Lisa Carlson: “No life is too short, no career too brief, no contribution too small,” July 16, 2023

NOAA Teacher at Sea

Lisa Carlson

NOAA Ship Bell M. Shimada

July 5, 2023 – July 19, 2023

Mission: Fisheries: Pacific Hake Survey (More info here)

Geographic Region: Pacific Ocean, off the coast of California

Date: July 16, 2023

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Weather Data from the Bridge

July 14 (1200 PT, 1500 EST)
Location: 38° 34.9’ N, 123° 42.7’ W
15nm (17mi) West of Stewarts Point, CA

Visibility: <1 nautical miles
Sky condition: Overcast, fog
Wind: 19 knots from NW 330°
Barometer: 1014.6 mbar
Sea wave height: 3-4 feet
Swell: 5-6 ft from NW 300°
Sea temperature: 11.0°C (51.8°F)
Air temperature: 13.1°C (55.6°F)
Course Over Ground: (COG): 330°
Speed Over Ground (SOG): 10 knots

July 15 (1200 PT, 1500 EST)
Location: 38° 56.3’ N, 124° 02.1’ W
13nm (15mi) West of Point Arena Lighthouse, Point Arena, CA

Visibility: 10 nautical miles
Sky condition: Overcast
Wind: 20 knots from NW 340°
Barometer: 1013.1 mbar
Sea wave height: 3-4 feet 3-4
Swell: 7-8 ft from NW 320°
Sea temperature: 10.8°C (51.4°F)
Air temperature: 13.3°C (55.9°F)
Course Over Ground: (COG): 270°
Speed Over Ground (SOG): 9 knots

July 16 (1200 PT, 1500 EST)
Location: 39° 36.2’ N, 124° 01.6’ W
14nm (16mi) Northwest of Fort Bragg, CA

Visibility: 10 nautical miles
Sky condition: Overcast
Wind: 29 knots from NW 320°
Barometer: 1011.4 mbar
Sea wave height: 3-4 feet
Swell: 5-6 ft from NW 320°
Sea temperature: 11.3°C (52.3°F)
Air temperature: 13.9°C (57.0°F)
Course Over Ground: (COG): 280°
Speed Over Ground (SOG): 7 knots

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Science and Technology Log

Without a vessel and without a crew, none of this mission would be possible. As I’ve said before, this crew is special. Like any job, employees are required, but that does not mean that you will work well cohesively and passionately towards a goal. The two weeks I’ve been spending with this crew who is so wholeheartedly excited about their job and role, while being on the ocean, has been so rewarding and inspiring. More later, this is starting to remind me of crying along with my sobbing fourth graders on the last day of school.

While I’ve discussed a lot of the daily operations of the crew and ship, and what I’ve been learning and working on myself, however, I have not discussed the vessel and agency that has made all of this possible. Many people question, “What is NOAA?” when I explain this opportunity.

About NOAA

NOAA logo: a circle bisected by the outline of a seagull, dark blue above the seagull's wings and lighter blue below. Around the circle read the words: National Oceanic and Atmospheric Administration, U.S. Department of Commerce.

“The National Oceanic and Atmospheric Administration (NOAA) is a U.S. government agency that was formed in 1970 as a combination of several different organizations. The purpose of NOAA is to study and report on the ocean, atmosphere, and coastal regions of Earth.”

National Geographic Education: “National Oceanic and Atmospheric Administration (NOAA)

“Our mission: To understand and predict changes in climate, weather, ocean, and coasts, to share that knowledge and information with others, and to conserve and managecoastal and marine ecosystems and resources.”
NOAA: “About Our Agency”

NOAA: “About Our Agency”

NOAA Ship Bell M. Shimada can carry a total crew of 24, which include NOAA Corps officers, engineers, other crew members, and scientists.

“The NOAA Commissioned Officer Corps (NOAA Corps) is one of the nation’s eight uniformed services. NOAA Corps officers are an integral part of the National Oceanic and Atmospheric Administration (NOAA), an agency of the U.S. Department of Commerce, and serve with the special trust and confidence of the President.”

NOAA OMO: “NOAA Commissioned Officer Corps

The Vessel

NOAA Ship Bell M. Shimada, commissioned in 2010, is a fisheries survey vessel designed to produce a low acoustic signature, built to collect data on fish populations, conduct marine mammal and seabird surveys, and study marine ecosystems. The quiet operation provides scientists the ability to study fish and marine mammals without significantly altering their behavior.

Stats and Specs (Link for more information)
Length: 208.60 ft
Beam (width): 49.2 ft
Draft (bottom of the lowered centerboard to waterline): 29.7 ft
Displacement (full load): 2,479 tons (4,958,000 lbs)
Speed: 11.00 knots
Endurance: 40 days
Range: 12,000 nautical miles
Home port: Newport, Oregon
Crew:
– 24 (5 NOAA Corps officers, 4 licensed engineers, and 15 other crew members)
– Plus up to 15 scientists

Namesake

“[Dr.] Bell M. Shimada (1922-1958), served with the United States Fish and Wildlife Service and the Inter-American Tropical Tuna Commission, and was known for his studies of tropical Pacific tuna stocks.”

Wikipedia: “NOAAS Bell M. Shimada

The ship’s namesake was known for his contributions to the study of Tropical Pacific tuna stocks, which were important to the development of West Coast commercial fisheries following World War II. Dr. Bell Shimada and colleagues at Pacific Oceanic Fisheries Investigations (POFI) Honolulu Laboratory were among the first to study the population dynamics of tunas and the oceanography affecting their abundance and distribution.

a man (Dr. Shimada) wearing a white t-shirt, shorts, and red baseball cap stands holding a penguin. He grasps the penguin securely beneath its wings, which are spread out to each side. The man, and the penguin, look at the camera. He appears to be on a vessel - we can see some ocean water in the background - and we can tell that two other people are behind him, mostly obscured.

Dr. Bell M. Shimada, circa 1957.
Wikipedia: “Bell M. Shimada

“In her remarks at the christening and launch, [Dr. Shimada’s daughter] Julie Shimada offered the following, “I hope the Bell M. Shimada is a lasting testament that no life is too short, no career too brief, no contribution too small, to make a difference.”

NVC Foundation: “NOAA Honors Nisei With Launch of Fisheries Vessel “Bell M. Shimada””

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Interviews with the Crew
(Part 1 of 2)

(Take note of the similarities and differences between how these crew members chose an ocean-related career and got to be assigned to NOAA Ship Bell M. Shimada)


A photo of a photo in a wooden frame with a name plaque reading CDR Laura Gibson. The photo is a portait of a woman posing in a survival suit, hands in the air. She's wearing a navy blue hat that says Bell M Shimada R-227.

Executive Officer
Commander Laura Gibson

What is your role aboard NOAA Ship Bell M. Shimada?
CDR Gibson’s role includes a lot of administrative work, handling the budget, standing bridge watches as the Officer on Duty (OOD), along with other executive duties.

What do you enjoy the most about your role?
The mission and camaraderie of the crew, as well as getting to know the ship and happy, successful operations.

When did you know you wanted to pursue an ocean-related career?
CDR Gibson enjoys Scuba diving and grew up on lakes. She worked on a research ship in college and continued working on the water which led her to NOAA. She mentions her Dad as a large motivator and inspiration of wanting to pursue an ocean-related career.

What do you think you would be doing if you were not working for NOAA?
Working a boring 9-5 desk job!

Favorite animal
Rhinoceros

Fun Fact: she brings a stuffed animal dog with her from her son, named Barfolomew.

His nickname is Barf!

a stuffed animal (a brown dog with long black ears) photographed against a carpet

A photo of a photo in a wooden frame with a name plaque reading LT Nicole Chappelle. The photo is a portait of a woman wearing a blue jacket.

Operations Officer
Lieutenant Nicole Chappelle

What is your role aboard NOAA Ship Bell M. Shimada?
Coordinate with scientists to make the plan of the day, assist in navigation and operation of the vessel.

What do you enjoy the most about your role?
Nicole enjoys seeing all of the sea life and creatures, and hearing and learning what the scientists are doing and why.

When did you know you wanted to pursue an ocean-related career?
She originally wanted to work with animals, which she did as a member of a rehabilitation team at Sea World. She then wanted to join uniformed service. Nicole chose NOAA’s uniformed service (NOAA Corps) because their science missions aligned with her interests.

What do you think you would be doing if you were not working for NOAA?
Working with animals and marine life or being a scuba instructor.

Do you have an outside hobby?
Horseback riding, Scuba diving, jogging, kayaking, hiking.

What’s something you were surprised to see or learn about living and working onboard when you first started?
Nicole remarked on the times she’s been out in the ocean, hundreds of miles away from shore, and how few other vessels you see there. She says it gave her a much greater appreciation for just how big the ocean is.

