Well, it has been a tremendous journey. Our ship arrived safely to port on Saturday in Panama and everyone, including the ship's crew, was very excited to hit dry land again. On Sunday, the scientists began flying home, while a few stayed behind to spend time in and around Panama. The ship soon began its week-long return trip through the Panama Canal to its home port in Fort Pierce, Florida. The work continues as the ship must be unloaded and its cargo - rich now with scientific data - returned to the scientists at their home research labs and institutions. It will take many months and years to examine the specimens and data obtained from the research cruise. All the hard work at sea has enabled scientists to return with a wealth of scientific information which they can now examine at their own pace in their research labs. Thank you for joining us on this incredible journey. If you have any questions or comments, please send them to: etpcruise@yahoo.com.
Monday, November 26, 2007
Friday, November 16, 2007
Happy Birthday Ruth!
On Wednesday, November 14th, we celebrated Ruth Coffey’s birthday. And how do you celebrate a birthday at sea? With cake, of course! Ruth was treated with a chocolate multi-layer cake from the galley complete with “magic” candles. The crew surprised Ruth with a photo of our current home, the R/V Seward Johnson and a Seward Johnson t-shirt while she watched one of her favorite flicks, Indiana Jones and the Last Crusade in the lounge. While you should be sure to celebrate again with Ruth when she gets home, don’t feel too bad for her for being away at sea on her special day – she said that this was the most fun she ever had on her birthday! Happy Birthday Ruth!
Wednesday, November 14, 2007
What a day!
We continue to steam on towards our port of Panama. Most scientists have begun to pack up their equipment and laboratory supplies, while others are completing experiments that began while we were on station at the Costa Rican Dome. Because the waters of the Dome are so productive, wildlife viewing has been fantastic even as we transit out of our research station. In a matter of hours, dozens of turtles had been sighted, and manta rays were seen leaping throughout the day. We had a very special treat yesterday when not one, but two different pods of dolphins joined us for some bow riding, and amazed us with their acrobatic leaping and porpoising around the boat. Bottlenose dolphins were the first to arrive and were so close during bow riding that we could hear their underwater clicks and whistles! The Common dolphins arrived later and could be seen leaping so high in the air that they easily leaped twice their height out of the water. Tuna could also be seen jumping alongside them. Several of the Common dolphins came up to the boat to bow ride as well, providing excellent and exciting views of these beautiful creatures. It is a very exciting time as we travel through this incredible place, all the while knowing that much of our research and hard work aboard the ship has ended and we are finally heading home.
Sunday, November 11, 2007
Operation Shrinking Cups
It’s been a long few days here at our final station. The research has continued around the clock and sleep is again at a minimum. We are all trying to finish up our deployments and experiments before beginning our transit back to Panama on Tuesday. Some of the sampling systems have already decided that it's time for a vacation, keeping the ship’s senior technician busy with repairs. In the midst of all this activity, we launched Operation Shrinking Cups, decorating Styrofoam cups and sending them down with our deep cast CTD this morning. The cups returned a fraction of their original size; a stunning example of the immense pressures exerted onto objects at 1500 meters. Tonight Dr. Brad Seibel and his crew resumed their nightly tradition of squid jigging, shining bright lights onto the waters surrounding the ship. The light attracts and highlights small organisms, which attracts larger predators, which move in toward the surface to feed. Tonight we had company as four bottlenose dolphins joined in on the hunt. They provided us with an excellent exhibition of their speed and maneuverability. The research continues now with SCUBA divers in the water and a midnight running of the MOCNESS. It’s never a dull moment on the R/V Seward Johnson here at the Costa Rican Dome.
Friday, November 9, 2007
Sea turtle rescue at sea!
