Title: CTENOPHORA
1CTENOPHORA
2Common Names
- Ctenophores are often called comb jellies, sea
gooseberries, sea walnuts, or Venuss
girdles.
3Examples
- There are two classes in the phylum Ctenophora
- Tentaculata, of which the most characteristic
species is Hormimorpha plumosa - Nuda, of which the most characteristic species is
Beroe punctatus. - The most commonly seen ctenophores are of the
genus Pleurobrachia. There are about one hundred
species of Ctenophora that have been discovered.
4Characteristics
- All organisms in Ctenophora have comb rows that
are actually large cilia used for transportation.
These are the largest cilia any organism uses.
Ctenophores lack the ability to sting and instead
use tentacles covered by colloblasts . All
ctenophores are bioluminescent, meaning they are
capable of producing light. Some have the
appearance of rainbow coloration. This is caused
by the beating of their combs, causing the
diffraction of light to form a rainbow.
Classification is generally done through
comparative morphology.
5Characteristics (continued)
- Ctenophores have two digestive openings, but
rarely use the anus for defecation - Biradial symmetry and three germ layers
(epidermis, gastrodermis, mesoglea if included) - Mesoglea holds muscle cells and amoebacytes
- Digestive system consists of mouth, pharynx, and
stomach with a canal system - Have no CNS or brain, but a nerve net
- Use an aboral sense organ with a statocyst to
maintain balance - Balance is maintained by mood (turn toward prey
if in danger) - All Ctenophores have a distinct larval form
before adulthood
6Morphology
- Most ctenophores are round or spherical in body
shape. They generally have two large tentacles
and eight rows of comb plates. Their tentacles
have the adhesive colloblasts to capture prey and
they have a stomach, mouth, pharynx, and anal
pores. They have a nerve network that is rather
complex and an apical sense organ. All
ctentophores are hermaphrodites and most
reproduce sexually. They generally range in size
from .6 cm to 30.5 cm.
7Colloblasts (Morphology)
Colloblasts are microscopic, sticky structures
used to adhere to the prey of a ctenophore.
Usually the classes Cydippida and Lobata have
colloblasts on their tentacles. After a prey is
caught by a colloblast, the tentacle is
contracted and the prey is brought by the
predators mouth. There the prey is released and
ingested.
8Cydippids (Morphology)
- Egg-shaped bodies
- Order includes pleurobrachia
- Tentacles on opposite sides of body
- Body can be flattened to increase range of
tentacles - Tentacles have tentilla (small tentacles) with
colloblasts - Generally coil around prey to kill
- Combs are spaced evenly around the body
- From each statocyst balancer, two combs are moved
at once - Movement is dependent on water disturbances
9Lobata (Morphology)
- Order also called Lobates
- Have pair of muscular lobes extending from mouth
- Tentacles in grooves on lobes, have auricles
between lobes and mouth - Auricles have cilia to create current and flush
prey into the mouth - Two comb rows on each lobe and two on each side
between lobes - Comb movement dependent on nerves rather than
water movement - Some can clap combs to push water rapidly and
move opposite - Generally prey on plankton
10Beroids (Morphology)
- Order also known as Nuda
- No feeding appendages, but pharynxes have
macrocilia - Marcocilia are large bundles of cilia that work
to bite off pieces of whatever is being consumed - Prey on other ctenophores
- When not eating, a ridge shuts the mouth by
connecting with the other part of the ridge
11Embryology
- When the egg is fertilized, development of the
embryo begins. Cleavage occurs completely but
unequally, first producing two cells, then four,
then eight, and so on until the embryo is full
developed. The embryo forms within the egg cover.
It develops double rows of cilia, a pair of
lateral tentacles, and a large, apical
sense-organ. The ectodermal layer of the
gastrovascular system undergoes Epiauxesis.
Epiauxesis involves the flattening and extension
of the ectoderm germ layer in the gastrovascular
system. Soon, the cilia begin to function and
the developed larva breaks the egg shell and
enters the water. The following pages are
detailed steps to the process of initial cleavage
and development.
12Development (Embryology)
13Development (Embryology)
14Biochemical Evidence
- Little biochemical evidence exists regarding the
phylogeny of Ctenophora. However, by using 18S
ribosomal RNA for comparison, it has been
determined that the ctenophores are a distinct
monophyletic group that is closest related to the
cnidarians. The ancestral ctenophore seems to
have been like Cydippida. Thus, it was
determined that Cydippida is a polyphyletic
group, all other orders having been secondarily
derived from the ancestor. The relatively close
distance between the 18S ribosomal RNA sequences
leads to the conclusion that ctenophores are
derived from a recent common ancestor.
15Life History
- Mnemiopsis leidyi is a ctenophore of the order
Lobata. These have a distinctive level of
bioluminescence that makes them appear to glow
even more than others. Locomotive flappers hide
the phosphorescent cells within the meridional
canal, perpendicular to the plane of the comb
plate. It exists in various morphological forms,
chiefly where transparence is inversely
proportional to body size. They can be up to 5-7
cm long and always live in a marine environment.
16Life History (continued)
M. leidyi is a hermaphroditic and are capable of
self-fertilization. They are considered
developed when capable of producing offspring,
even though they have not ceased growing yet.
When reproduction begins, the gonads in the
meridional canals produce one spermatophore and
one to four eggs. The auricalular gonads produce
only one egg. The egg is covered in a thick
membrane one minute after seawater contact.
17Life History (continued)
When embryogenesis begins, the eggs are spherical
and soft. After the larvae is formed, the egg is
covered with a thick membranous cuticle. The
embryo experiences epiboly, gastrulation, ctenes
appear, apical organs grow, tentacles grow, and
the embryo enters the tentacular stage. Here,
the larval form hatches and continues
development. Complete embryonical development
takes 20-24 hours.
18Life History (continued)
After hatching, the M. leidyi enters the lobate
stage. Next, the meridional canal meets and the
auricles begin to grow out. At this point, the
M. leidyi is capable of reproduction and
considered an adult.
19Life History (continued)
M. leidyi are capable of regeneration of damaged
body parts. After damage is done, the cells
begin dividing to reform the organ by doubling.
M. leidyi feeds on fish eggs and larvae,
phytoplankton, and holoplankton. It ingests any
organism it can grasp with its oral lobes. They
are generally considered carnivores but have been
known to consume phytoplankton when needed.
Their feeding on phytoplankton and zooplankton
has reduced their populations as well as those of
the kilka in the Caspian ecosystem. Thus, the
economy in Caspian countries has suffered due to
the loss of kilka.
20Life History (Digestion)
- Enzymes and contractions of pharynx liquidize
prey - Cilia move the resultant mush into the stomach
canal system - Nutritive enzymes break down the mush in the
stomach - Ciliary rosettes in canal transfer nutrients to
muscles in mesoglea - Most waste is ejected through the mouth, rarely
through the anal pores. - Exact mode of excretion is unknown
21Summary
- Are ctenophores carnivorous, herbivorous, or
omnivorous? - How do ctenophores capture prey?
- How do ctenophores reproduce and what organs do
they have for such? - To what phylum are ctenophores most closely
related? - What is the function of a colloblast?
- When are ctenophores considered fully developed?