentian Trough

In vivo observations in laboratory mesocosms and aquaria, accompanied with in situ photographic surveys, have shown that the burrowing shrimp Calocaris templemani has a significant impact on bottom sediment dynamics and geochemistry in the St. Lawrence Estuary. This burrowing shrimp establishes and maintains complex semi-permanent burrows made up of several interconnected, ‘U-shaped’ galleries with generally four or more openings to the sediment surface. In the Estuary, at 345 m depth, Calocaris average density was estimated at 3.4 individuals m^?2. Observed individual burrows reached a maximum volume of 0.54 L. C. templemani displaces this volume of mostly anoxic sediments from the subsurface layers (down to 15 cm) to the sediment surface, thereby obscuring some of the natural stratification patterns. With an estimated turnover rate of about 8 L m^?2 year^?1 of sediment, our calculations suggest that over a period of about 18.75 years, all the sediment to a depth of 15 cm will have been reworked by C. templemani alone.     

Modelling the effect of fibropapilloma disease on the somatic growth dynamics of Hawaiian green sea turtles

The effect of the tumour-forming disease, fibropapillomatosis, on the somatic growth dynamics of green turtles resident in the Pala’au foraging grounds (Moloka’i, Hawai’i) was evaluated using a Bayesian generalised additive mixed modelling approach. This regression model enabled us to account for fixed effects (fibropapilloma tumour severity), nonlinear covariate functional form (carapace size, sampling year) as well as random effects due to individual heterogeneity and correlation between repeated growth measurements on some turtles. Somatic growth rates were found to be nonlinear functions of carapace size and sampling year but were not a function of low-to-moderate tumour severity. On the other hand, growth rates were significantly lower for turtles with advanced fibropapillomatosis, which suggests a limited or threshold-specific disease effect. However, tumour severity was an increasing function of carapace size—larger turtles tended to have higher tumour severity scores, presumably due to longer exposure of larger (older) turtles to the factors that cause the disease. Hence turtles with advanced fibropapillomatosis tended to be the larger turtles, which confounds size and tumour severity in this study. But somatic growth rates for the Pala’au population have also declined since the mid-1980s (sampling year effect) while disease prevalence and severity increased from the mid-1980s before levelling off by the mid-1990s. It is unlikely that this decline was related to the increasing tumour severity because growth rates have also declined over the last 10–20 years for other green turtle populations resident in Hawaiian waters that have low or no disease prevalence. The declining somatic growth rate trends evident in the Hawaiian stock are more likely a density-dependent effect caused by a dramatic increase in abundance by this once-seriously-depleted stock since the mid-1980s. So despite increasing fibropapillomatosis risk over the last 20 years, only a limited effect on somatic growth dynamics was apparent and the Hawaiian green turtle stock continues to increase in abundance.     

Growth and production of new recruits and adult individuals of Ascophyllum nodosum in a non-harvested population at its southern limit (Galicia,NW Spain)

Populations near the geographic distribution limits of the species are considered to live under suboptimal conditions, and hence, slight environmental changes can be critical for their survival. The potential sensitivity to disturbances of the long-living macroalga Ascophyllum nodosum was analyzed by the determination of growth, recruitment, mortality, and production of biomass of a population near its southern distribution limit. Recruitment, survival and growth rates of <2 years old individuals were determined in a new population growing in experimentally denudated squares. Demographic data for >2 years old individuals were obtained from individuals in the original population after estimating their age from the number of gas bladders in the thallus. Growth and survival were described as continuous nonlinear functions of age applied to the population and were further used to make demography-based production estimates. Recruitment of A. nodosum in denudated substrates seemed to require a previous cover of other macroalgae (as Fucus vesiculosus) as the only cohort detected during the 26-month period of the study was observed after F. vesiculosus individuals started to increase. The low production estimates (2,033 g m^?2 for a 10 year period) and poor recruitment may indicate a slow recuperation of this population to denudation. However, the large variability observed in the estimated growth curves of different populations along this southern distribution area suggests a large influence of local conditions that may help to overcome environmental changes at regional scales.