Tag Archives: 2025

Day 5: Presentations, leafcutter ants, night hike and more!

We spent the morning going over the results of our cecropia tree experiments and making a poster to present those results to the instructors. The results were mixed—while some of the leaves did appear eaten, others actually seemed to have gained mass. We chalked this up to the leaves rehydrating in the containers, as there was also water inside for the herbivorous insects. It also seemed like the leaves from the young, uncolonized tree lost more mass, although difference was slight. This surprised me—I had assumed that, without ants to defend them, the young cecropia trees had developed some other defense mechanism. There were lots of factors we weren’t able to control for which added confounding variable, such as the species of herbivore and the age of the cecropia tree. It would also probably be better to sample more trees. We came up with a theoretical laboratory follow-up in which we grew cecropia trees and prevented one from being colonized, giving us more control over the conditions.

BIOS 319 students weighing leaves and recording observations.
Unpacking the herbivory chambers and recording observations
Working on the poster for the cecropia experiment.
Making progress on the poster!

We also were treated with a presentation from Rafael Manzanero, the director of FCD (Friends for Conservation and Development), the organization that manages oversees Las Cuevas. He told us about the different types of work FCD does, from resource management to research to protection. He also told us about some of the challenges FCD faces, particularly since Covid.

After lunch, we had student lectures and a presentation from Yasmini Manzanero, who does cultural heritage work with FCD. She went into more detail about the history of the caves as well as the cultural and natural wonders which can be found inside. FCD works together with the Belizean Institute of Archeology to document and manage the caves, and we learned about how that relationship works as well. It really showcased another side of the work being done in this place—the work of the karst team is so fascinating,

Later the afternoon, we set out to investigate leafcutter ant fungal gardens. Basically, leafcutter ants will bring leaves back to their colony feed a fungus which they then eat. Mature colonies can have tens or hundreds of fungal garden chambers. We first went to a young leafcutter and colony, probably just over one year old, and excavated the fungal garden. We hit it pretty quickly, and we were able to pull it out intact. It had the queen right on it, along with many workers. It was too young to have any soldiers, though. After inspecting it, we moved on to a mature colony. The immature colony was in the clearing with the research station, but to find an ideal mature colony we ventured down the road a bit. We wanted one that was raised so we wouldn’t have to dig deep to find the fungal garden. The mature colony was well-defended and after only a few strokes with the shovel the soldier ants came pouring out. We had to keep stomping our boots to shake them off. Eventually, though, we uncovered the fungal garden and pulled out a sample of the fungus. It was really interesting to see nests of such radically different sizes.

Dr. Solomon kneels down by an excavated leafcutter anthill and reaches in to bring out the fungal garden.
Dr. Solomon excavating the fungal garden of a small leafcutter ant colony.
Sam dogs a large leafcutter ant colony.
Sam works to excavate the large leafcutter ant colony.

We ended the day with a night hike. We did the Maya trail which goes in a loop, and we walked slow so we could see as much wildlife as possible It had been so dry that we were limited in what we were able to see, but there was still a huge diversity of insects that were super active. We also got to see two anoles and. One interesting thing we came across was some fake snakes (made of clay) being used for research purposes. By far the best part, in my opinion, was when we all turned our headlamps off and and stayed quiet for a minute to listen to the forest. It was so peaceful and the stars were beautiful! What a way to end our day.

Day 5: Please I’m a Starrrr

Today was the second day I was able to get up to go birding! Let’s hope we can keep this streak up. This time, we got to see toucans, amazons, parrots, and more macaws!

We then began wrapping up our research project from yesterday, where we massed the weight of our leaves and calculated the average difference between. We found that the average difference between uncolonized leaves was greater than the difference between the colonized leaves. After lunch, we gave our first poster presentation! One down, many more to go.

The director of Friends for Conservation and Development (FCD) also stopped by and gave us a presentation on both the grassroots start of the organization and the differences between Belizean rangers and US rangers. We also learned a little more about the caves we’ll be exploring tomorrow, which I’m super excited for.

