Highlights of the 2018 Conservation Science course

The 2018 Conservation Science course

The Conservation Science course aims to provide an exciting and hands-on introduction to the field of conservation science, covering changes in biodiversity, threats to biodiversity, protected area management, people-oriented conservation and more! With lots of engaging discussions, conservation hot topics, activities on ecological theory, decision-making and quantitative analyses, the semester sure has flown by! Here, we will reflect on our highlights from the 2018 Conservation Science course. Thanks everyone for making Conservation Science an awesome course!

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Part of the 2018 Conservation Science class during our field trip to the Cairngorms

Back to ecological first principles

Conservation Science is a young field, but it has already changed a lot, and continues to evolve. Despite what kind of conservationist you are, we can all benefit from every once in a while going back to first principles – take something you believe to be true, and ask yourself why. A theory was once an idea, and ideas, especially big ones, rarely go uncontested – is there a major criticism, an opposing theory? What about any theories in the making? What contributions can conservation science make along the journey of idea – stylised fact – theory, and do the classic theories conservation rests upon still hold true today? Pondering these questions was a reoccurring theme in our tutorial groups and activities.

Island Biogeography Theory

As has become a tradition in the course, we tested one of ecology’s classics – MacArthur and Wilson’s Island Biogeography Theory – hands-on, with these hands full of tiny plant and animal species (and the odd star!) made of cereal. The distribution and abundance of species on Earth is one of ecology’s eternal questions, and you might be surprised to find out that a question so big can be summarised using three two simple items – tupperware and cereal. Imagine an archipelago (the little grassy area outside our classroom) and in it islands of various sizes (students with tupperware containers), each at different distances from the mainland (a line we drew on the ground). On that particular Tuesday morning, it was raining species – students threw cereal in the air from the mainland towards the islands – species colonisation in action!

We set out our hypotheses, measured, counted, and then went through a quick coding exercise to unwrap the data presents!

Population dynamics

Populations change – across space, across time. One of the goals of conservation science is to reverse population declines, and to do so effectively, we first have to understand how and why populations are changing in the first place. We went back to theory – visiting concepts such as exponential growth and decay, among the many suggested models for population change, and then filled our hands with cereal again. This time, our goal was to count how many individuals of different species there are in Kluane National Park. We added a third tool to our set of tupperware containers and cereal, and designed a mark-recapture experiment. We discussed experimental design, as well as its implications for precision, accuracy and ultimately conservation actions.

This is our fourth year of using cereal to test ecological theory and estimate population size, and in addition to looking at how our different groups did, it’s also interesting to compare among the different years of the course – for example, who’s our ultimate winner with the most precise and accurate estimate of population abundance in Kluane? Does Island Biogeography theory still hold true when you add in temporal replication of our experiment?

Stay tuned for next year, when we will reveal all of that, with a planned blog post titled: “Five years of cereal and conservation – lessons learned and ways forward.”

Until then, you can check out our blog posts on island biogeography and population dynamics here – 20152016 (island biogeography)2016 (population dynamics)2017.

The Politics of Conservation

There is much more to conservation than science. Conservation is an activity that is driven by particular values and ideas about the way the world should be and how that can be achieved. It’s important to recognise that no matter how ‘objective’ conservation science may appear to be, those values may not be shared by everyone. Throughout the course students had several opportunities to engage in discussions about the values they hold and why they want to ‘do’ conservation. We looked at how different values are shaping the conservation agenda, and how this might conflict with the interests of other stakeholders, such as governments, business, and local people. These conflicts were most vividly brought to life during the conservation role-playing game where students adopted the perspectives of these stakeholders and tried to negotiate a land-use plan for a Tanzanian landscape. These games illustrated just how difficult it can be to make decisions that satisfy all stakeholders, and that some form of compromise might be needed. It also showed that not all groups are equally powerful, and that we as conservationists need to take care to think about how we impact on others, especially on the poorest who often most depend on natural resources.

New tools, big data and long-term monitoring

Conservation problems are often complex, and innovation can go a long way in terms of providing a new perspective, or even better a new solution, to issues such as habitat loss, protected area designation and more. As more and more scientists make their data publicly available, the breadth and scale of questions we can ask grow larger. Questions that transcend biomes, taxa and large temporal periods are now possible – thanks to long-term monitoring at sites around the world, and technological advances helping us analyse growing amounts of data. We live in an exciting time, and in the Conservation Science course we want to keep up and give students a taste of all the new angles from which you can approach conservation science.

