All posts by fah3

Faith Hill Rice University; Wiess Bioscience Pre-med Class of 2025

Going to Miss This Place (Final Blog)

Hi all, it’s Faith with some closing remarks…

Reflecting on this trip, I learned a lot about rainforests, coral reefs, and biodiversity. You may have heard the phrase that “coral reefs are the rainforests of the ocean” or the other way around, and now, I know why! I got to see first hand how both ecosystems are house so much biodiversity. Both ecosystems house a majority of the earth’s biodiversity and rely on complex interspecies relationships. They are homes to a variety of specialists, that have evolved to reduce competition with other species, and both are incredibly valuable.  I observed how tree density means nothing if the tree species present aren’t native to the environment, and how hard corals provide structures and homes for an immeasurable amount of species whereas soft corals were more “space-fillers.” From the deforestation line at the Belize-Guatemalan border to the veins of coral disease at Glover’s, I saw how  humans negatively impact our environments. I even learned that these two seemingly different environments are connected: long, long ago, the sea creatures with calcium carbonate skeletons laid the foundations for the rainforests soil. This lead to the forests having numerous soils types and massive cave systems beneath them. Furthermore, the rainforest is equally dependent on abiotic factors like nutrient availability, temperature, and  soil (or water) type as coral reefs! In my eyes, the largest difference between these two ecosystems are the dominating species, as trees are plants and most corals are cnidarians!

The most surprising fact I learned from this trip is how nutrient deficient the reefs and rainforests are. This seems contradictory because organisms need nutrients to live, and these two ecosystems house most of the words biodiversity. So, one would assume that they were plentiful in nutrients. However, these ecosystem’s nutrient scarcity allows them to be diverse. Organisms have evolved to maximize their ability to get nutrients, and this results and mega-specific symbiotic interactions like fig wasps with fig trees and corals with dinoflagellates. These specific interactions create specialized niches that reduce competition and allow many different species to coexist!

However, this system also makes the rainforests and reefs extremely fragile. On this trip, we got to listen to Dr. Alavero, and hear his research on scarlett macaws. He emphasized that the jungles are equally impacted by climate change as coral reefs. Humans tend to overlook climate change’s effects when they aren’t directly visible, but the environments current changes have made the weather unpredictable which disrupts the life cycles of land animals and marine animals. Scarlett macaws utilize different areas when mating and foraging, and they use the weather to help determine when to mate and migrate. Similarly, corals, trees, and insects (like termites), “coordinate” their reproductive cycles around the climate. The world’s changing climate, has cause reduced reproductive success in macaws and is harming other species as well. With global warming and ocean acidification, we actively see the weakening of coral skeletons and coral bleaching. The decline of these species then causes the decline of their symbionts, and because everything is interconnected, this can cause great losses of biodiversity. Just seeing the extreme differences between the health of an mpa reef and a non-mpa reef indicates how harmful we are to our planet. I will never forget the impact we have on the planet, and I now understand how difficult it is to save intricate ecosystems. Because of their complexity, There is no “one-size-fits-all” solution to restoring these ecosystems. However, we should all do our part to be eco-friendly, and reduce our impact.

When I look back, I imagine that I’ll remember how this trip “opened my eyes” per se. When you first enter the water or forest, everything looks the same. But after you look a little more closely and learn a little about taxonomic groups, you begin to realize that the biodiversity lies not in the major differences but the minor ones.  In only 2 days, I was just as excited to see a new species of grasshopper as I would have been to see a jaguar. Likewise, being able to differentiate between Diploria labyrinthiformis, Grooved brain coral, and  Diploria strigosa, Symmetrical brain coral, is extremely cool.  It’s hard to grasp the differences between similar species and their ecological niches without seeing them in person. Textbooks do a great job of summarizing these specific species’ interactions, yet being surrounded by them provides a true understanding about how dynamic our world is. And now, I feel like  I could identify these interactions in my own community.

Here are a few other facts (that are a little less sentimental) that I’ll never forget.

  • Ecosystems are entirely different at night due to temporal differentiation
  •  You have to be at least 5’2″ to enroll in the Belizean coast guard
  • The barrier reef GREATLY protects us from wave activity (you have no idea)
  • The different tree-top layers provide homes to unique animals, and some fauna will only live in specific tree species
  • If you order a fish in Belize, it will be served whole!