In the evening, we went out to examine the fungus gardens in leafcutter ant colonies, and even saw a queen!

We also went on our first night hike today! We saw some more crickets, but I did not get a picture fast enough. A katydid also flew right over my head, which sounded like a mini helicopter whir. But I did get a picture of an anole and it’s dewlap!

We also found a black orchid by the tree in the middle of the clearing, which was super pretty. It’s also the national flower of Belize.

A couple friends and our guide went back out to see if we could find some ripe breadnuts, and on our way we saw a blue morpho caterpillar.

We went stargazing as well, and made out the Big Dipper. That was about all we recognized so we started making up a couple constellations, finding a spiral and even seeing plenty of shooting stars. I never realized just how fast they move!

That’s all for today, see y’all in the caves!

Ian C

Me and Stella

Hello again. We just got back from our night hike, and it was quite lovely. Although we didn’t see a snake, we did smell some sort of big cat where some people had heard cat sounds before, so we think there’s a puma or ocelot around. I really hope our camera traps get a picture. We also saw a few cool bugs. We found lots of moths, but it was difficult for me to identify them or get a good picture because they are moving so fast. Sadhana got a picture of a really big one, so I plan to ID it later. Another cool bug we saw was a weevil. I covered weevils in my presentation today on plant insect interactions in the tropics, so it was nice to see one out in the field.

Earlier in the day, we saw another example of an insect plant mutualism from my presentation, which is leaf cutter ants! We excavated a young mound first and found the fungal garden and the queen. This mutualism is so cool because despite leaf cutter ants being known for their ability to cut and carry leaves, these leaves are actually to feed the fungus that they maintain in their own garden of sorts. As fungivores, these leaves fungus is their source of food. The queen that we saw started her nest by taking a piece of fungus from her origin nest, initiating a mating flight, and then finding a new spot to start laying eggs for her colony. The success rate of these new colonies are low, but they can be maintained for dozens of years, like the next mound that we excavated to find the fungal garden, which was ENORMOUS. I was really nervous about how we were standing right in the midst of all these giant, angry ants with giant mandibles, but the boots did a great job at keeping us safe.

While not a mutualism, my favorite part of the day was finding a stick bug friend that hung around with us for a little bit. His names is Stella, and he seemed to enjoy crawling up and down our faces and backs.

Fungi, Ants, and Caves…Oh My!

Hey y’all,

Today was a bit different than the past few days because we spent most of it indoors for a bunch of reasons. First, we finished the trials with the insects in the leaf containers. After releasing the insects, we found that the leaves from the ant-guarded trees had been eaten less than the leaves from unguarded trees. I was shocked because I would have thought that the leaves usually guarded by ants would be easy to eat once the ants were gone, but what we saw indicates otherwise.

We then got two big surprises: The directors of the Friends for Conservation and Development talked to us about their work in preserving the wildlife of the Chiquibul Forest, especially the Scarlet Macaw, and the Chiquibul Cave System! This is the largest cave system in Central America with at least 40 miles of passages mapped out! We’re even gonna explore some of it tomorrow morning! I’m super excited because there are a whole bunch of different animals that only live in caves and a lot of sites with ancient Maya artifacts!

Our project for the day was to find fungi gardens inside Leafcutter Ant colonies. We first found a small one that was around one year old, and the fungi colony was about the size of a tennis ball with an enormous queen!

Then, we found a colony that we thought was between 10-25 years old. While digging for the colony, ant soldiers swarmed out of the hole like lava out of a volcano, and I was hopping the entire time to keep them off of my boots!

I did not see a bunch of spiders today except for a Wolf Spider and another bigger spider carrying babies on her back! Sadly, the mama spider crawled underground before I could snap a picture of her, but here’s a cool picture of the Wolf Spider below.

While I’m a little nervous for my arachnid presentation tomorrow, I think it should be pretty fun to finally share with my classmates what I’ve learned about arachnids!

Keep it Cool!

