Emilisa Saunders: Finding the rhythm aboard the Oregon II, May18, 2013

NOAA Teacher at Sea

Emilisa Saunders

Aboard NOAA ship Oregon II

May 14, 2013 – May 30 2013

Mission: SEAMAP Spring Plankton Survey

Geographical Area of Cruise:  Gulf of Mexico

Date: May 18, 2013

Weather Data: Wind Speed: 13.94 knots; Surface water temperature: 25.4;  Air temperature: 26.4; Relative humidity: 87%; Barometric pressure: 1,015.33 mb

IMG_1991

Science and Technology Log:

For the scientists on board the Oregon II, each shift follows roughly the same routine.   When we start our shift, we check in at the dry lab to see how much time we have until the next sampling station.  These stations are points on the map of the Gulf of Mexico; they were chosen to provide the best coverage of the Gulf waters.  Our ETA, or estimated time of arrival, is determined by how fast the ship is moving, which is influenced by wind and currents, which you can see in the map below.  A monitor mounted in the dry lab shows us a feed of the route mapping system that is used by the crew on the Bridge to drive the ship.  This system allows us to see where we are, where we are headed, and what our ETA is for the next station.  We also get warnings from the Bridge at one hour, at thirty minutes, and at ten minutes before arrival.

Gulf Currents

The currents in the Gulf of Mexico, plus our planned route.  Image courtesy of NOAA.

At the 10-minute mark, we put on our protective gear – more on that later in this post – and bring the cod ends up to the bow of the boat, where we attach them to the ends of the appropriate nets.  Then, we drop the Bongo nets, the regular Neuston net, the Sub-surface Neuston net, and the CTD into the water, in that order.  These all go down one at a time, and each one is pulled out and the samples collected before the next net goes in.

Neuston

Towing the Neuston net on the night shift

The idea of dropping a net into the water probably sounds pretty simple, but it is actually a multiple-step process that requires excellent teamwork and communication amongst several of the ship’s teams.  The scientists ready the nets by attaching cod ends and making note of the data that tracks the flow of water through the net.  Because the nets are large and heavy, and because of the strong pressure of the water flowing through the nets, they are lifted into the water using winches that are operated by the ship’s crew.  The crew members operate the machinery, and guide the nets over the side of the ship.  While this is happening, the crew members communicate by radio with the Bridge, providing them with information about the angle of the cable that is attached to the net, so that the Bridge can maintain the a speed that will keep the net at the correct angle. At the same time, a scientist in the dry lab monitors how deep the net is and communicates with the deck crew about when to raise and lower the nets.  This communication takes place mostly over walkie-talkies, which means that clear and precise instructions and feedback are very important.

Operating the winches

Crewmember Reggie operating the winch, while crewmember Chris measures the angle of the cable

When each net is pulled back out of the water after roughly 5-10 minutes, we use a hose to spray any little creatures who might be clinging to the net, down into the cod end.  At stations where we run the MOCNESS, we head to the stern of the ship, where the huge MOCNESS unit rests on a frame.  Lowering the MOCNESS takes a strong team effort, since it is so large.  After we retrieve each net, we detach the cod ends and bring them to the stern, where a station is set up for us to preserve the specimens.  I’ll go into more detail about the process of preserving plankton samples in a later post.

Hosing down the nets

Alonzo, hosing down the Bongo nets before bringing them aboard.

We’ve had a couple of nights of collecting now, and so far it has been completely fascinating.  I’m in awe of the variety of organisms that we’ve come across.  The scientists on my shift, Glenn and Alonzo, are super knowledgeable and have been very helpful in explaining to me what we are finding in the nets.  Although this is a Bluefin Tuna study, we collect and preserve any plankton that ends up in the nets, which can include copepods, myctophids, jellies, filefish larvae and eel larvae, to name a few.  When we get the samples back to shore, they will be sent to a lab in Poland, where the species will be sorted and counted; then, the tuna larvae will be sent back to labs in Mississippi or Florida for further study and sometimes genetic testing.

My favorite creature find so far has been the pyrosome.  While a pyrosome looks like a single, strange creature, it is actually a colony of tiny creatures called zooids that live together in a tube-shaped structure called a tunic.  The tunic feels similar to cartilage, like the upper part of your ear.  Pyrosomes are filter feeders, which means they draw in water from one opening, eat the phytoplankton that passes through, and push out the clean water from the other end.  So far on the night shift, we’ve found two pyrosomes about four inches in length and one that was about a foot long; the day crew found one that filled two five-gallon buckets!

