Egg production, hatching rates, and abbreviated larval development of Campylonotus vagans Bate, 1888 (Crustacea: Decapoda: Caridea), in subantarctic waters

Early life history patterns were studied in the caridean shrimp, Campylonotus vagans Bate, 1888, from the subantarctic Beagle Channel (Tierra del Fuego). As a consequence of very large egg size (minimum 1.4 mm), fecundity was low, ranging from 83 to 608 eggs per female (carapace length [CL] 11-22.5 mm). Egg size increased continuously throughout embryonic development, reaching prior to hatching about 175% of the initial diameter. Due to low daily numbers of larval release, hatching of an egg batch lasted for about 2-3 weeks. The complete larval and early juvenile development was studied in laboratory cultures fed with Artemia sp. nauplii. At 7.0±0.5 °C, development from hatching to metamorphosis lasted for about 6 weeks. It comprised invariably two large zoeal stages and one decapodid, with mean stage durations of 12, 17, and 15 days, respectively. Larvae maintained without food survived on average for 18 days (maximum: 29 days), but did not reach the moult to the zoea II stage. Size increments at ecdysis were low in all larval stages (2.1-3.9%), indicating partial utilisation of internal energy reserves. A clearly higher increment (14%) was observed in the moult from the first to the second juvenile stage. Low fecundity, large size of eggs and larvae, an abbreviated mode of larval development, high larval survival rates during absence of food, demersal behaviour of the early life history stages, and an extended hatching period with low daily release rates are interpreted as adaptations to conditions typically prevailing in subantarctic regions, namely low temperatures (causing long durations of development) in combination with a pronounced seasonality in plankton production (i.e., short periods of food availability).     

Are blackcaps current winners in the evolutionary struggle against the common cuckoo?

Blackcaps Sylvia atricapilla reject artificial cuckoo eggs, and their eggs vary little in appearance within clutches, whereas among clutches eggs vary considerably. Low variation within clutches facilitates discrimination of parasitic eggs, whereas high variation among clutches makes it harder for the cuckoo to mimic the eggs of a certain host species. These traits have most probably evolved as counteradaptations against brood parasitism by the common cuckoo Cuculus canorus, even though blackcaps are not regularly parasitised today. In this study, we investigated how fine-tuned the rejection of parasitic eggs is in this species by introducing three types of eggs into their nests: a real non-mimetic egg the approximate size of a cuckoo egg, an artificial mimetic egg the size of a cuckoo egg and a real conspecific egg. As the rejection frequency of both mimetic and non-mimetic artificial cuckoo eggs has been shown to be high in previous studies, the variation in rejection behaviour between individuals is low, indicating that most individuals within the population are able to reject parasitic eggs. Thus, we predict that (1) the intraclutch variation in egg appearance should be generally low in all individuals, and that (2) regarding conspecific eggs, rejection decisions should be highly dependent on the degree of mimicry between parasitic and host eggs. We found support for these predictions, which indicates that due to their highly sophisticated countermeasures against brood parasitism, blackcaps can probably be regarded as current winners of the arms race with the common cuckoo. Furthermore, the high and consistent rejection frequency of cuckoo eggs found throughout Europe for this species supports the spatial habitat structure hypothesis, which claims that woodland-nesting species breeding near trees, like blackcaps, presumably experienced a high level of parasitism throughout their range in the past and, therefore, their rejection behaviour, once evolved, spread rapidly to all populations.     

THE SOCIABLE WEAVER,PART 3: BREEDING BIOLOGY AND MOULT

Maclean, G. L. 1973. The Sociable Weaver, Part 3: Breeding biology and moult. Ostrich 44: 219–240.

Rain or some associated phenomenon is the principal Zeitgeber releasing breeding in the Sociable Weaver. The species does not breed in the absence of rain. The same nest chambers are used for breeding as are used for roosting throughout the year. The Sociable Weaver is monogamous. The clutch size varies from two to six eggs, larger clutches being more common after good rains than in relatively poorer breeding periods. Food supply may therefore be the proximate factor regulating clutch size. Replacement clutches are not necessarily smaller than first clutches. The mean clutch size within a breeding period decreases with an apparent decrease in food supply. The parents share parental duties about equally. Up to four successive broods may be raised in a single breeding period; a breeding period may last up to nine months and may occur at any time of the year according to the somewhat erratic rainfall which averages about 226 mm per year in the study area.

