Copepods: Rice of the Sea

Of all plankton groups, probably most is known about the copepods. They represent a critical link in the food chain and are consumed by diverse animal community ranging in size from small fish, chaetognaths, and ctenophores all the way up to large whales (the right whale is a voracious copepod feeder). Because of their small size and importance as food, copepods are affectionately known as “the rice of the sea.” Copepods are effectively captured by plankton nets because they have hard exoskeletons, and scientists have good estimates of their abundances and distributions. Although copepods are all relatively small (0.5 mm – 5 mm in length), they comprise over 200 families and 10,000 different species.

CopepodsTogether

Examples of typical copepods. Note to the two large appendages on the top of the head with small sensory hairs

Copepods consume both phytoplankton and microzooplankton in two different ways: suspension feeding and raptorial feeding. Suspension feeding is relatively passive and performed by beating small appendages that draw a current through a feeding chamber. Copepods then select which particles encountered are food and discard others. Raptorial feeding is used to actively capture prey. Many copepods have small sensors on their first appendages to detect water disturbances produced by prey and also predators. They can use these relatively large appendages to “hop” through the water and capture an unsuspecting prey item or to quickly escape a predator.

Copepod reproductive strategies vary greatly and are adapted towards the ability to withstand the variable conditions that characterize the ocean environment. For example, many copepod eggs have the ability to enter a phase of diapause where they remain viable on the bottom for several months or even years, only hatching with conditions are favorable (high concentrations of food). Some copepods carry their eggs, allowing them to develop a bit before releasing them into the water column. The timing of copepod reproduction is especially important for the life cycle of fishes because most fish larvae depend on the recently hatched copepod nauplii for food. If there are not enough copepod nauplii present when fish larvae are abundant, there could be mass starvation events causing few fish larvae to reach their juvenile stage. Because of this, the copepod life cycle is extremely important to fish populations and overall ocean ecosystem health.

This image was taken from a thin layer near Stellwagen Bank offshore of Massachusetts, USA. Each one of the white particles is a copepod. The concentration of organisms in this image corresponds to ~400,000 individuals per cubic meter! That is some good eating for a right whale!

This image was taken from a thin layer near Stellwagen Bank offshore of Massachusetts, USA. Each one of the white particles is a copepod. The concentration of organisms in this image corresponds to ~400,000 individuals per cubic meter! That is some good eating for a right whale!

One of the most remarkable characteristics of copepods is their tendency to aggregate in discrete thin layers within the water column. Sometimes >90% of the copepod biomass will be confined these thin layers, which are a maximum of 5 m thick. ISIIS and other systems that sample on small scales are ideal for detecting these layers of copepods, and the function of the formation and dissipation of copepod thin layers is not well understood. Copepods have been shown to be attracted to strong changes in current direction and speed, potentially allowing them to feed at a faster rate within these zones (Woodson et al. 2005). The changes in environmental variables associated with aggregations of copepods are of great interest to marine ecologists. With your help, we can better understand how these extremely important organisms are distributed throughout our oceans!

References:

Johnson WS, Allen DM (2005) Zooplankton of the Atlantic and Gulf coasts: A guide to their identification and ecology. Johns Hopkins University Press. Baltimore, MD.

Woodson CB, Webster DR, Weissburg MJ, Yen J (2005) Response of copepods to physical gradients associated with structure in the ocean. Limnol Oceanogr 50:1552-1564

Advertisements

Pteropods By Dorothy Tang

Pteropods are a group of organisms that we’re not focusing on because they are not very abundant in the Plankton Portal dataset. Nevertheless, you may have run across a few of those fascinating little creatures.

Pteropod, which means ‘wing-foot’ in Greek, is a group of free-swimming pelagic gastropods (snails). Officially, the word ‘pteropod’ is no longer used in taxonomy; it is a collective term which refers to two clades of gastropods—thecosome (shelled body) and gymnosome (naked body). Pteropods are quite unique because in order to adapt to life in the water column, their foot is modified into two wing-like flippers used for swimming. Their body size ranges from a few millimeters to several centimeters – so they’re easily imaged by ISIIS. They can be quite abundant in certain regions of the world’s oceans, and are typically found near surface waters.

The first group of pteropods, thecosomes, are also known as the sea butterflies. They have a pair of large ‘wings’ and swims by continually flapping them. Their body is encased in a delicate and translucent shell.The shell can be coiled, needle-like, triangular, and globed.

51d1bda13ae74008a40111d7

Thecosomes are omnivores. Their diet consists of diatoms, dinoflagellates, and zooplanktons such as copepods, tintinnids, and other gastropod larvae. They capture food by secreting a spherical mucus web several times larger than their body. Scientists believe that the use of the large size mucus web is to capture large, fast swimming prey, such as copepods. The web acts as a filter: particles that are too large for ingestion are removed. During feeding, the mucus web is suspended above the animal while the animal remains motionless below. Ciliary action draws back the web to the mouth and the whole web is ingested.

51d1bda43ae74008a4012a44

Thecosome reproductive biology is quite unusual. The animal first matures and functions as male. The male pteropod mates with another male and the sperm is stored until the animal changes into a female. When the animal turns into female; its male reproductive organs degenerate. The female lays fertilized floating egg mass that later hatch into swimming larvae (veliger).

