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SLIDE 21

Scr.., .Lu, e. o €

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_._<._-r<.
  • Frc. 4. Diagram
  • f a verricrr

c--.:^- -t I I muscte fibres'

  • - -' - ''itical section through the ssca
  • f L. oborifera. Aftows indicate

the position of smooth

\\gggutYii

N\=

slide-22
SLIDE 22

Melanocefus johnsonii Cryptosarus couesi

slide-23
SLIDE 23

RaP re- scnta 4't"vL

Ce..ot i

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S,rb ow!-c,r Ccuq,€io f cJer \ o Fa.mlli cs tv <O E peci c5

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slide-24
SLIDE 24

1xl

  • 1o

1x1Os

1 x 1 0 8 1 x 1 0 7

1x106

t xf Osg

Controls Fig.2. Results

  • f bacterial

luciferase assays. Mean activ- ity of each sample is plotted. Abbreviations (Table 1) identify sample sourses, Multiple sanrples rvere available for some spe. cies. Solid bars, bacterial and symbiotic light organ controls;

  • pen

bars, myctophid and stomiiform samples grouped ac-

BIOLUNIINESCENCE OF MID\ryATER FISHES Gut

229

Pg

GF, dg

cording to tissue

  • type. Pp, \Ih, means
  • f all basterial

con. trols; +, -, V harueyi extract plus or minus photophore ex.

  • tract. The lowest activity samples

(Sa gut, Lt and Sa photophores) had no detectable activity and are plotted at the level

  • f

the detection limit. Photophores Gi[ Liver M.G.IIAYG Negative- Control

230

I symbiotic

I Luminous Bactcria I Light Organs v l-] Vf Pp Vh Pl Bs Ak Cc

m r r

  • a

LI CW Sb AA Sd Photo Liver Gut

  • Fig. 3. Dot blot of DNA from positive and negative

con- trols (top rorv) and tissues from myctophid and stomiiform fishes probed rvith a lu.t fragment analogous to pHU870. Ab- breriations

  • fspecies

identification as in Table 2.

slide-25
SLIDE 25

PETER '. HERRING

c _ I / \ l PH Ii

')l,i

/rN '. 'ojrt

, f i R

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{.

X: Chcu\roc't'rf I = Ar5lroYJct't1

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