Academic literature on the topic 'Copepod life-cycle'

The morphology of the developmental stages of Neobrachiella robusta (Wilson, 1912) (Copepoda: Siphonostomatoida) is described. The copepod is parasitic on the gill rakers of Sebastes alutus (Gilbert, 1890) (Teleostei: Scorpaeniformes). The life cycle of this copepod consists of a copepodid stage, followed by four chalimus stages and a relatively long preadult stage, which undergoes extensive metamorphosis. The copepods aggregate on the outer row of long gill rakers of the first gill arch, as many as 97% of them being attached to these rakers. Some of the rakers become distorted, but a connection between the presence of N. robusta and these abnormalities could not be established.

AbstractThe cestode parasite Schistocephalus solidus' growth is limited by the size of its second intermediate host, the three-spined stickleback, Gasterosteus aculeatus. S. solidus should thus prefer a large stickleback as host. Since the stickleback is a predator of the parasite's previous intermediate host, a small copepod, the stickleback that consumes the infected copepod will probably be of a size for which this copepod has the optimal prey size. The optimal foraging decision of the stickleback may or may not be compatible with the parasite's preference. Infected copepods are present in early summer when both many size classes of young of the year and adult sticklebacks are potential predators. We offered laboratory bred three-spined sticklebacks of four size classes individually the choice among five prey types: two size classes of copepods, two classes of Daphnia of corresponding size as alternative prey and a third Daphnia size class that was larger than the larger copepod. We found that small copepods, the potential hosts of S. solidus, were most accepted by the smallest sticklebacks of about 1.5 cm of length, larger fish consumed a decreasing proportion; fish larger than 3.8 cm did not consume them at all. Experience with copepods over several weeks increased the acceptance for this prey to some extend but hardly in the largest fish. This suggests that S. solidus will end up usually in sticklebacks that are too small for the parasite so that it has to allow its host's further growth after infection to reach its definitive size.

AbstractLernaeenicus radiatus, a mesoparasitic pennellid copepod, has long been known in the northwest Atlantic with metamorphosed females infecting the muscle of marine fish. The study herein is the first to identify a definitive first host, black sea bass Centropristis striata, for L. radiatus supporting larval development to adults and sexual reproduction in the gills. This finding suggests a two-host life cycle for L. radiatus, with black sea bass as the first host. Heavy infections in the gill were associated with considerable pathology related to a unique and invasive attachment process that penetrated the gill and selectively attached to the gill filament cartilage. The morphology of the developing copepod was highly conserved with that of a related pennellid copepod, Lernaeocera branchialis, though was distinguished by the attachment process, unique pigmentation and other morphologic features described herein. Sequencing the small and large subunits of the ribosomal RNA and mitochondrial cytochrome c oxidase subunit I genes demonstrated L. radiatus to share closer identities with Lernaeocera and Haemobaphes spp. pennellid copepods rather than other Lernaeenicus spp. available in GenBank to date. Taxonomy of L. radiatus is discussed in relation to life cycles, tissue tropism, morphology and genetics of other closely related pennellid copepods.

SUMMARYTo facilitate the completion of their life-cycle, many helminth parasites have evolved the ability to manipulate the behaviour of their intermediate host in order to make it more likely to be eaten by the parasite's definitive host. Here, we determined whether the cestode Eubothrium salvelini modifies the behaviour of its intermediate host, the copepod Cyclops vernalis, and makes it more susceptible to predation by brook trout, Salvelinus fontinalis, the parasite's final host. Following the experimental infection of copepods, the spontaneous activity of infected and control subjects was quantified weekly. In addition, we regularly quantified predation by individual brook trout fry on known numbers of infected and control copepods. At approximately the time when the cestode larvae became infective to fish (2–3 weeks following infection), the infected copepods started to swim more actively than uninfected controls. Also at that time, infected individuals became more likely to be captured by fish than uninfected ones. Copepod size and intensity of infection had no significant effect on their behaviour or their risk of being eaten by fish. Thus cestode- induced changes in copepod swimming activity can lead to infected copepods becoming highly vulnerable to fish predators, and may have resulted from selection on the parasite to increase its transmission success