Overall, this course was way more fun than I expected, and now I can say that I’m proud to be an Ebio major! I really enjoyed excavating the leaf-cutter ant colony, posing with the queen, exploring the Belize Zoo, and touring Caracol. Honestly, the only activity I didn’t enjoy on this trip was having to pee in a vial and sort the arthropods that fell in, but, alas, sometimes you must pee in a cup in the name of science. I learned so much, and I definitely see both the rainforest and coral reefs in a new light. I even accomplished some of my goals and one of my life goals (seeing a wild mantis shrimp), so how could I not love this trip?!

Bye bye Chiquibil!!!

Leaving Las Cuevas (Day 12)

Hi all, it’s Faith with Day 12 updates from the 2022 Belize trip…

This morning we woke up and prepared to leave Lac Cuevas. I enjoyed my morning hot-chocolate-coffee, and then joined the group at 8 to collect our pee samples from the forest.

We didn’t see any reptiles on out hike, but we did see lots of fungi from the rains. We did this hike rather speedily, so I don’t have much to report on. Afterwards, we worked on out poster and analyzed our findings. Our data supported our hypothesis by 66%. We did find more arthropods on the forest floor, and more were attracted to the pee samples over all. However, the ratios between pee:water on the floor was actually greater than that of the canopy. Our study had many limitations such as a short data collection time, inability to identify some insects, and having flagging tape on our trees. All of these could have skewed our data.

After we analyzed the data, or group split into two teams. One team went and collected the cameras, while my team stayed and packed up camp. By 3:00, we were all packed and ready to leave Las Cuevas. My team did make a quick run to the frog pond to grab the last camera; however, we didn’t see any fauna on that trip either. I wish I could have gone on the hike to retrieve the cameras, but our teams method was much more efficient

After a 4 hour car ride, we made it to Midas Resort in San Ignacio. We plan on staying here until our flight tomorrow… I’m so sad that tomorrow will be my last Belizean breakfast; I will miss the  fryjacks, eggs, and beans.

Goodbye Belize!

QOTD: “If you really have to, you could pee in a waterbottle. We are all really good at that now.”

Luna the cat at Midas Resort
Our Pee Project Poster

 

Canopee!!! (Day 11)

Hi all, it’s Faith with Day 11 updates from the 2022 Belize trip!!!

Today we had another round of early morning bird watching, and it seems we keep adding more and more coffee to our cups. Because of the fog, we didn’t see much, so we had and nice morning chat.

After breakfast, we went over to the classroom to watch Micheal’s presentation on soil (specifically soil, not dirt). After the presentation the professors told us we had to pee in vials to put out in the rainforest… and then count the arthropods that are attracted to it. I wasn’t happy about it, but sometimes you have to pee in the rainforest in the name of science. This is actually one of our experiments.

We hypothesized that arthropods would be 1) more attracted to the pee vials than the water vials, 2) more arthropods would be on the forest floor than canopy over all, and 3) that a higher ratio of canopy arthropods would be in the pee vials than the water vials than the ground arthropods. After filling the vials, we set out to place 16 stations in the forest, at least 10 feet apart. One of each vial type (water and pee) were placed on the ground and in the trees at each station. We plan on checking them tomorrow to collect our findings.

Even thought this experiment was…. Something else … I was glad we went on the Mayan trail because I saw a jumping pit viper (Atropoides mexicanus)! Phoenix was walking and happened to notice it shuffling through the path leaves. It was nearly identical to the deal leaves’ color, and it was unusually small. We got plenty of pictures. After seeing it, I asked the professor if they had ever seen an elusive eyelash viper on the trip, to which he said “we’ve never seen one on a Belize trip.” I had figured that would be the case since these vipers are hard to find. Literally as he said that, Elena yelled that there was another snake. You guessed it, sitting on a log about 1ft above the ground was a lichen-colored eyelash viper (Bothriechis schlegelii). I was almost afraid to identify it as one because I was in disbelief! Of all the reptiles to find, this was one of the best. Later on, we got to show the lead park ranger the viper because he hadn’t seen a wild one even after working here for 12 years! This was only the begging if of our luck…

After lunch we searched around the research station for leaf cutter and mounts. We found a few by the far cabins, and we began to dig them up! We started with a small 1 yo mound and eventually found the fungus growing room and Queen! After becoming ant finding experts (not really lol), we tried digging  up another nest and got nothing but spiders! Nevertheless, Prof. Solomon convinced us to keep digging saying that the ants would get here eventually. Instead of ants, however, we duh up a Mexican burrowing toad!!! He was so gelatinous!!! He was defiantly one of the trips coolest finds.

