shrimp – Page 4 – NOAA Teacher at Sea Blog

June 29, 2012August 11, 2021

Andrea Schmuttermair: Tows Away! June 26, 2012

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

Mission: Groundfish Survey
Geographical area of cruise: Gulf of Mexico
Date: June 26, 2012

Ship Data from the Bridge:
Latitude: 2805.26N
Longitude: 9234.19W
Speed: 10mph
Wind Speed: 5.86 knots
Wind Direction: E/SE
Surface Water Salinity: 35.867 PPT
Air Temperature: 28.8 C
Relative Humidity: 86%
Barometric Pressure: 1010.51 mb
Water Depth: 96.5 m

Science and Technology Log

Opisthonema oglinum, Lagadon rhomboides, Chloroscombus chrysurus…..yes, I have officially started dreaming about taxonomic names of our fish. It’s day 4 and I now have a much better grasp at identifying the variety of critters we pull up in our trawls. I am always excited to be out on deck when they bring up the trawl to see what interesting critters we catch. Surprises are great!

Do you want to know where the Oregon II is headed?

Check out Ship Tracker at http://shiptracker.noaa.gov/

If you click on the link above, you can see the path that our ship is taking to hit all of our stations for the survey. We often have station after station to hit- meaning as soon as we are done sorting and measuring, we have to bring in the next catch. Because some stations are only 3-5 miles apart, we sometimes have to do “double dips”, where we put in the trawl for 30 minutes, pull it up, and put it right back in again.

It’s been interesting to note the variety of our catches. Croakers, bumperfish, and shrimp have been in high abundance the last 2 days as we were in shallower water. Before that we had a couple of catches that had a high abundance of pinfish. When we take our subsample, we typically enter data for up to 20 of that particular species. We take length measurements on each fish, and on every fifth fish. We will also weigh and sex it (if sexing is possible).

Shrimp in the Gulf — A comparison of the various sizes of shrimp we pull up from our trawls.

Shrimp waiting to be measures — A relatively small catch in comparison to the 200+ we’ve been pulling up recently.

When we were in shallower waters, we had a significant increase in the number of shrimp we brought up. Tuesday morning was the first catch that did not have well over 200 shrimp (this is because we’ve been moving into deeper waters). For the 3 commercial shrimp, white (farfantepenaeus setiferus), pink (farfantepenaeus duorarum), and brown (farfantepenaeus aztecus), we take 200 samples, as opposed to our high-quantity fish, where we will only take 20 samples. For each of the commercial shrimp we catch, we measure, weigh and sex each shrimp. I’ve gotten very good at identifying the sex of shrimp- some of the fish are much more difficult to tell. The information we get from this survey will determine the amount of shrimp that boats can take during the shrimping season in Louisiana and Mississippi. During the first leg of the groundfish survey, the data collected determined the amount of shrimp that could be caught in Texas. The groundfish survey is crucial for the shrimping industry and for ensuring that shrimp are not overfished.

Students- think of the food chain. What would happen if we overfished and took out too many shrimp? (Hint: Think of predators and prey.)

We’ve now started doing 2 different tows in addition to our trawls. Some of the stations are trawl stations, whereas others are plankton stations.

The trawl on deck — Alex, Alonzo and Reggie unloading the trawl net.

At a trawl station, we lower the trawl from the stern down to the ocean floor. The trawl net is meant for catching larger critters that live at the bottom of the ocean. There is a chain, also known as a “tickler”, which moves lightly across the ocean floor to lure fish to leave their hiding spots and swim into our net. The trawl is down for 30 minutes, after which it is brought back on deck to weigh the total catch, and then brought back into the wet lab for sorting.

Another important mission of the groundfish survey is to collect plankton samples. To do this, we use a Neuston tow and a bongo tow.