Me holding a pyrosome.  So neat!

Me holding a pyrosome. So neat!

Alonzo and the pyrosome

Alonzo holding the pyrosome

Challenge Yourself:

Hello, Nature Exchange Traders!  Pick one of the of the zooplankton listed in bold above, and research some facts about it: Where does it live?  What does it eat?  What eats it?  Write down what you find out and bring it in to the Nature Exchange for bonus points.  Be sure to tell them Emmi sent you!

Gumby Suit

In the Gumby suit, practicing the Abandon Ship drill. Photo by Glenn Zapfe

Personal Log:

Safety is the top priority on board the Oregon II.  We wouldn’t be able to accomplish any of our scientific goals if people got hurt and equipment got damaged.  We started our first day at sea with three safety drills: the Man Overboard drill, the Abandon Ship drill and the Escape Hatch drill.  For Man Overboard, everyone on board gathered, or mustered, at specific locations; for the Science team, our location was at the stern, or back of the ship.  Aft is another word for the back.  From there, we all scanned the water for the imaginary person while members of the crew lowered a rescue boat into the water and circled the Oregon II to practice the rescue.

For the Abandon Ship drill, we all grabbed our floatation devices and survival suits from our staterooms and mustered toward the bow, or front of the ship.  I got to practice putting on the survival suit, which is affectionately called a Gumby suit.  In the unlikely event that we would ever have to abandon ship, the suit would help us float and stay relatively warm and dry; it also includes a whistle and a strobe light so that aircraft overhead can see us in the water.

For the Escape Hatch drill, we all gathered below deck where our staterooms are, and climbed a ladder, where crew members helped pull us up onto the weather deck (the area of the ship exposed to weather) on the bow of the ship.  This is meant to show us how to escape dangers such as fire or flood below deck.

Safety gear

Safety gear on; ready for station!  Photo by Glenn Zapfe

But safety isn’t just practiced during drills; it’s pretty much a way of life on the ship.  Whenever winches or other machinery are in operation, we all have to wear hard hats and life jackets; that means that we wear them every time we reach a station and drop the nets.  We are also all required to wear closed-toed and closed-heeled shoes at all times, unless we’re sleeping or showering.  Another small safety trick that is helpful is the idea of, “keep one hand for yourself and one hand for the ship.”  That means we carry gear in one hand and leave one free to hold onto the swaying ship.  This has been really useful for me as I get used to the ship’s movements.

Until next time, everyone – don’t forget to track the Oregon II here: NOAA Ship Tracker

Emilisa Saunders: Away We Go! May 13, 2013

NOAA Teacher st Sea
Emilisa Saunders
Aboard NOAA Ship Oregon II
May 14th – 30th, 2013

Mission: SEAMAP Plankton Study
Geographical area of cruise: Gulf of Mexico
Date: Monday, May 13th, 2013

Science and Technology Log:

Boarding the Oregon II

Me and the Oregon II (and the silly crewmember in the background). Photo by Kaela Gartman

I’m finally aboard the Oregon II!

Today I got a sneak preview from the lead scientist, Andy, of the labs and some of the equipment that we’ll be using to collect plankton once we’re underway.  There are three labs where we’ll be doing science for the next 17 days: the dry lab, the wet lab, and the chem lab.  The dry lab, where I’m sitting and typing right now, is a room with computers that are used to remotely monitor the depths of the nets once they have been dropped, and to record data about those drops.  The wet lab is where samples of plankton are preserved in jars to be sent back to shore and studied.  The chem lab is where chlorophyll is separated from plankton samples.

I got to see the CTD, which is a unit that collects water at specific depths in order to measure physical characteristics of the water, such as salinity, fluorescence, temperature, and dissolved oxygen.  I’m looking forward to learning more about this physical data and why it is important once we are underway.

CTD

The CTD collects water samples for testing

Andy also showed me the nets we will use to collect plankton.  All of the nets are large and heavy and are raised and lowered by winches that are operated by the ship’s crew.  The first is a Bongo net.  If you’ve ever seen bongo drums, you can get a sense of what this unit looks like: two side-by-side nets with round openings.  The nets themselves are shaped like cones, and we’ll attach a bottle called a cod end on the end of each to capture all of the plankton from the nets.  Then there are two Neuston nets, which have large, rectangular openings.  The regular Neuston net will be towed along the surface, and the Subsurface Neuston will be towed in a pattern at various depths, as will the Bongo.  The unit that I am most excited about is the MOCNESS.  This big frame holds up to ten nets, which can be opened and closed at certain depths; that way, we can collect samples from various depths and monitor plankton at separate locations and at specific depths in the water column.  In the other nets, you know what you get and where it came from, but not how deep it was.

