Professional Documents
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PRODUCED BY:
IN COLLABORATION WITH:
FIELD STAFF: Danny Guy, Thijs Claes, Stephanie Butera, Peter Lichtenthal, Sara Conlon,
Brandon Dembs
Cited as
Hawkins, V. 2018. Species inventory and biodiversity comparison for the area of Jalova,
Tortuguero National Park, Costa Rica.
Submitted in whole to
With thanks to all the staff and volunteers who contributed to the Incidentals Project
during the study period and since its commencement in 2010.
The research during the study period was conducted with the help of the following
volunteers:
Bandon Dembs, Corne Slemmer, Zoe McCallum, Jack Glover, Baley Good, Eoin Donohoe,
Jurgen Vincke, Alice Hirons, Emma Wagner, Danielle Small, Peter Lichtenthal, Timothy
Carlson, Brandon Dembs, Zarah Ehlin, Eleanor Green, Emma Brown, Diane Leishman, Amber
Searcy, Rebecca Barber, Tess Nelson, Emily Larmer, Freya Savage, George Buchanan,
Amanda Maretto, Jenna Scherger, Marlena Ryzyk, Emiel Zaandam, Daniela Campama, Lara
Lehnen, Kevin Goulart, Joris Giglio, Ethel Mery, Connor Dupree-Sood, Amanda Schultz,
Alice Douvillez, Tom Panneman, Kieran Bose Rosling, Alex Bartlett, Matt Smith, Elijah
Denham, Michelle Welch, Selina Mellin, Simon Thel, Brian Milne, Willem Van Doorninck,
Krijn Bresser, Matthew Webb, Madison McLatchie, Rachel Hetherington, Mara Ramirez,
Lauren Chappel, Ben Cozens, Alice Palmer, Christine Davison, Erin Gleason, Rob Harris, Ira
Epstein, Lucy Shephard, Leah Cole, Andrew Ujifusa, Jennifer Ujifusa, Christina Coyle, Sofia
Hedman, Karin Jermer, Spencer Kielar, Anna Westwood, Bethany Ball, Alex Willis, Zoe
Mathurin, Marcin Oksinski, Martin Schamberger
Central America acts as a natural land bridge between North and South America; as such
species from both continents are represented as well as endemic species (Baltensperger &
Brown 2015). The large number of life zones and ecoregions which provide a multitude of
habitat types explains the high biodiversity found in this region (Stiles and Skutch 1989;
Garrigues and Dean 2007). It is well documented that habitat change, fragmentation and
deterioration often at the hand of anthropogenic forces are key drivers in the risk of
biodiversity loss (e.g. Baltensberger & Brown 2015, Hooper 2008). Therefore, it is crucial to
understand habitat change, particularly in regards to regeneration of secondary habitats and
within plantations (Beirne et al. 2013). Costa Rica has experienced high levels of deforestation
with up to a 50% loss of forests since 1950 (Baltensberger & Brown 2015). As a result of this
the landscape is fragmented and now consists of a mosaic of habitats. One way to tackle this
issue was to instigate a national network of protected areas encompassing a multitude of
habitat types (Wainwright & Arias 2007).
In the 1970’s as part of this national network, Torutugeuro National Park (TNP) was
established (Boza 1993). The park was originally established to protect a valuable nesting site
for green turtles (Chelonia mydas) but as a consequence of this new status the tropical forest
was also preserved, and former plantations were acquired and turned back into forest (Boza
1993). A high level of biodiversity was discovered in the park, increasing its value and ensuring
its protection. Almost 44% of the known biodiversity found in Costa Rica is found in TNP
(Bermudez 2006). Specifically, this includes 375 species of aves, 125 of mammalia, and 124 of
reptilia and amphibian. However, one consequence of a protected area network is that it can
result in the patch effect. Species are unable to move from one protected area to another
resulting in their increased isolation (Cabrera-Guzman and Reynoso 2012). It was therefore
vital to establish connectivity between these sites to ensure habitat continuity. The San Jan –
La Selva Biological Corridor which includes TNP was established to prevent fragmented
populations and secondary growth forests play a large role in conservation for this reason
(Hooper 2008).
