goals! 1 1.!!plankton!sampling! 2 1a …...ocean&410/430&thompson&cruise&...

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Ocean 410/430 Thompson Cruise Name:________________________________________ 30 September 2013 1 GOALS 1 1. PLANKTON SAMPLING 2 1A.ZOOPLANKTON VERTICAL NET TOW 3 1B.PHYTOPLANKTON NET TOW 4 1C.PHOTOSYNTHESIS &RESPIRATION:BOTTLE INCUBATIONS. 5 2. WATER COLUMN STRUCTURE 7 3. MORPHOLOGIC FEATURE IDENTIFICATION 8 5. BOX AND KASTEN CORING 10 6. MULTIBEAM SONAR EXERCISE 11 Goals Learn to identify phytoplankton and zooplankton in Elliot bay Measure phytoplankton respiration rates with a bottle incubation experiment Understand the morphologic and subbottom features in Elliot Bay through the examination of two landslides Interpret different kinds of sediment cores Learn to plan a multibeam survey Be safe and have fun! (you’re on a boat!)

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Page 1: GOALS! 1 1.!!PLANKTON!SAMPLING! 2 1A …...ocean&410/430&thompson&cruise& name:_____& 30&september&2013& & 1&! goals! 1! 1.!!plankton!sampling! 2! 1a.!zooplankton!vertical!nettow!

Ocean  410/430  Thompson  Cruise   Name:________________________________________  30  September  2013  

  1  

 

GOALS   1  

1.    PLANKTON  SAMPLING   2  

1A.  ZOOPLANKTON  VERTICAL  NET  TOW   3  1B.  PHYTOPLANKTON  NET  TOW   4  1C.  PHOTOSYNTHESIS  &  RESPIRATION:  BOTTLE  INCUBATIONS.   5  

2.  WATER  COLUMN  STRUCTURE   7  

3.  MORPHOLOGIC  FEATURE  IDENTIFICATION   8  

5.  BOX  AND  KASTEN  CORING   10  

6.  MULTIBEAM  SONAR  EXERCISE   11  

Goals  -­‐ Learn  to  identify  phytoplankton  and  zooplankton  in  Elliot  bay  -­‐ Measure  phytoplankton  respiration  rates  with  a  bottle  incubation  experiment  -­‐ Understand  the  morphologic  and  sub-­‐bottom  features  in  Elliot  Bay  through  the  

examination  of  two  landslides  -­‐ Interpret  different  kinds  of  sediment  cores  -­‐ Learn  to  plan  a  multibeam  survey  -­‐ Be  safe  and  have  fun!  (you’re  on  a  boat!)  

     

Page 2: GOALS! 1 1.!!PLANKTON!SAMPLING! 2 1A …...ocean&410/430&thompson&cruise& name:_____& 30&september&2013& & 1&! goals! 1! 1.!!plankton!sampling! 2! 1a.!zooplankton!vertical!nettow!

Ocean  410/430  Thompson  Cruise   Name:________________________________________  30  September  2013  

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1.    Plankton  Sampling     What  are  plankton?  Plankton  consist  of  plants  and  animals  that  drift  with  water  currents  and  can  make  no  significant  swimming  movements  against  a  current.  Plankton  are  not  uniformly  distributed  in  the  sea,  instead  they  tend  to  have  patchy  distributions  (i.e.  they  show  clumped  or  aggregated  distribution).  In  general,  plankton  may  be  categorized  according  to  size  (picoplankton,  nanoplankton,  microzooplankton,  etc.).  They  may  also  be  characterized  by  functional  role  in  the  environment:   Phytoplankton –  the  plant-­‐like  photosynthesizing  component  of  the  plankton  (microscopic,  mainly  unicellular  algae)   Zooplankton –  the  animal  component  of  the  plankton,  which  range  from  microzooplankton  to  megaplankton  (i.e.  jellyfish!)   Phytoplankton  and  zooplankton  distributions  in  the  water  column  are  commonly  sampled  using  plankton  nets.  Many  plankton  nets  are  conical  in  shape,  tend  to  be  made  of  nylon  (or  nitex)  and  are  woven  into  a  consistent  mesh  size  so  that  the  holes  between  the  threads  are  of  equal  size.  The  mesh  size  of  the  net  determines  what  type  of  plankton  is  retained  when  towing  the  net.  Nets  with  a  finer  mesh  size  retain  phytoplankton  and  small  zooplankton  and  nets  with  a  coarser  mesh  size  retain  larger  zooplankton.  In  order  to  estimate  the  concentration  of  different  types  of  plankton,  it  is  necessary  to  take  counts  of  plankton  species  of  interest  caught  in  the  nets  and  also  have  an  idea  of  the  volume  of  water  filtered  by  the  net.   Beyond the scope of this cruise (but still totally cool!), there are also bacterioplankton (bacteria) in the water column. They are diverse in their functions in the environment and are sampled using water bottle (niskin) samples. For the exercise, we are going to attempt to identify several species in the sample and estimate their concentrations in the water column.

