20,000 Larvae Under the Sea

April 28th, 2022. It’s nearly the end of our long journey in the southwest Pacific. While we would be diving at Mariner, the southernmost site in the Eastern Lau Spreading Center, weather said otherwise. Instead, for our last site we are currently near West Mata, a volcano southwest of the Samoas. A 40-hour transit from Tu’i Malila. While this site is outside of our original sites, it hosts some of the snail species we’ve been studying. Since we are looking at the interactions between the geology, chemistry, and symbionts on adult snail distributions, we can compare with this additional location. Alviniconcha sp. also host unique groups of symbionts, so it will be interesting to compare the free-living symbionts communities between our sites and a new location.

For those unfamiliar with the term, a larva is the immature form of an organism before it metamorphoses into a physiologically different form. This means many larvae can look completely different from their adult forms. Think of a caterpillar turning into a butterfly. Caterpillars are larvae!

Gastropod veliger photos by Tessa Beaver (WWU) and Avery Calhoun (OIMB). Edited and arranged by Dexter Davis (WWU)

On this cruise we are particularly interested in finding the larvae of the Alviniconcha and Ifremeria sp. snails we are studying. This is not an easy thing to do. With the samples collected by Jason, Sentry’s SyPRID, and the McLane pump, our team of sorters pick through water, sediment, and snail bucket dregs searching for them. We work day and night. If any of our deployments come up at 2am, then we sort all morning. We plan accordingly though, taking naps, getting snacks, and playing music to keep us awake and focused. Here’s a photo of 9 different larval snails, gastropod veligers, we’ve found on this cruise that highlight the beauty and diversity of these organisms. The middle veliger has its “velum” out, a lobe covered in small hairs that it swims with. However, we are not confident on which species these veligers belong to. We’ve actually identified 23 different gastropod veligers so far! Unfortunately, we won’t be able to confirm their mysterious identities confidently until we do DNA sequencing on these individuals back on land.

Gastropod veligers are not the only larval type we’ve been finding on this cruise though. We pick out every larval type we find, separated by morphotype (form). Since they are so tiny, we are sorting these samples under dissecting microscopes where we have to fight the rocking and shaking of the ship’s movements to grab them. While some larval forms, like gastropod veligers, may look like their adult forms (or at least like a snail), here are some others that look different. The in the top-left of the left collage there is a larval crab and shrimp, also known as zoea. The top-right is a bivalve pediveliger (veligers are mollusc larvae) that will develop into a mussel. You can see its foot sticking out, one of the ways it moves around. The bottom left is a nectochaete, which will turn into a polychaete. From a golden-winged angel into a marine worm! In the right collage the top-left is another morphotype of nectochaete we’ve found. Even within a larval type the morphotypes can vary drastically. The top-right is a parenchymella, which will turn into a sponge. The bottom two pictures are the larval forms of a barnacle. They look completely different, right? The bottom-left is the nauplius stage, with distinct horns, and the bottom-right is the cyprid form. These amazing photos were taken on a compound microscope by Tessa Beaver (WWU) and Avery Calhoun (OIMB).

Top left: Crab zoea. Top right: Bivalve veliger. Bottom left: Nectochaete. Bottom right: Shrimp zoea. Photos by Tessa Beaver (WWU) and Avery Calhoun (OIMB). Edited and arranged by Dexter Davis (WWU).
Top left: Nectochaete. Top right: Parenchymella. Bottom left: Barnacle nauplius. Bottom right: Barnacle cyprid. Photos by Tessa Beaver (WWU) and Avery Calhoun (OIMB). Edited and arranged by Dexter Davis (WWU).

One particular larva we’ve been focusing on during this cruise is from one of our study snails, Ifremeria nautilei. The Warén’s larva. These “fat Y”-shaped larvae are uniquely brooded by female Ifremeria within a brood pouch in their foot. Little is known about these larvae, but we’ve been setting up live cultures throughout the cruise to research their developmental stages and temperature sensitivity. It’s been very exciting to map out the different stages we’re seeing, watching as a culture changes from one day to the next. We do not know at what stage these larvae are released from the adult, whether it’s as a veliger, or earlier in the Warén’s stage. Excitement within the science party occurred when we produced the first culture of larvae to develop the larval shell, documenting the transition into a veliger. Using a broken pair of polarized sunglasses found while snorkeling during our shelter in place, we were able to see the birefringence of the shell reflecting back at us under the scope. Why is this exciting? Because it also might be the first time someone has seen this development occur.

