Andrea Schmuttermair: A Lesson in Chemistry, July 1, 2012

NOAA Teacher at Sea
Andrea Schmuttermair
Aboard NOAA Ship Oregon II
June 22 – July 3, 2012

Mission: Groundfish Survey
Geographical area of cruise: Gulf of Mexico
Date: July 1, 2012 

Ship  Data from the Bridge
Latitude: 2957.02N
Longitude: 8618.29W
Speed: 10 knots
Wind Speed: 9.65
Wind Direction: S/SE
Surface Water Salinity:35.31
Air Temperature: 28.2 C
Relative Humidity: 76%
Barometric Pressure: 1017 mb
Water Depth:  57.54 m

Science and Technology Log

water from CTD
Here I’m filling up the BOD jar with our salt water samples from the CTD cast.

Reminiscent of my days in high school chemistry, today I had the opportunity to work with our Chief Scientist, Brittany, on completing the daily titration. If you remember, getting readings on the dissolved oxygen in the water is an important part of this survey as we locate any hypoxic (less than 2 mg of oxygen per liter of water) zones or anoxic (no oxygen) zones. This is done with a computerized device on the CTD, but we want to make sure that our readings are accurate. Because “chemistry never lies”, this is how we ensure our readings are accurate.

With our CTD, we have the ability to collect water samples at various depths. We do not collect water samples at every CTD, but rather one or two a day during the daytime hours. We collect water from the bottom to see if there is any expansion of hypoxia.

orion meter
Using the Orion dissolved oxygen meter to measure the amount of dissolved oxygen in our sample.

When the CTD comes back up, we use an Orion dissolved oxygen meter, which is a handheld device, to get a dissolved oxygen reading from our samples. We put the probe on the end of the meter gently into the containers of water on the CTD to get our reading. We will use this number in conjunction with the information sent from the CTD to our dry lab to check against our titration results.

Once we have the reading with the probe, we are ready to take some samples for our titration. We then take the water samples in the cylinders, rinse out our 300 mL BOD (biological oxygen demand) glass bottles a few times with that water, and then fill the botttles up with the sea water from the bottom. These samples are brought back to our Chem Lab (short for chemistry, as I’m sure you figured out) where we will test the amount of dissolved oxygen.

adding manganese sulfate
Adding the manganese sulfate to our sample.
This is after I’ve added the manganese sulfate and iodide. Now we have to wait for it to settle.

We are using the Winkler method to find the amount of dissolved oxygen in our water samples. The first step in this process is to put 2mL of manganese sulfate into the bottle. After that, we also add 2 mL of azide- iodide. With those 2 chemicals added, we carefully replace the stopper and give the bottle a good shake. We then can wait about 10-15 minutes for the chemicals to settle at the bottom. Pipettes are used to add the liquids and allow us to be very precise in our measurements.

after settling 1
Here is our sample after it has settled.

After the particles have settled at the bottom, we add 2 mL of sulfuric acid (which can be a dangerous chemical if used inappropriately), replace the stopper, and shake the bottle again gently. The sulfuric acid “fixes” the solution. Finally we add 2 mL of starch to the solution, which is a blue indicator when we put it in but turns the solution a burnt orange color. Now we are ready to titrate!

adding to beaker
Our sample solution being poured into the beaker, ready for the titration. Inside the beaker is a magnetic stirrer.
finished titration
Now you can see the solution is clear in color, meaning our titration is finished. We are ready to determine the amount of dissolved oxygen.

Prepared beforehand was a burette filled with phenylarsine oxide, what we use to drip into the sample. We pour the sample into a beaker and place it on a magnetic plate. We’ve placed a magnetic stirrer in the beaker so it gently stirs the solution while we are titrating. We let the phenylarsine oxide slowly drip into the sample  until it turns clear. When it does this, we note the amount of phenylarsine oxide that we put in the sample (which is equivalent to the amount of oxygen in the water), and the number should match (or be very close) to the reading of dissolved oxygen that we received from the CTD and the Orion dissolved oxygen meter.

This process is quite simple yet yields important results and is just one of the ways scientists verify their data.