First broods help their parents to feed later broods; fourth brood chicks may therefore be fed by as many as 11 birds (nine young and two parents). This has survival value especially toward the end of a breeding period when food is scarce. Of similar value is the habit of starting incubation with the first or second egg of the clutch; in a relatively poor season older chicks will survive while younger ones will starve, thereby effectively and quickly reducing brood size. Young birds moult into adult plumage at four months, but do not normally leave the home colony. The sexes are indistinguishable at all ages, but there is an approximate ratio of eight males to five females in the study area.

Wing moult is slow: each remex takes about a month for replacement. Body moult occurs within the space of a month, usually after rain while the birds are breeding. Primary remiges are moulted proximo-distally from 1 to 9; secondaries are moulted disto-proximally from 1 to 6. Body moult is antero-posterior with the dorsal surface slightly in advance of the ventral surface.     

The timing, duration and pattern of moult and its relationship to breeding in a population of the European Greenfinch Carduelis chloris

Moult was studied in 1 year among Greenfinches trapped in a garden in east‐central England. Over the period June–December 2003, 333 captures of 179 individual adults provided information on breeding condition, moult, body weight, sex and age (yearling or older adult, equivalent to birds in their second or later calendar years, respectively). About 95% of all birds (sex and age groups combined) started primary feather moult from 2 July to 14 August, and finished from 10 October to 22 November. The mean date of moult onset in the population as a whole was 24 July. On average, males began 8 days before females, and yearlings began 6 days before older birds. The mean duration of moult was 100 days, whether the figure was calculated for the population as a whole or just for the 36 individual birds that were caught more than once during moult. However, moult rate was slightly slower, and moult duration slightly longer, in yearlings than in older adults of both sexes. No evidence was found for any systematic relationship between moult onset date and rate (duration). Breeding and moult overlapped by up to 5 weeks or more in individual birds, and some birds probably started to moult as early as the incubation stage of their last clutch of the season. The cloacal protuberance (taken as indicative of breeding condition) had regressed in all males by the time the fifth primary was shed, and the brood patch had regressed and re‐feathered in all females by the time the fourth primary was shed. The bulk of feather replacement in the secondary, tail and body tracts occurred in the second half of primary moult, and after cloacal protuberances and brood patches were completely regressed. In all birds examined near the end of primary moult the secondaries were still growing, and would have continued growth for up to another 19 days or more, extending the end of the moulting season into December. Body mass during moult was affected significantly by sex and age, as well as by time of day, amount of food in gullet, reproductive condition and date. No firm evidence emerged that body mass was affected by moult stage, after allowing for effects of date and other variables (although there was a non‐significant negative relationship between moult stage and body mass in males). In the population as a whole, the breeding season (from first egg‐laying to independence of last young) was spread over 21 weeks and moult over 24 weeks. With an overlap between the two events at the population level of up to 9 weeks, the two processes together took up to 36 weeks, some 69% of the year.     

Reproduction of astacid crayfish in captivity—current developments and implications for culture,with special reference to Ireland and Spain

Summary

Astacid crayfishes, native to western Eurasia and western North America, are iteroparous and long-lived (6–12 years), reaching final sizes of about 30–500 g and 90–200 mm total length, depending on species. While economically valuable, their low fecundity and slow growth makes economic aquaculture difficult. In Spain and Ireland the relatively small native white-clawed crayfish Austropotamobius pallipes (Lereboullet) carries around 70 eggs for 8–9 months and reaches first maturity at 3–4 years and 50 mm total length. The larger signal crayfish Pacifastacus leniusculus Dana, introduced to Europe from California, matures at about 70 mm and 2 years and carries some 200 eggs for 8 months. A. pallipes alone occurs in Ireland; both species in Spain. We have investigated fecundity, oviposition and subsequent egg development of diese species in field and laboratory and developed strategies to maximize egg survival in artificial incubators. Temperature manipulations may be used to maximize juvenile survival and also to modify incubation period. For successful aquaculture critical phases in captivity are mating and fertilization, pleopodal egg attachment, late embryo survival and moult from Stage 1 hatchlings to free-living Stage 2 juveniles.     