Favorite animal
Horses


A photo of a photo in a wooden frame with a name plaque reading Deb Rose. This is a photo of woman wearing a green NOAA t-shirt, a purple bandana, and sunglasses.

Junior Engineer
Deb Rose

What is your role aboard NOAA Ship Bell M. Shimada?
Junior Engineer Deb Rose (in her words) handles the “hotel services” of the vessel. Her role includes plumbing, electrical work, repairs, and many other behind the scene tasks to keep the vessel running safely.

What do you enjoy the most about your role?
I get to fix stuff! Troubleshooting, figuring out what’s wrong, and fixing the problem were among steps that she described as part of her work onboard.

When did you know you wanted to pursue an ocean-related career?
While working at Firestone, Deb met and befriended Jason who became a wiper on NOAA Ship Oscar Elton Sette. She saw pictures and heard his stories of how he is now a licensed engineer, and decided to follow in his footsteps! She mentions Jason as a motivator that inspired her to pursue an ocean-related career.

What do you think you would be doing if you were not working for NOAA?
Continue to work on the Alaska Marine Highway ferries. (These ferries cover 3,500 miles of Alaska’s coastline.)

Outside hobbies: Video games, Scuba diving, swimming, fishing

What’s something you were surprised to see or learn about living and working onboard when you first started?
How few women there still are in the industry. Deb has often been the only or one of the only female crew members both on land and at sea. She hopes that this trend will keep changing and that women will be in more engineering industries.

Favorite animal
Her favorite animals are the Jackson Chameleon and dogs.

Fun Fact: Humans are more related to salps than any other creatures we catch. She can also identify 12 Rockfish species!


A photo of a photo in a wooden frame with a name plaque reading Connor Rauch. The photo is a portrait of a man with glasses standing against a wall.

Deck Department
Connor Rauch

What is your role aboard NOAA Ship Bell M. Shimada?
Connor is a General Vessel Assistant as part of the Deck Department. He helps deploy and recover the trawl net and CTD rosette, stands watch as a lookout, helps keep the ship clean, and much more! He took classes at Seattle Maritime Academy for one year and is now applying his education on his first NOAA vessel!

What do you enjoy the most about your role?
He is enjoying his first assignment on a NOAA vessel and traveling up and down the Pacific coast. He says he is also enjoying being on the water, applying new knowledge to tasks, and training to a real ship. He also enjoys learning about trawling and commented on how nice the people onboard are.

When did you know you wanted to pursue an ocean-related career?
He wanted to try something new after working for a non-profit group during the Covid-19 pandemic assisting those in need. He decided to work on the water since he grew up sailing and kayaking. He thought of working on local ferries, but after taking classes at Seattle Maritime Academy, he had the confidence to apply for NOAA.

Do you have an outside hobby?
Reading, kayaking, camping, and hiking.

What’s something you were surprised to see or learn about living and working onboard when you first started?
Connor said he was pleasantly surprised at how tight the crew is, how easy it is to sleep, how comfortable the ship is, and the good food!

Favorite animal
Beavers and dog

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Personal Log

As this experience comes to the end, I reflect on all parts of this mission. The crew, vessel, marine life, food, sleep, friendships, and more. I’m so thankful I was able to have this experience and share NOAA’s Teacher at Sea program more with coworkers, family, friends, and my students. Meeting and talking with the crew resulted in long conversations and plenty of laughs and connections amongst each other that they previously had not known.

Winds and swells picked up over the weekend and on Sunday July 16 we only caught six Hake. After that trawl and an increase in marine mammals being sighted when we were trying to trawl, fishing was called off for the rest of the Leg. At 1020 Monday July 17, we completed our last transect for Leg 2 of the Survey and headed due North for the long trek to Newport, Oregon. We still found ways to entertain ourselves, nap, snack, share stories and riddles, take photos of sunsets and marine mammals, watch shooting stars and have a movie night. Below are photos of our art craft: fish prints of two Chilipepper Rockfish!

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Did You Know?

NOAA Ship Bell M. Shimada has an endurance, the amount of time the vessel can be at sea in a row, of forty days. This is not because the ship can’t make its own fresh water through reverse osmosis from sea water, or a lack of fuel, oil, extra parts, or a way to exhume waste and trash in an environmentally friendly way…

but because of food!

Our galley crew is amazingly talented and spoils us with a huge all you can eat buffet, desserts, and drinks every day! But, as per various laws and for the safety of the crew, they are lawfully entitled to fresh fruit, vegetables, meat, etc. within set guidelines and window of time.


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Animals Seen Today

Pacific White-Sided Dolphins! Although these energetic friends caused us to abandon a trawl attempt after multiple marine mammal watches ended early because of their presence, they were so much fun to watch! I brought my DSLR camera up to the bridge deck and eventually sat down on the deck watching them jump and race through the ocean waters next to the hull. Below are some of my favorite photos I took of the pod.

Lisa Carlson: One Fish, Two Fish, Rockfish, Hake fish! July 10, 2023

NOAA Teacher at Sea

Lisa Carlson

NOAA Ship Bell M. Shimada

July 5, 2023 – July 19, 2023

Mission: Fisheries: Pacific Hake Survey (More info here)

Geographic Region: Pacific Ocean, off the coast of California

Date: July 10, 2023

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Weather Data from the bridge:

July 7 (1200 PT, 1500 EST)
Location: 36° 00.4’ N, 122° 05.9’ W
16nm (21mi) West of Big Sur, CA

Visibility: 10 nautical miles
Sky condition: Overcast
Wind: 20 knots from NW 330°
Barometer: 1013.1 mbar
Sea wave height: 3-4 feet
Swell: 6-7 ft from NW 320°
Sea temperature: 14.0°C (57.2°F)
Air temperature: 14.4°C (57.9°F)
Course Over Ground: (COG): 323°
Speed Over Ground (SOG): 10 knots

July 8 (1200 PT, 1500 EST)
Location: 36° 34.5’ N, 122° 05.3’ W
17nm (20mi) Southwest of Monterey, CA

Visibility: 10 nautical miles
Sky condition: Few clouds
Wind: 19 knots from NW 330°
Barometer: 1013.8 mbar
Sea wave height: 5-6 feet
Swell: 6-7 ft from NW 330°
Sea temperature: 14.0°C (57.2°F) 13.7
Air temperature: 14.4°C (57.9°F) 14.3
Course Over Ground: (COG): 089°
Speed Over Ground (SOG): 10 knots

July 9 (1200 PT, 1500 EST)
Location: 37° 06.8’ N, 123° 00.5’ W
30nm (35mi) West of Pigeon Point Light Station, Pescadero, CA

Visibility: 10 nautical miles
Sky condition: Overcast
Wind: 13 knots from NW 332°
Barometer: 1016.0 mbar
Sea wave height: 2-3 feet
Swell: 4-5 ft from NW 310° 4-5
Sea temperature: 14.3°C (57.7°F)
Air temperature: 15.2°C (59.4°F)
Course Over Ground: (COG): 093°
Speed Over Ground (SOG): 10 knots

July 10 (1200 PT, 1500 EST)
Location: 37° 26.7’ N, 123° 06.4’ W
32nm (37mi) West of Pescadero, CA

Visibility: 8 nautical miles
Sky condition: Overcast, fog in vicinity
Wind: 20 knots from NW 330°
Barometer: 1015.9 mbar
Sea wave height: 2-3 feet
Swell: 3-4 ft from NW 320°
Sea temperature: 14.5°C (58.1°F)
Air temperature: 13.6°C (56.5°F)
Course Over Ground: (COG): 314°
Speed Over Ground (SOG): 3 knots

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Science and Technology Log

Lisa poses for a photo in the wet lab with a hake fish. She's wearing heavy-duty orange overalls and large orange gloves. With her right hand, she grasps the fish by its open mouth, and her left hand holds on to the tail. We can see metal tables and equipment in the background.
Me holding a Hake before sorting. After observation, we determined this was a developmentally mature female, measuring 50cm (20in) long!

In my July 6 blog post, I explained how NOAA Ship Bell M. Shimada is equipped to collect acoustic data in the form of echo grams. The acoustics team uses the data to determine if there are enough return signals to suggest fish are present and attempt a trawl. In this blog post, I will explain how we get the fish onboard, and what we do with the sample of marine life once it is collected from the net.

One question I had after learning about the acoustics and environmental DNA (eDNA) pieces of the survey mission was, “How does physically collecting and researching Hake samples fit into the puzzle of understanding their ecosystem and supporting sustainable fisheries?” (NOAA Fisheries quick facts and video here)

“While echosounders are useful, they do not provide certain quantitative data that researchers need to understand the ecology of these organisms and the midwater zone. To collect quantitative data, such as biomass, length and weight, and age class distributions, researchers must gather representational samples and take direct measurements of them. The best way to do this is by employing trawls.”