Bongo nets

Bongo nets

Subsurface Neuston

Subsurface Neuston Net

The water column is an idea that scientists use to think about and study the ocean from top to bottom, or from the surface to the ocean floor.  When you think about the water column, imagine the ocean as an aquarium, and you’re looking into it and seeing the organisms that live at different depths and what the water is like at those depths.

The reason that the MOCNESS is so exciting to me is that it reminds us that the water in the ocean is not just a uniform mixture all throughout; different creatures live at different depths, and in different numbers at those depths.  It’s easy to imagine that creatures that are benthic – meaning, they live on the ocean floor – will vary depending on where they are in the world and how deep the ocean floor is in that spot.  It’s harder to imagine that pelagic organisms – those that live in the water column, neither at the very surface, nor at the bottom or at the shore – will also vary greatly depending on depth and location.  The water itself is different as well; the temperature of the water and the amount of salt, light and oxygen changes with depth.

Challenge Yourself:  Here’s a challenge for my Nature Exchange Traders: go on into the Nature Exchange and explain the terms water column, benthic and pelagic to earn some bonus points.  Tell them Emmi sent you!

NOAA Oregon II

The journey begins! Photo by Kaela Gartman

Personal Log

Flying over Alabama on the descent into Mobile on Sunday, I was struck by how much water there was everywhere below me.  Everywhere I looked, there were slow, meandering rivers, sparkling ponds, lakes and streams.  At times when I thought I was looking down on a forest, I saw the sun reflecting off of water blanketing the ground beneath the trees and shrubs.  I was even struck by the number of puddles in parking lots and lining the streets.  I kept thinking that, living in the desert, I’m just not used to seeing so much water – and I hadn’t even reached the harbor yet!  It was as if I was being slowly introduced to the world that I’m about to live in for the next 17 days.

I’ve been aboard the Oregon II at dock for just a few hours now, and I’m already overwhelmed with fascination, excitement, curiosity, and anticipation.  I started the morning at my hotel feeling very nervous, knowing that I was about to experience a rush of newness: new people, places, sights, sounds, rules, routines, you name it.  I told myself just to take a deep breath and take it in one thing at a time, and that really helped me to enjoy the experience.  Now the nerves are mostly gone and I’m just very much looking forward to the ship’s departure tomorrow afternoon!

To my great fortune, I’ve already found everyone I’ve met to be incredibly kind and friendly.  I got to meet some of the NOAA lab scientists who study the plankton that is collected from the Gulf, as well as field scientists Alonzo and Glenn, with whom I’ll be working the night shift on the Oregon II.  Last but not least is Andy, the lead scientist for this cruise, who helped plan logistics for my arrival, gave me a tour of the ship and helped me get situated on board.

The folks I’ve met on board are from all over the United States.  Some of them came to Pascagoula to work for NOAA to study the effects of the Deepwater Horizon oil spill; some came as part of their graduate school studies.   Everyone I’ve met either has or is pursuing an advanced degree, so the intelligence on board the ship is impressive.  As challenging as it can be to for the scientists to be away from home for more than a hundred days out of the year, all of them have some level of appreciation for doing field work.  Not all of the scientists who study plankton in Pascagoula are able to leave the lab to go on the cruises, so I am even more grateful that I have the honor of taking part.  I’m also extremely grateful to learn that I will be of help to the team.  Because of limited staffing and budgets, the science team depends on teachers, like me, to provide extra sets of hands during the field work.

Stateroom 5

My stateroom on the Oregon II

I’ll be staying in Stateroom 5 for this cruise, which I’ll share with a volunteer scientist named Jana.  “Stateroom” is the word used for a bedroom on a ship.  The stateroom is small, as expected, but it actually feels like it’s the perfect size.  All of my belongings are unpacked in drawers and cabinets, and they all fit just fine.  There’s a bunk with two beds, a sink, and three storage cabinets.  Two of the cabinets are entirely for our use, and one mostly holds safety gear and flotation devices.  There is enough floor space that I could lay on the floor and do snow angels, so there will be plenty of room to move around.  I don’t expect to be spending all that much time in the stateroom once we are underway.