Waren’s Larvae. Photo taken by Maia Heffernan (WWU).
Shelled veliger of Ifremeria nautilei. Photo taken by Avery Calhoun (OIMB).

Alviniconcha strummeri

As the next part of our creature feature, I’d like to show you the second of our three Alviniconcha species, Alviniconcha strummeri. This punk rock snail is named after a member of the punk rock band, the Clash, Joe Strummer. Named by: Shannon Johnson (punkrocksnails on Instagram/Twitter) A fitting name for these snails that have adapted to live in one of the most extreme habitats on the planet. This species is easily identifiable by the spines on its shell. This species only has long spines of the same length, while the other species have varying lengths. A. strummeri dominates the more southern of our sites along with A. kojimai from the last post. One interesting aspect about Alviniconcha is that under their periostracum (the outer layer of the shell), their shell is gold! You can see at the apex of this individual a little bit of it sticking out. However, we are only collecting these snails for the scientific wealth they hold. Here’s an article about them if you want to learn more: https://www.npr.org/2014/12/20/372052995/a-snail-so-hardcore-its-named-after-a-punk-rocker


Snail Cruise 2: The Seaquel

April 20th, 2022. The science team is now on the second round through conducting science at our six sites in the Lau Basin. While we’ve already been out at sea for almost a month and we’ve still got 3 weeks to go! The time between each of these sites has varied between 35 minutes to 8 hours. Sometimes we would get a nice break between samples collected from Jason and Sentry. Other times we would have a quick turn around and would need to sleep in shifts to get samples processed in time. Even the transit from our southernmost site, Mariner, back to our northernmost site, Kilo Moana, was only 12 hours! Now it’s time to do it all over again. Although this time, we now know how all our sites look, and where the good collection locations are.

I want to walk you through some of the sights we’ve seen so far. When we first arrived, the first thing we saw at our sites were not snails, but instead was what we presumed was ash! Since we are so close to the Hunga Tonga Hunga Ha’apai volcano, we are assuming that this could be from the recent eruption. We’re currently communicating with some geologists in Tonga and around the world to collect observations and samples. The depth has varied across and between sites, but at Kilo Moana one of the manipulator hands on Jason disappeared completely into the ash. The ash turned our rocky sites into snow-capped mountains. At first, we were worried that all vent animals were covered. As we further explored our sites, we found concealed refuges of resilient snails. Here’s a photo at ABE, our biggest site, of a group of chimneys covered in Ifremeria nautilei, Alviniconcha sp., and some vent crabs. One thing to notice is at the apex (the smallest whirl / point of the shell) of many of these snails it’s white where the shell has broken off. It’s tough living at the bottom of the ocean on rocky volcanoes!

This next photo takes us to another site, Tu’i Malila that was very mountainous. Throughout the dive we were surrounded by huge walls of basalt with diffuse, weak, flows of vent fluid. These pockets of hydrothermal energy were inhabited by groups of animals, like these Alviniconcha strummeri here. If you look closely towards the center of the image you can actually see the shimmering water that indicates these diffuse flows mixing with the seawater. This site had many patches like this, some snail patches surrounded by groups of Bathymodiolin mussels, creating a nest-like appearance. At this site we also found many creatures peering out from between the rocks like this curious little pink sea toad.

Ash at Kilo Moana
Chimney of snails at ABE.
Alviniconcha at Tu’i Malila | Pink Sea Toad

The final site I’ll show you this time is from our final site, Mariner. This site, while active (has flowing vent chimneys), does not host our study snail species. This site will act as a control group to collect background vent data (looking for symbionts / larvae) in a place without snails. While devoid of snails, this site has some of the most spectacular vent chimney structures. Chimneys towering over 15 meters, one called the toilet bowl, “black smokers” – chimneys spewing heavy metal rich hydrothermal fluid, in all sorts of shapes. Here’s a photo of the spiky top of one of these chimneys, where you can see the irregular shape that they form in. You might also notice the long purple organism wrapped inside, which happens to be a sea cucumber! This site still had many different types of organisms, just not the snails we are studying on this snail cruise. Here’s another photo of a rock we found covered in these beautiful puffball / lollipop sponges. These little dandelion-looking creatures are actually a type of carnivorous sponge. Those long spicules radiating from the center act as a net collecting passing plankton that can be consumed by the individual. In the bottom left corner there’s also a small squat lobster.

Tall spiky chimneys at Mariner.
Puffball sponges at Mariner.

