Trevor Hance: Water, Water Everywhere… Time for a Bath(ology), June 17, 2015

NOAA Teacher at Sea
Trevor Hance
Aboard R/V Hugh R. Sharp
June 12 – 24, 2015

Mission: Sea Scallop Survey
Geographical area: New England/Georges Bank
Date: June 17, 2015

Science and Technology Log

We’re now at the half-way point of this journey and things continue to run well, although the weather has picked up a bit.  I mentioned to one of my fellow crew members that the cloud cover and cool weather reminded me of “football and gumbo” and he said, “Yeah… around here, we just call it ‘June’.” Touché, my friend.

“June,” huh…. Hey, this guy got jokes!

I am continually impressed by both the ship’s crew and the science party’s ability to identify work that needs to be done and set a course towards continued, uninterrupted success of the mission.  The depth and breadth of knowledge required to navigate (all puns intended!) extended scientific expeditions requires professional dedication matched with a healthy sense of humor, and it is truly an honor to be invited to participate in this unique opportunity for teachers. I am learning volumes each day and will forever treasure this wonderful adventure.  Thanks again, NOAA!

Remember students, don’t kiss frogs.  Gigantic lobsters?  Well…
Remember students, don’t kiss frogs. Gigantic lobsters? Well…

Science and Math

My instructional path is rooted in constructivist learning theory, and I work diligently to secure resources for my students to have authentic, project-based learning experiences where they determine budgets, necessary tools and physically build things that we use on our campus.

Most recently, my math class designed and built some raised mobile garden beds that will be used by the youngest students on our campus as well as those with unique mobility challenges.  Through these hands-on learning experiences, I expect my students to develop a solid working-level of mathematic and scientific literacy, and I’m proud of the fact that when I present a new concept, my students never ask “When am I going to have to use this in real life?”

My students doing math.  More doing, more learning...
My students doing math. More doing, more learning…

I believe fifth grade students can understand any science concept, and I am seeing additional opportunities to test that idea using what I learn out here, so thought I’d share a few examples of some of the things I’ve learned as they will be presented in my G5 classroom starting this fall.

With a basic understanding of the objective for this survey presented in the last blog, I’ll explore some of the geographic and hydrodynamic concepts associated with this part of the world in this post.  In the next blog, I’ll dive deeper into a specific study of scallops and lobsters, and in the fourth post I’ll talk more about the effects of current marine/fisheries management practices, with particular focus on those relating to closed areas (somewhat akin to the Balcones Preserve behind our campus.)

This is a Sculpin Longhorn, distantly related to BEVO
This is a Sculpin Longhorn, distantly related to BEVO

Georges Bank…water, water everywhere, time for a bath(ology)

We all know that water is central to our survival, and “playing” with water provides a strong anchoring point (am I pushing the puns too far?) for understanding systems relationships as students progress through their educational path.  For the past couple of years, I have been accepted to participate in a “Scientist in Residence” program offered through the University of Texas’ Environmental Science Institute, which pairs local teachers with a graduate level scientist for an entire school year.  In my first year, I was paired with (recently graduated) Dr. Kevin Befus, whose work focuses on hydrology.  Through my work with Kevin (note to students:  I can call him Kevin, you call him Dr. – he’s earned it!), I learned much about water and the importance of “flow,” and when you understand some of the “flow” relating the world’s most productive fishery, Georges Bank, I think you’ll agree with me.

Dolphin splashin’, getting everybody all wet
Dolphin splashin’, getting everybody all wet

Georges Bank is an oval shaped shoal, which is essentially a submerged island that lies about 60 miles off the coast of Cape Cod, and covers nearly 150 square miles.  “The Bank,” or “Georges,” as many people aboard the vessel refer to it, is only recently submerged (i.e. – within the last 100,000 years).  As recently as ten years ago scientists found mastodon tusks on the Bank, and legend holds that in the early 1900s, fishing vessels would stop on an island in Georges Bank (now submerged to about 10m) and play baseball (note:  I have yet to find a bat and ball aboard the Sharp, but hope remains!)

Just like good soil helps support plant life, good water helps support marine life, and the key to the abundant life along Georges Bank lies in the nutrient rich water that is pushed towards the surface as it approaches Georges from the north and south.  On three sides of Georges Bank, the sea floor drops dramatically.  To the north sits the Gulf of Maine, which drops to approximately 1000m deep, and to the east and south, the Atlantic Ocean quickly reaches depths of over 2500m.

NASA photo
NASA photo

Almost all water enters Georges Bank from the north via the Gulf of Maine. The Gulf of Maine is fed via natural river discharges (including those from the Damariscotta and Merrimack Rivers) and the Labrador Currents that hug the coastline south around Nova Scotia before turning west into the Gulf of Maine.  Water also enters the Gulf of Maine through The North Channel on the east side of Maine from the Gulf Stream and that very salty, warm water is important, particularly when it comes to the biology of Georges Bank (as we’ll look at more in the next blog entry.)

Much of the water exiting the Gulf of Maine enters The Great South Channel, which is something like a “river in the ocean” that runs between Cape Cod and Georges Bank.  Deep within the Channel is a “sill,” which is a type of landform barrier, similar to a fence that doesn’t reach up to the surface.  The sill rises quickly from the sea floor and extends across the Great South Channel, effectively blocking the deepest, densest water, resulting in strong, deep, cold currents that are pushed east around the outer edge of Georges Bank before returning towards the United States’ east coast in a clockwise path, resembling “from 11 until 7” on a clock’s face.  Yes students, I do mean an analog clock!

After the deep currents make their way back to southern Massachusetts, they head south on the Longshore Coastal Current, which is like a “jet” of water that sprints southbound right along the eastern United States coastline (note:  those of us from the Gulf Coast frequently hear friends wonder why the Atlantic Ocean is so cold when they visit Florida, and this is partly why!)