Time has taken on a whole new meaning in the past two days.  Yesterday morning I left Las Vegas in the Pacific Time Zone and flew to Atlanta in the Eastern Time Zone, then to Mobile in the Central Time Zone.  It was almost like time travel.  After we embark tomorrow, I’ll start my work schedule, which will have me on duty from midnight to noon every day.  Work goes on around the clock on NOAA vessels.  This schedule will take some getting used to, but as a morning person, I am excited that I’ll be awake and active for my favorite part of the day, and I’ll get to watch the sun rise.  Right now, I’m attempting to stay awake for my entire first night on the ship so that I can get on my work schedule right away.  To add another level of confusion to my sense of time, ship crews observe 24-hour military time instead of using AM and PM.  Numbers are difficult for me and don’t come naturally, so this will take some getting used to.

Military time

The clocks on the ship show the 24-hour military time system.

Just being on the ship feels quite surreal.  As I write this at 23:33hrs, there are just a handful of people on board, and we are still at dock.  Every once in a while some subtle movement reminds me that this is a ship in the water, but mostly it feels like solid ground.  I know that will change once we get moving.  Aside from the obvious signs, there are other little reminders that this is a ship, where everything must be secured for rougher waters.  Computers and monitors are strapped and bolted to the tables, there are gripper pads spread out on tables and in drawers, and every door, from drawers and cabinets to staterooms, has to be latched shut and unlatched to open, and open doors have to be secured with a hook so that they don’t slam shut when the ship shifts.   There’s also a constant hum of noise on the Oregon II.  I’m interested to see how loud it is when we’re actually moving!

The adventures in science begin tomorrow!

Sunset at Dock

Sunset at dock, from the dry lab of the ship

Did you know?

Bluefin tuna plankton are a type of ichthyoplankton, which comes from the Greek words for “fish drifters.”  For those of you in Nevada, think of our state fossil, the ichthyosaurus, which means “fish lizard!”

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


Sunrise

Sunrise on the Oregon II

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.)

Sunrise

The trawl net at sunrise

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.

neuston tow

The Neuston tow about to pick up a lot of Sargassum- oh no!

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.

Bongo tow

The bongo tow on deck waiting to be sent down to about 3m from the ocean floor.

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

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:

cownose ray

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!

-

Atlantic sharpnose shark

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

Sharksucker
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?

Christopher Faist: Endless Horizon, July 26, 2011

NOAA Teacher at Sea
Chris Faist
Aboard NOAA Ship Henry B. Bigelow
July 20 — August 1, 2011

Mission: Cetacean and Seabird Abundance Survey
Geographical Area: North Atlantic
Date: July 26, 2011

Weather Data
Air Temp:  20 ºC
Water Temp: 20 ºC
Wind Speed: 3 knots
Water Depth: 4141 meters

Science and Technology Log

To quantify sea conditions, scientists use the Beaufort Scale.  Calm waters with no wind is a Beaufort state of zero but when the wind speed increases and white caps start to form the Beaufort state raises to a 4.  Good observation conditions for sighting marine mammals fall between sea state 0-3.  When the white caps form it gets difficult to distinguish between a white cap and a dolphin splash, decreasing our chances of seeing all the animals in our survey area.

Today, the sighting conditions were good with the sea state varying from a 1-3 over the course of the day.  While the conditions were good we did not see any animals for hours.  This was surprising to many of the scientists so we looked more closely at the conditions in the water to investigate the lack of sightings.

Bongo Net

Bongo Net being deployed

Three times a day (morning, noon and night) a system of nets with a probe attached is deployed to sample the water under the ship.  The net is called a Bongo net, due to its dual net design that looks similar to a Bongo drum.  The net is made of a fine mesh that catches small animals swimming below the ship.  The probe, attached to the net, is called a CTD, which stands for conductivity, temperature and depth.  Scientists can use the combination of the animals found in the net and the readings from the CTD to make conclusions about the productivity of the waters around the ship.  The data collected at our noon deployment gave great insight into our lack of visual and acoustic sightings.

During our noon Bongo net deployment an interesting phenomenon was seen in the data.  First, the nets that typically collect animals were nearly empty.  Secondly, the CTD data showed very little change in water density between the surface and 200m.  This lack of change tells scientists that there is very little mixing of the ocean currents in this area of the North Atlantic.  Mixing usually causes colder, nutrient rich water to move toward the surface supplying animals with the oxygen and nutrients they need to grow and reproduce quickly.  When mixing is absent small animals are not as abundant eliminating the food source for the rest of the food chain.  With no food, dolphins and whales move out of the area to more fertile waters.  Hopefully, we will move to more productive areas and increase our cetacean sightings.