Plasticity of brood patch development and its influence on incubation periods in the yellow-eyed penguin Megadyptes antipodes: an experimental approach

In many bird species, eggs laid late in the laying period hatch after a shorter incubation period than early-laid eggs. However, the mechanisms that explain these seasonal declines in incubation periods among clutches remain poorly understood. In this study we investigated the plasticity of brood patch development during incubation in yellow-eyed penguins Megadyptes antipodes and established whether differences exist in brood patch formation among early, mean and late-breeding penguins. We also examined whether brood patch development was influenced by sex and age of birds. We then placed an artificial egg in nests a few days prior to egg laying to investigate whether the presence of an egg influences brood patch development and whether an advanced brood patch development at the time of egg laying causes declines in incubation periods. Initial brood patch width on the day the first egg was laid was dependent on sex and age, while the development of brood patch width after first egg laying was slower in early-laying birds than in mean- and late-laying birds. Initial brood patch temperature as well as temperature throughout incubation was largely dependent upon sex, whereby males had higher brood patch surface temperatures than females. Placement of an artificial egg in nests stimulated successfully brood patch development in manipulated birds, so that by the time they laid their own first egg, their brood patches were wider and had higher temperatures than those of control birds. Moreover, incubation periods of first eggs from manipulated nests were significantly shorter (43.5 days) than were those from control nests (47.3 days). Thus, variation in brood patch development and related differences in incubation temperature during early incubation could contribute to seasonal declines in incubation periods.     

The growth, development and reproduction of a deep sea cumacean (Crustacea: Peracarida)

A single sample of over 1000 individuals of Leuconjonesi Bishop, 1982, taken at a depth of about 1500 m on the continental slope off Surinam, was studied. The carapace length of individuals in the first postmarsupial instar was already about half that of brooding females. Growth increments at early moults were of 20–25. Males reached the final morphological form in the sixth postmarsupial instar. A prepuberty moult was recognized between the third and fourth male instars. Females reached the preparatory stage in the fourth postmarsupial instar. Brooding condition occurred for the first time after the next moult. The brooding form could then alternate at successive moults with an inter-brood form, resembling the preparatory female, with small, non-overlapping oostegites. Preparatory and inter-brood females were morphologically separable; vitellogenesis was restricted to these instars. Broods were of 6–12 young. The individuals in each brood probably completed marsupial development, and were released, one by one. The copepod parasite Sphaeronella infested 10", of brooding-form females.     

Development ofEuvarroa sinhai (Acarina: Mesostigmata), a parasitic mite ofApis florea,onA. mellifera worker brood

The development ofEuvarroa sinhai Delfinado and Baker, a parasite ofApis florea F., onA. mellifera worker brood was demonstrated for the first time. The mite fed, lived and reproduced onA. mellifera worker brood as a new host in addition toA. florea. Fertile females used once in the experiment produced 1–8 offspring (x 4.30±1.7) per cell. The actual and potential reproduction rates ofEuvarroa in honeybee worker brood cells were 3.62 and 3.95, respectively. Developmental period from egg to adult was 5 and 6–7 days for males and females, respectively. The female commences to mate soon after her deutonymph/adult moult. Copulation was observed in 18 cases.     

Growth in the crayfish Austropotamobius pallipes (Crustacea: Astacidae)

SUMMARY. The growth of Austropotamobius pallipes was studied in the River Ouse during 1976–78. Growth of mature crayfish (>2.5 cm carapace length) was followed by determining the relationship between the growth increment at moult and premoult carapace length, together with the frequency of moulting of different categories of crayfish. These data are supplemented by the recapture of marked individuals and the measurement of crayfish held in corves in the river. Growth was limited to the period May–October when water temperatures exceeded 10°C. Growth rates of male and female crayfish are similar until maturity is reached, thereafter males moult twice per year and the majority of females moult once. No crayfish in excess of 3.7 cm carapace length has been observed to moult more than once per year. Growth of juveniles (<2.5 cm carapace length) was estimated from size frequency distributions constructed from regularly taken samples. Growth rates of juveniles showed great variation both between and within year classes. In the hot dry summer of 1976, juveniles exhibited faster growth rates (instantaneous growth rates (G) for 0+ and 1 + crayfish were 0.029 and 0.013 mg mg⁻¹ day⁻¹. respectively) than in other years. Laboratory experiments on the effect of temperature on the growth rate of 0 + crayfish were undertaken; for crayfish at 15°C. G = 0.0138 (0–53 days) and at 10°C, G = 0.0003 (0–90 days). Crayfish held at 10°C failed to undergo a single successful moult. At 20°C crayfish exhibited exponential growth over the first 40 days, with G = 0.0189. declining thereafter to G = 0.012 (40–90 days).     