Serenity

Day 4: Poaching and Logging

Last night was cockroach-mania in my bedroom. We accidentally left the light on while showering/listening to lectures and ended up attracting a cacophony of cockroaches. Although I have been hoping to spot more of the little creatures, seeing three crawl out of my pillowcase was not the grand introduction I expected. Nevertheless, we persevered. Many of them appeared to be German Cockroaches (Blattella germanica) under the glow of my flashlight. I think a few of them may have been brown-banded roaches (Supella longipalpa), and a few others were likely the Smokybrown cockroach (Periplaneta fuliginosa), as they were significantly bigger than the others. Many of them were quite little, and I believe they were not full-grown, but still in the nymph stage of development.

This morning’s activity was quite different from yesterday’s, as it involved each of our urine being placed out in viles in hopes of trapping invertebrates. We called back on the knowledge we gained from the previous lectures on canopy life and tropic soil in an effort to better understand the question: how does the structure of the forest impact Nitrogen availability in invertebrates? In order to observe both the abundance and richness of species and see how nitrogen-limited invertebrates are up in the canopy compared to the forest floor, we utilized pitfall traps. Our hypothesis was that the forest floor may demonstrate a greater abundance in the Nitrogen pitfall trap than the canopy, and that in the canopy there would be a greater visible difference between the Nitrogen and water pitfall traps. Our methods involved each student placing 4 viles in the rainforest. Each person tied two viles to a tree: one with urine (a Nitrogen-heavy substance), the other one with water; and digging two holes with a trowel near the tree to place counterpart urine and water viles. My tree was over a tarantula den, which was a bit less than desirable for an activity which involved kneeling and digging into the ground for several minutes! In a couple of days, we will return to our viles and collect them to measure the invertebrates collected in each.

After a lunch of fried chicken and veggie rice, we turned to a study of plant-animal interactions. Specifically, the relationship between cecropia trees and ants. These two organisms have a special, co-evolved relationship, as the trees provide a perfect, compartmentalized home for the ants complete with nutrition in exchange for the ants’ defense. Our study aims to understand whether there is a difference in the tree’s defense mechanisms pre vs post-ant colonization. To do this, we decided to go directly to the source and ask herbivores themselves. We collected samples from two different cecropia trees (one with an ant colony and one without), measured the leaves using a penetrometer and scale, and placed the leaves in containers with a few different Orthoptera species: crickets, grasshoppers, and katydids. Tomorrow morning, we will return to this study and note the eating patterns in the cecropia trees without an ant colony and those with an ant colony.

The hike to collect these cecropia samples was packed-full of fun and creepy creatures! Notably, a scorpion, the molten skin of a tarantula, and two cute leaf-cutter bugs sharing a drink of tree juice. Honestly, it made me quite sad to see the ant colony flee from their home when we chopped down the cecropia tree (hence my title for today). I wished that there had been another way to go about the experiment, and it was hard to watch them grab the larvae and run from their tree, knowing they would all die quite soon. The tarantula under the tree was also carring an egg sack and I can only hope that her fate is somewhat better than the poor ants.

.

Dinner was absolutely delicious and tonight’s lectures featured beetles, amphibians, and the Chiquibul cave system! I learned that the Chiquibul cave system is composed of carbonate limestone deposits dating back to 200 million years ago. Many of the cave creatures we may encounter on our expedition have quite uniquely adapted features to life in the dark such as rudimentary/absent eyes, specialized secondary organs, a lack of pigmentation, and modified appendages. I think I am most excited for our day in the caves, and am truly looking forward to spotting many of the subterranean species that dwell there.

It is really hard to believe we’ve only spent two full days in the rainforest so far. I hope to wake up early for bird watching tomorrow morning and spot some of the iconic colorful feathers that help define jungle biodiversity.

-Emily

Day 3: Into the thick of it!

Wow. Today really felt like a marathon: an awesome, sweaty, exhausting, educational marathon. Most of the day we spent setting up camera traps. This effort involved countless machete hacks, tons of bug spray, and a lot of good laughs.