NOAA Ocean Exploration: “Trawls

So, although acoustics and eDNA research is important to the overall survey, they are only pieces of the puzzle, and the puzzle is not complete without conducting trawls and physically researching samples. NOAA Ship Bell M. Shimada uses a midwater trawl net that is deployed from the stern over the transom, and towed behind the vessel. As the name suggests, midwater trawls occur in the middle section of the water column, versus surface and bottom trawls. The net is conical in shape and uses two metal Fishbuster Trawl Doors, and two sets of heavy chain links called Tom weights, in order to keep the trawl in the middle of the water column.

a simple and stylized monochrome illustration of a fishing vessel towing a midwater trawl behind it. The net in tow is conical, attached at four points to two bars that hold the opening apart, and these bars are attached to lines (ropes) extending back from the vessel. This net is capturing two fish and missing a third.
NOAA Fisheries: “Fishing Gear: Midwater Trawls

“The midwater region is especially important because the creatures that inhabit it constitute the majority of the world’s seafood. Understanding the ecology of midwater organisms and their vast environment can provide us with better information to manage these important natural resources and prevent their overexploitation.”

NOAA Ocean Exploration: “Trawls

Deck department assisting in recovering the trawl net after a successful deployment.

Two deck crewmembers work with an orange and white fishing net on the aft deck of NOAA Ship Bell M. Shimada. They are wearing foul weather gear, life vests, and hard hats. At right, one leans over the net, searching for remaining captured fish. The other approaches from the left, looking down at the net, to assist. We can see a cloud-capped mountain range in the distance beyond the water.

Once the net is onboard, the net is emptied one of two ways depending on the size of the sample. For large samples, marine life is deposited into a hopper and subsequent conveyor belt. For smaller samples, the Hake will be put into a large basket then divided into smaller baskets of approximately 100 Hake each. Any other marine life like Salps, Myctophids, Pyrosomes, Rockfish, King of the Salmon, and small bony fish, etc. are recorded in the database and returned to the ocean.

“The ship’s wet lab allows scientists to sort, weigh, measure and examine fish. The data is entered directly into the ship’s scientific computer network.”

NOAA Office of Marine and Aviation Operations (OMAO): “Bell M. Shimada
a large black plastic bin filled with fish - mostly hake, but a few splitnose rockfish (eyes bulging from the pressure change) stand out for their red color. An orange-gloved hand reaches toward the basket from the upper left corner of the image.

Large basket containing a sample of Hake with a few (red) Splitnose Rockfish.

With our boots and bright orange rubber pants and gloves on, our first task is to distribute the sample of Hake into baskets of about 100 each. Based on how many baskets we fill, a random selection of baskets will be kept, and the others will be returned to the ocean. With the remaining groups of Hake, we determine their sex and length.

In order to do this, we use a scalpel to make an incision on the underside/belly of the Hake. Once open, we are able to examine their organs, including the gonads to determine if the fish is male or female, and if they are developmentally immature or mature. Young Hake are difficult to sex, and it takes practice to get over any initial fears of cutting into an animal; let alone being able to locate and identify the gonads. Hake usually spawn in early winter, so many of the smaller Hake we sample from during the summer are age one or younger.

Our largest Hake thus far was a developmentally mature female, measuring 50cm (20in). In order to accurately and consistently measure the length of the sample, we use a waterproof, magnetic plastic board with metric (centimeter and millimeter) markings called an Ichthystick (think: high-tech meter stick). The fish is placed on the board with its mouth touching the black board at 0cm, then a magnetic stylus is placed at the fork of the fish’s tail. Once the magnetic stylus is placed on the board, the length to the nearest millimeter is displayed on the LCD screen and automatically entered into the database program. The length data is grouped with the date, time, and identified sex for later observation and comparison.

Additional information, abstracts and outline about Ichthystick here

Ichthystick’s LCD display, motherboard, magnetic board, and magnetic stylus. Digital scale in background.

Ichthystick’s LCD display, motherboard, magnetic board, and magnetic stylus. Digital scale in background.

An even smaller subgroup is then selected and examined to record weights of individual Hake, collect ear bones called Otoliths for aging, stomach samples for diet, liver for RNA, and ovaries for maturity development. Otolith bones help determine the age of the Hake because they grow a new “layer” of bone each year, similar to coral structures and annual tree rings. Organs and bones removed from the Hake are sent to NOAA Fisheries centers for analysis and included in databases with the date, identified sex, length, weight, and location in which they were collected.

This data is used to build more of the puzzle, along with acoustical information, water samples, and eDNA data in order to further understand the ecosystem, biomass, diet, and

“support sustainable populations of Pacific hake on the West Coast.” (…)
“It provides vital data to help manage the migratory coastal stock of Pacific hake. The hake survey, officially called the Joint U.S.-Canada Integrated Ecosystem and Pacific Hake Acoustic Trawl Survey, occurs every odd-numbered year.”

NOAA Fisheries: “Joint U.S.-Canada Integrated Ecosystem and Pacific Hake Acoustic Trawl Survey

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Personal Log

Although this subtopic of explaining the Integrated Ecosystem and Pacific Hake Acoustic Trawl Survey is a bit easier to understand than my July 6 Acoustics Lab post, it certainly does not mean it’s an easy task!

When I had a tour on July 4, I remarked how clean and
organized the Wet Lab is. I hadn’t see it in action yet, but noticed how everything had its place and use. On July 6 we conducted our first trawl and collected a sample of 11 baskets of Hake (approximately 1,100 Hake since we group about 100 Hake together in each basket.) From that sample, we kept four baskets and counted, sexed, and measured 541 Hake.

Five of us were working together in the Wet Lab for that haul. I’ll admit I probably
didn’t sex 100+ Hake. It took a few minutes of watching the others carefully and swiftly cut into the underside of a fish, open the two sides, and know what to look for to determine the sex of very young Hake. Eventually I found the courage to slice in and take a look. By the fourth or fifth Hake, the uneasiness had subsided and I found the process very interesting and educational. Although young samples are hard to sex as they are often undeveloped, the others encouraged me and answered my questions and guesses with enthusiasm and support.

While working on measuring the lengths of our samples, one Science Team member paused and remarked how beautiful he found the fish. Although they do not have vibrant, bold colors, shimmering scales, or anything else particularly remarkable, he found the beauty in them. He digressed into a conversation of their role in the ecosystem, how they are living and breathing creatures, and how they probably all have their own personalities and slight physical differences. I noticed some of their eyes were shiny and sparkling, and how their faces and expressions were
noticeably unique the more you looked. That “down to earth”, heartfelt discussion was very special and demonstrated how the crew respects the process of catching and sampling Hake, while keeping each other and marine mammals safe.

From the NOAA Corps Officers, to the deck department, to the engineers,
electronics, science team, survey team, galley crew, volunteers, and everyone in between; the crew on NOAA Ship Bell M. Shimada is special. They take pride in their vessel and job, and always seem to have a smile and kind greeting. Being away from land and loved ones for weeks and months at a time will certainly take a toll on the body and mind, but this team is there for each other. To all of the crew, thank you for making me feel so welcomed and appreciated. We’re almost halfway through the mission, and as tired as I may get after (sometimes) 12+ hour days, I sleep well knowing the crew trusts their vessel and each other; and look forward to learning and becoming more and more acquainted each day with the people that make this mission possible. Thank you!

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Did You Know? (FAQs)

1. Are you finding schools of them?

We’ve had seven successful trawls out of nine attempts for Pacific Hake fish. They often come with pyrosomes (Sea Pickle) myctophids (Lanternfish), and salps in the net too. Some trawl attempts are successful without a hitch, but more often than not we have to restart our Marine Mammal watches a few times before deploying in order to keep our ocean life safe and not get tangled in the net. Two trawl attempts have been abandoned because of the amount of persistent marine mammal life and playfulness near the ship. (I think they know we’re watching and show off for our cameras.)

2. What’s your average depth?

The transects (Set and numbered longitudinal east-west lines NOAA Ship Bell M. Shimada navigates on while collecting acoustic data) usually range from 50m – 1,500m (164ft – 4,921ft) in depth.

  • However, right now one of the displays in the Acoustics Lab, the depth reading is 3,240m which is about 10,630ft or just over two miles deep! 
  • This depth is only 1,870ft shallower than the wreck of the RMS Titanic! 
  • (We were on a long transect, we do not often see depths this great.)

3. Have you gotten seasick? Seasickness should subside after about 3 days.

I’ve never gotten seasick thankfully! Knock on wood and all the other premonitions, please.