Same data, different interpretations

Long-term data of how populations and ecological communities are changing through time at sites around the world are extremely valuable for conservation science. As data accumulates, it’s important to remember that people can have different interpretations of the same data, which can potentially influence decision-making in conservation. To see if this really is the case, we opened our (made up) journal AQMCS (Advanced Quantitative Methods in Conservation Science, pronounced aq-mecs) for its second round of publications, following the inaugural issue last year.

We gave students the same dataset, coming from the Niwot Ridge Long-term Ecological Research Site – a montane site whose flora and environment have been monitored for decades to understand ecological processes in high-elevation mountain ecosystems. Each group then independently thought of a question, completed a quick analysis to find the answer, and submitted their 1-page manuscript to our journal. Each group was also a member of our editorial board, so once all the manuscripts were in, we presented our key findings and voted on which manuscript to accept for publication.

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This year’s candidate papers for our AQMCS journal!

We think that this experiment is telling us that different scientists do make different interpretations when presented with the same data. You can check out this study that found the same result with analyses of football (soccer) data. We at AQMCS think that the way forward is to make sure our data, code and science are as open as possible, so that we can promote thorough investigations of data and their transparent interpretations in the literature.

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A word cloud of all the titles of the 1-page manuscripts using the same data, collated over four years. Interestingly, “increase” is just as common as “decrease”, similarly some people found “dramatic” change, others “varying” change!

You can find our 2015 blog post about the “Same data, different results” activity here and the 2017 blog post here.

The Google Earth Engine

Towards the end of the course, we got hands-on experience with an exciting tool – the Google Earth Engine! Conservation problems are tough, and powerful tools like the Google Earth Engine can help us get closer to the answers. Through the Earth Engine, we explored a place we had recently visited, the Cairngorms National Park, and in just minutes, we managed to extract the amount of forest loss and gain using the Hansen et al. Global Forest Change dataset.

cairngorms_forests

Forest loss in the Cairnforms has fluctuated over the years, and the magnitude of loss is much larger than the magnitude of gain.

Seeing the power of the Earth Engine automatically makes you want to do more and more! We split into small groups to find out how forest cover has changed over the last 16 years in national parks around the world.

Pixel by pixel, we gained insight into where forest gain and loss and occurring, and we pondered why that might be. Are those naturally occurring changes in habitat, or are they driven by anthropogenic actions? Are there any patterns? We put our results in the context of different types of protected areas and different management strategies. Are certain types of protected areas better at preventing loss of forest habitat? Here are our data presents!

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Forest cover gain and loss in four national parks in different parts of the world – spot anything surprising or unexpected? You can find the data and the R script to generate these plots on GitHub.

Sankuru, as we found out, is actually a nature reserve, not a national park, and is a category 2 protected area in the Democratic Republic of Congo. Sankuru Nature Reserve lost the most forest cover, and interestingly, Manu National Park (also category 2!) lost the least forest cover. After zooming into where forest loss and gain did occur in Manu NP, we suspect that those are naturally occurring changes in forest cover due to river bed moving. We were surprised that there hasn’t been more forest gain in Yellowstone – the classic example of how forests come back after wolf reintroduction.

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Forest loss (purple) in Peru – one of the areas we explored in the Google Earth Engine. Within Manu National Park, forest loss mainly occurred along river beds and on hill slopes, suggesting naturally occurring tree loss due to river bed moving and land slides.

Keen to learn more about coding, models and data visualisation? Here are a few relevant Coding Club tutorials:

A course conference with biscuits – preparing for the real world

The Conservation Science course focuses on teaching students about the latest in conservation research, including methods, issues and debates. Whilst this is essential for a career in the field, we also want to take this further, in order to prepare students for the real world. Finishing their undergraduate studies, students should not only be knowledgeable; they should be able to inform, educate and inspire others. If we are to use our research to change the world for the better, we must acquire the communication skills necessary to share our findings and passion.

Therefore, we held a course conference in November, where students presented a ‘hot topic’ of their choice with a poster and short presentation. Attempting to mimic other conferences, students presented their work repeatedly in a short space of time, with others asking questions about the topic. There were also snacks- a highlight of any true conference. Hopefully, this recreation of a conference setting accurately conveyed the intensity and high pressure of the real thing. Not only this, but conferences should be an enjoyable experience. Being able to share our findings with others is one of the true privileges of a career in research. Education is exciting!

