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 Centruroides vittatus is nocturnal and generally
finds refuge during the day under bark,
beneath vegetation, in holes in the ground
(Polis 1990).
 C.vittatus and other bark scorpions rarely dig
their own burrows (Polis 1990).
 C.vittatus do not emerge from their refuge
every night, but when they do they actively stalk
their prey (Hadley and Williams 1968)
 The study was conducted on the campus of
Texas A&M International, Laredo,TX.
 The habitat of the study site is described as
thorny brush (Blair 1950) or chaparral.
 An area of approximately 0.3 hectares was
flagged.
 Used previously for C.vittatus studies
(McReynolds 2004, 2008)
© 2010 Google maps – Map data © 2010 Europa Technologies , Geocentre Consulting, INEGI
|______|
100 m
 Microhabitat use can be associated with
seasonal changes in prey availability and
predation risk.
 Microhabitats can serve multiple functions for
C.vittatus, but a particular habitat can be
preferred for a certain function such as refuge,
foraging, or feeding.
 Black brush (Acacia rigidula)
 Burt (1943) defined the home range as the area
used by the individual to carry out daily
activities like foraging, mating, and caring for
young.
 The size of the home range may vary with sex
or other factors and different individuals may
have overlapping home ranges (Burt 1943).
 The home range may change during the life of
the individual;essentially by abandoning one
home range for another (Burt 1943)
 Observed surface activities of North American
scorpions in relation to feeding.
 Differences in foraging behavior between
Vejovidae and Buthidae.
 Vejovidae would assume a stationary position
around their burrow.
 Buthidae would actively forage, moving
continously.
 Area seemed to be limited in scope and a
similar range was covered by the same
scorpion each night of activity.
 These observations suggested the likelihood of
home ranges in scorpions, even non-burrowing
forms.
 Conducted a study on the home range of the
desert scorpion Smeringus mesaensis (formerly
Paruroctonus).
 Home range was circular with older, and larger,
scorpions occupying more space than younger
ones.
 Possible factors affecting home range included
prey distribution, energy requirements, and risk
of predation.
 Study was conducted
from Feb. 2009 to Feb
2010.
 Observations began
at 20:30 and ended
at 00:30 that night.
 UV lamps were used
to locate scorpions.
 Observations began by selecting one flagged
area to search.
 Every area was searched until the entire study
site was covered.
 The search pattern was randomized each
observation night so that each area was
searched at different times of the night.
 Only scorpions found on the surface of the
ground or on vegetation were used for the
study.
 There was no removal of debris, bark, or rocks
to uncover scorpions in refuges.
 Scorpion size class was determined by length.
• Class I - < 5 mm
• Class II - 5 to 10 mm
• Class III - 10 to 15 mm
• Class IV - > 15 mm
 Only size class IV was collected.
 Females carrying young were not collected.
 Scorpions were collected with forceps and
placed in a Whirl-Pak® (Nasco).
 The scorpions were measured with calipers and
rounded to the nearest 1 mm.
 The sex was determined by size and sexual
dimorphism of metasomal segments.
 Scorpions were marked with Sharpie® markers
on the last segment of the mesosoma and two
segments of the metasoma.
N McReynolds 2009
 Marked scorpions were released the next
morning where collected.
 Data was obtained and recorded for every
“recaptured” scorpion
 Recorded data included date and time
observed, height of scorpions on vegetation,
position relative to flags, prey captured, prey
taxa, and behavior.
 The most common and easiest method for
estimating home range.
 Method consists of using points of data to
create a convex polygon that includes all data
points (Mohr 1947).
 The area of the polygon is the home range
estimate (used for 31 individuals).
 This method is used to identify hard
boundaries (e.g. a river) when estimating
home ranges (Getz and Wilmers 2004).
 Polygons (hulls) are created within the home
range using the k-1 nearest neighbors of each
data point.
 These hulls are then combined to estimate the
home range.
 Calculate the “center of activity” of an animal
(Hayne 1949).
 Create concentric circles around the center point.
 The space between circles are considered
probability contours (zones) within which the
animal spends varying proportions of its time.
 Calculating the area of the circle that contains up
to 99% of the data points is the home range.