On the trails, Scott and Kory turned over a couple of logs which revealed the homes of a couple cockroaches! From my taxon ID card I think they were either Smokybrown cockroaches or Oriental cockroaches, but they ran away quickly so it was a bit difficult to tell.  I can’t believe I’m actually starting to get excited about seeing those little creatures. We also spotted a large cat paw-print on the trail, and decided to get creative by making an even larger footprint of own.

It was really awesome to see all of the micro-habitats on the rainforest floor. It seems like each and every leaf conceals a unique habitat and lifecycle of its own. I also loved noticing all of the twisting and turning vines and plants I had only seen in expensive houses before.

Tonight’s lectures were quite interesting and spotlighted orthoptera, reptiles, and the history of biogegraphic development in Central America. I learned about the jumping mechanisms of grasshoppers (something we get to see in action each day in the field/LCRS), stridulation, and the significance of orthopera in reflecting broader microclimatic conditions. It was also fascinating to hear about all of the unique species of reptiles just in the Belizian rainforest.

Tomorrow will be another big nature day and I am excited to get back out there!

-Emily

Day 4 (LCRS Day 2): Pee, Cecropia Trees, and even more ants!

May 19, 2025
Hey hey hey! Today was, like yesterday and the day before, a fantastic day. We worked on two projects today, the first being a pitfall trap experiment to assess nitrogen limitation in arthropods in the canopies versus the forest (underlying assumption: canopies have less nitrogen. Hypothesis: arthropods of the canopies will exhibit more signs of nitrogen limitation (be more attracted to nitrogen-rich fluid (human pee) than arthropods of the forest floor.) In the afternoon, we began an experiment with Cecropia trees. This was exciting for me, because I am the ant man. These trees, like the Bull’s Horn Acacia mentioned earlier this week, are protected by a colony of Azteca family ants living inside them (except Bull’s Horns have Pseudomyrmex ants in them.) The experiment considered whether young Cecropias found other ways to protect themselves from herbivores before they were inhabited by ants, so the experiment didn’t directly involve ants, but that didn’t stop us from studying how the colony moves about the tree.
The first tree we found was inhabited by a whole colony, and it was so cool to see them swarm to protect the tree and to see the tree’s structure to provide a home for them. The second tree we found, after a long search, was much younger and had only one inhabitant: the queen. She was laying larvae, and the tree was not yet colonized, so we sued it for our experiment and called it day there.
However, throughout the day, we saw many cool ants. In the morning, doing the nitrogen-limitation pee experiment (where we peed in tubes to see if arthropods would be more attracted to our nitrogen-rich pee compared to water,) we saw a leafcutter ant colony that must have been 30-40 feet long across the trail. SUPER cool. Right next to the colony (or right above,) there was a Bull’s Horn Acacia Tree coexisting with the Leafcutter colony. We decided to run a fun experiment by putting a leafcutter soldier on the acacia tree to see what would happen. Unfortunately, while attempting to rouse the ants who lived on the tree, the leafcutter soldier fell off so the experiment was cut short. We got to see it run away from one of the Pseudomyrmex guard ants though, which was pretty cool.

In the afternoon, when looking for a cecropia tree, we naturally ran into the cecropia ant inhabitants. Our afternoon experiment will test whether or not young (not colonized by ants) cecropia trees will develop alternate (chemical, physical) defenses to herbivorous predators before they are colonized by ants and benefit from that defense. When we happened upon an adult cecropia tree, we got to see how they swarm out when it falls, and how the tree has evolved a hollow structure inside of it for the ants to live. The structure is an akin to the ants having high-rise apartments, because that tree is tall! Cecropia ants all fall under the Azteca family, and I think we saw Azteca alfari based on the looks. After we saw the big cecropia tree & colony, we set out to find the young uncolonized tree. While we searched, we happened upon two more really cool ant phenomena. The first, we saw a young leafcutter ant colony. We could tell it was young for two reasons: a) the colony entrances were small. there were multiple, indicating an age greater than one year, but still relatively small and therefore young. b) the ants were bicolored (red head and abdomen and a darker thorax.) Dr. Solomon did some inconclusive research as to why leafcutter ants may be discolored, but he discovered that ants were bicolored when the colony was young, which is how I know that colony is young! After the young colony, we saw an ant I hadn’t seen yet or even researched: theCamponotus sericeiventris, or Carpenter ant (but it directly translates to “Golden butt” ant, which is more fitting.) After we saw these two ants, we found the young cecropia tree, which was supposed to be uncolonized, but the one we found had one singular inhabitant: the queen! It was super cool to see her working in the little tree before her colony and her tree grew (her colony and tree did not grow because we cut it down unfortunately.) Overall, it was another fun and interesting day to be the ant man, and I know tomorrow will be even better as we are to spend the afternoon investigating leafcutter ant colonies! What a treat!