Bioluminscence

One other interesting thing happened the other night on one of our shifts. We had brought in a bongo tow and were looking into the codends to see what we got. When Alex began rinsing the sample with some salt water, the whole codend began to illuminate. Why did it illuminate? Bioluminescence.  Bioluminescence is essentially a chemical reaction that produces light. Many marine critters can produce bioluminescence, as seen below.

bioluminescence
Bioluminescence in our bongo tow.

Personal Log

One of the things I’ve probably enjoyed the most about my trip so far are the relationships I’ve formed with the people on board. As a teacher, one of my top priorities is to build and maintain relationships with my students, both past and present. That became a bit more of a challenge to me this past year as I took on a new position and began teaching 600 students rather than the 30 I was used to.

Alonzo
Our watch leader, Alonzo, waiting to weigh our next catch.

I’ve come to love working with the scientists on the night watch, as each of them brings something to the table. Our watch leader, Alonzo, has a wealth of knowledge that he gladly shares with each of us, pushing us to learn more and find the answer for ourselves. I’ve improved immensely on identifying the different fish, crabs and shrimp we find (thanks to Lindsey, who is my partner in crime for making up silly ways to remember these crazy Latin names for all our species). Where I came in knowing names of very few if any types of Gulf critters, I can now confidently identify 15-20 different species. I’m learning more about how to look for the subtle differences between different species, and Alonzo has been able to sit back and be that “guide on the side” while we work and input all of our data. His patient demeanor has allowed all of us to become more self-sufficient and to become more confident in the knowledge we have gained thus far on this trip.

Alex
Alex with a sharksucker

Alex, another one of the scientists on my watch, shows an endless enthusiasm for marine science. He shares in my excitement when a trawl comes up, and the both of us rush out there to watch the net come up, often guessing how big we think the catch is going to be. Will it fill one basket? Two? Six? It’s even more exciting when we get inside and lay it out on the conveyor belt and can really examine everything carefully. His wish finally came true today as we are now in the eastern part of the Gulf. Alex is studying lionfish (Pterois volitans) for his research, and of course has been hoping to catch some. Today we caught 4, along with a multitude of other unique critters that we have not seen yet. Alex’s enthusiasm and passion for science is something I hope my students can find, whether it be in marine science, biology, or meteorology- whatever it is they love is what I hope they pursue.

Lindsey
Lindsey and Alex, getting ready to work.

Lindsey and Renee are both graduate students. Rene wanted to gain some experience and came on the ship as a volunteer. What a better way to get a hands-on experience! Lindsey has joined us on this cruise because she is doing research on Sargassum communities. She has been able to collect quite a few Sargassum  samples to include in her research for her thesis. Lindsey, like Alex, is very passionate and excited about what she does. I’ve never seen someone more excited to pull up a net full of Sargassum (which I’m sure you remember is a type of seaweed) in order to sift through and find critters. She has a great eye, though, because she always manages to find even the tiniest of critters in her samples. Just yesterday she found a baby seahorse that couldn’t have been more than a few millimeters long! Outside I hear her giggle with glee- I know this is because she has found a Sargassum fish, which is her all-time favorite.

deck crew
Our night shift deck crew- Tim, Chuck and Reggie

Our night watch would not be complete without the deck crew, Tim, Reggie and Chuck, who are responsible for helping us lower the CTD, Neuston and bongo tows, and for the trawl net. Our work could not be done without them.

William, one of our engineers, took me down into the engine room the other day. First impressions- it was hot and noisy! It was neat to see all the different machines. The ship makes its own water using a reverse osmosis system, which takes water from the ocean and converts it into drinking water for us (this water is also used for showers and sinks on board). One interesting note is that the toilets actually use salt water rather than fresh water so that we conserve our fresh water.

reverse osmosis
Our reverse osmosis systems.

I cannot believe how fast this leg has gone and that we only have a few more shifts to go before we return to the Oregon II’s  home port of Pascagoula. As we’ve moved into the eastern waters of the Gulf, we have seen a lot of different types of critters. On average, our most recent trawls have been much more brightly colored. We are near some coral reefs too- in our trawls we have pulled up a bit of coral and sponge. The markings on some of the fish are very intriguing, and even fish we’ve seen before seem to be just a little brighter in color out here.