Structural study of the ovary,oogenesis and brooding in Tonicia lebruni (Polyplacophora Chitonidae) from Patagonia

Tonicia lebruni, a common, lower intertidal and subtidal chiton inhabiting Patagonian rocky shores, is a gonochoristic iteroparous species producing large eggs (≈ 400 μm in diameter), which are fertilized and brooded within the pallial groves until released as juveniles. A free larval stage is absent, despite this, T. lebruni is widely distributed along the south‐western Atlantic. At Puerto Deseado, T. lebruni has a marked seasonality in the reproductive cycle, reproducing only once a year. The reproductive period is quite short and defined in time: spawning and brooding take place during the late austral winter and beginning of spring. Recovery of the female gonad starts very soon after spawning. Oogenesis takes about 10–11 months for completion. Brood size is correlated with length of maternal individual. The number of embryos per brood varied between 785 and 5945. Extensive resorption of abortive eggs is viewed as related to limitation of space available for brooding. The egg hull is formed by a large number of minute pentagonal or hexagonal plates each one bearing a short spine bent onto the egg surface. The morphology and the surface of the hull could contribute to the cohesiveness of the brooded egg mass within the pallial grooves.     

Egg rejection and clutch phenotype variation in the plain prinia Prinia inornata

Avian hosts of brood parasites can evolve anti‐parasitic defenses to recognize and reject foreign eggs from their nests. Theory predicts that higher inter‐clutch and lower intra‐clutch variation in egg appearance facilitates hosts to detect parasitic eggs as egg‐rejection mainly depends on the appearance of the egg. Therefore, we predict that egg patterns and rejection rates will differ when hosts face different intensity of cuckoo parasitism. We tested this prediction in two populations of the plain prinia Prinia inornata: Guangxi in mainland China with high diversity and density of cuckoo species, and Taiwan where there is only one breeding cuckoo species, the oriental cuckoo Cuculus optatus. As expected, egg patterns were similar within clutches but different among clutches (polymorphic eggs) in the mainland population, while the island population produced more uniform egg morphs. Furthermore, the mainland population showed a high rate of egg rejection, while the island population exhibited dramatically reduced egg grasp‐rejection ability in the absence of parasitism by the common cuckoo Cuculus canorus. Our study suggests that prinias show lower intra‐clutch consistency in egg colour and lose egg‐rejecting ability under relaxed selection pressure from brood parasitism.     

THE MIGRATION SYSTEM OF THE CURLEW SANDPIPER CALIDRIS FERRUGINEA IN AFRICA

Elliot, C: C. H., Waltner, M., Underhill. L. G., Pringle, J. S. & Dick, W. J. A. 1976. The migration system of the Curlew Sandpiper Calidris ferruginea in Africa. Ostrich 47:191-213. Data on ringing and recoveries of Curlew Sandpiper, mainly from the Cape, South Africa are presented. Possible migration routes to the breeding grounds are considered in the light of these and other recoveries from the rest of Africa. Retraps show that the species exhibits ortstreue and some evidence is presented which suggests that some birds may travel together and stay in the south in the same flock during one and subsequent migrations. Sex ratio statistics show an excess of females. Adults complete a full primary moult in the Cape between September and February, taking about 140 days but there is a lot of individual variation. Data from Mauritania show primary moult starting faster, a month earlier than in the Cape, and arrested moult in a few adults. The difference may be because Mauritanian birds move on further south while the Cape is the end point of the migration. Kenyan moult records from the Rift Valley follow the Cape pattern except that some birds arrest moult and finish later. Juvenile moult is shown to be different from that of adults, involving only a moult of the outer primaries and taking place during the overwintering period, April to August. All juveniles in the Cape are thought to overwinter and the modified moult to be an adaptation to this behaviour. The weight of adults but not juveniles increases markedly in the six weeks before migration. Fat and protein analyses suggest that the increase is entirely due to deposition of migratory fat. Kenyan birds have lower mean weights and deposit fat about two weeks later than those at the Cape. The nearer the non-breeding quarters are to the breeding grounds, the earlier moult starts and the later fat deposition takes place.     

CHAIRMAN'S REPOST, 1954–55

Brown, C. R. 1986. Feather growth, mass loss and duration of moult in Macaroni and Rockhopper Penguins. Ostrich 57:180-184.

The development of new feathers, loss of body mass and the duration of moult were investigated in Macaroni Penguins Eudyptes chrysolophus and Rockhopper Penguins E. chrysocome at Marion Island, southern Indian Ocean. New feathers began developing under the skin before the birds returned ashore to moult, and only began protruding through the skin about five days later when they were already over half their final length. Feather synthesis was complete by 21 days after the birds returned ashore. Loss of body mass was similar to previous observations for the species, but previous reports on the duration of moult do not take into account that moult begins while the birds are still at sea.     