4. What is the Hake role in the ecosystem?

More info on this coming in later posts after explaining our Chemistry lab and technology aboard! 

  • However, as predators, they can be cannibalistic towards their own kind. 
  • As far as their role in human consumption: They are often used as a substitute for Cod and Haddock, and in fish sticks and imitation crab meat.

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Animals seen July 5-July 10:

Mammals: Sea Lions, Harbor Seals, Dall’s Porpoise, Risso’s Dolphins, Pacific White-Sided Dolphins, Northern Right Whale Dolphins, Humpback Whales

Birds: Gulls, Black-Footed Albatross

Bony Fish: Hake, Lanternfish (Myctophid), Flatfish, King of the Salmon, Split Nose Rockfish, Chili Pepper Rockfish

Other Marine Life: Giant or Humboldt Squid (15 foot tentacles in trawl), Spiny Dogfish Shark, Shrimp, Plankton, Krill, Sea Pickle (Pyrosome), Salp, Eel Larva

Lisa Carlson: Come Out, Come Out, Wherever You Are, Hake! July 6, 2023

NOAA Teacher at Sea

Lisa Carlson

NOAA Ship Bell M. Shimada

July 5, 2023 – July 19, 2023

Mission: Fisheries: Pacific Hake Survey (More info here)

Geographic Region: Pacific Ocean, off the coast of California

Date: July 6, 2023

Weather Data from the Bridge:

— July 5 Departure
(1800 PT, 2100 EST)

Location: 37° 44.9’N, 122° 39.2’W
Docked at Pier 30/32
San Francisco, CA

Visibility: 10 nautical miles
Sky condition: Overcast
Wind: 17 knots from NW 300°
Barometer: 1012.8 mbar
Sea wave height: 1-2 feet
Swell: 2-4 ft from W 270°
Sea temperature: 14.2°C (57.6°F)
Air temperature: 14.7°C (58.5°F)
Course Over Ground: (COG): N/A
Speed Over Ground (SOG): N/A

— July 6 (1200 PT, 1500 EST)
Location: 35° 38.2’ N, 121° 18.9’ W
16nm (18mi) West of San Simeon, CA

Visibility: 10nm
Wind: 6 knots from 330°
Barometer: 1013.9
Sea wave height: 1-2ft
Swell: 2-4ft from 280°
Sea wave temperature: 14.4°C (57.9°F)
Air temperature: 14.9°C (58.8°F)
Course Over Ground: (COG): W 270°
Speed Over Ground (SOG): 10 knots

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Science and Technology Log

On July 6, our first full day at sea, we gathered in the acoustics lab to observe and keep watch on data from various screens. Data includes our current course plotted on a digital chart, a camera showing current sea state, measurements of the wind speed and direction, and displays of the multiple frequencies at which the Simrad EK80 transmitter emits sound. The EK80 is used while traveling on numbered longitudinal east-west lines called transects. NOAA Ship Bell M. Shimada navigates on these lines while collecting acoustic data along the west coast of the U.S. and into Canada, in hopes of finding schools of Hake to collect for surveying.

A topographic map of a portion of the coast of California. The topographies of the both the land (beige and green scales) and water (blue scale) are depicted. Black dots mark the locations of three coastal cities: Crescent City, near the top of the map; San Francisco, a little more than halfway down; and Morro Bay, toward the bottom of the map. Black horizontal lines mark transects extending west from the coast line. The black lines are marked with red or black x's (showing previous sampling locations, perhaps) and a couple have green triangles.
Map showing transects 1-45 off the coast of California. Transect 1 is south of Morro Bay, CA and transect 45 is near Crescent City, CA.
(We hope to survey transects 8-35 by Cape Mendocino, CA before traveling north to dock in Newport, OR.)

“For acoustic surveys, the ship uses a multibeam echo sounder (MBES) that projects a fan-shaped beam of sound that bounces back to the ship. The ship’s MBES—one of only three systems of its type worldwide—acquires data from both the water column and the sea floor.”

NOAA Office of Marine and Aviation Operations (OMAO): “Bell M. Shimada

The Simrad EK80 emits sound waves from the hull of the vessel down to the sea floor. The process is very similar to a dolphin or bat using echolocation to find prey. Any object the signal hits that has a different density and reflectivity than the surrounding water will cause the waves to bounce back to the ship. An image, called an echo gram, is pieced together each time this occurs and the acoustics team is able to use this information to determine if there are enough return signals that suggest fish are present to attempt a trawl.

Fish that have swim bladders, like bony fish, reflect or echo the sound wave back to the vessel very strongly. Other marine life such as myctophids and zooplankton also have a different density than the sea water, and reflect sound, although not as strongly as fish with air-filled swim bladders. The sea floor itself also reflects sound very strongly, because of the density difference between water and rocks, sand, and mud.

Marine life that have swim bladders (represented in blue) reflect or echo the sound wave back to the vessel. Examples of such marine life include bony fish, myctophids, and zooplankton, as well as the sea floor itself, which has a different density than the sea water.

Image: Cross section example of a Black Sea Bass to show a swim bladder.

an illustrated diagram of the internal anatomy of a bony fish (perhaps a black sea bass). Labels mark the locations of the gills, kidney, swim bladder, urine bladder, gonad, intestine, spleen, stomach, liver, and heart.

If the acoustics team determines there is enough marine life (that they are interested in surveying) to attempt a haul, they will notify the bridge deck and officers that they would like to have the fishing net deployed.

Before an attempted haul, the science team conducts a marine mammal watch for ten minutes. In this time window, several pairs of eyes are observing from the bridge deck and stern for any signs of dolphins, whales, sea lions, seals, and any other marine mammals that are within 500 meters of the vessel. If any marine mammals are spotted within the ten minute observation, we will stand down and wait ten minutes before restarting the marine mammal watch. Net deployment cannot occur until the full observation window has completed.

First haul July 6:
1422-1432 Mammal watch, no marine mammals spotted.
The net deployment started, at which time the vessel continues forward at two knots. Vessel speed increases to three knots when the net is fully deployed with doors and weights in the water, which assist in opening the conical shaped net outwards linearly and laterally. During this time the science team watches displays of the EK80 frequencies and observe the linear width and depth of the net. Scientists can compare these displays to determine if the net is in the correct position to have the best chance of collecting fish.

Hauling back the net occurs after several minutes, at which time the vessel returns to a speed of two knots, and we estimate how many fish were collected. The amount of time in which the net is submerged depends on the depth of the water and acoustic information about the size of the school of fish the net is (hopefully) sampling. After recovery, the haul is deposited into a hopper which feeds onto a conveyor belt in the wet lab, then into large baskets and the wet lab team takes over.

During the first attempt, two sea lions were spotted which required the haul attempt to be paused. We restarted the ten minute marine mammal watch from 1500-1510, the deck department retrieved and reset the net, and the vessel was turned around to return to the start of the noted longitudinal transect. With no marine mammals spotted during the observation period, the second attempt was successful and resulted in:

– 1604-1634: 30 minute haul at 350m depth.

– 11 baskets of Hake collected.

– 4 sample baskets kept at random.

– 541 Hake counted and studied in the wet lab.

Photo: Two deck department members about to open the net to allow the sample to drop into a large collection basket.

Two crewmembers, dressed in orange paints and black and neon yellow coats, face away from the camera, toward a large orange net suspended from above. They may be working to empty the net.

– – ⚓ – –

Personal Log

On July 4 I arrived to pier 30/32 in San Francisco, CA to board NOAA Ship Bell M. Shimada. Although I grew up volunteering on the 441’ WWII Liberty Ship SS John W. Brown in Baltimore, MD, seeing a new ship still resulted in a mix of emotions, nervousness, adrenaline, excitement, and everything in between. After five and a half years, finally seeing the 208’ vessel that would become my home for the next two weeks was a core memory and feeling I will always remember.

NOAA Ship Bell M Shimada in port, as seen from a point on the dock beyond the bow. We can see the NOAA logo and read: NOAA R 227. The water is calm and turqoise; the sky is blue with clouds. A portion of what may be the Golden Gate Bridge is visible in the background.
NOAA Ship Bell M. Shimada docked at Pier 30/32 in San Francisco, CA on July 4

Once onboard, I met Chief Scientist Steve de Blois and Wet Lab Lead Ethan Beyer. I was given a tour of the acoustic, chem, and wet labs and shown to my cabin. After dinner ashore, I joined some of the crew on the flying bridge to watch the July 4th fireworks. I met additional science team members and enjoyed a long night’s rest.