The Neuston tow has a large, rectangular frame with a fine mesh net attached to it. At the end of the net is a large cylindrical bucket, called a codend, with a mesh screen meant for catching the organisms. In comparison to the trawl net, which has openings of 41.4mm , the Neuston’s mesh is only 0.947mm. This means the mesh is significantly finer, meant for catching some of the smaller critters and plankton that would otherwise escape the trawl net. The Neuston tow is put on the surface of the water and towed for 10 minutes. Half the tow is in the water while half is out. We end up picking up a lot of Sargassum, or, seaweed, that is found floating at the water’s surface. When we gather a lot of Sargassum, we have to sift through it and spray it to get out any of the organisms that like to hide in their protective paradise.

After we’ve completed the Neuston tow, we do the bongo tow. The bongo’s mesh is even finer than the Neuston tow’s mesh at only 0.333mm. The bongo has 2 parts- a left and a right bongo (and yes they do look a little like bongo drums- hence their name). The top part of the bongo is a large cylinder with an open bottom and top. The net is attached to this cylinder, and again at the bottom of each side is cylindrical tube called codends meant to catch the plankton. The bongo tow is meant to take a sample from the entire water column. This means that instead of riding on the surface of the water, it gets sent down to about 3 meters from the ocean floor (there is a sensor at the top that is 2m from the bottom of the net) and brought back up immediately.

Sifting through the sieve — The remnants from our Neuston tow. This is the sieve we use to weed out what we want and don’t want.

bongo leftover — Here are our 2 samples from the bongo tow. The left one is preserved in ethanol and the right is preserved in formaldehyde (10% formalin and sea water)

Neuston tow samples — Here is a sample from the Neuston tow. Carefully camouflaged are thousands of crab megalops, aka juvenille crabs.

For both tows, it is important to rinse the nets to get any lasting organisms we might not see with our own eyes into our sample. Once we’ve done this, we bring the tubes back into the wet lab where we continue to rinse them through a sieve so that only certain items are leftover. In the Neuston, we often find small fish (usually less than 3mm), baby shrimp, crabs and Jessica’s favorite, the Sargassum fish. Most recently a few flying fish got caught in our Neuston tow. Prior to pulling it up, I was enjoying watching them flit across the water- they were about all we could see in the water in the middle of the night. After being rinsed thoroughly through the sieve, we preserve them by placing the sample in a glass jar with either ethanol or formaldehyde solutions. They are preserved in ethanol for DNA work and in formaldehyde for long-term preservation. These samples are then saved to send to a lab in Poland, which is the sorting center for the SEAMAP samples.

Flying fish we pulled up in our Neuston tow at nighttime.

Personal Log

My stateroom — My sleeping quarters (top bunk), also known as a stateroom. My roommate is Kristin, one of the scientists on board.

Well, I think I am finally getting used to the schedule of working the night shift. I am thankful that my bunk is on the bottom floor of the ship- which means it is completely dark- so that I can sleep during the daytime. Yesterday was probably one of the least busy days we’ve had so far, and because we were in deeper waters, our trawls were much smaller. This means I had a little more time to work on my blogs, which at times can be hard to fit in. It amazes me that we have internet access on the ship, and it’s not even as slow as I expected. It goes down from time to time, especially when the waters are rough. We’ve been fortunate to have pretty calm waters, aside from the first day.

You may have heard about Hurricane Debby on the news as it prepared to hit the Gulf. On Sunday, we were heavily debating heading back to Galveston to “bunker down” and ride out the storm. However, the storm that was forming seemed to dissipate and head in a different direction, thank goodness. I was not thrilled about the possibility of heading back to port!

We had our first drills the day after we set sail. The drills- fire and abandon ship are distinguished by different types of bells, similar to using Morse code. The abandon ship drill was fun. We got to put on our survival suit, which is like a big orange Gumby suit. It not only protects you in cold water, but also makes you highly visible. I remember reading some of the former TAS blogs, and this picture was always in. Of course, I’ve got to add mine as well.

Survival Suit — Here I am in my survival suit. Judd also decided to be in the picture. 🙂

I’ve been having fun exploring different areas of the ship, even though there is only so far you can go on the ship. Yesterday, I went up to the bridge, which is the front of the ship where the captain or the NOAA Corps officers steer the ship from. You can think of it like a control center of an airplane. There are navigation charts (both computerized and paper) and radars that help guide the ship so it knows what obstacles are out there. There is a great view from the bridge that you don’t get anywhere else on the ship. It’s also fun to watch the folks down on deck when they are deploying the CTD or either of the 2 tows.

