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Revista de biología marina y oceanografía

versión On-line ISSN 0718-1957

Rev. biol. mar. oceanogr. v.43 n.3 Valparaíso dic. 2008 


Revista de Biología Marina y Oceanografía 43(3): 607-613, diciembre de 2008


Molting behavior and growth in the giant barnacle Austromegabalanus psittacus (Molina, 1782)

Muda y crecimiento en el cirripedio gigante Austromegabalanus psittacus (Molina, 1782)


Daniel A. López1*, Eduardo A. Espinoza1, Boris A. López1 and Alexis F. Santibañez1

1Universidad de Los Lagos, Departamento de Acuicultura y Recursos Acuáticos, Avenida Fuchslocher 1305, Casilla 933, Osorno, Chile


Se evaluó, bajo condiciones controladas, el efecto de la temperatura y el fotoperiodo sobre la producción de mudas en ejemplares juveniles del cirripedio Austromegabalanus psittacus (Molina, 1782). El crecimiento fue determinado tanto en condiciones controladas como naturales. Se midió la frecuencia de muda, periodo de intermuda y las tasas instantáneas de crecimiento en el largo carino-rostral de ejemplares sometidos a dos condiciones de temperatura (10ºC y 16ºC) y fotoperiodo (8 horas luz: 16 horas oscuridad y 16 horas luz: 8 horas oscuridad). El crecimiento de ejemplares en condiciones naturales fue evaluado en sustratos suspendidos de balsas en Bahía Metri (41°36' S; 72°43' W), a dos niveles de profundidad entre 1 y 2 m y entre 4 y 6 m, durante las estaciones de otoño-invierno y primavera-verano. La frecuencia de mudas fue mayor a 16ºC que a 10ºC, sin que se evidenciaran variaciones por el fotoperiodo. Los periodos de intermuda fueron mayores a 10ºC que a 16ºC y a fotoperiodos de 8:16 que a 16:8. Las tasas instantáneas de crecimiento, en cambio, fueron mayores a 10ºC que a 16ºC y bajo condiciones de fotoperiodo 8:16 que a 16:8. No se observó relación entre la tasa instantánea de crecimiento y la frecuencia de muda. En condiciones naturales, se observó un mayor incremento del largo en individuos creciendo a mayor profundidad. Los resultados obtenidos en ambiente controlado y en el medio natural fueron congruentes, porque el mayor crecimiento obtenido en sistemas suspendidos a mayores profundidades se asoció a condiciones de menor luminosidad y temperatura, donde fue mayor el crecimiento bajo condiciones controladas.

Palabras clave: Balanidae, picoroco, temperatura, fotoperiodo, Chile


The effect of temperature and photoperiod on molt production in juvenile specimens of the acorn barnacle Austromegabalanus psittacus (Molina, 1782) was evaluated under controlled conditions. Growth was determined both under controlled and natural conditions. The molt frequency, intermolt period and instantaneous growth rates of the carino rostral lengths were measured in specimens subject to two temperature conditions (10oC and 16oC) and photoperiods (8 hours light: 16 hours darkness and 16 hours light: 8 hours darkness). Growth of specimens in natural conditions was evaluated in substrates suspended from floating rafts in Metri Bay (41o36'S; 72o43'W) at two depths: between 1 and 2 m and between 4 and 6 m, during the autumn-winter and spring-summer seasons. Molt frequency was greater at 16oC than at 10oC, with no evidence of variations due to photoperiod. The intermolt periods were greater at 10oC than at 16oC and during the photoperiods 8:16 than at 16:8. Instantaneous growth rates, on the other hand, were greater at 10oC than at 16oC and under photoperiod conditions of 8:16 than at 16:8. No relation was observed between instantaneous growth rate and molt frequency. Under natural conditions, a larger increase in length was observed in individuals growing at greater depths. The results obtained in a controlled environment and in the natural environment were consistent, given that the higher growth reported in suspended systems at greater depths, was associated with lower luminosity conditions and lower temperatures; a similar situation was observed under controlled conditions.