In the morning on July 5, we had a welcome aboard meeting, various trainings, a safety meeting and orientation, fire and abandon ship drills, and a science team meeting. We introduced ourselves, took an official team photo, and soon departed pier 30/32 for our 14 day mission. After passing under the Golden Gate Bridge and heading to the Pacific Ocean, our cold hands were warmed by a wonderful hot dinner of chicken, steak, fresh veggies, salad, and desserts from our galley crew. After dinner, we settled in for our first night at sea, waiting with anticipation for our first trawl on July 6.

– – ⚓ – –

Did You Know?

an orange-gloved hand holds a hake (fish) up so that it faces the camera. We can see the another smaller hake hanging limply across its open mouth

– Hake can be cannibalistic!
– Some larger Hake we have collected have had a smaller Hake in their mouth, throat, or stomach!
– Their very sharp teeth often stick to our thick rubber gloves.

– – ⚓ – –

New Terms/Phrases:

“Salp: Barrel-shaped, planktonic tunicate in the family Salpidae. It moves by contracting, thereby pumping water through its gelatinous body.”

Wikipedia: “Salp

“Myctophid: Lanternfish (or myctophids, from the Greek μυκτήρ myktḗr, “nose” and ophis, “serpent”) are small mesopelagic fish (…) Lanternfishes are aptly named after their conspicuous use of bioluminescence.”

Wikipedia: “Myctophid

Simrad EK80: Multibeam Echo Sounder (MBES) transducer that emits sound waves from the hull of the vessel down to the sea floor. It allows scientists to observe and study returned sound wave signals that may suggest marine life is present.

Transect: Set and numbered longitudinal east-west lines NOAA Ship Bell M. Shimada navigates on while collecting acoustic data.

Karah Nazor: Sorting Protocol and the Ubiquitous Tunicates of the Central CA Coast: Salps and Pyrosomes, May 30, 2019

NOAA Teacher at Sea

Karah Nazor

Aboard NOAA Ship Reuben Lasker

May 29 – June 7, 2019


Mission: Rockfish Recruitment & Ecosystem Assessment

Geographic Area: Central California Coast

Date: May 30, 2019

Last night I fell asleep, twice, at the lab bench in between trawls, since I am still adjusting to being on the night shift.  We worked from 9:00 P.M. to 6:30 A.M. After the shift I had a nice hot shower and slept a solid 9 hours from 7:00 AM to 4:00 PM.  Hopefully, I will be less drowsy tonight!

Upon waking, I went to the galley and grabbed some Raisin Bran and coffee and took it up to the flying bridge to hang out with Ornithologist Brian Hoover.  Our current location is in the middle of the Channel Islands, an area I know something about because my friend Evan Morrison, mentioned in my first blog, helps with the Channel Islands Swimming Association, and I would like to swim between these islands one day.  Lauren Valentino, Flora Cordoleani, Ily Iglesias and I congregated on the flying bridge and decided we should exercise. We joined Flora in her squat challenge (80 squats on this particular day), followed by 5 minutes of planking and a bit of erging.  Half of female members of the fish sorting team are avid rock climbers. They did lots of pull-ups using the rock ring climbing training holds that are installed there.

It felt nice and warm when the ship stopped for deployment of the Conductivity, Temperature and Depth (CTD) Rosette, and it got chilly again as the wind picked up when the ship started moving again. We saw a few whale spouts in the distance and at 5:30 P.M. we went down to the galley for a delicious meal of steak and mashed potatoes.  I am beginning to really appreciate how nice this whole experience has been in terms of amenities. The NOAA Reuben Lasker first set launch in 2014 and is a state of the art fisheries vessel with a sophisticated acoustics lab, fish lab, dynamic positioning system, CTD, etc., but is ALSO equipped with creature comforts including a movie lounge, an ice cream cooler loaded with ice cream sandwiches, snickers, fruit pops, you name it, and my personal favorite – a coffee bar where all coffee is freshly ground, an espresso machine, and all varieties of milk and creamers, including Reese’s cup whipped cream. The mattress in my stateroom bunk is quite comfortable and the shower gets hot within seconds! I doubt it can get much better than this for a research experience at sea?

Game Plan and Trawling Line: Point Sal line with five 15 minute hauls.

I am familiar with the sorting protocol now. The catch is dropped from the net into the bucket by members of the deck crew and survey tech, with the oversight of Keith Sakuma, Chief Scientist and NOAA Operations Officer Keith Hanson.  The bucket is immediately placed in the fish lab and this is when the fish sorting team starts our work.

Cobb Trawl net
Dropping the catch from the Cobb Trawl net into the bucket.
fish on a sorting tray
A volume of fish just placed on a sorting tray. This catch has a lot of anchovies, krill, and California smoothtongues.
Separating the krill
Separating the krill from the myctophids, Northern anchovies, and California smoothtongues.
Sorting fish group photo
Team Red Hats sorting fish. NOAA’s Keith Hanson in the rear left side.


SORTING AND COUNTING METHOD

We start by carefully picking through a 2000 mL or 5000 mL volume of the harvest, depending on Keith Sakuma’s initial assessment of the species density and volume in the bucket.  The first volume of catch to be sorted is evenly dispersed onto four white sorting trays arrayed on the main lab bench. Once you have a pile of the catch on your tray, you start to separate them into piles of different types of organisms, such as Northern anchovies, ctenophores, krill, salps, pyrosomes, Californian smoothtongues, squid, rockfish, myctophids, and young of year (YOY) fish.  I prefer to use my hands for sorting while others use forceps. Once sorted, we count the number of individuals for each species. If we have difficulty identifying an animal that we have not yet seen, we ask Keith Sakuma or a more experienced team member to help with identification. YOY fish, some in larval form, are particularly difficult for me.

Once sorted and counted, we verbally call out the common name and number of organisms to Keith Sakuma who manually records the data in a 3-ring binder for the lab hard-copy.   For smaller organisms, such as krill or salps, or in hauls with a high number of any particular species, it would be quite tedious to pick out and count each individual in the total haul.  This is why we start with a small subsample volume or 0.5, 2 or 5L, count the individuals in that small volume, establish the ratio for the number of individuals in that volume, and then extrapolate and calculate by the total volume of the haul.  For example, if we counted 97 pyrosomes in the initial 5L sort, and we collected a total of 1000L, then we can say that there are 19,400 pyrosomes in the haul.

Chief Scientist Keith Sakuma
Chief Scientist Keith Sakuma recording the data from a haul during sorting.

Once 20 individuals of each species have been called out, we no longer have to count that species since the ratio for this catch has already been established and to expedite sorting the rest of the volume.  Following sorting, the length of the twenty representatives of each species is measured using electronic calipers and the values populate on an Excel spreadsheet. After measuring, specimens requested by various research institutes including Scripps Institution of Oceanography, Moss Landing, and Monterey Bay Aquarium Research Institute (MBARI) are collected, labelled and frozen.

Flora Cordoleani
Flora Cordoleani keeping track of which specimens are to be preserved for various research groups.
Keith Sakuma bagging specimens to send to collaborators.

Creature(s) feature: Salps and Pyrosomes. 

Salps What are these strange gelatinous organisms in our catch that look like little puddles of clear jelly with a red, green, yellow, and brown digestive organ in the center?  They are goopy, small and slippery making them difficult to pick up by hand. They float on the sea surface and are ubiquitous in our hauls BUT NOBODY KNOWS ABOUT THEM.

These creatures are called salps and belong to the subphylum Tunicata. Tunicates have a notochord in their early stage of life which makes them members of the phylum Chordata, to which humans also belong. Having a transparent body is a way escape being preyed upon.

A group of salps. This species is dime to quarter sized and this number of salps occupies a volume of ~10-15 ml once placed in a beaker.
Salp digestive organs.

Salps are planktonic tunicates  That can be found as individual salps or in long chains called blastozooids.   The salps shown in the photo below were individuals and were notable in most of our hauls. Individual salps in this pile are dime to quarter sized and occupy a volume of ~10-15 ml. We measured the volume of salps in every haul.

While on the topic of salps, I will tell you about a cool 1 inch long salp parasite I found on my sorting tray (see image below). Keith Sakuma explained that it was a deep sea amphipod called Phronima which is a parasitoid that takes up residence inside of a salp’s body, eats the salp’s organs, and then lays its eggs inside of the salp. The King-of-the-salmon, Trachipterus altivelis, (which we are also catching) uses its protrusible jaw to get inside of the salp just to eat this amphipod!

Phronima amphipod
Phronima amphipod – lives and reproduced in salp after eating the salp’s organs. King-of-the-salmon fish use their protrusible jaws to eat the amphipod.
King-of-the-salmon
King-of-the-salmon, Trachipterus altivelis
King-of-the-salmon jaw protruded
King-of-the-salmon, Trachipterus altivelis, who preys upon phronima living inside of salp, with jaw protruded.
A large haul full of salps.