The gut structure and ultrastructure of Neoergasilus japonicus (Harada, 1930), a copepod from the family Ergasilidae (Copepoda, Poecilostomatoida) and a parasite of fish, were compared at different periods of the life cycle: in free-living specimens in October and after attaching to fish in January and June. Differences in the depth of the intestinal epithelium were prominent and other cellular characteristics appeared seasonally variable. We relate these to changes in the physiological activity. Preliminary data from stable-isotope analyses of attached specimens suggest nutritional contribution from parasitism. The possibility of a diapause in the life cycle, as well as the relationship between the morphology of the gut and early evolutionary parasitism of N. japonicus, are discussed.

SUMMARYThe paramyxean parasite Marteilia refringens infects several bivalve species including European flat oysters Ostrea edulis and Mediterranean mussels Mytilus galloprovincialis. Sequence polymorphism allowed definition of three parasite types ‘M’, ‘O’ and ‘C’ preferably detected in oysters, mussels and cockles respectively. Transmission of the infection from infected bivalves to copepods Paracartia grani could be experimentally achieved but assays from copepods to bivalves failed. In order to contribute to the elucidation of the M. refringens life cycle, the dynamics of the infection was investigated in O. edulis, M. galloprovincialis and zooplankton over one year in Diana lagoon, Corsica (France). Flat oysters appeared non-infected while mussels were infected part of the year, showing highest prevalence in summertime. The parasite was detected by PCR in zooplankton particularly after the peak of prevalence in mussels. Several zooplanktonic groups including copepods, Cladocera, Appendicularia, Chaetognatha and Polychaeta appeared PCR positive. However, only the copepod species Paracartia latisetosa showed positive signal by in situ hybridization. Small parasite cells were observed in gonadal tissues of female copepods demonstrating for the first time that a copepod species other than P. grani can be infected with M. refringens. Molecular characterization of the parasite infecting mussels and zooplankton allowed the distinguishing of three Marteilia types in the lagoon.

The vertical distribution, abundance, population structure and life cycle of the ice-associated copepod, Paralabidocera antarctica was studied in the fast ice near Syowa Station (69°00'S, 39°35'E) in the eastern part of Lützow-Holm Bay in 1970, 1975 and 1982. The results indicated that P. antarctica inhabited the ice-seawater interface throughout the year with a one year life cycle and was actually present in the sea ice for most of the year except the summer. P. antarctica overwintered as naupliar stages (NIV-NV) with slow development in sea ice during winter. P. antarctica population then developed rapidly and attained adulthood in the water just beneath the sea ice during spring-summer. P. antarctica depended entirely on ice algae for food throughout its whole life-span, suggesting that the ice-seawater interface provides favourable food conditions for P. antarctica. The slow development in naupliar stages in sea ice and short copepodite life span in the water suggest that P. antarctica may adapt its growth strategy to suit the varying fast ice/water interface environment.