Key words: Balanidae, giant barnacle, temperature, photoperiod, Chile


Temperature and photoperiod generate functional and behavioral changes in barnacles that can be expressed not only in the condition of individuals, but also at a population level (Clare 1987, Sarojini & Nagabhushanan 1999). It has been reported that photoperiod and temperature can directly and synergistically affect metabolic activities, and also cause specific endogenous behavior, influencing growth and molt frequency in specimens of various intertidal species, such as Semibalanus balanoides, Balanus amphitrite, Balanus eburneus and Balanus trigonus (Crisp & Patel 1960, El-Komi & Kajihara 1991). Furthermore, their effect and the result of any interaction between them may vary according to the seasonal variations of these factors (Barnes & Stone, 1974). Austromegabalanus psittacus (Molina, 1782) is a species of endemic barnacle distributed along the entire Chilean coastline, from southern Peru (6oS) to the Straits of Magellan (58oS), including the Juan Fernández archipelago (Nilsson-Cantell 1957, López et al. 2007a) and the southern zone of the Atlantic coast (Young 2000). This species mainly inhabits the subtidal zone, between 5 and 7 m depth (Pilsbry 1916, Santelices 1991), forming dense groups that can reach large dimensions (López et al. 2007b). This species is economically important in Chile, because it is traditionally consumed as human food. At present culture technologies are being developed that require knowledge of the factors that affect biomass production, growth and periodic changes in the exoskeleton or molt. Although it is not possible to directly relate biomass growth to molt production frequency in barnacles (Costlow & Bookhout 1956, Sarojini & Nagabhushanam 1999), ecdysis processes permit an understanding of the functioning of the neuroendrocrine system associated with growth. Studying the effects of environmental variables that fluctuate seasonally, such as temperature and photoperiod, can help to determine how these marine organisms adjust functionally and behaviorally to the physical-chemical factors present in the environment. This information could, secondarily, be considered both in the design and development of efficient culture technologies, or in the management of natural populations. In this species, it has been established that molt frequency is affected by fluctuations in salinity and hydrocarbon concentrations in the water. Thus, evidence indicates that molting frequency was greater at 30 psu than at 20 psu, while diesel concentrations of 0.1% v/v, produce an increase in molting production frequency with respect to concentrations of 0.5% v/v and treatments without petroleum (López & López 2005).

The aim of this study was to establish the effects of variations in temperature and photoperiod on the production of molts and the growth of Austromegabalanus psittacus juveniles, maintained under controlled conditions, comparing this with observations made on growth in the natural environment.



Experiments in controlled environments

Sixty Austromegabalanus psittacus juveniles were collected from Metri Bay in southern Chile (41 o36'S; 72o42'W), during August and October, 2005. Size range fluctuated between 0.7 cm and 1.0 cm carino-rostral length (maximum distance between the carinal plate and the rostral plate), which is a density-independent measurement of age (López et al. 2007b). They were transported to aquaria in the Marine Aquaculture Laboratory of the Universidad de Los Lagos, after eliminating sediments and epibionts. They were acclimatized for a period of 15 days in 15 l trays with sea water and a constant air supply at an environmental temperature (15 ± 2oC), a natural photoperiod and fed ad libitum with the microalga Dunaliella tertiolecta.

To evaluate molting behavior, a binary factorial experimental design was used, at two photoperiod regimes (8 hours light: 16 hours darkness and 16 hours light, 8 hours darkness) and two temperature conditions (10oC and 16oC). Temperature values were selected according to the range of surface water temperatures present in southern Chile, that fluctuate between an average of 10oC in the winter and 16oC in summer. Similarly, photoperiod regimes were selected based on the seasonal fluctuations of this factor in the same area. For each treatment, juvenile specimens were placed individually in 1 L glass containers, with filtered seawater (0.45 µm) and a constant air supply. Fifteen replicates were undertaken for each treatment, over a total experimental period of 60 days. The individual specimens in each experimental treatment were fed three times weekly with the microalga Dunaliella tertiolecta, at average concentrations of 50,000 cells mL-l. The number of light and dark hours in each of the experimental treatments was regulated by using two structures (`black boxes') that contained a luminosity system consisting of two 20W fluorescent tubes. Each of the structures was connected to a digital electronic timer, permitting automatic regulation (on/off) of the light source, according to photoperiod. A constant temperature was maintained, to ± 0.1oC accuracy. Daily controls were undertaken to determine molting frequency, quantifying the number of exuviae produced by each of the individuals over the total 60-day period. The intermolt periods per individual (time lapse between one molt and another) were expressed in days. Similarly, specimen growth was evaluated, calculating the instantaneous growth rates (d) of the increase in carino-rostral length, according to the formula: d = 1n FS - 1n IS / Dt, where FS = final size at the end of the period, IS = initial size at the beginning of the period and Dt = period in days.