The regeneration of forested areas can take up to 100-180 years to recover fully back to
primary status after anthropogenic disturbance (Chazdon et al. 2009) One way to monitor the
success of regrowth is to look at changes to the fauna species assemblages (e.g. Takano 2014).
As the forest develops and matures, species assemblages also change from generalist species
to ones which are more specialised (Devictor et al. 2008, Christian et al. 1998). However,
many studies of these systems are limited to young regenerating forests, and therefore it is
important to get more information on maturing secondary forest, and more long term studies
on species assemblages (Chazdon et al. 2009; Hooper 2008).
Knowing where specific species occur within a managed area is also useful for maximising
tourist experience whilst minimising interference with sensitive or vulnerable species (Bryan
2014). Species inventories can assist conservation by signifying the ecological status of an
area, particularly some assemblages of indicator species, which are indicators of good
ecological health and the condition of the habitat (Stotz et al. 1996). Some bird species are
often considered good indicator species because they can have specific requirements for
areas they live in i.e. nesting sites, certain types of fruit or seeds and canopy cover (Stotz et
al. 1996). Amphibians are also useful indicator species because of their high sensitivity to
pollution, and their need for complex microhabitats (Wilson and McCranie 2003).
The aims of the project undertaken by Global Vision International (GVI) at the southern end
of TNP are to build a species inventory of the vertebrate species found here. This inventory
will increase the knowledge and understanding of the species assemblages and therefore
inform management decisions. The Jalova research station is in the unique position of being
able to compare directly disturbed habitat types with secondary and primary forest habitat.
As a result, a further aim of the research undertaken here is to monitor the changes in species
assemblages and the habitat zones found here to gain understanding on how well the forest
is regenerating.
OBJECTIVES
Incidentals Project:
The Incidentals Project collects data on the presence of all mammal, aves, reptile, and
amphibian species found within the southern tip of TNP. The main aim of the project is to
construct a thorough species inventory for MINAE so that there is a record of every species
identified within the area and date of first sighting. A secondary aim of the project is recording
habitat types that species are encountered in to compare number of sightings in different
areas, and compose a database that can be used to compare trends over time.
STUDY AREA
The Jalova Biological Research Station is operated by Global Vision International and is located
in the southern tip of the Tortuguero National park. Tortuguero National Park is located on
the Caribbean coast of Costa Rica as shown in figure 1, includes 76 000 ha of protected land
and sea (26 000 ha land) and is classified as a tropical rainforest. The topography of the area
ranges from 0 to 311m above sea level, and the average rainfall is near 6000mm per year with
an average temperature of 26̊C (Lewis et al. 2010; Bermúdez and Hernández 2004; Bermúdez
2006). Within this area are several different habitat types including several different types of
swamp forest (some dominated by several palm species, some more species rich including
high canopy tree species), herbaceous marshes, coastal forest (has a more open canopy, often
dominated by sea grape - Coccoloba uvifera), dense forest (drier than the swamp forest areas
often dominated by Ficus species) coconut plantation and beach (Halewood et al. 2013; Lewis
et al. 2010; Ramsar 2006).
Within the study area there are seven main trails that are used to survey the forest habitats,
as well as two trails within the coconut plantation that were added within the last year (figure
2). Trails are as follows;
Kingfisher: (600m) Dense Forest. Starts at the edge of coconut plantation and winds through
dense forest ending at the estuary. Dominated by high canopy trees with a reasonably open
mid canopy layer, and a lot of smaller palms and ferns at lower levels. It is well drained most
of the year with only a small amount of standing water present in the wetter seasons.
South Boundary: (580m) Swamp Forest. Starts in the coconut plantation near kingfisher and
heads north west, this trail is one of the wettest we have and most of the year there is
standing water and in the driest periods there is still thick mud. A lot of palm species are
present but with a variety of larger trees forming a high canopy in most places.
North Boundary A: (650m) Dense Forest. Starts in the coconut plantation and travels
perpendicular to the plantation. A dry trail at most times of the year with only one spot
subject to standing water in rainy periods. More open forest than in kingfisher with a sparser
mid canopy and less understory vegetation, at points gets very near to the plantation.
North Boundary B: (400m) Swamp forest. Dominated by raffia palms (Raphia taedigera), low
canopy for most of it, some parts are very open with a lot of herbaceous species such as peace
lilies (spathiphyllum friedrichsthalii). Most of the year is inundated and even in dry periods
has mud and a few pools of water.