We’ve caught such an abundance of critters, I thought I’d share some of my favorite catches thus far:

Here I am holding a cownose ray (Rhinoptera bonasus)- my favorite catch yet. He weighed about 25lbs! This one was the highlight of my day as rays are some of my favorite ocean critters!

–

One of the 4 Atlantic sharpnose sharks (Rhizoprionodon terraenovae) we’ve caught so far.

A sharksucker (Echeneis naucrates)- these guys hang onto sharks to catch a ride- he’s still alive so is able to hang onto my arm!

Sharksucker — One of the 4 Atlantic sharpnose sharks (Rhizoprionodon terraenovae) we’ve caught so far.

A sharksucker (Echeneis naucrates)- these guys hang onto sharks to catch a ride- he’s still alive so is able to hang onto my arm!

Critter Query Time!

Critter Query #1: What is a fathom (in your own words please)?

Critter Query #2: What are the differences between skates and rays?

June 26, 2012August 11, 2021

Andrea Schmuttermair: Out to Sea, June 24, 2012

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

Mission: Groundfish Survey
Geographical area of cruise: Gulf of Mexico
Date: June 24, 2012

Ship Data from the Bridge
Latitude: 2858 N
Longitude: 9310.96 W
Speed: 10 mph
Wind Speed: 6.77
Wind Direction: N/NE
Surface Water Salinity: 30.9
Air Temperature: 28.5 C
Relative Humidity: 79%
Barometric Pressure: 1009.84 mb
Water Depth: 24.3 meters

Personal Log

And the journey has begun! I arrived in Houston on Thursday afternoon, only to be whisked away by Chief Scientist Andre DeBose to meet a few of the other scientists and crew for dinner. I had a great time getting to know a few of the people I will be working with over the next couple of weeks. We arrived to the port at Galveston about 10pm, where I got a quick tour of the Oregon II, my home for the next 2 weeks. Exhausted from traveling, I made myself at home in my stateroom before turning in for the evening.

Because we weren’t scheduled to set sail until 1400, I had a bit of time in the morning to explore Galveston. Being the adventurous type , I took this time to explore the land I would soon be leaving. The Oregon II is docked at Pier 21, located on “The Strand”, a strip filled with historic buildings and tourist shops. I spent most of my morning snapping photos, checking out the shops, and tracking down a good breakfast burrito at one
of the many Mexican food places that don the strip.

Once back at the ship, we were briefed on the “Do’s and Don’ts” while on board, and what our shifts would look like. I am on the night watch, which means I will be working from midnight until noon each day. This will be a tough schedule to get used to, but I’m hoping we’ll see some neat things at night, and that it will be a little cooler out. I knew I should get to sleep as soon as we set sail, however I couldn’t help hanging out on deck for a little while as we left the port. I was rewarded for this opportunity by watching the pelicans and dolphins seeing our ship out of the port. I snapped a few more photos, enjoyed the cool breeze, and then headed down for bed.

I had quite a blast on my first night shift. I think keeping busy was a good thing, even though it was exhausting. I enjoyed getting to know my team a little better, and of course, checking out all the critters! Some of my favorites were the squid, sharp-nose and dogfish sharks, lizardfish, and my all-time favorite so far – the bashful crab.

Why do you think he is called the "bashful crab"? — Why do you think he is called the “bashful crab”?

Science and Technology Log

I am always under the mindset that if you want to learn something, you need to throw yourself in head first. Well, that’s exactly what I did on my very first shift on the Oregon II. We are split up into 2 shifts — midnight to noon or noon to midnight. On my watch, I am working with our watch leader, Alonzo, 2 scientists, Lindsey and Alex, and a volunteer, Renee. Our Field Party Chief Scientist (FPC), Andre, had to leave unexpectedly. Our new FPC, Brittany, was with us a bit of this first watch to make sure we understood our tasks, as I had lots of questions! Not only did I get the privilege to work the nightshift (I know you’re probably wondering why I said privilege — I’ll explain soon), but we also had one of the busiest shifts we’re anticipated to have for the length of this cruise. Just after midnight on Saturday morning, we pulled up our first trawl and conducted our first CTD.