Since today ended kind of early, we did presentations before dinner, I presented on reptiles!

I’ll update you for our next hike, till then!

QOTD: “mark is real” no

“Ohhhh tomorrows day is father day!”

Mexican Burrowing Toad
Eyelash Viper (Bothriechis schlegelii)
Tiny jumping viper (Atropoides picadoi)
The horrific vials *shudder*

Trapping a Jaguar!!! (On camera, hopefully) (Day 10)

Hi all, it’s Faith with Day 10 updates from the 2022 Belize trip!!!

Today we woke up extra early (mostly on accident) to birdwatch from Las Cuevas Deck! We didn’t see any macaws, but we saw two- four toucans flying across the sky. They were gorgeous!

Then we went to plan out next research project. For our question, we chose “which area (trails, jungle, roads) will each animal group (large predators, small predators, large prey, small prey) use the most measured by relative abundance?” Our hypothesis was that big cats would be the dominant animals using paths and roads whereas small prey and mammals would stay under forest cover. We planned on using trap-cameras to get photos of animals as they cross the trails. By the way, while we were planning, we saw 4 scarlet macaws flying around!

Then we set off to se tho the cameras. Our first trip out we ran into our first of three white lipped turtles (Kinosternon leucostomum). This one was easy to identify because of its white lip, it looked just like one of the ones on my taxa sheet, and we found it swimming in a muddy puddle after the morning rains. After we saw the turtle, I set up my first camera on the “shortcut path” back to Las Cuevas. Because I went first, I was deemed the “camera soldier” and had to fix/ mess with lots of peoples cameras.

We did so much in this hike: set up cameras, use gps markers, walk through the jungle, eat termites, climb a bird tower, trip on Mayan stairs, see huge cave spiders, the list is endless.

I didn’t see my taxa again until after a light evening rain, and they were two mud turtles swimming around in mud puddles. I’m finding that these turtles vary greatly in shell appearance and patterning. The last two turtles lacked the classic white lip coloring, which caused me to misidentify them at first. However, their “bridge shell pattern” between the carapace and bottom shell indicated their true species. Plus, they were found in the same environment as the other white lipped mud turtle!

I’m hoping to see other types of mud turtles, like the Tabasco turtle. The wet season is proving to be good for turtle hunting but bad for reptiles and snakes. I’ll let you know what we see next!

Til’ Tomorrow!

QOTD:

“ if you leave me I’m signing up for an online orphanage”

Giant Cave Spiders
The view at Las Cuevas
One of the three white-lipped mud turtles! (Generously picked up by Caio)
Scarlett Macaw!

 

 

The Ruins of Caracol!!! (Day 9)

Hi all, it’s Faith with Day 9 updates from the 2022 Belize trip!!!

Today we left the TEC to visit Caracol, one of the largest Mayan cities. I got kind of car sick on the way there, but it was OK because we sighted a Morelet’s crocodile (crocodylus moreleti). While I couldn’t get the exact size, it was obviously a younger crocodile. It even had the black tail bands that characterize young morelet’s. We saw it sunbathing on a rock near a freshwater river in the Chiquibil. What an exciting find!

After that, I fell asleep and awoke at Caracol. This ancient Mayan city was home to over 200k people at one point and spans over 7 miles. The temples are in a pyramidal shape and come in groups of threes and sixes. The property had a wide variety of trees. One of them produces fruit that are locally called horse balls, and the fruit have a sticky glue-like sap. We also saw a gumbo limbo tree wrapped in a strangling fig. The last cool tree we saw was a Ceiba tree. They can live for over 200 years, and they dominate the emergent layer of the rainforest (highest portion of the canopy). We all looked so small compared to the twin ceiba trees! The highlight of Caracol, for me at least, was seeing a bat! I love bats, so I was the first and last person out of the Mayan cave-room! He was so small (pictured below)!