Despite the mountain of assignments that students have to face at this time of year, they put on a fantastic conference. With beautiful posters and dynamic presentations, the atmosphere was charged with information exchange. If this conference was anything to go by, we can get very excited about the future of conservation science.

Conservation in action – Field trip to Cairngorms National Park

We celebrated our fourth trip to the Cairngorms on the Conservation Science course! Each year so far has definitely been a highlight of the course, and it’s always great to learn more about conservation practices with beautiful autumnal colours as a backdrop!

Special thanks to Glen Feshie EstateCairnGorm MountainPeter Cosgrove and Badaguish Outdoor Centre and our bus driver Keith for supporting our trip!

We learned from Peter Cosgrove, local conservation expert, about the most important species in shaping British history – the freshwater pearl mussel and the conservation actions being taken today to preserve the species in Scotland.

We visited the Glen Feshie estate and discussed natural woodland regeneration, estate management and control of deer populations. We got great views of the deer and Highland cows and very much enjoyed learning more about the estate and its conservation views!

We took a hike around the Cairngorm Mountain and talked about alpine flora. Here you can tell from where the prevailing wind direction is based on tree shapes, and trees seldom grow to be taller than us people. Though short, some of the trees we saw have decades of life behind them!

It’s been a great year for the Conservation Science course, thanks to everyone involved and we’re excited to see how conservation science continues to develop, perhaps in the future with the help of some of our course alumni!

All photos by the ConSci teaching staff.

Same data – different results? ConSci 2017 introduces AQMCS!

A question that I have always had, is what happens when you give different scientists the same data and ask them to analyses those data. Do different scientists come up with different answers? Do they ask different questions? How much does our scientific interpretations depend on individual perspectives?

In the Conservation Science course we set out to test this question in our activity “Same data, different results?” We used data from the Niwot Ridge Long-term Ecological Research Site – a montane site whose flora and environment have been monitored for decades to understand ecological processes in high-elevation mountain ecosystems. Students and tutors worked in small groups to complete a speed data analysis and write-up activity – a quick and exciting journey though picking a research question, deciding on the methods that best address it, opening the data present, interpreting what it all means, AND writing a one page manuscript.

We love quantitative analysis, and we don’t shy away from statistics and coding – in the past we have counted Pokemon to calculate different biodiversity metrics, we have tested island biogeography theory, and we have gone through live coding exercises in class. Among all those blog posts, we often say we are “getting quantitative” – well, it is an exciting time of the year now, and not just because the holidays are approaching, but because now we can say that we are quantitative! So quantitative, in fact, that we couldn’t resists day-dreaming about a conservation journal highlighting different quantitative methods. And of course, Gergana couldn’t resist making a logo, so we are proud to present AQMCS (pronounced ack-mecs),  Advanced Quantitative Methods in Conservation Science, our course fictional journal!

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Our dream journal – Advanced Quantitative Methods in Conservation Science. Though an official impact factor hasn’t been calculated yet, we have observed many students honing their quantitative skills, which can be quite significant.

We all rushed to write up our reports and submit them to AQMCS’s editors – after all, the sooner you submit a manuscript, the sooner you will get your reviews back. We had to wait only a mere three weeks, so as far as journals go, we would like to commend AQMCS’s quick turnaround time. All of out five manuscripts got sent out to review (phew, no straight-away rejections!), and in the final Conservation Science session, we all got to experience the peer-review process firsthand! And though the journal might be fictional, let us assure you that our editorial boards scrutinised the manuscripts and explored them in detail, making for some intense peer-reviewing!

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AQMCS’s editors-in-chief, Myers-Smith and Keane, setting the scene for an intense round of peer-review.

Tasked with selecting just one manuscript for publication (publication in AQMCS is very competitive!), students worked away in small groups. Manuscript after manuscript, students thought critically of the studies’ key questions and findings, as well as the methods used to obtain them. Does the manuscript meet the journal guidelines (e.g. a one page format), is the science exciting and novel, does the take-home message contribute to our understanding of biodiversity change?

Some of the submitted manuscripts were over the one page limit – we would like to remind their authors that should they need to present extra information, they can do so in Supplementary Information, which would be published online alongside the manuscript, should it be accepted for publication. One manuscript did not include a methods section – given our journal’s strong methodological focus (it is after all, Advanced Quantitative Methods in Conservation Science), we recommend those authors to implement our suggested revisions (i.e. outline what methods were used and how they advance conservation science) and re-submit. Just like in the real world, co-authorship dynamics were interesting to ponder – who is first author, who is last? One group included an authorship contribution statement, which we appreciated.