The CTD warming up just below the water's surface — The CTD warming up just below the water’s surface

A CTD, if you remember from my first blog, stands for Conductivity, Temperature, and Depth. We put the device overboard in the front of the ship (the bow), and let it sit just below the surface for about 3 minutes so the sensors can warm up before we drop it to its scheduled depth. Then we lower it so it is as close to the ocean floor as possible. We do this at every station to collect important information about the oxygen level in the water in these areas. This information is important because we want to find out what the optimal conditions (temperature, salinity and oxygen levels) are for the specimens we collect. Knowing what environmental conditions suit each species allows us to see how shifts in the environment can impact populations. The data from the CTD is displayed on the computer in our dry lab, where the data points are plotted on a graph.

The dry lab is where we process a lot of our data both from the CTD and the sampling. We can monitor our CTD casts and find the weather information here. It is also the area where scientists go when there is a bit of downtime to relax before the next catch is brought in.

Bringing up the trawl- this was a big catch! — Bringing up the trawl — this was a big catch!

Over in the back of the ship, also known as the stern, the trawl picks up all sorts of critters from the ocean bottom. When we’re ready, the deck crew helps us bring up the trawl and dump our catch into large buckets on deck. We had so much on the first catch that they dumped it out on the floor and we shoveled it into buckets like we were shoveling snow. We then weighed our catch before bringing it in and sorting it. Our first few catches were quite large — we had 6 or 7 baskets full of critters! Each basket can hold roughly 25kg. So, mathematicians, about how many kilograms were our first couple of catches? The nighttime brings on some interesting animals, and there is a certain excitement to staring out at the pitch black ocean.

Our troughs full of the catch, waiting to be sorted

With these large catches, jumping in head first was exactly what I had to do. I got a quick crash course in how to identify and sort the fish. I had no idea there would be so many different types! From the entire catch, we were to pull out red snapper, shrimp (pink, white and brown only), blue crabs, and anything unusual. We did this by dumping all the fish in a large trough, which we would then dig through to find our samples and place them in separate baskets.

We are pulling out samples primarily of shrimp because that is one of the main focuses of our survey this summer. The estimated abundance of shrimp, calculated from the trawl catches, is used to set limits for the commercial fishermen.

In addition to sorting out these important critters, we would also take what we call a subsample, the size of which is determined by the size of our total catch. Of this subsample, we sorted out everything in this section of the catch. We often had over 20 different types fish or crustaceans! Once the subsample was sorted, Alonzo would then weigh the total weight of a certain species and enter the data into our computer system. From here the fun part really began.

Lindsey is measuring, weighing and sexing the catch while I enter the data into the computer.

We would measure the length of each critter on our measuring board, which uses a magnetic wand to capture the data and send it directly to the computer database. For most of the species, we would also take the weight of the first fish and every fifth fish thereafter, and, if possible, also determine its sex and stage of maturity. All this information was entered in the database. We typically worked in teams of 2 with one person measuring and weighing the fish and the other entering information into the computer. We were a bit slow to start, but after the first catch we had a system down. Once we had all of our data, we bagged up some of the fish that people have requested for samples while the rest headed back to the ocean. Fish from our survey will go to scientists in lab across the country to study further.

Because all the stations were about 2-5 miles apart on our first watch, we were working nonstop from midnight until about 11am. We pulled up about 7 catches, and almost always had a catch waiting to be sorted on deck.

Got Questions?

Don’t forget, you can leave your questions in the “Comments” section below, and I’ll do my best to answer them!

Critter Query:

Students: Don’t forget to put your name in your response. Remember, the first one to respond correctly will receive a prize in the fall!

Critter Query #1: What’s the biggest commercial shrimp found in the Gulf of Mexico and what is its scientific name?