Personal Log

Chris Processing Bongo

Chris Processing the Bongo Sample

We have been at sea for 5 days now.  I have figured out my routine and I am really enjoying being away from land.  Surprisingly for a ship, internet speeds are quick, DirectTV is crystal clear and the laundry facilities are efficient.  (It pays to be on one of the newer, technologically advanced ships in NOAA’s fleet. )  The food has been outstanding and I am making some new friends.  Getting up early, 5am, may bothersome, but the sunrises and clear air have made the mornings a great part of the day.  After dinner the crew has a variety of games to pass the time including ladder golf, bean bag toss and darts.  If you think these games are challenging on land, adding the roll of the ship adds a new level of difficulty.

Bruce Taterka, July 4, 2010

NOAA Teacher at Sea: Bruce Taterka
NOAA Ship: Oregon II

Mission: SEAMAP Summer Groundfish Survey
Geographical Area of Cruise: Gulf of Mexico
Date: Sunday, July 4, 2010

Out in the Gulf

Weather Data from the Bridge

Time: 1000 hours (10:00am)
Position: Latitude = 27.58.38 N; Longitude = 096.17.53 W
Present Weather: partly cloudy, haze on the horizon
Visibility: 8-10 nautical miles
Wind Speed: 17 knots
Wave Height: 2-4 feet
Sea Water Temp: 28.6 C
Air Temperature: Dry bulb = 29.2 degrees Celsius; Wet bulb = 26.1 C
Barometric Pressure: 1011.1 mb

Science and Technology Log

The purpose of the SEAMAP Summer Groundfish Survey is to collect data for managing commercial fisheries in the Gulf of Mexico. SEAMAP stands for Southeast Area Monitoring and Assessment Program.

Right now we’re working along the Gulf Coast of Texas, far from the BP Deepwater Horizon oil spill, so we’re not seeing any effects of oil here. However, part of our mission is to collect fish for testing to make sure that oil spill has not impacted the marine life in this area and that the fish and shrimp from Texas are safe to eat. We’re also collecting water samples from this area to use as baseline data for the long-term monitoring of the impact of the oil spill in Gulf.

Analyzing a water sample in the Oregon II’s lab.

There are four main ways the Oregon II is gathering SEAMAP data on this cruise, and we’ve already learned how to use all of them. The main way we collect data is by trawling, and this is where we do most of our work on the Oregon II. In trawling, we drag a 42’ net along the bottom for 30 minutes, haul it up, and weigh the catch.

Hauling in the trawl net.

We then sort the haul which involves pulling out all of the shrimp and red snapper, which are the most commercially important species, and taking random samples of the rest. Then we count each species in the sample and record weights and measurements in a computer database called FSCS (Fisheries Scientific Computer System).

Logging a sample into FSCS.

Here on the Texas coast, where we’re working now, the SEAMAP data is used to protect the shrimp population and make sure that it’s sustained into the future. Since 1959, Texas has been closing the shrimp fishery seasonally to allow the population to reproduce and grow. The SEAMAP data allows Texas to determine the length of the season and size limits for each species. Judging by our trawls, the Texas shrimp population is healthy.

Another tool for data collection is the CTD, which stands for Conductivity, Temperature, and Depth. The CTD also measure dissolved oxygen, chlorophyll and other characteristics of the marine ecosystem and takes measurements from the surface to the bottom, creating a CTD profile of the water column at our trawling locations. These data are important to assess the extent of the hypoxic “dead zone” in the Gulf of Mexico, and to relate the characteristics of our trawling hauls to dissolved oxygen levels. SEAMAP data collected since the early 1980s show that the zone of hypoxia in the Gulf has been spreading, causing populations to decline in hypoxic areas.

We also use Bongos and Neustons to gather data on larval fish, especially Bluefin Tuna, Mackerel, Gray Triggerfish, and Red Snapper. The Neuston is a rectangular net that we drag along the surface for ten minutes to collect surface-dwelling larval fish that inhabit Sargassum, a type of seaweed that floats at the surface and provides critical habitat for small fish and other organisms.

Examining the results of a Neuston drag.

Bongos.

We drag the Bongos below the surface to collect ichthyoplankton, which are the tiny larvae of fish just after they hatch. The Neuston and Bongo data on fish larvae are used for long-term planning to maintain these important food species and keep fish stocks healthy.