Brood care among basommatophorans: a unique reproductive strategy in the freshwater limpet snail Protancylus (Heterobranchia: Protancylidae), endemic to ancient lakes on Sulawesi, Indonesia

In molluscan taxa inhabiting marine environments oviparity and reproduction via planktonic larvae is predominant while incubation and viviparity is most frequently found in taxa inhabiting brackish or freshwater aquatic habitats. Brooding has evolved repeatedly and independently in several limnic taxa among Bivalvia and Gastropoda. However, among basommatophoran gastropods no such cases were yet known. We here report on a unique reproductive strategy involving brood care in the lacustrine freshwater limpet genus Protancylus, endemic to the ancient lakes on central Sulawesi (former Celebes), Indonesia, namely the Lake Poso and the Malili lake system, because this constitutes the first known case of this behaviour among the Basommatophora. Protancylus live exclusively as epizoans on those pachychilid gastropods of the viviparous genus Tylomelania, also a Sulawesi endemic species, that inhabit mostly soft substrates. We found that the two known species Protancylus pileolus from Lake Poso and P. adhaerens from the Malili lake system both retain gelatinous egg strings underneath their outer mantle, where up to 15 (mostly eight or nine) shelled juveniles are brooded. Nourishment is provided within the egg capsule only. Thus, brood care in Protancylus resembles the reproductive strategy found recently among pachychilid gastropods Jagora from the Philippines, but differs from euviviparous (i.e. matrotrophic) incubation among thiarid gastropods possessing a brood pouch with juveniles being nourished via a ‘pseudoplacenta’ in several taxa.     

Ontogenetic changes in the carapace shape of the non-marine ostracod Eucypris virens (Jurine)

Developmental changes in carapace form (size+shape) during ontogeny have been explored in Eucypris virens (Crustacea, Ostracoda) using elliptic Fourier analysis. Clones from different geographic localities raised under controlled constant conditions (temperature and photoperiod) were used to characterize developmental pathways in the species. A larger data set including field populations and laboratory populations cultured under a range of environmental conditions were used to infer influence of environmental factors on carapace shape changes during ontogeny. Size changes between consecutive juvenile stages support empirical laws describing the doubling of ostracod volume at each moult. Ontogenetic changes point out the remarkable influence of environmental conditions on carapace shape.     

Egg Discrimination and Sex-Specific Pecking Behaviour in Parasitic Cowbirds

We studied egg‐pecking behaviour in males and females of three cowbird species: the shiny cowbird (Molothrus bonariensis), a host generalist brood parasite, the screaming cowbird (M. rufoaxillaris), a host specialist brood parasite, and the bay‐winged cowbird (Agelaioides badius), a non‐parasitic species. We conducted three experiments in which we offered each bird an artificial nest with two plaster eggs and recorded whether egg pecking occurred and the number of pecks on each egg. In expt 1, we tested if there were species and sex differences in egg‐pecking behaviour by offering the birds two spotted eggs of similar pattern. Shiny and screaming cowbirds responded in 40.3% and 44% of the trials, respectively, with females and males presenting similar levels of response. In contrast, bay‐winged cowbirds did not show any response. In expt 2, we tested if shiny cowbirds responded differentially when they faced a choice between one host and one shiny cowbird egg, while in expt 3, we tested if screaming cowbirds responded differentially when they faced a choice between one shiny and one screaming cowbird egg. Shiny cowbirds pecked preferentially host eggs while screaming cowbirds pecked more frequently shiny cowbird eggs. Our results show that egg‐pecking behaviour is present in both sexes of parasitic cowbirds, but not in non‐parasitic birds, and that parasitic cowbirds can discriminate between eggs of their own species and the eggs of their hosts or other brood parasites.     

Proximate Determinants of Reproductive Skew in Polygyne Colonies of the Ant Formica fusca

Understanding the determinants of reproductive skew (the partitioning of reproduction among co‐breeding individuals) is one of the major questions in social evolution. In ants, multiple‐queen nests are common and reproductive skew among queens has been shown to vary tremendously both within and between species. Proximate determinants of skew may be related to both queen and worker behaviour. Queens may attempt to change their reproductive share through dominance interactions, egg eating and by changing individual fecundity. Conversely, workers are in a position to regulate the reproductive output of queens when rearing the brood. This paper investigates queen behaviour at the onset of egg laying and the effect of queen fecundity and worker behaviour on brood development and reproductive shares of multiple queens in the ant Formica fusca. The study was conducted in two‐queen laboratory colonies where the queens produced only worker offspring. The results show that in this species reproductive apportionment among queens is not based on dominance behaviour and aggression, but rather on differences in queen fecundity. We also show that, although the queen fecundity at the onset of brood rearing is a good indicator of her final reproductive output, changes in brood composition occur during brood development. Our results highlight the importance of queen fecundity as a major determinant of her reproductive success. They furthermore suggest that in highly derived polygyne species, such as the Formica ants, direct interactions as a means for gaining reproductive dominance have lost their importance.     