Lernaeocera branchialis (L., 1767) is a parasitic copepod that parasitises a range of gadoids by anchoring in the proximity of the branchial chamber of its host, deriving nutrition from the blood of its host and causing serious pathogenic effects. This study investigates the taxonomy of the juvenile free-swimming stages and host location behaviour in the pre-metamorphosed adult female. The large size and distinctive appearance of the metamorphosed adult female stage, coupled with the wide exploitation and commercial importance of one of its principle final gadoid hosts, the cod (Gadus morhua L.), means that this species has long been recognised in the scientific literature, and here the extensive literature concerning this potentially important and damaging pathogen is re-examined to provide an up to date overview, which includes both aquaculture and wild fisheries perspectives. Due to disagreements between several descriptions of the L. branchialis juvenile stages, and because the majority of the descriptions are over 60 years old, the juvenile free-swimming stages are re-described, using current terminology and a combination of both light and confocal microscopy. The time of hatching and moults in these stages is also examined. Techniques for the automated creation of taxonomic drawings from confocal images using computer software are investigated and the possibilities and implications of this technique are discussed. The method of host location in L. branchialis is unknown but is likely to involve a variety of mechanisms, possibly including chemo-reception, mechano-reception and the use of physical phenomena in the water column, such as haloclines and thermoclines, to search for fish hosts. In this study the role of host-associated chemical cues in host location by adult female L. branchialis is investigated by analysing the parasites behavioural responses to a range of host-derived cues, in both a choice chamber and a 3D tracking arena. To analyse the data from the experiments, specialised computer software (“Paratrack”) was developed to digitise the paths of the parasites’ movements, and calculate a variety of behavioural parameters, allowing behaviour patterns to be identified and compared. The results show that L. branchialis responds to host-associated chemical cues in a similar way to many copepods in the presence of chemical cues. Of the different cues tested, gadoid conditioned water appears to be most attractive to the parasites, although the wide variation in behavioural responses may indicate that other mechanisms are also required for host location. The different behavioural responses of parasites to whiting (Merlangius merlangus L.) and cod (Gadus morhua) conditioned water, which are both definitive hosts, provide some evidence for sub-speciation in L. branchialis. The role of chemical cues in host location of L. branchialis, and the relative importance of chemical and physical cues in host location are discussed. As well as demonstrating several techniques, which show potential for further development, this work has improved our knowledge of the biology and life-cycle of L. branchialis. Further study of this, and other areas of L. branchialis biology and its host-parasite interactions, should assist the development of contingency plans for the effective management and control of this widespread and potentially devastating pathogen.

Studies in the USA have reported that species of meiobenthic copepods can be used as bioindicators of sediment-associated contaminants. The main objective of this research project was to develop and validate methods to assess the effects of estuarine pollution, using the marine benthic copepod Robertsonia propinqua as a bioindicator of environmental health in New Zealand intertidal / estuarine areas. Cultures of R. propinqua were set up and maintained in the laboratory and individuals used in 96h acute and full life-cycle chronic bioassays using the pre-selected contaminants atrazine and zinc sulphate. From the 96h acute experiments it was found that the lethal doses at which 50% mortality occurred (LC50) for exposed nauplii and adult individuals were 7.5 mg/L and 31.8 mg/L, respectively for atrazine and 1.7 mg/L and 2.7 mg/L, respectively for zinc sulphate. This indicated that the nauplii life stage was more sensitive than were the adult life stages for exposure to both contaminants. Based on the 'trigger' values reported (atrazine = 0.013 mg/L, zinc = 0.015 mg/L) in the Australian and New Zealand guidelines for fresh and marine water quality, which provide values at which concentrations of contaminants can occur in the environment before they begin causing effects on aquatic fauna, it is unlikely that the calculated LC50s in the current research will induce biological effects in exposed copepods in the short-term. The calculated LC50 results were then used to further investigate the effects of chronic exposure of sediment-associated contaminants on the complete life-cycle (egg-reproductive adult) of R. propinqua. In a laboratory-based full life-cycle toxicity test, field-collected sediments from polluted sites in the Auckland and Bay of Plenty regions reduced reproductive output (nauplii and copepodite production) of R. propinqua individuals, but the number of males and females, gravid females, clutch size per female and the number of eggs produced were not affected by either the polluted or non-polluted (reference) sediment samples from both field regions. Field investigations of meiofauna community composition in polluted and non-polluted field sites were carried out in 2004 in the Auckland and Bay of Plenty field regions in New Zealand. Greater sediment organic content and a correspondingly deeper redox potential discontinuity layer occurred in all polluted field sites compared with the non-polluted sites. However, species composition could not be used to characterise polluted and non-polluted sites, as there were no dominant taxa which were representative of these sites. The results presented in this thesis indicate that R. propinqua has strong potential to be a good candidate species as a bioindicator of environmental contamination. Furthermore, the full life-cycle toxicity test could be used as a rapid test to detect immediate changes in individual reproduction and development as well as long-term population effects. The technologies developed as part of this research may eventually provide additional tools for commercial environmental consultancies and may compliment existing standard operating procedures for environmental assessments involving pollution of estuarine ecosystems.

