The Schaus Swallowtail Habitat Enhancement Project: An
Applied Service-Learning Project Continuum from Biscayne
National Park to Miami–Dade County Public Schools
Jaeson Clayborn, Suzanne Koptur, George O’Brien, and Kevin R.T. Whelan
Southeastern Naturalist, Volume 16, Special Issue 10 (2017): 26–46
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Vol. 16 Special Issue 10
The Schaus Swallowtail Habitat Enhancement Project: An
Applied Service-Learning Project Continuum from Biscayne
National Park to Miami–Dade County Public Schools
Jaeson Clayborn1, Suzanne Koptur1,*, George O’Brien2, and Kevin R.T. Whelan3
Abstract - Urbanization in Miami–Dade County has modified large tracts of suitable
habitats into smaller patches and increased distance between habitats. As a result, the
endangered Heraclides aristodemus ponceanus (Schaus Swallowtail), which historically
inhabited subtropical dry forests in south Florida and the Florida Keys, is now restricted
to several islands in the Florida Keys and its numbers are precipitously declining. Here we
report on a project that combined a remote in situ restoration project with a communityoutreach
component that brought the restoration effort to local urban elementary schools.
The Schaus Swallowtail Habitat Enhancement Project in Biscayne National Park utilized
volunteers to remove exotic plants and plant over 3000 Amryis elemifera (Sea Torchwood)
and Zanthoxylum fagara (Wild Lime), which are host plants for the Schaus Swallowtail.
After planting and initial establishment, we monitored growth and survival of host plants.
We developed the Schaus and Coastal Hardwood Hammock curriculum unit in partnership
with teachers and university faculty, and implemented it at 8 locations including 5 public
schools in an ex situ outreach and education program. Lesson plans aimed to: (1) inform
students about the Schaus Swallowtail, (2) increase the number and size of native-plant butterfly
gardens at schools and homes, and (3) thwart “extinction of experience” in nature for
school children. Teachers implement applied activities modeled on the habitat enhancement
project in Biscayne National Park in the classroom and on school grounds, and used them
to illustrate the butterfly life cycle, species’ niche requirements, biodiversity, and restoration
and conservation of south Florida habitats. Ongoing engagement with school gardens
through maintenance and project-based assignments can help students achieve academically
and become responsible environmental stewards.
Introduction
Charismatic, “flagship” species such as butterflies have been used to raise
awareness and promote conservation and biodiversity of organisms, ecosystems,
and resources in the US and other countries (Leader-Williams and Dublin 2000,
Walpole and Leader-Williams 2002). South Florida hosts over 100 species of butterflies;
temperate and tropical species coexist in various habitats, ranging from
residential neighborhoods to subtropical dry forests (Minno and Emmel 1993).
Urbanization in south Florida has reduced large tracts of viable habitats into
1Biological Sciences and International Center for Tropical Botany, Florida International
University, 11200 SW 8th Avenue, Miami, FL 33199. 2Teaching and Learning, Florida International
University, 11200 SW 8th Avenue, Miami, FL 33199. 3South Florida/Caribbean
Network, Inventory and Monitoring, National Park Service, Suite 419, 18001 Old Cutler
Road, Miami, FL 33157. *Corresponding author - kopturs@fiu.edu.
Manuscript Editor: Richard Baird
The Outdoor Classroom
2017 Southeastern Naturalist 16(Special Issue 10):26–46
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smaller patches (Alonso and Heinen 2011). Habitat loss is a major factor that has
contributed to the decline of insect species globally (Bender et al. 1998, Ricketts
2001, Ricketts et al. 2008, Taki and Kevan 2007). Anthropogenic development has
modified the natural environment through habitat simplification, expanded matrix
(unsuitable surrounding habitat), and increased distance between viable habitats
(Rosa et al. 2004). As a result, many insect species, often habitat specialists, have
declined to very low numbers.
Many butterfly species have experienced significant population reductions
(Calhoun et al. 2002, Loftus and Kushlan 1984, USFWS 2008), including Heraclides
aristodemus ponceanus (Schaus Swallowtail), a species symbolic of the
plight of many insect species in south Florida. Historically, the Schaus Swallowtail
inhabited subtropical dry forests in both peninsular south Florida and
the Florida Keys, but it is now restricted to several islands in the Florida Keys
(Fig. 1). The Schaus Swallowtail, endemic to south Florida and the Bahamas, was
among the first insects given federal protection; listed as threatened in 1976, it
was reclassified as endangered in 1984 (Smith et al. 1994; USFWS 2008, 2015).
Many butterflies, including federally and state-listed species, inhabit subtropical
dry forests (known as hardwood hammocks in Florida; Snyder et al. 1990). Hardwood
hammocks in the northern Florida Keys are vital to the Schaus Swallowtail
because the preferred host plant, Amyris elemifera (Torchwood), exists primarily in
this particular habitat (Minno and Emmel 1993, Rutkowski 1971). Torchwoods are
Figure 1. Current range of the Schaus Swallowtail Butterfly in south Florida. Map generated
by Helena Giannini.
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subcanopy trees that thrive in gaps in the interior and along the edges of hardwood
hammocks (Jameson 2002, Ray et al. 1998, Ross et al. 2001). Hardwood hammocks
in the Florida Keys experienced timber harvests from the 1700s until the
20th century, followed by agricultural cultivation (early 1900s), and a transition to
human habitation and tourism uses (Snyder et al. 1990, Strong and Bancroft 1994).
Development and tourism have had direct and indirect deleterious effects on local
flora and fauna. Direct effects include loss of land area, habitat degradation, and
pollution; indirect effects include the spread of invasive species and the impacts of
mosquito abatement treatments (Hoekstra et al. 2005, Janzen 1988, Roe et al. 1997).
As a result, some native species in the Florida Keys are now im periled or extinct.
The Schaus Swallowtail Habitat Enhancement Project in Biscayne National Park
(BNP) is an ongoing project on Elliott and Adams Keys—2 islands protected within
the boundaries of BNP—since 2011. National parks can provide refugia for imperiled
insects to thrive and flourish; the protection of natural habitats and restoration
of degraded areas are 2 of many solutions available to protect Earth’s biodiversity
(Hoekstra et al. 2005, Oliver et al. 2010). Hardwood hammocks are protected in
BNP from both development and mosquito abatement. Biscayne National Park is
home to imperiled species extirpated from the Floridian mainland, and continues to
protect the Schaus Swallowtail from deleterious, anthropogenic impacts. The project
was designed by National Park Service (NPS) staff to enhance the habitat of the
endangered butterfly. They planned to restore degraded habitat overgrown with invasive
plant species within the butterfly’s prime territory by planting and nurturing
large numbers of host plants, mainly Torchwood (Whelan 2011). The distribution of
larval host plants is clustered (Jameson 2002, Whelan 2011); therefore, another goal
of the project was to more widely distribute larval host plants across the landscape
to help increase overall butterfly population stability, by mitigating against negative
stochastic episodes that might impact the current limited population of larval host
plants (Whelan 2011).
We also sought to raise public awareness of the importance of these natural areas
in the conservation of threatened and imperiled species, and instill stewardship in
project volunteers. Information explaining the human and natural history of south
Florida, especially with regard to hardwood hammocks and the Schaus Swallowtail,
are readily available at the BNP nature center, and are also featured on the
interpretive trail at Elliott Key. The decrease in visitors to this and other parks is
symptomatic of the disconnection between humans and nature which has increased
over time in south Florida (Pergams and Zaradic 2008, Zaradic and Pergams 2007).