Critter Query #2: Name 3 types of shark found in the Gulf of Mexico. (more than one correct response — all correct responses will receive a prize providing there are no repeats)

June 11, 2012August 11, 2021

Andrea Schmuttermair: Eager Anticipation from Land-locked Colorado, June 7, 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 (between Galveston TX and Pascagoula, MS)
Date: June 7, 2012

Personal Log (pre-cruise)

What does

+ + = ?

That’s right! Ms. Schmuttermair is heading to sea this summer as a participant in NOAA’s Teacher at Sea Program!

Hi! My name is Andrea Schmuttermair, and I am a 3-6 grade science teacher at The Academy in Westminster, CO. I just finished up my first year in this position, and absolutely love engaging my students in important science concepts. Outside of the classroom, I can be found hiking, biking, and exploring the mountains of beautiful Colorado with my dog, Wesson.

Growing up in San Diego, CA, I would definitely consider myself an “ocean lover”. I grew up spending countless hours at the beach, checking out the sea life that washed up in the tide pools and snorkeling in La Jolla Cove. When I heard about the Teacher at Sea program, I knew it was right up my alley. Living in land-locked Colorado, I strive to bring both my love and knowledge of the ocean to my students. One of the most memorable teaching moments for me this year was seeing my 3^rd graders have that “Aha!” moment when they realized what we do here in Colorado greatly affects our oceans, even though they are hundreds of miles away.

Now, in just a couple short weeks, I will don my sea legs, leave dry land behind, and set sail on the Oregon II. The Oregon II, one of NOAA’s 11 fishery vessels, conducts fishery and marine research to help ensure that our fish population in the ocean is sustainable. Fishery vessels work with the National Marine Fisheries Service to provide important information about fish populations and what regulations about fishing practices need to be in place.

This summer, we will be conducting the summer groundfish survey, a survey that has been conducted for the past 30 years. This particular survey is conducted during the summer months between Alabama and Mexico. On this second leg of the survey, we will be sailing from Galveston, TX to the Oregon II’s home port of Pascagoula, MS.

What exactly is a groundfish survey, you ask? When I first received my acceptance letter, they informed me that this was the “critter cruise”, and I, being the critter lover, was thrilled! The main goal of this survey is to determine the abundance and distribution of shrimp by depth. In addition to collecting shrimp samples, we may also collect samples of bottomfish and crustaceans. It will also be important to collect meteorological data while out at sea. I am excited to see what kind of critters we pull up!

NSTA 11 (36) — Ms. Schmuttermair LOVES critters, as seen here with Rosy the scorpion.

How will we be catching all of these critters and collecting data while out at sea? The Oregon II has a variety of devices to help collect information about the ocean, including bottom trawls and a CTD. The bottom trawl is a large net that is towed to collect shrimp and other bottom dwellers that will be sorted once the catch is brought aboard. A CTD (stands for Conductivity, Temperature, and Depth) is an instrument that can collect a wide variety of data, including temperature, salinity and oxygen content. I can’t wait to learn how some of these tools are operated!

What are my goals while out at sea?

To learn as much about the environment I am in as possible.
To ask the scientists plenty of questions about their research, and why collecting data is so important.
To take many pictures to bring back to my students
To get to know the crew on board, and how they came to work on the Oregon II
Not getting seasick!

Now it’s your turn: What would YOU like to know more about? Is it more about the animals we bring up in our trawls? Maybe it’s to learn more about life on the Oregon II, and specifications about this ship. Perhaps you’d like to know how to become a scientist with NOAA and work on board one of their many ships. Leave your questions in the “Comments” section below (you are welcome to do this in any of my entries), and I’ll do my best to answer them!

Don’t forget to keep an eye out for the challenge questions, which from this point forward I will refer to as the “Critter Query”.