Another type of salp we keep catching is Thetys vagina, a large solitary species of nektonic salp that feeds on plankton, such as diatoms, and is an important carbon sink in the ocean. Thetys has an external surface, or test, that is covered with bumps and ridges, as seen in the photo below.

Thetys vagina, the twin-sailed salp.
Thetys vagina, the twin-sailed salp.
internal filtering organ
The internal filtering organ of Thetys vagina.
Kristin Saksa examining a larger Thetys
Kristin Saksa examining a larger Thetys vagina, or the twin-sailed salp. The dark colored tentacles are downward facing. This is the siphon where water enters the sac-filled body.

Pyrosomes Pyrosoma atlanticum are another type of planktonic tunicate which are very numerous in most of our hauls. Pyrosomes look like bumpy pink hollow tubes with openings on both ends. They are rigid in structure and easy to pick up by hand, whereas salps are goopy and difficult to pick up by hand.  We have collected some pyrosomes that are 13 inches long, while most are in the 4-6 inch range. The small pyrosomes look like clear Tic Tacs, but they do not taste as such.

Pyrosoma atlanticum
Pyrosoma atlanticum, with an ~6 inch specimen on the left and small pyrosomes on the right.

How can pyrosomes be so ubiquitous just 20 miles or so off of the Central California Coast, but I have never seen one that has floated up on the beach or while swimming?

Pyrosoma atlanticum are also planktonic tunicates, but are colonial organisms made up of many zooids held together by a gelatinous structure called the tunic. One end of the tube is wide open and filters the water for zooplankton and phytoplankton, while the other end is tighter and resembles a diaphragm or sphincter. The pyrosomes we harvested appeared in diverse array of pinks and purples.  Pyrosomes are believed to harbor intracellular bioluminescent bacteria. Pyrosomes are drifting organisms that swim by beating cilia lining the branchial basket to propel the animals through the water and create a current for filter feeding. 

Pyrosome rainbow
Pyrosoma atlanticum assorted by color.
Kristin Saksa
Moss Landing Graduate Student Kristin Saksa excited about the large haul of Pyrosoma atlanticum.
high-five
Pyrosoma atlanticum high-five.

Julia West: Science Is About the Details, March 29, 2015

NOAA Teacher at Sea
Julia West
Aboard NOAA ship Gordon Gunter
March 17 – April 2, 2015

Mission: Winter Plankton Survey
Geographic area of cruise: Gulf of Mexico
Date: March 29, 2015

Weather Data from the Bridge

Time 1600; clouds 35%, cumulus; wind 170 (S), 18 knots; waves 5-6 ft; sea temp 24°C; air temp 23°C

Science and Technology Log

We have completed our stations in the western Gulf! Now we are steaming back to the east to pick up some stations they had to skip in the last leg of the research cruise, because of bad weather. It’s going to be a rough couple of days back, with a strong south wind, hence the odd course we’re taking (dotted line). Here’s the updated map:

sampling stations 3/29/15
Here’s where we are as of the afternoon of 3/29 (the end of the solid red line. We’ve connected all the dots!

 

I had a question come up: How many types of plankton are there? Well, that depends what you call a “type.” This brings up a discussion on taxonomy and Latin (scientific) names. The scientists on board, especially the invertebrate scientists, often don’t even know the common name for an organism. Scientific names are a common language used everywhere in the world. A brief look into taxonomic categories will help explain. When we are talking about numbers, are we talking the number of families? Genera? Species? Sometimes all that is of interest are the family names, and we don’t need to get more detailed for the purposes of this research. Sometimes specific species are of interest; this is true for fish and invertebrates (shrimp and crabs) that we eat. Suffice it to say, there are many, many types of plankton!

Another question asks what the plankton do at night, without sunlight. Phytoplankton (algae, diatoms, dinoflagellates – think of them like the plants of the sea) are the organisms that need sunlight to grow, and they don’t migrate much. The larval fish are visual feeders. In a previous post I explained that they haven’t developed their lateral line system yet, so they need to see to eat. They will stay where they can see their food. Many zooplankton migrate vertically to feed during the night when it is safer, to avoid predators. There are other reasons for vertical migration, such as metabolic reasons, potential UV light damage, etc.

Vertical migration plays a really important role in nutrient cycling. Zooplankton come up and eat large amounts of food at night, and return to the depths during the day, where they defecate “fecal pellets.” These fecal pellets wouldn’t get to the deep ocean nearly as fast if they weren’t transported by migrating zooplankton. Thus, migration is a very important process in the transport of nutrients to the deep ocean. In fact, one of the most voracious plankton feeders are salps, and we just happened to catch one! Salps will sink 800 meters after feeding at night!

Salp
Salp caught in the neuston sample. Salps are a colony of tunicates (invertebrate chordates for you biology students – more closely related to humans than shrimp are!)

Now it’s time to go back into the dry lab and talk about what happens in there. I’ll start with the chlorophyll analysis. In the last post I described fluorescence as being an indicator of chlorophyll content. What exactly is fluorescence? It is the absorption and subsequent emission of light (usually of a different wavelength) by living or nonliving things. You may have heard the term phosphorescence, or better yet, seen the waves light up with a beautiful mysterious light at night. Fluorescence and phosphorescence are similar, but fluorescence happens simultaneously with the light absorption. If it happens after there is no light input (like at night), it’s called phosphorescence.

phosphorescence
An example of phosphorescence. We haven’t seen it yet, but I hope to! (From eco-adventureholidays.co.uk)

Well, it is not just phytoplankton that fluoresce – other things do also, so to get a more accurate assessment of the amount of phytoplankton, we measure the chlorophyll-a in our niskin bottle samples. Chlorophyll-a is the most abundant type of chlorophyll.

We put the samples in dark bottles. Light allows photosynthesis, and when phytoplankton (or plants) can photosynthesize, they can grow. We don’t want our samples to change after we collect them. For this same reason, we also process the samples in a dark room. I won’t be able to get pictures of the work in action, but here are some photos of where we do this.

chlorophyll lab
This is the room where we do the chlorophyll readings.

We filter the chlorophyll out of the samples using this vacuum filter:

chlorophyll filter
Each of these funnels filters the sea water through a very fine filter paper to capture the chlorophyll.

The filter papers are placed in test tubes with methanol, and refrigerated for 24 hours or so. Then the test tubes are put in a centrifuge to separate the chlorophyll from the filter paper.

filter paper for chlorophyll
Some of the test tubes for chlorophyll readings, and the filter paper. This box costs about $100!

The chlorophyll values are read in this fancy machine. Hopefully the values will be similar to those values obtained during the CTD scan. I’ll describe that next.

Fluorometer
This fluorometer reads chlorophyll levels.

While the nets and CTD are being deployed and recovered, one person in the team is monitoring and controlling the whole event on the computer. I got to be this person a few times, and while you are learning, it is stressful! You don’t want to forget a step. Telling the winch operator to stop the bongos or CTD just above the bottom (and not hit bottom) is challenging, as is capturing the “chlorophyll max” by stopping the CTD at just the right place in the water column.

Bongo graph
This is the graph that comes back from the SeaCAT on the bongo. We are interested in the green line, which shows depth as it goes down and comes back up.

The dry lab
Here I am trying my hand at the computers. The monitor on the left is the live video of what is happening on deck (see the neuston net?). Photo by A.L. VanCampen

 

CTD scan
This is the CTD graph after it has been completed. The left (magenta) line is the chlorophyll, and the horizontal red lines are where we have fired a bottle and collected a sample. Notice the little spike partway down. That is the chlorophyll max, and we try to capture that when bringing it back up. The colored chart shows columns of continuous data coming in.

Here’s another micrograph of larval fish. Notice the tongue fish, the big one on the right. It is a flatfish, related to flounder. See the two eyes on one side of its head? Flatfish lie on the bottom, and have no need for an eye facing the bottom. When they are juveniles, they have an eye on each side, and one of the eyes migrates to the other side, so they have two eyes on one side! Be sure to take the challenge in the caption!

Larval fish 2
There is a cutlass fish just right of center. Can you find the other one? How about the lizard fish? Hint – look back at the picture in the last post. Photo credit Pamela Bond/NOAA

Personal Log

It’s time to introduce our intrepid leader, Commanding Officer Donn Pratt, known as CO around here. CO lives (when not aboard the Gunter) in Bellingham, WA. He got his start in boats as a kid, starting early working on crab boats. He spent 9 years with the US Coast Guard, where he had a variety of assignments. In 2001, CO transferred to NOAA, while simultaneously serving in the US Navy Reserve. CO is not a commissioned NOAA officer; he went about his training in a different way, and is one of two US Merchant Marine Officers in the NOAA fleet. He worked as XO for about seven years on various ships, and last year he became CO of the Gordon Gunter.

