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A communication network is formed when more than one receiver can intercept the signal produced by a signaller, and when more than one signal reaches a receiver at the same time (McGregor & Dabelsteen, 1996). Communication network theory broadens the consideration of selection pressures on signallers and receivers to include selection on signallers by receivers other than the primary or target receiver, and selection on receivers when they receive more than one signal simultaneously or intercept a signal that was not targeted at them (McGregor & Dabelsteen, 1996; McGregor & Peake, 2000).
A mudflat full of male fiddler crabs (genus Uca, family Ocypodidae), all rhythmically waving their enlarged claw, seems a perfect example of a communication network: there are several signallers and receivers in close proximity, and many signals are being produced simultaneously. However, this human perception of a coordinated network may be partly a product of our excellent visual ability and large size in relation to these small crabs. What about the crabs themselves: how many receivers does a signal reach, and how many signals can individuals receive simultaneously? Is our impression that they form signalling networks simply an illusion caused by our extreme size and high visual acuity? Most importantly, what can we learn about the communication system of fiddler crabs by considering networks of signallers and receivers rather than simple sender–receiver dyads?
We are both spectators and actors in this great drama of existence
Niels Bohr
Introduction
Poeciliid fishes such as green swordtails Xiphophorus helleri and guppies Poecilia reticulata aggregate in social groups called shoals. In addition to reducing predation risk and increasing foraging efficiency (e.g. Magurran & Pitcher, 1987; Ranta & Juvonen, 1993), fish shoals promote the transfer of social information within the group. For instance, information about foraging routes is transmitted from trained individuals to naive fish in guppy shoals (Laland & Williams, 1997; Swaney et al., 2001; Brown & Laland, 2002). The type of information transfer demonstrated in the social learning and foraging literature involves the transmission of signals from one or more individuals to the remaining group members. Investigations of social foraging and anti-predator behaviour have demonstrated that poeciliids attend to a variety of cues emitted by both conspecifics and heterospecifics (e.g. predators: Brown & Godin, 1999; Mirza et al., 2001; Brosnan et al., 2003). Although social learning and anti-predator responses constitute important aspects of group living in poeciliids, this chapter focuses more on how individuals gain information from observing interactions that occur in their social environment. Indeed, the concept of communication networks was founded on the premise that the information exchanged during social interactions (e.g. agonistic or courtship displays) may be available not only to the participants but also to bystanders within signal detection range (McGregor, 1993; McGregor et al., 2000).
Embryos of Crepidula dilatata develop within egg capsules where they feed on nutritive eggs also deposited within the capsules. Nutritive eggs permit the embryos to develop to a juvenile stage at hatching without passing through a pelagic larval phase. The juveniles enter the local population in posession of a well developed radula and gill filaments covered by lateral, ventral, and dorsal cilia. Initial feeding by the juveniles, employing both the radula and the gill, occurs from the first day of release from the capsule. The radular band of recently hatched snails is functional from the first day in the benthos, and is used for grazing the substrate, driving the mucus cord from the neck-canal to the mouth, and also for extracting mucus balls produced in the food pouch. The gill is active in particle collection from the first day of the free living juvenile, and is noted by the presence of well developed dorsal and ventral ciliature, active in moving mucus and particles over the gill lamellae to form the mucus string at the extreme ends of the gill filaments. The food pouch becomes active two to three days after initiation of production of mucus cords. All the functions associated with feeding, such as the numbers of mucus cords, radular strokes, and mucus balls increase in activity with progressive development of the juveniles.
This review provides insights into the distribution and impact of oestrogens and xeno-oestrogens in the aquatic environment and highlights some significant knowledge gaps in our understanding of endocrine disrupting chemicals. Key areas of uncertainty in the assessment of risk include the role of estuarine sediments in mediating the fate and bioavailability of environmental (xeno)oestrogens (notably their transfer to benthic organisms and estuarine food chains), together with evidence for endocrine disruption in invertebrate populations.
Emphasis is placed on using published information to interpret the behaviour and effects of a small number of ‘model compounds’ thought to contribute to oestrogenic effects in nature; namely, the natural steroid 17β-oestradiol (E2) and the synthetic hormone 17α-ethinyloestradiol (EE2), together with the alkylphenols octyl- and nonyl-phenol (OP, NP) as oestrogen mimics. Individual sections of the review are devoted to sources and concentrations of (xeno)oestrogens in waterways, sediment partitioning and persistence, bioaccumulation rates and routes, assays and biomarkers of oestrogenicity, and, finally, a synopsis of reproductive and ecological effects in aquatic species.
The first occurrence of a giant squid Architeuthis sp. specimen in Portuguese waters is noted and another reference set of biological and biometrical data provided which may in future be used in conjunction with others to further elucidate important aspects of the identity, biology and ecology of the species. The fact that the specimen is a male is relevant, since males have been much less frequent in the reports in the scientific literature than have females. Additionally, this is the most southerly report of a male known to have occurred in the Atlantic Ocean.
The influence of several environmental factors on the abundance and spatial–temporal distribution of the shrimp Artemesia longinaris were investigated from January 1998 to December 1999 in the Ubatuba region of São Paulo State, Brazil. Collections were performed monthly in the bays of Ubatumirim (UBM), Ubatuba (UBA) and Mar Virado (MV). Six sampling transects were established in each bay, four were parallel to the shore line, and two were next to the rocky shores. A commercial shrimp fishing boat equipped with two ‘double-rig’ nets was used. A total of 11,503 individuals was collected, including 1633 from UBM, 6344 from UBA and 3526 from MV. The majority of the captured specimens came from the deeper areas (15 to 20 m) with high salinity (34 to 36 ppt). The highest abundance of A. longinaris in Ubatuba bay was recorded in areas where fine and very fine sand comprised more than 70% of the sediment. Moreover, the abundance of A. longinaris followed a seasonal trend, being higher during the summer, when intrusions of cold South Atlantic Coastal Waters (SACW) are frequent. Thus, type of sediment, temperature and salinity are determinant factors in the distribution of A. longinaris in the studied region.
Regular sea temperature measurements have been made since 1975 at Gravelines (French coast of the Southern Bight of the North Sea) within the framework of a research programme aimed at monitoring the influence of the thermal discharge of a nuclear power plant. The sampling has yielded a 28-year time-series. Pluriannual natural fluctuations of temperature show cyclic patterns and long-term trends in good accordance with global climatic changes as revealed by the NAO (North Atlantic Oscillation) annual index.
Crepipatella fecunda is a benthic, primarily suspension-feeding gastropod that occurs in great abundance along the Chilean coast. It is a protandrous species whose reproduction involves brooding of an encapsulated embryonic stage followed by the release of free-living planktotrophic larvae. Because its close sister species, C. dilatata, co-occurs with C. fecunda, understanding the details of reproduction in this species might shed light on differences in reproductive features that correlate with divergences in mode of development. In southern Chile, brooding occurs throughout the year except for May and June, and each female produces 3–7 broods. The smallest brooding female was 28·2 mm in shell length and the largest was 56·3 mm. All full-grown eggs from the ovary are deposited at one time in a single brood, and only smaller oocytes remain in the gonad after the female finishes ovopositing. Those females that host pinnotherid crabs do not deposit eggs. All the eggs develop into embryos whose intracapsular development is similar to Crepidula fornicata and Crepipatella lingulata. Planktotrophic larvae hatch at a mean shell length of 329·5 μm (SD=27·09) after 4–5 weeks. During the pelagic stage the shell and velum of the larvae grow, but little other morphological development is visible externally. The pelagic stage lasts for 15–16 days at 17°C, during which the larvae grow ∼20·7 μm d−1. Observations of cultured larvae and protoconchs of field-collected juveniles show that settlement occurs when the larvae reach a shell-length of 650 μm (SD=28·3 μm).
The sex ratio of 100 immature Kemp's ridley turtles (Lepidochelys kempi) captured in Gullivan Bay, Ten Thousand Islands, south-west Florida was determined through radioimmunoassay analysis (RIA) of plasma testosterone levels. We determined the sex ratio to be 1·9F:1·0M, corroborating the female dominance reported from other studies. The mean sizes of female (N=57) and male turtles (N=30) were 40·9 cm (±6·9 SD) and 41·9 cm (±6·2 SD), respectively. There were an additional 13 turtles (41·3 cm±6·5 SD) for which sex could not be determined by this technique. Female-biased sex ratios are not uncommon in reptiles with temperature dependent sex determination. If fecundity is not male-limited, the occurrence of a female-biased sex ratio could enhance the recovery of the endangered Kemp's ridley turtle.
This paper reports the first study of breeding in the boreo-arctic barnacle Semibalanus balanoides in which latitudinal variation in timing of egg mass hardening has been examined simultaneously over the geographical scale involved, thereby excluding temporal confounding of the data. The timing of autumn egg mass hardening on the middle shore was established in 2002 and 2003 at ten stations ranging latitudinally from Trondheim (63°24′N) to Plymouth (50°18′N). To assess variation at local scale (<10 km), breeding was studied on three shores at each of two Irish locations (Cork and Galway). At Oban (Scotland) and Cork, the effect of shore height on timing of breeding was investigated. A strong influence of latitude and day length on timing of breeding was found in both 2002 and 2003. In both years, barnacles bred much earlier (when day length was longer) at high rather than low latitudes. No significant effect of environmental temperature or insolation on timing of breeding was detected. Shores no more than 10 km apart showed minimal difference in middle shore breeding date (<4 days). However, upper shore barnacles bred significantly earlier (by 7–13 days) than middle shore animals. The data indicate that breeding is controlled by period of daily darkness, with high shore animals encountering longer effective ‘nights’ because of the opercular closure response to emersion (which will reduce light penetration to tissues). Predictions concerning the effects of global changes in climate and cloud cover on breeding and population distribution are made. It is suggested that increased cloud cover in the northern hemisphere is likely to induce earlier breeding, and possibly shift the present southern limit of Semibalanus southwards.
A molecular assay was designed to distinguish the common sea louse Caligus elongatus from its sympatric relatives. The method identifies the parasites at all developmental stages. Fragments of the mitochondrial Cytochrome C Oxidase 1 (COI) gene from identified adult caligids were amplified by polymerase chain reaction (PCR) and sequenced. Analysis of sequence data from unknown samples permitted identification by clustering of the samples with their appropriate genetic relative. Nucleotide sequences obtained were used for preliminary investigations of the population genetic structure of Caliguselongatus. Aligned sequences from the COI gene from this speciesindicate that our C. elongatus material divides into two distinct clades, possibly revealing two closely related species. The two genotypes do not appear to be associated with sample site, parasite gender, sample time or host species. Parasites from both groups were found on Atlantic salmon (Salmosalar), sea trout (Salmotrutta), pollack (Pollachiuspollachius), saithe (Pollachiusvirens), and Atlantic herring (Clupeaharengus).
Mobile lice levels of two species of sea lice, Lepeophtheirus salmonis and Caligus elongatus, were examined on two samples of Atlantic salmon from the west coast of Ireland. The samples examined were taken two weeks apart from salmon caught by drift net in June 2003 at two different locations off the west coast of Ireland, one in the north-west and one in the west. Both samples of salmon caught were comparable in terms of numbers of total lice counted. No significant differences in male, female and ovigerous L. salmonis levels between the two samples were recorded, however, a significant difference was recorded between juvenile L. salmonis levels. Morphometric comparisons of male and ovigerous L. salmonis examined for each of the two salmon samples examined revealed some differences. There was a significant difference in male L. salmonis in terms of cephalothorax length between the samples. In the females significant differences were found between cephalothorax length, overall total length and egg length. Significant positive correlations within samples were also observed, between total female body length and both total egg number and egg string length in one of the samples examined.
The population biology and reproduction of the hermit crab Clibanarius longitarsus were studied with emphasis on size structure, sex ratio, breeding season and fecundity. Specimens were sampled monthly over a period of one year (January–December 2003) at Costa do Sol mangrove, Maputo Bay, southern Mozambique. A total of 597 individuals was obtained of which 202 were males, 192 non-ovigerous females and 203 ovigerous females. Annual size–frequency distributions were polymodal for males and bimodal for non-ovigerous and ovigerous females, respectively. Sexual dimorphism was recorded by the larger average size attained by males in relation to females. Sex ratio was female-biased during most months of the study. Clibanarius longitarsus showed a higher reproductive activity with two major peaks (March and October). Juvenile recruitment was continuous throughout the study period. Clutch size was positively associated with female size. The high number of ovigerous females as obtained in the present population may evidence a higher reproductive activity displayed by C. longitarsus at Costa do Sol mangrove.
Six specimens of an unknown Argulus species were found on a cod caught off the coast of Finnmark in northern Norway. All six were found to be sixth stage male larvae, ∼2·6 mm long and 1·6 mm wide. Argulus has not previously been recorded from cod and this is also the first record of a marine Argulus from Norwegian waters. The Argulus sp. from cod can be easily distinguished from other marine species found in northern European waters, and also from Norwegian freshwater species of Argulus. It is believed that it represents a new species, but a complete species description must await the finding of adult stages.
A new species of the planktonic copepod Tortanus (Atortus) (Calanoida: Tortanidae), T. (A.) magnonyx is described from the Seychelles, Mauritius and Madagascar. This is the sixth species of the Indian Ocean recticauda species group, of the Indo-West Pacific recticauda species complex, that has been described from the western Indian Ocean. The inshore areas where these copepods are found have been poorly surveyed, so the number of species found implies a high diversity.
Thirty-six boat surveys were conducted in Guanabara Bay, south-eastern Brazil, from October 2002 to June 2004 in order to investigate marine tucuxi group characteristics. The average and the range of tucuxis group size in the Guanabara Bay are similar with areas where small group sizes have been recorded. Group size ranged between one and 40 individuals (13·0±9·5; median=10·0). Groups of two to ten dolphins were the most common (53·9% of observations). Group size and the maximum number of dolphins sighted in each survey day did not vary between seasons (Kruskal–Wallis test, H3,36=3·249; P=0·355). Spatial geometry varied with group size and mixed groups were the largest (Kruskal–Wallis test, H3,218=57·149; P<0·001). The presence of calves had a great effect on group size, and nursery groups (mean =14·3±9·1; median=13·0) were twice as large than non-calf groups (mean=7·1±5·2; median=6·0). It is suggested that larger groups may aid in the calves development and learning. Group size changed frequently, resulting in 82·2% of observations with no constant size. Group size of marine tucuxi was not affected by the dolphins' behaviour (Kruskal–Wallis test, H2,215=5·626, P=0·06) neither by water depth (R2=0·012; F1,219=2·82; P=0·094).
Shell growth of the whelk Nassarius (=Hinia) reticulatus was studied in the Ria de Aveiro (north-west Portugal) between 1995 and 1998. Temporal analysis of shell height frequency distributions demonstrated that growth occurs during the first five years of life, whelks attaining a size of 6·7–7·8 mm in the 1st year, 12·1–14·5 mm in the 2nd year, 18–19·5 mm in the 3rd year, 22·7–23·6 mm in the 4th year and by the 5th year males have achieved an average size of ∼25 mm whilst females have reached ∼27 mm. Age estimates from internal microscopic annual growth lines present in the shell lip suggest that large whelks may achieve a longevity of at least 11 years. External annual rings become less discernible as the whelks increase in size and estimates of their age based solely on ring counts can underestimate their age. In males sexual maturation is reached between the 3rd and 4th years whilst in females it is attained between the 4th and 5th years. Imposex was visible in ∼2 year old females and attained maximum development by the 5th year.
Reproduction of newly established populations of the warm-water Atlantic Mediterranean wrasse Thalassoma pavo is here reported for the first time in the Ligurian Sea, and mating behaviour is described in detail. The reproductive season (May to October) may be divided in three stages: (1) pre-mating (mid-May to the end of June), during which terminal-phase (TP) males establish territories and start courting females; (2) mating (end of June to the end of August), with a mean frequency of up to one spawning event ind−1 h−1; and (3) post-mating (September to mid-October), when TP males remained inside territories but no spawning events were recorded. Mating followed two distinct modalities: pair spawning and group spawning, the latter replacing the former when population density exceeded 10 ind 100 m−2. Four phases have been distinguished in both modalities: (1) approach (pair) or gathering (group), to establish the contact between potential partners; (2) acceptance (pair) or priming (group), in which partners establish a common behavioural pattern; (3) ascent to near the sea surface; and (4) spawning. The saddled sea-bream Oblada melanura has been seen to predate intensively on the large cloud of sexual products released by groups.
Methods for assessing the occurrence and recency of mating are important for the management and conservation of exploited brachyuran crabs. Using multiparous females of the snow crab Chionoecetes opilio, we evaluated by experiment the efficacy of three indicators of recent mating: a white deposit in the spermathecae, extended mate-guarding, and fresh grasping marks on the female pereiopods. This was done by contrasting sperm counts between the left and the right spermatheca of females that were exposed to males with the right gonopod ablated, at treatment sex ratios of 20[female]:3[male] or 50[female]:3[male]. We expected that sperm reserves would be balanced between the two spermathecae of non-mated females and larger in the right than in the left spermatheca of mated females. Although no mating indicator was infallible, the presence of a white deposit was the most accurate because it maximized the median difference of sperm counts between the two spermathecae for the group of presumably mated females and minimized it for the group of presumably non-mated females. The use of grasping marks overestimated the mating frequency and resulted in the misclassification of a large proportion of females. Extended mate-guarding was a slightly better mating indicator than grasping marks, but it is not practical for field studies. Classification errors associated with each indicator can be explained mostly by female and male behaviours and may vary in magnitude with sociosexual context.
Laboratory breeding of the dog-whelk, Nucella lapillus, has established that the male-sterilizing Dumpton Syndrome (DS)—underdevelopment, or non-development (aphally), of the penis, incomplete formation (non-closure) of the vas deferens, resulting in a split prostate—can be readily observed in male F1 progeny. Cultivated under high ambient concentrations of the antifouling agent tributyltin (TBT), DS-carrying females can be recognized by their lesser degree of masculinization (imposex): sterilization is thereby avoided. When Dumpton females are crossed, under high ambient TBT, with individuals from a non-DS-affected population (Bude, North Cornwall) DS is absent from both sexes. Crosses of these F1 progeny result in F2 progeny exhibiting the classic DS symptoms in both sexes. A Mendelian mechanism for DS inheritance is suggested by the data.