 The overall recapture rate of Centruroides
vittatus was about 50%.
 Of those recaptured, 46% were male and 54%
were female.
 Smaller scorpions (15-17 mm) had the highest
rate of no recapture.
 MCP areas of males and females were
compared. (Female: µ = 25.41, n = 21, sd =
5.23; Males: µ= 91.65, n = 10, sd = 4.27).
 An unpaired t-test using natural log
transformation showed that the areas among
males and females were significantly different
(t = 2.095, df = 29, P < 0.05).
 Males had significantly larger areas than
females.
 Mean distances travelled between recaptures
of males and females were compared (Female:
µ = 819.31, n = 21, sd = 564.19; Males: µ=
1619.9, n = 10, sd = 1151.6)

 (Mann-Whitney Test, U = 55.0, U’ = 155.0, P <
0.05)
 Males moved significantly greater distances
between recaptures.
 Why was recapture rate so low?
• 15-17 mm scorpions were recaptured the least.
 Penultimate scorpions (molted the mark)
 Intra-guild predation
• Male and female recaptures were about the same.
 Male recapture should have been higher because they are
more active during mating season.
 Males may have wandered out of the study site.
• Low levels of surface activity are common for both
male and female scorpions.
 Why do males have larger home ranges?
• Males occupy more space in search of mates
• Female carrying young will hide to protect the offspring
 What is the difference in home range shape
between Centruroides vittatus and Smeringus
mesaensis?
• Desert scorpions have a circular home range while C.
vittatus have irregular home range shapes.
• Sandy desert habitats are homogenous while chaparral
habitats are heterogeneous.
• C.vittatus do not make their own burrows, so they must
find refuge wherever they can.
 How did the methods work in the area?
• MCP
 Outliers affect outcome
 Home range is overestimated
 Helps establish size for study area of C.vittatus. At least 1
hectare.
• LoCoH
 Requires at least 6 points to create two polygons (per
individual)
 Small polygons within home range show areas of higher use.
 Can be compared to distribution of vegetation or other
factors.
• CPZ
 Requires at least 10 data points
 Would work better with desert scorpions because of circular
home range
 Assumes a normal distribution from a central point of activity
(e.g. burrow)
 Irregular shapes with a more linear distribution can be
overestimated
 Method works when there are multiple centers of activity
 Larger study area.
 Observations on consecutive nights.
 Seasonal changes in home range.
 Compare home range to distribution of
vegetation.
 Use other methods for estimating home range.
 Audy, J.R. and J.L. Harrison. 1954. Collections made in Malaya by
the Colonial Office Scrub Typhus Research Unit. Studies from
the Institute for Medical Research, Malaya, 26:1-22.
 Blair, W. F. 1950. The biotic provinces of Texas. Texas Journal of
Science 2:93-117.
 Burt, W.H. 1943. Territoriality and home range concepts as applied
to mammals. Journal of Mammalogy 24:346-352
 Getz, W.M. and C.C. Wilmers. 2004. A local nearest-neighbor
convex-hull construction of home ranges and utilization
distributions. Ecography 27:489-505.
 Hadley, N. F. and S. C. Williams. 1968. Surface activities of some
North American scorpions in relation to feeding. Ecology
49:726-734.
 Hayne, D.W. 1949. Calculations of size of home range. J. Mammal.
46:398-408.
 McReynolds, C. N. 2004. Temporal patterns in microhabitat use for
the scorpion Centruroides vittatus (Scorpiones:Buthidae).
Occasional Publications in Scorpiology 17:35-45.
 McReynolds, C. N. 2008. Microhabitat preferences for the errant
scorpion, Centruroides vittatus (Scorpiones, Buthidae). The
Journal of Arachnology 36:557-564.
 Mohr, C.O. 1947. Table of equivalent populations of North American
small mammals. Am. Midl. Nat. 37:223-249.
 Polis, G. A., C. N. McReynolds, and R. Glenn Ford. 1985. Home
range geometry of the desert scorpion Paruroctonus mesaensis.
Oecologia 67:273-277.
 Polis, G. A. 1990. Ecology. Pgs. 247-293 in G. A. Polis, ed. The
Biology of Scorpions. Stanford University Press, California.