Each editorial group presented the criteria they used in the selection process, and finally announced the manuscript selected for publication. It was a close race, and it was up to the last editorial group to break the tie between “Long-term study in Niwot Ridge, Colorado reveals greater increases in spatial and temporal homogeneity within, but not between sites” and “Unprecedented biodiversity changes in continental divide at Niwot Ridge, Co, US”. Though informative, the group felt that the title of the first manuscript was a bit too long, and in the end, they decided that in its next issue, AQMCS will publish “Unprecedented biodiversity changes in continental divide at Niwot Ridge, Co, US” – the first publication in this exciting new journal!

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Accepted for publication in AQMCS – “Unprecedented biodiversity changes in continental divide at Niwot Ridge, Co, US”!

The two activities, “Same data, different results” and the AQMCS peer-review session, stirred up many thoughts on biodiversity change, how we quantify it and how we can attribute it to different drivers. We also honed our speed writing skills, and finally, our critical thinking skills – a winning combination!

Isla has been collected the titles of the same data different results papers throughout the years and here they are below.

2017:

  • Unprecedented biodiversity changes at the continental divide at Niwot Ridge, CO, US
  • Long-term study in Niwot Ridge, Colorado reveals greater increases in spatial and temporal homogeneity within, but not between sites
  • Baby It’s Hot Outside – Change in alpha diversity over elevational gradients due to temperature increase?
  • Nowhere to go: Biodiversity change at Niwot Ridge, CO, US
  • Potential trends and effects of temperature on species richness on four sites

2016:

  • Evidence of adaptation of high elevation plant species to dramatic climate change
  • Increased variance in species richness over time in montane forest-tundra environments
  • Disturbance causes varying levels of species richness change across alpine latitudinal gradients
  • Human activities cause species declines and increases across elevational gradients
  • Higher temperatures decrease biodiversity in alpine habitats
  • Local mountain biodiversity increases by 7% over time

2015:

  • Evidence of high-elevation plant community shifts to dramatic climate change
  • Increased variance in species richness over time in montane forest-tundra environments
  • Disturbance causes varying levels of species richness change across alpine latitudinal gradients
  • Human activities cause species declines and increases across elevational gradients
  • Higher temperatures decrease biodiversity in alpine habitats
  • Local mountain biodiversity increases by 7% over three decades

You can also check out our 2015 blog post about the “Same data, different results” activity: Same data different interpretations?

I think this experiment is telling us that different scientists do make different interpretations when presented with the same data. You can check out this study that found the same result with analyses of football (soccer) data. We at AQMCS think that the way forward is to make sure our data, code and science are as open as possible, so that we can promote thorough investigations of data and transparent interpretations in the literature.

By Gergana, Isla and the Cons. Sci. 2017 class

Getting quantitative & testing Island Biogeography Theory

Ecological theories and breakfast cereal naturally go hand in hand, at least for us Conservation Science folks. We have a tradition of using cereal for scientific experiments (check out our results from 2015 and 2016), testing MacArthur and Wilson’s Island Biogeography Theory, and some of us among the teaching staff have been known to play “Guess the theory” during breakfast – a stimulating start of day putting your ecological knowledge to the test!

This Tuesday morning, though, there was no question as to which theory we were referring to – Island Biogeography. In particular, we tested the ideas that the bigger an island is, the more species it can support, and the more isolated an island is, the fewer species that will have the opportunity to colonise.

The premise of our experiment is simple. While in our usual day to day lives it may be true that no man (or woman) is an island, for the purpose of this experiment, everyone was indeed an island, or at least they were responsible for one. Each student grabbed a container of a particular size and placed it at a random distance from the “mainland”. We then temporally abandoned our islands, returned to the mainland, which happened to be supporting a great abundance of breakfast cereal species. With hands full of cereal and lined up along the mainland, we turned our backs to our islands, and threw the cereal in their direction.

We set out our hypotheses, measured, counted, and then went through a quick coding exercise to unwrap the data presents!

Fig. 1.  Species-area and species-isolation relationships presented using different analytical approaches.

