Anatomy of Bivalves and Crustaceans

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    Invertebrateanatomy

    Invertebrate

    anatomy

    KU022Physiology of Aquatic organismBent Vismann

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    cnidarians

    sponges

    ctenophores

    flatworms

    annelids

    gastropoda

    bivalves

    chelicerates

    crustaceans

    bryozoans

    Echinoderms

    ascidians

    nemerteans

    pogonophorans

    cephalopods

    pygnogonida

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    cnidarians

    sponges

    ctenophores

    flatworms

    annelids

    gastropoda

    cheliceratesbryozoans

    Echinoderms

    ascidians

    nemerteans

    pogonophorans

    cephalopods

    bivalves

    crustaceans

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    Phyllum: Mollusca

    Gastropoda Bivalvia Cephalopoda

    Protobranchia Lamellibranchia

    TAXONOMYTAXONOMY

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    Edible cockle(Cerastoderma sp.)

    Jackknife clam ( Ensis sp.)

    Blue mussel(Mytilus edulis )

    Pacific Oyster

    (Crassostrea gigas )European oyster ( Ostrea edulis )

    Venus clams ( Venus , Mercenaria, Cyclina sp.)

    Scallops (Pectinidae)

    (Pecten maximus )

    Some commercially exploited species

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    App. 5 kg and siphon up to 2 meter

    Siphon

    Geoduck

    (Panope generosa )

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    Adult blue mussels

    egg

    sperm

    embryo

    Veliger larvaeTrochophore

    larvae

    Pediveliger larvae

    spat In e.g. oystersthis takes placeat the gills

    (i.e., it is the veliger

    larvae that comesout from the adultbivalve)

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    W-shapedgill

    stomach

    Heart

    mantle

    MantlecavityAfferentcavity

    Efferent cavity

    Digestive gland

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    Frontal cilia

    Laterofrontal

    cilia

    Ciliary

    junctionsLateral cilia

    Food grove

    Interlamellar

    junctions

    Branchial

    vessels

    http://mblserver3/bvismann/officefiler/powerpoint-filer/Physiology%20of%20aquatic%20organisms/FilibranchBivalve_tegnefilm.swf
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    How to measure filtration?How to measure filtration?

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    FR: Filtration rate(or Pumping rate)

    The water volumepumped per time unit

    CR: Clearance rate

    The water volume

    cleared for particlesper time unit

    RE: Retention efficiency

    The gills efficiency to retain

    particlesCR = FR * RE

    When RE = 1

    CR = FR

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    In order to know how many algae is present(or removed) we need to quantify the algae

    Microscope and counting chamber Cells ml -1

    Coulter counter (electric registration of particles sucked through an orifice) Cells ml -1

    Spectrophotometer (extraction of chlorophyll) g Chl a ml-1

    Fluorometer

    (excitation of chlorophyll and measuring the fluorescence) Volt

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    Y = aX b

    Cl

    L2

    Allometric

    equation:

    Relation between size and shape

    W

    L3 L

    W1/3

    Now turning to the bivalve

    A bivalve is not just a bivalve; i.e., size matters for any given physiological activity

    0

    0.5

    1

    1.5

    2

    2.5

    0 10 20 30 40 50 60 70

    Shell length (mm)

    S o

    f t p

    a r t

    ( g )

    W = 3.3 * 10-6

    L3.16

    Mhlenberg & Riisgrd 1979

    0

    2

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    0 10 20 30 40 50 60 70 80Shell length (mm)

    C l e a r a n c e

    ( l h - 1 )

    Cl

    = 0.0012 L 2.14

    Kirboe & Mhlenberg 1981

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    02468

    101214161820

    0 0.5 1 1.5 2 2.5

    Soft parts (g)

    C l e a r a n c e

    ( l h - 1

    g - 1 )

    Cl

    (W 1/3 )2

    W2/3

    W0.67

    Cl

    L2

    and when L

    W1/3

    So, when measuring clearanceit is important to realize that theclearance rate is dependent onthe bivalve being measured.In other words, the clearance

    rate must be given in a form,which can be related to other studies.Also remember the same holds

    true for experimental conditions

    0

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    0 0.5 1 1.5 2 2.5

    Soft parts (g)

    C l e a r a n c e

    ( l h - 1 )

    Cl

    = 7.45 W 0.66

    Jones et al. 1992

    Cl d t

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    0

    0.5

    1

    1.5

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    2.5

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    3.5

    4

    0 10 20 30 40 50 60

    Time (min)

    A l g a e

    ( 1 0 0 0 c e

    l l s m l

    - 1 )