Comparisons of accumulated molt frequencies were analysed using the Kruskal-Wallis non-parametric test (Sokal & Rohlf 1979). In the case of the intermolt periods and instantaneous growth rates, comparisons between treatments were undertaken by 2-way variance analysis, after complying with normality and homocedasticity assumptions, using the Shapiro-Wilk and Bartlett tests, respectively. Significant differences were analysed according to an a posteriori Tukey test. Furthermore, the relationship between molting frequency and growth was determined by carrying out lineal regression analysis and Pearson correlation (Sokal & Rohlf 1979). The STATISTICA 6.0 (StatSoft 2001) computer statistical package was used for statistical analysis.


Experiments in natural systems

During February and September, 2005, artificial substrates, suspended from a floating raft, were installed for cypris larval settlement and subsequent growth of Austromegabalanus psittacus specimens in Metri Bay (41o36'S; 72o42'W), southern Chile. This is a wave-protected location, with average tidal fluctuations of 7 m. Two types of growth systems were designed: - four 33 cm x 33 cm polyethylene plates, 0.6 cm thick, separated by a distance of 30 cm, and joined by a polypropylene cord (n = 5); - three polyethylene tubes, 70 cm long and 10 cm diameter, placed 50 cm apart, and joined by a 6 mm polypropylene cord (n = 5).

These systems were located at two depths: between 1 and 2 m and between 4 and 6 m. Surface temperature fluctuated between 9 and 17oC on average. As depth increased, temperature decreased by between 1oC and 3oC. Average natural photoperiod during this season of the year was 16:8. At depths between 4 and 6 m, the relationship was inverse. Growth was determined bimonthly in samples of 100 specimens, according to depth, and the increase in carino-rostral length was determined with a caliper, to 0.01 accuracy, over a total period of 20 months.

Comparison of the average increases in carino-rostral length according to depth was carried out by one-way variance analysis, with repeated measurements (Zar 1999).



Experiments in controlled environments

a) Molting frequency

Temperature modified molting frequency, which was greater at 16oC than at 10oC (H de Kruskal-Wallis = 25.017; g.l. = 1.41; P<0.05). Nevertheless, there were no statistically significant variations under different photoperiod regimes (H de Kruskal-Wallis = 0.023; g.l. = l.41; P = 0.877) (Fig.1).

Figure 1. Molting frequency (average + 1 SD) in juvenile Austromegabalanus psittacus individuals subject
to two photoperiod regimes (8 h light: 16 h darknessand 16 h light: 8 h darkness) and temperatures
(10ºC and 16ºC)
Figura 1. Frecuencia de muda (promedio + 1 SD) en individuos juveniles de Austromegabalanus psittacus sometidos a
dos regímenes de fotoperiodo (8 h luz: 16 h oscuridad y16 h luz: 8 h oscuridad) y temperatura (10ºC y 16ºC)


b) Intermolting periods

Statistically significant differences occurred in intermolting periods according to photoperiod regime. The intermoulting periods were longer at photoperiod 8 h light: 16 h darkness than at 16 h light: 8 h darkness. Temperature also significantly modified this variable, which was more prolonged at 10oC than at 16oC. No significant interaction was observed between photoperiod and temperature (Table 1, Fig. 2).

Table 1. Two-way variance analysis of the intermolt period of Austromegabalanus psittacus specimens in laboratory experiments subject to two photoperiods (8 h light:16 h darkness and 16 h light: 8 h darkness) and two temperatures (10ºC and 16ºC). The asterisks indicate significant differences (n=41)
Tabla 1. Análisis de varianza de dos vías para el periodo de intermuda de los ejemplares de Austromegabalanus psittacus en laboratorio, sometidos a dos fotoperiodos (8 h luz: 16 h oscuridad y 16 h luz: 8 h oscuridad) y dos temperaturas (10ºC y 16ºC). Los asteriscos indican diferencias significativas (n=41)


Figure 2. Intermolt period (average + 1 SD) in Austromegabalanus psittacus juveniles, with photoperiod regimes (8 h light:16 h darkness and 16 h light: 8 h darkness) and temperatures (10ºC and 16ºC)
Figura 2. Periodo de intermuda (promedio + 1 SD) expresado en días, en individuos juveniles de Austromegabalanus psittacus sometidos a dos regímenes de fotoperiodo (8 h luz: 16 h oscuridad y 16 h luz: 8 h oscuridad) y temperatura (10ºC y 16ºC)


c) Instantaneous growth rate

Significant differences were observed between the two photoperiod regimes, with greater growth at photoperiod 8: 16 than at 16: 8. Similarly, statistically significant differences in growth occurred between temperatures, being greater at 10°C than at 16°C. Interaction between photoperiod and temperature was not significant (Table 2, Fig. 3).