Ttylxox,
Sam
Images:
Me with my Pee tubes for the nitrogen limitation experiment:
Huge leafcutter ant colony
Bull’s Horn Acacia directly next to/ on top of huge leafcutter colony
Colonized Cecropia tree filleted open
Bicolored leafcutter ant (Image from https://leafcuttingants.com/forum/viewtopic.php?t=531&start=10)
Golden butt carpenter ant (Image taken by Dr. Solomon) (I know it doesn’t look gold, the gold part has mostly fallen off)
Young Cecropia tree filleted open showing only the queen inhabitant

Day 4: Crickets, Grasshoppers, Katydids and More!

Today was the day I finally got up early to go birding! And boy was it worth the 5:30AM wake up. We got to see a bunch of parrots, hummingbirds, and even a couple woodpeckers! The morning view was also super pretty.

After breakfast, we began setting up the first of two research projects of the day, involving nitrogen pitfall traps! During our pre lab discussion, we found a live scorpion, named Sean, hiding inside one of the drawers at our desks.

Anyways, back to the pitfall traps. We set them up on trees and in the ground along a trail, and while we were setting them up, we saw this super cool bug eating another one.

We also found this super long Liana hanging from a tree, and took turns swinging on it!

In the afternoon, we started a second project, looking at Cecropia tree defenses with animals before and after they’re colonized by ants. When looking for an uncolonized tree, we found one with a new queen hiding inside it.

While looking for Cecropia, we found this super cool tarantula molt and it’s chilicerae.

Some other cool finds of the day include another dead (this time fully grown) scorpion and a spider with an egg sac!


We also found and captured a bunch of Orthoptera, including two species of katydids (angle-winged and common true), a South American lesser field cricket (I think), a spotted winged grasshopper, and three other grasshoppers that I couldn’t identify. It was a great day for Orthoptera!

Tomorrow we might have the opportunity to go on a night hike, which I’m super excited about. See y’all then!!

Ian C

Day Four(est… get it, forest?): Poking Holes and Picking Bugs

As I type this up, I have swatted away 15 bugs of different sizes, including two true bugs from my bright screen amid the dark screen. I think two are about to battle out for the space or try feeding on my screen (they’re debating). 

I literally cannot believe we’re already 4/14 of the way into our trip. To be fair, it’s only the second day in LCRS, so we’ve still got a ton of time, but that’s already 28% of our trip! It’s been so so fun getting to know everyone and their tasks along our trip. From Sam’s ant catching to Dyllan’s butterfly trapping (always so close, it’s really really hard though), to Claire C’s insane ability to spot anything from a mile away. And also, Elise can tie super crazy knots (figures she was an Eagle scout). But we’re only getting closer as we complete more and more projects together. And today, we had two of them!

But not to get ahead of myself! First, at 6 we saw a group of parakeets–it was so cool to watch them fly above in formation. There were also a lot of bright green parrots and something called Morelet’s seedeater… makes me think they eat seeds lol. They were this really pretty shade of brown though I loved it. After this, we had a yummy, yummy breakfast of fryjacks with eggs and beans. Miss Angie has never missed on a meal, like plate scraped and everything. Now would also be a good time to mention the dishwashing station. There are three areas, a bin to scrub your plate with soap water, one to rinse off the water, and one with a mild bleach solution. We all wash our plates and utensils, and throw out any food scraps. While we did have sinks and stuff, this is actually a pretty similar system to one I use in India visiting my grandparents. All scraps need to be composted because they won’t be drained otherwise. And all food is washed outside to prevent insects from potentially entering indoors. But back to the point. 