Page 3: GOALS! 1 1.!!PLANKTON!SAMPLING! 2 1A …...ocean&410/430&thompson&cruise& name:_____& 30&september&2013& & 1&! goals! 1! 1.!!plankton!sampling! 2! 1a.!zooplankton!vertical!nettow!

Ocean  410/430  Thompson  Cruise   Name:________________________________________  30  September  2013  

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1a.  Zooplankton  Vertical  Net  Tow    Station #:_____________ Latitude:________________ Longitude:_____________

Depth of tow: _____________________________

Diameter of net: ____________________________

Volume of water filtered, in liters (area of mount of net x distance towed): __________________

Mesh size of net:___________________________

Take a known volume of the sample (maybe 2-3 ml) and estimate the abundance of two types of zooplankton in this sample using the following steps: Identify 2 organisms of interest and sketch them. Name: Name: Abundance in _______ ml: Abundance in _______ ml: Now, scale these abundances back to the total volume to determine abundance in the area of the water column sampled. To do this, first you have to figure out abundance in the total sample. This can be determined by first figuring out what fraction of the total sample you examined and then dividing the number of organisms you observed by this fraction. Then to figure out how many zooplankton are in 1 liter of water all you have to do is divide this value by volume of water filtered to get organisms/L. Zooplankter 1: Zooplankton 2:

DON’T FORGET: Record your results on the cruise datasheet!!

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Ocean  410/430  Thompson  Cruise   Name:________________________________________  30  September  2013  

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1b.  Phytoplankton  Net  Tow    Station #:_____________ Latitude:________________ Longitude:_____________

Diameter of net: ____________________________

Volume of water filtered, in liters (area of mount of net x distance towed): __________________

Mesh size of net:___________________________

Draw and identify four phytoplankton you observed in the sample. Name: Name:

Name: Name:

Phytoplankton require light to photosynthesize so it is extremely important that you stay up in the well-lit portion of the water column. Examine the structures of the different phytoplankton you observed. List and explain possible adaptations, if any, each phytoplankton has to help them resist sinking out of the photic zone.          

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Ocean  410/430  Thompson  Cruise   Name:________________________________________  30  September  2013  

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1c.  Photosynthesis  &  Respiration:  Bottle  Incubations.   The total amount of organic material produced through photosynthesis is termed gross primary productivity (GPP). Because phytoplankton respire some of their organic matter, not all of the organic matter they produce is available for consumption by higher trophic levels. The total carbon fixed during photosynthesis minus that part which is respired is termed net primary productivity (NPP). A method to measure the respiration and photosynthetic rates is to incubate in ambient light and temperature conditions a portion of a water sample in a clear bottle (“light bottle”) and another portion in an opaque bottle which light cannot penetrate (“dark bottle”). We will measure oxygen concentrations in the bottles, and how the oxygen concentration changes from the start until the end of the incubation period. 1.) What process(es) is/are occurring in the “light bottles”? (Circle all that apply)

Photosynthesis Respiration

2.) What process(es) is/are occurring in the “dark bottles”? (Circle all that apply)

Photosynthesis Respiration

3.) The change in O2 concentration in the light bottle indicates: (Circle answer)

Gross Primary Production Net Primary Production Total Respiration

4.) The change in O2 concentration in the light bottle – Final O2 concentration in the dark bottle

indicates: (Circle answer)

Gross Primary Production Net Primary Production Total Respiration

5.) The change in O2 concentration in the dark bottle indicates: (Circle answer):

Gross Primary Production Net Primary Production Total Respiration

6.) What was the initial oxygen concentration of the sample water? _____________________

7.) What is the final O2 concentration in the “light bottle”? __________________________

8.) What is the final O2 concentration in the “dark bottle”? __________________________

9.) Using the results of your experiment, calculate the respiration rate. Your answer should be in

mg O2 L-1 hr-1.

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Ocean  410/430  Thompson  Cruise   Name:________________________________________  30  September  2013  

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10.) Using the results of your experiment, calculate net primary production (NPP). Your

answer should be in mg O2 L-1 hr-1.

11.) Using the results of your experiment, calculate gross primary production (GPP). Your

answer should be in mg O2 L-1 hr-1.