CO is well known on the Gunter for having strong opinions, especially about food and music. He loves being captain for fish research, but will not eat fish (nor sweet potatoes for that matter). A common theme of meal conversations is music; CO plays drums and guitar and is a self-described “music snob.” We have fun talking about various bands, new and old.

CO Donn Pratt
CO Don Pratt on the bridge.

One of the most experienced and highly respected of our crew is Jerome Taylor, our Chief Boatswain (pronounced “bosun”). Jerome is the leader of the deck crew. He keeps things running smoothly. As I watch Jerome walk around in his cheerful and hardworking manner, he is always looking, always checking every little thing. Each nut and bolt, each patch of rust that needs attention – Jerome doesn’t miss a thing. He knows this ship inside and out. He is a master of safety. As he teaches the newer guys how to run the winch, his mannerism is one of mutual respect, fun and serious at the same time.

Jerome has been with NOAA for 30 years now, and on the Gunter since NOAA acquired the ship in 1998. He lives right in Pascagoula, MS. I’ve only been here less than two weeks, but I can see what a great leader he is. When I grow up, I want to be like Jerome!

Jerome Taylor
Chief Bosun Jerome Taylor, refusing to look at the camera. No, he’s not grilling steaks; he’s operating the winch!

 

Challenge Yourself!

OK, y’all (yes, I’m in the south), I have a math problem for you! Remember, in the post where I described the bongos, I showed the flowmeter, and described how the volume of water filtered can be calculated? Let’s practice. The volume of water filtered is the area of the opening x the “length” of the stream of water flowing through the bongo.

V = area x length.

Remember how to calculate the area of a circle? I’ll let you review that on your own. The diameter (not radius) of a bongo net is 60 cm. We need the area in square meters, not cm. Can you make the conversion? (Hint: convert the radius to meters before you calculate.)

Now, that flow meter is just a counter that ticks off numbers as it spins. In order to make that a usable number, we need to know how much distance each “click” is. So we have R, the rotor constant. It is .02687m.

R = .02687m

Here’s the formula:

Volume(m3) = Area(m2) x R(Fe – Fs) m

Fe = Ending flowmeter value; Fs = Starting flowmeter value

The right bongo net on one of the stations this morning had a starting flowmeter value of 031002. The ending flowmeter value was 068242.

You take it from here! What is the volume of water that went through the right bongo net this morning? If you get it right, I’ll buy you an ice cream cone next time I see you! 🙂

sunset
Sunset from the Gordon Gunter as we are heading east.

 

Mary Anne Pella-Donnelly, September 18, 2008

NOAA Teacher at Sea
Mary Anne Pella-Donnelly
Onboard NOAA Ship David Jordan Starr
September 8-22, 2008

Mission: Leatherback Use of Temperate Habitats (LUTH) Survey
Geographical Area: Pacific Ocean –San Francisco to San Diego
Date: September 18, 2008

Weather Data from the Bridge 
Latitude: 3543.3896 N Longitude: 12408.3432 W
Wind Direction: 129 (compass reading) SE
Wind Speed: 7.8 knots
Surface Temperature: 17.545

Blue shark seen on 9/18
Blue shark seen on 9/18

Science and Technology Log 

Today was an exciting one scientifically. The team has been examining all of the oceanographic data so far in order to pinpoint frontal edges for further data collection. They selected a point last night that might contain a biologically rich layer and hopefully, with jellies. After closely looking over every thing they have learned on this trip so far and plotting a destination to sample, we traveled to that station. We found an ocean water ‘river’ full of kelp, moon jellies, sea nettles and pelagic birds! It was exactly where the team predicted there might be a biotic stream!! This confirmed that offshore habitats can be found using oceanographic data and satellite imaging.  There certainly were offshore areas that would give leatherbacks a chance to eat their fill.  And through that period, the sun came up!  With only a slight breeze, the flying deck was warm and relaxing. It put us all into excellent spirits.

Personal Log 

Ray Capati shows off his Turtle Cake. (photo by Karin Forney)
Ray Capati shows off his Turtle Cake.

A few days ago, the chief steward made a cake- there are daily baked goods offered in the mess hall. This cake, however, was decorated for the LUTH Survey with turtles, kelp and jellyfish!  Today would have been another good day for that treat.  It is also time to get some pictures with C.J. our school mascot.  He was pretty happy to get out and see the ship.  He even tried to help up on the flying bridge, but without thumbs, it was hard for him to enter in observation comments.

Animals Seen Today 
Moon jellies Aurelia labiata, Sea nettle jellies Chrysaora fuscescens, Salps Salpida spp., Sea gooseberries Pleurobrachia bachei, Red phalaropes Phalaropus fulicaria, Cuvier’s beaked whales Ziphius cavirostris, Common dolphins Delphinus delphis, Blue sharks Prionace glauca, and Arctic terns Sterna paradisaea.

C.J. helps out on the flying bridge.
C.J. helps out on the flying bridge.

Questions of the Day 

  1. What might be some oceanographic conditions that would create a water mass filled with kelp and jellyfish?
  2. What other organisms (than we observed) might be attracted to such a water mass?

Rebecca Bell, August 16, 2008

NOAA Teacher at Sea
Rebecca Bell
Onboard NOAA Ship Delaware II 
August 14-28, 2008

Mission: Ecosystems Monitoring Survey
Geographical Area: North Atlantic
Date: August 16, 2008

Weather Data from the Bridge 
Time:   1807 (GMT)
Latitude:  36.05.40 N Longitude: 75.24.30 W
Air Temp 0C: 25.3 0C
Sea Water Temp:  26.7 0C

On left: small barrel-shaped copepods; Center: white, arrow worms; Top right: amphipods
On left: small barrel-shaped copepods; Center: white, arrow worms; Top right: amphipods

Science and Technology Log 

The most common zooplankton we have seen so far are salps, amphipods, arrow worms and copepods. Pteropods (sea butterfly) have been in a number of samples but are not numerous. Salps look like clear, jelly-like marbles. We’ve encountered these animals in warm, shallow water. They are holoplanktonic relatives of sea squirts (Urochordata). Salps are filter feeders, using cilia to move suspended particles from the water. They feed by pumping water through a sieve to remove bacteria and nanoplankton, and are thus, a very important link in the food chain. Some species of salps form huge chains by budding. They show both sexual and asexual life stages. For more about salps and photos see this website.

Amphipods are also extremely common crustaceans. There is no carapace (shell-like covering), but their bodies are flattened side-to-side, much like a shrimp.  Their bodies are segmented with 6 segments in the head, 8 in the thorax and 6 in the abdomen.1 They have a brood pouch on their thoracic limbs. They have a variety of limbs used for feeding, crawling or jumping. One group lives off a host, feeding on salp tissues. Some types live in tubes; others use their back legs to anchor themselves while they sway to and fro in the water column. Some species swim rapidly while others stay near the bottom of the ocean. Many will move vertically in the water column, moving near the surface during the day, and sinking again at night. The species we are catching has large compound eyes that can be seen by the naked eye. For more about amphipods, visit this website. 

Becky examines the catch using a hand lens.
Becky examines the catch using a hand lens.

Copepods are very common crustaceans, with more than 200 species and 10,000 families. 2 We have found more of these than any other organism. Copepods are omnivorous. Some groups graze on microplankton; other groups of copepods prey on larger plankton, including other copepods. They are an important link in the food chain as well, moving carbon from a microscopic level to a larger trophic (feeding) level. They are eaten by jellyfish, fish, comb jellies and arrow worms. Copepods have “antennae” that have special sensors that detect water movement around them. They are able to move toward prey by contracting a muscle that runs in a circle around their bodies. For more about copepods, visit this website.

Arrow worms (Chaetognatha) are common along coasts, but we did not catch any out away from shore. Arrow worms are classified in their own group, distinct from Annelids (earthworms), round worms and flatworms, which are all separate groups of worms. They are predators, often waiting to ambush their prey. When their cilia detect prey, usually copepods, the arrow worm contracts 2 muscles that run dorsally and ventrally (top to bottom) to strike. Their mouths have spines that grab the prey and smaller “teeth” produce a venom that subdues the prey. The prey is swallowed whole. Arrow worms, in turn, are eaten by jellyfish, copepods and fish.

Sea Butterflies were not common, but they are very interesting. Sea butterflies (pteropods) are holoplanktonic mollusks, related to snails. Basically, they are shell-less snails. Their foot is modified into winglike structures (ptero= winged) that they flap as they swim through the water. Their bodies are tube-shaped and clear. The bodies and wings of the species we have seen are an orange-pink color. They are predators and are preyed upon by fish, sea birds and whales.