Table 2. Two-way variance analysis for growth (cm day-1) of the carino-rostral length (CRL) of the Austromegabalanus psittacus specimens in laboratory experiments, subject to two photoperiods (8 h light: 16 h darkness and 16 h light: 8 h darkness) and two temperatures (10ºC and 16ºC). Asterisks indicate significant differences (n=41)
Tabla 2. Análisis de varianza de dos vías para el crecimiento (cm día-1) del largo carino-rostral (LCR) de los ejemplares de Austromegabalanus psittacus en laboratorio, sometidos a dos fotoperiodos (8 h luz: 16 h oscuridad y 16 h luz: 8 h oscuridad) y dos temperaturas (10ºC y 16ºC). Los asteriscos indican diferencias significativas (n=41)


Figure 3. Instantaneous growth rate (average + 1 SD) of the carino-rostral length in Austromegabalanus psittacus juveniles, with two photoperiod regimes (8 h light: 16 h darkness and 16 h light: 8 h darkness) and temperatures (10ºC and 16ºC). Capital letters on the bars indicate significant differences between experimental treatments
Figura 3. Tasa instantánea de crecimiento (promedio + 1 DE) del largo carino-rostral en individuos juveniles de Austromegabalanus psittacus sometidos a dos regímenes de fotoperiodo (8 h luz: 16 h oscuridad y 16 h luz: 8 h oscuridad) y temperatura (10ºC y 16ºC). Las letras mayúsculas sobre las barras indican diferencias significativas entre los tratamientos experimentales


d) Relation between molting frequency and growth in carino-rostral length

Molting frequency and instantaneous growth rate in carino-rostral length were not related. The Pearson correlation coefficient (r) between these variables was 0.27; the lineal regression slope was not statistically significant (P = 0.086) (Fig. 4).

Figure 4. Relationship between instantaneous growth rate (cm day-1) of the carino-rostral length and the molting frequency of Austromegabalanus psittacus individuals in laboratory experiments with two photoperiod regimes (8 h light: 16 h darkness and 16 h light: 8 h darkness) and two temperatures (10ºC and 16ºC) (n=41)
Figura 4.
Tasa instantánea de crecimiento (cm día-1) del largo carino-rostral, en función de la frecuencia de muda de individuos de Austromegabalanus psittacus bajo condiciones de laboratorio sometidos a dos regímenes de fotoperiodo (8 h luz: 16 h oscuridad y 16 h luz: 8 h oscuridad) y temperatura (10ºC y 16ºC) (n=41)


Experiments in natural systems

The increase in carino-rostral length differed significantly between specimens growing at different depths (F = 5.6; gl = 1;198; P<0.05). After 20 months, average size of specimens growing at a depth of between 4 and 6 m was 3.4 ± 0.17 cm carino-rostral length, while average carino-rostral length of those that grew a depths of between 1 and 2 m was 2.92 ± 0.14 cm (Fig. 5).

Figure 5. Growth in carino-rostral length (average + 1 SD) of Austromegabalanus psittacus specimens in field experiments placed in suspended systems at two depths (1-2 m and 4-6 m) in Metri Bay over 20 month period (n=100)
Figura 5. Crecimiento en longitud carino-rostral (promedio + 1 DE) de ejemplares de Austromegabalanus psittacus en experimentos de campo dispuestos en sistemas suspendidos a dos profundidades (1-2 m y 4-6 m) en Bahía Metri por un periodo de 20 meses (n=100)



