Skip to main content
Advertisement

Main menu

  • Home
  • Articles
    • Accepted manuscripts
    • Issue in progress
    • Latest complete issue
    • Issue archive
    • Archive by article type
    • Special issues
    • Subject collections
    • Interviews
    • Sign up for alerts
  • About us
    • About JEB
    • Editors and Board
    • Editor biographies
    • Travelling Fellowships
    • Grants and funding
    • Journal Meetings
    • Workshops
    • The Company of Biologists
    • Journal news
  • For authors
    • Submit a manuscript
    • Aims and scope
    • Presubmission enquiries
    • Article types
    • Manuscript preparation
    • Cover suggestions
    • Editorial process
    • Promoting your paper
    • Open Access
    • Outstanding paper prize
    • Biology Open transfer
  • Journal info
    • Journal policies
    • Rights and permissions
    • Media policies
    • Reviewer guide
    • Sign up for alerts
  • Contacts
    • Contact JEB
    • Subscriptions
    • Advertising
    • Feedback
  • COB
    • About The Company of Biologists
    • Development
    • Journal of Cell Science
    • Journal of Experimental Biology
    • Disease Models & Mechanisms
    • Biology Open

User menu

  • Log in

Search

  • Advanced search
Journal of Experimental Biology
  • COB
    • About The Company of Biologists
    • Development
    • Journal of Cell Science
    • Journal of Experimental Biology
    • Disease Models & Mechanisms
    • Biology Open

supporting biologistsinspiring biology

Journal of Experimental Biology

  • Log in
Advanced search

RSS  Twitter  Facebook  YouTube  

  • Home
  • Articles
    • Accepted manuscripts
    • Issue in progress
    • Latest complete issue
    • Issue archive
    • Archive by article type
    • Special issues
    • Subject collections
    • Interviews
    • Sign up for alerts
  • About us
    • About JEB
    • Editors and Board
    • Editor biographies
    • Travelling Fellowships
    • Grants and funding
    • Journal Meetings
    • Workshops
    • The Company of Biologists
    • Journal news
  • For authors
    • Submit a manuscript
    • Aims and scope
    • Presubmission enquiries
    • Article types
    • Manuscript preparation
    • Cover suggestions
    • Editorial process
    • Promoting your paper
    • Open Access
    • Outstanding paper prize
    • Biology Open transfer
  • Journal info
    • Journal policies
    • Rights and permissions
    • Media policies
    • Reviewer guide
    • Sign up for alerts
  • Contacts
    • Contact JEB
    • Subscriptions
    • Advertising
    • Feedback
Research Article
Propulsion in hexapod locomotion: how do desert ants traverse slopes?
Toni Wöhrl, Lars Reinhardt, Reinhard Blickhan
Journal of Experimental Biology 2017 220: 1618-1625; doi: 10.1242/jeb.137505
Toni Wöhrl
Friedrich Schiller University Jena, Seidelstraβe 20, 07749 Jena, Germany
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: toni.woehrl@uni-jena.de
Lars Reinhardt
Friedrich Schiller University Jena, Seidelstraβe 20, 07749 Jena, Germany
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Reinhard Blickhan
Friedrich Schiller University Jena, Seidelstraβe 20, 07749 Jena, Germany
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & tables
  • Info & metrics
  • PDF
Loading

ABSTRACT

The employment of an alternating tripod gait to traverse uneven terrains is a common characteristic shared among many Hexapoda. Because this could be one specific cause for their ecological success, we examined the alternating tripod gait of the desert ant Cataglyphis fortis together with their ground reaction forces and weight-specific leg impulses for level locomotion and on moderate (±30 deg) and steep (±60 deg) slopes in order to understand mechanical functions of individual legs during inclined locomotion. There were three main findings from the experimental data. (1) The hind legs acted as the main brake (negative weight-specific impulse in the direction of progression) on both the moderate and steep downslopes while the front legs became the main motor (positive weight-specific impulse in the direction of progression) on the steep upslope. In both cases, the primary motor or brake was found to be above the centre of mass. (2) Normalised double support durations were prolonged on steep slopes, which could enhance the effect of lateral shear loading between left and right legs with the presence of direction-dependent attachment structures. (3) The notable directional change in the lateral ground reaction forces between the moderate and steep slopes implied the utilisation of different coordination programs in the extensor–flexor system.