Despite an increase in “baby boomer” visitors, overall visitation to national parks
has steadily declined over the years. The low attendance rates among young people
foreshadow an uncertain future for the conservation and preservation of natural resources
(NPS 2015; Pergams and Zaradic 2006, 2008; Stevens et al. 2014). People
who are introduced to natural areas as children are more likely to value them as
adults (Bögeholz 2006, Duda et al. 1998, Hungerford and Volk 1990, Louv 2008,
Pergams and Zaradic 2008, Wells and Lekies 2006). When children have repeated
exposure to nature, they often grow up to be adults that advocate for the protection
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of natural areas and biodiversity conservation (Chawla 1998, Hungerford and Volk
1990, Matthews and Riley 1995, Wells and Lekies 2006).
The Schaus Swallowtail Habitat Enhancement Project in BNP has involved
volunteers since 2011 to help restore patches of land by removing widespread
exotic, invasive vegetation and replanting native butterfly-attracting plants
(Whelan and Atkinson 2015). A similar model can be applied in local communities
(Mathew and Anto 2007); schools, community centers, businesses, and residences
can enhance habitat by constructing butterfly gardens with a focus on native plants
(Vickery 1995). These places provide opportunities to expose legions of young
people to the national parks through in situ field trips to natural areas and ex situ
activities in the classroom or schoolyard, with activities ranging from exploratory
observations to service-learning projects.
Based on the Schaus Swallowtail Habitat Enhancement Project in BNP, J.
Clayborn designed the Schaus and Coastal Hardwood Hammock curriculum unit
(containing multiple lesson plans) to connect students in Miami–Dade County to
their local environment in south Florida. Participating professors and veteran teachers
from Air Base K–8 Center, Coral Terrace Elementary, Florida International
University, and Gateway Environmental K–8 Learning Center provided comments
to improve the initial draft. The curriculum uses the charismatic Schaus Swallowtail
as a flagship species to demonstrate habitat restoration, a process which can
also be applied locally at schools and homes to collectively benefit other butterfly
and invertebrate species. Many students were unaware that south Florida’s remnant
ecosystems were historically expansive and exist now only as fragments outside
of BNP, Big Cypress National Preserve, and Everglades National Park (Myers and
Ewel 1990). This disconnect in understanding of the significance of native ecosystems
can be detrimental to many organisms if anthropogenic constructs replace
natural ecosystems.
As part of the newly developed curriculum, schoolyard gardens were created
in most of the schools involved; most students active in this ex situ outreach and
educational program did not participate in the Schaus Swallowtail Habitat Enhancement
Project in BNP. Enhancing areas such as schools and community centers
by planting native plants, removing invasive plants, and minimizing pesticide application
can provide suitable habitats that protect butterflies (including imperiled
taxa) and other species (especially arthropods) from urbanization (Ricketts 2001).
Host plants are critical for all butterflies to maintain their populations (Dennis et al.
2004, Minno and Emmel 1993, Vickery 1995); adult butterflies are less abundant
in areas lacking such plants (Mathew and Anto 2007). Outreach programs that integrate
habitat restoration projects with habitat rehabilitation projects in backyards,
parks, and schoolyards can simultaneously help thwart extinction of species of
imperiled butterflies in south Florida and “extinction of experience” in nature for
children in urban areas (Louv 2008, Miller 2005, Pyle 1978).
The project at BNP and those carried out in other communities had the following
objectives:
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Schaus Swallowtail Habitat Enhancement Project
• Establish supplemental plantings of host species Torchwood and Zanthoxylum
fagara (Wild Lime) in various locations at BNP.
• Restore critical hardwood hammock habitat by removing invasive plant species
and planting native species.
• Provide volunteer-based in situ outreach and education programs to increase
public awareness of Schaus Swallowtail habitat and instill stewardship values.
Schaus and Coastal Hardwood Hammock curriculum unit
• Replicate the Schaus Swallowtail Habitat Enhancement Project in the Schaus
and Coastal Hardwood Hammock curriculum unit created for urban schools
and communities in south Florida.
• Construct native plant butterfly gardens with high plant diversity, and observe
and identify different butterfly species; in some cases, track the movement of
butterflies from school grounds to adjacent communities.
• Implement an ex situ education and outreach program to promote the use of
native plants and awareness of the negative implications of pesticide application
for butterflies.
Note that complete lists of all species mentioned in this paper including the
authorities and common names are provided in Appendices 1 and 2.
Field-site Description
Originally established as Biscayne National Monument in 1968, BNP became a
national park in 1980. There is limited terrestrial area in BNP; 95% of the park is
comprised of marine environments. The terrestrial area consists of a narrow strip
of land on the mainland and 42 islands, the majority of which are dominated by
mangrove forest (2400 ha).
Hardwood hammocks are dense, evergreen, subtropical dry forests dominated
by broad-leaved trees that occur primarily in the southern portion of Florida (Ross et
al. 1992, Snyder et al. 1990). Hardwood hammocks of the northern and middle Keys
have marine-based limestone outcroppings (Key Largo limestone), which are partially
covered with a shallow layer of endogenous soil (Armentano et al. 2002, Horvitz
and Koop 2001). Coastal hardwood hammocks in BNP cover about 723 ha (23%) of
the terrestrial lands (Whelan et al. 2013). The largest island, Elliott Key, is roughly
7 miles long and nearly a mile wide; the hardwood hammock covers 68% of its area
and 43% of Adams Key (Whelan et al. 2013). Many of these keys are currentl y impacted
by exotic, invasive plant and animal species (FISP 2017, Invasive.org 2017).
Approximately 500,000 people visit BNP each year (NPS 2015).
For this study, we established 2 site locations in BNP: Adams Key (AK) and
Elliott Key (EK) (Fig. 2). Other parts of this research were conducted at Florida International
University’s (FIU) nature preserve, greenhouse, and the Ziff Education
Building; the Miami-Dade College Hialeah Campus (MDC); and the Open House
Ministries Community Center (OHM). We also had sites at 5 public schools: Air
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Base K–8 Center (AB), Coral Terrace Elementary (CTE), Gateway Environmental
K–8 Learning Center (GEL), North Hialeah Elementary School (NHE), and Whispering
Pines Elementary School (WPE) (Fig. 2).
Figure 2. Study-site locations in Miami–Dade County (Biscayne National Park is outlined
on the bottom right in the map). See text for site abbreviation s.
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Methods
Establishment of Torchwood corridors in Biscayne National Park, Elliott Key,
and Adams Key
The enhancement project involved planting Torchwood in restoration areas, and
along a 8.05-km (5-mile) north–south trail down the middle of Elliott Key to provide
a corridor of host plants (2 ha [4.94 ac]) between known Schaus Swallowtail
locations and restoration areas. The 2 restoration areas were initially dominated by
2 invasive plant species, Colubrina asiatica (Latherleaf) and Neyraudia reynaudiana
(Burma Reed), that had become established after disturbances at the sites.