References: 

Information for these paragraphs were modified and combined from the following sources: 1 Newell, G.E. and Newell, R.C.; Marine Plankton: A Practical Guide; 5th edition; 1977; Hutchinson & Co; London.2 Johnson, William S. and Allen, Dennis M.; Zooplankton of the Atlantic and Gulf Coasts: A Guide to Their Identification and Ecology; 2005; Johns Hopkins University Press.

Personal Log 

This morning we saw dark clouds in the distance. You could see rain falling from the clouds. Nearby we could see the tail of a water spout disappearing into the clouds.  We sampled our southern-most station and are now heading north along the coast just south of Chesapeake Bay. The samples we are pulling now have a lot of diatoms.

Rebecca Bell, August 15, 2008

NOAA Teacher at Sea
Rebecca Bell
Onboard NOAA Ship Delaware II 
August 14-28, 2008

Mission: Ecosystems Monitoring Survey
Geographical Area: North Atlantic
Date: August 15, 2008

Weather Data from the Bridge 
Latitude:  3846.7 Longitude: 7302.1
Temp 25.4 C

Bongo net
Bongo net

Science and Technology Log 

In the last post, I explained WHY we are collecting zooplankton. This post will illustrate HOW the samples are taken.

The samples are collected using a device called a bongo net (Yes, like the musical instrument).  You can see the metal rings and the nets hang from the metal rings. One net is marked with red and the other green. This allows you to tell the two nets apart. The samples from the red side will be used for the ichthyoplankton study. The samples from the green side will be used for the zooplankton study.

The white device is the CTD (Conductivity, Temperature, Depth). You attach it to the bongo net frame and turn it on. The CTD takes measurements on the way into the water and on the way out of the water. When the bridge clears you, the computer operator (inside) tells the hydraulics operator to start letting out the line and at what speed to let it out and bring it in. You calculate the amount of time in and out using a chart that is based on changing depth. You have to calculate it so you get at least a 5-minute tow.

The CTD
The CTD

Now the bongo nets are raised on the A-frame. You can see the CTD above the bongos (right picture) and there is a lead weight beneath and between the nets. Next, the A-frame moves the nets over the side of the ship and they are lowered into the water. You cruise for at least 5 minutes. The idea is to get within 5 meters of the bottom, then start bringing the nets back in. The computer operator keeps track of where the bottom is. The idea is to stop the line going out in time so the nets don’t hit the bottom and pull up a bunch of sand. Then you just have to wait for the tow, and eventually for the nets to come back up.

The bongos are removed from the A-frame and brought into the wet lab. You use the hose to wash the plankton down to the bottom of the net. The bottom of the net is put into the sieve. When the net is hosed down to the sieve end, you untie the bottom of the net and let the plankton wash into the sieves. The mesh captures zooplankton, but lets smaller phytoplankton through. Finally you rinse the plankton from the sieves into a jar with 5% formalin for preservation. A label is put into the jar as well as on top of the jar, stating station number, date and time.

NOAA Teacher at Sea, Becky Bell, assists in deploying the bongo nets.
NOAA Teacher at Sea, Becky Bell, assists in deploying the bongo nets.

Personal Log 

We had a fire drill and an “abandon ship” safety drill. In the picture to the right, I am wearing a survival suit, lovingly known as a “Gumby suit”. If you abandon ship, you have to run to the deck and put on this suit. It is one piece, with inflatable neck rest, whistle and flashing pocket light so you can be spotted. You have to lay the suit out on deck, and sit down in it. Feet go in first, then you stand up and pull the rest over your head, find the arms etc. Look at the look on my face. Not too sure about this! The front flap closes to show only your eyes–on me a little higher. You should try zipping the front zipper with thick rubber gloves that are too big for you. It reminds me of the astronauts trying to fix the space station. I have a new appreciation for how difficult it is too, like, HOLD anything. The best news yet–we get to practice next week again.

Deploying the Bongo net
Deploying the Bongo net

The A-frame
The A-frame

The nets begin to emerge from the water.
The nets begin to emerge from the water.

Becky waits for the nets to come back up after the tow
Waiting for the nets to come back up after the tow

Becky rinsing down the net
Becky rinsing down the net

Then she puts the plankton into a jar for preservation
Then she puts the plankton into a jar for
preservation

Becky dons her survival suit during a safety drill.
Becky dons her survival suit during a safety drill.

 

Rebecca Bell, August 14, 2008

NOAA Teacher at Sea
Rebecca Bell
Onboard NOAA Ship Delaware II 
August 14-28, 2008

Mission: Ecosystems Monitoring Survey
Geographical Area: North Atlantic
Date: August 14, 2008

Weather Data from the Bridge 
Time:   134628 (GMT)
Latitude:  40.33.06N Longitude: 72.47.36W
Air Temp 0C: 22.1
Sea Water Temp:  22.3 0C

NOAA Ship Delaware II
NOAA Ship Delaware II

Science and Technology Log 

We sailed from Woods Hole, MA on Wednesday, August 13, 2008 on the first of three legs as part of the Ecosystem Monitoring Program. There are two main objectives of the cruise. The first is to see how well the fish population is doing by sampling and counting fish larvae. The number of fish is important to the fisheries industry- those folks who bring cod and other fish to your table. The second objective is to monitor the zooplankton population. Fish feed on the zooplankton, so a healthy zooplankton population may mean a healthier fish population. We also are monitoring the physical properties of the water; in this case, salinity and temperature. These influence where fish larvae and zooplankton can survive and where and how far they can be dispersed.

There are 125-130 sites randomly selected for sampling. At each site, a pair of bongo nets are dropped and the two samples are collected side-by-side, for a total of 250-260 samples. One sample is designated for the ichthyoplankton (fish larvae) study, and the other for the study of zooplankton composition, abundance and distribution. Near-surface along-track chlorophyll-a fluorescence, which indicates abundance of phytoplankton (i.e. food for the zooplankton), water temperature and salinity are constantly measured with the vessel’s flow-through sampling system. We will also be collecting a separate set of samples as we approach the Chesapeake Bay. These will be used to study aging of fish larvae.

Zooplankton include both unicellular and multicellular organisms. Many can easily be seen with the naked eye. Zooplankton can be classified in a number of ways. One way is to classify them by life history. Holoplankton are those that are planktonic during their entire life cycle (lifers). Meroplankton refers to those plankton in a developmental stage, like eggs and larvae (shorttimers). These larvae will grow into larger organisms such as jellyfish, mollusks, fish, starfish and sea urchins, crustaceans, copepods and amphipods.

The term “plankton” comes from a Greek word for “wanderer” or “drifter”.1 This may imply that these organisms are passively moved about by currents. However, many can power around on their own, using several different methods such as cilia, muscle contraction, or appendages on the head, thorax or abdomen. They also move vertically in the water column, up toward sunlight during daylight hours and downward at night. Krill (whale food), on the other hand, do the opposite- travel downward during the day and up at night.

The first two samples contained a vast number of salps. A salp is holoplanktonic and is related to sea squirts (urochordates). They are filter feeders, catching bacteria and extremely small plankton in mucous-covered “nets” that act as sieves. Salps are an important part of the ocean food chain.

Samples 3-5 show a greater variety of organisms- comb jellies (ctenophores), arrow worms (Chaetognatha) fish larvae and amphipods. Samples 6-8 are dominated by copepods. There are salps, too, but not nearly as many (about 1/3 fewer) as we saw in the first 2 samples.

So I am looking at these results and wondering: Are there patterns to the distribution of these assemblages? Are salps found in warm water or cooler water?  Does temperature matter at all? Do they like deeper water?  Higher or lower salinity? Combinations of any of these? Are they found where another organism is found?

Personal Log 

We began our first work shift today, er, last night, um, this morning at 3 a.m. I work the 3 a.m. to 3 p.m. shift. That means to bed around 7pm., rise and shine at 2:30 a.m. Well, rise, anyway. Not much shining till later.

As I sat on the deck in darkness, waiting to reach our first sample site, I spotted the light from another ship on the horizon. I watched as the light traveled up a wave, then down a wave then up, up, up, up, still up. I could not believe how high it was going, knowing we were doing the same thing. It’s a good thing it doesn’t feel like that. We are now heading south, back towards the Chesapeake Bay. It is getting hotter and muggier, just like home.

We saw dolphins today. A large leatherback turtle was spotted from the bridge. The 3pm- 3am. shift reported seeing flying fish.

Animals Seen Today 

  • Salps
  • Amphipods
  • Copepods
  • Ctenophores
  • Chaetognaths (arrow worms)
  • Fish larvae
  • Sea butterfly
  • Dolphins
  • Gulls (4 species)

1 Source: Online Etymology Dictionarywww.etymologyonline.com.