There is growing concern about the fate and biological effects of chemical contaminants in the marine environment. In the United Kingdom, the present ability to detect the potential longterm effects of contaminants is limited by the lack of suitable laboratory methods for measuring chronic toxicity. The harpacticoid copepod Tisbe battagliai was selected as a candidate test organism and a suite of chronic toxicity test methods was developed for measuring the effect of chemical contaminants on individual copepods (postembryonic development, reproduction and life-table analysis) and populations of T battagliai. The development of chronic test methods proceeded alongside investigations of the influence of key environmental variables (temperature and food availability) on the biology of this species. These investigations provided a valuable insight into the potential importance of these environmental factors for influencing the development of populations of T battagliai in the field, and helped to define the optimum conditions for the culture and chronic toxicity testing of this species in the laboratory. The methods were further evaluated using pentachlorophenol (PCP) as a reference toxicant and the aim was to investigate the potential interaction between toxicant (PCP), environmental factors (temperature and food availability), and their effects on the population dynamics of T battagliai. In summary, results showed that temperature, and food quantity and quality, were important determinants of population dynamics. There were significant interactions between the chosen environmental variables (e. g. temperature), PCP, and subsequent biological effects on Tisbe battagliai, and results highlighted some important differences in toxicity testing approaches based on the measurement of individuals and populations of copepods. Established laboratory toxicity test procedures do not take account of the degree of complexity in the natural environment and this underlines the Miculty in extrapolating from laboratory. results to the field situation. In conclusion, the project was successful in its primary objective of developing a suite of techniques that can be used to measure the potential chronic toxicity of chemical contaminants in the marine environment. The methods using Tisbe battagliai are relatively simple to perform, are amenable to standardisation and provide relatively cost-effective measurements of chronic toxicity. The test methods can be used to provide chronic toxicity data but, more importantly, they can be used to address some of the current limitations associated with single species laboratory tests. For example, used in conjunction with key environmental variables, the methods provide a greater understanding of the potential interaction between contaminants and abiotic variables, thereby, improving the extrapolation of laboratory results to the field situation. The ability to carry out measurements on individual and populations of T. bauagliai provides a valuable insight into the predictive links between effects at different levels of biological organisation.

Os Copepoda constituem a maior classe de pequenos crustáceos, com mais de 8.500 espécies descritas. Dentre as cinco ordens de Copepoda de vida livre, as espécies pertencentes à ordem Calanoida apresentam um forte endemismo, com uma restrita distribuição geográfica. Além disso, os Copepoda Calanoida são particularmente sensíveis a contaminantes contidos na coluna de água devido ao seu hábito planctônico. No presente trabalho foram realizados estudos ecotoxicológicos com duas espécies de Copepoda Calanoida, particularmente com as espécies Argyrodiaptomus furcatus Sars, 1901 e Notodiaptomus iheringi Wright, 1935. Estas espécies foram comparadas com relação à sensibilidade e desempenho como organismos-teste na avaliação da qualidade da água em ecossistemas de água doce. Foram testadas e adaptadas metodologias de cultivo em laboratório, e foram estudados os principais aspectos da biologia destes em condições ambientais controladas. Além disso, foram analisados aspectos referentes à dinâmica populacional. A sensibilidade das duas espécies de Calanoida às substâncias de referência sódio, potássio e zinco na forma de cloreto (\'NA\'CL\', \'K\'CL\' e \'ZN\'CL IND.2\', respectivamente), ao dicromato de potássio (\'K IND.2\'CR IND.2\'O IND.7\') e ao sulfato de alumínio (\'AL IND.2\'(\'SO IND.4\')IND.3\'), aos surfactantes dodecilsulfato de sódio (\'C IND.12\'H IND.25\'NA\'O IND.4\'S\') e ácido dodecil benzenosulfonato de sódio (\'CH IND.3\'(\'CH IND.2\')IND.11\'C IND.6\'H IND.4\'S\'O IND.3\'NA\'), foram avaliadas. Além disso, avaliou-se a toxicidade aguda de diferentes amostras ambientais e das toxinas da cianobactéria Microcystis aeruginosa após tratamento por irradiação. Os resultados dos testes ecotoxicológicos foram expressos em concentração efetiva (CE(I)50). Para o cálculo estatístico da CE50 foi utilizado o programa Trimmed Spearman-Karber. Os resultados relativos ao ciclo de vida mostraram que N. iheringi tem um menor tempo de desenvolvimento do que A. furcatus, com tempos de duração do desenvolvimento do ovo determinados pelos métodos indireto e direto. Verificou-se que a espécie de N. iheringi, de menor tamanho, apresentou tempo de desenvolvimento pós-embrionário menor do que a espécie de maior tamanho, A. furcatus. As taxas intrínsecas de crescimento populacional foram mais elevadas para a espécie A. furcatus do que para N. iheringi. Pelos resultados obtidos observou-se que N. iheringi além de atingir tamanhos menores, possui um desenvolvimento mais rápido e ciclo de vida mais curto. Em relação à sensibilidade destes Copepoda Calanoida às substâncias tóxicas observou-se que em relação aos sais, estas duas espécies foram mais sensíveis ao cloreto de potássio (\'K\'CL\'). Em relação aos metais, o grau de toxicidade aos Copepoda decresceu na sequência zinco > cromo > alumínio. Já com em relação aos surfactantes, a espécie N. iheringi foi mais sensível do que A. furcatus, e a toxicidade diminui à medida que o estágio de desenvolvimento dos indivíduos se torna mais avançado. Os náuplios são mais sensíveis à maioria das substâncias de referência testadas (sais, surfactantes, cromo e zinco) do que os estágios de desenvolvimento mais avançados. A espécie N. iheringi é mais sensível aos diversos agentes tóxicos do que a espécie A. furcatus, no entanto, N. iheringi foi mais resistente às cianotoxinas do que A. furcatus. Os resultados apresentados corroboram a idéia de que os calanoides A. furcatus e N. iheringi apresentam elevada sensibilidade a uma variedade de substâncias tóxicas de referência, o que torna viável sua utilização como organismos-teste em ensaios ecotoxicológicos. Estes estudos podem proporcionar maior entendimento sobre a estrutura das comunidades aquáticas e das alterações na dinâmica das populações, no sentido de se poder verificar como as espécies respondem às alterações na qualidade da água e o porquê das modificações na estrutura das comunidades, permitindo, dessa forma, ações de manejo e de conservação visando a preservação da biodiversidade das águas doces.
Copepods constitute the largest class of small crustaceans, with more than 8,500 described species. Among the five orders of free-living copepods, the species belonging to the order Calanoida show strong endemism, with a restricted geographic distribution. Additionally, they are particularly sensitive to contaminants in the water column due to their planktonic habit. In the present study ecotoxicological studies with two species of Calanoida copepods were performed, particularly with the species Argyrodiaptomus furcatus Sars, 1901 and Notodiaptomus iheringi Wright, 1935. These species were compared for sensitivity and performance as test organisms in assessing water quality in freshwater ecosystems. Methods of cultivation in the laboratory were tested and adapted, and the main aspects of these species biology were studied under controlled temperature and photoperiod. In addition, aspects related to population dynamics were also analyzed. The sensitivity of the calanoids to a number of reference substances as: sodium, potassium and zinc in the form of chlorides (\'NA\'CL\', \'K\'CL\' and \'ZN\'CL IND.2\', respectively), potassium dichromate (\'K IND.2\'CR IND.2\'O IND.7\') and aluminum sulfate (\'AL IND.2\'(\'SO IND.4\')IND.3\'), and to the surfactant sodium dodecyl sulfate (\'C IND.12\'H IND.25\'NA\'O IND.4\'S\') and sodium dodecyl benzenesulphonate (\'CH IND.3\'(\'CH IND.2\')IND.11\'C IND.6\'H IND.4\'SO IND.3\'NA\') were evaluated. Also the toxicity of environmental samples and of the cyanobacteria Microcystis aeruginosa toxin after irradiation treatment was tested. The results of ecotoxicity tests were expressed as effective concentrations (EC(I)50). The statistical calculation of the EC50 was carried out by the Trimmed Spearman-Karber program. The results regarding the copepods life cycle showed that N. iheringi has a shorter development time and duration of egg development, by both indirect and direct methods, than A. furcatus. It was found that small sized N. iheringi, had a post-embryonic development faster than the larger species, A. furcatus. The intrinsic rates of population increase were higher for the species A. furcatus than for N. iheringi. The results indicated that N. iheringi besides reaching smaller sizes, has a faster development and shorter life cycle. Regarding the sensitivity of these two species to toxic substances it was observed that in relation to the salts the calanoids were more sensitive to the potassium chloride (\'K\'CL\'). Compared to metals, toxicity to copepods followed the sequence zinc> chromium> aluminum. However, regarding surfactants the species N. iheringi was more sensitive than A. furcatus, and toxicity decreased with the advance in developmental stages. The nauplii were more sensitive to most of the reference substances tested (salts, surfactants, chromium and zinc) than the more advanced developmental stages. The species N. iheringi was more sensitive to various toxic agents than A. furcatus, but N. iheringi was more resistant to the cyanotoxins than A. furcatus. The results support the hypothesis that the calanoid copepods A. furcatus and N. iheringi have high sensitivity to a variety of toxic reference substances, what makes them feasible to be used as test organisms in ecotoxicological tests. The study performed may provide further understanding about the structure of aquatic communities and changes in population dynamics, contributing for the understanding of how species respond to changes in water quality by changes in community structure, subsidizing management actions aiming the conservation of freshwater biodiversity.

Ergasilus sieboldi has been reported from a number of trout fisheries in England and Wales. The population dynamics of this parasitic copepod in Rutland Water, a large reservoir in Central England was studied from 2003 to 2005. A combination of angler and net caught fish were examined to record numbers of adult females and egg production throughout each year. The parasite overwintered in large numbers on trout and commenced egg production in April which then continued until October/November. The prevalence of infection and the abundance of the parasite were very high in overwintered rainbow trout but these parameters then decreased in March as large numbers of uninfected fish were stocked into the reservoir. The parasite population then increased until October. Infection levels in 2004 and 2005 were significantly lower than in 2003. Infections of cage-held rainbow trout showed that E.sieboldi could become ovigerous within two weeks of attachment to trout in July and August. New infections occurred from June until November. Several species of coarse fish examined were also shown to be infected by the parasite. Cage trials showed that triploid rainbow trout were infected by significantly higher numbers of the parasite than diploid rainbow, brown trout or “blue” rainbow trout. Observations of infected fish in experimental tanks showed that overwintering parasites were stimulated to commence oviposition by increasing water temperatures. Photoperiod had no noticeable effect on the parasite. Egg viability and rate of development was studied using tank held infected fish and in vitro incubation techniques. Viability of eggs in sacs detached from the adult parasite was greater than those remaining attached. The rate of egg development was modelled and was shown to be predicted by temperature. Development of eggs was estimated to commence at 3.6ºC. Eggs developed more rapidly at higher temperatures and at peak production, inter-clutch interval was between 0 and 0.5 days. Egg production models estimated that an overwintered parasite could produce up to 19 clutches of eggs between April and October under normal temperature regimes measured at the reservoir. Ovarian development during the winter was confirmed using classifications of ovary size and shape based on parameters measured using image analysis techniques. The life span of E.sieboldi was estimated at 10-12 months. Nauplii culturing techniques were compared, and nauplii to stage V were successfully developed. Nauplii hatched from the eggs of adult parasites occurring in the spring were larger and conditioned to develop at lower temperatures than those hatched later in the year. Nauplii were fed on 4 different types of algae held in monocultures but development occurred only in algal polycultures. A comparison was made of nauplii feeding preferences and development with algae recorded in Rutland Water in 2003 and 2005 but no correlations were found. Fish stock assessment was carried out using models of angler catch, effort and stocking figures from the fishery. Parasite numbers on the overwintered fish were estimated at 12 million parasites in April 2003, 8.3 million in April 2004 and 1.2 million in April 2005. Stock assessments suggested a reduction in number of overwintering trout and effects of stocking policy to be at least partially responsible for the decline in the parasite population. The results of this study formed a management strategy for the operation of the trout fishery.

Etude consacree dans la premiere partie a la taxonomie et a la biogeographie des eladoceres du lac tchad et du bassin moyen de l'orenoque. Une deuxieme partie etudie le zooplancton de 9 lacs d'altitude des pyrenees (cladoceus et copepodes) notamment la repartition des especes, leur cycle evolutif regi par le facteur thermique, la dynamique des populations

Adult Diphyllobothrium latum is acquired by consumption of raw fish by persons living around lakes/reservoirs/rivers. Hymenolepis nana can have a direct life cycle so eggs produced by adults in man are important in transfer between humans. The contribution of rodents and the indirect life cycle through arthropods need re-evaluation. Other minor adult cestode infections are described.Man can be an intermediate host for tissue metacestodes. Taenia multiceps and related species are that acquired from canids and produce a coenurus. Spirometra spp. pleurocercoids are acquired from copepod or reptile/amphibian/mammalian intermediate hosts. Other metacestode infections are very rare.

This chapter describes the taxonomy of copepods. Copepods are small aquatic crustaceans and are considered to be one of the most abundant and diverse multi-cellular organisms on earth. Populating a wide range of aquatic habitats, from the deep ocean floor to high Himalayan freshwater lakes, copepods have many free-living as well as highly modified parasitic forms. The chapter covers their life cycle, ecology, and general morphology. It includes a section that indicates the systematic placement of the taxon described within the tree of life, and lists the key marine representative illustrated in the chapter (usually to genus or family level). This section also provides information on the taxonomic authorities responsible for the classification adopted, recent changes which might have occurred, and lists relevant taxonomic sources.

Guinea-worm disease (dracunculiasis)—now limited to sub-Saharan Africa—is caused by the nematode Dracunculus medinensis, whose life cycle involves water-borne copepod crustaceans and humans, who acquire the infection when they drink water containing infective larvae. Clinical presentation is usually with a skin blister, most often on the leg, sometimes preceded by allergic prodromal symptoms. Bacterial infection is a common complication. Most patients in endemic areas recognize their condition, but irrigation of ulcers can reveal larvae. Treatment is by physical removal of the worm; anthelmintics have no role in management. Provision of safe water for drinking is the key to prevention....

Guinea worm disease (dracunculiasis)—now limited to sub-Saharan Africa—is caused by the nematode Dracunculus medinensis, whose life cycle involves aquatic copepod crustaceans. Humans are infected when they drink water containing infective larvae. Adult worms enter subcutaneous tissue and can reach a metre in length. Clinical presentation is usually with a skin blister, most often on the leg, sometimes preceded by allergic prodromal symptoms. Bacterial infection and local scarring with disability are common complications. Most patients in endemic areas recognize their condition, but irrigation of ulcers can reveal larvae. Treatment is by physical removal of the worm; anthelmintics have no role in management. Provision of safe water for drinking is the key to prevention. The disease is now nearing eradication.