June 30, 2011April 28, 2021

Steven Wilkie: June 29, 2011

NOAA TEACHER AT SEA
STEVEN WILKIE
ONBOARD NOAA SHIP OREGON II
JUNE 23 — JULY 4, 2011

Mission: Summer Groundfish Survey
Geographic Location: Northern Gulf of Mexico
Date: June 29, 2011

Ship Data

Latitude	28.06
Longitude	-96.43
Speed	8.40 kts
Course	89.00
Wind Speed	13.90 kts
Wind Dir.	71.56 º
Surf. Water Temp.	27.80 ºC
Surf. Water Sal.	24.88 PSU
Air Temperature	29.30 ºC
Relative Humidity	76.00 %
Barometric Pres.	1013.73 mb
Water Depth	26.00 m

Science and Technology Log

Plankton Sample — A preserved plankton sample from one of the Oregon II's bongo nets.

So now that we have an understanding of abiotic factors, let’s talk biotic factors, and for the most part, those biotic factors are going to be fish and plankton. The majority of our plankton (plankton are organisms–plants or animals–that are too small to fight against the current and thus drift along with it) samples come from the neuston and bongo nets. After we have our bongo or neuston nets back on board, the science crew goes to work preserving the specimens.

Something common in the neuston net, is Sargassum a type of brown algae belonging to the Kingdom Protista and the Phlyum phaeophyta (kingdoms and phylums are associated with the science of taxonomy or classification). If you are familiar with kelp, then you are familiar with brown algae. Kelp is a long algae that fastens itself to the bottom of the seafloor with a root of sorts called a holdfast. Sargassum, however, does not hold fast, but rather drifts out in the open ocean. It can stay afloat because Sargassum has little tiny gas-filled floats called pneumatocysts. These clumps of algae can provide much needed hiding places for small marine organisms out in the open ocean. Because so many organism might live in, on or around the mats of Sargassum whenever we capture Sargassumin our nets we have to be sure to wash them down thoroughly in order to ensure that we get as many of the creatures off of the blades as possible.

The currents of the Gulf of Mexico and the Atlantic actually concentrate the Sargassum into a giant mass in the middle of the North Atlantic ocean, commonly referred to as the Sargasso Sea. So significant is the Sargassum, that Christopher Columbus feared for the safe passage of his ships because of the thick mass of algae.

The adventures of Captain Nemo as penned by Jules Verne in the late 19th century even commented on the nature of this floating mass of algae: “This second arm–it is rather a collar than an arm–surrounds with its circles of warm water that portion of the cold, quiet, immovable ocean called the Sargasso Sea, a perfect lake in the open Atlantic: it takes no less than three years for the great current to pass round it. Such was the region the Nautilus was now visiting, a perfect meadow, a close carpet of seaweed, fucus, and tropical berries, so thick and so compact that the stem of a vessel could hardly tear its way through it. And Captain Nemo, not wishing to entangle his screw in this herbaceous mass, kept some yards beneath the surface of the waves. The name Sargasso comes from the Spanish word “sargazzo” which signifies kelp.”

As interesting and important as Sargassum is to the ocean environment, it is not our targeted organism, which is, for the most part fish! Although not a fish, crustaceans are still an important fishery, and few are more significant than Panaeus aztecus (brown shrimp), Panaeus setiferus (white shrimp) and Panaeus duorarum (pink shrimp). Chances are if you are dining on shrimp cocktail you are eating one of these three species.

Panaeus aztecus (the brown shrimp) Waiting to be Measured — One of many (so many) brown shrimp to be measured. We measure from the length of the rostrum (the point part by their eyes) to the tip of their (tail).

Lutjanus campiechanus (or the red snapper) is another commercially important species that scientists are particularly interested in. Species like the red snapper are of particular concern because, according to NOAA’s Fish Watch website, the population is currently at low levels prompting NOAA to establish temporary restrictions on fishing this species in past years.

It is the work of the crew aboard the Oregon II to collect the data that helps scientists predict population trends in species such as these which allows government regulations to be based on sound science. Although sometimes unpopular with the local fishing industry the temporary ban on fishing for some species is aimed at providing a long-term sustainable population for future generations.

Although not a primary target of this fish survey, cartilaginous fish (Class Chondricthyes…there’s that taxonomy again) like sharks, rays and skates are also organisms of particular concern. Unlike the majority of the fish we bring on board, which are bony fish belonging to the Class Osteicthyes, the majority of cartilaginous fish reproduce internally. This means that a female shark, ray or skate, might have much fewer offspring in a given year, but those offspring might be more mature once they are born. Bony fish on the other hand often lay eggs externally by the thousands, but only a small percentage survive.