51d1be2e3ae74008a402f99b

When a thecosome dies, its shell sinks to the bottom of the sea and forms sediment called pteropod ooze. The shell is composed of aragonite, an unstable form of carbonate mineral. Anthropogenic ocean acidification is one of the challenges that pteropods face. The increase of anthropogenic carbon dioxide level in the atmosphere reduces pH and carbonate ion concentration in the ocean, thus decreasing the calcium carbonate saturation level. As a result, the production of biogenic carbonate becomes more difficult. Overall, they have a hard time secreting their protective shell because of ocean acidification.

The second group of pteropods, or gymnosomes, are more commonly known as sea angels. They have much smaller wings which appear as side lobes. They are more robust and lack a shell. Unlike their thecosome relatives, gymnosomes are carnivores. They are active hunters and exclusively prey on thecosome pteropods. A combination of hooks and a toothed radula are employed to extract the flesh from the thecosomes’ shells.

The reproductive anatomy of gymnosome pteropods is similar to thecosomes pteropods. The only difference: the male reproductive organs do not degenerate in females. Gymnosomes has two distinct larvae forms. Eggs are hatched into shelled veliger. The veliger metamorphoses into a shell-less polytrochous larvae. The polytrochous larvae are initially wingless and movement is achieve by three ciliary bands. They gradually grow wings and lose the ciliary bands as they become adults.

Here is a very nice video about Pteropods.

Plankton Chronicles Project by Christian Sardet, CNRS / Noe Sardet and Sharif Mirshak, Parafilms. See Plankton Chronicles interactive site: planktonchronicles.org

Salps and Doliolids

Salps and doliolids (class Thaliacea) are interesting animals because they are in the phylum Chordata, which includes all animals with a notochord during development (e.g., humans, fish, cats), but thaliaceans have a vastly different appearance and feeding strategy compared to most vertebrates. A salp or doliolid body is essentially a giant pumping muscle that forces water through a mucous net filter that collects phytoplankton and is ingested periodically. Both groups have limited mobility, with salps using muscular contractions to scoot through the water, while doliolids use tiny beating cilia to propel themselves.

salpsolo

A salp in the process of forming a new chain of clones for asexual reproduction (see white coil)

The life history of salps and doliolids is remarkable and complex. Similar to plants, their life cycle alternates between sexual and asexual generations. The solitary phase reproduces asexually by budding off clones of itself. On salps, a chain of these clones develops on the solitary animal that is then released and reproduces sexually with other salp chains. The chains first mature as female and then change sexes to become male when they are larger! These chains release small solitary salps that then begin asexual budding once they are a certain size. Doliolids on the other hand produce short-lived tadpole larvae that are not seen in salps. When you consider that a chain of salps contains an average of ~28 individuals, it is no surprise that these organisms are capable of extremely fast reproductive rates and can double their populations in hours (Heron 1972). Some scientists think their remarkable reproductive rates can overwhelm other phytoplankton grazers, which could explain the fact that large salp aggregations are often associated with low biomass of other grazers (Alldredge and Madin 1982).

Doliolids images offshore of Monterey Bay showing asexual budding

Doliolids imaged offshore of Monterey Bay showing asexual budding

Because of their ability to reproduce quickly, salps are often very abundant near steady supplies of phytoplankton, such as at ocean fronts (zones where two water masses with differing physical properties meet) and eddies (Deibel and Paffenhöfer 2009). However, these organisms cannot tolerate extremely dense aggregations of phytoplankton because their mucous filters will become clogged with prey, which severely decreases their feeding efficiency. Salps and doliolids can “bloom” like other jellies, and when these blooms die off the dead salp bodies can export a large amount of carbon into deeper waters. Because of salps and doliolids close evolutionary relationship to vertebrates, scientists are also very interested in their developmental biology. Scientists are trying to use salps as a model organism to study the development of complex nervous systems in all vertebrate animals (Lacalli and Holland 1998).

Check out this video from Plankton Chronicles on these remarkable animals!

Plankton Chronicles Project by Christian Sardet, CNRS / Noe Sardet and Sharif Mirshak, Parafilms. See Plankton Chronicles interactive site: planktonchronicles.org

References:

Alldredge AL and Madin LP (1982) Pelagic tunicates: Unique herbivores in the marine plankton. Bioscience 32:655-663

Deibel D and Paffenhöfer GA (2009) Predictability of patches of neritic salps and doliolids (tunicata, thaliacea). J Plankton Res 31:1571-1579

Heron AC (1972) Population ecology of a colonizing species: The pelagic tunicate Thalia democratica – I. individual growth rate and generation time. Oecologia 10:269-293

Lacalli TC and Holland LZ (1998) The developing dorsal ganglion of the salp Thalia democratica, and the nature of the ancestral chordate brain. Philosophical Transactions of the Royal Society B: Biological Sciences 353:1943-1967

Drifter science!!

Here is a very funny educational video from the Carthe group (University of Miami). How physical oceanographers study and track currents and why it is important.

Very useful data if you want to know where our precious plankton is going! Just watch! funny and instructive.

Video credit: Laura Bracken (CARTHE), Patrick Rynne (Waterlust) and Fiona Graham (Waterlust), Sharon Chinchilla (CARTHE) and Jennah Caster (Waterlust)