Tonight we had a dramatic example of how floating marine debris, in particular, lost fishing gear can harm and kill marine life. Upon setting out to deploy our Tucker trawl, the ship’s crew spotted a large fishing net floating in the water with two sea turtles ensnarled in the gear and floating helplessly with it. The boat moved alongside the turtles to assist and upon further inspection found that one of the turtles was dead while the other was alive, but wrapped heavily in fishing line across its neck and front flippers. The fishing gear wrapped so tightly around the turtle’s front right flipper that it was completely severed from its body. One of the crew members immediately used a knife to free the line from the live turtle. The dead turtle was brought on board for inspection and the fishing gear removed from the water for proper discharge on land. The two turtles appear to be Olive Ridleys, which are quite abundant in this area (off the Pacific coast of Mexico and Costa Rica) and are believed to be the most abundant sea turtle in the world. Nonetheless, the loss and maiming of these beautiful animals struck a blow to all onboard. Floating fishing gear kills countless birds, mammals and sea turtles every year, in addition to fish and other marine life. This destructive act is termed “ghost fishing”, for its continual capture of marine life, which can carry on for years after the gear has been lost or abandoned. Sea turtles around the world have suffered dramatic population losses from their entanglement in lost and active fishing gear. For more information on sea turtles and what you can do to help, visit The Blue Ocean Institute’s website at http://www.blueocean.org/ or the Riverhead Foundation’s (New York state’s marine mammal and sea turtle stranding program) at http://www.riverheadfoundation.org/.
Wednesday, November 7, 2007
The Costa Rican Dome
We made it to our last long station - the Costa Rican Dome - located at 9°and 90°W. This station lies inside a highly productive upwelling system, receiving its name from the doming of the isobars (lines of constant pressure) that result from the upwelling of cold, nutrient water towards the surface. These nutrients support abundant phytoplankton growth (also known as primary productivity) which in turn supports higher-than-usual abundances of zooplankton and higher trophic levels, including dolphins and whales. So it was no surprise when our ship encountered a couple of whales just an hour before reaching the station last night, welcoming us to our last stop. We are all excited to reach our final station and to be in such a highly productive region. The flurry of activities began immediately last night with CTD casts, Tucker trawl and SIPPER deployment, continuing into the morning with the launching of the MOCNESS, and continued deployment of the CTD and SIPPER. So the race for sleep is on, but it is always exciting to reach a long station and resume research, especially in such a special place.
Tuesday, November 6, 2007
Monday, November 5, 2007
Rockin' and a rollin'
The ship ran into some rough seas last night, which resulted in the cancellation of the night’s activities and a decision to move forward to our other stations. The waves were pounding onto the deck as the scientists tried to maneuver the CTD back from the sea onto the deck. Dr. Stuart Wakeham and his CTD team were splashed repeatedly by the angry seas in a scene similar to those on ‘Deadliest Catch’ (only with warmer water)! Inside, chairs and unsecured items went flying or toppling over. This made matters worse on deck since it was already dark and the scientists deploying equipment would not be able to see the large waves before they strike – a dangerous position to be in, and hence the reason sampling for the night was scrubbed. Other students working inside confined laboratories were fighting bruises and seasickness as the rough seas tossed their samples and themselves about as the boat continued to rock throughout the night. We arrived briefly at an intermediate station today to run a quick CTD cast and now continue on to our next short station, which will be reached tonight during the smaller hours of the morning. The seas have finally calmed a bit making sampling, working, and sleeping easier on all of us.
Sunday, November 4, 2007
Short Station
We are presently at our third short station located at approximately 10° N latitude and 96° W longitude. Dr. Stuart Wakeham and Heidi continue pumping water at depth during the CTD casts while the boat remains motionless (a necessity for pumping and collecting water). After the CTD is brought back up later this evening, the SIPPER, MOCNESS and Bongo nets – all of which require the ship to be in motion – will be deployed. In the meantime, scientists continue to catch up on sleep, enter data, and make any necessary repairs to their equipment. Sleep at station is a bit of a commodity, and many of the staterooms are unfortunately not immune to the loud noises of the winches and tuggers that operate the cables during equipment deployment. The crew continues to take good care of us feeding us three ‘squares’ a day and regularly provide fresh baked cookies at snack time (around 3:30) and an assortment of desserts after dinner. Last night was steak night (a Saturday tradition) followed by an ice cream bar! Fortunately for all of us, there is also a gym onboard with weights, a stationery bike and a treadmill to burn off the munchies and keep us from feeling guilty in devouring them!
Saturday, November 3, 2007
Friday, November 2, 2007
update from Heidi (Wakeham lab)
So Stuart and I worked all night and successfully got all 4 of our pumps to work! And we just recently left station 1 and are steaming to our next stop. I have samples to filter during the transit but it will be a nice break for roughly 24 hours. We’ll have to stock up on sleep for the next station.