At this point, I’m going to take a moment and speak directly to my students:   Just as the water flows into and mixes at Georges Bank from different directions, I’m hopeful that your thoughts are starting to swirl as you recognize the connection to concepts we have studied relating to energy, weather and climate, mixtures and solutions, salinity (and conductivity/resisitivity) and density (and buoyancy) – they are all evident and part of this story! And YES — this WILL be on the test!

b3g - 4 shells
I pulled these four scallops from one of our dredges to show the unique, beautiful patterns we find while sorting

While the deep-water currents that circle around Georges Bank’s edges exist year-round, in the winter there isn’t tremendous difference in the three primary water measurements (“Conductivity, Temperature and Density,” or “CTD”) between the water in The Great South Channel versus that sitting atop Georges Bank.  As you might recognize, in normal conditions, there shouldn’t be much cause for warm or fresh water to be added to the area during the cold winter months, as our part of the world seems to slow down and a goodly amount of water freezes.  In the spring, however, the northern hemisphere warms and ice melts, adding lots of warmer-and-fresh water to the Labrador Current and river discharges I mentioned above, ultimately sending that water south towards Georges Bank.  At this point, things get really interesting…

The new, warmer water is less dense than the deeper water. The warm and cold water ultimately completely decouple and become fully stratified (i.e. – there are two distinct layers of water sitting one on top of the other.)  The stratified layers move in separate currents:  the deeper, colder, more-dense layer continues its clockwise, circular path along the outer edge of the Bank before heading south; and the top, “lighter” layer gets “trapped” in a clockwise “gyre,” which is the formal word for a swirling “racetrack” of a current that sits on the Bank. This gyre goes full-circle atop Georges Bank approximately 2.5 to 3 times per summer season.

Bigelow and Bumpus:  Going with the Flow

The stratified/gyre relationship was confirmed almost 90 years ago by Henry Bigelow (note: those familiar with NOAA will no doubt recognize his name for several reasons, including the fact that a ship in the NOAA fleet is named after him).  Essentially, Bigelow used a type of “weighted-kite-and-floating-buoy” system to observe and confirm the two layers.  Bigelow’s “floating-buoy” was tied to the “weighted-kite” (actually called a drogue) and set at various depths, with each depth tested as an independent variable.  Once set, Bigelow drogued the water, chasing after the floats-and-kites, ultimately confirming that the stratified currents did in fact exist.  When you look at our dry lab here on the Sharp, complete with dozens of computers constantly monitoring hundreds of variables, Bigelow’s paper-and-pencil study aboard a 3-masted schooner is pretty awesome, and makes me feel a little lazy!

Source:  Bigelow, HB (1927): Physical Oceanography of the Gulf of Maine
Source:  Bigelow, HB (1927): Physical Oceanography of the Gulf of Maine

In a different study conducted later in the 1900s that perhaps might evoke romantic images of the sea, physical oceanographer Dean Bumpus performed a study similar to Bigelow’s, but in a slightly different fashion. Over the course of a few years, Bumpus put notes in over 3,000,000 test-tubes and set them adrift from Georges Bank.  The notes provided instructions on how to contact Bumpus if found, and he used the returned notes to determine things like current speed and direction.  While I’m not sure if Bumpus also used this methodology to find true love, the experiment did reinforce the idea of the currents that exist around Georges Bank!

b3i - Bumpus

Yep, it’s pretty cool to hear stories of those old-school scientists getting their names in the history books by just going with the flow.

Gulf Coast Style Kicking It Up North

One other unique hydrologic influence on Georges Bank relates to “meanderings” by the Gulf Stream.  Normally, as the Longshore Coastal Current sprints southbound along the east coast faster than a recent retiree snowbirding to Florida, a little further offshore, the Gulf Stream is heading north, bringing with it warm water.  As the water moves towards Georges Bank, the bank does its thing, acting as a berm (my BMX students might better identify with that term), and pushes that water off towards the east.  The warm water ultimately reaches England, and when mixed with the cool air there, causes the cloudy conditions and fog we frequently associate with life in the U.K.

Shark!
Shark!

The unique aspect of this relationship occurs when, from time to time, the Gulf Stream misses the turn and a “slice” of the Gulf Stream breaks away.  When this happen, the split portion spins in a counter clockwise fashion and breaks into Georges Bank, bringing with it warm water — and all the chemistry and biology that comes with it.  More on that later…

Water Summary 

So, in a nutshell, that’s the system.  The coldest water at the headwaters of rivers in Maine and that in the arctic freezes and becomes ice.  Deep water doesn’t have access to the warm sunlight, so it stays colder than the warm, less dense water at the surface that is hoping for the chance to boil over and soar up into the skies as water vapor.  Newton tells us that things like to stay still, but will stay in motion once they get started.  Things like sills and submerged islands get in the way of flowing water (yeah, more Newton here), resulting in mixtures and unique current patterns.

From a biological standpoint, the traditional currents associated with Georges Bank bring the deep, nutrient rich waters to the surface. As that water is pushed to the surface, algae and phytoplankton grow in great numbers.  Phytoplankton attracts zooplankton, fish larvae eat the zooplankton, and eventually, “circle gets a square,” the trophic pyramid is complete, and nature finds its equilibrium.

If only it was that easy, right?

Unfortunately, the frequency of warmer weather over the past century has had an impact on the ecology of Georges Bank.  Scientists have noticed more warm water from the north as ice continues to melt and increased frequency of the Gulf Stream meandering from the south. I’m told that 20 years ago, Red Hake were rare here, but I’ve noticed very few of our dredges where Red Hake weren’t at least the plurality, if not majority, of fish we caught.  As Mr. Dylan says, “the times, they are a changin’.”

Okay.  That’s it!  Congratulations students! You have passed Oceanography: Hydrodynamics Short Course 101 and it is time to move on to Oceanography:  Shellfish Biology 101, which we will cover in the next blog.