Due to the fact that we are finding very different critters, my list of favorites for today has greatly increased! Here are just a few:

scorpion fish
The mouth of a scorpion fish. We’ve caught a bunch of these since we hit the eastern Gulf.
sea horse
A baby seahorse we pulled out of our Neuston tow. He was hiding in the Sargassum.
red snapper
One of our biggest red snappers.
box crab
This is another type of bashful crab, also known as the flame-streaked box crab (Calappa flammea).
octopus
This octopus sure liked my hard hat!

Justin Czarka, August 16, 2009

NOAA Teacher at Sea
Justin Czarka
Onboard NOAA Ship McArthur II (tracker)
August 10 – 19, 2009 

Mission: Hydrographic and Plankton Survey
Geographical area of cruise: North Pacific Ocean from San Francisco, CA to Seattle, WA
Date: August 16, 2009

Weather Data from the Bridge 

Sunrise: 6:29 a.m.
Sunset: 20:33 (8:33 p.m.)
Weather: no significant weather (wx)
Sky: partly to mostly cloudy
Wind direction and speed: north-northwest 20-25 knots; (kt) gusts to 30 kt
Visibility: unrestricted, reduced to 1-3 nautical miles (nm) in mist
Waves: north-northwest 6-9 feet
Air Temperature: high 18°C, low: 12°C
Water Temperature: 15°C

Science and Technology Log 

Wow! I stayed up past 2:30 a.m. this morning, but it was well worth it.  I witnessed one of the most spectacular displays of nature’s beauty.  There was a bioluminescent bloom, where patches of ocean glowed as if hundreds of Halloween glow sticks floated in the ocean.  While bioluminescence happens from time to time, this display of a glowing sea was unique.  Crew and scientists aboard the McArthur II, some who have been on ships for 30+ years, say that they have never seen a bloom like this.  As far as the eye could see (12 miles in every direction), for over four hours, there were huge patches of ocean glowing blue green. As you scanned toward the horizon, it became nearly solid green-yellow.   And to think that I almost missed it!

The turbulence in the McArthur II’s wake shines blue-green during a bioluminescent bloom 175 nautical miles off the Oregon coast.  The ship was lit up as if by lamps lit underwater.
The turbulence in the McArthur II’s wake shines blue-green during a bioluminescent bloom 175 nautical miles off the Oregon coast. The ship was lit up as if by lamps lit underwater.

Scientists ad crew were in the lounge watching a movie when the XO (Executive Officer) LT John A. Crofts rushed in saying, “You have to check this out! Come up to the bridge.” We thought it was some joke, but we hurried up the stairs three levels, entering the pitch-black darkness of the Bridge.  Looking out, you could see a panoramic view of hundreds upon hundreds of floating, glowing patches on wave crests. On top of this, it was a clear, dark night where you could see the entire Milky Way galaxy and star clusters never seen near any human settlement (due to light pollution). It was a fantastic, otherworldly experience, as if we had sailed into the sunset, entered dark, and found ourselves in a new universe.  Words are insufficient.

In scientific terms, what we were spectator to was a bioluminescent dinoflaggellate bloom. Dinoflagellates are a type of plankton. When the water is disturbed, it excites the dinoflagellates, causing them to emit the colors at night.  They are often seen close to shore, but not this far out in the Pacific. Or it could be that not many observers on a regular basis get out this far to see…

Personal Log 

Justin Czarka and Morgraine McKibben try on their survival suits during drills aboard the McArthur II.
Justin Czarka and Morgraine McKibben try on their survival suits during drills aboard the McArthur II.