Our data were quite zero-inflated as you can see from the first set of plots above. Overall, there was a trend for more species on bigger islands, and fewer species on more isolated islands. After seeing the plots, we discussed how we can improve our cereal experiment in the future. Perhaps we should have used more cereal and repeated our colonisation processes a few times to increase our sample size. It probably didn’t help that we were colonising our islands as hurricane Ophelia was passing through the UK – the winds could have carried away our cereal species in unpredictable directions. Most of the students chose small containers, so we had few data points for islands with large areas. On the third plot above, which we made by fitting a smooth curve,  you can spot an interesting hump-shaped species-isolation relationship. Well, we think we know why! Our islands may have been a bit too close to the mainland, so when we threw the cereal in the air, it would fly over the closest islands and be more likely to land in the islands at an intermediate distance.

ConSci_biogeo4
Fig. 2. Species-area (A) and species-isolation (B) relationships for brown and white species.

Our breakfast cereal species came in different colours – brown (chocolate) and white (honey), but colour didn’t seem to affect the species-area and species-isolation relationships.

We wrapped up our morning of island hopping with another visit to the mainland, with our metaphorical mainland being Kluane National Park this time. We then took the roles of conservation scientists, tasked with estimating the size of the local brown bear population. Our resources were limited – a box of cereal, a tupperware container, a marker and our minds. Working in small groups, we designed a mark-recapture experiment. Here are the results:

mark_recapture
Fig. 3. Population estimates of the brown bear population in Kluane National Park in Canada. Numbers derived using a mark-recapture technique and cereal as a proxy for bears. Black dots indicate actual population numbers. Error bars show standard deviations for Isla and Gergana’s groups, and standard errors for Mariana’s group.

We discussed experimental design, as well as its implications – for example Pedro and Zac’s groups didn’t calculate a measure of uncertainty around their estimates, and Gergana’s group ate their cereal, so they couldn’t count the actual population. Mariana’s group got the most accurate answer, and the first method Gergana’s group used led to the most precise estimate. The first method Gergana’s group used was to mark only 20 individuals, then for their second method, they marked 40, thinking that as more individuals are marked, the estimates become more precise, not the case this time though!

You can download the data we collected during this week’s ConSci session here – Island Biogeography dataset and Bear population dataset.

You can download our R Script here.

Keen to learn more about coding, models and data visualisation? Here are a few relevant Coding Club tutorials:

By Gergana

Stand up and be counted

Imagine. You’re a consulting company hired by Kluane National Park in the Yukon Territory to conduct a survey of the Grizzly Bear population in the park by the Canadian Government. You have been given one summer to conduct the field data collection and a fixed amount of helicopter time – no you cannot just go and count every individual!  You need to provide a population estimate.

grizzly-bear-861962_1280

Now imagine, that the bears are Pom-Bears (crisps) in a bowl rather than a National Park and the tools you have to hand are a coloured pen and your own mathematical knowhow.  That is the scenario that each of the Edinburgh Conservation Science students were faced with a few weeks back.

pombears

Not only did the Cons. Sci. students need to figure out how to sample a population to estimate the total population of individuals. They had to figure out the mathematical formula to make their estimates without the aid of the internet. There were moments of struggle as numbers were jotted down, then crossed out, and sums done by hand, then checked with a calculator and minorly adjusted. But in the end six different tutorial groups came up with six different estimates with error for their populations of Grizzly Bears using a technique known as mark-recapture.

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How close did each group come to the true number of bears in the park?  I will let the numbers speak for themselves!

markrecapture

Lots of samples or more marked individuals increases the accuracy of your estimate, but in the real world tagging extra bears is expensive. Most groups came quite close to estimating their populations, but some were farther off and some (Sandra’s group) forgot to count their bears to see how close they got! What did we learn – that precision and accuracy aren’t necessarily the same thing. Emiel’s group’s estimates are pretty precise, but not super accurate!

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In summary, Pom bears are tasty and coming up with accurate population estimates can be challenging, if field sampling of real populations is limited by resources and time.

By Isla

Data for figure:

Group Tutor Estimate Error Actual Marked Samples
Group 1 Isla 114 34.81 105 20 4
Group 2 Zac 156.82 38.57 133 18.57 7
Group 3 Emiel 102.37 6.31 154 21.14 7
Group 4 Haydn 224 72.03 134 NA 4
Group 5 Sandra 130 14 NA NA 4
Group 6 Rose 129 24.72 134 21 5