    Mussels pumping at aconstant rate are placedin a tank with presenceof algae

    Algae = a *e (mt)

    0

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    0 10 20 30 40 50 60Time (min)

    L n

    ( a l g a e

    ) ( 1 0 0 0 c e

    l l s m

    l - 1 )

    Ln(Algae) = ln(a) + mtThis one can verify by alinear regression analysis

    Closed system

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    0

    500

    1000

    1500

    2000

    25003000

    3500

    4000

    0 10 20 30 40 50 60

    Time (min)

    A l g a e

    ( c e

    l l s m

    l - 1 )

    C1

    C2

    In steady state:

    Cl

    = F * (C 1-C 2)/C 2 = 0.174 * (3500-1500)/1500 = 0.232 l min -1

    F = 174 ml min -1 W = 4 g = 13.92 l h -1

    = 3.48 l h -1 g -1

    Weight specific clearance

    basic experimental set up

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    basic experimental set-up

    Interface

    Remotecontrolled

    peristalticPump

    PC & Labtech Notebook

    Flow-troughfluorometerPump

    Pump

    Algaestock

    solution

    input

    Closed loopControlOutput(on/off)

    Analog input

    Data on disk

    L o g f u

    n c t i o

    n

    The set-up can be used in two modes:A) Continously clearance rateB) Intermittent clearance rate

    output

    Flow-troughfluorometer

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    Where n = number of mussels (or biomass); t = time; v p = dosing pumprate; t p = dosing pump active; C 1 = algae concentration in stock solution;C2 = algae concentration in aquaria

    Cl

    = 1/(n * t) * (v p * tp* C1)/ C 2

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    500

    1000

    15002000

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    3000

    3500

    4000

    0 10 20 30 40 50 60

    Time (min)

    A l g a e

    ( c e

    l l s m

    l - 1 )

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    0

    500

    1000

    1500

    20002500

    3000

    3500

    4000

    0 10 20 30 40 50 60

    Time (min)

    A l g a e

    ( c e

    l l s m

    l - 1 )

    Cl

    = V/(n*t) * ln(C 0/C t)

    V = volume; n = number of mussels (or biomass); C 0 and C t = algae concentrationat time 0 and t, respectively

    Particles clearedParticles cleared

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    RR

    In connection with growth and activity someof the energy contained in the assimilatedfood is lost through respiration

    (R)

    FF

    A part of the ingested food is not absorbedby the bivalve but is excreted as faeces

    (F)

    Energy balance: I

    = P

    + R

    + U

    +

    F

    P

    = I ( R

    + U

    + F)

    PP The remaining part of the absorbed foodis called the assimilated food and is used

    for growth = Production ( P ).

    A part of the absorbed food is excreted asurine, mucus mm. ( U)

    UU

    II

    Particles retained by the gills can either beingested ( I)

    or rejected

    as

    pseudofaeces(PF )

    PFPF

    Particles clearedParticles cleared

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    Sejr et al. 2004

    Max clearance at 2000 cells ml -1

    AE = (I -

    (U + F))/I

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    Energy: Algae = 1.75 J cell -1; O 2 = 14 J mg -1; NH 4 = 0.025 J g -1

    P = I

    (R + U + F) AE = (I -

    (U + F))/I P = (I * AE) - R

    -0.5

    0

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    3.5

    0 5000 10000 15000 20000 25000 30000

    Algae concentration (cells ml -1)

    E n e r g y

    ( J o u l e

    h - 1 )

    ingestionRespirationExcretionproduction

    Zero production at app. 21000 cells ml -1

    Optimal production

    6000 cells ml -1

    In situ P

    I = Cl

    * [algae]

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    Phyllum: ArthropodaPhyllum: Arthropoda

    TrilobitomorphaTrilobitomorpha ChelicerateChelicerate ArachnidaArachnidaMandibulataMandibulata

    PycnogonidaPycnogonida

    CrustaceaCrustacea InsectaInsectaChilopodaChilopoda DiplopodaDiplopoda

    CopepodaCopepoda CirripediaCirripedia MalacostracaMalacostraca

    MysidaceaMysidacea CummaceaCummacea IsopodaIsopoda AmphipodaAmphipoda

    EucaridaEucarida

    EuphausiaceaEuphausiacea

    DecapodaDecapoda

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    Telson

    Uropods

    Abdomen

    Pleopods 4. walking leg 1. walking leg Cheliped

    Eye Rostrum 1. antenna

    2. antennaMaxillipedCarapace

    Cervicalgroove

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    Gills

    Heart

    artery

    Hemocoel

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