After breakfast, we got to working. Dr. Solomon taught us about pitfall traps. These are super useful to collect specimen in understanding the abiotic factors of the rainforest. One of these is nitrogen richness in the canopy vs. the forest floor. With the sheer mass of leaf litter, soil-breaking organisms, and roots on the ground, much can vary between this area and the canopy, which is dense, and often quite isolated. This includes nitrogen content, which can really change the mass of producers, and thus herbivorous and predatory invertebrates along the forest floor and the canopy. To understand these dynamics and how they varied species biodiversity and abundance, we decided to place a nitrogen source and regular fluid in the pitfall traps. We would add these to the base of trees to capture forest floor dynamics and the tree trunk to get the expansive canopy above. And what better trail than the 50 hectare plot. Funny enough, each spot was about 50 ft away from the other. Coincidence? I think not…

Ok, ok, but what was our nitrogen source? If you’ve read any of the other blogs, don’t spoil it. OK. 

3..

2..

1…

 

…pee? 

Yup! And so the process began. We were actually really speedy with the setup. And obviously, as the best person ever, I was first to go (we ran out of vials, and long story short my very makeshift pitfall needed to be placed quick). But it was really a cute setup. And writing coordinates and marking spots, we were done in time for lunch!

Featuring my pee!

One beautiful stirfry rice later, it was time for our second experiment of the day. A key characteristic of plants in the rainforest are their symbiotic relationships with insects. And one unique one is the Cecropia Tree and Cecropia ant. These ants burrow deep into the Cecropia, making multilevel chambers to lay their pupa in, gaining nutrition from the numerous extrafloral nectaries (little knobs on the tree surface). In return, the tree get’s protection from the ants against other herbivores. 

We wanted to test out if there was more that was keeping the herbivores away from the tree. As ants habited the tree, did the tree physically and chemically change? To solve this mystery, we needed leaves from an uninhabited and an inhabited Cecropia tree. We would also need several general herbivores to compare this. 

So off we went to the San Pastore and Las Cuevas Roads, hunting for both Cecropia and herbivores. But first off, (the royal) we caught to big, green katydids for each group. They were literally right there, and massive skill from Serenity, Dyllan, and Claire C. really paid off. Bug and leaf hunt time!

My favorite frolick yet. Remember those bright red nymph/beetle things from yesterday? We saw so many of them and it was giving herbivore so we stuck them all into one bin to pick apart later. Then, we were off on a cricket and grasshopper hunt. And Ian was really put to the test today with all of these species. I’d never caught bugs before this and it was a brain chemistry-altering experience. Crouching below, getting them with my bare hands, it was so fun. At one point I caught what we thought was an ant but turned out to be a tiger beetle, which is a lot more bitey and a lot less fun. Eventually, we got a high rise of the bugs. I like to think they were all like roommies back at the dorm, some better than others. Speaking of bitey though, we got to see a tarantula exoskeleton! They’re super hairy (the hair is a defense tactic!) and their fangs are a glossy black. It was so interesting to hold, because you know the tarantula is now bigger than this exoskeleton (a bigger shell of itself, one might say).  

Tarantula exoskeleton!

Ian, the Orthoptera expert!

Also though, we got to cut open a Cecropia. It was so insane to see the layered chambers, as I’ll add below. And also, there were tarantula holes on the base of these trees. Crazy stuff. Try and try as we could though, we couldn’t get the young, uncolonized Cecropia. That is, until we literally walked 10 feet into Las Cuevas Road. And there it was, ready for Claire C. to spot it. Legendary stuff. Punching the leaves with a penetrometer to test physical resistance was definitely the most satisfying part of it all. I can’t wait to see how our insects do as we collect biomass of the leaves they eat tomorrow. But yeah, check out the leaves below!