After Caracol we made the 2 hour drive to Las Cuevas research center. On the way it began to rain, and the gravelly- dirt roads became faint puddles. In those puddles, we saw three turtles! One I identified as a red cheeked mud turtle (K. scorpiodes). I determined his species by noting his habitat and appearance.  I even saw a glimpse of his bright red cheeks! Because of the speed we passed them with and their small sizes, I wasn’t able to identify the other two turtles we passed. They were also living their best life in road ponds. I also couldn’t get pictures of these turtles because of the moving car 🙁

Las Cuevas seems cool for now, but I guess I have all week to figure that out. I’ll let you know what happens next!

Till Tomorrow!

QOTD

““You guys are gonna make me touch the horse balls?”

“Micheal pees! How could he?”

This is the site we saw a morelet’s crocodile! It is in this picture I will add a close up of the crocodile once I receive is from Dr. Solomon
The Giant Ceiba Tree!
THE BAT!!!
Morelet’s crocodile sunbathing!

De-bris-ing Glovers (Day 6)

Hi all, it’s Faith with Day 6 updates from the 2022 Belize trip!!!

We woke up to gloomy, grey skies with fierce winds, but that did not stop us from conquering the fore reef! Diving the fore reef was incredibly unique, it was unlike any of the shallow patch reefs we usually see. The water was a dark, royal blue, similar to the color of pen ink, and the waves were intense. Usually, the reefs are only a few feet below us, but the fore reef was around 40-50 ft below. Because of the depth, there was no color discrimination unless you swam really close to the reef. I saw lots of new sponge types, but the most interesting was the Giant Barrel Sponge. I saw it close to the “deep drop” towards the edge of the reef; it was on the much deeper side. Because the reef was so far below us, I didn’t see any echinoderms; however, I saw a sea turtle! It was too far away to identify, but from the shape of its bill and fins, I believe it was a loggerhead sea turtle (Caretta caretta). It lacked the hawksbill pattern. The turtle was chilling under/ next to some coral, and it didn’t move even as we all approached it. I assume he was in the area because of the jellyfish swarm above us. Because the waves were so rough, we only stayed out four 20 minutes, and we swam through the jellyfish on our way back to the boat.

When we got back to glovers, I got to see some brown anoles (A. sangrei) because Dr. Correa’s son was catching them and letting us hold them. You can tell they are brown anoles because they are brown and have bright orange dewlaps (throat fans) that lack dots. I don’t know where he was catching them, but I assume they were crawling around the station.

After our much needed break, we made a research question to answer. We asked “How much of the trash that washes up on Glover’s reef can be disposed of on island, where is it located, and which area is the most efficient to clean?”

Our “trash” hypothesis was that the most debris would be located at the coral graveyard and that 50% would need to be taken off-island to dispose of. Our hypothesis really was trash because WE WERE COMPLETELY INCORRECT!!! After garbage collection and sorting, we found that 88% of trash could be disposed of on-island via burning, and we found that the mangroves behind the kitchen collect the most garbage by mass. Therefore, if we are going to do more beach cleanups at glovers, we should have volunteers focus on the areas near those mangroves.

While we were collecting the trash, Nate made an interesting find– an almost intact cow fish skeleton?!  I got to carry it back because everyone else thought it was gross. I mean, it is, but that wasn’t going to stop me! (Pictured below)

After listening to talks of Annelids, hydroids, ocean debris, and anemones, our group got to watch a hermit crab change shells! (Nate also found the shell while gathering trash, and he kindly gave it to the hermit crab). We all got very emotional, and it was the perfect way to end this reef day.

Till Tomorrow! P.s. I’m not sure why this blog didn’t get published on the day I wrote it, but it’s up now that we have better wifi, sorry!!!

QOTD: “I can’t explain it but our group gets really emotional over hermit crabs”

“Ugh, I lost my brainblast”

The Turtle we saw on the reef; as you can see, it is very far away. Potentially a Caretta caretta (Loggerhead)
The land hermit crab we saw change shells. The shell it is wearing is the one that Nate picked out!
The Cowfish skeleton Nate found!
Our Poster!!!
The 64kg of trash we collected from 3 different sites on Middle Key

The Reptiles of Belize Zoo (Day 8)

Hi all, it’s Faith with Day 8 updates from the 2022 Belize trip!!!I dropped my phone in a line of lead cutter ants!!! But, a lot happened before that, so let me tell you!