North Trail A and North Trail B (Originally one trail of 1050m now divided into two different
trails of 700 m each; the habitat of these trails is very similar) Coastal Forest. Travels parallel
to the beach though coastal forest, a much drier trail than any of the others, canopy is
dominated by sea grape (Coccoloba uvifera) and tropical almond (Terminalia catappa), very
sparse understory. Very open and exposed, the widest and most used trails within the study
as it is often used by rangers on quad bikes and is maintained by rangers with strimmer’s,
machetes, and chainsaws.
Juana Lopez: (700m this trail was originally 990m, but the length of the survey was reduced
to be more comparable with other trails and to ensure only habitat consistent with dense
forest was included) Dense Forest. Located the furthest away from the base of all the trails
within the study it is the least used by GVI of all our trails. It starts 300 metres from the beach
at mile 15 and goes west though dense forest to end at the canal Cano Negro. This trail has
some of the oldest and least impacted forest that we survey, dominated by Figus spp. with a
dense canopy and mid canopy. At several points it travels though small herbaceous wetland
areas.
Cocos Back Trail: (650m) Coconut Plantation. This trail starts outside the base and is shielded
from the beach by the base and a thick hedge of vegetation. It travels through coconut
plantation that is bordered by dense forest. This is very open and dry habitat dominated by
coconut palms (Cocos nucifera) with a few other fruit trees interspersed, the grass is kept low
by a small herd of cows and manual slashing.
Cocos Front Trail: (700m) Coconut Plantation. Starting at the front gate to the base this trail
runs through the coconut plantation that boarders the beach, at points this trail is very close
to a mixed vegetation hedge that separates two areas of coconuts. Other than this the
dominant tree is coconut palms (Cocos nucifera) and it is a very open and dry habitat. The
grass is kept low by a small herd of cows and manual slashing. Because this trail is in full sight
of the beach at many points it will never be surveyed at night time during the turtle season
due to potential disturbance for nesting marine turtles.
Methodology: For full methodology please see: Hawkins, V. & Guy, D. 2017. Anteproyecto
2017 Inventario de biodiversidad en el área de Jalova.
An ANOVA was used to test the sample means for the incidental species sightings data against
the zone that the sightings occurred in. Analysis was also carried out by class to discern the
distribution of species better. Individual species of interest were analysed using a fitted line
regression to examine the relationship between the number of sightings recorded and the
years in which they were recorded to determine any trends over time.
Descriptive and visual statistics were carried out in Microsoft Excel and statistical testing in
Minitab 2017.
The observation of six new species during this study period confirms the success of the
primary aim of the incidental project which is too build a species inventory. It is worth noting
that after seven years building this inventory, new species are still being added. Four of the
bird species found this year we would expect to see in this area as they are either forest edge
dwellers, open habitat specialists or prefer foraging at second growth (Garrigues & Dean
2007). However, the Rose-throated becard usually prefers dry forest habitat, but they are
known to forage at forest edges (Garrigues & Dean 2007) and this one was seen in the Coco
plantation. It is also possible that some new species are moving in to the area, which would
be expected in secondary forest as it matures into more complex habitat (Chazdon et al 2009;
Baltensperger and Brown 2015). The reptile added to the inventory is locally abundant on the
Caribbean shoreline where it prefers open disturbed habitat, particularly stands of coconuts
(Savage 2002). Therefore, it is a surprise that it hasn’t been recorded here previously.
A total of 9,283 sightings were recorded during the study period with a total of 287 individual
species. This amounts to 50.45 sightings of species per day on average. There is a statistically
significant difference between the number of sightings and each zone (df = 8, f =11.96, p =
0.000). The Cocos (C) zone differed significantly from all the other zones except Base (A).
Likewise, the Swamp Forest differed significantly to the rest of the zones too in terms of the
number of sightings. Coastal forest (CF), Dense forest (DF) Estuary (E), Flyover (F), Canals (C)
and Beach (B) all had a similar number of sightings over the study period. The Cocos zone (C)
had the most sightings at 2,315, followed by base (A) which has 1,799. The swamp forest (SF)
had the least sightings at 325.