The old Cecropia (top) and young Cecropia (bottom)

What a fun, tiring day. I got to present my topic lecture which was fun. I did have a lot more info than I thought and had to skim through it, but I hope it was decent! Also, some fungi/lichen updates! Today was kind of a slow day. I got to see some more Dirinaria in interesting places. Also, there was a Turkey Tail right at the end of the 50 hectare plot. It was like a reward (after the long day of potting up everything). Plus, my first few termite mushroom of the day, with hollow, funnel pileus and white coloration. And a really interesting one, Claire C. spotted a series of black shelf fungi on a high up tree. I couldn’t tell you what it was, but I would love to climb it and find out at some point.

Some fruticose lichen with cool apothecia!
spot the mushrooms in the tree!
Love u Dyllan thanks for the candid <3

P.S. Speaking of climbing, check out this vine I swung through. #gains #tarzan #allnatural #cleangirlaesthetic

What came first, Sohee or the leaf?

Mysterious ecology experts

More to come!

mutualisms and morphos

It seems fitting that my topic presentation is tomorrow because today we saw so many great example of plant insect interactions that I plan to discuss in my presentation! 

To start of the day, we set up pitfall traps around the forest to collect insects. We made one set of traps using our own pee as a source of Nitrogen to attract the bugs that are nutrient deficient. When Dr. Solomon first said we had to use our pee, I totally thought it was a joke, but no. We did in fact hide vials of our pee on trees and in the ground to observe how forest structure impacts nutrient limitation. 

On this hike, I saw another blue morpho, which I was able to get a (blurry) picture of. In real life, the butterfly is big, metallic, and majestic, but in the photo is more of a blue blur. 

Another cool thing we saw was lichen  growing with visible sporophytes. These little adorable contraptions allow the lichen to reproduce by releasing spores for the gametophytes. I’ve read about this process, but it was so cool to actually see it!

After lunch, we went out on a hunt for a colonized and uncolonized cecropia tree, as well as 6 herbivore insect generalist for our next project. Me, Serenity, and Claire immediately caught to katydids in the station and then we set out to find the rest.

We found our first cecropia tree pretty quickly, and we cut it down. Immediately, the ants that live inside of it began to swarm, defending they home and source of food. This symbiotic relationship is covered in my presentation tomorrow, so it will be a cool call back. Additionally, next to this tree, was an Acacia tree that also started swarming with ants once we disturbed it. This is the first of a few Acacia trees that we have seen, which is so exciting because this is another classic relationship that I will cover in upcoming presentation. As we searched for the uncolonized tree, we found a bug fig tree, where we discussed the fig tree and fig wasp relationship, where the wasp eggs are placed in the fig and develop within the fig— yet ANOTHER classic relationship that I will talk about tomorrow. Studying these relationships up close is so cool after learning about them for so long. 

Along our walk, we made many pitstops to try and catch some flighty insects. This was so fun for me. At this point, the weather was much nicer and we were essentially just wandering around trying to catch some useful bugs. We were trying to find two individuals in the same species of orthoptera, but instead we found and caught 4 different species of grasshoppers and one cricket. While this wasn’t what we wanted, it ended up working and it was a blast running around trying to catch them. I also caught a bunch of nymphs and adults of this red insect that we keep seeing hundreds of on all of our paths. I thought at first we could use them in our experiment, but I soon saw that they have haustellate mouths instead of mandibulate, which would be more ideal for our experiment. While we couldn’t definitively ID them, We think they were true bugs. I kept collecting them because I thought they were cool. I thought they were even cooler when they started fighting hunger games style, with the larger ones sucking the bug juices of the smaller ones. We kept them in a jar to see who is the final winner tomorrow. 

In addition to these bugs, I saw another Dirce beauty on the road, and I got a good picture and came so close to catching it! I don’t think butterfly catching is particularly my strong suite, but I still have hope. Maybe tomorrow will be the day.