The watch leader of my watch, Brittany Palm, realizes the significance of the reproductive habits of these organisms (follow this link to review Brittany and her fellow authors extensive work) and has used much of her expertise gained through NOAA cruises like this one to publish scientific papers in peer-reviewed journals.

If you recall, one of the steps of the “scientific method” is to share your results, and there is no better way than to publish your findings in journals for other scientists to read. Although writing a paper may sound simple, this is not your average high school term paper–there is considerably more effort required. Brittany and her fellow authors labored for close to four years to finally draft and submit the paper for publishing.

Angelshark — An example of a cartilaginous fish, the Atlantic angelshark (Squatina dumeril) was brought on board as part of one of our trawls.

Although we may not write anything as extensive at the high school level, good sound scientific investigations will always end up with you sharing your results, and as a result, well-researched background information is always essential. To all my past and future students out there, feel free to take note of the reference section of the paper and remember how important references and good research is in backing up your work!

Personal Log

It has not taken long to get into the rhythm of things aboard ship. Although I thought that the waves might lead to a little sea sickness, I now find them quite soothing, and am curious as to how I might feel once back on shore as I struggle to get my land legs back. Sleeping with the waves is a slightly different story. At times they can lull you off to sleep (or it might simply be the twelve hours of sorting, measuring and weighing the catch that does that); other times they can roll you right into your bunk wall and snap you awake. My bunk is on the top, so the wall is better than the floor I suppose!

Although the waves have been soothing up to this point, we are possibly facing some inclement weather as the first tropical storm of the season, Arlene, is to our southwest heading towards the Mexican coast. If the weather picks up too much we may have to head in shore to work up some of the shallower stations while the Gulf settles back down. Either way we will be kept busy, measuring fish or measuring the waves!

Tropical Storm Arlene, the first tropical storm of the Atlantic season is headed for the Mexico coast in the next few days.

June 21, 2011April 28, 2021

Jason Moeller: June 19-20, 2011

NOAA TEACHER AT SEA
JASON MOELLER
ONBOARD NOAA SHIP OSCAR DYSON
JUNE 11 – JUNE 30, 2011

NOAA Teacher at Sea: Jason Moeller
Ship: Oscar Dyson
Mission: Walleye Pollock Survey
Geographic Location: Gulf of Alaska
Dates: June 19-20, 2011

Ship Data
Latitude: 54.29 N
Longitude: -165.13 W
Wind: 12.31 knots
Surface Water Temperature: 5.5 degrees Celsius
Air Temperature: 6.1 degrees Celsius
Humidity: 97%
Depth: 140.99 meters

Personal Log

Welcome aboard, explorers!

To be honest, there is not a great deal to write about for the personal log. My daily schedule has settled in quite nicely! I get off work at 4 in the morning, shower, sleep until 2:30 in the afternoon, and then head down to the acoustics room where we track the fish. When we are processing a catch (see the science and technology section of this blog), I am in the fish lab wearing bright orange waterproof clothes that make me resemble a traffic cone.

The rest of the time is down time, which is spent reading, working on the blog, learning about the ship, and dreaming up lesson plans that I can use to torment my students. I hope they are interested in a summer fishing trip, as that is the one I am currently planning.

Most of the blog work involves running around and taking photographs. My wife’s camera was soaked beyond repair during the prank that was pulled (see the previous post) as Sarah was holding the camera when the wave came over the railing. Fortunately, there was another camera on board.

Our survey is keeping us very close to the coast and islands of Alaska. As a result, I’ve gotten some gorgeous photos. This place is just beautiful.

Wind — Jason in front of an island. It was a bit windy, but at least it was sunny!

view — Mountaintops visible just above the island coast. Jake took this photo while I was in the fish lab.