Zone comparison
3000
2500
2000
1500
1000
500
0
A - Base B - Beach C - Cocos CF - Coastal DF - Dense E - Estuary F - Flyover R - Canals SF - Swamp
Forest Forest Forest
Fig. 4. Mean (± 95% CI, n = 287) distribution of the number of sightings of species per zone.
The distribution of species sightings was further divided by class (Figure 5) over this study
period. Aves makes up the majority of sightings in each zone but particularly in the Cocos,
Base and on the canals. This is not unexpected given the nature of the disturbed habitats in
and around base and on the plantation. This disturbed habitat is more open and suited to
generalist bird species who forage in open habitat areas and along forest edges. The nature
of this open habitat also makes their observation easier (Henderson, C. 2010). However, it
must be considered that both the Base and Cocos zone will have a time effort bias because
the project and its volunteers will spend more time observing here than any other zone. The
combination of this and the habitat preferences of the species encountered on a regular basis
explains the higher number of sightings in these two zones. For similar reasons, the canals
have higher Aves sightings with one additional factor that there is an active study undertaken
regularly on the canals surveying for target bird species. Finally, because of the species
richness in the Aves class (where there are more species of bird found in Costa Rica than any
other class (Garrigues and Dean 2007)), it is unsurprising that the Aves class dominates the
recorded species sightings across all zones.
The distribution of the remaining species sightings is relatively even indicating that sightings
in these areas are consistent with a more constant surveying effort. The three forest types
are explored in more detail during the Forest Biodiversity project results.
2500
2250
2000
1750
1500
1250
No. of species sighted
1000
Reptilia
750
500 Mammalia
250 Aves
0
Amphibia
E - Estuary
C - Cocos
R - Canals
A - Base
F - Flyover
SF - Swamp Forest
B - Beach
CF - Coastal Forest
DF - Dense Forest
Zone
Fig. 5. Distribution of sightings by Class in the zones they were sighted.
Figure 6 shows that the number of sightings of White-lipped peccary has doubled overall since
the project’s inception in 2010. Although the record of sightings has fluctuated over the last
seven years and no statistical significance can be drawn from the results (R² = 0.4067, df = 7,
f = 4.11, p = 0.08), the number has not decreased below an average of 20 recorded sightings
per year. The population of this species has declined in the region over the last 50 years as
their home ranges contract. As such they are now known to be ranging further afield to reach
dispersed resources (Reyna-Hurtado et al. 2009) and depend upon protected areas more and
more (Zeller 2011). This could account for the fluctuations in sightings during this study.
However as this is not a dedicated study on the population or abundance of the White-lipped
peccary we cannot infer too much from the data regarding a population trend, but it is
promising that the last three years indicates a higher encounter rate than the previous four
years.
For the other species in the vulnerable category, the American Crocodile (Crocodylus acutus)
and Great Curassow (Crax rubra), the trend is relatively stable and there is no statistically
significant difference in the number of sightings across the years (R² = 0.2492, df = 7, f = 1.99,
p = 0.208 and R² = 0.3529, df = 7, f = 3.27, p = 0.120 respectively). There is a peak in sightings
in 2014 for the Great Curassow but the number of sightings soon became consistent for the
last three years. It is welcome that the trend in sightings is constant for these birds as they
are well known to be sensitive to disturbance (Thornton et al 2012). This potentially indicates
that the overall health of the ecosystem in the study area is in a favourable condition for large
bodied birds. The American Crocodile sightings declined over the years reaching a low in 2016
but it is auspicious that the number of sightings have risen this year. The population of
American crocodile have declined in recent decades due to over hunting and a depletion of
suitable nursey and nesting habitat (Mauger et al. 2012). Another factor potentially impacting
sightings of the American Crocodile is high speed boat traffic. Populations can be driven out
or if suitable habitat is not available in other areas, remain in disturbed habitats resulting in a
reduced fitness (Grant and Lewis 2010). Overall, not enough data is available to say for certain
what the population trend is here, but it is promising that the number of sightings have risen
again in 2017 after declines in previous years.
Fig. 6. IUCN vulnerable species that are regularly sighted during the study period. The plot is based on the
means with R² value determined from the raw data.