I had a good talk with Linda Halderman, the wiper aboard the McArthur II. A wiper is a person who does many different tasks in the engine department.  She was talking to me about Personal Protective Equipment (PPE).  She mentioned that PPE has “become really big. I’ve just started learning about it while on the job, but it would be really good for students to learn from the start.”  It was a great conversation about safety equipment required for different jobs and the relevant cleanup. Safety has been of utmost important aboard the McArthur II. Alarms are tested daily.  Life jackets, safety harnesses, and hardhats are required during “ops” on the deck.  We even practice drills in the event that a fire would occur, someone fell overboard, or we would need to abandon ship. Everyone is delegated a role in the event of an emergency.

Vocabulary 

Dinoflagellate- a marine (ocean) plankton that propels itself with two flagella (bands around the organism) that provide propulsion and steering. Bioluminescence- “bio-“ meaning life; “-luminescence” meaning light.  An organism than emits light through an internal chemical reaction.

Did You Know?   

According to Bill Peterson, chief scientist, plankton (small plant and animal organisms in the ocean) are so prolific in quantity that the Long Island Sound is actually filtered completely every three days! In order to obtain nutrients from the ocean, these small organisms either pump water through their bodies or propel themselves through the water, and consequently the water through their bodies.  One doliolid filters about a liter of water every single day!  While small individually, these organisms truly play a significant role in the ocean ecosystem.  This is why the researchers are aboard the McArthur II.

Jennifer Fry, July 16, 2009

NOAA Teacher at Sea
Jennifer Fry
Onboard NOAA Ship Miller Freeman (tracker)
July 14 – 29, 2009 

Mission: 2009 United States/Canada Pacific Hake Acoustic Survey
Geographical area of cruise: North Pacific Ocean from Monterey, CA to British Columbia, CA.
Date: July 16, 2009

Here is Dr. Chu using a sonar readout to determine where the hake are located.
Here is Dr. Chu using a sonar readout to determine where the hake are located.

Weather Data from the Bridge 
Wind speed: 20 knots
Wind direction: 358°from the north
Visibility: foggy
Temperature: 15.2°C (dry bulb); 13.4°C (wet bulb)

Science and Technology Log 

We conducted several sea trawls for hake and other various fish species.   First, the scientists conduct an acoustic survey using 4 different frequencies. Then the nets are lowered and drug at depth. The fun begins when we don our rubber overalls, gloves, and galoshes and count, identify and, weigh the fish. The most numerous fish in the trawls were myctophids (see photo), bioluminescent fish with some species having 2 headlights in front of their eyes to help attract prey.

Here we are sorting the catch.
Here we are sorting the catch.

HAB/ Harmful Algal Blooms Test:  Throughout the day we took HAB samples, “harmful algae blooms”, which measures the toxins, domoic acid, and chlorophyll levels in the water (which correspond to the amount of plankton present). The HAB sample entails collecting sea water and putting it through a filtering process. Julia Clemons, a NOAA Oceanographer, and I conducted the HAB survey (pictured below).  Fifty milliliters of sea water is measured into a graduated cylinder then filtered.

This is a type of fish called a myctophid. They are bioluminescent.
This is a type of fish called a myctophid. They are bioluminescent.

Sea water is collected at specific times during each transect or line of study.  The sea water goes through a filtering process testing domoic acid and chlorophyll levels.  These results will be evaluated later in the lab. One thing that strikes me is the importance of careful and accurate measurement in the lab setting. The harmful algal bloom samples are conducted 5-6 times daily and accuracy is essential for precise and definitive results.  Later scientists will review and evaluate the data that was collected in the field.  It is very important that the scientists use the same measurements and tools so that each experiment is done the same way. Making accurate data collection makes for accurate scientific results.

Animals Seen Today 
Numerous albatross circling the stern of the ship, Viper fish, Octopi (approx. 6 inches in length), Squid (approx. 3 inches in length), and Myctophidae (see photo).

Zooplankton
Zooplankton
Here I am observing Julia as she filters a HAB sample.
Here I am observing Julia as she filters a HAB sample.