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Ocean  410/430  Thompson  Cruise   Name:________________________________________  30  September  2013  

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2.  Water  column  structure   Station #: Latitude: Longitude: Secchi disk: The secchi disk is a very simple device used to measure the transmission of visible light in the upper watch column. It is basically a white and black disk about 30 cm in diameter (although size can very) attached to a rope that is marked off at some depth interval (perhaps 0.5 or 1 meter). To estimate how well light is transmitted in the water column you lower the secchi disk over the sunny side of the boat until it can just no longer be seen. As you pull the disk back up, record how deep you could see the secchi disk. This provides a simple measure of turbidity, which can be used for a relative comparison from station to station. Secchi disk reading: _____ m Does this seem like a lot or a little visibility? And What are some factors that might influence the transmission of light in the water column? CTD cast: Sketch the water column profile you observed during the CTD cast. Include: Salinity, Temperature, Transmissivity, PAR and Fluorescence. You might need to make a couple sketches – one with salinity and temperature and another with transmissivity, fluorescence and PAR Do you think the weather of the past week has had any influence on the water column structure you observed today? Why or why not? Does the water column appear to be well mixed or stratified? Explain.          

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Ocean  410/430  Thompson  Cruise   Name:________________________________________  30  September  2013  

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3.  Morphologic  feature  identification  Identify and label morphologic features such as dredge spoils, canyon, landslide scarp, etc. on the following two bathymetric maps.

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Ocean  410/430  Thompson  Cruise   Name:________________________________________  30  September  2013  

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Page 10: GOALS! 1 1.!!PLANKTON!SAMPLING! 2 1A …...ocean&410/430&thompson&cruise& name:_____& 30&september&2013& & 1&! goals! 1! 1.!!plankton!sampling! 2! 1a.!zooplankton!vertical!nettow!

Ocean  410/430  Thompson  Cruise   Name:________________________________________  30  September  2013  

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5.  Box  and  Kasten  coring  Is  there  any  physical  layering  present  in  the  cores  we  collected?    What  would  be  an  effective  approach  to  investigate  layering?              Describe  the  sediment  properties  observed  in  at  least  one  of  the  cores.    What  mechanisms  caused  these  properties?              In  the  core  logs  below,  sketch  the  major  features  from  one  of  the  cores  we  collected  (e.g.,  layering  if  present,  grain  size,  color).    Is  there  anything  else  you  notice  that  could  be  important  when  interpreting  geological  significance?          Core  location:  

Date:  

Water  depth:    

Depth  in  core  cm                      

 cm                      

 cm  

cm                      

cm                      

cm  

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Ocean  410/430  Thompson  Cruise   Name:________________________________________  30  September  2013  

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6.  Multibeam  sonar  exercise    Multibeam  sonars  are  used  to  map  the  seafloor  by  sending  out  a  fan  of  beams  to  measure  depth  in  a  profile  in  the  across-­‐ship  direction.  The  maps  on  pages  8-­‐9  were  created  using  data  collected  using  a  multibeam  sonar.    For  this  exercise,  you  will  determine  how  long  it  would  take  do  a  multibeam  survey  of  Elliot  Bay  using  an  EM302  (the  same  system  that  is  on  the  Thompson).  The  survey  will  be  conducted  to  the  right  (East)  of  the  red  line  below.  For  simplicity,  you  may  assume  an  average  water  depth  of  100m.    

                             1  nm    You  need  100%  overlap  between  adjacent  swaths.  This  means  that  the  edge  of  your  swath  must  “touch”  the  center  of  the  line  beside  it  (see  the  following  figure  for  an  illustration  of  this  concept).    

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Ocean  410/430  Thompson  Cruise   Name:________________________________________  30  September  2013  

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   1)  What  is  the  swath  width  of  the  EM302  system,  as  a  multiple  of  water  depth?  Hint:  you  can  find  this  in  the  EM302  specifications,  or  if  you  ask  the  multibeam  operator  nicely,  he/she  may  help  you  out.          2)  Using  the  swath  width  specification  from  the  previous  question,  calculate  the  swath  coverage  (S)  for  your  assumed  water  depth.    Use  S  to  calculate  H,  the  horizontal  spacing  between  lines.        3)  Using  approximate  dimensions  from  the  map  above,  calculate  how  many  North-­‐South  survey  lines  you  would  need  to  do  (an  approximate  is  fine,  this  is  just  to  get  the  concept).          4)  What  would  be  the  average  length  of  the  lines  (again,  a  decent  approximate  is  fine  here)?        5)  From  the  previous  two  questions,  calculate  the  total  length  of  the  survey,  in  meters.        6)  If  the  ship  can  survey  at  4.5  kts,  how  long  would  it  take  to  run  your  survey?  (Just  the  lines,  don’t  worry  about  turning  time).