While we’ve been enjoying our time at sea, seeing fantastical habitats in an unfamiliar world, working with amazing scientists, and getting to use frontier scientific instruments, we are disconnected from our daily lives. This past week we missed Easter, usually a time to spend with family, so we celebrated on board. We brought candy and easter eggs that we placed all around the ship. Hidden under microscopes, within coffee mugs in the galley, and within storage cabinets. If an egg was found it would be re-hid with new contents, creating a constant easter egg hunt as we’re all awake and active at different times throughout the day. Everyone could participate. Timed with some maintenance on the ROV Jason, this gave us a fun break day to decorate Styrofoam cups instead of our traditional easter eggs. These cups will go down on the side of Jason or Sentry and will shrink under the pressure from a dive. Here’s a few of the ones we crafted.


Alviniconcha kojimai

Keeping up with the pattern from the last post, I’d like to introduce another of our study species, Alviniconcha kojimai. This was one of the first of our Alviniconcha sp. that we found on this expedition. As I introduce the rest of the snails from this group, you’ll see they look very similar to each other. There are a few ways to differentiate them, I prefer to do it through the spines on their periostracum (the outer shell layer). On kojimai between each of the tall spikes there are three smaller spikes. They also have the reddest coloration on their snout and cephalic tentacles (those long protrusions). This species is found in our more southern sites, where the geology is more andesitic and hydrogen sulfide concentrations in the vent fluid decrease. Whether these changes are impacting their distribution is one of the questions we are exploring.

Entries of A Hydrothermal Journal

April 9th, 2022. It’s been a while, but we made it to the Lau Basin! It’s located just northwest of the Kingdom of Tonga, and near the Hunga-Tonga Hunga-Ha’apai volcano that erupted in February. Within this basin there are a series of hydrothermal vents (underwater volcanoes) along a north-south axis. We will be visiting 6 different sites across it, twice, once to deploy equipment, and a second to recover them.  Currently, we are at our third site. We started at Kilo Moana, a site where there’s no active venting, then we went to Tow Cam, and are now at Tahi Moana. One interesting feature of these sites is that there is a geological gradient transitioning from basaltic rock in the north to andesitic rock in the south. In the samples we’ve been sorting so far there’s been a lot of small pieces of basalt. This gradient has been linked to a gradient in vent fluid geochemistry as well, which we are curious to the impacts on our target snails’ bacterial symbionts.


Sample Collection Methods

To get all of our samples we are making use of three different methods: the Autonomous Underwater Vehicle (AUV) Sentry, the McLane pump, and the Remote Operated Vehicle (ROV) Jason.

AUV Sentry

AUV Sentry works independently of the ship with a pre-programmed course mapped out. As it travels it hovers at a set altitude and filters water through two “plankzookas”, collecting plankton and hopefully our target larvae. It communicates acoustically via “chirps” to a team on board, sending updates on location, vehicle status, and science equipment status. The team can send small messages back altering the mission, small changes to the course, control the science equipment, or even abort the mission.

McLane Pump

The McLane pump is within a metal frame and pumps water at a rate of 30 liters per minute for 24 hours over a 60µm sieve. The pump has a weight stack with an acoustic release and a float pack overhead that allows us to deploy it over the side of the ship and release it off the seafloor without guiding it. Once the pump is on the seafloor, ROV Jason will move it next to a chimney to collect more larvae and is programmed to pump during Sentry’s dive. This pump so far has been most efficient at collecting live larvae, that we can try to raise and preserve on the ship.

ROV Jason

ROV Jason is attached to the ship with a cable, where it can be controlled from a storage container (“van”) on board. Within this van, members of the science party can watch live footage from the vehicle. They can communicate with the Jason pilot, co-pilot, navigator, and data manager to collect samples, deploy instruments, explore sites, and take videos / pictures. Jason has two manipulator arms that are controlled by the pilot and can use a multitude of tools including scoops, temperature probes, a slurp, mussel pots, and the SuPR sampler. This allows us to collect adult and juvenile target species, deploy / recover other instruments, and sample water for free-living bacterial symbionts in the environment.


Explorations of the Natural World

With the aid of all these instruments and vehicles, we’ve begun to explore our study sites, filled with excitement and anticipation. For many of us this is the first time really seeing hydrothermal vents, habitats many of us have dreamt of seeing since childhood. An unrivaled experience is driving up to a massive rock chimney jutting out of the seafloor, spewing hydrothermal fluid. Covered in sea stars, crabs, and snails. The sheer size of it towering over the ROV, understanding this fluid sustains unique ecosystems. After over an hour and a half descent to get to these 2600m deep sites also instills a sense of how remote and hard to reach these vents are. The vent fluid shimmers in the water, highlighting the hot temperatures and chemical richness spewing out. Even though we are still on the ship, within the van surrounded by screens with different cameras and vehicle information, it feels like we are in the ROV seeing these sights firsthand.

One amazing experience happened at 2am at our dive in Tow Cam. After we placed the McLane pump down, we realized we were within a ring of hydrothermal vents, surrounded by rocky peaks. We began to explore the surfaces up and down, searching for our target snails, and surveying the area. As we exited the center, we came face to face with a brilliant orange dumbo octopus. The van erupted into excited gasps and panic to get the cameras rolling. It was a rare sight to see, and one that will stick with all of us in the van forever.

Another cool creature came to us not during a dive, but during the recovery of Jason. When ascending, sometimes fish will get caught on the vehicle and during our Tahi Moana recovery, we accidentally snagged this majestic dragonfish. With an iridescent body and long pointy teeth, it’s certainly nothing like the fish we’ve seen before. We all gathered around to observe it, a deep fish that’s made it to the surface, in relatively good condition for a 2.5km pressure change (about 255 atmospheres!). Unfortunately, we are not here for fish and do not have a permit for keeping them, so we couldn’t hold on to it, and said our goodbyes.

Ifremaria nautilei

I want to end this post by highlighting one of the snail species we’re studying on this cruise, as we’ve been collecting a lot of them, and have been spent a lot of time on their processing. Ifremaria nautilei is a species of deep-sea provannid snail that can be found across all our active sites in this arc-basin, and even in other vent sites like the North Fiji Basin. Here are some headshots of some models collected from Tahi Moana. The bigger ones are about the size of a baseball! What makes these snails so interesting is their unique reproduction. Within their foot (the muscle they crawl around on) they have a brood pouch to raise the embryos. However, these embryos are transported along a ciliated groove (ciliated = moving hairs) into the pouch that expose them to the environment prior to development. They then develop into unique “Waren’s larva”, which have only recently been described. As all of our study snails at these sites have bacterial symbionts that allow them to survive on vent fluid, we are interested to explore when Ifremaria get their symbionts. Whether or not symbionts are acquired during this external movement of embryos to the brood pouch, or during their free-swimming larval stage is something to be explored. Little is known about the Waren’s larva as well, and we hope to learn more about them and potentially culture them on this cruise.


Crossing Lines of Space and Time

April 1st, 2022. During our long transit across the Pacific Ocean there have been a few exciting moments on the ship relating to our path. From Hawaii to the Kingdom of Tonga, the ship crossed over the International Date Line, as well as crossing over the Equator. This ties into sailing traditions of sailor tattoos, earning tattoos representative of the achievements in their career. For instance, when one crosses the Equator, a sailor now earns the right to wear a shellback tattoo. During this cruise the science party is ticking off a few of these achievements: crossing the Internal Date Line earns the golden dragon, sailing to Hawaii (on the way back) earns a hula girl, and a swallow is earned for every 5,000 miles sailed. Many of us have talked about getting some of these when we get back to commemorate this long expedition.

The science party participated in another sailing tradition, or ritual, when crossing over the Equator. To earn the shellback title, graduating from a pollywog, there’s typically a crossing event that takes place. These events can be fairly traumatic and are more like hazing events. Crew members being taken from their berthing rooms, food waste dumped on them, or physically abused. We did not do this, instead, we did a voluntary ceremony to be cleansed with “equator water”. No hazing here. We filled up a bucket for each scientist, with some members of the Jason and Sentry parties joining, lined up against the side of the ship, and baptized ourselves under King Neptune. As we dumped the water, we were welcomed across the boundary separating the North and the South, granting access to the Southern Hemisphere. After the ceremony we received certificates noting the time and place we crossed, 167 25.0 West on March 28th, and our place of respect within the realm of Neptunus Rex. It was a bonding moment for the family of scientists, taking lots of photos and videos of the event. To the right is a lab group photo, it was all of our first times sailing across the Equator.


The day before, we crossed the International Date Line on March 27th / March 28th where we only changed our time, not the day. We went back one hour but we were supposed to move forward a day, instead deciding to keep the day the same to avoid mix-ups in our continuous tracking of days and events at sea. This caused some confusion among the science party, as now when we are connected to the internet all our messages and notifications are coming from the future, telling us we posted in 20 hours, or our messages from yesterday, are actually today. Some of us entered a philosophical state, joking about the human constructs of time, entering a state of temporal limbo. It was nice to get an extra hour of sleep though! Time at sea already feels so different, none of us can remember what day of the week it is, and soon when sampling starts it will only get more difficult to keep track of time. We will all be on different ROV Jason watches, 6 4-hour shifts for round the clock science as well as having separate responsibilities to be available for the different instruments. This will inevitably set us all on different sleeping schedules, and time will become meaningless to us. It doesn’t help that while we are all coordinating with “ship time”, the ROV Jason operates under UTC time. Today we’ll be finally reaching our first site, Kilo Moana. We’ve been split into our respective teams of dissecting and microscopy, to divide and conquer all the snails we will be collecting for this grant. Now all the instrumentation we brought will be put to the test and after 10 days of transit, we’re ready to start the science.

Leaving Vacation for a New Destination

From city skylines, to unobstructed ocean horizons.

March 27th, 2022. While our shelter in place in Hawaii was very comfortable, sunbathing in between work and diving into the local cuisine, the purpose of our time on Oahu had come to an end. After three COVID tests – pre-flight, post-flight, and before mobilization, we were cleared to join the vessel, the R/V Thomas G. Thompson. After a brief delay waiting for a part for the ship, we set sail towards the Lau Basin. When the cruise was initially planned, we aimed to leave out of Tonga or Tahiti for easier access, now leaving from Hawaii means we will begin our cruise with a 10-day transit across the Pacific Ocean. If you want to see where we are along this journey or throughout the cruise, click here!

As we boarded the ship, we said our final goodbyes to land. We won’t be making any stops during this voyage, the next time we set back on land will be around May 10th, back in Honolulu. It was a good thing to be staying on such a lush island, as we won’t be seeing much green out on the ocean. The only respite will come from a small succulent we brought on board, our little lab plant.

We crossed the gangway with all of our luggage to friendly crew members welcoming us on board. To some, the Thompson is an old friend, participating on another cruise just last May, but to many this was a new introduction. We made our way to the main lab where we began to familiarize ourselves with our new home. We learned where we would be sleeping, our berthing rooms, where we would eat, the galley, our meeting spot, the library, and other amenities on the ship including a small gym, the laundry room, and a movie lounge.

Once we were moved in, the first step was to set up the lab. Before heading to sea it’s important to ensure everything is tied down properly, avoiding any expensive crashes resulting from the rocking of the waves. We set down grippy shelf liner, drilled holes into the tables and secured equipment with rope, and ratchet strapped larger bins and technologies under tables and to the walls. We also set up our respective lab spaces for the different processing we’d be doing, and organized our equipment to avoid future headaches of digging through our various deep containers.

Now at sea, with such a long transit time to our study sites, it begs the question, what are our scientists up to? Here’s a list of what we’ve been doing to keep ourselves busy:

  • Science meetings – informal presentations about the various project goals from the inter-institution science party.
  • Writing proposals and preparing for post-cruise presentations.
  • Setting up our equipment and running tests.
  • Many board and card games including Rummikub, Ligretto, Egyptian Rat Screw, King’s Corner.
  • Lab group photos.
  • Movie nights – “Nausicaa of the Valley of the Wind”, “O Brother, Where Art Thou”, “The Goonies”, “Ghostbusters”.
  • Stargazing out on the bow.
  • Lifting weights and running on the treadmill in the gym (getting off a treadmill on a rocking boat is a very disorienting feeling).
  • Curling up with a good book (I’m currently reading The Shining, maybe not the best book when being *voluntarily* trapped somewhere remote).
  • Drawing analog and digital art.
  • Journaling and reflecting on times in Hawaii and life at sea.
  • Getting to know each other – sharing stories and comparing the different regions we’re from.
  • German lessons from Livia.
  • Texting and calling our friends and family (yes we have internet all the way out here!).
  • Sunset watching.
  • Searching for whales and watching flying fish off the boat. Apparently humpback whales are currently migrating to Alaska from Hawaii.
  • An intense hula hooping contest (current record of 303.74 seconds held by Melissa Betters of Temple University).

We’ve managed to keep ourselves occupied, enjoying the free time to pursue our hobbies and make friends before the hectic science begins. We will have a lot of different processing to do, and around the clock work to ensure everything is done before the next batch of science is brought up. While we will be spending nearly two months together, the science party is already becoming a family, and staying relatively sane on this metal home in the middle of the ocean. The first challenge on this cruise however, will be overcoming the noises of the ship. Down in the berthing rooms, we have constant booms from the waves crashing into the metallic hull, reverberating through the structure. Eventually it will become a soothing, familiar sound, for now, a constant anxious reminder of the strength of the ocean around us.