This morning we woke up and had to say goodby to Middle Key, it was really sad, but we knew it was coming. The boat ride back to the the mainland was 3.5 hours, and then we waited at the Calypso restaurant for 2.5 hours trying to get lunch. What a chaotic start to traveling…

After stopping at a convenience store to restock on snacks, we arrived at the Tropical Education Center and Belize Zoo! The cabins we stay in here are so cute!!!

We quickly set our stuff down then headed up to the classroom for a presentation from Dr.  about his research on Scarlett Macaws. He was super informative about the species, and explained to us how important the Chiquibil is to their breeding and how crucial the red band area is for their foraging. His research clearly has many practical applications for conservation biology and informs us about were we should allocate preservation efforts.

In between dinner and the zoo, I noticed a few reptiles at the TEC, but none of them were living. The TEC classroom has Hickatee shells (Dermatemy mawii) , and two preserved snakes on display. The two snakes are a fer-de-lance (Borthops asper) and a jumping viper (Atropoides nummifer). Additionally, a sign in the kitchen gave me hope: 2 Hickatees were seen last week in a pond. I might get to see one of the critically endangered Central American river turtles!

After dinner, our group took trucks to the Belize zoo where we got a taste of the Belizean forest’s biodiversity. We saw “nomming” ocelots, rolling jaguars, climbing ant-eaters, Mexican raccoons (coatimudnis), and a tapir! We got to feed the tapir, and as I was grabbing the carrot from our guide, I dropped my phone into a trail of leafcutter ants! I was terrified. (Thankfully Dr. Correa kindly retrieved it for me).

The Belize Zoo also provided me the opportunity to see many reptiles that I might not get to see in the wild. The first reptile we saw was the American Saltwater Crocodile (Crocodylus acutus); he was a massive 13.5 feet! This crocodile was older than me, and he was relatively calm. He laid unbothered in the water until our guide tossed a piece of chicken for him to munch; he moved very fast in pursuit.

Later on in the reptile cages, we saw a live tommygoff (Borthops asper), Boa constrictor, and a Chicken/rat snake (Spilotes pullatus). The tommygoff was curled up in a ball inside a dark log, so I couldn’t get a clear picture of it. However, the boa constrictor and chicken snake were both out on top of logs, so I have added their pictures below. This boa constrictor was actually quite small, but his patterning was the perfect example with dark and light brown spots. Likewise, the rat snake had a beautiful pattern, and the lack of red scales indicated that he was a Chicken/rat snake and not a Yellow-red rat snake.

Now that we are away from glovers, we won’t see any more echinoderms. I’m just glad I got to post a sea star for you all.

Till Tomorrow!!!

QOTD: “It’s like edgy sprite”

The internet here won’t let me upload photos, so I’ll have to add them at Las Cuevas. :'(

Chicken Snake at Belize Zoo, Spilotes pullatus
Boa Constrictor at Belize Zoo
Crocodylus acutus (American saltwater crocodile) at Belize Zoo!

Today we ate a Snack, Appetizer, and Main Course!!! (Day 7)

Hi all, it’s Faith with Day 7 updates from the 2022 Belize trip!!!

Today we woke up and gathered our last non-mpa reef data. The waves were brutal; McKenna described them as, “being thrown in a washing machine.” The reef was about 5 feet deep, and it was mostly sand. The winds made this data collection positively  horrendous! It was really hard to keep our quadrats in place, and the transect tape kept coming undone. I EVEN GOT FIRE CORALED (or “fire hydroided” since fire corals are actually hydroids). Nevertheless, we powered through.

The urchin collecting went surprisingly well. Today we collected 177 E. viridis (Reef boring urchins). per usual, we found them burrowed in tight niches of branched hard corals and under rocks. We found some exceptionally large ones today being 1.25 inches + !!! Even though there are always urchins we can’t grab, I usually notice more species variation on the reef. However, this patch reef only had E. viridis; there were no pencil slate urchins or boring urchins in sight!