Lisbeth Uribe, August 5, 2008

NOAA Teacher at Sea
Lisbeth Uribe
Onboard NOAA Ship Delaware II
July 28 – August 8, 2008

Mission: Surfclam and quahog survey
Geographical Area: Southern New England and Georges Bank
Date: August 5, 2008

Chief Scientist Vic Nordahl, Chief Boatswain Jon Forgione and Chief Engineer Patrick Murphy discussing the best way to reattach the pump power cable to the dredge.
Chief Scientist Vic Nordahl, Chief Boatswain Jon Forgione and Chief Engineer Patrick Murphy discussing the best way to reattach the pump power cable to the dredge.

Ship Log 

In the last 48 hours the engineers, crew and scientists have had to re-attach the power cable to the dredge (see photograph), fix the cracked face plate of the pump, replace the blade and blade assembly, change the pipe nozzles that direct the flow of water into the cage, and work on the dredge survey sensor package (SSP). Dredging is hard on the equipment, so some mechanical problems are to be expected. The main concern is for lost time and running out of critical spare parts.  So far we have had great success with making the repairs quickly and safely.

Science and Technology Log 

Collecting Tow Event and Sensor Information for the Clam Survey 
Over the weekend I was moved up to the bridge during the towing of the dredge. I was responsible for logging the events of each tow and recording information about the ship and weather in a computerized system called SCS (Scientific Computer System). I listened carefully to the radio as the lab, bridge (captain) and crane operator worked together to maneuver the dredge off the deck and into the water, turn on the pumps, tow the dredge on the seafloor bottom, haul the dredge up, turn off the pump and bring the clam-filled dredge back on deck. It is important that each step of the tow is carefully timed and recorded in order to check that the tows are as identical as possible.  The recording of the events is then matched to the sensor data that is collected during dredge deployment. As soon as the dredge is on deck I come downstairs to help clean out the cage and sort and shuck the clams.   

Lisbeth is working on the bridge logging the events of each tow into the computer system.
Lisbeth is working on the bridge logging the events of each tow into the computer system.

My next job assignment was to initialize and attach to both the inside and outside of the dredge the two mini-logger sensors before each tow. Once the dredge was back on deck I removed both mini-loggers and downloaded the sensor data into the computers. Both sensors collect pressure and temperature readings every 10 seconds during each tow. Other sensors are held in the Survey Sensor Package (SSP), a unit that communicates with onboard computers wirelessly.  Housed on the dredge, the SSP collects information about the dredge tilt, roll, both manifold and ambient pressure & temperature and power voltage every second. The manifold holds the six-inch pipe nozzles that direct the jets of water into the dredge.  Ideally the same pump pressure is provided at all depths of dredge operation. In addition to the clam survey, NOAA scientists are collecting other specimens and data during this cruise.

Two small black tubes (~3 inches long), called miniloggers, are attached to the dredge. The miniloggers measure the manifold (inside) and ambient (outside) pressure and temperature during the tow.
Two small black tubes (~3 inches long), called miniloggers, are attached to the dredge. The miniloggers measure the manifold (inside) and ambient (outside) pressure and temperature during the tow.

NOAA Plankton Diversity Study 
FDA and University of Maryland Student Intern Ben Broder-Oldasch is collecting plankton from daily tows.  The plankton tows take place at noon, when single-celled plants called phytoplankton are higher in the water column. Plankton rise and fall according to the light. Plankton is collected in a long funnel-shaped net towed slowly by the ship for 5 minutes at a depth of 20 meters. Information is collected from a flow meter suspended within the center of the top of the net to get a sense of how much water flowed through the net during the tow. Plankton is caught in the net and then falls into the collecting jar at the bottom of the net.  In the most recent tow, the bottle was filled with a large mass of clear jellied organisms called salps. Ben then filters the sample to sort the plankton by size. The samples will be brought back to the lab for study under the microscope to get a sense of plankton species diversity on the Georges Bank.

An easy way to collect plankton at home or school is to make a net out of one leg of a pair of nylons. Attach the larger end of the leg to a circular loop made from a metal clothes hanger.  Cut a small hole at the toe of the nylon and attach a plastic jar to the nylon by wrapping a rubber band tightly around the nylon and neck of the jar.  Drag the net through water and then view your sample under a microscope as soon as possible.