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THESIS DEFENSE

  • 2.  Centruroides vittatus is nocturnal and generally finds refuge during the day under bark, beneath vegetation, in holes in the ground (Polis 1990).  C.vittatus and other bark scorpions rarely dig their own burrows (Polis 1990).  C.vittatus do not emerge from their refuge every night, but when they do they actively stalk their prey (Hadley and Williams 1968)
  • 3.  The study was conducted on the campus of Texas A&M International, Laredo,TX.  The habitat of the study site is described as thorny brush (Blair 1950) or chaparral.  An area of approximately 0.3 hectares was flagged.  Used previously for C.vittatus studies (McReynolds 2004, 2008)
  • 4. © 2010 Google maps – Map data © 2010 Europa Technologies , Geocentre Consulting, INEGI |______| 100 m
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  • 6.  Microhabitat use can be associated with seasonal changes in prey availability and predation risk.  Microhabitats can serve multiple functions for C.vittatus, but a particular habitat can be preferred for a certain function such as refuge, foraging, or feeding.  Black brush (Acacia rigidula)
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  • 9.  Burt (1943) defined the home range as the area used by the individual to carry out daily activities like foraging, mating, and caring for young.  The size of the home range may vary with sex or other factors and different individuals may have overlapping home ranges (Burt 1943).  The home range may change during the life of the individual;essentially by abandoning one home range for another (Burt 1943)
  • 10.  Observed surface activities of North American scorpions in relation to feeding.  Differences in foraging behavior between Vejovidae and Buthidae.  Vejovidae would assume a stationary position around their burrow.  Buthidae would actively forage, moving continously.
  • 11.  Area seemed to be limited in scope and a similar range was covered by the same scorpion each night of activity.  These observations suggested the likelihood of home ranges in scorpions, even non-burrowing forms.
  • 12.  Conducted a study on the home range of the desert scorpion Smeringus mesaensis (formerly Paruroctonus).  Home range was circular with older, and larger, scorpions occupying more space than younger ones.  Possible factors affecting home range included prey distribution, energy requirements, and risk of predation.
  • 13.  Study was conducted from Feb. 2009 to Feb 2010.  Observations began at 20:30 and ended at 00:30 that night.  UV lamps were used to locate scorpions.
  • 14.  Observations began by selecting one flagged area to search.  Every area was searched until the entire study site was covered.  The search pattern was randomized each observation night so that each area was searched at different times of the night.
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  • 16.  Only scorpions found on the surface of the ground or on vegetation were used for the study.  There was no removal of debris, bark, or rocks to uncover scorpions in refuges.
  • 17.  Scorpion size class was determined by length. • Class I - < 5 mm • Class II - 5 to 10 mm • Class III - 10 to 15 mm • Class IV - > 15 mm  Only size class IV was collected.  Females carrying young were not collected.  Scorpions were collected with forceps and placed in a Whirl-Pak® (Nasco).
  • 18.  The scorpions were measured with calipers and rounded to the nearest 1 mm.  The sex was determined by size and sexual dimorphism of metasomal segments.  Scorpions were marked with Sharpie® markers on the last segment of the mesosoma and two segments of the metasoma.
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  • 21.  Marked scorpions were released the next morning where collected.  Data was obtained and recorded for every “recaptured” scorpion  Recorded data included date and time observed, height of scorpions on vegetation, position relative to flags, prey captured, prey taxa, and behavior.
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  • 23.  The most common and easiest method for estimating home range.  Method consists of using points of data to create a convex polygon that includes all data points (Mohr 1947).  The area of the polygon is the home range estimate (used for 31 individuals).
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  • 25.  This method is used to identify hard boundaries (e.g. a river) when estimating home ranges (Getz and Wilmers 2004).  Polygons (hulls) are created within the home range using the k-1 nearest neighbors of each data point.  These hulls are then combined to estimate the home range.
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  • 28.  Calculate the “center of activity” of an animal (Hayne 1949).  Create concentric circles around the center point.  The space between circles are considered probability contours (zones) within which the animal spends varying proportions of its time.  Calculating the area of the circle that contains up to 99% of the data points is the home range.