Outside of the urchin hunt, we didn’t find any other echinoderms. I’ve really enjoyed being the urchin- identifier on the urchin counting team for the past few days. I realize I haven’t described it much, but that is because we usually only find Reef urchins and the occasional sea egg. Today, however, I got to throw the urchins back into the sea. They look like little soot sprites as they float to the bottom.

After the data dive, we went on a recreational snorkel. I was also fire coraled here, but I’ll forgive it. This reef had significantly less urchins than the non-mpa reef we had snorkeled earlier. The ones I saw were E. viridis and they were burrowed in coral crevices. Even though we didn’t do a formal collection, the reef had a visibly lower urchin count.

This reef also surprised us with 2 Caribbean reef squid (the only squid in the Caribbean), 2 spiny lobster, and a lionfish! (I found the lionfish btw)

Back on land, Caio showed me how to catch lizards so that I would be prepared for seeing them in Las Cuevas. (I think he likes me more now that he knows I’m the reptile taxon). According to the Caio technique, you have to cup the lizard with your hands when they can’t see you. Then, you let the front legs perch on two fingers while you press (lightly) on their torso with your thumb. I put a picture of me holding one below! The lizards we caught we brown anoles (A. sangrei), and they were climbing the trees behind the kitchen.

Later in the day, we analyzed our data about corals and urchins, answering the question, “how does the sea urchin population correlate with the live coral count, and how does this change across mpa and non-mpa reefs?” Our data was mostly inconclusive because of our improved ability to find sea urchins and environmental factors.

Last but not least, we dissected the 3 lionfish we hunted! Liliana got to dissect the big one; meanwhile, Maegan, Michiel, Ava, and I dissected “Snack,” the small 23.6g immature female. We didn’t get much data besides that, but she did eat a tiny fish in her limited years. Snack, Appetizer, and MC (main course) made a great ceviche. Also MC was a giant lionfish weighting 680g!

Anyways I’m about to enjoy some ceviche, till tomorrow!

QOTD: “Surchin af”

“BRB I’m gonna go rub this book on my head”

E. Viridis from urchin hunting!
Ceviche Prep!!!
Dissecting Snack, the small lionfish
Me holding an Anolis sangrei, brown anole
Caribbean Reef squid I found

I got really scared by an eel (Day 5)

Hi all, it’s Faith with Day 5 updates from the 2022 Belize trip!!!

DISCLAIMER: I just wrote this whole blog, and then the draft didn’t save, so here is an abridged version of what got deleted since we wake up at 6am and its almost 11 and I’m really tired 🙂

Today we woke up and continued collecting data to answer our research question. We did two snorkels on MPA reefs ( we called them MPA reefs 1 and 2, boring I know). These reefs had more cover than the non-mpa protected areas; however, they also had a lot of algae growth. Because these reefs were deeper and the tide was calmer, it was easier to measure the % live and dead coral. We also were way more successful at catching urchins. We caught about 113 total with the majority being E. viridis. However, we also saw 3 pencil slate urchins E. tribuloides, a west indian sea egg Tripneustes ventricosus (We had a bond. He latched onto me with his tube feet and held on for dear life, so I named him Fuzzy), and a super special live Clypeaster rosaceus sea biscuit. (We usually find them dead so we got very excited).  Lastly, but not least the Marine sea offcicers found some brittle stars for me since I can’t ever find them. We saw a common spiny brittle star Ophicoma echinata and a O. cinera, a banded brittle star. They were both found under rocks and coral. We only found one Diadema antillarium today and he was under some coral. We did see a nice eel on this reef (pictured below) he didn’t scare me. I decided to call him Floyd.

After the boat drove us back, we watched 3 presentations on crustaceans, green algae, and climate change’s effects on coral. Then we enjoyed some relaxation before out next dive.

Our final dive of the day was at the seagrass beds and barrier reef behind our dorms. I noticed big differences between the two areas even though they were right next to each other! The seagrass beds were extremely warmer with ample algae and a greenish water color. Meanwhile, the barrier reef was freezing cold with a pretty aqua color. It had dead coral piled up the the surface,  but sea urchins and other small creatures made their homes in the rubble. I didn’t see any echinoderms in the seagrass beds, but we saw a an eel, a stingray, 3 lionfish, 3 lobster, a white anemone, spaghetti worms (which are very fun to mess with), and a pufferfish. The pufferish and eel scared the living daylight out of me because I found them by being directly above them (which made them very upset). The eel snapped at me, but the pufferfish just stayed in place. It was scary… I named the scary eel Jade, and he has no picture.