I have written a lot about our interest in particulate organic matter and the in situ pumping system that Stuart and I are using. We are also interested in matching the particulate organic matter with the microbiology of the water column. By microbiology I mean the different types and amount of bacteria and archaea that live in the ocean. The types of bacteria and archaea change as you move down the water column. For example, there are populations that like to live in the light and high oxygen concentration of the surface and others who live in the low oxygen in the dark subsurface waters. So we collect water samples with the CTD at different depths for DNA analysis and fluorescent in situ hybridization (FISH) microscopy.
For DNA analysis we collect 20 L of water and filter it with a pump to capture the microbes. Then when we are back on land at our lab we can extract the DNA off the filter and see which types of microbes lived in the water we filtered. For FISH samples we collect 200 mL of water and filter them with a hand pump so that the cells are gently collected and not broken. Then, back at the lab we take the filter through a short process that adds dyes to the microbes. Next, you look at the filter under a microscope the bacteria will glow in one color and the archaea will glow in a different color. This makes it easy to count the different types of microbes. For an example, see micrograph image at bottom right (of photo cluster above) and click on to enlarge.
I have written a lot about our interest in particulate organic matter and the in situ pumping system that Stuart and I are using. We are also interested in matching the particulate organic matter with the microbiology of the water column. By microbiology I mean the different types and amount of bacteria and archaea that live in the ocean. The types of bacteria and archaea change as you move down the water column. For example, there are populations that like to live in the light and high oxygen concentration of the surface and others who live in the low oxygen in the dark subsurface waters. So we collect water samples with the CTD at different depths for DNA analysis and fluorescent in situ hybridization (FISH) microscopy.
For DNA analysis we collect 20 L of water and filter it with a pump to capture the microbes. Then when we are back on land at our lab we can extract the DNA off the filter and see which types of microbes lived in the water we filtered. For FISH samples we collect 200 mL of water and filter them with a hand pump so that the cells are gently collected and not broken. Then, back at the lab we take the filter through a short process that adds dyes to the microbes. Next, you look at the filter under a microscope the bacteria will glow in one color and the archaea will glow in a different color. This makes it easy to count the different types of microbes. For an example, see micrograph image at bottom right (of photo cluster above) and click on to enlarge.
Transit time
We finally left our first long station last night after a final MOCNESS tow sampling the lower portion of the oxycline. There is rest to come for some of us as we make our way towards several intermediate (short) stations, but the work continues for many others. The past 3 nights have been excellent for star gazing and with no manmade lights for hundreds of miles around, the Milky Way shown clear across the night’s sky. Transit time means catching up on a good night’s sleep, entering data, cleaning up, and preparing for the next station. But it also provides time to catch a movie in the lounge, continue dart tournaments which began earlier in our transit days (have you ever tried throwing a dart in rough seas?), and keep watch for dolphins as they ride the bow waves created by the moving ship. Check out Dr. Brad Seibel and his Ph D. student Amy Maas jamming on their guitars during some down time. They're really good!
Thursday, November 1, 2007
Happy Halloween!
Happy Halloween from the eastern tropical Pacific! In honor of the holiday, several scientists and crew dressed up in costume, including our very own Leann Birden and Rebecca Williams with their loyal intern, Dr. Stuart Wakeham as Team Zissou. There were also pirates and witches to be found on the prowl for some of the gremlins that have been hiding out in our equipment the past few days. At night, the chip’s stewards announced the winners to a costume contest, with the recipients receiving an R/V Seward Johnson t-shirt. And our very own SIPPER was equipped with a witch (OK, it was a pez dispenser) to ward off any spirits in the depths as it was deployed this Hallow’s Eve. So maybe no trick or treating here at sea, but we made the most of it, and had plenty of candy to prove it!
Wednesday, October 31, 2007
Blog from Christine Cass (Daly lab)
In the eastern tropical Pacific, there is a very prominent oxygen minimum zone at intermediate depths of the water column (from about 300-600 m). Oxygen levels in this oxygen minimum zone are extremely low and many organisms cannot survive under such conditions. This leads to a vertically layered water column, where some marine life is confined to the well-oxygenated shallow water, while other organisms seem to tolerate low-oxygen conditions and are found within or near the oxygen minimum layer. It appears that even closely related species can reside in very different oxygen environments.
My work examines aspects of the biochemistry and physiology of copepods which reside in different oxygen environments in the water column. I will compare substrate usage (whether lipids, carbohydrates or proteins are primarily used for energy), body composition and feeding preferences between three closely related species of eucalanoid copepods. Hopefully, these analyses will allow us to better understand adaptations of copepods to low-oxygen conditions in the water column.