Enhancement project collaborators removed invasive plants and replaced them with
native vegetation at 2 sites: 1 on Elliott Key (0.58 ha [1.43 ac]) and 1 on Adams
Key (0.27[0.66 ac]). The establishment of native plants can prevent, or substantially
reduce, the reestablishment of invasive species (Berger 1993, Egan and Howell
2001). Numerous Torchwood and Wild Lime seedlings (host plants for Schaus
Swallowtail), as well as other species of typical hardwoods, were planted to allow
development of upper-canopy vegetation in the restoration area.
Establishment of supplemental host plants
National Park Service (NPS) staff, John Pennekamp State Park staff (Key Largo,
FL), volunteers, and a commercial nursery operator collected Torchwood and Wild
Lime fruits from native populations. The fruits were transported to a native plant
nursery in Homestead, FL, in 2011–2013, where the globose Torchwood berries
were processed by removing the fleshy outer coat, scarifying the seed, and planting
them in germination trays. Project personnel removed Wild Lime seeds from
the follicles, and placed single seeds directly into germination trays, and grew the
resulting seedlings in a greenhouse for a year before transporting them to Elliott and
Adams Keys for planting.
J. Clayborn gave volunteers a brief lecture about insect conservation and the
plight of the Schaus Swallowtail before they began fieldwork. Volunteers and
other project personnel proceeded to the field for hands-on service-learning work
in the restoration areas. Their tasks included digging, planting, watering, and
tracking host-plant growth and survival at both Elliott and Adams Keys. Upon
completion of the fieldwork in the restoration sites, volunteers surveyed the
planted Torchwood and Wild Lime for eggs and caterpillars by scanning newly
emerged leaves.
We conducted volunteer fieldwork days with a number of groups, including the
Sierra Club of Miami, FIU biology students, FIU Insect Conservation Club, University
of Miami (UM) Ecosystem Science and Policy undergraduates, UM Alternative
Fall Break Group, Miami Dade College Environmental Science class, and Doral
High School 11th and 12th graders. Before volunteers left the field site, we gave them
t-shirts with a graphic that read Schaus Swallowtail Habitat Helper to reward their
hard work and to raise public awareness of the project and miss ion.
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Ex situ outreach and educational program
Five public schools, 1 university, 1 community college, and 1 community center
participated in the Schaus and Coastal Hardwood Hammock curriculum unit. The
curriculum unit followed the Learning Cycle Teaching Approach to actively engage
students, in which we created lessons for the student investigations modeled
on the “5 Es” (engage, explore, explain, extend, evaluate; Bybee 2002, Settlage
and Southerland 2012). The lesson design highlighted several important aspects of
teaching toward the Next Generation Science Standards (Achieve, Inc. 2013, Bybee
2014): (a) establishing meaningful context, (b) engaging in scientific inquiry,
(c) collaborating to share/refine understanding, (d) utilizing learning tools, and
(e) creating class/individual artifacts. Each participating school followed the same
curriculum protocol for 3 months.
Lesson 1. The plight of the butterfly (historical lessons about Biscayne National
Park). Students formed small groups and constructed a model of an island,
considered ways to attract and maintain a population of Schaus Swallowtails, and
proposed possible solutions to ameliorate extinction after 3 kinds of disturbances
(anthropogenic habitat development, application of mosquito insecticides, and
tropical storms).
Lesson 2: Pin the Schaus Swallowtail in the right habitat. After an interactive lecture
presentation on imperiled butterflies of south Florida (including basic butterfly
information, native plant gardening, and insect conservation), students participated
in an activity titled “Place the Schaus Swallowtail in its habitat (current range).” A
randomly selected student was blindfolded and given a butterfly magnet. The remaining
students brainstormed a plan to navigate the blindfolded student with the butterfly
to the appropriate location on a large poster map displaying the historic and current
range of the Schaus Swallowtail (Fig. 1). Students were only allowed to communicate
nonverbally, by using musical instruments (harmonica, flute, kazoo, and tambourine),
until the blindfolded person placed the butterfly on the map.
Lesson 3: Habitat rehabilitation on school grounds. Students performed a butterfly
survey on their school grounds using south Florida butterfly identification
guides. The guides also served as a reference to let students see what host plants
were appropriate for recruitment of new species and to encourage increases in local
butterfly populations. Most of the species students planted in the butterfly gardens
naturally occur in hardwood hammocks and pine rockland ecosystems—globally
imperiled ecosystems found in south Florida (Alonso and Heinen 2011, Janzen
1988, Ross et al. 2009, Snyder et al. 1990). Several months after garden completion,
students conducted another butterfly survey to compare and contrast species
recruitment and abundance with their initial observations.
Lesson 4: Hardwood hammock restoration and butterfly monitoring project. FIU
education students restored parts of the FIU Nature Preserve by planting native
hardwood hammock and pine rockland plants, and, with training, participated in an
on-campus butterfly monitoring project (including tagging, release, and retrieval;
MonarchWatch 2014). These students (different groups each semester) learned
how to estimate population size using mark–recapture techniques. They tagged
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Heliconius charithonia (Zebra Longwing), a common and slow-flying species of
butterfly found in hardwood hammocks, in the FIU Nature Preserve for 3 semesters
(Fall 2014, Spring 2015, and Summer 2015) to track butterfly movement on campus,
monitor their population, and learn new skills useful for careers in education
and science. Students captured Zebra Longwings with butterfly nets and placed a
non-toxic label (with a specific code) on the hindwing of the butterfly. Tagged butterflies
were released back into the preserve; 2 weeks later, students again caught
Zebra Longwings to see how many were recaptured (Fig. 3).
Results
Schaus Swallowtail habitat enhancement project
This project utilized over 150 volunteers from the general public; the volunteers
spent 2670 field hours (valued at ~$60,000, in 2015 dollars). Overall, participants
planted more than 3200 plants at Elliott and Adams Keys. The main species used in
restoration was Torchwood (Table 1), which participants planted in the hardwood
hammock near trails at Elliott Key, connecting wild Torchwood patches to the main
restoration site.
On 16 May 2015, a Schaus Swallowtail egg was documented on 1 of the planted
Torchwoods in the main restoration site at Elliott Key (Fig. 4). Students documented
recruitment (larvae and eggs) of 2 species closely related to the Schaus
Swallowtail, Heraclides cresphontes (Giant Swallowtail) and Heraclides andraemon
(Bahamian Swallowtail).
Figure 3. Tagged Zebra
Longwing ready for release
at the Florida International
University nature preserve.
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Ex situ outreach and educational program (schools and community center)
Overall, we distributed 34 plant species (31 native) to the schools and community
center (Table 2). Most of the plants were used to rehabilitate the school grounds;
however, students at Miami–Dade County Hialeah Campus were encouraged to plant
seedlings at home and establish their own butterfly garden. Twenty-one of the plant
species used were butterfly host plants (Table 3); the other 13 plant species were nectar-
producing and structural plants for insects and other garden inhabitants.
When the results of the pre- and post-surveys conducted by students at 5 of the
7 survey locations were compared, we found that butterflies increased in abundance
(Table 4). Students had learned a considerable amount about butterflies and they
conducted the post-survey without assistance from their instructors; the instructors
were present only to validate the post-survey results.
Table 1. Number of plants including Torchwood, Wild Lime, and nectar plants planted at Elliott and
Adams Keys. Numbers are shown per restoration area. Column on right shows total number of plants
planted per restoration area.