Molting in barnacles includes discarding the prosoma, cirrus, penis, digestive tract teguments and internal mucous membrane (Darwin 1854). The main factors that affect the molting cycle are temperature, photoperiod and food availability (Clare 1987, Sarojini & Nagabhushanam 1999). Costlow & Bookhout (1953, 1956) reported that Balanus improvisus and Balanus amphitrite niveus juveniles maintained in laboratory under different photoperiod conditions and at a temperature of 20oC, molted during periods of 2-3 days and shell growth was continuous; similarly, they established that individuals subject to total darkness conditions reached a higher growth rate (shell basal area) than those kept under continuous light conditions. In relation to food availability, Crisp & Patel (1960) observed that molting frequency in Semibalanus balanoides individuals starving for a period of 30 to 50 days, declined considerably. On contrast, specimens fed with Artemia sp. larvae, continued molting at the same frequency. These authors also verified that molting frequency in individuals that were fed, linear to temperature increase, from 3oC to 20oC, while in those animals without food, this effect was only produced from 3oC to 12oC, decreasing considerably at higher temperatures. In Austromegabalanus psittacus, molting frequency in juveniles was affected by temperature, with greater molting frequency at 16oC than at 10oC. This could be due to decreasing metabolism at lower temperatures or to effects at the neuroendocrine system level, associated with the molting cycle. These results are congruent with those reported by Crisp & Patel (1960) and El-Komi & Kajihara (1991), who, in their studies of other species of barnacles, established that molting frequency increased as temperature increased up to a certain level, depending on the species; above this temperature level, molting frequency began to decrease drastically. It is probable that thermal regimes in the natural environment are an influencing factor. Average winter temperatures in southern Chile are around 10oC and in summer, 16oC. On the other hand, molting frequency did not differ according to photoperiod regimes (8:16 and 16:8). This fits well with observations made by Crisp & Patel, (1960) and Barnes & Stone (1974) in S. balanoides, and Costlow & Bookhout (1953, 1956) in B. improvisus and B. amphitrite niveus, with regard to the absence of molting frequency variations in individuals exposed to different photoperiod regimes (24 hours light; 24 hours darkness; 12 hours light and 12 hours darkness). Nevertheless, constant illumination during the reproductive intermolt led to the rapid reestablishment of molting frequency, thus indicating the importance of an adequate photoperiod during this condition (Barnes & Stone 1974). According to Darwin (1854), molting frequency would be related to growth rate. Nevertheless, in studies undertaken on Balanus improvisus and Balanus amphitrite niveus, Costlow & Bookhout (1953, 1956) established that shell growth is not associated with molting frequency. Similarly, in Austromegabalanus psittacus, no association was found between these variables, given that molting frequency was not higher in those individuals that grew more. The instantaneous growth rate of A. psittacus was affected by variations in temperature and photoperiod. However, no interaction was observed between both variables. Instantaneous growth rates were greater at 10oC than at 16oC. Since individuals kept at temperatures of 10oC have lower molting frequencies than those maintained at 16oC, they also have lower energetic expenditure (Newell 1979). Among the environmental factors, temperature tends to increase growth in many species of marine invertebrates (Newell 1979). However, the metabolic costs could change this pattern. Growth depends, for the most part, on the way species distribute energy obtained from food towards the different physiological processes (Diaz & Martinez 1992). Austromegabalanus psittacus has accelerated growth rates at an early age, with a subsequent and considerable decrease during further age. In the natural environment, growth was higher at greater depths, where temperature and quantity of light hours are lower. If feeding is similar at different depths, a drop in energetic costs could imply increased energy available for growth. Growth in individuals subject to the 8:16 photoperiod was greater than in those maintained at 16:8 photoperiods. Given that the 8:16 photoperiod has a greater number of dark hours (2/3) than the 16:8 photoperiod (1/3), this result could be explained by the fact that availability of carbonates for shell growth is lower at greater luminosity conditions, due to the consumption of carbon dioxide provided by the unicellular algae used as food for specimens, both under laboratory and natural conditions. The opposite occurs when the darkness period is increased. Growth obtained under laboratory conditions cannot be entirely extrapolated to natural conditions, given that the different environmental factors are not fixed and interact with a complex series of variables. Nevertheless, A. psittacus growth in suspended systems was higher at greater depths than at surface level, which is congruent with the results obtained under controlled conditions. The information gathered from the results obtained is applicable to the future culture of A. psittacus. At present, cultures are being carried out on a semi-industrial scale, taking advantage of the favorable biological characteristics of this species (López et al. 2005). The molting period is considered to be a highly vulnerable stage for crustaceans, due to their greater propensity to infectious diseases that tends to increase mortality rates. The results show that molting frequency is greater at higher temperatures and that the opposite occurs with growth. Thus, lower temperatures would favor the growth and survival of juveniles of A. psittacus juveniles. On the other hand, greater growth was observed during the photoperiod 8 h light: 16 h darkness than at photoperiod 16 h light: 8 h darkness, indicating that biomass production in cultures would be higher under conditions of longer darkness hours. As a consequence, during the fattening phase, cultures should be undertaken at depths of 4 to 6 m, where temperatures are more stable throughout the year, bordering on 10oC, and, furthermore, luminosity conditions are low.



This study was financed by FONDEF project D03I1116 and DIULA project No 00205F. The collaboration of Cecilia Pino, Alejandra Valenzuela, Mónica Neculman and Nicolás Castro in the laboratory experiments, and of Sergio Arriagada, Oscar Mora, Mauricio Pineda and José Uribe in the field activities, is gratefully acknowledged. Similarly, the cooperation of Susan Angus in the translation of the manuscript is also acknowledged. The comments and suggestions of an anonymous referee are also appreciated.



* Invited author



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Recibido el 17 de julio de 2008 y aceptado el 10 de noviembre de 2008


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