Code for figure:

library(ggplot2)

data

ggplot() +
geom_point(data=data, aes(x=Tutor, y=Actual, colour=”Actual Pop.”), size=6, pch = 17, show.legend=TRUE) +
geom_errorbar(data=data, aes(x=Tutor, ymin=Estimate-Error, ymax=Estimate+Error), width=.1, colour = “black”, show.legend=FALSE) +
geom_point(data=data, aes(x=Tutor, y=Estimate, colour=”Est. Pop.”, shape = 2), pch = 19, size=6, show.legend=TRUE) +
labs(y = “Population Estimate\n”, x = “\nTutorial Leader”) +
theme_bw() +
theme_classic() +
theme(legend.title = element_blank(), legend.text=element_text(size=25), axis.line.x = element_line(colour = ‘black’), axis.line.y = element_line(colour = ‘black’), axis.title.x = element_text(size=25), axis.text.x = element_text(size=25), axis.title.y = element_text(size=25), axis.text.y = element_text(size=25), axis.ticks.length = unit(0.3, “cm”)) +
scale_colour_manual(values = c(“Est. Pop.” = “black”, “Actual Pop.” = “red”), name = “Legend”) +
guides(colour = guide_legend(override.aes = list(size=6, shape = c(17,19))))

# Code credit to Anne for figuring out the tricky stuff to make the legend work!

Go forth and multiply

Despite the autumn rains settling in, we spent one of our last classes island hopping. From Myasia to McIsland, Spiceland to Big Isi we wondered at the vast variety of life. And yet stopping off at Elbario, Demonstrator Island and Little Joe, we found them barren, desolate, in some cases with no life at all. Why could this be?

As you may have guessed, this week we were looking into a classic theory in ecology: Island Biogeography. Back in the 1960s, heart-throb scientists Robert MacArthur and Edward Owen Wilson were puzzling over the differences in diversity between islands – differences that seemed to show predictable patterns. They discovered that larger islands tended to have a much larger variety of species than smaller ones, but also that isolated islands had fewer species than those close to the mainland. The resulting trade-off has been a cornerstone of ecological theory ever since.

islandbiogeography

Island biogeography in graphical form.

One of the main challenges to testing this theory is the challenge of conducting experiments. Ethics boards are less than keen on allowing researchers to wipe out all island life nowadays (not that it hasn’t happened in the past – see Simberloff & Wilson, 1969 – https://www.jstor.org/stable/1934856), while waiting for recolonisation is not always within the realms of a typical three year PhD project. Of course, these issues become less problematic if you replace animals with cereal and natural dispersal mechanisms with a class-full of students.

The experiment conducted by our Edinburgh Conservation Science class was remarkably simple. Each student chose a tupperware container (henceforth ‘island’) and placed it in the grassy ocean outside the classroom. From a single point of dispersal on the ‘mainland’ we all threw cereal at the ocean, subjecting its chance of survival to fate and the reasonably stiff October breeze. Everyone then claimed their island, counted the number of colonising ‘species’, and measured both island size and distance from the dispersal point.

As a class we now had data to test the theory of island biogeography. We found that:

  1. Species richness decreases with distance from the mainland (linear model slope=-0.77, p<0.05)
  2. Species richness increases with larger island area (linear model slope=0.016, p<0.001)

In other words, a success! MacArthur and Wilson can breathe a sigh of relief.

ibfig

The relationships between ‘island’ species richness, distance from the ‘mainland’ (left), and size of island (right).

We also discussed some of the problems with this dataset. Many of our islands were ambitiously distant in their grassy ocean, resulting in a highly zero-inflated dataset. This might give us the appearance of more certainty in our results that we actually have. In fact, if we remove islands without any species at all, the relationship between richness and distance is no longer significant (p=0.46). Another problem is the shape of the relationship. Just as expected by theory, cereal animal species increased non-linearly with proximity and area; fitting the relationship linearly therefore might not be appropriate. This is extremely important if we want to predict change or extrapolate from our data.

Finally, not all creatures are created equal. Some can swim, some can fly, some leave all the travelling to their offspring. While our cereal showed little of this diversity, we still had a go at seeing if there were differences between chocolate ovoids (Cereala cocoa) and pale corn-moons (Cereala lupina). There’s really too few data for anything to be statistically significant (and they’re in the same genus anyway so probably have similar dispersal mechanisms), but lupina seems to do better on large islands and have a greater dispersal capability. But we’ll be making no conservation management decisions based on this fact alone.

ibfig2

Difference in dispersal and colonisation ability for the two cereal ‘species’.

So all and all, what did we find? Whether it is breakfast cereal and tupperware or real species and real islands, the theory of Island Biogeography holds up!