Wild Nectar Total
Island Restoration area Torchwood Lime plants plants to date
Elliott Key Elliott Main 598 116 60 774
Elliott Breezeway 433 102 2 537
Elliott Spite Highway North 824 - - 824
Elliott East 58 - - 58
Elliott West 151 - - 151
Adams Key Adams Main 414 104 15 533
Adams Breezeway 275 64 17 356
Total 2753 386 94 3233
Figure 4. (A, left). Schaus Swallowtail egg on Torchwood in the main restoration site at Elliott
Key in Biscayne National Park; (B, right). Giant Swallowtail caterpillar on Wild Lime
in the main restoration site at Adams Key.
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Participants tagged a total of 63 butterflies. Of these, 1 female Zebra Longwing
tagged on 21 October 2014 in the FIU Nature Preserve was recaptured by a student
425 m away, near the center of campus on 16 November 2014. Four Zebra Longwings
tagged on 4 June 2015 were recovered (3 males, 1 female) 2 weeks later (18
June 2015) near the same location in the FIU Nature Preserve.
Discussion
BNP is a sanctuary for the Schaus Swallowtail and other imperiled organisms
that depend on healthy hardwood hammocks. Because BNP maintains the largest
Table 2. Plants planted in the butterfly gardens and FIU Nature Preserve. Note: MDC students were
given plants to take home. Asterisks (*) denote exotic plants. See text for site abbreviations.
Site
Plant species MDC FIU OHM AB CTE GEL NHE WPE Total
Alvaradoa amorphoides 6 5 3 0 4 5 0 0 23
Amyris elemifera 0 4 1 0 2 0 0 0 7
Angadenia berteroi 14 7 6 3 8 6 0 4 48
Aristolochia gigantea* 0 0 0 0 2 0 2 2 6
Asclepias curassavica* 0 0 3 0 4 15 4 1 27
Asclepias incarnata 10 0 0 0 0 0 0 2 12
Asclepias tuberosa 12 10 0 0 1 3 0 0 26
Bourreria succulenta 4 0 0 1 0 0 2 0 7
Byrsonima lucida 6 5 3 3 3 0 0 3 23
Cardiospermum corindum 2 0 0 0 0 0 0 0 2
Chamaecrista fasciculata 0 0 0 0 8 0 0 12 20
Citharexylum spinosum 0 0 0 0 0 4 0 0 4
Coccothrinax argentata 0 0 0 0 2 0 0 0 2
Colubrina elliptica 0 0 0 0 0 0 3 3 6
Cordia sebestena 3 0 0 0 3 0 4 0 10
Croton linearis 0 4 3 0 2 9 0 4 22
Cynophalla flexuosa 2 6 0 3 5 4 0 1 21
Ficus aurea 0 0 0 0 2 1 0 0 3
Flaveria linearis 0 2 0 2 8 4 0 6 22
Guaiacum sanctum 5 0 0 2 3 4 0 3 17
Guapira discolor 8 2 0 0 2 0 0 0 12
Jacquinia keyensis 0 0 0 16 0 0 0 0 16
Lantana involucrata 10 8 0 4 4 0 0 6 32
Passiflora suberosa 14 3 3 10 20 8 5 20 83
Physalis walteri 3 6 0 2 6 5 0 4 26
Pithecellobium unguis-cati 4 1 1 1 3 2 0 0 12
Plumbago zeylanica 1 0 0 0 3 1 2 0 7
Psychotria nervosa 4 3 0 0 4 0 0 0 11
Ruta graveolens* 0 0 0 0 3 3 2 0 8
Senna mexicana 3 8 4 5 2 4 10 4 40
Solidago sempervirens 9 0 0 0 0 0 0 4 13
Varronia globosa 2 0 0 0 0 2 0 0 4
Zamia integrifolia 0 0 10 6 4 28 4 6 58
Zanthoxylum fagara 10 4 0 3 3 2 2 2 26
Total 132 78 37 61 111 110 40 87 656
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Table 3. Host plants planted in the gardens and Lepidoptera (but terflies, moths, and skippers) attracted to them. Asterisks denote exotic plants.
Host plants Butterfly, moth, and skipper species that depend on each host plant
Alvaradoa amorphoides (Mexican Alvaradoa) Pyrisitia dina (Dina Yellow)
Amyris elemifera (Sea Torchwood) Heraclides aristodemus ponceanus (Schaus Swallowtail), Heraclides andraemon (Bahamian
Swallowtail), Heraclides cresphontes (Giant Swallowtail)
Angadenia berteroi (Pineland Golden Trumpet) Syntomeida epilais (Polka-Dot Wasp Moth)
Aristolochia gigantea* (Brazilian Dutchman’s Pipe) Battus polydamas (Polydamas Swallowtail)
Asclepias species*(Milkweed) Danaus plexippus (Monarch), Danaus gilippus (Queen), Danaus eresimus (Soldier)
Byrsonima lucida (Locustberry) Ephyriades brunnea (Florida Duskywing)
Capparis flexuosa (Limber Caper) Glutophrissa drusilla neumoegenii (Florida White), Ascia monuste (Great Southern White)
Cardiospermum corindum (Balloonvine) Chlorostrymon simaethis (Silver-Banded Hairstreak)
Chamaecrista fasciculata (Partridge Pea) Hemiargus ceraunus (Ceraunus Blue), Phoebis sennae (Cloudless Sulphur), Eurema nicippe
(Sleepy Orange), Pyrisitia lisa (Little Yellow)
Citharexylum spinosum (Fiddlewood) Epicorsia oedipodalis (Fiddlewood Leafroller)
Coccothrinax argentata (Silver Palm) Asbolis capucinus (Monk Skipper)
Croton linearis (Pineland Croton) Anaea troglodyta floridalis (Florida Leafwing), Strymon acis bartrami (Bartram’s Scrub-Hairstreak)
Ficus aurea (Strangler Fig) Marpesia petreus (Ruddy Daggerwing)
Guaiacum sanctum (Lignum-Vitae) Kricogonia lyside (Lyside Sulphur)
Passiflora suberosa (Corkystem Passionflower) Heliconius charithonia (Zebra Longwing), Dryas iulia (Julia), Agraulis vanillae (Gulf Fritillary)
Pithecellobium unguis-cati (Catclaw Blackbead) Leptotes cassius (Cassius Blue), Phoebis agarithe (Large Orange Sulphur)
Plumbago zeylanica (Doctorbush) Leptotes cassius (Cassius Blue)
Ruta graveolens* (Rue) Heraclides cresphontes (Giant Swallowtail), Papilio polyxenes (Black Swallowtail)
Senna mexicana (Chapman’s Senna) Phoebis philea (Orange-Barred Sulphur), Phoebis sennae (Cloudless Sulphur)
Zamia integrifolia (Coontie) Eumaeus atala (Atala)
Zanthoxylum fagara (Wild Lime) Heraclides aristodemus ponceanus (Schaus Swallowtail), Heraclides andraemon (Bahamian
Swallowtail), Heraclides cresphontes (Giant Swallowtail)
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Schaus Swallowtail population in the Florida Keys, it is imperative to maintain the
park’s ecological integrity (Saunders and Hobbs 1989, USFWS 2008). As human
populations continue to increase, land is continually developed, and there is pressure
on the tracts surrounding protected areas. In addition, people are increasingly
engulfed in cocoons provided by their enhanced mobile technology, and many have
become disconnected from nature. A negative feedback pattern has been generated
by these phenomena, where species may persist in protected parks but still face the
threat of habitat loss and degradation near park boundaries (Pergams and Zaradic
2006, Wiersma et al. 2004).
This intensive, multi-year, service-learning project raised awareness about a
federally endangered butterfly, and demonstrated memorable hands-on approaches
to proactive solutions. Habitat restoration efforts led to visitation of sites and oviposition
on planted Torchwood by Schaus Swallowtails (Fig. 4), as well as oviposition
Table 4. Before garden construction, butterfly-species counts (pre-survey) were conducted (numbers
indicated in parenthesis) at each site. Several months later, a post-survey was conducted in the same
area at each site. Asterisks (*) denote an increase in butterflies from the pre-survey. Note: Students at
MDCHC did not construct a butterfly garden.
Site
Butterfly species MDCHC OHMCC AB K-8 CTE GEL K-8 NHE WPE Total
Agraulis vanillae (0)0 (0)1 (5)0 (0)2 (1)5 (0)3 (2)3 (8)14*
Anartia jatrophae (3)4 (5)2 (4)0 (6)3 (5)5 (2)2 (4)3 (29)19
Asbolis capucinus (0)0 (0)0 (0)4 (0)0 (3)2 (0)1 (0)1 (3)8*
Ascia monuste (0)0 (0)1 (0)0 (0)0 (0)0 (0)3 (0)1 (0)5*
Battus polydamas (0)0 (0)0 (0)0 (0)1 (0)0 (0)0 (1)3 (1)4*
Danaus gilippus (0)0 (0)0 (0)0 (0)0 (2)2 (0)0 (2)1 (4)3
Danaus plexippus (0)0 (0)3 (3)0 (5)2 (3)12 (1)5 (4)5 (16)27*
Dryas iulia (0)0 (0)2 (1)0 (0)0 (0)1 (0)0 (1)3 (4)6*
Electrostrymon angelia (0)0 (1)1 (0)0 (0)0 (0)1 (0)0 (0)0 (1)2*
Eumaeus atala (0)0 (0)0 (2)3 (0)0 (0)0 (0)0 (0)0 (2)3*
Eurema daira (0)2 (5)3 (0)2 (8)3 (0)0 (4)2 (0)0 17(12)
Heliconius charithonia (0)0 (0)0 (4)6 (0)0 (0)1 (0)0 (3)5 (7)12*
Hemiargus ceraunus (0)0 (0)0 (1)1 (0)2 (5)2 (0)0 (2)1 (8)6
Hylephila phyleus (0)0 (0)1 (0)3 (0)0 (0)0 (0)0 (0)0 (0)4*
Junonia coenia (0)0 (0)1 (1)1 (0)0 (2)1 (0)0 (2)1 (5)4
Leptotes cassius (3)1 (0)2 (1)0 (3)3 (6)8 (1)3 (0)2 (14)19*
Marpesia petreus (0)0 (0)0 (0)1 (0)0 (0)0 (0)0 (1)1 (1)2*
Nathalis iole (0)0 (3)1 (2)0 (1)4 (0)3 (0)1 (0)0 (6)9*
Papilio cresphontes (0)0 (0)0 (1)0 (0)1 (0)0 (1)1 (0)0 (2)2
Papilio polyxenes (0)0 (0)0 (0)0 (0)0 (0)1 (0)0 (0)0 (0)1*
Phoebis agarithe (2)1 (4)2 (3)2 (0)0 (10)9 (1)0 (0)0 (20)14
Phoebis philea (0)0 (0)0 (0)1 (0)1 (2)1 (0)0 (0)0 (2)3*
Phoebis sennae (0)0 (0)0 (0)0 (0)2 (0)1 (0)1 (0)0 (0)4*
Phyciodes phaon (0)0 (1)1 (1)0 (0)0 (1)1 (0)0 (2)1 (5)3
Polites vibex (0)0 (0)0 (0)1 (0)0 (0)0 (1)0 (0)1 (1)2*
Pyrgus oileus (0)0 (1)1 (0)0 (0)0 (0)0 (0)0 (1)1 (2)2
Urbanus proteus (0)0 (1)0 (0)0 (0)0 (0)0 (0)1 (0)1 (1)2*
Total (8)8 (21)22* (29)25 (23)24* (40)56* (11)23* (27)34* (159)192*
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2017 Vol. 16, Special Issue 10
by the rare Bahamian Swallowtail Butterfly. Project volunteers saw many other
species at the restoration sites, including native bees, flies, resident and neotropical
migrant birds, and giant land and hermit crabs, exposing them to BNP’s terrestrial
biodiversity. Every participating volunteer at BNP, the schools, and community
center became aware of the Schaus Swallowtail’s conservation status, as well as
other butterflies and their native host plants.
The schools that integrated the Schaus and Coastal Hardwood Hammock curriculum
unit into their lesson plans engaged students in the garden and used field
guides to identify and count various butterfly species. Students of all ages were
able to conduct the butterfly count without the aid of teachers and other experts,
and were able to identify more species during the post-survey, a prime example of
“scaffolding.” Scaffolding refers to students accomplishing something they, under
other circumstances, would be unable to achieve, with only minimal support from a
teacher (Settlage and Southerland 2012). This teacher support is temporary, and can
be withdrawn as students acquire confidence, skills, and knowledge. At participating
schools, students absorbed the information and used it in a multitude of ways,
taking ownership and sharing with others, and working as scient ists themselves.
The gardens still flourish, and both new and veteran students continue to add
native plants each year while maintaining their gardens through weeding, watering,
and edging. Each garden serves to enhance academic achievement, social
capital, and environmental quality through active learning, applied and practical
science, and self-governing responsibilities (student-driven ownership; Blair 2009,
Sobel 2005). Students who value habitat preservation for wildlife in their school
garden become protective of the plants they nurtured after placing them to the
ground. Teachers use the garden not only for science, but also for activities in other
subject areas such as mathematics, writing, and art.
Schools can raise awareness and motivate large numbers of people to think
globally by acting locally. School grounds can be more ecologically valuable than
the traditional grass monoculture bordered with several exotic plant species. By
establishing butterfly gardens during the project, these areas became complex,
multi-layered, verdant landscapes harboring diverse insect species. Teachers can
use the school’s surroundings as a framework upon which students can build their
own learning while also increasing the biodiversity of organisms (Lieberman and
Hoody 1998, Skelly and Bradley 2000). Projects involving schoolyard habitats can
also encourage further activities by families and lifelong compassion for the environment,
as well as provide guidelines for our behavior towards other people in
the outdoors and our behavior towards nature (Matthews and Riley 1995, Waliczek
and Zajicek 1999). By greening their school grounds and neighborhoods, teachers,
students, and families can help butterflies and other insect species overcome habitat
loss in areas that still harbor imperiled species.
South Florida and the Keys provide extreme examples of human ha bitation and
development at the expense of native wildlife (Alonso and Heinen 2011, Bancroft
et al. 1995, Karim and Main 2009). Education can bring about change through an
increased understanding of the importance of maintaining wildlife habitat, and a
Southeastern Naturalist
J. Clayborn, S. Koptur, G. O’Brien, and K.R.T. Whelan
2017
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Vol. 16 Special Issue 10
sense of empowerment that individuals can do something, even on a small scale,
to help promote species diversity (Miller 2005). Butterflies can be used as flagship
species to educate and raise public awareness of many important environmental
issues because they are charismatic and provide attractive models for conservation
(Guiney and Oberhauser 2009, Leader-Williams and Dublin 2000, Walpole and
Leader-Williams 2002). The establishment of butterfly gardens, such as those created
for the Schaus and Coastal Hardwood Hammock curriculum unit, can provide
habitat for other vulnerable species and generate an “umbrella” that can protect
multiple species against negative human impacts (Guiney and Oberhauser 2009,
Malone et al. 2015, Mathew and Anto 2007, Vickery 1995).
Acknowledgments
We thank S. Zona, Y. Reynaldo, and the editors and anonymous reviewers for helpful
suggestions on the manuscript; Biscayne National Park and National Park Service personnel
for providing access to the study sites (study numbers BISC-00041 and BISC-00046 under
permits BISC-2014-SCI-0031, BISC-2015-SCI-0023, and BISC-2016-SCI-0044), and their
continued commitment to protecting the jewels in the National Parks. We are grateful to
all volunteers from the Sierra Club, Florida International University, University of Miami,
Doral High School, John Pennekamp State Park, Biscayne National Park, and the National
Park Service for their assistance in this project; and the faculty and teachers at Miami–Dade
County schools and FIU for improving the Schaus and Coastal Hardwood Hammocks curriculum
unit. This work was supported by the US Fish and Wildlife Service, and the FWS
South Florida Coastal Program provided partial funding. This paper is contribution # 326 to
the Tropical Biology Program at Florida International University, Maiami, FL.
Literature Cited
Achieve, Inc. 2013. Next generation science standards (NGSS). Available online at
http://www.nextgenscience.org/next-generation-science-standards. Accessed 5 September
2015.
Alonso, J., and J.T. Heinen. 2011. Miami–Dade County’s environmentally endangered
lands program: Local efforts for a global cause. Natural Areas Journal 3:183–189.
Armentano, T.V., D.T. Jones, M.S. Ross, and B.W. Gamble. 2002. Vegetation pattern and
process in tree islands of the southern Everglades and adjacent areas. Pp. 225–282, In
F.H. Sklar and A. Van Der Valk (Eds). Tree Islands of the Everglades. Kluwer Academic
Publishers, Dordrecht, The Netherlands. 541 pp.
Bancroft, G.T., A.M. Strong, and M. Carrington. 1995. Deforestation and its effects on
forest-nesting birds in the Florida Keys. Conservation Biology 9:835–844.
Bender, D.J., T.A. Contreras, and L. Fahrig. 1998. Habitat loss and population decline: A
meta-analysis of the patch-size effect. Ecology 79:517–533.
Berger, J.J. 1993. Ecological restoration and nonindigenous plant species: A review. Restoration
Ecology 1:74–82.
Blair, D. 2009. The child in the garden: An evaluative review of the benefits of school gardening.
The Journal of Environmental Education 40:15–38.
Bögeholz, S. 2006. Nature experience and its importance for environmental knowledge,
values, and action: Recent German empirical contributions. Environmental Education
Research 12:65–84.
Southeastern Naturalist
41
J. Clayborn, S. Koptur, G. O’Brien, and K.R.T. Whelan
2017 Vol. 16, Special Issue 10
Bybee, R. 2002. Learning Science and the Science of Learning: Science Educators’ Essay
Collection. National Science Teachers Association Press, Arlington, VA. 158 pp.
Bybee, R.W. 2014. NGSS and the next generation of science teachers. Journal of Science
Teacher Education 25:211–221.
Calhoun, J.V., J.R. Slotten, and M.H. Salvato. 2002. The rise and fall of tropical blues in
Florida: Cyclargus ammon and Cyclargus thomasi bethunebakeri (Lepidoptera: Lycaenidae).
Holarctic Lepidoptera 7:13–20.
Chawla, L. 1998. Significant life experiences revisited: A review of research on sources of
environmental sensitivity. Environmental Education Research 4:369–382.
Dennis, R.L., J.G. Hodgson, R. Grenyer, T.G. Shreeve, and D.B. Roy. 2004. Host plants and
butterfly biology. Do host-plant strategies drive butterfly status? Ecological Entomology
29:12–26.
Duda, M.D., S.J. Bissell, and K.C. Young. 1998. Wildlife and the American Mind: Public
Opinion on and Attitudes toward Fish and Wildlife Management. Responsive Management,
Harrisonburg, VA. 804 pp.
Egan, D., and E.A. Howell (Eds.). 2001. The Historical Ecology Handbook: A Restorationist’s
Guide to Reference Ecosystems. Island Press, Washington, DC. 457 pp.
Florida Invasive Species Partnership (FISP). 2017. Florida Keys Invasive Exotics Task
Force. Available online at https://www.floridainvasives.org/Keys/. Accessed 5 August
2017.
Guiney, M.S., and K.S. Oberhauser. 2009. Insects as flagship conservation species. Terrestrial
Arthropod Reviews 1:111–123.
Hoekstra, J.M., T.M. Boucher, T.H. Ricketts, and C. Roberts. 2005. Confronting a biome
crisis: Global disparities of habitat loss and protection. Ecol ogy Letters 8:23–29.
Horvitz, C.C., and A. Koop. 2001. Removal of nonnative vines and post-hurricane recruitment
in tropical hardwood forests of Florida. Biotropica 33:268 –281.
Hungerford, H., and T. Volk. 1990. Changing learner behavior through environmental education.
Journal of Environmental Education 21:8–21.
Invasive.org. 2017. Florida Keys Invasive Species Task Force – List of invasive plants.
Available online at https://www.invasive.org/species/list.cfm?id=82. Accessed 5 August
2017.
Jameson, A. 2002. Host plants and habitats of the Schaus Swallowtail Butterfly (Papilio
aristodemus ponceanus). M.Sc. Thesis. University of Miami, Coral Gables, FL. 51 pp.
Janzen, D.H. 1988. Tropical dry forests: The most endangered major tropical ecosystem.
Pp. 130–137, In E.O. Wilson and F.M. Peter (Eds.). Biodiversity. National Academies
Press, Washington, DC. 521 pp.
Karim, A., and M.B. Main. 2009. Habitat fragmentation and conservation strategies for a
rare forest habitat in the Florida Keys archipelago. Urban Ecos ystems 12:359–370.
Leader-Williams N., and H. Dublin. 2000. Charismatic megafauna as “flagship species”.
Pp. 53–81, In A. Entwistle and N. Dunstone (Eds.). Priorities for the Conservation of
Mammalian Diversity: Has the Panda had its Day? Cambridge University Press, Cambridge,
UK. 457 pp.
Lieberman, G.A., and L.L. Hoody. 1998. Closing the achievement gap: Using the environment
as an integrating context for learning. Research report. State Environment and
Education Roundtable, San Diego, CA. 21 pp.
Loftus, W., and J. Kushlan. 1984. Population fluctuations of the Schaus Swallowtail (Lepidoptera:
Papilionidae) on the islands of Biscayne Bay, Florida, with comments on the
Bahaman Swallowtail. Florida Entomologist 67:277–287.
Southeastern Naturalist
J. Clayborn, S. Koptur, G. O’Brien, and K.R.T. Whelan
2017
42
Vol. 16 Special Issue 10
Louv, R. 2008. Last Child in the Woods: Saving our Children from Nature-deficit Disorder.
Algonquin Books, New York, NY. 323 pp.
Malone, K.C., W. Wilber, G. Hansen, J.C. Daniels, C. Larsen, and E. Momol. 2015. Community
butterfly-scaping: How to move beyond butterfly gardening to create a largescale
butterfly habitat. University of Florida IFAS Extension. Available online at http://
edis.ifas.ufl.edu/ep420. Accessed 9 September 2015.
Mathew, G., and M. Anto. 2007. In situ conservation of butterflies through establishment
of butterfly gardens: A case study at Peechi, Kerala, India. Current Science 93:337–347.
Matthews, B.E., and C.K. Riley. 1995. Teaching and evaluating outdoor-ethics education
programs. Descriptive report. National Wildlife Federation, ERIC Document Reproduction
Service No. ED 401 097, Vienna, VA. 118 pp.
Miller, J.R. 2005. Biodiversity conservation and the extinction of experience. Trends in
Ecology and Evolution 20:430–434.
Minno, M.C., and T.C. Emmel. 1993. Butterflies of the Florida Keys. Scientific Publishers,
Gainesville, FL. 168 pp.
MonarchWatch. 2014. MonarchWatch: Migration and tagging. Available online at http://
monarchwatch.org/tagmig/tag.htm. Accessed 16 March 2014.
Myers, R.L., and J.J. Ewel (Eds.). 1990. Ecosystems of Florida. University of Central
Florida Press, Orlando, FL. 765 pp.
National Park Service (NPS). 2015. National Park Service visitor-use statistics. Available
online at https://irma.nps.gov/Stats/Reports/Park/BISC. Accessed 9 September 2015.
Oliver, T., D.B. Roy, J.K. Hill, T. Brereton, and C.D. Thomas. 2010. Heterogeneous landscapes
promote population stability. Ecology Letters 13:473–484.
Pergams, O.R., and P.A. Zaradic. 2006. Is love of nature in the US becoming love of electronic
media? 16-year downtrend in national park visits explained by watching movies,
playing video games, internet use, and oil prices. Journal of Environmental Management
80:387–393.
Pergams, O.R., and P.A. Zaradic. 2008. Evidence for a fundamental and pervasive shift
away from nature-based recreation. Proceedings of the National Academy of Sciences
105:2295–2300.
Pyle, R.M. 1978. The extinction of experience. Horticulture 56:64–67.
Ray, G.J., F. Dallmeier, and J.A. Comiskey. 1998. The structure of two subtropical dry forest
communities on the island of St. John, US Virgin Islands. Pp. 367–384, In F. Dallmeier
and J.A. Comiskey (Eds.). Forest Biodiversity in North, Central, and South America,
and the Caribbean: Research and Monitoring, Man and the Biosphere series. Vol. 21.
UNESCO and the Parthenon Publishing Group, Camforth, Lancashire , UK. 768 pp.
Ricketts, T. 2001. The matrix matters: Effective isolation in fragmented landscapes. The
American Naturalist 158:87–99.
Ricketts, T.H., J. Regetz, I. Steffan-Dewenter, S.A. Cunningham, C. Kremen, A. Bogdanski,
B. Gemmill-Herren, S.S. Greenleaf, A.M. Klein, M.M. Mayfield, L.A. Morandin,
A. Ochieng, and B.F. Viana. 2008. Landscape effects on crop-pollination services: Are
there general patterns? Ecology Letters 11:499–515.
Roe, D., N. Leader-Williams, and D.B. Dalal-Clayton. 1997. Take only photographs, leave
only footprints: The environmental impacts of wildlife tourism (No. 10). The International
Institute for Environment and Development, London, UK. 8 6 pp.
Rosa, E., R. York, and T. Dietz. 2004. Tracking the anthropogenic drivers of ecological
impacts. AMBIO: A Journal of the Human Environment 33:509–512.
Ross, M.S., J.J. O’Brien, and L.J. Flynn. 1992. Ecological site classification of Florida Keys
terrestrial habitats. Biotropica 24:488–502.
Southeastern Naturalist
43
J. Clayborn, S. Koptur, G. O’Brien, and K.R.T. Whelan
2017 Vol. 16, Special Issue 10
Ross, M.S., M. Carrington, L.J. Flynn, and P.L. Ruiz. 2001. Forest succession in tropical
hardwood hammocks of the Florida Keys: Effects of direct mortality from Hurricane
Andrew. Biotropica 33:23–33.
Ross, M.S., J.J. O’Brien, R.G. Ford, K. Zhang, and A. Morkill. 2009. Disturbance and the
rising tide: The challenge of biodiversity management on low-island ecosystems. Frontiers
in Ecology and the Environment 7:471–478.
Rutkowski, F. 1971. Observations on Papilio aristodemus ponceanus (Papilionidae). Journal
of Lepidopterist Society 25:126–136.
Saunders, D., and R. Hobbs. 1989. Corridors for conservation. N ew Scientist 121:63–68.
Settlage, J., and S.A. Southerland. 2012. Teaching Science to Every Child: Using Culture
as a Starting Point. Taylor and Francis, New York, NY. 383 pp.
Skelly, S.M., and J.C. Bradley. 2000. The importance of school gardens as perceived by
Florida elementary school teachers. Horticultural Technology 10:229–231.
Smith, D.S., L.D. Miller, J.Y. Miller, and R. Lewington. 1994. The Butterflies of the West
Indies and South Florida. Oxford University Press, New York, NY. 264 pp.
Snyder J.R., A. Herndon, and W.B.J. Robertson. 1990. South Florida rockland. Pp. 230–
277, In R.L. Myers and J.J. Ewel (Eds.). Ecosystems of Florida. University Press of
Florida, Orlando, FL. 765 pp.
Sobel, D. 2005. Place-based education: Connecting Classrooms and Communities. The
Orion Society, Great Barrington, MA. 116 pp.
Stevens, T.H., T.A. More, and M. Markowski-Lindsey. 2014. Declining national park visitation.
Journal of Leisure Research 46:153–164.
Strong, A.M., and G.T. Bancroft. 1994. Patterns of deforestation and fragmentation of
mangrove and deciduous seasonal forests in the upper Florida Keys. Bulletin of Marine
Science 54:795–804.
Taki, H., and P.G. Kevan. 2007. Does habitat loss affect the communities of plants and
insects equally in plant–pollinator interactions? Preliminary findings. Biodiversity and
Conservation 16:3147–3161.
US Fish and Wildlife Service (USFWS). 2008. Schaus Swallowtail Butterfly (Heraclides
aristodemus ponceanus) 5-year review: Summary and evaluation. Available online at
http://ecos.fws.gov/docs/five_year_review/doc1983.pdf. Accessed 23 Oct 2013.
USFWS. 2015. Environmental conservation online system (Schaus Swallowtail Butterfly).
Available online at https://ecos.fws.gov/ecp0/profile/speciesProfile?spcode=I016. Accessed
8 September 2015.
Waliczek, T.M., and J.M. Zajicek. 1999. School gardening: Improving environmental attitudes
of children through hands-on learning. Journal of Environmental Horticulture
17:180–184.
Walpole, M.J., and N. Leader-Williams. 2002. Tourism and flagship species in conservation.
Biodiversity and Conservation 11:543–547.
Wells, N.M., and K.S. Lekies. 2006. Nature and the life course: Pathways from childhood
nature experiences to adult environmentalism. Children, Youth, and Environments
16:1–24.
Whelan, K.R. 2011. Schaus Swallowtail Butterfly (Heraclides aristodemus ponceanus)
habitat enhancement in Biscayne National Park. Project report. Funded by FWS South
Florida Coastal Program. National Park Service, Palmetto Bay, FL. 9 pp.
Whelan, K.R.T., and A. Atkinson. 2015. Schaus Swallowtail Butterfly (Heraclides aristodemus
ponceanus) habitat enhancement in Biscayne National Park. South Florida Coastal
Program project progress report. NPS/SFCN. National Park Servic e, Palmetto Bay, FL.
24 pp.
Southeastern Naturalist
J. Clayborn, S. Koptur, G. O’Brien, and K.R.T. Whelan
2017
44
Vol. 16 Special Issue 10
Whelan, K.R.T., P.L. Ruiz, R.B. Shamblin, P.A. Houle, M.S. Ross, A.J. Atkinson, J.M.
Patterson, and J. Alonso. 2013. Biscayne National Park vegetation map project. Natural
resource technical report. NPS/SFCN/NRTR – 2013/774. National Park Service, Fort
Collins, CO. 352 pp.
Wiersma, Y.F., T.D. Nudds, and D.H. Rivard. 2004. Models to distinguish effects of landscape
patterns and human population pressures associated with species loss in Canadian
national parks. Landscape Ecology 19:773–786.
Vickery, M.L. 1995. Gardens: The neglected habitat. Pp. 123–134, In A.S. Pullin (Ed.).
Ecology and Conservation of Butterflies. Springer, Dordrecht, The Netherlands. 363 pp.
Zaradic, P.A., and O.R. Pergams. 2007. Videophilia: Implications for childhood development
and conservation. Journal of Developmental Processes 2:130 –144.
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Appendix 1. Latin names, taxonomic authority, and common names of butterfly, moth, and
skipper species mentioned in this paper.
Scientific name Common name
Abaeis nicippe (Cramer) Sleepy Orange
Agraulis vanillae nigrior Michener Gulf Fritillary
Anaea troglodyta floridalis F. Johnson & W.P. Comstock Florida Leafwing
Anartia jatrophae guantanamo Munroe White Peacock
Asbolis capucinus (Lucas) Monk Skipper
Ascia monuste (L.) Great Southern White
Battus polydamas lucayus (Rothschild and Jordan) Polydama Swallowtail
Chlorostrymon simaethis (Drury) Silver-banded Hairstreak
Danaus eresimus tethys W. Forbes Soldier
Danaus gilippus berenice (Cramer) Queen
Danaus plexippus (L.) Monarch
Dryas iulia largo Clench Julia
Electrostrymon angelia (Hewitson) Fulvous Hairstreak
Ephyriades brunnea floridensis E. Bell & W. Comstock Florida Duskywing
Epicorsia oedipodalis (Guenée) Fiddlewood Leafroller
Eumaeus atala Poey Atala
Eurema daira (Godart) Barred Yellow
Glutophrissa drusilla neumoegenii (Skinner) Florida White
Heliconius charithonia tuckeri W. Comstock & F. Brown Zebra Longwing
Hemiargus ceraunus antibubastus Hübner Ceraunus Blue
Hylephila phyleus (Drury) Fiery Skipper
Junonia coenia Hübner Common Buckeye
Kricogonia lyside (Godart) Lyside Sulphur
Leptotes cassius theonus (Lucas) Cassius Blue
Marpesia petreus (Cramer) Ruddy Daggerwing
Nathalis iole Boisduval Dainty Sulphur
Papilio (Heraclides) andraemon (Hübner) Bahamian Swallowtail
Papilio (Heraclides) aristodemus ponceanus (Schaus) Schaus Swallowtail
Papilio (Heraclides) cresphontes Cramer Giant Swallowtail
Papilio polyxenes asterius (Stoll) Black Swallowtail
Phoebis agarithe maxima (Neumoegen) Large Orange Sulphur
Phoebis philea (L.) Orange-barred Sulphur
Phoebis sennae (L.) Cloudless Sulphur
Phyciodes phaon (W.H. Edwards) Phaon Crescent
Polites vibex (Geyer) Whirlabout
Pyrgus oileus (Linnaeus) Tropical Checkered-Skipper
Pyrisitia dina helios (D. Bates) Dina Yellow
Pyrisitia lisa (Boisduval & Le Conte) Little Yellow
Syntomeida epilais (Walker) Polka-Dot Wasp Moth
Strymon acis bartrami (W. Comstock and Huntington) Bartram’s Scrub-Hairstreak
Urbanus proteus (L.) Long-tailed Skipper
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Appendix 2. Latin names, taxonomic authority, and common names of plants mentioned
in this paper.
Scientific name Common name
Alvaradoa amorphoides Liebm. Mexican Alvaradoa
Amyris elemifera L. Sea Torchwood
Angadenia berteroi (A.DC.) Miers Pineland Golden Trumpet
Aristolochia gigantea Mart. & Zucc. Brazilian Dutchman’s Pipe
Asclepias curassavica L. Tropical Milkweed
Asclepias incarnata L. Swamp Milkweed
Asclepias tuberosa L. Butterfly Milkweed
Bourreria succulenta Jacq. Bahama Strongbark
Byrsonima lucida (Mill.) DC. Locustberry
Cardiospermum corindum L. Balloonvine, Heartseed
Chamaecrista fasciculata (Michx.) Greene Partridge Pea
Citharexylum spinosum L. Florida Fiddlewood
Coccothrinax argentata (Jacq.)L.H. Bailey Florida Silver Palm
Colubrina asiatica (L.)Brongn. Asian Nakedwood, Latherleaf
Colubrina elliptica (Sw.)Brizicky & W.L.Stern Soldierwood
Cordia sebestena L. Largeleaf Geigertree
Croton linearis Jacquin Pineland Croton
Cynophalla flexuosa (L.) J. Presl Bayleaf Capertree, Limber Caper
Ficus aurea Nuttall Strangler Fig
Flaveria linearis Lag. Narrowleaf Yellowtops
Guaiacum sanctum L. Holywood Lignumvitae
Guapira discolor (Spreng.) Little Beeftree, Blolly
Jacquinia keyensis Mez Joewood
Lantana involucrata L. Buttonsage
Neyraudia reynaudiana (Kunth) Keng ex Hitchc. Burmareed, Silkreed
Passiflora suberosa L. Corkystem Passionflower
Physalis walteri Nutt. Walter’s Groundcherry
Pithecellobium unguis-cati (L.) Benth. Catclaw Blackbead
Plumbago zeylanica L. Doctorbush
Psychotria nervosa Swartz Wild Coffee
Ruta graveolens L. Rue
Senna mexicana var. chapmanni (Isely) H.S. Irwin Chapman’s Wild Sensitive Plant
& Barneby
Solidago sempervirens L. Seaside Goldenrod
Varronia globosa Jacq. Butterflybush, Curacao Bush
Zamia integrifolia L. Coontie
Zanthoxylum fagara (L.) Sarg. Lime Pricklyash, Wild Lime