Life history of a dipteran predator (Scathophagidae: Acanthocnema) of insect egg masses in a northern California stream

1. Little is known about the predators of insect eggs in fresh waters. This study describes aspects of the life history of a scathophagid fly (Acanthocnema sp.), whose larvae are predators of aquatic insect eggs. 2. Because the Acanthocnema predator oviposits its eggs on the surface of aquatic insect egg masses, all insect egg masses were collected regularly within a 200‐m reach of Redwood Creek (California, U.S.A.) between September 2003 and June 2007. Acanthocnema predators were found predominantly within egg masses of the caddifly Neophylax rickeri (Trichoptera: Uenoidae). 3. There was a mean of 0.25 Acanthocnema individuals per N. rickeri egg mass (n = 2367 egg masses). In general, N. rickeri egg masses were more commonly found clustered in aggregations (93.7%) than singly (6.3%), and Acanthonema were found more often within the aggregations of N. rickeri (98.7%) compared to singly laid egg masses (1.3%). 4. The duration of the Acanthocnema predator life stages was: egg 2.9 ± 0.8 (mean ± SD) days, larva 15.6 ± 10.2 days, pupa 80.3 ± 24.9 days and adult 7.2 ± 4.8 days. The short duration of the Acanthocnema egg stage (1–7 days) compared to that of its prey N. rickeri (2–4 weeks) raises the probability that the undeveloped eggs of N. rickeri would be available to the young predators upon hatching. Egg consumption of N. rickeri eggs by Acanthocnema averaged 262.6 eggs per larval period. 5. Acanthocnema had a bivoltine life cycle in which the first generation fed exclusively on N. rickeri egg masses in the winter and the second generation fed on the egg masses of several species, including other Trichoptera (Brachycentridae) and Diptera (Ceratopogonidae, Chironomidae) in the spring. These findings suggest differing feeding strategies by the first and second generations of Acanthocnema in response to the seasonal availability of prey species. This type of autecological information is important for understanding mechanisms of community interactions.     

Alloparental care between catfishes in Lake Tanganyika

A bagrid catfish Auchenoglanis occidentalis cared for its brood, deposited within an accumulation of shells and gravel in the centre of a large saucer-like depression, for up to 2 weeks in Lake Tanganyika. Adults of another catfish Dinotopterus cunningtoni (Clariidae) persistently came to A. occidentalis nests near days of host spawning. Eggs of D. cunningtoni were found in the host nests on the day and within 2 days of host spawning. During and for a few days after the end of host brooding, associate species' young of much older ages than the host brood were often found in the nests together with those of a similar age to the host young. Associate young were rarely found in nests before spawning and in unused nests. These findings suggested that this brood-mixing has two origins: egg dumping by associate adults and voluntary intrusion of large associate young into host nests. Possible benefits to the associate species are to take advantage of nest preparation and parental behaviour of the host species and to feed on the host brood.     

Biology of <Emphasis Type="Italic">Grapsus grapsus</Emphasis> (L<Emphasis Type="SmallCaps">innaeus</Emphasis>, 1758) (Brachyura,Grapsidae) in the Saint Peter and Saint Paul Archipelago,Equatorial Atlantic Ocean

Eleven expeditions were undertaken to the Saint Peter and Saint Paul Archipelago to study the reproductive biology of Grapsus grapsus, providing additional information on limb mutilation and carapace colour. MATURE software was used to estimate morphological maturity, while gonadal analyses were conducted to estimate physiological maturity. The puberty moult took place at larger size in males (51.4 mm of carapace length) than in females (33.8 mm), while physiological maturity occurred at a similar size in males (38.4 mm) and in females (33.4 mm). Above 50 mm, the proportion of red males increased in the population, indicating that functional maturity is also related to colour pattern. Small habitat and high local population density contributed to the high rate of cannibalism. The low diversity of food items, absence of predators of large crabs and high geographic isolation are the determinants of unique behavioural and biological characteristics observed in the G. grapsus population.