By Haydn

Data: islandbiogeog2016

Code: island_bio

Pokémon Go – Gotta count ’em all

Biodiversity is a grand and wonderful thing, but it is also a notoriously hard thing to measure. What makes a habitat or landscape “diverse”? This was the topic of last week’s Cons. Sci. lecture, which touched upon patterns of biodiversity and the different metrics we use to quantify biological diversity in the world around us.

To make the lecture more interactive, we thought we would calculate diversity metrics live in class (*code and files below*), as we talked about them, on a dataset collected by the students. However, sending the students out “in the field” would have been impractical in the time frame we had – and frankly, Scotland in October is not the best time to wander around with a butterfly net. Instead, phone in hand, we sent them in the wondrous virtual world of Pokémon Go to see what they could find.

fig-0

Our Pokébiologists had to record all the Pokémon species found in their vicinity every day for a week.

Students (and devoted tutors) had a week to make a daily screenshot of the Pokémon’s found around them, and were then asked to compile the species observed along with the time and location of “sampling”. Our research question was: “Does the diversity of Pokémon species vary across campuses of the University of Edinburgh?”

fig-1

Abundance of Pokémon species recorded on Central and Kings Buildings campuses.

From a quick glance at our data above, we see that many more species were sighted at King’s Buildings, the southern campus, compared to the Main campus. However, this seemed mostly due to the fact that observers were mostly based at KB, which biased our sampling effort. We also noticed that some species were seen more often than others. Those Pidgeys, Weedles and Rattatas are everywhere!

We first calculated the alpha diversity in each building where observations were made, and although we did not follow up with a statistical test it seems that the Main Library was less Pokémon-rich than other places.

fig-2

Alpha diversity of Pokémon species in buildings across the King’s Buildings (turquoise) and the Central (red) campuses. “n” represents the number of “plots” (i.e. screenshots) at each location. The Main Library appears less species-rich than the other buildings.

We then calculated the Shannon-Wiener index, which considers evenness (i.e. whether we have many species with similar abundances or just a few dominant species making most of the individuals recorded). The Shannon-Wiener index was 0.88 for both campuses, which means that the assemblages in both cases are quite diversified and even.

Finally, we wanted to have an idea of how these assemblages varied spatially: did buildings that are close together hold more similar communities than those further apart? We calculated pairwise Jaccard’s distances, which indicate dissimilarity, and confirmed our hypothesis that buildings from different campuses were indeed more dissimilar.

fig-3

The Jaccard’s distance shows that buildings that are on different campuses (e.g. Drummond St vs KB Centre, or Main Library vs KB Centre) are dissimilar, that is, they do not share many Pokémon species. Buildings that are very close together (e.g. Murray Library and KB Centre) have more similar communities.

Although simple, this exercise allowed us to put into practice some diversity metrics, test hypotheses, learn bits of R code and reflect on sampling bias and the challenges of monitoring biodiversity.  What do these same sampling biases mean for biodiversity data collection in the real world?  – Our in class discussions taught us that this is a big issue facing biodiversity science, if we want a global monitoring programme to capture how biodiversity is changing on planet earth.

We have since then found out that another course had designed a – rather more ambitious – protocol to explore community ecology in New York City, also using Pokémon Go. We can’t wait to see their results!

By Sandra

*If you want to have a closer look at the code, you can download the R script and data files here

Same data different interpretations?

In the activity in today’s Biodiversity Change session, each of our five tutorial groups were given the same dataset from the Niwot Ridge Long-term Ecological Research site and asked to summarize the biodiversity trends and potential drivers of change.

We wanted to know if you give five different collaborative groups of scientists the same data will they come up with the same findings and interpretations.  And the answer was… we spotted many of the same trends, but our interpretations were sometimes quite different (see summaries below)!  Sure this was a speed science activity, as we had to do our analyses in 45 min or less, but I think this might have held true even if we had been given more time.

There are many different papers coming out of the Niwot LTER site that attribute the different trends in vegetation change being observed there to a variety of factors, so even the experts have different interpretations of pretty much the same data!

Niwot

Niwot Ridge in the mountains of Colorado

Summaries of our different findings

Group 1
Species richness: Sites A1+B1 richness is increasing overall
Driver: Temperature and may be suppressed by another factor before the mid-1990s

  • Logging?
  • Fire?
  • Nutrient Availability?