My students get scribbled maps like this from me all the time. I didn’t draw this one, but it did make me feel good about my methods!
My students get scribbled maps like this from me all the time. I didn’t draw this one, but it did make me feel good about my methods!

Lagniappe:  Dr. Scott Gallager

My students and friends know that I am continually working to learn new things.  I am surrounded by experts on this cruise and I need to go ahead and admit it:  I feel sorry for these folks because they are trapped and can’t escape the questions I’ll wind up asking them about their incredibly interesting work!

As I mentioned earlier, depth of knowledge is important to success of these missions, but, breadth is equally important.  Addressing challenges and solving problems from different perspectives is essential, and it sure would be nice to have a Boy Scout out here.  Oh wait, we actually have a long time Scout Master among us, Dr. Scott Gallagher.  There, I feel better already…

Scott is a scientist at the Woods Hole Oceanographic Institution (“WHOI”), where his work focuses on biological and physical interactions in oceanography, which can perhaps be a little better explained as “working to understand the physical properties and processes of the ocean that impact biological abundance and populations (aka – distributions).”  In other words, “where are the scallops, how many are there, and why are they there and at that number?”

From a scientific perspective, there are three primary controls to analyze when studying shellfish populations:  the total amount of larvae spawned; the transportation, or “delivery”, of the larvae through the water column to the place where they settle; and, post-settlement predatory relationships (aka – the sea stars, crabs, and humans all out to feast on these delicious creatures)… Seems like an easy-peasy career, right? (I kid. I kid.)

This is a shot of the specimen count in the wet lab
This is a shot of the specimen count in the wet lab

Scott cut his teeth as an undergrad at Cornell, starting off in electrical engineering, and ultimately earning degrees in both pre-med and environmental science (see, I told you he could see things from a variety of perspectives!).  In his environmental science courses, Scott studied the Seneca and Cayuga Lakes, and after graduating from Alfred University/Cornell University, moved on and earned a master’s degree in Marine Biology at the University of Long Island.  Over the next several years, he worked at Woods Hole as a research assistant, first working in bivalve (shellfish) ecology, and quickly moving up through the ranks to research specialist.  After a couple of years at WHOI, the magnitude and awesome wonder of the life in our oceans presented Scott with more questions than answers, and he realized it was time to return to school and obtain his PhD so he could start answering some of the questions swimming around in his head (okay, no more puns, I promise).

In our discussion, Scott described the challenge of decoupling the biological processes of the ocean as a fascinating mystery novel that never ends, and never allows you to put the book down or stop turning the pages to see what comes next.  After only a week out here with these good folks, it is evident that passion and curiosity exists in each of them, and it is really cool to feel their continued excitement about their work.

Our live aquarium
Our live aquarium

Aboard the ship, I’ve been fortunate to spend some time working with Scott in the wet-lab, where he helps conduct a more intensive study of a sample of 5-7 scallops from each dredge, according to survey protocol: taking photos, measuring the scallop size and weight, and recording whether it is male or female.

While the survey work is the mission of this cruise, it was the development and operational support for the HabCam that really got Scott working aboard these cruises, and members of his team are aboard each of the three legs every summer to participate in the survey work and provide technical assistance for the HabCam.  I think of my time driving the HabCam of what it must be like to explore Mars with Curiosity.

In addition to his mission-specific field-work, Scott has set up an onboard live aquarium in one part of the deck, using nothing more than an air hose, fresh sea water, and a tote.  The aquarium is a temporary home for many of the unique species we’ve caught on our dredge.  Most species are only kept long enough for me to nerd-out and take some photos, and it has been very interesting to see the interaction of the animals in the confined habitat that would normally only be seen on the sea floor.

Photoblog:

The pasta-looking stuff on the top of the clam shell are wavedwelk eggs. You can see a black-and-white wavedwelk poking out of the shell just to the right of the clam
The pasta-looking stuff on the top of the clam shell are wavedwelk eggs. You can see a black-and-white wavedwelk poking out of the shell just to the right of the clam
Sea urchins.  We catch many of these.  Zoom in on the one on the right.  Yeah, that’s its mouth.  Life’s at sea is tough!
Sea urchins. We catch many of these. Zoom in on the one on the right. Yeah, that’s its mouth. Life’s at sea is tough!
An ocean pout.  They crush sand dollars and eat them for breakfast.
An ocean pout.  They crush sand dollars and eat them for breakfast.
The smaller birds were enjoying that fish until the big dog bombed them and stole it away. Katie said it was cleptoparasitism; Fancy Nancy would approve.
The smaller birds were enjoying that fish until the big dog bombed them and stole it away. Katie said it was cleptoparasitism; Fancy Nancy would approve. 
Barnacles growing atop this scallop.  I think this was one of the designs tossed around for NASA’s recent “UFO” launch
Barnacles growing atop this scallop.  I think this was one of the designs tossed around for NASA’s recent “UFO” launch
It’s remarkable watching these guys zig-and-zag through rough seas, their wings not ever touching the water, but sometimes too close to it to see light peeking through from the other side
It’s remarkable watching these guys zig-and-zag through rough seas, their wings not ever touching the water, but sometimes too close to it to see light peeking through from the other side
I kept looking for a button to push and see if it would sing “Feliz Navidad”
I kept looking for a button to push and see if it would sing “Feliz Navidad”
Stars on the water
Stars on the water
Don't be a skater-hater
Don’t be a skater-hater

Dredge playlist:  Metallica, Dierks Bentley, Spoon, The National

Special thanks to Dr. Gallager for his help with this one.

Okay, that’s it, class dismissed…

Mr. Hance

Tom Savage: Whales to the Left, Whales to the Right, June 12, 2015

NOAA Teacher at Sea
Tom Savage
On Board NOAA Ship Henry B. Bigelow
June 10 – 19, 2015

Mission: Cetacean and Turtle Research
Geographic area of Cruise: North Atlantic
Date: June 12, 2015

Weather Data from the Bridge
Air temperature: 18 C
Wind speed: 10 knots
Wind direction: coming from north west
Relative humidity: 90%
Barometer: 1015 millibars

Personal Log

Today is my second day at sea and I can finally walk to various places on the ship in less time. I have found sleeping on the ship to be very easy as the ship rocks back and forth. I really enjoy being at sea; it is very tranquil at times and I am not rushed to go anywhere except my assigned duty locations. While on deck observing, the sights and smell of the ocean invokes memories of my former home in Bar Harbor, Maine.

After a full day of observing whales in the sunshine I was very excited to conduct some star-gazing at night. At 2200, as I opened the first hatch outside, I walked into a wall of fog and was reminded quickly that I am miles offshore on Georges Bank in June!

Science and Technology Log

Sighting whales yesterday was very slow, but today made up for it. The weather was perfect, as the sky was mostly sunny with few high cirrus clouds early. Today I was assigned to the Flying Bridge for observations all day. There are three stations and we rotate every thirty minutes. The stations are Big Eyes on port and starboard sides and a computer in the center for data entry. We use different terms for orientation on the ship. For instance, the front of the ship is called the bow. While facing the bow, the left side is called the port and the right side starboard.

DiscussingSightings
Discussing sightings on the “Fly Bridge”

My rotation began on the port side of the ship using the “Big Eyes”. After a half hour, your eyes become tired, strained and shifting to the computer to enter whale sighting helps. At the computer we enter whale sighting data called out by observers.

LookingThroughBigEyes
Looking through the “Big Eyes”. Do you see anything?

In addition to recording the identification of animals; other important attributes are called out by the observers such as bearings and direction headings. Looking through the “big eyes”, a range finder is located from center with a scale from 0 – 24, and is called the reticle. To properly calculate distance, the observer needs to adjust the “Big Eyes” to align zero with the ocean horizon. This is very difficult since the ship is always in motion. The “Big Eyes” in the image above is not correctly aligned. There is a chart we used to translate the reticle values to distance.

An early morning break was followed by an amazing hour of multiple whale sightings. Fin, humpback whales and pods of Atlantic white-sided dolphin sightings were all around the ship. One humpback whale came within twenty feet of the boat. The afternoon was less active but we tracked pilot whales later which were not seen during morning rotations.

ViewFlyBridge
View from the “Fly Bridge” looking down on the “Rolling Bridge”

 

Until next time, happy sailing!

~ Tom

 

Tom Savage, Introduction, June 2, 2015

NOAA Teacher at Sea
Tom Savage
     (Almost)  On Board NOAA Ship Henry B. Bigelow
        June 10 – 19, 2015

Mission: Cetacean and Turtle Research
Geographic area of Cruise:  North Atlantic
Date: June 2, 2015

Personal Log

Greetings from Western NC.  My name is Tom Savage, and I am a Science teacher at the Henderson County Early College in Flat Rock, NC. I currently teach Chemistry, Earth Science, Biology and Physical Science. In a few days I will be flying to Rhode Island and boarding NOAA ship Henry B. Bigelow, a research vessel. We will be traveling in the North Atlantic region, mostly in Georges Bank which is located east of Cape Cod and the Islands.  The research mission will focus on two types of whales: Sei and Beaked Whales. Our primary goals will be photo-ID and biopsy collection, acoustic recording, and prey sampling.  I am looking forward to learning about the marine life and ocean ecosystem, and I look forward to sharing this knowledge with my students.

This will not be the first time that I have been out to sea.  A few years ago, I spent a week with eighteen other science teachers from across the county, scuba diving within the Flower Garden Banks National Marine Sanctuary. This week long program was sponsored by the Gulf of Mexico Foundation and NOAA.  This exceptional professional development provided an opportunity to explore, photograph and develop lesson plans with a focus on coral reefs. I also learned about how important the Gulf of Mexico is to the oil industry.  I had the opportunity to dive under an abandoned oil platform and discovered the rich, abundant animal life and how these structures improve the fish population.

Prior to becoming a teacher, I worked as a park ranger at many national parks including the Grand Canyon, Glacier and Acadia. Working at these national treasures was wonderful and very beneficial to my teaching.

Providing young adults with as many experiences and career possibilities is the hallmark of my teaching. During the year, I arrange a “Discover SCUBA” at the local YMCA. Students who have participated in this have gone on to become certified. In the fall I have offered “Discover Flying” at a local airport, sponsored by the “Young Eagles” program. Here students fly around our school and community witnessing their home from the air. A few students have gone on to study various aviation careers.

Flying
“Discover Flying”

 

I am very excited in learning about the many career opportunities that are available on NOAA research vessels. It would be very rewarding to see a few of my students become employed with the NOAA Corps or follow a career in science due to this voyage.

Regards,

~  Tom

 

 

DJ Kast, Bongo Patterns, June 1, 2015

NOAA Teacher at Sea
Dieuwertje “DJ” Kast
Aboard NOAA Ship Henry B. Bigelow
May 19 – June 3, 2015

Mission: Ecosystem Monitoring Survey
Geographical areas of cruise: Mid Atlantic Bight, Southern New England, George’s Bank, Gulf of Maine
Date: June 1, 2015

Science and Technology Log:

Bongo Patterns!

Part of my job here on NOAA Ship Henry B. Bigelow is to empty the plankton nets (since there are two we call them bongos). The plankton is put into a sieve and stored  in either ethanol if they came from the small nets (baby bongos) or formalin if they came from the big nets (Main bongos).

What are plankton? Plankton is a greek based word that means drifter or wanderer. This suits these organisms well since they are not able to withstand the current and are constantly adrift. Plankton are usually divided by size (pico, nano, micro, meso, macro, mega). In the plankton tows, we are primarily focused on the macro, meso and megaplankton that are usually with in the size range of 0.2- 20 mm  (meso), 2-20 cm (macro), and above 20 cm (mega) respectively.

Group Size range Examples
Megaplankton > 20 cm metazoans; e.g. jellyfish; ctenophores; salps and pyrosomes (pelagic Tunicata); Cephalopoda; Amphipoda
Macroplankton 2→20 cm metazoans; e.g. Pteropods; Chaetognaths; Euphausiacea (krill); Medusae; ctenophores; salps, doliolids and pyrosomes (pelagic Tunicata); Cephalopoda; Janthinidae (one family gastropods); Amphipoda
Mesoplankton 0.2→20 mm metazoans; e.g. copepods; Medusae; Cladocera; Ostracoda; Chaetognaths; Pteropods; Tunicata; Heteropoda
Microplankton 20→200 µm large eukaryotic protists; most phytoplankton; Protozoa Foraminifera; tintinnids; other ciliates; Rotifera; juvenile metazoansCrustacea (copepod nauplii)
Nanoplankton 2→20 µm small eukaryotic protists; Small Diatoms; Small Flagellates; Pyrrophyta; Chrysophyta; Chlorophyta; Xanthophyta
Picoplankton 0.2→2 µm small eukaryotic protists; bacteria; Chrysophyta
Femtoplankton < 0.2 µm marine viruses

(Omori, M.; Ikeda, T. (1992). Methods in Marine Zooplankton Ecology)

We will be heading to four main geographical areas. These four areas are: the Mid Atlantic Bight (MAB), the Southern New England (SNE), Gulf of Maine (GOM), and George’s Bank (GB). I’ve been told that the bongos will be significantly different at each of these sites.  I would like to honor each geographical area’s bongos with a representative photo of plankton and larval fish.  There are 30 bongos in each area, and I work on approximately 15 per site.

DJ Kast holding the large plankton net. Photo by Jerry P.
DJ Kast holding the large plankton net. Photo by Jerry Prezioso
Bongos in the Sunset. Photo by DJ Kast
Bongos in the Sunset. Photo by DJ Kast

Here is a video of a Bongo launch.

 

Flow Meter Data. It is used how to count how far the plankton net was towed. Used to calculate the amount of animals per cubic meter. Photo by DJ Kast
Flow Meter Data. It is used how to count how far the plankton net was towed to calculate the amount of animals per cubic meter. Photo by DJ Kast

 

The plankton nets need to be wiped down with saltwater so that the plankton can be collected on the sieve.

 

Day 1: May 19th, 2015

My first Catch of Plankton! Mostly zooplankton and fish larvae. Photo by: DJ Kast
My first Catch of Plankton! Mostly zooplankton and fish larvae. Photo by: DJ Kast
Day 1: Fish Larvae and Copepods. Photo by: DJ Kast
Day 1: Fish Larvae and Copepods. Photo by: DJ Kast

 

 

Day 2: May 20th, 2015

Larval Fish and Amphipods! Photo by: DJ Kast
Larval Fish and Amphipods! Photo by: DJ Kast

Day 3: May 21st, 2015

IMG_7096
Day 3, the plankton tows started filling with little black dots. These were thousands of little sea snails or pteropods. Photo by DJ Kast
IMG_7100
Clogging the Sieve with Pteropods. Photo by DJ Kast
IMG_7110
Close up shot of a Shell-less Sea Butterfly. Photo by: DJ Kast
IMG_7121
Glass Eel Larva. Photo by DJ Kast

 

Day 4: May 22nd, 2015

Butterfly fish found in the plankton tow. Photo by; DJ Kast
Butter fish found in the plankton tow. Photo by; DJ Kast
IMG_7187
Baby Triggerfish Fish Larvae Photo by: DJ Kast
Swimming Crab. Photo by DJ Kast
Swimming Crab. Photo by DJ Kast
IMG_7174
Megalops or Crab Larva. Photo by: DJ Kast
IMG_7176
Polychaete Worms. Photo by: DJ Kast
IMG_7165
Salp. Photo by: DJ Kast

 

Day 5: May 23, 2015

Unidentified organism Photo by DJ Kast.
Unidentified organism
Photo by DJ Kast.
Sand Lance Photo by DJ Kast
Sand Lance Photo by DJ Kast
Polychaete worm. Photo by DJ Kast
Polychaete worm. Photo by DJ Kast
3 amphipods and a shrimp. Photo by DJ Kast
3 amphipods and a shrimp. Photo by DJ Kast
Such diversity in this evenings bongos. Small fish Larva, shrimp, amphipods. Photo by DJ Kast
Such diversity in this evening’s bongos. Small fish Larvae, shrimp, amphipods. Photo by DJ Kast
Small fish Larva. Photo by DJ Kast
Small fish Larvae. Photo by DJ Kast

Below are the bongo patterns for the Southern New England area.

I have learned that there are two lifestyle choices when it comes to plankton and they are called meroplankton or holoplankton.

Plankton are comprised of two main groups, permanent or lifetime members of the plankton family, called holoplankton (which includes as diatoms, radiolarians, dinoflagellates, foraminifera, amphipods, krill, copepods, salps, etc.), and temporary or part-time members (such as most larval forms of sea urchins, sea stars, crustaceans, marine worms, some marine snails, most fish, etc.), which are called meroplankton.

Day 6: May 24th, 2015

Copepod sludge with a fish larva. Photo by: DJ Kast
Copepod sludge with a fish larva. Photo by: DJ Kast
Baby Bongo Sample in ethanol. Photo by: DJ Kast
Baby Bongo Sample in ethanol. Photo by: DJ Kast
Megalops? Photo by: DJ Kast
Megalops?
Photo by: DJ Kast
Fish Larvae. Photo by: DJ Kast
Fish Larvae. Photo by: DJ Kast
Side station sample from the mini bongos on the sieve. Photo by: DJ Kast
Sample from the mini bongos on the sieve. Photo by: DJ Kast

Day 7: May 25th, 2015

???? Photo by DJ Kast
???? Photo by DJ Kast
Tiny Snail. Photo by DJ Kast
Tiny Snail. Photo by DJ Kast

Georges Bank- It is a shallow, sediment-covered plateau bigger than Massachusetts and it is filled with nutrients that get stirred up into the photic zone by the various currents. It is an extremely productive area for fisheries.

Photo by: R.G. Lough (NEFSC)
Photo by: R.G. Lough (NEFSC)

Today, I learned that plankton (phyto & zoo) have evolved in shape to maximize their surface area to try and remain close to the surface. This makes sense to me since phytoplankton are photosynthesizers and require the sun to survive. Consequently, if zooplankton are going to consume them, it would be easier to remain where your food source is located. I think this would make for a great lesson plan that involves making plankton-like creatures and seeing who can make them sink the least in some sort of competition.

Photo by DJ Kast
Photo by DJ Kast
Harpactacoid Copepod. Photo by DJ Kast
Harpactacoid Copepod. Photo by DJ Kast
The Biggest net caught sand lance (10 cm). Photo by DJ Kast
The Biggest net caught sand lance (10 cm). Photo by DJ Kast
Fish Larvae. Photo by DJ Kast
Fish Larvae. Photo by DJ Kast

Day 8: May 26th, 2015 Very Diverse day,  Caprellids- skeleton shrimp, Anglerfish juvenile, Phronima inside of salp! Photo by DJ Kast

Photo by: DJ Kast
Juvenile Anglerfish aka Monk Fish. Photo by: DJ Kast
IMG_7483
Sand Shrimp. Photo by DJ Kast
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A tiny krill with giant black eyes. Photo by DJ Kast
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A small jellyfish! Photo by: DJ Kast
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A phronima (the bee looking thing inside the translucent shell) that ate its way into a salp and is using the salp as protection. Photo by: DJ Kast

Video of the phronima:

Caprellids or Skeleton Shrimp. Photo by DJ Kast
Caprellids or Skeleton Shrimp. Photo by DJ Kast

Video of the Caprellids:

Day 9:  May 27th, 2015= Triggerfish and colorful phronima (purple & brown). Our sieves were so clogged with phytoplankton GOOP, which is evidence of a bloom. We must be in very productive waters,

Evidence of a Phytoplankton bloom in the water, Photo by: DJ Kast
Evidence of a Phytoplankton bloom in the water. Photo by: DJ Kast
Juvenile Triggerfish. Photo by: DJ Kast
Juvenile Triggerfish. Photo by: DJ Kast

Day 10: May 28th, 2015= change in color of copepods. Lots of ctenophores and sea jellies

A Sea jelly found in George's Bank. We are in Canada now! Photo by: DJ Kast
A comb jelly (ctenophore) found in George’s Bank. We are in Canada now! Photo by: DJ Kast
Gooseberry: a type of ctenophore or comb jelly. Photo by DJ Kast
Sea Gooseberry: a type of ctenophore or comb jelly. Photo by DJ Kast

Did you  know? Sea Jellies are also considered plankton since they cannot swim against the current.

Day 11: May 29th, 2015: Border between Georges Bank and the Gulf of Maine!

Krill found in the Gulf of Maine. Photo by DJ Kast
Krill found in the Gulf of Maine. Photo by DJ Kast
Callenoid Copepods. Photo by DJ Kast
Callenoid Copepods- its so RED!!! Photo by DJ Kast

Gulf of Maine! Water comes in from the North East Channel (the Labrador current), coast on one border and George’s  Bank on the other. Definitely colder water, with deep ocean basins. Supposed to see lots of phytoplankton. Tidal ranges in the Gulf of Maine are among the highest in the world ocean

Gulf of Maine currents! Photo by NEFSC NOAA.
Gulf of Maine currents! Photo by NEFSC NOAA.

Day 12: May 30th, 2015: day and night bongo (Just calanus copepods vs. LOTS of krill.)

Krill, Krill, Krill! Photo by DJ Kast
Krill, Krill, Krill! Photo by DJ Kast

Krill are normally found lower in the water column. The krill come up at night to feed and avoid their predators and head back down before dawn. This daily journey up and down is called the vertical migration.

Video of Krill moving:

Day Sample. Photo by DJ Kast
Day Sample. Photo by DJ Kast
Night Sample. Photo by DJ Kast
Night Sample (look at all those krill). Photo by DJ Kast

Day 13: May 31th, 2015: Calanoid Copepod community.  Calanoida feed on phytoplankton (only a few are predators) and are themselves the principal food of fish fry, plankton-feeding fish (such as herring, anchovies, sardines, and saury) and baleen whales.

Calanious Community. Its so RED! Photo by DJ Kast
Calanus Community. It’s so RED! Photo by DJ Kast

Day 14: June 1st, 2015:

Brittle Stars caught in the Plankton Tow. Photo by DJ Kast
Brittle Stars caught in the Plankton Tow. Photo by DJ Kast
Tusk shell. Photo by DJ Kast
Tusk shell. Photo by DJ Kast
Side profile of Shrimp caught in the plankton nets. Photo by DJ Kast
Side profile of Shrimp caught in the plankton nets. Photo by DJ Kast
Shrimp Head. Photo by DJ Kast
Shrimp Head. Photo by DJ Kast
Shrimp Tail with Babies. Photo by DJ Kast
Shrimp Tail with Babies. Photo by DJ Kast

Day 15: June 2nd, 2015: Last Day

Gooey foamy mess in the sieve with all the phytoplankton. Photo by DJ Kast
Gooey foamy mess in the sieve with all the phytoplankton. Photo by DJ Kast
Gooey foamy mess in the net with all the phytoplankton. Photo by DJ Kast
Gooey foamy mess in the net with all the phytoplankton. Photo by DJ Kast
Gooey foamy mess in the jar with all the phytoplankton. Photo by DJ Kast
Gooey foamy mess in the jar with all the phytoplankton. Photo by DJ Kast
Map of all the Bongo and CTD/ Rosette Stations. Photo by DJ Kast.
Map of all the Bongo and CTD/ Rosette Stations (153 total). Photo by DJ Kast.