My work examines aspects of the biochemistry and physiology of copepods which reside in different oxygen environments in the water column. I will compare substrate usage (whether lipids, carbohydrates or proteins are primarily used for energy), body composition and feeding preferences between three closely related species of eucalanoid copepods. Hopefully, these analyses will allow us to better understand adaptations of copepods to low-oxygen conditions in the water column.
Blog from Heidi (Wakeham lab)
So last entry I was a bit brief on what Stuart and I are actually doing. I’ll try and explain in further detail below. But, I am excited to say we have actually collected some good samples and are scheduled to pump again tonight starting at 1AM!
Stuart and I are collecting filters of seawater at various depths in the ocean. The filtering units consist of a steel frame, a battery unit (black cylinder), a vacuum pump, a filter stand (smaller black cylinder), and a flow meter. So the water is slowly sucked through the filter stand, then through the flow meter and then back out to the open ocean. We trap the particles, bacteria, and archaea on our filter. The filter stand has a mesh grill to catch any larger animals or objects that get sucked in, followed by a 53 micrometers filter to catch small animals, and then a 0.7 micrometer glass fiber filter that we collect for our sample. The glass filters have been heated to 450 °C to burn any organic material off them so that they are completely clean when we put them in the filter stand. Therefore we know our results our just from the ocean.
The CTD is a machine lowered on a steel cable that has twenty-four 10 L bottles attached that can collect water at specific depths in the water column. It has sensors attached that can measure the salinity, O2 concentration, and depth. We use the cable for the CTD and it’s depth meter to lower our filtering pumps to the layers of water we want to collect. This is a tricky process. The CTD gets lowered into the water and then we have to coordinate with the crane operator to lower the cable a certain distance and then we lean over the side of the boat (with safety lines tied to our life vests) and attach the 100 lb. filter pump onto the cable. It is a little scary when the weather is bad and the waves are high.
So far, we have collected 9 depths from station 2 and 4 depths from station 1. We are scheduled to pump again the next two days so we should end up with 12 depths from station 1. The filters are stored in the -80 C freezer. We will transport the lipids back to our lab frozen and then extract the filters for bacterial and archaeal lipids.
We are interested in the particles in the ocean because the particles sink to the bottom and form mud, the mud becomes sediment, and the sediment over geologic time becomes sedimentary rock. We study the particles to see what will eventually be compressed into the sedimentary rock. If we can understand this process in the modern times we can get useful information about paleoclimate and paleoecology from the sedimentary rocks of the past.
Stuart and I are collecting filters of seawater at various depths in the ocean. The filtering units consist of a steel frame, a battery unit (black cylinder), a vacuum pump, a filter stand (smaller black cylinder), and a flow meter. So the water is slowly sucked through the filter stand, then through the flow meter and then back out to the open ocean. We trap the particles, bacteria, and archaea on our filter. The filter stand has a mesh grill to catch any larger animals or objects that get sucked in, followed by a 53 micrometers filter to catch small animals, and then a 0.7 micrometer glass fiber filter that we collect for our sample. The glass filters have been heated to 450 °C to burn any organic material off them so that they are completely clean when we put them in the filter stand. Therefore we know our results our just from the ocean.
The CTD is a machine lowered on a steel cable that has twenty-four 10 L bottles attached that can collect water at specific depths in the water column. It has sensors attached that can measure the salinity, O2 concentration, and depth. We use the cable for the CTD and it’s depth meter to lower our filtering pumps to the layers of water we want to collect. This is a tricky process. The CTD gets lowered into the water and then we have to coordinate with the crane operator to lower the cable a certain distance and then we lean over the side of the boat (with safety lines tied to our life vests) and attach the 100 lb. filter pump onto the cable. It is a little scary when the weather is bad and the waves are high.
So far, we have collected 9 depths from station 2 and 4 depths from station 1. We are scheduled to pump again the next two days so we should end up with 12 depths from station 1. The filters are stored in the -80 C freezer. We will transport the lipids back to our lab frozen and then extract the filters for bacterial and archaeal lipids.
We are interested in the particles in the ocean because the particles sink to the bottom and form mud, the mud becomes sediment, and the sediment over geologic time becomes sedimentary rock. We study the particles to see what will eventually be compressed into the sedimentary rock. If we can understand this process in the modern times we can get useful information about paleoclimate and paleoecology from the sedimentary rocks of the past.
