The heterotrophic dinoflagellate Protopemdinium cf. divergens, known as prey for adult copepods, itself feeds on copepod eggs and early naupliar stages. One to several P. cf. divergens can attack an egg or nauplius larger than themselves. The time for an egg to be digested was proportional to the number of P. cf. divergens attacking it. Ingestion rates of P, cf. djvergens on Acartia tonsa eggs ...

Increased atmospheric CO(2) concentrations are causing greater dissolution of CO(2) into seawater, and are ultimately responsible for today's ongoing ocean acidification. We manipulated seawater acidity by addition of HCl and by increasing CO(2) concentration and observed that two coastal harpacticoid copepods, Amphiascoides atopus and Schizopera knabeni were both more sensitive to increased ac...

We studied the coastal zooplankton community structure of six waterbodies of Mathbaria and Bakerganj from January 2008 to June 2009. In total 35 zooplankton species were identified under 26 genera under 20 families under 8 orders from Mathbaria. Among them 6 were protozoans, 24 were rotifers, 3 were copepods, 1 was cladocerans and 1 was ostracods. From Bakergonj a total of 42 zooplankton specie...

The development of the nematode Procamallanus saccobranchi Karve, 1952, a parasite in the stomach of the fish Heteropneustes fossilis (Bloch), was studied in Mesocyclops crassus (Fischer) and Mesocyclops leuckarti (Claus). After being ingested by the copepods the nematode first-stage larvae penetrated into the haemocoel of the intermediate host; there they moulted twice (on days 3 and 5 p.i. at...

We link a two-dimension coastal upwelling circulation hydrodynamic-ecosystem (NPZ) model with an individualbased model (IBM) for an intermediate sized (ca. 2.5 mm) copepod capable of diel vertical migration (DVM) at larger sizes. The NPZ model is that of Franks, Wroblewski and Flierl (1986), with the zooplankton state variable parameterized for macrozooplankton. IBM simulations are done with di...

Southern Mexico and Central America have many water bodies of different morphology and water chemistry with an interesting zooplankton fauna, originating from North or South America. A set of 63 samples, taken in 2005 and 2008, from water bodies of the Yucatan Peninsula karst, Belize and Guatemala, were studied for the content of calanoid copepods. Old and recent literature was used to determin...

Diatoms are key phytoplankton organisms and one of the main primary producers in aquatic ecosystems. However, many diatom species produce a series of secondary metabolites, collectively termed oxylipins, that disrupt development in the offspring of grazers, such as copepods, that feed on these unicellular algae. We hypothesized that different populations of copepods may deal differently with th...

Calanoid copepods are among the most abundant metazoans in the ocean and constitute a vital trophic link within marine food webs. They possess relatively narrow swimming capabilities, yet are capable of significant self-locomotion under strong hydrodynamic conditions. Here we provide evidence for an active adaptation that allows these small organisms to adjust their motility in response to back...

Oithona spp. is considered the most abundant and ubiquitous copepod genus in the marine environment, often outnumbering calanoid copepods throughout the year. Previous studies have argued that one of the reasons for such success is that the respiration rate of Oithona spp. is insensitive to temperature changes and lower than in calanoids. However, comprehensive data on the thermal biology of th...

Copepod-bacteria interactions include permanent and transient epi- and endobiotic associations that may play roles in copepod health, transfer of elements in the food web, and biogeochemical cycling. Microbiomes of three temperate copepod species (Acartia longiremis, Centropages hamatus, and Calanus finmarchicus) from the Gulf of Maine were investigated during the early summer season using high...