Figure 7 (below) shows the trend in species sightings for those species seen regularly that are
assessed as endangered by IUCN. The Great Green Macaw shows a significant and steady
increase in sightings year on year (R² = 0.7915, df = 7, f = 22.8, p = 0.003). After a serious
decline in the species populations last century, they have started to recover in this area which
may explain the increased regularity of the sightings in this study area. This recovering
population is due in part to The San Juan – La Selva biological corridor project which started
in the 1990’s (Chassot 2010). The Great Green Macaw is considered as an umbrella species
and is therefore considered a key indicator species for setting management priorities (IUCN
WCPA 2012).
Baird’s Tapir are secretive and elusive mammals (e.g. Foerster & Vaughan 2002) so most
sightings here are through encountering tracks, therefore these findings are not a reliable
assessment of the population. However, the number of sightings does remain stable (R² =
0.3152, df = 7, f = 2.76, p = 0.148) over the seven-year study period which is encouraging.
Fig. 7. IUCN endangered species that are regularly sighted over the study period. The plot is based on the means
with R² value determined from the raw data.
Finally, figure 8 represents the high number of sightings of the endangered Central American
Spider Monkey. These sightings have increased significantly year on year (R² = 0.6362, df = 7,
f = 10.49, p = 0.018). This bucks the trend seen elsewhere where the species has declined 50%
in the last 45 years (Caurón et al. 2008). They require a large home range (Gonzalez-Zamora
et al 2008) and tend to occupy regenerating forest areas 60 – 80 years later than other
primates (Sorensen & Fedigan 2000). It is well documented that Spider monkeys are highly
sensitive to disturbance due to their frugivory diet, need for extensive home range and slow
reproductive cycles (Sorensen & Fedigan 2000).
Central American Spider Monkey
300
R² = 0.6362
250
No of sightings
200
150
100
2010 2011 2012 2013 2014 2015 2016 2017
Year
Fig. 8. IUCN endangered species, Central American Spider Monkey. It is separate because the number of times
it is sighted each study period are much higher than the other species being compared. The plot is based on
the means with R² value determined from the raw data.
The regular sighting of all these at-risk species within the study area is a positive sign for the
local populations ongoing health and stability. It is encouraging that although some sightings
trends are stable, some are increasing. These species all have in common their sensitivity to
disturbance be it through hunting pressure, habitat change/loss or their complex dietary
requirements. It is therefore a positive sign for the park and its management that they are
present here and being seen with increasing regularity in the majority of cases. It is a good
indication that the forest is regenerating and recovering well enough to supply these complex
needs across the keystone and umbrella species.
The richness of species on individual trails was compared and found to be statistically
different (df = 8, f = 2.30, p = 0.019). A Tukey test revealed that species richness of the Cocos
front trail was significantly different to the south boundary trail (see Table 1 below). Cocos
front had the highest frequency of species observations, but the other trails did not differ
significantly in terms of species richness found. North Boundary B had the lowest number of
species sightings per survey. It is probable that this is because it is the shortest trail in length
and consequently less time is spent surveying that trail.
Trail N Mean Grouping
Coco Front 388 1.3608 A
North Trail A 455 1.2725 A B
Coco Back 366 1.2708 A B
Juana Lopez 284 1.2500 A B
North Trail B 372 1.2419 A B
North Boundary A 389 1.2262 A B
Kingfisher 336 1.1429 A B
South Boundary 294 1.1088TrailAcomparison
B
0.45 Boundary B
North 173 1.1040 A B
0.4
Table 1. The species richness of each trail. Means that do not share a letter are significantly
Frequency of occurrence
0.35
different.
0.3
0.25
0.2
0.15
0.1
0.05
0
CB CF JLO KF NBA NBB NTA NTB SB
Trail
Fig. 9 Mean distribution of species across each trail type.
When this is broken down by class (see figure 10), Aves again dominates the community,
particularly so for the two Cocos trails. This form of biotic homogenisation is to be expected
in a disturbed open habitat. It has often been observed that species richness decreases
whilst bird abundance increases with disturbance (Garaffa 2009). Furthermore, the forest
edge surrounding the plantation may be facilitating a greater movement of birds in a
fragmented habitat and accommodates those bird species that are classified as edge
dwellers better than an enclosed forest setting (Ries et al. 2004, Garrigues & Dean 2007).