Shelter in Paradise

Diamond Head Viewpoint, Oahu, Hawai’i

March 18th, 2022. Aloha! Welcome to paradise, or that’s what it feels like to the Arellano Lab. This warm, lush island is a little different to what our lab is typically experiencing during March in Washington. Currently the lab is sheltering in place in Waikiki, Oahu, HI, until March 21st when we board the R/V Thomas G. Thompson. After years of set backs, the Arellano Lab is finally heading to the Lau Basin to study how symbionts influence species distributions of Provannid snails at southwestern Pacific hydrothermal vents.

During this cruise, the lab will work closely with scientists from multiple institutions including the University of Rhode Island (URI), University of Oregon (UO), Temple University, and the Gollner Lab at NIOZ. This multi-institutional crew will also work with a plethora of deep-sea instruments including ROV Jason, AUV Sentry, a McLane High Volume Pump, Suspended Particulate Rosette (SuPR) samplers, and Field Recruiment Isolation Enviroments (FRIEs) to collect samples.

Left to right, top to bottom; Dexter Davis (WWU), Livia Brunner (NIOZ), Avery Calhoun (UO), Marcus Chaknova (UO), Michelle Bauer (URI), Johann Becker (URI), Aubrey Taradash (UO), Tanika Ladd (WWU), Sebastian Bergen (UO), Lauren Rice (UO), Roxanne Beinart (URI), Shawn Arellano (WWU), Caitlin Plowman (UO), Vanessa Jimenez (WWU), Emily Cowell (Temple), Tessa Beaver (WWU), Maia Heffernan (WWU), and Melissa Betters (Temple)

We will be collecting many different types of samples, and we’ll go into depth about what all these will tell us later in the cruise blog. The focus of this cruise will be on two main groups of snails found at our sites; Alvinoconcha sp., and Ifremaria nautilei. Relying on symbiotic bacteria that feed off the vent fluid, their distributions follow patterns throughout our sites, and we want to find out why. To explore this question we will be dissecting adult snails to retrieve gill tissues, we will sort through plankton samples searching for larval and juvenile snails, and we will collect and filter water samples. Additionally, we will take lots of photos and videos of our sites and the organisms that inhabit them.

For many of us this is the longest cruise, or the first cruise we have been on. Spending a total of 51 days on the ocean, without stopping at any ports, we will put to the test our dedication to unraveling the mysteries of the deep-sea.

Before we head out on our expedition, with long nights and hard work, we’re enjoying the Hawaiian experience, much different than our home towns. Staying COVID conscious, and avoiding people, we are delving into the tropical natural world around us.

Many of us are spending time at the beach where we read, draw, swim, and tan (actually more like burn..) in the 82 °F sun. This tropical climate also allows us to experience all sorts of different flora and fauna, exciting for a group full of biologists and nature lovers. Hiking through forests of palm trees and large fronds, volcanic craters, along the coast with cerulean waters and sandy beaches, Oahu is full of fantastical habitats to explore.

On top of the nature, we are inquiring on the local cuisine. A new variety of local fruits consisting of guava, papaya, lilikoi, longan berries and many others stimulating our tastebuds. The accessibility of local fish provide delicious poké and sushi dishes to try. Of course we also have been trying other Hawaiian specialties including musubi, hula dogs and malasadas. Staying in the Waikiki area supplies many different international cuisines as well such at Korean BBQ across the street, udon and ramen shops down the strip, empanada food trucks, and burgers for our dining pleasure. We are certainly making the most of our shelter in place.

To follow along with our journey search for our Instagram and Twitter posts including the hashtag #veligervoyage

Koko Head, Oahu, Hawai’i

NDSF User Spotlight: Shawn Arellano

The Arellano lab is proud to be showing off the hard work we do! Dr. Shawn Arellano was chosen to be interviewed by the National Deep Submergence Facility (NDSF) for her work at cold seeps. Through working at these sites, she has been able to work with all three of the NDSF’s prized deep-sea vehicles; HOV Alvin, ROV Jason, and AUV Sentry. Check out NDSF’s post and learn more about how these vehicles have helped us with our project!

https://ndsf.whoi.edu/shawn-arellano/

Rolling in the Deep, Goodbye Cold Seeps

June 18th and 19th, 2021

Some of us stayed up all night, wanting to spend as much time together as possible before returning to our homes. For some this was routine on the night shift, for others, we tried to stay up as long as we could. Staying up was worth it to reminisce on the memories we’ve built on the past month, and see a beautiful sunrise to close out our expedition at sea. We all packed out backpacks and suitcases, cleared out our berthing rooms and swapped out linens, and gathered in the lab. Here we talked about future plans to meet up back home, hopes to see each other on the next cruise, and wished everyone the best in any path they pursue.

Together, we packed up all the science we needed to quickly ship including live organisms and thermally sensitive samples and creates piles near the door. First came the moving truck where we stocked our mail and made sure our science would get home safely. Then, the shuttles arrived, and we all waited on the deck of the ship, a waving goodbye party to our fellow shipmates. Eagar to get home and return to our own beds and lives, we departed the ship, but we knew we’d miss conducting science at sea together. Not all of us left as once however, some of us were flying out on the 18th, and the rest of us flew out on the 19th. For those that stayed behind, we had one more night aboard the ship to hang out and say farewell to the crew and ship.

Interview with the Scientists

How are our scientists feeling now that they’re back home?

“Definitely happy to be on dry land!! Loving the fresh tree smell!” -Laura Murray

“Glad to be in my own bed, but I miss the people and the science!” -Avery Calhoun

“Miss the people and work, but I think I miss the sound of bow thrusters going while I’m trying to sleep the most!” -Liam Patrick

“Enjoying the green but missing the 360 ocean and amazing sunsets” -Sinja Rist

“I literally cannot stop thinking about spending time out on the bow, the laughs, being on the ship with everyone!” -Carmen Sanchez-Reddick

“I thought I was over the dock rock but then I fell over tying my shoe yesterday and started to miss people and the boat all over again.” -Casey Barnard

“Enjoying the comforts of home, miss driving with Jason” -Ian Grace

“I had forgotten that the seasons kept changing without me, it’s suddenly warm and green in Washington. Miss the sunsets, dolphins, and people, among other things.” -Fiona McBride

“Happy to be home and sleeping, but missing sunsets on the bow” -Lauren Rice

After first contact with land, stressful connecting flights, and changing time zones, we all managed to return to our home states. With the TGT behind us, the ship will continue traveling at sea, down through the Panama Canal, and up the western US to return to its home in Seattle, WA. With the Arellano lab back in Washington, we began our late night journey back to the Anacortes and Bellingham areas, where we can rest before unpacking and getting ready to analyze our science! We’re so grateful to be part of an inter-institution project and really enjoyed working with other amazing scientists each with unique perspectives. Contributing to deep sea research and building strong connections on board has been a dream come true.

With that being said, I hope you all enjoyed the blog! If you want to continue following along with our projects visit the project’s main page here: https://sites.google.com/ncsu.edu/salt  or follow our Instagram: @larvallab and Twitter: @LarvalLab

Thank you to:

The Thomas G. Thompson and crew for aiding us in our data collection.

All the scientists in the science party and on the submersible teams for working so hard throughout this cruise.

Western Washington University, University of Oregon, North Carolina State University for supporting our students and faculty in participating in this cruise.

University of Washington School of Oceanography for coordinating COVID-safety and communications.

Marine Biological Laboratory for providing quarantine housing pre-cruise.

NSF for funding this project.

Readers for your interest in our work!

 

If you are curious about me, you can follow me on Instagram: @djdavis123 or Twitter: @dexterity_no.

See you next time!

We’ll Be Home Shore-tly

June 17th, 2021

All good things must come to an end, and today marks the last day of our research cruise. Early this morning we recovered Sentry for the last time and began our transit to Gulfport, Mississippi, where we are departing the Thomas G. Thompson. It has been such a privilege to work with both the ROV Jason and the AUV Sentry throughout this past month. Without their help we wouldn’t have been to conduct such incredible science to answer our research questions about cold seep larval dispersal. While working with Sentry, we would bring up water samples and sort through them to identify different larval types. In total, we found 232 different types of larvae, and found 1,885 total larval individuals with the SyPRID sampler. To collect these larvae, we sieved through the equivalent of 30 seconds of water gushing over the Niagara Falls in total. Our collections would happen right above the seafloor, and then a midwater depth both onsite and offsite. While we sorted through these samples, Sinja Rist would take pictures of the larvae we found and determine whether or not the individual was part of a new morphotype. In this picture you can see we would print out the larval types and put them around the microscopes for reference. We ended up having a beautiful gallery of Atlantic and Gulf of Mexico larvae that we found during this cruise.