We came back to watch 2 presentations: 1 by the coast guard and 1 by the island manager. I learned lots of interesting facts about how they keep the island “human-free.” But the most interesting fact to tell all of you is that I’m too short to join the Belizean coast guard. You have to be 5’3″ to apply as a girl and 5’5″ to apply as a guy!!!

Till tomorrow!

QOTD: “It’s commiting crabicide!” … “Did you just say crab-i-cide?”

“What does TBF mean?” (TBF, aka Tropical Field Biologists, aka what we have been called since our first meeting in March)

Banded Brittle Star O. cinera
Live Sea Biscuit Clypeaster rosaceus
The puffer that scared me terribly. I was chasing after a stingray, and next thing you know I’m in a pufferfish’s personal space
Floyd, the nice eel

Research? More like reef-search!!! (Day 4)

Hi all, it’s Faith with Day 4 updates from the 2022 Belize trip!!!

Today we started our attempt to answer our new research questions: “ What is the correlation between percent live coral and the sea urchin population?” and “How does that correlation change between mpa and non mpa reefs?”

Our hypothesis are as follows:  we think that areas with moderate amounts of sea urchins will have the highest percentage of live reefs. Additionally, we think that the unprotected reefs  will have an abundance of sea urchins and therefore have less live coral. We think this because unprotected reefs are susceptible to overfishing, which reduces the amount of creatures that prey on sea urchins.

Our methods were to lay out 50ft of transect tape in random, radial direction s from one central point. Then, at every 5 meters we would count the squares of live coral and dead coral using a quadrat. Our final part, would be collecting as many sea urchins as possible in 10 minutes, which we would identify later.

This method sounds easy in practice, but let me tell you. Counting. The. Corals. Was. Hellish. Don’t try to tell me,  “Corals are delicate, don’t touch them because they’ll get hurt.” * I now know the truth. They will cut you, burn you, and make you lose your quadrat to the current. If I wasn’t wearing a wetsuit, I would be covered in the wrath of a fire coral right now. So, yeah, getting the data from the West patch reef was very difficult, but collecting the sea urchins wasn’t easy either. Most of the time, the sea urchins were 1cm-2inches burrowed in the remains of hard corals (specifically the ones with a little algae overgrowth). They were hard to see at first, but after awhile they were easy to find. I saw many types, and as the echinoderms expert, I knew exactly what they were (mostly). The most common find was a Common reef urchin, Echinometra viridis, identifiable by the dark body, orange spikes, and small white rings on their spines. We saw a few reef burrowing urchins, Echinometra lucunter, and 2 pencil slate urchins, Eucidaris tribuloides. We found so many urchins that I could hardly count the ones in the wild, but we brought back 20 to classify.  My three favorite finds of this trip were a Flamingo tongue snail, a lobster trio(featured picture), and the donkey dung sea cucumber (Holothuria mexicana). I found the sea cucumber under a coral, and I got to hold him, he was very squishy and started molding to the shape of my hands. I couldn’t identify any particular behavior that he was doing, but maybe he just needed a nap.

Our other daily activity was making a taxa showcase! We gathered lots of creatures from the seagrass beds behind the kitchen. We found one Spiny Sea Urchin, Diadema antillarum, and Kaiu graciously scooped it up for me to talk about. He hardly stole the show though because we found so many types of green algae, a lobster, and two mantis shrimp!

Oh, and did I mention that Prof. Solomon speared a lionfish? Looks like we might have ceviche tomorrow!

Till then!

QOTD: “You made the *dumb* graph, this is on you

The first mantis shrimp I’ve ever seen. Everytime I go to an aquarium they don’t have them, and they are supposed to be really hard to find. I finally accomplished my life goal (twice in one day!!!)
Me and the Donkey Dung Sea Cucumber, Holothuria mexicana
Black long-spined sea urchin, Diadema antillarum, somehow being carried in a tiny net
Some of the guides we used to identify the sea urchins. I made the one on the left!!!
My teacher speared a lionfish in front of me … I LOVE BIOLOGY

* please do not intentionally touch corals its a) illegal and b) bad for corals