South Boundary and North Boundary B have the most even spread of richness across the four
classes and both are swamp forest habitats. This explains the difference found previously in
the trail species richness between the cocos and south boundary trails. The presence of open
areas, standing water areas and dense canopy found in swamp forest provides a variety of
niches for all classes to occupy (Chazdon et al. 2009) and could explain why the species
richness is more even here. There is also a higher presence of Amphibian species on these
two trails (as well as on Juana Lopez) than the other trails. Amphibians need shade and
moisture to thrive (Savage 2002) which is provided in this habitat type.
Kingfisher trail, North trail A and North trail B have a greater presence of reptiles which is
consistent with their ectothermic regulation behaviours (Hertz 1992). These trails have wide
open spaces with a sparser canopy covering allowing greater levels of sunshine to penetrate
to the forest floor. More recent studies have also shown that reptile richness was positively
related to higher humidity, closed canopy cover, large patch size and the presence of leaf
litter (Cabrera-Guzmán & Reynoso 2012). These factors help explain why they are the second
largest class and are present on all trails as all their ecological needs are catered for by all the
forest types found in the study area.
0.45
0.4
Frequency of occurrence
0.35
0.3
0.25
0.2
Reptilia
0.15 Mammalia
0.1 Aves
0.05 Amphibia
0
Trail
To further explore the trail comparison analysis, it was divided into the four forest types found
in the study area (See table 2). This analysis returned similar results to the trail analysis and
in all probability for the same reasons examined above. The Coconut plantation and the
Coastal forest were significantly different to the Swamp Forest type (df = 3, f = 5.02, p = 0.02)
in terms of species richness. Dense Forest and Swamp forest were similar in species richness.
Again, with similar results to the above trail analysis, Aves dominated the community
composition for Coconut plantation and Swamp and Dense forest had the most even
distribution of richness (Figure 11).
1000
Species richness
800
Reptilia
600
Mammalia
400 Aves
Amphibia
200
0
Coastal forest Coco Plantation Dense Forest Swamp Forest
Forest type
Finally, the year on year trends for species richness and community composition were
examined to discern any longer term trends in populations. Two and half years of data has
been collected for the Forest Biodiversity project. Firstly, the Class trend was investigated
(Figure 12) and no significant difference was found in the species richness over this time
period (df = 4, f = 0.93, p = 0.447). This suggests that the populations when examined by Class
have been consistent with no significant increase or decrease. However, in terms of difference
between Class, it is clear that Aves and Mammalia have the highest frequency of occurrence
and Reptillia and Amphibia the lowest over the last two and a half years (df = 3, f = 34.52, p =
0.000). This result is expected following on from the previous analysis undertaken on
community class composition (Figure 10) and also matches what was found in the Incidental
project analysis (Figure 5). The high skew towards mammals is almost certainly due to the
high frequency of observations of the Central American Spider Monkey which can be seen
when compared to the two other primate species that occur in TNP (Figure 13.). The lower
sightings of amphibians may be due in part to the fact that the identification of this class is
extremely difficult. Only species that can be identified with 100% accuracy are recorded. For
identification of some groups of frogs such as rain-frogs or litter-frogs or of juvenile frog’s key
features include things like toe pads and measurements of body parts (Savage 2002; Browne
2014). This would require handling the frogs which is not permitted here. For this reason, the
numbers of species and sightings of amphibians are unlikely to be an accurate representation
all species that can be found here.
Trends over time by class
1.4
1.2
1
Species richness
0.8 Amphibia
0.6 Aves
Mammalia
0.4
Reptilia
0.2
0
2015b 2016a 2016b 2017a 2017b
Year
Primates
0.12
0.1
0.02
0
2015b 2016a 2016b 2017a 2017b
Fig. 13. Primate species richness from the start of the project in 2015 to present.
However, when the year on year trend is examined for species richness by trail, the results
differ significantly from the six month data comparison. The trail Juana Lopez (JLO) is
significantly different to South Boundary (SB) and North Boundary B (NBB) (df = 9, f = 2.56, p
= 0.006) in terms of the species richness during this study period. The Coconut plantation
trails do not differ from the other trails in this comparison. The main factor for these
differences is because not all trails were surveyed evenly throughout the two and half years
and some were newly introduced a year ago. Therefore, these are preliminary results and as
they stand are not reliable enough to draw major conclusions from yet. It will be interesting
to see how the community composition changes on the trails as the study progresses.