Through rough seas and some amazingly calm days, we have all persevered as a crew and we have done a lot of science over the last 16 days. We went through 153 stations total. I have learned so much and I would like to thank Jerry, the chief scientist for taking me under his wing and training me in his Ecosystem Monitoring ways.  I would also like to thank Dena Deck and Lynn Whitley for believing in me and writing my letters of recommendation for the Teacher at Sea program. I would love to do this program again! -DJ Kast

DJ Kast, Interview with Jessica Lueders-Dumont, May 22, 2015

NOAA Teacher at Sea
Dieuwertje “DJ” Kast
Aboard NOAA Ship Henry B. Bigelow
May 19 – June 3, 2015

Mission: Ecosystem Monitoring Survey
Geographical area of cruise: East Coast

Date: May 22, 2015, Day 4 of Voyage

 

Interview with Jessica Lueders-Dumont

Who are you as a scientist?

Jessica Lueders-Dumont is a graduate student at Princeton University and has two primary components of her PhD — nitrogen biogeochemistry and historical ecology of the Gulf of Maine.

Jessica Lueders- Dumont, graduate student at Princeton cleaning a mini bongo plankton net for her sample.
Jessica Lueders- Dumont, graduate student at Princeton cleaning a mini bongo plankton net for her sample. Photo by: DJ Kast

 What research are you doing?

Her two projects are, respectively,

A) Nitrogen cycling in the North Atlantic (specifically focused on the Gulf of Maine and on Georges Bank but interested in gradients along the entire eastern seaboard)

B) Changes in trophic level of Atlantic cod in the Gulf of Maine and on Georges Bank over the history of fishing in the region. The surprising way in which these two seemingly disparate projects are related is that part A effectively sets the baseline for understanding part B!

She is co-advised by Danny Sigman and Bess Ward. Danny’s research group focuses on investigating climate change through deep time, primarily by assessing changes in the global nitrogen cycle which are inextricably tied to the strength of the biological pump (i.e. biological-mediated carbon export and storage in the ocean). Bess’s lab focuses on the functional diversity of marine phytoplankton and bacteria and the contributions of these groups to various nitrogen cycling processes in the modern ocean, specifically as pertains to oxygen minimum zones (OMZs). She is also advised by a Olaf Jensen, a fisheries scientist at Rutgers University.

In both of these biogeochemistry labs,  nitrogen isotopes (referred to as d15N, the ratio of the heavy 15N nuclide to the lighter 14N nuclide in a sample compared to that of a known standard) are used to track nitrogen cycling processes. The d15N of a water mass is a result of the relative proportions of different nitrogen cycling processes — nitrogen fixation, nitrogen assimilation, the rate of supply, the extent of nutrient utilization, etc. These can either be constrained directly via 15N tracer studies or can be inferred from “natural abundance” nitrogen isotopic composition, the latter of which will be used as a tool for this project.

Nitrogen Cycle in the Ocean. Photo credit to: https://wordsinmocean.files.wordpress.com/2012/02/n-cycle.png
Nitrogen Cycle in the Ocean. Photo credit to: https://wordsinmocean.files.wordpress.com/2012/02/n-cycle.png

On this cruise she has 3 sample types — phytoplankton, zooplankton, and seawater nitrate — and two overarching questions that these samples will address: How variable is “baseline d15N” along the entire eastern seaboard, and does this isotopic signal propagate to higher trophic levels? Each sample type gives us a different “timescale” of N cycling on the U.S. continental shelf. She will be filtering phytoplankton from various depths onto filters, she will be collecting seawater for subsequent analysis in the lab, and she will be collecting zooplankton samples — all of which will be analyzed for nitrogen isotopic composition (d15N).

Biogeochemistry background: 

Biogeochemists look at everything on an integrated scale. We like to look at the box model, which looks at the surface ocean and the deep ocean and the things that exchange between the two.

The surface layer of the ocean: euphotic zone (approximately 0-150 m-but this range depends on depth and location and is essentially the sunlit layer); nutrients are scarce here.

When the top zone animals die they sink below the euphotic zone and into the aphotic zone (150 m-4000m), and the bacteria break down the organic matter into inorganic matter (nitrate (NO3), phosphate (PO4) and silicate (Si(OH)3.). In terms of climate, an important nutrient that gets cycled is carbon dioxide.We look at the nitrate, phosphate, and silicate as limiting factors for biological activity for carbon dioxide, we are essentially calculating these three nutrients to see how much carbon dioxide is being removed from the atmosphere and “pumped” into the deep sea.  This is called the biological pump. Additionally, the particulate matter that falls to the deep sea is called Marine Snow, which is tiny organic matter from the euphotic zone that fuels the deep sea environments; it is orders of magnitude less at the bottom compared to the top.

Cycling
Visual Representation of the aphotic and euphotic zones and the nutrients that cycle through them. Photo by: Patricia Sharpley

 

Did you know that the “Deep sea is really acidic, holds a lot of CO2 and is the biggest reservoir of C02 in the world?” – From Jessica Lueders- Demont, graduate student at Princeton.

One of the most important limiting factors for phytoplankton is nitrogen, which is not readily available in many parts of the global ocean. “A limiting nutrient is a chemical necessary for plant growth, but available in quantities smaller than needed for algae and other primary producers to increase their abundance. Organisms can grow and reproduce only when they have sufficient nutrients. For algae, the carbon source is CO2and this, at least in the surface water, has a constant value and is not limiting their growth. The limiting nutrients are minerals (such as Fe+2), nitrogen, and phosphorus compounds” (Patricia Sharpley 2010).

