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As with most animals and plants,
tunicates come in all shapes and sizes. Benthic
ascidians are usually sessile in their adult lives and
prefer substrates on rocky shores or in subtidal
habitats. Pelagic tunicates, highly efficient
filter-feeders, are dispersed throughout plankton,
living as motile or floating organisms (Pearse V. et
al. 1987). Benthic tunicates make up the majority of
the subphylum urochordata and are what struck my
interest upon visiting the rocky intertidal zone of
Nahant, MA. Below are interactive diagrams of the adult
and larval stage of these ultimately sessile ascidians.
Move the mouse
over the words to see explanations...
In addition to the organs listed above, tunicates have
several other integral entities. The squirting that
earns tunicates their nickname is regulated by the
nervous system, a large ganglion being the primary
component. The nervous system is able to slow or halt
feeding due to its control of the beating pharyngeal
cilia (Pearse, V. et al. 1987). In addition to
the nervous system, tunicates also have a heart capable
of reversing the direction of blood flow. This unique
characteristic is found in all tunicates, but its
importance is not understood. The blood is carried
throughout the organism, supplying the pharynx and
tunic. Different cells in the blood aid in distribution
of nutrients, storage of excretory products, and
production of tunic (Pearse, V. et al. 1987).
Certain tunicates
produce self-defense mechanisms capable of protecting
them from predators such as crabs and fish. Some species
contain high concentrations of toxic compounds like
sulfuric acid and vanadium compounds in their tunic
cells (Pearse, V. et al. 1987). Other tunicates
are decorated with spiny projections that help fend off
large snails (Pearse, V. et al. 1987).
This is the opening of the tunicate where water enters.
Water is forcefully expelled out of both the oral opening (incurrent siphon) and atrial opening (excurrent siphon). This clears away any gathered debris.
Covers the pharyngeal pouch and opens to the outside,
allowing the water that leaves the pharyngeal slits to exit the tunicate.
A sieve-like sac that has cilia lining it, creating a current. Water flows into the mouth and out through the pharyngeal slits. Mucoid sheets that lay against the pharyngeal walls trap food particles, thus allowing the tunicate to filter-feed.
This covering surrounds and protects the inside components of the body. However, it acts as a connective tissue and contains many different cells and sections of the circulatory system.
Water is forcefully expelled out of both the oral opening (incurrent siphon) and atrial opening (excurrent siphon). This clears away any gathered debris.
Digested food exits the gut via the anus, opening into the atrium.
Food is flushed from the mucous sheets into the esophagus and stomach, where food is digested extracellularly.
This key chordate characteristic runs parallel below the nerve cord. The notochord facilitates swimming.
This is a well-developed entity that is anteriorly enlarged. It is one characteristic that places tunicates in the phylum Chordata.
The muscular tail of a tunicate is another chordate characteristic. When it undulates, the tadpole is propelled through the water.
Tunicates
may be solitary, compound, or colonial, though
little is different in the morphology of the
zooid
itself. Individual compound and colonial tunicates
are smaller than solitary tunicates, and are
connected primarily by blood vessels (Pearse V.
et al. 1987). When individual zooids are
embedded in a common tunic, or test, and share a
single atrial opening, the colony is considered to
be compound (“Sea squirt”, 2005). This is the
highest degree of organization among colonial
tunicates (Pearse V. et al. 1987). B.
Schlosseri appears as a star or flower, the
zooids in circular clusters. B. violaceus
zooids are arranged in elongated clusters, often in
double rows. These two species are firm and maintain
their system structure. However, it is also
possible for individuals to be loosely bound by the
tunic (see pictures from Bermuda on left).
B.
schlosseri and B. violaceus are examples
of these colonial organizations that allow for
extraordinary growth and reproduction. Individuals
in a colony may live for only a couple days as they
mature and release their young, then die, all in
near synchrony (Pearse V. et al. 1987). It
has been recorded that B. schlosseri may live
for approximately 3 months when larvae settle in the
spring, and 8 months when larvae settle in the fall
(Cohen, 2005).

B.
schlosseri and B. violaceus are founded
by sexual reproduction while the colonies grow
through asexual budding. Tunicates, with rare
exceptions, are hermaphroditic, producing both the
egg and sperm. Once a zygote is formed, a
tadpole develops. This tadpole larva can swim for as
little as a few minutes or up to a few days, using
sensory guides such as chemical and tactile
receptors and a light-sensing eye to assist in
settlement (Pearse V. et al. 1987). Once the
tadpole has attached itself to a firm surface by its
anterior end, it begins rapid metamorphosis, loosing
its chordate characteristics (dorsal nerve cord,
tail, and notochord) and developing other organs
such as its heart, digestive system, atrium, and
nerve ganglion (Cohen, 2005; Pearse V. et al.
1987). Following metamorphosis, the oozooids produce
buds (blastogenesis) simultaneously, just as the
organisms died simultaneously (Grosberg, 1988).
Blastogenesis leads to colony mats that can encrust
and overgrow other organisms. These colonies are
able to grow until bud production exceeds adult
zooids (Yund and Stires, 2002).
Taxonomy of B.
schlosseri:
Phylum: Chordata
Subphylum: Tunicata
Class: Ascidacea
Order: Pleurogona
Suborder:
Stolidobranchia
Family: Styelidae
Genus: Botryllus
Species: schlosseri
Taxonomy of
B. violaceus:
Phylum: Chordata
Subphylum: Tunicata
Class: Ascidiacea
Order:
Pleurogona
Suborder: Stolidobranchia
Family: Styelidae
Genus: Botrylloides
Species: violaceus
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