Species richness: D1 richness is decreasing
Driver: Temperature because extinction rates are greater than recruitment rates – species have nowhere to go

Future Research:

  • Migration between sites (species composition change with temperature)
  • Corridors
  • Community Assemblages

Group 2
Species richness: Change is different between subsites
Driver: NO3 deposition?, No strong evidence for temperature as a driver

Group 3
Species richness: Goes up, down and stays the same at different subsites
Driver: No trend in temperature over the long-term, temperature goes down from 2006 to 2014, Deposition data is variable and seems to track climate, but the change at the alpine site D1 could be due to pocket gopher herbivory and burrowing!

Group 4
Species richness: No clear trends
Driver: Nitrogen deposition – NH4 is increasing, NO3 is decreasing, climate?

Group 5
Species richness: Different trends for different plots – increase is greater for B1 > A1 > C1(negative) > D1 (negative)
Driver: General warming trend, increasing NH4 but decreasing NO3, glacier melt, tree cover change, and human disturbance might also be factors

By Isla and all five groups

Getting quantitative in conservation science

The theme of this weeks class was the quantitative side of conservation science with a lecture on population ecology, the theory of island biogeography and metapopulations.  We talked maths, stats and computers covering the topics of matrix algebra, demography, stochasticity, hierarchical models, programming in R and more. I hope we learned that being quantitative doesn’t have to be scary, as maths aren’t really that hard, and they can even be fun!

island_biogeog1

Coordinating the data collection from our archipelago of tupperware containers in our island biogeography experiment.

We also got hands on with being quantitative and tested the theory of island biogeography by setting up our own archipelago of tupperware containers in the grass outside of the Crew Annex and pitching handfuls of star-shaped chocolate breakfast cereal our species immigration from a point representing our mainland.  We even used a laser range finder to measure the distances between the “mainland” and our “islands” to calculate our species area and species isolation relationships!  We learned that the theory of island biogeography holds pretty well for our model tupperware-breakfast cereal system with significant relationships for both the species-area and species-isolation curves in our data.  Check out our data, R script (see bottom of post) and super cool figures (see below) that we coded in about 5 minutes or less, the first intro to programming for some members of our class.

Then we broke off into tutorial groups to try our hands at mark recapture to estimate the number of grizzly bears (animal-shaped cereal) in populations in Banff National Park (five large tupperware containers) over time.  I asked the students to derive their own equations for the mark recapture experiment and that was somewhat of a challenge given the short amount of time that we had for the activity.  My group had some moments of frustration exclaiming that maths were indeed “hard, too hard” – but they worked through that to get some solid population estimates together. And, by the end of class, all five groups had produced estimates with error of the populations over time (see figure below from the whiteboard).  We learned that population censuses using mark-recapture techniques are a trade off between the number and sizes of the samples you collect and the precision of your results, and that there can be a lot of error when you don’t standardize your methods in advance!

mark_recapture1

The hand-drawn figure of our mark recapture data – check out those error bars and that outlier measurement in 2005!

So all and all, I hope we learned that conservation science is a quantitative science and that maths and being quantitative shouldn’t be something to be afraid of, but something that we all can embrace as ecologists/conservation scientists in training!

Our very first class R script:


## Island Biogeography
## Conservation Science 20-10-2015

# Set the working directory to the folder on your computer where you saved the data
setwd(“path to the folder here”)

# Load the data – convert from .xlsx to .csv before uploading
data <- read.csv(file=”Island_Biogeo.csv”,head=TRUE,sep=”,”)

# Make sure the dataset has loaded properly. “Island” is the name of your island, “Size” is the area of the bottom of your container (in cm2), “Distance” is the distance from your standing point to your island (in m) and “Immigration” is the number of species that were found in your container
head(data)

# Plot the species-area relationship – pch = 19 makes the points filled circles, col = sets the colour of the points
plot(data$Immigration ~ data$Size, pch = 19, col = “red”, ylab = “Immigration”, xlab = “Size”)

# Is the relationship significant?
lm1 <- lm(Immigration ~ Size, data=data)
summary(lm1)

# Plot the regression line on the graph
abline(lm1)

# Plot the species-isolation relationship – pch = 19 makes the points filled circles, col = sets the colour of the points
plot(data$Immigration ~ data$Distance, pch = 19, col = “blue”, ylab = “Immigration”, xlab = “Distance”)

# Is the relationship significant?
lm2 <- lm(Immigration ~ Distance, data=data)
summary(lm2)

# Plot the regression line on the graph
abline(lm2)

# Further beautification of these figures could occur such as relabling the axes, adding error around the linear model, etc.