With our Sentry samples completed, we shifted our focus to finishing the samples collected by Jason. We dissected and preserved our final mussels. We sorted our final biobox samples, larval tube trap samples, and Technicap samples. Just like that we had come to an end of our science at sea. Having the opportunity to work closely with such exotic species and conduct deep sea research has been incredible. As students we’ve learned so much about the scientific process in practice. We developed our lab and field skills, we experienced the importance of scientific collaboration, and we were able to work with career scientists and engineers while building a community. To commemorate this impactful month at sea we took a group photo on the bow of the TGT.

With the rest of the night ahead of us, we began packing up all our equipment and making arrangements for shipping our gear along with specimens returning to our home labs. While we were involved in a complex Tetris game to get everything to fit in boxes, our minds were reflecting on the experiences we gathered while at sea. In the name of science we all worked incredibly hard in the past month, forgoing adequate sleep, having limited contact with the outside world or our loved ones, and missing events and milestones in our own lives. In return we gathered so much data, built strong relationships, acquired applicable marine science skills, worked with high-end submersibles, and saw things many don’t get to see in their lives. This was such a unique and impactful experience. If I’m saying it a lot, it’s because it’s true!

We made sure to take time to appreciate the final sunset on board, and we were also lucky enough to get a tour from one of the engineers on board to see behind the scenes of the ship. For a vessel that spends months at sea at a time, the ship has all the systems necessary for smooth sailing. As we went through the engine room we were shown the various systems that make life at sea possible. But first we had to put earplugs in because it’s extremely loud inside! In the engine rooms we observed the cooling systems that allow us to survive the heat of the Gulf. We were shown the reverse osmosis machine that converts seawater into available freshwater. We got to see the large engines that allow for our dynamic positioning to hover above site. We also saw the Z-drive that powers the propellers on the back of the ship. At the end we got to see the control room, where all the power in the ship is diverted. There’s enough power on this vessel to run a small town! During this tour we also learned some cool trivia! This vessel can travel at maximum 16.7 knots and can hold 280,000 gallons of fuel! Tomorrow we begin flying home, but it was a great way to end our time with the Thomas G. Thompson by exploring how this ship made everything possible!

Don’t Abandon Your Canyon Companions

June 16th, 2021

Today begins the end of the cruise. After spending three and a half weeks at sea, we returned to our final site, Mississippi Canyon. We launched our final Jason dive around 8 in the morning, after scrambling to finish cups to shrink. We placed our final deployments in Jason’s basket and saluted Jason as it was picked up by the winch and released into the water. At 1074 meters deep, Mississippi Canyon represents our midwater site compared to the shallow trifecta sites, and the deep Florida Escarpment site.

When we reached the bottom, we were met with a deserted landscape. It felt like an alien planet. With mud volcanoes and small canyons, the occasional fish or patch of bacterial mat, it was an unfamiliar habitat. We trekked through this wet desert scanning for our target mussels, with this site containing two different kinds: Bathymodiolus childressi and Bathymodiolus brooksi. We want to collect both kinds to understand the differences between the species. They look fairly similar, while brooksi has a chalkier texture and a bump on the umbo (the hinge of the mussel), so we had to look carefully. While we searched for mussels, Dr. Young set up an early Father’s Day present by preparing a Zoom with his dad to livestream the main science camera we use during our dives. Deep-sea habitats are bizarre, and we try to share the exploration with those we can, like this blog attempts to.

Here’s a video that Avery Calhoun created on the last research cruise highlighting the Mississippi Canyon site:

During the dive we did struggle to find our mussels, these deep-sea sites aren’t entirely understood or predictable. Luckily, we knew of another potential location from another deep-sea cruise and headed that way after scanning our original site. We traveled northwest and eventually found a large mussel bed where we collected our specimens, finding both of the target species, and deployed our equipment. After completing those objectives, we had the task of recovering our equipment from the last cruise, which was a ways away. On the last cruise the dive was cut short due to weather and the equipment was not an optimal location. On the way back we stumbled across a natural wonder, a brine river! We’ve seen a few brine pools, and a lot of brine puddles, but this river of brine extended across our whole view from the van. After crossing the salty stream, we picked up our equipment and resurfaced. With Jason back on deck, and with heavy hearts, we began sorting our samples for the last time.

As our time comes to an end in the Gulf, it’s been interesting to see a new perspective on human activity. When we look around, we are surrounded by oil rigs. With the oil that is seeping out at our research sites, the number of rigs was not surprising. However, as we move from site to site, there’s always a few oil rigs on the horizon. At night they come alive, and the horizon is dotted with these small cities on the water. Even the open ocean is still bustling with activity.

Tonight, we deploy Sentry for the last time. As we sort through the final samples, sort the last mussels, and take our final morphotype pictures, we’re getting ready to start packing up and heading home.