In the subphylum Crustacea, species from most major clades have independently evolved symbiotic relationships with a wide variety of invertebrate and vertebrate hosts. Herein, we review the life cycle disparity in symbiotic crustaceans. Relatively simple life cycles with direct or abbreviated development can be found among symbiotic decapods, mysids, and amphipods. Compared to their closest free-living relatives, no major life cycle modifications were detected in these clades as well as in most symbiotic cirripeds. In contrast, symbiotic isopods, copepods, and tantulocarids exhibit complex life cycles with major differences compared to their closest free-living relatives. Key modifications in these clades include the presence of larval stages well endowed for dispersal and host infestation, and the use of up to 2 different host species with dissimilar ecologies throughout their ontogeny. Phylogenetic inertia and restrictions imposed by the body plan of some clades appear to be most relevant in determining life cycle modifications (or the lack thereof) from the “typical” ground pattern. Furthermore, the life cycle ground pattern is likely either constraining or favoring the adoption of a symbiotic lifestyle in some crustacean clades (e.g., in the Thecostraca).

In this chapter, we explore the different patterns of development following the hatching of the crustacean larvae. For many groups of crustaceans, the free-living, postembryonic, and prejuvenile phase is by far the most important part of their life cycle, providing the link between different life modes in successive phases (e.g., between a sessile adult life and the need for long-range planktonic dispersal). Among the aspects covered, we discuss the specific criteria for what a “larva” is, including the necessity for defining specific larval traits that are lacking in other phases of the life cycle. We examine the typical anamorphic and hemianamorphic developmental patterns based on larval examples from a wide selection of groups from Decapoda to Copepoda, Thecostraca to Branchiopoda. In these groups, we examine the most common larval development patterns (including intraspecific variability) of, for example, the zoea, furcilia, copepodite, nauplius, and cypris larvae. We also expand on the importance of the molting cycle as the main driver in larval ontogeny and evolution. Finally, we discuss some of the more general trends of crustacean larval development in light of the general patterns and latest knowledge on tetraconate and arthropod evolution.

Crustacea (or Pancrustacea) have explored virtually all possible milieus in different parts of their life cycle, including freshwater, marine, and terrestrial habitats, and even the air (pterygote insects). Many crustacean taxa display complex life cycles that involve prominent shifts in environment, lifestyle, or both. In this chapter, the overwhelming diversity of crustacean life cycles will be explored by focusing on changes in the life cycles, and on how different phases in a life cycle are adapted to their environment. Shifts in crustacean life cycles may be dramatic such as those seen in numerous decapods and barnacles where the development involves a change from a pelagic larval phase to an adult benthic phase. Also, taxa remaining in the same environment during development, such as holoplanktonic Copepoda, Euphausiacea, and Dendrobranchiata, undergo many profound changes in feeding and swimming strategies. Numerous taxa shift from an early larval naupliar (anterior limbs) feeding/swimming system using only cephalic appendages to a juvenile/adult system relying almost exclusively on more posterior appendages. The chapter focuses mainly on nondecapods and is structured around a number of developmental concepts such as anamorphosis, metamorphosis, and epimorphosis. It is argued that few crustacean taxa can be characterized as entirely anamorphic and none as entirely metamorphic. Many taxa show a combination of the two, even sometimes with two distinct metamorphoses (e.g., in barnacles), or being essentially anamorphic but with several distinct jumps in morphology during development (e.g., Euphausiacea and Dendrobranchiata). Within the Metazoa the Crustacea are practically unrivalled in diversity of lifestyles involving, in many taxa, significant changes in milieu (pelagic versus benthic, marine versus terrestrial) or in feeding mode. Probably such complex life cycles are among the key factors in the evolutionary success of Crustacea.