Biological Toxin Studies 

NOAA Scientist Amy Nau hauls the plankton net out of the water using the A-frame. (Upper insert: flow meter; lower insert: plankton in the collection bottle after the tow).
NOAA Scientist Amy Nau hauls the plankton net out of the water using the A-frame. (Upper insert: flow meter; lower insert: plankton in the collection bottle after the tow).

Scientists from NOAA and the Food & Drug Administration (FDA) are working together to monitor clams for biological toxins. Clams and other bi-valves such as oysters and mussels, feed on phytoplankton. Some species of phytoplankton make biological toxins that, when ingested, are stored in the clam’s neck, gills, digestive systems, muscles and gonadal tissues.  If non-aquatic animals consume the contaminated clams, the stored toxin can be very harmful, even fatal.  The toxin affects the gastrointestinal and neurological systems. The rate at which the toxins leave the clams, also known as depuration rate, varies depending on the toxin type, level of contamination, time of year, species, and age of the bivalve. Unfortunately, freezing or cooking shellfish has no effect on the toxicity of the clam. The scientists on the Delaware II are collecting and testing specimens for the two biological toxins that cause Amnesia Shellfish Poisoning (ASP) and Paralytic Shellfish Poisoning (PSP).

NOAA Amnesia Shellfish Poisoning (ASP) Study 
A group of naturally occurring diatoms, called Pseudo-nitzschia, manufacture a biological toxin called Domoic Acid (DA) that causes Amnesia Shellfish Poisoning (ASP) in humans.  Diatoms, among the most common organisms found in the ocean, are single-celled plankton that usually float and drift near the ocean surface. NOAA scientist Amy Nau collects samples of ocean water from the surface each day at noon. By taking water samples and counting the numbers of plankton cells, in particular the Pseudo-nitzschia diatoms, scientists can better determine if a “bloom” (period of rapid growth of algae) is in progress. She filters the sample to separate the cells, places the filter paper in a test tube with water, adds a fixative to the tube and sets it aside for further study in her lab in Beaufort, NC. 

Scientist Amy Nau filters seawater for ASP causing dinoflagellates.
Scientist Amy Nau filters seawater for ASP causing dinoflagellates.

FDA Paralytic Shellfish Poisoning (PSP) Study 
Scientists aboard the Delaware II are also collecting meat samples from clams for an FDA study on the toxin that causes paralytic shellfish poisoning. When clams ingest the naturally occurring dinoflagellate called Alexandrium catenella, they accumulate the toxin in their internal organs. When ingested by humans, the toxin blocks sodium channels and causes paralysis. In the lab, testing for the toxin causing PSP is a lengthy process that involves injecting a mouse with extracts from shellfish tissue.  If the mouse dies, scientists know the toxin is present. The FDA is testing the accuracy of a new quick test for the toxin called the Jellet Test Kit. After measuring and weighing a dozen clams from each station on the Georges Bank, Ben and Amy remove and freeze the meat (internal organs and flesh) from the clams to save for further testing by scientists back on land. At the same time, they also puree a portion of the sample and test it using the Jellet strips for a quicker positive or negative PSP result.

Personal Log 

Pilot whales sighted off the bow!
Pilot whales sighted off the bow!

The problems that we have experienced with regard to the dredge over the past few days are an important reminder of the need for the scientists and crew to not only be well prepared but also flexible when engaged in fieldwork. All manner of events, including poor weather and mechanical difficulties, can and do delay the gathering of data. The Chief Scientist, Vic Nordahl, is constantly checking for inconsistencies or unusual patterns, particularly from the dredge sensor readings, that might need to be addressed in order to ensure that the survey data is consistent and accurate. The time required to repair the dredge meant I was able to do a load of laundry. Dredging is very dirty work! Good thing I am using old shirts and shorts. I also caught up on a few emails using the onboard computers. Though the Internet service can be slow at times it is such a luxury to be able to stay in touch with friends and family on land. I still have two very special experiences that I wish to share before ending my log.