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  • 30.  The overall recapture rate of Centruroides vittatus was about 50%.  Of those recaptured, 46% were male and 54% were female.  Smaller scorpions (15-17 mm) had the highest rate of no recapture.
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  • 35.  MCP areas of males and females were compared. (Female: µ = 25.41, n = 21, sd = 5.23; Males: µ= 91.65, n = 10, sd = 4.27).  An unpaired t-test using natural log transformation showed that the areas among males and females were significantly different (t = 2.095, df = 29, P < 0.05).  Males had significantly larger areas than females.
  • 36.  Mean distances travelled between recaptures of males and females were compared (Female: µ = 819.31, n = 21, sd = 564.19; Males: µ= 1619.9, n = 10, sd = 1151.6)   (Mann-Whitney Test, U = 55.0, U’ = 155.0, P < 0.05)  Males moved significantly greater distances between recaptures.
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  • 45.  Why was recapture rate so low? • 15-17 mm scorpions were recaptured the least.  Penultimate scorpions (molted the mark)  Intra-guild predation • Male and female recaptures were about the same.  Male recapture should have been higher because they are more active during mating season.  Males may have wandered out of the study site. • Low levels of surface activity are common for both male and female scorpions.
  • 46.  Why do males have larger home ranges? • Males occupy more space in search of mates • Female carrying young will hide to protect the offspring  What is the difference in home range shape between Centruroides vittatus and Smeringus mesaensis? • Desert scorpions have a circular home range while C. vittatus have irregular home range shapes. • Sandy desert habitats are homogenous while chaparral habitats are heterogeneous. • C.vittatus do not make their own burrows, so they must find refuge wherever they can.
  • 47.  How did the methods work in the area? • MCP  Outliers affect outcome  Home range is overestimated  Helps establish size for study area of C.vittatus. At least 1 hectare. • LoCoH  Requires at least 6 points to create two polygons (per individual)  Small polygons within home range show areas of higher use.  Can be compared to distribution of vegetation or other factors.
  • 48. • CPZ  Requires at least 10 data points  Would work better with desert scorpions because of circular home range  Assumes a normal distribution from a central point of activity (e.g. burrow)  Irregular shapes with a more linear distribution can be overestimated  Method works when there are multiple centers of activity
  • 49.  Larger study area.  Observations on consecutive nights.  Seasonal changes in home range.  Compare home range to distribution of vegetation.  Use other methods for estimating home range.
  • 50.  Audy, J.R. and J.L. Harrison. 1954. Collections made in Malaya by the Colonial Office Scrub Typhus Research Unit. Studies from the Institute for Medical Research, Malaya, 26:1-22.  Blair, W. F. 1950. The biotic provinces of Texas. Texas Journal of Science 2:93-117.  Burt, W.H. 1943. Territoriality and home range concepts as applied to mammals. Journal of Mammalogy 24:346-352  Getz, W.M. and C.C. Wilmers. 2004. A local nearest-neighbor convex-hull construction of home ranges and utilization distributions. Ecography 27:489-505.  Hadley, N. F. and S. C. Williams. 1968. Surface activities of some North American scorpions in relation to feeding. Ecology 49:726-734.  Hayne, D.W. 1949. Calculations of size of home range. J. Mammal. 46:398-408.
  • 51.  McReynolds, C. N. 2004. Temporal patterns in microhabitat use for the scorpion Centruroides vittatus (Scorpiones:Buthidae). Occasional Publications in Scorpiology 17:35-45.  McReynolds, C. N. 2008. Microhabitat preferences for the errant scorpion, Centruroides vittatus (Scorpiones, Buthidae). The Journal of Arachnology 36:557-564.  Mohr, C.O. 1947. Table of equivalent populations of North American small mammals. Am. Midl. Nat. 37:223-249.  Polis, G. A., C. N. McReynolds, and R. Glenn Ford. 1985. Home range geometry of the desert scorpion Paruroctonus mesaensis. Oecologia 67:273-277.  Polis, G. A. 1990. Ecology. Pgs. 247-293 in G. A. Polis, ed. The Biology of Scorpions. Stanford University Press, California.