Tuesday, October 30, 2007
Long Station - Day 4
The flurry of activity continues here on day 4 at our first long research station. Scientific processes occur 24/7 with one deployment after another made of CTD, MOCNESS, SIPPER, Tucker trawls, Bongo nets, and underwater pump systems. Usually there is also a morning SCUBA dive to collect delicate organisms, however tonight will be the first night dive of the trip! The labs are packed with scientists and are almost never empty even in the early morning hours. Some of the scientists work together on crews for a specific project and take shifts, but there is a lack of sleep felt on everyone. The long stations are busy, without a doubt, but we will soon have a break as we transit to our next short station in the upcoming days. This will provide some necessary rest for all of us.
Sunday, October 28, 2007
SIPPER
The Shadowed Image Particle Profiling and Evaluation Recorder (SIPPER) is an in-situ plankton imaging system developed by the University of South Florida College of Marine Science (USF-CMS) and Center for Ocean Technology (USF-COT). The SIPPER operates by imaging plankton and other suspended particles in the water as they pass through a collimated light sheet casting their shadow and outline onto a high speed line scan camera. Ancillary data from other sensors such as CTD, fluorometer, transmissometer, oxygen and sensor diagnostics are embedded in the image data so that every imaged particle has corresponding environmental data associated with it. Plankton image data can then be either manually identified or classified using our Plankton Image Classification and Extraction Software (PICES). During this cruise, the SIPPER will be deployed in a series of vertical profiles on a small towbody on standard 0.322 CTD cable. Andrew Remsen from USF-COT will be the biologist operating the system and Kurt Kramer from the USF College of Engineering will be optimizing the PICES software.
And the research goes on
This morning began with Dr. Seibel and his team of scientific research divers (who are also his graduate students) heading out on the boat’s Zodiak for a morning SCUBA dive. They came back with many delicate gelatinous zooplankton, such as ctenophores and salps, which are best collected by hand. His team continues to deploy tucker trawls and tries to dip net any squid that venture into the well-lit surface waters surrounding the research vessel during any down time during the night. There are many experiments in progress throughout the boat, as water sampling continues and scientists scoop up important organisms from the MOCNESS tows and tucker trawls. Our research vessel, the R/V Seward Johnson provides us with the opportunity to send these nets to incredible depths and catch glimpses of a sometimes bizarre and alien world. In these dark depths of the ocean, gelatinous zooplankton and transparent squid abound. Parasitic amphipods (a type of crustacean), which inspired the movie The Alien (true story!) can be brought up in the tucker trawls and invisible fish larvae and crustaceans are frequently seen in plankton net samples. It’ll be a series of long days and short nights for the scientists here at our first “long” station, but the effort and the research that becomes of it will be all worth it.
Saturday, October 27, 2007
Station #1
What a day! Here we are at Station #1 located at 13° latitude and 105° longitude, a few hundred miles off the Pacific coast of Mexico. This research vessel has been swirling with activity since we arrived here yesterday afternoon. Immediately, a CTD equipped with a Nisken bottle rosette was deployed to collect water. Soon other sampling equipment went sent overboard. Dr. Stuart Wakeham and Heidi deployed pumps which filter water and their constituents onto a filter at various depths. Dr. Brad Seibel and his team ran a tucker trawl to collect small organisms at varying levels in the water column, including many see-through squid, shrimp, fish and gelatinous zooplankton. Dr. Karen Wishner and her team sent out a MOCNESS to capture zooplankton throughout the water column from depths as deep as 1200 meters (approximately 3600 feet!). The ship's crew and its scientists are definitely keeping busy.
Friday, October 26, 2007
Technical Difficulties
Our apologies... Blogspot is currently experiencing technical difficulties and we are unable to upload and send photos at this time. Please stay tuned for exciting research updates and images. Thanks for your patience!
Thursday, October 25, 2007
Science!
At long last, we arrived at our first research station today. We are over approximately 4000 meters of water (that’s more than 12,000 feet!). We successfully deployed a series of CTD casts, involving a rosette of Nisken bottles to collect water at various depths and the CTD instruments which record Conductivity (which is a proxy for salinity), Temperature, and Depth. Everyone on board is busy, but happy, to be doing science again! Also deployed were a series of pumps which will concentrate particles in the water column onto special filters for later chemical analysis. It’s going to be a long night and early morning for many of us here on board, but we are glad to be a part of this exciting research.
Tuesday, October 23, 2007
Almost there!
Well, we are still on schedule for arriving at our first test (or "short") sampling station tomorrow morning. Everybody is happy that they will be able to begin their research, but since things will get very busy once that happens, most are also enjoying the free time we are afforded en route. A few students continue to fish off the stern, occassionally providing dinner for the scientists and crew. The smaller ones are thrown back but not after we have had a chance to look at these beautiful creatures. A few of us tested our MOCNESS today, which stands for "Multiple Opening and Closing Net Environmental Sampling System" and contains 8 large zooplankton nets which can be opened and closed at varying depths. This instrument will be crucial for our sampling at multiple depths once we reach the stations. Having everything in running order is important for effective sampling and is also a great way to keep us busy during this long transit to our first site.
Monday, October 22, 2007
Curse of the meatloaf
Well, it is finally a beautiful day here at sea. The seas have calmed and there are blue skies all around. We had suspected that our bad luck was caused by the "curse of the meatloaf", which is rumored to have conjured up rough seas the last time it was cooked, too. Turns out, however that tropical storm-turned hurricane Kiko just north of us was the cause for all the foul weather. As we continue steaming to our site, we continue to spot dolphins, manta rays, and billfish, and of course fying fish, which are everywhere here in the ETP. We are practicing deploying our nets and other sampling systems, which will be of the utmost importance once we reach our sampling stations. And we are all hoping this good weather continues...
ETP blog Wakeham group
Today has had calmer weather but we are still behind schedule. We will get to the first station on Wednesday morning. But today we learned how to set the bottles on the CTD, how we are going to do O2 and salt analysis from the CTD, and most importantly how we will get the CTD off the deck and into the water without killing anyone or the CTD. All of my samples are dependent on the CTD casts so I was excited to learn how everything works today. Now we just have to get to the station. Hopefully the weather will cooperate. Currently there is a hurricane over the second stop!
Sunday, October 21, 2007
What a night!
Last night, the boat aimed its bright lights down onto the water and we went squid jigging! Jumbo (also known as Humboldt’s) Squid were immediately attracted to the lights and were appearing around the boat. Squid jigs – a type of lure with upturned hooks and glow-in-the-dark light sticks – were dropped into the water and immediately attracted the squid, which took the "bait" and were reeled inside. Dr. Brad Seibel and his team of biologists quickly went to work, taking blood samples from the squid for use in blood oxygen profiles. Smaller squid were also captured with dip nets and used for onboard experiments. However, most of the squid were captured and released, allowing us an excellent opportunity to interact with these beautiful creatures. Also attracted to the lights were flying fish, which surrounded the boat, and flew high above the water as if they were birds in flight. One even landed on deck! It was a beautiful experience here in the eastern tropical Pacific.
Saturday, October 20, 2007
Dolphins and tuna
It's day 3 at sea and we are still steaming to our first research station. The seas are still a bit rough and it continues to rain. In spite of the foul weather, many of us have been fortunate to spot yellowfin tuna jumping and dolphins leaping alongside. A couple of manta (devil) rays have also been spotted leaping from the surface. The crew is feeding us well and remind us that it is Saturday with steak night tonight! We are all also excited about plans for squid jigging tonight, which will be used for research projects back in the lab.
ETPblog Wakeham Group
Today we are anxiously awaiting our first station. Our equipment is mostly set up and ready we just need to load batteries into the pumps and prime them. So while we are awaiting our first destination we have been keeping busy by helping other groups setting up and catching up on sleep. The boat has a terrific crew and everything has been going fine except for some rough weather. So it’s been a rough start to my first ever cruise but hopefully the weather will improve before we get to the first station.
Green on a Sea of Blue
Day 2 of our cruise: We are still in rough seas and many of even the most experienced seafaring scientists are turning green. It has been raining all day (and night) which is not unusual since it is the rainy season here in the tropics. While we are in transit to our first station, the scientists continue to prepare for their research. On deck, many of us keep our eyes on the water looking for signs of life. Some have already had their first dolphin encounter of the trip, while others routinely spot seabirds. We are all fed well on the ship and even have access to the ship’s ice cream, which nearly everyone has taken advantage of.
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