Late in the evening a couple of days ago, as we steamed toward our next tow station, I was invited to peer over the bow. The turbulence in the water was causing a dinoflagellate called Noctiluca to sparkle and glow with a greenish-blue light in the ocean spray.  The ability of Noctiluca and a few other species of plankton and some deep-sea fish to emit light is called bioluminesense. A few days later we had the great fortune to see five pilot whales about 100 meters away, gliding together, their black dorsal fins slicing through the water, occasional plumes of air bursting upward through their blowholes (nostrils located on the tops of their heads).

Answers to the previous log’s questions: 

1. What is the depth and name of the deepest part of the ocean? The Mariana Trench in the Pacific Ocean is 10,852 meters deep, (deeper than Mount Everest is tall – 8,850 meters).  Speaking of tall mountains, the tallest mountain in the world is not Mount Everest, but the volcano Mauna Kea (Hawaii).  It reaches 4,200 meters above sea level, but its base on the sea floor is 5,800 meters below sea level.  Its total height (above base) is therefore 10, 000 meters!

2.What is the longest-lived animal on record? In 2007, an ocean quahog was dredged off the Icelandic coast.  By drilling through and counting the growth rings on its shell, scientists determined it was between 405 and 410 years old. Unfortunately it did not survive the examination, so we do not know how much longer it would have lived if left undisturbed. This ancient clam was slightly less than 6 inches in width.

Elizabeth Eubanks, August 2, 2007

NOAA Teacher at Sea
Elizabeth Eubanks
Onboard NOAA Ship David Starr Jordan
July 22 – August 3, 2007

Mission: Relative Shark Abundance Survey and J vs. Circle Hook Comparison
Geographical Area: Pacific Ocean, West of San Diego
Date: August 2, 2007

Weather Data from the Bridge 
Visibility: 10+ miles
Air temperature: 20.3 degrees C
Sea Temperature at 500 m:
Sea Temperature at surface: 19.8 degrees C
Wind Direction: 280 W
Wind Speed:  17 kts
Cloud cover: partially cloudy–alto cumulus
Sea Level Pressure: 1015.7 MB
Sea Wave Height: 1-2 ft
Swell Wave Height: 2 ft

Bow Chamber
Bow Chamber

Science and Technology Log 

The Bow Chamber! Wow! The Bow Chamber is in the bulbous bow. It is located in the very front of boat where the V hull is. Basically this area breaks up the water pressure to create less drag. The chamber is actually a little room about 20 feet down below the main deck. It has port holes/windows so you can see aquatic life. Currently the windows have a lot of algae on them so it is hard to see out of them during the day. A group of us went down after dark and we could see bioluminescent creatures zipping by. We were seeing things such as dinoflagelletes/ plankton and jelly fish. It was so beautiful to watch.

Personal Log 

Doctoral student Dovi Kacev and NOAA Teacher at Sea Elizabeth Eubanks look down into the bow chamber.
Doctoral student Dovi Kacev and NOAA Teacher at Sea Elizabeth Eubanks look down into the bow chamber.

Great day. I got up at 5:30am to watch and learn a little more about the CTD, which I wrote about yesterday. We completed our 2 final sets and I gathered goodies to bring back to school. We had the perfect ending to our last set. One of the very last hooks we pulled in possessed a huge, enormous Blue Shark. He was the biggest that we had caught so far, in length (229 cm) and girth. He gave a huge fight while in the water and even threw up a little (but thankfully not his stomach) before they got him onto the cradle. The best part of this was that the rest of the scientists could watch the people on the platform work with the shark, because the long line hauling was finished. It was truly the perfect ending to the perfect adventure.

Question of the Day 

How do bioluminescent creatures shine? 

Question of the trip: Which hook, the J or Circle, will catch more sharks? 

Please make a hypothesis. Utilize resources to justify your hypothesis. ———Yes, you get extra credit for this. 

A big Blue Shark.  Graduate student Heather Marshall holds the tail while Dr. Jeff Graham helps Dr. Suzi Kohin with the bolt cutters as Dr. Russ Vetter retains the head.
A big Blue Shark. Graduate student Heather Marshall holds the tail while Dr. Jeff Graham helps Dr. Suzi Kohin with the bolt cutters as Dr. Russ Vetter retains the head.