Personal Log

This is a great learning experience, not only about marine science but also about living and working on a ship. The Oregon II is literally a well-oiled machine, and the operation of the ship and the SEAMAP study depends on a complex effort and cooperation among the science team, the crew, the officers, engineers, and the steward and cook. Everyone seems to be an expert at their job, and the success of our survey and our safety depends on that. It’s a different feeling from life on land.

Life aboard the Oregon II is comfortable, especially now that I’ve gotten my sea legs.(I was hurting after we set out on Friday in 4’ to 6’ swells, but by Saturday afternoon I felt fine.) The food is excellent and most of the ship is air conditioned. The Gulf – at least the Gulf Coast off of Texas right now – is beautiful. The seas are deep green and blue and teeming with marine life. I’m looking forward to spending the next 2 weeks on board the Oregon II and being part of the effort to study the marine ecosystem in the Gulf and how it’s changing.

View of Gulf of Mexico

View of Gulf of Mexico

Mechelle Shoemake, June 29, 2010

NOAA Teacher at Sea
Mechelle Shoemake
Onboard NOAA Ship Oregon II
June 19 – 30, 2010

Mission: SEAMAP Groundfish Survey
Geographical Area of Cruise: Northwestern Gulf of Mexico
Date: Tuesday, June 29, 2010

Weather Data from the Bridge
Time: 0000 hours (12:00pm)
Position: Latitude = 28.45.067 N; Longitude = 091.35.189 W
Present Weather: cloudy
Visibility: 6 nautical miles
Wind Speed: 8 knots
Wave Height: 4-6 foot swells
Sea Water Temp: 29.8 degrees Celsius
Air Temperature: Dry bulb = 27.3 degrees Celsius;
Wet bulb = 26.2 degrees Celsius

Science and Technology Log

The Groundfish Survey’s purpose is to find out what species are here in the Gulf how many, and their size, sex, and maturity status. On average the trawl produces at least 20-40 different species on each tow. The type of trawl used on the Oregon II is the Bottom Otter Trawl. The deck hands put the net out, it trawls for around 30 minutes, and it is then pulled back in by the deck hands. The catch is then placed in basket where it is weighed and then separated by species Each species is then individually weighed, measured, and sexed.

This is a red snapper I’m sorting out of the catch

We caught a nice red snapper that will be sent back to the lab for testing. It will also be determined if the oil spill had any effect on the fish, shrimp, crabs, and other species we caught. We also took some more water samples using the CTD to determine how much oil is in the water. We We used the Neuston net and the Bongo nets to gather plankton, which is also being collected for testing. The Neuston gathers plankton on the surface while the Bongo nets gather plankton all the way from the bottom of the gulf to the surface. This plankton is then placed inglass jars with a preservative Twenty-four hours later the plankton is transferred to a lesser preservative. The initial set sample is too strong for long storage. The plankton samples are then sent to Poland to a specialized plankton lab. In this lab, the plankton is identified to the family level. It is then sent back to the NOAA labs where it is identified to the species level. It was amazing to see all the little critters in the jar. There were so many of them.

Deploying the bongo net

Later in the day, we did another trawl….the catch of the day. Well it was a tire! It did have two little critters living in it, though. They were both identified and weighed and then frozen and packaged for the lab. The speculated reason for the trawl producing so few specis what’s called hypoxia. Hypoxia is the depletion of the oxygen in the water. If there is no oxygen,the fish and many other species cannot live. You can read more about hypoxia at http://www.ncddc.gov.

A frog fish

To the right is a frog fish that we found living in the tire. It has a trick to catch its food. The tentacle on the top of the head acts as a lure to attracts its prey. When a smaller fish comes by to eat what it thinks is food at the end of the frog fish’s lure…..well it gets caught and the frog fish eats the little fish. This frog fish still had its dinner in its mouth.

To the left is a picture of the last trawl that my shift made. You can see that this catch was full of shrimp and little crabs. We had to turn back towards Texas due to Tropical Storm Alex, which is forecasted by NOAA’s National Weather Service to become a hurricane by tomorrow. It’s too dangerous for the ship to be out in weather like that.

Some of the critters from out last trawl

Personal Log

Well, I can say that this has definitely been an adventure of a lifetime. I have enjoyed my voyage with all of my new NOAA friends. They have taught me a lot. As I am writing this, we are sailing back to port in Galveston, TX. As I said earlier, we had to cut our trip short due to Tropical Storm Alex. Believe me, I know he is out there. Our ship is rolling with the waves. I had a quick lesson in securing my belongings. You never know what you might encounter when you go to sea. Thanks to NOAA for giving me this opportunity.