Conversely, phosphorus is the limiting factor on land. The most common nitrogen is molecular nitrogen or N2, which has a strong bond to break and biologically it is very expensive to fix from the atmosphere. 

Biological, chemical, and physical oceanography all work together in this biogeochemistry world and are needed to have a productive ocean. For example, we need the physical oceanography to upwell them to the surface so that the life in the euphotic zone can use them.

Activities on the ship that I am assisting Jessica with:

  • Zooplankton collected using mini bongos with a 165 micron mesh and then further filtered at meshes: 1000, 500, and ends with 250 microns, this takes out all of the big plankton that she is not studying and leaves only her own in her size range which is 165-200 microns.
  • She is collecting zooplankton water samples because it puts the phytoplankton that she is focusing on into perspective.
The last of the mesh buckets that's filtering for phytoplankton. Photo by: DJ Kast
The last of the mesh buckets that’s filtering for phytoplankton. Photo by: DJ Kast
    • Aspirator pump sucks out all of the water so that the zooplankton are left on a glass fiber filter (GFFs) on the filtration rack.

 

  • Aspirator pump that is on the side sucks out all of the air so that the plankton get stuck on the filters at the bottom of the cups seen here. Photo by: DJ Kast
    Aspirator pump that is on the side sucks out all of the air so that the plankton get stuck on the filters at the bottom of the cups seen here. Photo by: DJ Kast
  • Bottom of the cup after all the water has been sucked through. Photo by: DJ Kast
    Bottom of the cup after all the water has been sucked through. Photo by: DJ Kast
  • Jessica removing the filter with sterilized tweezers to place into a labeled petridish. Photo by: DJ Kast
    Jessica removing the filter with sterilized tweezers to place into a labeled petri dish. Photo by: DJ Kast

    Labeled petri dish with GFF of phytoplankton on it. Photo by: DJ Kast
    Labeled petri dish with GFF of phytoplankton on it. Photo by: DJ Kast

Video of this happening:

Phytoplankton filtering:

Jessica collecting her water sample from the Niskin bottle in the Rosette. Photo by DJ Kast
Jessica collecting her water sample from the Niskin bottle in the Rosette. Photo by DJ Kast
Up close shot of the spigot that releases water from Niskin bottle in the Rosette. Photo by DJ Kast
Up close shot of the spigot that releases water from Niskin bottle in the Rosette. Photo by DJ Kast
DJ Kast helping Jessica collect her 4 L of seawater from the Niskin bottle in the Rosette. Photo by Jerry P.
DJ Kast helping Jessica collect her 4 L of seawater from the Niskin bottle in the Rosette. Photo by Jerry P.
DJ and Jessica collect her 4 L of seawater from the Niskin bottle in the Rosette. Photo by Jerry P.
DJ and Jessica collect her 4 L of seawater from the Niskin bottle in the Rosette. Photo by Jerry P.
Chief Scientist Jerry Prezioso and Megan Switzer next to the CTD and Rosette
Chief Scientist Jerry Prezioso and Megan Switzer next to the CTD and Rosette Photo by: DJ Kast

 

May 21, 14:00 hours: Phytoplankton filtering with Jessica.

In addition to the small bottles Jessica needs, we filled 4 L bottles with water at the 6 different depths (100, 50, 30, 20, 10, 3 m) as well.

We then brought all the 4 L jugs into the chemistry lab to process them. The setup includes water draining through the tubing coming from the 4 L jugs into the filters with the GFFs in it. Each 4 L jug is filtered by 2 of these filter setups preferably at an equal rate. The deepest depth 100 m was finished the quickest because it had the least amount of phytoplankton that would block the GFF and then a second jug was collected to try and increase the concentration of phytoplankton on the GFF.

Phytoplankton filtration setup. Photo by DJ Kast
Phytoplankton filtration setup. Photo by DJ Kast
The filter and pump setup up close. Photo by DJ Kast
The filter and pump setup up close. Photo by DJ Kast
Up close shot of the GFF within the filtration unit.
Up close shot of the GFF within the filtration unit. Photo by DJ Kast
Jessica keeping an eye on her filtration system to make sure nothing is leaking and that there are no air bubbles restricting water flow
Jessica keeping an eye on her filtration system to make sure nothing is leaking and that there are no air bubbles restricting water flow. Photo by DJ Kast
Here I am helping Jessica setup the filtration unit.
Here I am helping Jessica setup the filtration unit.Photo by Jessica Lueders- Dumont
The GFF with the phytoplankton (green stuff) on it.
The GFF with the phytoplankton (green stuff) on it. Photo by: DJ Kast

There are 2 filters for each depth, and since she has 12 filtration bottles total, then she would be collecting data from 6 depths. She collects 2 filters so that she has replicates for each depth.

Here they are all laid out to show the differences in phytoplankton concentration.

The 6 depths worth of GFFs. See how the 30 m is the darkest. Thats evidence for the chlorophyll max. Photo by: DJ Kast
The 6 depths worth of GFFs. See how the 30 m is the darkest. Thats evidence for the chlorophyll max. Photo by: DJ Kast

She will fold the GFF in half in aluminum foil and store it at -80C until back in the lab at Princeton. There, the GFF’s are combusted in an elemental analyzer and the resulting gases run through a mass spectrometer looking for concentrations of N2 and CO2. The 30 m GFF was the most concentrated and that was because of a chlorophyll maximum at this depth.

Chlorophyll maximum layers are common features of vertically stratified water columns. There is a subsurface maximum or layer of chlorophyll concentration. These are found throughout oceans, lakes, and estuaries around the world at varying depths, thicknesses, intensities, composition, and time of year.