Science and Technology Log

We finally started fishing! As I mentioned in my very first blog, the Oscar Dyson is surveying walleye pollock, which is an important fish species here in Alaska. Walleye pollock make up 56.3% of the groundfish catch in Alaska, and is eaten in fast food restaurants around the world such as Wendy’s, McDonalds, and Burger King. It is also used to make imitation crabmeat.

Our first catch had a little over 300 walleye pollock, and we processed all of them. Three hundred is an ideal sample size for this species. If, for example, we had caught 2,000 pollock, we would only have processed 300 of the fish, and we would have released the rest of them back into the ocean.

The photo captions below will provide a tour of the fish lab as well as introduce blog readers to the data we wish to collect and how scientists aboard the Oscar Dyson collect it.

Conveyer belt — This is the conveyor belt. After the catch is pulled on board, it is loaded onto this conveyor belt and moved down the belt and into the lab. At this point, the scientists separate the pollock from the rest of the sea life that was accidentally in the net. Today, the majority of the "extra" sea life were brittle stars, sponges, and a few squid.

Gender Box — Once the pollock and other sea life are separated, they are moved to this box to be sexed. In order to do this, we would have to cut the fish open and look at the internal organs of the fish. Once this was done, females would go over the yellow sign on the right and into the box that was hidden behind it. The males went into the box on the left.

Length Station — Once we had determined the pollock's gender, we moved to the measuring station, which was on the other side of the last station. We laid each individual fish on the table on top of the ruler, and then measured the fish from the head to the fork of its tail. We recorded the length by tapping the table at the fork of the fish's tail with a sensor that we carried in our hand. A sensor in the table recorded the data and sent it to the computer monitor seen above the table.

measuring pollock — Jason measures a pollock on the board!

From this catch (we will do this for any following catch as well) we also took and preserved twenty stomachs from random fish. This was done in order to later analyze what the pollock had eaten before they died. We also took forty otoliths from random pollock as well. An otolith is the ear bone of the pollock, and it is incredibly important to researchers as they will tell the pollock’s age in a similar manner to the way a tree’s rings will.

Stored Otoliths — After removing the otolith from the fish, they were put into these vials. Each pair of otoliths received their own vial.

While looking at pollock is the main focus of the survey, we did run into some other neat critters in this haul as well!

Atka Makerel — This is an Atka Mackerel. We also caught a salmon, but I didn't get a good look at it. Our kitchen grabbed it!

Basket Star — This is a basket starfish. We were trawling close to the bottom and pulled it up in the nets.

Lumpsucker — This is a lumpsucker! They spend their lives on the bottom where they eat slow-moving animals such as worms and mollusks.

Arrowtooth Flounder — This is an arrowtooth flounder. These are not very good eating fish, and are not the flounder found in the supermarket. Check out the nasty teeth in the photo below this one!

Flounder teeth — I wouldn't want to be bitten by this fish!

Species Seen

Albatross
Northern Fulmar
Gulls
Rockfish
Walleye Pollock
Lumpsucker
Arrowtooth Flounder
Atka Mackerel
Salmon
Pacific Grenadier
Squid
Shrimp
Basket Starfish

Reader Question(s) of the Day!

Today’s question is actually a request. It comes from Tish Neilson, one of our homeschool parents.

Hey Jason –
I had a super favor to ask of you. There is a little girl from Jackson’s school that is a 5th grader and she was recently diagnosed with leukemia. There have been some bracelets created for her that say “Going Bananas for Anna” to show support and several moms and I have gotten together and are putting together a scrapbook for her and trying to get as many people as possible wearing her bracelets in really cool places. Then we are having them take pictures to send to us to put in her scrapbook so she can she how far her bracelets have traveled and how many people are pulling for her. If it’s possible to do so and you would be willing to do it I would LOVE to try and get you a bracelet to take some pictures and send to me from Alaska. Her nickname is Anna Banana and she is always asking for pictures and such so that is why we came up with this idea.
Tish Neilson

Unfortunately, I had left for Alaska before I received the email, and as a result I do not have a bracelet. Hopefully, a sign will work just as well.

For Anna — Hi Anna! This is Unimak Island! It is one of the Aleutian Islands off the coast of Alaska! Hang in there, we are rooting for you!