0.00200
0.00175
0.00150
Species Richness
0.00125
0.00100
0.00075
0.00050
Fig. 14. Species richness by trail from 2015 to 2017 study period.
Overall, the forest biodiversity project has yielded some interesting results. The addition of
the Coconut plantation trails and being able to continuously observe a human disturbed
habitat in comparison with the recovering forest types has given greater understanding of the
diversity in the area. The main aim of the project was to gain information on species richness
and abundance and the direct comparison to the disturbed habitat has been invaluable for
achieving this aim. As the project progresses and the disturbed habitat changes this project
will produce increasingly valuable insights and offers great potential for individual species
studies in the future.
RECOMMENDATIONS
Both the Incidental project and the more focussed Forest Biodiversity project are invaluable
studies into the health and functioning of the ecosystem. With the added trails allowing for
direct comparison with a human disturbed habitat these projects will allow for a greater
understanding of the successional process of tropical rainforest regeneration. The
monitoring of this process has already begun and is set to continue as it encompasses an
area of plantation that has recently been abandoned. Therefore, habitat patches are
available for study at varying degrees of successional change.
To enhance this understanding, future analysis of both the projects will include a more in
depth study of the key indicator species associated with pristine or primary growth forest
habitats. The Aves class for example are already well documented in their habitat
preferences so by categorising this class into generalists or disturbed habitat users or
specialist/primary forest species will enable a more insightful analysis into the recovery of
the forest and the different use by species of these habitat patches.
The introduction of a butterfly project this year will further enhance this as a similar
categorisation already exists. By building an inventory of species and the trails where they
are found, knowledge of the condition of the ecosystem will also be improved.
The addition of allowing controlled handling of lizard species for identification purposes was
an asset in the surveys and helped make data collected for the forest surveys more accurate.
It was hoped within this data collection period to look at the differences in certain species of
lizards’ size and weight on the different trails to see if there was any effect of habitat on them.
However, this project was delayed due to logistical constraints but should now take place in
the next permit period. The night surveys were identified as being the best time of day for
this project to be carried out. Lizards are easier to capture when sleeping and are more docile
in the hand at this time of day. It would be beneficial if a more reliable method of identifying
amphibians was available as amphibians are well known to be good indicators of ecosystem
health and many species of them are at risk of being lost (Cabrera-Guzman & Reynoso 2012
Savage 2002) and they are the least well recorded of the classes in this study.
Finally, there is tremendous scope for further individual species investigating more closely
populations of species. This would have particular relevance for the IUCN species of interest
and the park’s focal target species. However, GVI do not have the resources to efficiently
execute these studies and therefore the support of outsiders such as students would be
beneficial in bringing these studies to fruition. The results of these studies would be valuable
for informing the park’s management plan and future initiatives for protecting and monitoring
key species. For example, the Baird’s tapir is a keystone browser and plays a crucial role seed
dispersal (Foerster & Vaughan 2015) and the white lipped peccary has begun to range further
and wider in search of key resources (Reyna-Hurtado et al. 2009). Both these species are good
indicators for the overall health of the forest and the success of management initiatives such
as the San Jan – La Selva biological corridor. These are but two examples, many more studies
could exist to further the knowledge of the park and how it functions. GVI would support such
studies and work together with the park if resources allow however, to gain insight into the
population and habitat use of the cryptic species new methods of surveying would have to be
developed.
A previous report for the incidental project noted the fact that we rely on tracks for the
recording of cryptic mammal species and recommended the use of camera trapping to
increase our recording of them, but after consultation with our partner project Coastal Jaguar
Conservation it was concluded that it would be duplicating data and the use of more camera
traps within the park was not going to be beneficial, so this was not carried out.
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APPENDIX 1
Species list Jalova, Tortuguero NP
Below is a comprehensive list of all species (476) observed since the commencement of the
Incidentals Project in January 2010 to December 2017. Species are divided by class and
sorted in alphabetical order, according to the common name.
Amphibians:
Mammalia:
Reptillia: