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Cite this article: Hallworth MT, Marra PP,
McFarland KP, Zahendra S, Studds CE. 2018
Tracking dragons: stable isotopes reveal the
annual cycle of a long-distance migratory
insect. Biol. Lett. 14: 20180741.
http://dx.doi.org/10.1098/rsbl.2018.0741
Received: 23 October 2018
Accepted: 23 November 2018
Subject Areas:
ecology, behaviour
Keywords:
Anax, common green darner, stable-hydrogen
isotopes, migration phenology
Author for correspondence:
Michael T. Hallworth
e-mail: [email protected]
Electronic supplementary material is available
online at https://dx.doi.org/10.6084/m9.
figshare.c.4320911.
& 2018 The Author(s) Published by the Royal Society. All
rights reserved.
Animal behaviour
Tracking dragons: stable isotopes reveal
the annual cycle of a long-distance
migratory insect
Michael T. Hallworth1,2, Peter P. Marra1, Kent P. McFarland3,
Sara Zahendra3
and Colin E. Studds1,2
1Migratory Bird Center, Smithsonian Conservation Biology
Institute, Washington, DC 20008, USA
2Department of Geography and Environmental Systems,
University of Maryland, Baltimore County, Baltimore,
MD 21250, USA
3Vermont Center for Ecostudies, White River Junction, VT
05001, USA
MTH, 0000-0002-6385-3815; PPM, 0000-0002-0508-7577;
KPM, 0000-0001-7809-5503;
CES, 0000-0001-5715-1692
Insect migration is globally ubiquitous and can involve
continental-scale
movements and complex life histories. Apart from select species
of
migratory moths and butterflies, little is known about the
structure of the
annual cycle for migratory insects. Using stable-hydrogen
isotope analysis
of 852 wing samples from eight countries spanning 140 years,
combined
with 21 years of citizen science data, we determined the full
annual cycle
of a large migratory dragonfly, the common green darner (Anax
junius).
We demonstrate that darners undertake complex long-distance
annual
migrations governed largely by temperature that involve at least
three gen-
erations. In spring, the first generation makes a long-distance
northbound
movement (further than 650 km) from southern to northern
range limits,
lays eggs and dies. A second generation emerges and returns
south (further
than 680 km), where they lay eggs and die. Finally, a third
resident gener-
ation emerges, reproducing locally and giving rise to the cohort
that
migrates north the following spring. Since migration timing and
nymph
development are highly dependent on temperature, continued
climate
change could lead to fundamental changes in the biology for
this and similar
migratory insects.
1. Introduction
Insects are the most species-rich and abundant group of
macroscopic organisms
on the planet, yet our understanding of the biological
underpinnings of their
annual cycles and migratory behaviours drastically trails behind
that of
vertebrate taxa [1]. Perhaps the best-known insect migrations
are the multi-
generational migrations of the monarch butterfly (Danaus
plexippus) in eastern
North America [2], and the painted lady (Vanessa cardui) in
Europe [3], which
migrate southbound each autumn from the northern reaches of
their distri-
bution into southern North America and Africa, respectively.
Monarchs wait
out the boreal winter [4] and the same individuals migrate
northbound the fol-
lowing spring into the southern parts of their distribution where
they lay eggs,
beginning the next generation that continues the northbound
progression of
their lifecycle [2,3,5,6].
Few migratory insects have had their full annual cycles
sufficiently
described despite their profound cultural [7], ecological [8] and
agricultural
importance [9]. This disparity is owing largely to the
difficulties with tracking
small organisms over space and time, as well as their complex
life histories that
often require both terrestrial and aquatic habitats [10]. Among
the migratory
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https://dx.doi.org/10.6084/m9.figshare.c.4320911
https://dx.doi.org/10.6084/m9.figshare.c.4320911
http://orcid.org/
http://orcid.org/0000-0002-6385-3815
http://orcid.org/0000-0002-0508-7577
http://orcid.org/0000-0001-7809-5503
http://orcid.org/0000-0001-5715-1692
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Biol.
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2
insects, almost all are suspected to employ complex multi-
generational migrations (but see [7,8]) similar to the monarch
butterfly and painted lady, where no single individual
completes the entire migratory circuit [2,3,5,6,10,11]. The con-
tinental distances travelled [12,13], small body sizes and
multi-generational aspect of their life histories pose signifi-
cant challenges to understanding the fundamental biology
of the full annual cycles of migratory insects. Adding to
this complexity, movements, timing and life-history strategies
are likely linked to photoperiod, weather, temperature and
other environmental forces [1,3,11,14 – 16].
The common green darner (Anax junius) is a ubiquitous,
charismatic migratory dragonfly found in North America.
Its complex life-history includes both resident and migratory
populations. The aquatic nymphs likely give rise to resident
and migratory phenotypes because they exhibit two distinct
developmental strategies [14]. Nymphs either undergo
rapid development and emerge within a single season or
develop slowly, enter diapause and emerge the following
summer [14]. The developmental strategy is governed by the
photoperiod experienced by the egg or early instars [17] and
temperature [14]. Therefore, the seasonal timing of oviposition
likely determines whether nymphs develop, emerge within a
single growing season and migrate, or enter diapause.
Darner migration is considered an adaptive strategy
because it spreads reproductive effort across multiple,
widely separated water bodies and ameliorates the risk of
predation, competition and drought [17,18]. Migratory move-
ments are commonly observed in autumn and have been
documented using direct [12] and indirect techniques [19].
Northbound migration in spring is suspected and supported
by anecdotal observations but is not well documented [20].
Although it is known that common green darners migrate,
no study to date has linked multiple populations over time
and space to better understand the phenology of the annual
cycle and the number of generations involved.
2. Methods and materials
We combined observational and stable-hydrogen isotope
data to identify the timing of migration and emergence ori-
gins of darners. Two publicly available datasets were
assembled to refine emergence assignments using stable iso-
topes. First, we acquired citizen science data on the first
observed migratory adult common green darners (first
flight dates) to determine the minimum temperature necess-
ary for darners to migrate (electronic supplementary
material, table S1). Daily mean temperature of the first
flight date was 9.178C, similar to the development threshold
(8.7 + 0.18C) reported by Trottier [14]. In addition to deter-
mining the temperature threshold for migratory flights, we
used occurrence records submitted by citizen scientists and
museum collections to generate a habitat suitability surface
that we included as prior information in the probabilistic
isotope-assignments [21] (see §2a).
(a) Emergence assignments
We obtained contemporary and museum specimens from 681
locations from eight countries ranging from the tropics to the
northern temperate zone (17.988 N to 51.148 N) that we used
to describe migration phenology and the number of gener-
ations within the annual cycle for the common green
darner. Specimens, which included exuviae, tenerals and
mature adults, were collected in every calendar month span-
ning over 100 years (electronic supplementary material, table
S2). Isotope analyses were performed on a small distal seg-
ment of the wing to determine where the captured
individuals emerged (see electronic supplementary material).
(b) Migratory distance
Determining the exact emergence origin from stable isotopes
is not possible given the uncertainty in geographical assign-
ment and lack of longitudinal variation in the underlying
isoscape. Therefore, we used a conservative distance estima-
tor as an index of migration distance. We determined the
minimum distance (kilometres) between the ‘likely’ emer-
gence origin surface and the location where the specimen
was collected (i.e. shortest possible distance travelled).
Migration distances were calculated using the gDistance
function in the rgeos [22] package in program R [23].
(c) Annual cycle
We summarized the emergence origins within the hardiness
zones (see electronic supplementary material, delineating
populations) for each calendar month to describe the pheno-
logy of the annual cycle. Isotope-based emergence origins
provide spatio-temporal information of adults but the
phenology of nymph development and emergence timing is
also needed to fully understand the annual cycle of darners.
3. Results
We combined data on stable-hydrogen isotopes of 852
common green darner museum and contemporary specimens
spanning 140 years (1874 – 2013) from eight countries with
citizen science observations to determine the emergence
origin, continental migrations and annual cycle of the
common green darner. Using citizen science observations,
we found that northbound darner migration closely tracks a
thermocline of 9.178C (figure 1). We then used this tempera-
ture-dependent flight phenology to refine stable-isotope
assignments, and found that adults originating from the
southern range margin migrate a minimum of 659.46 +
49.11 km to the northern range edge in March and April
(n ¼ 50; electronic supplementary material, figure S1a). Pre-
vious estimates of darner daily migration rates indicate this
journey would take 55.42 + 4.13 days to complete [12]. There-
fore, the first migratory individuals arriving in the north
likely emerge in the south in January and February. However,
prevailing wind patterns in spring favour northbound
migration, potentially allowing individuals to migrate faster
[24]. If darners use high-altitude migratory flights to take
advantage of fast-moving winds, the distances reported
above could be covered more rapidly [11,13,25].
Combining stable-isotope assignments and temperature-
related nymph development [14], we found the annual
cycle of common green darners is comprised of at least
three generations (figure 2). The first generation emerges
between January and May in the southern part of the distri-
bution and migrates north into the northern reaches of the
distribution. The first generation is complete by August, the
last month when darners with southern stable isotopic ori-
gins are captured in the north (figure 2, August). The first
60
34
GA
GA
GA
GA
ME
VT
CT
NC
NC
NC OK
MD
NJ
WV
NY
OH
IN
36 38 40 42
latitude of 9°C
44 46 48
80
fi
rs
t
ob
se
rv
ed
f
li
gh
t
(o
rd
in
al
d
ay
)
100
120
Figure 1. First flight date of adult common green darner and the
latitude of
the 9.178C thermocline. The mean latitude of the thermocline
was extracted
along the observation longitude from 1994 to 2014. Error bars
represent
the standard error in the latitude of the thermocline on the first
flight date.
Data represented in figure 1 can be found in electronic
supplementary material,
table S1. Graphic was drawn by Matthew Dodder
(https://neornithes.wordpress.
com) and used with permission. (Online version in colour.)
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Biol.
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20180741
3
cohort of the second generation—young from the previous
year that overwinter as late-stage instars and eclose between
May and July [14]—begin flying in May with 4% (2 of 53;
figure 2, May) of individuals assigned to where they were
captured. Spatio-temporal overlap exists between the first
and second generations as northbound migration continues
through July. The number of locally emerged darners in the
north increases throughout the season, peaking in September
when offspring of the first generation in April and early May
eclose (May: 4%, 2 of 53; June: 22%, 16 of 74; July: 29%, 15 of
52; August: 50%, 5 of 10; September: 86%, 6 of 7; October:
67%, 2 of 3; electronic supplementary material, figure S3).
This latter cohort of the second generation then migrates
south.
Second generation darners with northern isotopic signa-
tures are first detected in the south during August and
September (figure 2, September), suggesting southbound
migration begins in July and continues into October [12].
These southbound migrants are composed of darners that
overwinter as nymphs and emerge in June and July and dar-
ners who develop within a single growing season that eclose
in September. Southbound migration to the southern range
edge peaks in September and October, with 64% (7 of 11)
of green darners captured at least 680.97 + 178.84 km from
where they emerge in the north (electronic supplementary
material, figure S1b). The second generation composed of
individuals that emerge in the northern portion of the distri-
bution ends in late October (figure 2, October). After this
time, no individuals with northern isotopic signatures were
captured in the south (figure 2, November), suggesting they
die shortly after they arrive in the south. However, south-
bound migrants from mid-latitudes were captured in
November (43%, 3 of 7; figure 2, November) and December
(57%, 4 of 7), emerging a minimum of 226.13 + 108.50 and
232.03 + 93.28 km away from where they were captured,
respectively. A third, non-migratory generation occurs in the
south between November and January (figure 2, November –
January). This generation must be resident because adults
that emerge in November likely die before April and May
when the first migratory individuals are captured in the
north, based on the adult longevity reported for the species
(five to seven weeks [16]). Thus, third generation adults that
emerge in November likely give rise to the first generation of
migratory individuals that are captured in the north. Stable
isotopes, however, are unable to differentiate between the
first and proposed third generation.
4. Discussion
The annual cycle of green darners is composed of at least two
migratory and one non-migratory generations. In spring, the
first generation makes a long-distance northbound movement
(659.46 + 49.11 km) from southern to northern range limits,
lays eggs and dies. A second generation emerges and returns
south (680.97 + 178.84 km), where they lay eggs and die.
Finally, a third resident generation emerges, reproducing
locally and giving rise to the cohort that migrates north the
following spring.
During spring, individuals with southern emergence ori-
gins arrive at northern locations prior to those with origins
from mid-latitudes (electronic supplementary material,
figure S2). A similar pattern is observed in autumn, where
individuals with northern origins are captured in the
southern portion of their distribution before green darners
that emerge at mid-latitudes. This migratory phenomenon
could arise from several alternative life-history strategies.
First, such patterns could result if individuals spread repro-
ductive risk across multiple, widely separated water bodies
and reproduce during their migratory journey north [18].
Their offspring could take advantage of warm surface
waters, mature rapidly within the same growing season
and migrate northbound (electronic supplementary material,
figure S4). Such a strategy is akin to the multi-generational
migration of the monarch and painted lady butterflies [1,2],
however, the longevity and strong direct flights of darners
allow populations to be connected over larger spatial scales
compared to the northbound multi-generational progression
of migratory butterflies. The observed pattern of shortened
migratory distances as the season progresses also could
result if individuals reproduce during southbound migration.
If darners reproduce during the journey south, their eggs
would hatch but the nymphs would enter a state of diapause
as temperatures drop, emerge and migrate north the follow-
ing spring when suitable thermal conditions allow [14,18].
A combination of these strategies is likely. Plasticity in
nymph development further complicates discerning between
the two strategies. Eggs laid during migratory periods could
either (i) undergo rapid development after hatching and
emerge within the same season or (ii) hatch, enter diapause
as nymphs and emerge the following spring, depending on
the photoperiod experienced by the egg or early instar [17].
Stable-hydrogen isotope data cannot differentiate between
these competing hypotheses. Regardless of the strategy, the
timing of migratory movements allows for spatial and tem-
poral overlap of both migratory and non-migratory
populations, explaining the lack of genetic structure in this
species [18,26].
https://neornithes.wordpress.com
https://neornithes.wordpress.com
https://neornithes.wordpress.com
June
M
ay
A
pr
M
ar
Feb
Jan Dec
No
v
O
ct
S
ep
Aug
July
migr
ant and local
N
or
th
w
ar
d
m
ig
ra
tio
n
non-migratory
Southw
ard m
igration
generation 3
generation 2
ge
ne
ra
tio
n
1
Figure 2. The full annual cycle of the common green darner is
comprised of three generations. The first generation is
migratory, emerges in the south between
February and May and dies in the north. The second generation
emerges in the north, migrates south and dies. The third
generation, offspring of migratory
individuals in the fall, is non-migratory and emerges in the
south in November. The emergence origins of adults (colour
ramp; grey ¼ zero, red ¼ many) captured
at the sampling locations (black dots) in each month are shown
around the perimeter. Graphic was drawn by Matthew Dodder
(https://neornithes.wordpress.com)
and used with permission.
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Biol.
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20180741
4
Common green darner migration appears to be governed
in part by temperature. Northbound adult migration during
spring coincides with a daily mean thermocline of approxi-
mately 98C (9.178C) and the last observed adults in autumn
coincide with a similar thermocline (9.548C). These findings
are consistent with the short migratory movements of
tagged individuals following synoptic cold fronts [12]. In
addition, the 98C thermocline observed here is similar to
the development threshold of the final instar (8.7 + 0.18C)
[14]. Taken together, these findings suggest that temperature
is a key limiting factor to the northbound migration of
dragonflies in spring, the emergence of nymphs and south-
bound migration in autumn. Given the critical role of
temperature, a warming climate could induce earlier
spring flights, trigger later autumn flights and potentially
shorten migratory distances as the 98C thermocline moves
northbound, allowing adults to reside at higher latitudes
during the winter months. Further research is needed to
determine how a changing climate may alter the migratory
schedules and annual cycle of dragonflies and other
migratory insects.
Data accessibility. Museum holdings and specimen numbers and
data are
available from the Dryad Digital Repository:
http://dx.doi.org/10.
5061/dryad.17hf071 [27]. R code used to analyse data can be
found
at
https://github.com/MTHallworth/Hallworth_et_al_Anaxjunius.
Authors’ contributions. M.T.H., P.P.M., K.P.M. and C.E.S.
conceived and
designed the study. K.P.M. and S.Z. coordinated and collected
samples from field and museum specimens. M.T.H. and C.E.S.
ana-
lysed the data. M.T.H., P.P.M. and C.E.S. wrote the manuscript.
All
authors read, edited, approved the final version of the
manuscript
and agree to be held accountable for the content therein.
Competing interests. The authors declare no competing interests
exist.
Funding. Major funding was provided by the U.S. Forest
Service Inter-
national Programs and the Xerces Society for Invertebrate
Conservation.
Acknowledgements. This study was part of the Migratory
Dragonfly Part-
nership coordinated by The Xerces Society for Invertebrate
http://dx.doi.org/10.5061/dryad.17hf071
http://dx.doi.org/10.5061/dryad.17hf071
http://dx.doi.org/10.5061/dryad.17hf071
https://github.com/MTHallworth/Hallworth_et_al_Anaxjunius
https://github.com/MTHallworth/Hallworth_et_al_Anaxjunius
https://neornithes.wordpress.com
https://neornithes.wordpress.com
rsb
5
Conservation. Michael May, Desiree Narango and Dara
Satterfield
provided comments on a previous version of the manuscript. We
thank Desiree Narango and Tim Guida for preparing samples,
and
citizen scientists who contributed observations and samples. We
thank the many natural history, public and private collections
that
allowed us to sample from priceless specimens.
l.royalsociety
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http://dx.doi.org/10.1017/S0266467409006087
http://dx.doi.org/10.1098/rsbl.2006.0487
http://dx.doi.org/10.1098/rsbl.2006.0487
http://dx.doi.org/10.1371/journal.pone.0052594
http://dx.doi.org/10.4039/Ent1031671-12
http://dx.doi.org/10.4039/Ent1031671-12
http://www.nhbs.com/dragonflies-behaviour-and-ecology-of-
odonata-book
http://www.nhbs.com/dragonflies-behaviour-and-ecology-of-
odonata-book
http://www.nhbs.com/dragonflies-behaviour-and-ecology-of-
odonata-book
http://dx.doi.org/10.1007/s10841-012-9540-x
http://dx.doi.org/10.1007/s10841-012-9540-x
http://dx.doi.org/10.1371/journal.pone.0183508
http://dx.doi.org/10.1371/journal.pone.0183508
http://dx.doi.org/10.1111/j.2041-210X.2012.00202.x
http://dx.doi.org/10.1111/j.2041-210X.2012.00202.x
http://dx.doi.org/10.1674/0003-
0031(1998)140[0325:MSMODO]2.0.CO;2
http://dx.doi.org/10.1674/0003-
0031(1998)140[0325:MSMODO]2.0.CO;2
http://dx.doi.org/10.1890/04-0175
https://CRAN.R-project.org/package=rgeos
https://CRAN.R-project.org/package=rgeos
https://CRAN.R-project.org/package=rgeos
https://www.R-project.org/
https://www.R-project.org/
https://www.R-project.org/
http://dx.doi.org/10.1111/ele.12528
http://dx.doi.org/10.1111/j.1365-2311.2006.00813.x
http://dx.doi.org/10.1111/j.1365-2311.2006.00813.x
http://dx.doi.org/10.1046/j.1365-2311.2003.00521.x
http://dx.doi.org/10.1046/j.1365-2311.2003.00521.x
http://dx.doi.org/10.5061/dryad.17hf071
http://dx.doi.org/10.5061/dryad.17hf071Tracking dragons:
stable isotopes reveal the annual cycle of a long-distance
migratory insectIntroductionMethods and materialsEmergence
assignmentsMigratory distanceAnnual
cycleResultsDiscussionData accessibilityAuthors’
contributionsCompeting
interestsFundingAcknowledgementsReferences
Nishanth Padhma
Age: 24
Course: Computer Science
Year: 2015
Department: Computer Science
Goals and motivations
Nishanth Wants to become a good Game designer and after that
he want to play the Games as an E-sports player and want to
pursue the career in e-gaming. He is ambitious about the work
and want to contribute to the community he belongs to.
Lifestyle
Gaming , Gym, Cricket, Anime series, Singing, music
Nature of work
(Undergraduate, learning Game designing, Development in
Unity)
Experience and training
Worked as an internee at Quick Stack
Solution
s,
Python and C# expert with achievement of 2times programming
battle winner in interuniversity Competition
Environment
a day scholar and likes to spend the time in university
experiencing the time to use my skills to try new things and
play
IT skill level
Web Application Developer, Python developer, Java and XMl
mobile developer. Unity Developer for game designing
Attitude towards technology
Great – it’s easy to use and saves me time
I like it but it often falls short
I don’t like it but I have to use it
IT equipment
Mostly interested in PC and Console because of gaming and
also use mobiles for testing purpose for the game designs
How will this person use the application?
Judging from the personality, he would use the application for
the information collection through the application for the games
he plays and also plays the game or quiz game for fun too.
Because of the gaming player he likes to interact with the
applications and software. So he would be a positive user of my
application.
Key tasks
He needs to perform the survey to the application and provide
the feedback for the application soon. Also he reflects the
characteristics for the gamer and software developer which can
be a market target user for the application. A smart target for
the user review on the application.
Fears, Stress and Frustrations
Lack of Hard work is the fear for the future goals. Creative
working in own zone frustrates sometimes because achieving
something void and new burdens a lot. Although sometimes
achieves the. Failure stress me out at any level but I try to
overcome with distractions like achieving other things in
different grounds.
Aqsa khan
Age: 25
Course: Business and Finance
Year: 2012
Department: Management
Goals and motivations
Aqsa wants to become an Event manager and want to participate
in her family business grow afterwards. She wants to be a
designer and want to manage a boutique with her friends in an
entrepreneurship. She has very high goals and she is ambitious
to complete it.
Lifestyle
Music, Event Management, Social Media, Recitation and
political discussions
Nature of work
Graduate, Finance and event manager. Vice President women
student association in university of south Asia.
Experience and training
Worked as an Ittehad group of industries as an Internee,
Event Manager at Drift With Us with achievement of Gold
medallist and dean list Winner 2011 and 2010.
Environment
Research for more and thrives for the self-study and improving
own self to become a better person. Likes to work from home
but can manage an entire event with her team also. Hardworking
and anxious for more.
Attitude towards Hierarchy and Business
Great – always try new moves and new strategies to work
even fine.
No doubt sometime it fails but never stopped because of this
fear
didn’t had the courage to define myself in the top ones.
Business Expertise
Career counselling and designing the Trends for the current and
future generations. Expanding the business with a vision to
benefit someone else makes it even great.
How will this person use the application?
Judging from the personality, she would use the application for
the research and to check her calibre for herself to test her
knowledge about herself and about her expertise. This would
provide her to judge herself and place herself in her goals and
targets frame. So he would be a positive user of my application.
Key tasks
She needs to perform the survey to the application and provide
the feedback for the application soon. Also he reflects the
characteristics for the gamer and software developer which can
be a market target user for the application. A smart target for
the user review on the application.
Fears, Stress and Frustrations
Fears: technology will overcome the business fields which
would reduce the need of human in this field too. Could be in
upcoming years
Stress: presentations at any level stress me out.
Frustrations: No frustrations at all.
Revised Screens for Smart Quiz
1
Revised Screens for Smart Quiz Project
Screen 1: Welcome screen
The below screen is the first screen users sees when the
application is launched. It has a welcome banner, fields to enter
login credentials for existing users, login button and a button
for new user registration which directs user to sign up or
registration screen. The functionality of the screen is to test the
registered user’s login credentials and allow the user to access
the application
Screen 2: User Registration Screen
The second screen below is launched when user clicks on
register button, which has two buttons which allows user to sign
up to the application using there Google or Facebook accounts.
User has a choice to choose which account they want to use.
The functionality of the screen is to register the user and
provide login credentials to application.
Screen 3: Preferences Selection Screen
The preferences selection screen allows user to select their
preferred category in which they are interested. User can select
their preferences at the time of registration and it also to change
their preferences in the future use also. The functionality of the
screen is that user will get more questions from their preferred
category.
Screen 4: Quiz mode Selection
The below screen has 4 major buttons which allows the user to
play the game in different modes. The quiz is available in
modes like individual, challenge, league and daily mission.
The functionality of the screen is to allow the user to select the
type of game mode user is willing to launch. And the screen
also different common buttons at the bottom like settings, home
and messages which provides ease of navigation to users
through the application.
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3D%22%26lt%3Bh3%26gt%3B%26lt%3Bfont%20face%3D%26
quot%3BComic%20Sans%20MS%26quot%3B%20color%3D%26
quot%3B%23ffb570%26quot%3B%26gt%3BPlay%20Now%26lt
%3B%2Ffont%26gt%3B%26lt%3B%2Fh3%26gt%3B%22%20sty
le%3D%22labelPosition%3Dcenter%3BverticalLabelPosition%3
Dmiddle%3Balign%3Dcenter%3Bhtml%3D1%3Bshape%3Dmxg
raph.basic.shaded_button%3Bdx%3D10%3BfillColor%3D%23E
6E6E6%3BstrokeColor%3Dnone%3B%22%20vertex%3D%221
%22%20parent%3D%221%22%3E%3CmxGeometry%20x%3D%
22420%22%20y%3D%22647%22%20width%3D%22160%22%2
0height%3D%2243%22%20as%3D%22geometry%22%2F%3E%
3C%2FmxCell%3E%3C%2Froot%3E%3C%2FmxGraphModel%
3E
Screen 5: User Turn in league
The below screen provides the information of whose current
turn is to play in league mode of the game, users in the league
mode takes turns one after other to play. It has information
about both user and other participant’s information. It also has a
button to remind or poke other user, when waiting for others to
complete their turn.
Screen 6: Challenge mode
This screen is seen in the challenge mode of the quiz, user spins
the wheel which will automatically select a category for the
challenge between two users. The screen has a wheel with
different categories, pointer and a spin button. The screen also
provides information about the users participating the game at
the top. The functionality of the screen is when user clicks spin
button, the wheel spins and stops randomly at a category and
game is launched.
Screen 7: Quiz Main Screen
The below screen is the games main screen, which is launched
when the quiz starts, it has question highlighted the top,
followed by four different clickable buttons which are possible
answers and a countdown timer at the right top of the screen.
The functionality of the screen is user has to select a correct
answer form the 4 options provided with in the countdown time.
Screen 8: Result Screen:
The below screen is the result screen which appears when the
user selects an option for the question in the previous screen. It
provides the information if the selected option is right or
wrong, button to continue to next question, share button, report
button if user feels it as a wrong decision and also feedback
buttons.
References
Arhipova, A. (n.d.). Mobile UI Design:Basic Types of Screens.
Retrieved November 1, 2019, from
https://tubikstudio.com/mobile-ui-design-15-basic-types-of-
screens/.
Etermax. (n.d.). Trivia Crack. Retrieved from
https://www.triviacrack.com/.
NATS 1550
Assignment 3 – Write a short magazine article for the general
public (15%)
Due date: Nov. 28, 11.59pm
Please submit as a word or pdf file on Moodle
This assignment has a VERY strict word count (your article
absolutely has to be
within these limits, no exceptions), you will loose 50% of your
marks if you have
fewer or more words:
Minimum word count 450 words; Maximum: 550 words
(excluding title).
For this assignment you will be writing a short science-based
piece about migration for
the public in the form of a news or magazine article.
Most of the writing done by students in university science
follows a style and a set of
rules that are consistent with the scientific literature—
regimented, concise and technical.
Similarly, much writing done in university by non-science
students is also rule-bound as
required by the standards of scholarship in those disciplines.
However, it is also
important to be able to communicate academic ideas, including
scientific discoveries, in a
less intimidating and technical manner and this is what this
assignment is about.
In this assignment, you will be converting a research paper that
was published in a
scientific journal and deals with migration into a magazine
article. Choose ONE of the
scientific articles posted on Moodle in the Assignment 3 folder
for this, you decide which
one of these you want to use for this assignment, but only use
one. You will play the role
of a free-lance e-zine (=online magazine) science writer, and
you will be required to
reduce the paper to its essence by creating a non-illustrated*
magazine-style piece that
your editor requires to fit a space of 500 words, excluding your
catchy title. I will deduct
50% if your submission is less than 450 words or more than 550
words, no
exceptions! Editors would not publish pieces that are shorter or
longer than agreed upon.
I will post links to examples on Moodle that show you the type
of writing we are
seeking—no formal references, no essay styles! Make sure you
use your own words, do
not copy/paste or directly quote from the articles.
You need to have a catchy title that sparks interest. The writing
must capture the reader’s
attention immediately (you need to have a hook), and it must set
up the context almost as
fast. The writing should be precise, but not burdened by any
jargon. Imagine that you are
writing for well-informed adults, but who are not formally
trained in ecology or
environmental science or migration or biology etc..
Some comments on format:
Do not use the traditional subheadings of Introduction,
Methods, Results and Discussion.
Remember this is a magazine article NOT a lab report or
scientific journal article. It is up
to you whether you wish to use any sub-headings at all. No
specific font, size, or
paragraph formatting (but please use a standard font that is
readable) and it does not have
to be formatted like a newspaper article, it is the content that
counts.
NATS 1550
Do not use references; you never see formal referencing in
magazines or e-zines (online
magazines). If you do wish to refer to someone else’s work
within the body of your
article, simply do so, such as: “The researchers were interested
in following up on an idea
proposed by a Dutch group of scientists who had found...” Or,
refer to the posted
examples to give you an idea how to do this.
All words, excluding title (but including any subheadings, if
you have them), are part of
the word count (450 to 550 words)
You do not need to create a title page, but write your name and
student number and the
(original) name of the article you are using at the top of the
page. Below that should be
your magazine article including your own catchy title that you
created for it. At the end,
also include your word count.
*Note: If you wish to be creative you may add illustrations, but
I will ignore these and
not take these into consideration for marking.
What am I looking for?
Articles that
• Have a catchy title that immediately grabs a readers’ interest
• Right at the start grab my interest and make me want to read
on (without being
overly sensational) and hold my interest throughout
• Are written in the style of a reputable magazine or newspaper
article (not a lab
report or essay etc.)
• Are well-written, flow well and are easy and enjoyable to read
• Have a logical structure and present ideas clearly
• Do an excellent job accurately presenting the information from
the scientific
article and in getting the main points across, without loosing
themselves in
extraneous details
• Cater to a well-informed, but non-specialist audience, e.g. by
avoiding jargon
• Have good grammar and spelling
• Are within the allowed word count range of 450-550 words
you will loose 50%
of your marks if you have fewer or more words
Tip: ask your non-science friends or family to read it and give
you feedback on how
interesting and easy to read they found it!

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rsbl.royalsocietypublishing.orgResearchCite this article .docx

  • 1. rsbl.royalsocietypublishing.org Research Cite this article: Hallworth MT, Marra PP, McFarland KP, Zahendra S, Studds CE. 2018 Tracking dragons: stable isotopes reveal the annual cycle of a long-distance migratory insect. Biol. Lett. 14: 20180741. http://dx.doi.org/10.1098/rsbl.2018.0741 Received: 23 October 2018 Accepted: 23 November 2018 Subject Areas: ecology, behaviour Keywords: Anax, common green darner, stable-hydrogen isotopes, migration phenology Author for correspondence: Michael T. Hallworth e-mail: [email protected] Electronic supplementary material is available online at https://dx.doi.org/10.6084/m9. figshare.c.4320911. & 2018 The Author(s) Published by the Royal Society. All rights reserved.
  • 2. Animal behaviour Tracking dragons: stable isotopes reveal the annual cycle of a long-distance migratory insect Michael T. Hallworth1,2, Peter P. Marra1, Kent P. McFarland3, Sara Zahendra3 and Colin E. Studds1,2 1Migratory Bird Center, Smithsonian Conservation Biology Institute, Washington, DC 20008, USA 2Department of Geography and Environmental Systems, University of Maryland, Baltimore County, Baltimore, MD 21250, USA 3Vermont Center for Ecostudies, White River Junction, VT 05001, USA MTH, 0000-0002-6385-3815; PPM, 0000-0002-0508-7577; KPM, 0000-0001-7809-5503; CES, 0000-0001-5715-1692 Insect migration is globally ubiquitous and can involve continental-scale movements and complex life histories. Apart from select species of migratory moths and butterflies, little is known about the structure of the annual cycle for migratory insects. Using stable-hydrogen isotope analysis of 852 wing samples from eight countries spanning 140 years,
  • 3. combined with 21 years of citizen science data, we determined the full annual cycle of a large migratory dragonfly, the common green darner (Anax junius). We demonstrate that darners undertake complex long-distance annual migrations governed largely by temperature that involve at least three gen- erations. In spring, the first generation makes a long-distance northbound movement (further than 650 km) from southern to northern range limits, lays eggs and dies. A second generation emerges and returns south (further than 680 km), where they lay eggs and die. Finally, a third resident gener- ation emerges, reproducing locally and giving rise to the cohort that migrates north the following spring. Since migration timing and nymph development are highly dependent on temperature, continued climate change could lead to fundamental changes in the biology for this and similar
  • 4. migratory insects. 1. Introduction Insects are the most species-rich and abundant group of macroscopic organisms on the planet, yet our understanding of the biological underpinnings of their annual cycles and migratory behaviours drastically trails behind that of vertebrate taxa [1]. Perhaps the best-known insect migrations are the multi- generational migrations of the monarch butterfly (Danaus plexippus) in eastern North America [2], and the painted lady (Vanessa cardui) in Europe [3], which migrate southbound each autumn from the northern reaches of their distri- bution into southern North America and Africa, respectively. Monarchs wait out the boreal winter [4] and the same individuals migrate northbound the fol- lowing spring into the southern parts of their distribution where they lay eggs, beginning the next generation that continues the northbound progression of their lifecycle [2,3,5,6].
  • 5. Few migratory insects have had their full annual cycles sufficiently described despite their profound cultural [7], ecological [8] and agricultural importance [9]. This disparity is owing largely to the difficulties with tracking small organisms over space and time, as well as their complex life histories that often require both terrestrial and aquatic habitats [10]. Among the migratory http://crossmark.crossref.org/dialog/?doi=10.1098/rsbl.2018.074 1&domain=pdf&date_stamp=2018-12-19 mailto:[email protected] https://dx.doi.org/10.6084/m9.figshare.c.4320911 https://dx.doi.org/10.6084/m9.figshare.c.4320911 http://orcid.org/ http://orcid.org/0000-0002-6385-3815 http://orcid.org/0000-0002-0508-7577 http://orcid.org/0000-0001-7809-5503 http://orcid.org/0000-0001-5715-1692 rsbl.royalsocietypublishing.org Biol. Lett. 14: 20180741 2
  • 6. insects, almost all are suspected to employ complex multi- generational migrations (but see [7,8]) similar to the monarch butterfly and painted lady, where no single individual completes the entire migratory circuit [2,3,5,6,10,11]. The con- tinental distances travelled [12,13], small body sizes and multi-generational aspect of their life histories pose signifi- cant challenges to understanding the fundamental biology of the full annual cycles of migratory insects. Adding to this complexity, movements, timing and life-history strategies are likely linked to photoperiod, weather, temperature and other environmental forces [1,3,11,14 – 16]. The common green darner (Anax junius) is a ubiquitous, charismatic migratory dragonfly found in North America. Its complex life-history includes both resident and migratory populations. The aquatic nymphs likely give rise to resident and migratory phenotypes because they exhibit two distinct developmental strategies [14]. Nymphs either undergo rapid development and emerge within a single season or develop slowly, enter diapause and emerge the following
  • 7. summer [14]. The developmental strategy is governed by the photoperiod experienced by the egg or early instars [17] and temperature [14]. Therefore, the seasonal timing of oviposition likely determines whether nymphs develop, emerge within a single growing season and migrate, or enter diapause. Darner migration is considered an adaptive strategy because it spreads reproductive effort across multiple, widely separated water bodies and ameliorates the risk of predation, competition and drought [17,18]. Migratory move- ments are commonly observed in autumn and have been documented using direct [12] and indirect techniques [19]. Northbound migration in spring is suspected and supported by anecdotal observations but is not well documented [20]. Although it is known that common green darners migrate, no study to date has linked multiple populations over time and space to better understand the phenology of the annual cycle and the number of generations involved. 2. Methods and materials We combined observational and stable-hydrogen isotope
  • 8. data to identify the timing of migration and emergence ori- gins of darners. Two publicly available datasets were assembled to refine emergence assignments using stable iso- topes. First, we acquired citizen science data on the first observed migratory adult common green darners (first flight dates) to determine the minimum temperature necess- ary for darners to migrate (electronic supplementary material, table S1). Daily mean temperature of the first flight date was 9.178C, similar to the development threshold (8.7 + 0.18C) reported by Trottier [14]. In addition to deter- mining the temperature threshold for migratory flights, we used occurrence records submitted by citizen scientists and museum collections to generate a habitat suitability surface that we included as prior information in the probabilistic isotope-assignments [21] (see §2a). (a) Emergence assignments We obtained contemporary and museum specimens from 681 locations from eight countries ranging from the tropics to the northern temperate zone (17.988 N to 51.148 N) that we used to describe migration phenology and the number of gener-
  • 9. ations within the annual cycle for the common green darner. Specimens, which included exuviae, tenerals and mature adults, were collected in every calendar month span- ning over 100 years (electronic supplementary material, table S2). Isotope analyses were performed on a small distal seg- ment of the wing to determine where the captured individuals emerged (see electronic supplementary material). (b) Migratory distance Determining the exact emergence origin from stable isotopes is not possible given the uncertainty in geographical assign- ment and lack of longitudinal variation in the underlying isoscape. Therefore, we used a conservative distance estima- tor as an index of migration distance. We determined the minimum distance (kilometres) between the ‘likely’ emer- gence origin surface and the location where the specimen was collected (i.e. shortest possible distance travelled). Migration distances were calculated using the gDistance function in the rgeos [22] package in program R [23]. (c) Annual cycle
  • 10. We summarized the emergence origins within the hardiness zones (see electronic supplementary material, delineating populations) for each calendar month to describe the pheno- logy of the annual cycle. Isotope-based emergence origins provide spatio-temporal information of adults but the phenology of nymph development and emergence timing is also needed to fully understand the annual cycle of darners. 3. Results We combined data on stable-hydrogen isotopes of 852 common green darner museum and contemporary specimens spanning 140 years (1874 – 2013) from eight countries with citizen science observations to determine the emergence origin, continental migrations and annual cycle of the common green darner. Using citizen science observations, we found that northbound darner migration closely tracks a thermocline of 9.178C (figure 1). We then used this tempera- ture-dependent flight phenology to refine stable-isotope assignments, and found that adults originating from the southern range margin migrate a minimum of 659.46 + 49.11 km to the northern range edge in March and April
  • 11. (n ¼ 50; electronic supplementary material, figure S1a). Pre- vious estimates of darner daily migration rates indicate this journey would take 55.42 + 4.13 days to complete [12]. There- fore, the first migratory individuals arriving in the north likely emerge in the south in January and February. However, prevailing wind patterns in spring favour northbound migration, potentially allowing individuals to migrate faster [24]. If darners use high-altitude migratory flights to take advantage of fast-moving winds, the distances reported above could be covered more rapidly [11,13,25]. Combining stable-isotope assignments and temperature- related nymph development [14], we found the annual cycle of common green darners is comprised of at least three generations (figure 2). The first generation emerges between January and May in the southern part of the distri- bution and migrates north into the northern reaches of the distribution. The first generation is complete by August, the last month when darners with southern stable isotopic ori- gins are captured in the north (figure 2, August). The first
  • 13. 36 38 40 42 latitude of 9°C 44 46 48 80 fi rs t ob se rv ed f li gh t (o rd in al d ay )
  • 14. 100 120 Figure 1. First flight date of adult common green darner and the latitude of the 9.178C thermocline. The mean latitude of the thermocline was extracted along the observation longitude from 1994 to 2014. Error bars represent the standard error in the latitude of the thermocline on the first flight date. Data represented in figure 1 can be found in electronic supplementary material, table S1. Graphic was drawn by Matthew Dodder (https://neornithes.wordpress. com) and used with permission. (Online version in colour.) rsbl.royalsocietypublishing.org Biol. Lett. 14: 20180741 3 cohort of the second generation—young from the previous year that overwinter as late-stage instars and eclose between May and July [14]—begin flying in May with 4% (2 of 53; figure 2, May) of individuals assigned to where they were captured. Spatio-temporal overlap exists between the first
  • 15. and second generations as northbound migration continues through July. The number of locally emerged darners in the north increases throughout the season, peaking in September when offspring of the first generation in April and early May eclose (May: 4%, 2 of 53; June: 22%, 16 of 74; July: 29%, 15 of 52; August: 50%, 5 of 10; September: 86%, 6 of 7; October: 67%, 2 of 3; electronic supplementary material, figure S3). This latter cohort of the second generation then migrates south. Second generation darners with northern isotopic signa- tures are first detected in the south during August and September (figure 2, September), suggesting southbound migration begins in July and continues into October [12]. These southbound migrants are composed of darners that overwinter as nymphs and emerge in June and July and dar- ners who develop within a single growing season that eclose in September. Southbound migration to the southern range edge peaks in September and October, with 64% (7 of 11)
  • 16. of green darners captured at least 680.97 + 178.84 km from where they emerge in the north (electronic supplementary material, figure S1b). The second generation composed of individuals that emerge in the northern portion of the distri- bution ends in late October (figure 2, October). After this time, no individuals with northern isotopic signatures were captured in the south (figure 2, November), suggesting they die shortly after they arrive in the south. However, south- bound migrants from mid-latitudes were captured in November (43%, 3 of 7; figure 2, November) and December (57%, 4 of 7), emerging a minimum of 226.13 + 108.50 and 232.03 + 93.28 km away from where they were captured, respectively. A third, non-migratory generation occurs in the south between November and January (figure 2, November – January). This generation must be resident because adults that emerge in November likely die before April and May when the first migratory individuals are captured in the north, based on the adult longevity reported for the species (five to seven weeks [16]). Thus, third generation adults that emerge in November likely give rise to the first generation of
  • 17. migratory individuals that are captured in the north. Stable isotopes, however, are unable to differentiate between the first and proposed third generation. 4. Discussion The annual cycle of green darners is composed of at least two migratory and one non-migratory generations. In spring, the first generation makes a long-distance northbound movement (659.46 + 49.11 km) from southern to northern range limits, lays eggs and dies. A second generation emerges and returns south (680.97 + 178.84 km), where they lay eggs and die. Finally, a third resident generation emerges, reproducing locally and giving rise to the cohort that migrates north the following spring. During spring, individuals with southern emergence ori- gins arrive at northern locations prior to those with origins from mid-latitudes (electronic supplementary material, figure S2). A similar pattern is observed in autumn, where individuals with northern origins are captured in the southern portion of their distribution before green darners that emerge at mid-latitudes. This migratory phenomenon
  • 18. could arise from several alternative life-history strategies. First, such patterns could result if individuals spread repro- ductive risk across multiple, widely separated water bodies and reproduce during their migratory journey north [18]. Their offspring could take advantage of warm surface waters, mature rapidly within the same growing season and migrate northbound (electronic supplementary material, figure S4). Such a strategy is akin to the multi-generational migration of the monarch and painted lady butterflies [1,2], however, the longevity and strong direct flights of darners allow populations to be connected over larger spatial scales compared to the northbound multi-generational progression of migratory butterflies. The observed pattern of shortened migratory distances as the season progresses also could result if individuals reproduce during southbound migration. If darners reproduce during the journey south, their eggs would hatch but the nymphs would enter a state of diapause as temperatures drop, emerge and migrate north the follow-
  • 19. ing spring when suitable thermal conditions allow [14,18]. A combination of these strategies is likely. Plasticity in nymph development further complicates discerning between the two strategies. Eggs laid during migratory periods could either (i) undergo rapid development after hatching and emerge within the same season or (ii) hatch, enter diapause as nymphs and emerge the following spring, depending on the photoperiod experienced by the egg or early instar [17]. Stable-hydrogen isotope data cannot differentiate between these competing hypotheses. Regardless of the strategy, the timing of migratory movements allows for spatial and tem- poral overlap of both migratory and non-migratory populations, explaining the lack of genetic structure in this species [18,26]. https://neornithes.wordpress.com https://neornithes.wordpress.com https://neornithes.wordpress.com June
  • 21. d m ig ra tio n non-migratory Southw ard m igration generation 3 generation 2 ge ne ra tio n 1 Figure 2. The full annual cycle of the common green darner is comprised of three generations. The first generation is migratory, emerges in the south between February and May and dies in the north. The second generation emerges in the north, migrates south and dies. The third generation, offspring of migratory
  • 22. individuals in the fall, is non-migratory and emerges in the south in November. The emergence origins of adults (colour ramp; grey ¼ zero, red ¼ many) captured at the sampling locations (black dots) in each month are shown around the perimeter. Graphic was drawn by Matthew Dodder (https://neornithes.wordpress.com) and used with permission. rsbl.royalsocietypublishing.org Biol. Lett. 14: 20180741 4 Common green darner migration appears to be governed in part by temperature. Northbound adult migration during spring coincides with a daily mean thermocline of approxi- mately 98C (9.178C) and the last observed adults in autumn coincide with a similar thermocline (9.548C). These findings are consistent with the short migratory movements of tagged individuals following synoptic cold fronts [12]. In addition, the 98C thermocline observed here is similar to the development threshold of the final instar (8.7 + 0.18C) [14]. Taken together, these findings suggest that temperature is a key limiting factor to the northbound migration of dragonflies in spring, the emergence of nymphs and south-
  • 23. bound migration in autumn. Given the critical role of temperature, a warming climate could induce earlier spring flights, trigger later autumn flights and potentially shorten migratory distances as the 98C thermocline moves northbound, allowing adults to reside at higher latitudes during the winter months. Further research is needed to determine how a changing climate may alter the migratory schedules and annual cycle of dragonflies and other migratory insects. Data accessibility. Museum holdings and specimen numbers and data are available from the Dryad Digital Repository: http://dx.doi.org/10. 5061/dryad.17hf071 [27]. R code used to analyse data can be found at https://github.com/MTHallworth/Hallworth_et_al_Anaxjunius. Authors’ contributions. M.T.H., P.P.M., K.P.M. and C.E.S. conceived and designed the study. K.P.M. and S.Z. coordinated and collected samples from field and museum specimens. M.T.H. and C.E.S. ana- lysed the data. M.T.H., P.P.M. and C.E.S. wrote the manuscript. All authors read, edited, approved the final version of the manuscript and agree to be held accountable for the content therein.
  • 24. Competing interests. The authors declare no competing interests exist. Funding. Major funding was provided by the U.S. Forest Service Inter- national Programs and the Xerces Society for Invertebrate Conservation. Acknowledgements. This study was part of the Migratory Dragonfly Part- nership coordinated by The Xerces Society for Invertebrate http://dx.doi.org/10.5061/dryad.17hf071 http://dx.doi.org/10.5061/dryad.17hf071 http://dx.doi.org/10.5061/dryad.17hf071 https://github.com/MTHallworth/Hallworth_et_al_Anaxjunius https://github.com/MTHallworth/Hallworth_et_al_Anaxjunius https://neornithes.wordpress.com https://neornithes.wordpress.com rsb 5 Conservation. Michael May, Desiree Narango and Dara Satterfield provided comments on a previous version of the manuscript. We thank Desiree Narango and Tim Guida for preparing samples, and citizen scientists who contributed observations and samples. We thank the many natural history, public and private collections that allowed us to sample from priceless specimens. l.royalsociety
  • 25. References publishing.org Biol. Lett. 14: 20180741 1. Chapman JW, Reynolds DR, Wilson K. 2015 Long- range seasonal migration in insects: mechanisms, evolutionary drivers and ecological consequences. Ecol. Lett. 18, 287 – 302. (doi:10.1111/ele.12407) 2. Flockhart DTT, Wassenaar LI, Martin TG, Hobson KA, Wunder MB, Norris DR. 2013 Tracking multi- generational colonization of the breeding grounds by monarch butterflies in eastern North America. Proc. R. Soc. B 280, 20131087. (doi:10.1098/rspb. 2013.1087) 3. Stefanescu C et al. 2013 Multi-generational long- distance migration of insects: studying the painted lady butterfly in the Western Palaearctic. Ecography 36, 474 – 486. (doi:10.1111/j.1600-0587.2012.07738.x) 4. Wassenaar LI, Hobson KA. 1998 Natal origins of migratory monarch butterflies at wintering colonies in Mexico: new isotopic evidence. Proc. Natl Acad. Sci. USA 95, 15 436 – 15 439. (doi:10.1073/pnas.95. 26.15436) 5. Miller NG, Wassenaar LI, Hobson KA, Norris DR. 2012 Migratory connectivity of the monarch butterfly (Danaus plexippus): patterns of spring re-
  • 26. colonization in Eastern North America. PLoS ONE 7, e31891. (doi:10.1371/journal.pone.0031891) 6. Talavera G, Bataille C, Benyamini D, Gascoigne-Pees M, Vila R. 2018 Round-trip across the Sahara: Afrotropical painted lady butterflies recolonize the Mediterranean in early spring. Biol. Lett. 14, 20180274. (doi:10.1098/rsbl.2018.0274) 7. Common IFB. 1954 A study of the ecology of the adult bogong moth, Agrotis infusa (Boisd) (Lepidoptera: Noctuidae), with special reference to its behaviour during migration and aestivation. Aust. J. Zool. 2, 223 – 263. (doi:10.1071/zo9540223) 8. Warrant E, Frost B, Green K, Mouritsen H, Dreyer D, Adden A, Brauburger K, Heinze S. 2016 The Australian bogong moth Agrotis infusa: a long- distance nocturnal navigator. Front. Behav. Neurosci. 10, 77. (doi:10.3389/fnbeh.2016.00077) 9. Nagoshi RN, Meagher RL, Hay-Roe M. 2012 Inferring the annual migration patterns of fall armyworm (Lepidoptera: Noctuidae) in the United States from mitochondrial haplotypes. Ecol. Evol. 2, 1458 – 1467. (doi:10.1002/ece3.268) 10. Alerstam T, Chapman JW, Backman J, Smith AD, Karlsson H, Nilsson C, Reynolds DR, Klaassen RHG, Hill JK. 2011 Convergent patterns of long-distance nocturnal migration in noctuid moths and passerine birds. Proc. R. Soc. B 278, 3074 – 3080. (doi:10. 1098/rspb.2011.0058) 11. Anderson RC. 2009 Do dragonflies migrate across the western Indian Ocean? J. Trop. Ecol. 25,
  • 27. 347 – 358. (doi:10.1017/S0266467409006087) 12. Wikelski M, Moskowitz D, Adelman JS, Cochran J, Wilcove DS, May ML. 2006 Simple rules guide dragonfly migration. Biol. Lett. 2, 325 – 329. (doi:10. 1098/rsbl.2006.0487) 13. Hobson KA, Anderson RC, Soto DX, Wassenaar LI. 2012 Isotopic evidence that dragonflies (Pantala flavescens) migrating through the Maldives come from the Northern Indian subcontinent. PLoS ONE 7, e52594. (doi:10.1371/journal.pone.0052594) 14. Trottier R. 1971 Effect of temperature on the life- cycle of Anax junius (Odonata: Aeshnidae) in Canada. Can. Entomol. 103, 1671 – 1683. (doi:10. 4039/Ent1031671-12) 15. Corbet PS. 2014 Dragonflies: Behaviour and Ecology of Odonata. See http://www.nhbs.com/dragonflies- behaviour-and-ecology-of-odonata-book (accessed on 13 September 2017). 16. May ML. 2013 A critical overview of progress in studies of migration of dragonflies (Odonata: Anisoptera), with emphasis on North America. J. Insect Conserv. 17, 1 – 15. (doi:10.1007/s10841- 012-9540-x) 17. Matthews JH. 2007 Research in motion: patterns of large-scale migration in dragonflies and birds, pp. 62 – 91. PhD Dissertation, University of Texas. 18. May ML, Gregoire JA, Gregoire SM, Lubertazzi MA, Matthews JH. 2017 Emergence phenology, uncertainty, and the evolution of migratory
  • 28. behavior in Anax junius (Odonata: Aeshnidae). PLoS ONE 12, e0183508. (doi:10.1371/journal.pone. 0183508) 19. Hobson KA, Soto DX, Paulson DR, Wassenaar LI, Matthews JH. 2012 A dragonfly (d2H) isoscape for North America: a new tool for determining natal origins of migratory aquatic emergent insects. Methods Ecol. Evol. 3, 766 – 772. (doi:10.1111/j. 2041-210X.2012.00202.x) 20. Russell RW, May ML, Soltesz KL, Fitzpatrick JW. 1998 Massive swarm migrations of dragonflies (Odonata) in Eastern North America. Am. Midl. Nat. 140, 325 – 342. (doi:10.1674/0003- 0031(1998)140[0325:MSMODO]2.0.CO;2) 21. Andrew Royle J, Rubenstein DR. 2004 The role of species abundance in determining breeding origins of migratory birds with stable isotopes. Ecol. Appl. 14, 1780 – 1788. (doi:10.1890/04-0175) 22. Bivand R, Rundel C, Pebesma E, Stuetz R, Hufthammer KO, Giraudoux P, Davis M, Santilli S. 2018 rgeos: Interface to Geometry Engine - Open Source (GEOS). See https://CRAN.R-project.org/ package=rgeos. 23. R Core Team. 2016 R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing. See https:// www.R-project.org/. 24. Kranstauber B, Weinzierl R, Wikelski M, Safi K. 2015 Global aerial flyways allow efficient travelling. Ecol. Lett. 18, 1338 – 1345. (doi:10.1111/ele.12528)
  • 29. 25. Feng H-Q, Wu K-M, Ni Y-X, Cheng D-F, Guo Y-Y. 2006 Nocturnal migration of dragonflies over the Bohai Sea in northern China. Ecol. Entomol. 31, 511 – 520. (doi:10.1111/j.1365-2311.2006. 00813.x) 26. Freeland JR, May M, Lodge R, Conrad KF. 2003 Genetic diversity and widespread haplotypes in a migratory dragonfly, the common green darner Anax junius. Ecol. Entomol. 28, 413 – 421. (doi:10. 1046/j.1365-2311.2003.00521.x) 27. Hallworth MT, Marra PP, McFarland KP, Zahendra S, Studds CE. 2018 Data from: Tracking dragons: stable isotopes reveal the annual cycle of a long-distance migratory insect. Dryad Digital Repository. (doi:10. 5061/dryad.17hf071) http://dx.doi.org/10.1111/ele.12407 http://dx.doi.org/10.1098/rspb.2013.1087 http://dx.doi.org/10.1098/rspb.2013.1087 http://dx.doi.org/10.1111/j.1600-0587.2012.07738.x http://dx.doi.org/10.1073/pnas.95.26.15436 http://dx.doi.org/10.1073/pnas.95.26.15436 http://dx.doi.org/10.1371/journal.pone.0031891 http://dx.doi.org/10.1098/rsbl.2018.0274 http://dx.doi.org/10.1071/zo9540223 http://dx.doi.org/10.3389/fnbeh.2016.00077 http://dx.doi.org/10.1002/ece3.268 http://dx.doi.org/10.1098/rspb.2011.0058 http://dx.doi.org/10.1098/rspb.2011.0058 http://dx.doi.org/10.1017/S0266467409006087 http://dx.doi.org/10.1098/rsbl.2006.0487 http://dx.doi.org/10.1098/rsbl.2006.0487 http://dx.doi.org/10.1371/journal.pone.0052594 http://dx.doi.org/10.4039/Ent1031671-12
  • 30. http://dx.doi.org/10.4039/Ent1031671-12 http://www.nhbs.com/dragonflies-behaviour-and-ecology-of- odonata-book http://www.nhbs.com/dragonflies-behaviour-and-ecology-of- odonata-book http://www.nhbs.com/dragonflies-behaviour-and-ecology-of- odonata-book http://dx.doi.org/10.1007/s10841-012-9540-x http://dx.doi.org/10.1007/s10841-012-9540-x http://dx.doi.org/10.1371/journal.pone.0183508 http://dx.doi.org/10.1371/journal.pone.0183508 http://dx.doi.org/10.1111/j.2041-210X.2012.00202.x http://dx.doi.org/10.1111/j.2041-210X.2012.00202.x http://dx.doi.org/10.1674/0003- 0031(1998)140[0325:MSMODO]2.0.CO;2 http://dx.doi.org/10.1674/0003- 0031(1998)140[0325:MSMODO]2.0.CO;2 http://dx.doi.org/10.1890/04-0175 https://CRAN.R-project.org/package=rgeos https://CRAN.R-project.org/package=rgeos https://CRAN.R-project.org/package=rgeos https://www.R-project.org/ https://www.R-project.org/ https://www.R-project.org/ http://dx.doi.org/10.1111/ele.12528 http://dx.doi.org/10.1111/j.1365-2311.2006.00813.x http://dx.doi.org/10.1111/j.1365-2311.2006.00813.x http://dx.doi.org/10.1046/j.1365-2311.2003.00521.x http://dx.doi.org/10.1046/j.1365-2311.2003.00521.x http://dx.doi.org/10.5061/dryad.17hf071 http://dx.doi.org/10.5061/dryad.17hf071Tracking dragons: stable isotopes reveal the annual cycle of a long-distance migratory insectIntroductionMethods and materialsEmergence assignmentsMigratory distanceAnnual cycleResultsDiscussionData accessibilityAuthors’ contributionsCompeting
  • 31. interestsFundingAcknowledgementsReferences Nishanth Padhma Age: 24 Course: Computer Science Year: 2015 Department: Computer Science Goals and motivations Nishanth Wants to become a good Game designer and after that he want to play the Games as an E-sports player and want to pursue the career in e-gaming. He is ambitious about the work and want to contribute to the community he belongs to. Lifestyle Gaming , Gym, Cricket, Anime series, Singing, music Nature of work (Undergraduate, learning Game designing, Development in Unity) Experience and training Worked as an internee at Quick Stack Solution s, Python and C# expert with achievement of 2times programming battle winner in interuniversity Competition Environment a day scholar and likes to spend the time in university experiencing the time to use my skills to try new things and
  • 32. play IT skill level Web Application Developer, Python developer, Java and XMl mobile developer. Unity Developer for game designing Attitude towards technology Great – it’s easy to use and saves me time I like it but it often falls short I don’t like it but I have to use it IT equipment Mostly interested in PC and Console because of gaming and also use mobiles for testing purpose for the game designs How will this person use the application? Judging from the personality, he would use the application for the information collection through the application for the games he plays and also plays the game or quiz game for fun too. Because of the gaming player he likes to interact with the applications and software. So he would be a positive user of my application. Key tasks
  • 33. He needs to perform the survey to the application and provide the feedback for the application soon. Also he reflects the characteristics for the gamer and software developer which can be a market target user for the application. A smart target for the user review on the application. Fears, Stress and Frustrations Lack of Hard work is the fear for the future goals. Creative working in own zone frustrates sometimes because achieving something void and new burdens a lot. Although sometimes achieves the. Failure stress me out at any level but I try to overcome with distractions like achieving other things in different grounds. Aqsa khan Age: 25 Course: Business and Finance Year: 2012 Department: Management Goals and motivations Aqsa wants to become an Event manager and want to participate in her family business grow afterwards. She wants to be a designer and want to manage a boutique with her friends in an entrepreneurship. She has very high goals and she is ambitious
  • 34. to complete it. Lifestyle Music, Event Management, Social Media, Recitation and political discussions Nature of work Graduate, Finance and event manager. Vice President women student association in university of south Asia. Experience and training Worked as an Ittehad group of industries as an Internee, Event Manager at Drift With Us with achievement of Gold medallist and dean list Winner 2011 and 2010. Environment Research for more and thrives for the self-study and improving own self to become a better person. Likes to work from home but can manage an entire event with her team also. Hardworking and anxious for more. Attitude towards Hierarchy and Business Great – always try new moves and new strategies to work even fine. No doubt sometime it fails but never stopped because of this fear
  • 35. didn’t had the courage to define myself in the top ones. Business Expertise Career counselling and designing the Trends for the current and future generations. Expanding the business with a vision to benefit someone else makes it even great. How will this person use the application? Judging from the personality, she would use the application for the research and to check her calibre for herself to test her knowledge about herself and about her expertise. This would provide her to judge herself and place herself in her goals and targets frame. So he would be a positive user of my application. Key tasks She needs to perform the survey to the application and provide the feedback for the application soon. Also he reflects the characteristics for the gamer and software developer which can be a market target user for the application. A smart target for the user review on the application. Fears, Stress and Frustrations Fears: technology will overcome the business fields which would reduce the need of human in this field too. Could be in upcoming years
  • 36. Stress: presentations at any level stress me out. Frustrations: No frustrations at all. Revised Screens for Smart Quiz 1 Revised Screens for Smart Quiz Project
  • 37. Screen 1: Welcome screen The below screen is the first screen users sees when the application is launched. It has a welcome banner, fields to enter login credentials for existing users, login button and a button for new user registration which directs user to sign up or registration screen. The functionality of the screen is to test the registered user’s login credentials and allow the user to access the application Screen 2: User Registration Screen The second screen below is launched when user clicks on register button, which has two buttons which allows user to sign up to the application using there Google or Facebook accounts. User has a choice to choose which account they want to use. The functionality of the screen is to register the user and provide login credentials to application. Screen 3: Preferences Selection Screen The preferences selection screen allows user to select their
  • 38. preferred category in which they are interested. User can select their preferences at the time of registration and it also to change their preferences in the future use also. The functionality of the screen is that user will get more questions from their preferred category. Screen 4: Quiz mode Selection The below screen has 4 major buttons which allows the user to play the game in different modes. The quiz is available in modes like individual, challenge, league and daily mission. The functionality of the screen is to allow the user to select the type of game mode user is willing to launch. And the screen also different common buttons at the bottom like settings, home and messages which provides ease of navigation to users through the application. %3CmxGraphModel%3E%3Croot%3E%3CmxCell%20id%3D%2 20%22%2F%3E%3CmxCell%20id%3D%221%22%20parent%3D %220%22%2F%3E%3CmxCell%20id%3D%222%22%20value% 3D%22%26lt%3Bh3%26gt%3B%26lt%3Bfont%20face%3D%26 quot%3BComic%20Sans%20MS%26quot%3B%20color%3D%26 quot%3B%23ffb570%26quot%3B%26gt%3BPlay%20Now%26lt %3B%2Ffont%26gt%3B%26lt%3B%2Fh3%26gt%3B%22%20sty le%3D%22labelPosition%3Dcenter%3BverticalLabelPosition%3 Dmiddle%3Balign%3Dcenter%3Bhtml%3D1%3Bshape%3Dmxg
  • 39. raph.basic.shaded_button%3Bdx%3D10%3BfillColor%3D%23E 6E6E6%3BstrokeColor%3Dnone%3B%22%20vertex%3D%221 %22%20parent%3D%221%22%3E%3CmxGeometry%20x%3D% 22420%22%20y%3D%22647%22%20width%3D%22160%22%2 0height%3D%2243%22%20as%3D%22geometry%22%2F%3E% 3C%2FmxCell%3E%3C%2Froot%3E%3C%2FmxGraphModel% 3E Screen 5: User Turn in league The below screen provides the information of whose current turn is to play in league mode of the game, users in the league mode takes turns one after other to play. It has information about both user and other participant’s information. It also has a button to remind or poke other user, when waiting for others to complete their turn. Screen 6: Challenge mode This screen is seen in the challenge mode of the quiz, user spins the wheel which will automatically select a category for the challenge between two users. The screen has a wheel with different categories, pointer and a spin button. The screen also provides information about the users participating the game at the top. The functionality of the screen is when user clicks spin button, the wheel spins and stops randomly at a category and
  • 40. game is launched. Screen 7: Quiz Main Screen The below screen is the games main screen, which is launched when the quiz starts, it has question highlighted the top, followed by four different clickable buttons which are possible answers and a countdown timer at the right top of the screen. The functionality of the screen is user has to select a correct answer form the 4 options provided with in the countdown time. Screen 8: Result Screen: The below screen is the result screen which appears when the user selects an option for the question in the previous screen. It provides the information if the selected option is right or wrong, button to continue to next question, share button, report button if user feels it as a wrong decision and also feedback buttons.
  • 41. References Arhipova, A. (n.d.). Mobile UI Design:Basic Types of Screens. Retrieved November 1, 2019, from https://tubikstudio.com/mobile-ui-design-15-basic-types-of- screens/. Etermax. (n.d.). Trivia Crack. Retrieved from https://www.triviacrack.com/. NATS 1550 Assignment 3 – Write a short magazine article for the general public (15%) Due date: Nov. 28, 11.59pm Please submit as a word or pdf file on Moodle
  • 42. This assignment has a VERY strict word count (your article absolutely has to be within these limits, no exceptions), you will loose 50% of your marks if you have fewer or more words: Minimum word count 450 words; Maximum: 550 words (excluding title). For this assignment you will be writing a short science-based piece about migration for the public in the form of a news or magazine article. Most of the writing done by students in university science follows a style and a set of rules that are consistent with the scientific literature— regimented, concise and technical. Similarly, much writing done in university by non-science
  • 43. students is also rule-bound as required by the standards of scholarship in those disciplines. However, it is also important to be able to communicate academic ideas, including scientific discoveries, in a less intimidating and technical manner and this is what this assignment is about. In this assignment, you will be converting a research paper that was published in a scientific journal and deals with migration into a magazine article. Choose ONE of the scientific articles posted on Moodle in the Assignment 3 folder for this, you decide which one of these you want to use for this assignment, but only use one. You will play the role of a free-lance e-zine (=online magazine) science writer, and
  • 44. you will be required to reduce the paper to its essence by creating a non-illustrated* magazine-style piece that your editor requires to fit a space of 500 words, excluding your catchy title. I will deduct 50% if your submission is less than 450 words or more than 550 words, no exceptions! Editors would not publish pieces that are shorter or longer than agreed upon. I will post links to examples on Moodle that show you the type of writing we are seeking—no formal references, no essay styles! Make sure you use your own words, do not copy/paste or directly quote from the articles. You need to have a catchy title that sparks interest. The writing must capture the reader’s
  • 45. attention immediately (you need to have a hook), and it must set up the context almost as fast. The writing should be precise, but not burdened by any jargon. Imagine that you are writing for well-informed adults, but who are not formally trained in ecology or environmental science or migration or biology etc.. Some comments on format: Do not use the traditional subheadings of Introduction, Methods, Results and Discussion. Remember this is a magazine article NOT a lab report or scientific journal article. It is up to you whether you wish to use any sub-headings at all. No specific font, size, or paragraph formatting (but please use a standard font that is readable) and it does not have
  • 46. to be formatted like a newspaper article, it is the content that counts. NATS 1550 Do not use references; you never see formal referencing in magazines or e-zines (online magazines). If you do wish to refer to someone else’s work within the body of your article, simply do so, such as: “The researchers were interested in following up on an idea proposed by a Dutch group of scientists who had found...” Or, refer to the posted examples to give you an idea how to do this.
  • 47. All words, excluding title (but including any subheadings, if you have them), are part of the word count (450 to 550 words) You do not need to create a title page, but write your name and student number and the (original) name of the article you are using at the top of the page. Below that should be your magazine article including your own catchy title that you created for it. At the end, also include your word count. *Note: If you wish to be creative you may add illustrations, but I will ignore these and not take these into consideration for marking. What am I looking for?
  • 48. Articles that • Have a catchy title that immediately grabs a readers’ interest • Right at the start grab my interest and make me want to read on (without being overly sensational) and hold my interest throughout • Are written in the style of a reputable magazine or newspaper article (not a lab report or essay etc.) • Are well-written, flow well and are easy and enjoyable to read • Have a logical structure and present ideas clearly • Do an excellent job accurately presenting the information from the scientific article and in getting the main points across, without loosing themselves in extraneous details • Cater to a well-informed, but non-specialist audience, e.g. by avoiding jargon
  • 49. • Have good grammar and spelling • Are within the allowed word count range of 450-550 words you will loose 50% of your marks if you have fewer or more words Tip: ask your non-science friends or family to read it and give you feedback on how interesting and easy to read they found it!