2. INTRODUCTION
• The swim bladder, gas bladder or air bladder is an internal gas-
filled organ that contributes to the ability of many bony fish to control
their buoyancy, and thus to stay at their current water depth without
having to waste energy in swimming. Additionally, the swim bladder
functions as a resonating chamber, to produce or receive sound.
• The swim bladder is evolutionarily homologous to the lungs. Charles
Darwin remarked upon this in the Origin of Species. Darwin reasoned that
the lung in air-breathing vertebrates had derived from a more primitive
swim bladder.
• The gas/tissue interface at the swim bladder produces a strong reflection of
sound, which is used in sonar equipment to find fish.
• Cartilaginous fishes do not have swim bladders. Some of them can control
their depth only by swimming; others store fats or oils with density less
than that of seawater to produce a neutral or near neutral buoyancy, which
does not change with depth.
3. STRUCTURE AND FUNCTION
• The swim bladder normally consists of two
gas-filled sacs located in the dorsal portion
of the fish, although in a few primitive
species, there is only a single sac.
• It has flexible walls that contract or expand
according to the ambient pressure.
• The walls of the bladder contain very
few blood vessels and are lined
with guanine crystals, which make them
impermeable to gases.
• Due to the dorsal position it gives the fish
lateral stability.
• By adjusting the gas pressurizing organ using
the gas gland or oval window the fish can
obtain neutral buoyancy and ascend and
descend to a large range of depths.
4. • Depending on the condition of the swim-bladder, the teleosts are classified by older
taxonomists into two groups Physostomi and Physoclisti.
• In physostomous swim bladders, a connection is retained between the swim bladder
and the gut, the pneumatic duct, allowing the fish to fill up the swim bladder by
"gulping" air. Excess gas can be removed in a similar manner.
• In physoclistous swim bladders, the connection to the digestive tract is lost. In early life
stages, these fish must rise to the surface to fill up their swim bladders; in later stages,
the pneumatic duct disappears, and the gas gland has to introduce gas to the bladder to
increase its volume and thus increase buoyancy. Together with oxygen, other gases are
salted out in the swim bladder which accounts for the high pressures of other gases as
well.
• The combination of gases in the bladder varies. In shallow water fish, the ratios closely
approximate that of the atmosphere, while deep sea fish tend to have higher
percentages of oxygen. For instance, the eel has been observed to have 75.1% oxygen,
20.5% nitrogen, 3.1% carbon dioxide, and 0.4% argon in its swim bladder.
• Physoclistous swim bladders have one important disadvantage: they prohibit fast rising,
as the bladder would burst. Physostomes can "burp" out gas, though this complicates
the process of re-submergence.
5. • The swim bladder in fresh water fishes is interconnected with the
inner ear of the fish.
• They are connected by four bones called the Weberian
ossicles from the Weberian apparatus. These bones can carry the
vibrations to the saccule and the lagena . They are suited for
detecting sound and vibrations due to its low density in
comparison to the density of the fish's body tissues. This
increases the ability of sound detection.
• The swim bladder can radiate the pressure of sound which help
increase its sensitivity and expand its hearing.
• In red-bellied piranha, the swim bladder may play an important
role in sound production as a resonator. The sounds created by
piranhas are generated through rapid contractions of the sonic
muscles and is associated with the swim bladder.
• Teleosts are thought to lack a sense of absolute hydrostatic
pressure, which could be used to determine absolute
depth. However, it has been suggested that teleosts may be able
to determine their depth by sensing the rate of change of swim-
bladder volume.
6. EVOLUTION OF AIR BLADDER
• Swim bladders are evolutionarily homologous to lungs. Traditional wisdom has long held that
the first lungs, simple sacs connected to the gut that allowed the organism to gulp air under
oxygen-poor conditions, evolved into the lungs of today's terrestrial vertebrates and some fish
(e.g., lungfish) and into the swim bladders of the ray-finned fish.
• Primitive lungs gave an advantage by supplying the heart with oxygenated blood via the cardiac
shunt. This theory is robustly supported by the fossil record, the ecology of extant air-breathing
fishes, and the physiology of extant fishes.
• In embryonal development, both lung and swim bladder originate as an outpocketing from the
gut; in the case of swim bladders, this connection to the gut continues to exist as the pneumatic
duct in the more "primitive" ray-finned fish, and is lost in some of the more derived teleost
orders. There are no animals which have both lungs and a swim bladder.
• The cartilaginous fish split from the other fishes about 420 million years ago, and lack both lungs
and swim bladders, suggesting that these structures evolved after that split. Correspondingly,
these fish also have both heterocercal and stiff, wing-like pectoral fins which provide the
necessary lift needed due to the lack of swim bladders. Teleost fish with swim bladders have
neutral buoyancy, and have no need for this lift.
8. RISK OF INJURY
• Many anthropogenic activities or even Seismic wave, that could result
from climate change or natural causes, can create high-intensity
sound waves that cause a certain amount of damage to fish that
possess a gas bladder.
• Physostomes can release air in order to decrease the tension in the
gas bladder that may cause internal injuries to other vital organs,
while physoclisti can't expel air fast enough, making it more difficult
to avoid any major injuries.
• Some of the commonly seen injuries included ruptured gas bladder
and renal Haemorrhage. These mostly affect the overall health of the
fish.
9. WEBERIAN OSSICLE
• The Weberian apparatus is an anatomical structure
that connects the swim bladder to the auditory
system in fishes belonging to the
superorder Ostariophysi. When it is fully developed, the
elements of the apparatus are collectively referred to
as the Weberian ossicles.
• The structure consists of a set of minute bones that
originate from the first few vertebrae to develop in an
embryonic ostariophysan. These bones grow to
physically connect the auditory system, specifically
the inner ear, to the swim bladder.
• The structure acts as an amplifier of sound waves that
would otherwise be only slightly perceivable by the
inner ear structure alone.
10. STRUCTURAL ANATOMY AND FUNCTIONS
• The generalized structure of the
Weberian apparatus is similar to a
skeletal complex of bones and ossicles
that are physically connected to the
labyrinth auditory complex anteriorly
and the anterior most region of the swim
bladder posteriorly.
• The entire structure is derived from
skeletal elements of the first
four vertebrae. Together, the structure
interacts anteriorly with the lagenar
otolith set within the skull and posteriorly
with the swim bladder via the pleural rib.
11. FUNCTIONS
• The Weberian apparatus functions by transmitting auditory signals
straight from the gas bladder, through the Weberian ossicles and then
straight into the labyrinth structures of the inner ear.
• Volume change of the gas bladder cause the Weberian ossicles to
move in such a manner that pressure changes are transmitted to the
perilymph and then to the sensory cells of the inferior portion of the
labyrinth which is the seat of sound reception.
• The structure essentially acts as an amplifier of sound waves that
would otherwise be only slightly perceivable by the inner ear
structure alone.
• With the added function of the swim bladder as a resonating
chamber, signals are amplified to noticeable levels.