INTRODUCTION

Ants possess a large set of motor skills, such as moving within confined spaces in the soil (Gravish et al., 2013), traversing slopes (Seidl and Wehner, 2008; Weihmann and Blickhan, 2009), climbing (Endlein and Federle, 2015), swimming (Bohn et al., 2012) and even gliding (Yanoviak et al., 2005). Despite their wide range of body masses, which varies approximately from 0.008 mg (Kaspari and Weiser, 1999) to 480 mg (Linsenmair and Pfeiffer, 1998), ants as a family have adopted a common motion system that enables the lightest species to manoeuvre in a surface-dominated micro-environment where molecular forces predominate, and the heaviest species to prevail in a volume-dominated macro-environment where gravitational forces exceed molecular forces (Went, 1968).

One of the primary characteristics of their motion system is the alternating tripod gait, which was identified to be a relatively robust locomotion pattern for Hexapoda in different settings (e.g. Seidl and Wehner, 2008; Wahl et al., 2015; Zollikofer, 1994a,b,c) and probably helped them to inhabit various habitats. Because traversing slopes and climbing belong to the very basic routine of many worker ants, previous studies have already described either their kinematics over different inclines or their kinematics and forces for level locomotion and vertical climbing. For example, a kinematic study on desert ants found that the ground contact durations changed with the inclination of the slope, whereas the positioning of the legs was independent of the slope (Seidl and Wehner, 2008). Other studies have combined kinematics and forces and observed that wood ants and other hexapods such as cockroaches and stick insects pushed with both their front and hind legs for level locomotion (Cruse, 1976; Full et al., 1991; Reinhardt and Blickhan, 2014a), and identified the influence of surface on interactions between (pre)tarsal structures of weaver ants for level locomotion (Endlein and Federle, 2008). A separate study on vertically climbing weaver ants on a smooth surface found that the legs above the centre of mass (CoM) mainly held their body weight (Endlein and Federle, 2015). In order to overcome gravity and climb upward, their front legs used more pulling forces than the pushing forces of the hind legs in the fore-aft direction, while in climbing downward, their hind legs used more pulling forces than the pushing forces of the front legs. It was then concluded that weaver ants mainly utilised the distal-located arolia for pulling and the more proximally located third and fourth tarsomeres for pushing (Endlein and Federle, 2015).

A modelling study for a three-point climber with cockroach geometry has predicted that the slope angle for the push-pull transition of the front legs in the normal direction of the substrate could be increased from around 40 to 70 deg by lowering the relative height (body height per body length) from 0.2 to 0.1 (Günther and Weihmann, 2012). However, the transition between the pushing of the front and hind legs on level locomotion and the pulling by legs above the CoM on vertical climbing has not yet been supported with experimental data for any kind of hexapod. Therefore, the present study firstly examined the changes in the alternating tripod gait and ground reaction forces (GRF) of Cataglyphis fortis (Forel 1902) on different slopes to describe the kinematics and forces of ants during inclined locomotion.

In addition, we calculated the weight-specific leg impulses, which are the integrals of GRF over the time of foot contacts normalised by the body weight for each leg and direction, to determine the impact of individual legs on propulsion and load over stride cycles. While kinematic and GRF data can identify leg actions such as pulling (GRF vector points from the tarsi away from the CoM) and pushing (GRF vector points from the tarsi towards the CoM) at every point of time, they might not be sufficient to determine which pair of legs pulls or pushes the animals the most within one stride cycle in multi-legged locomotion. This is because one leg could generate relatively high force peaks for a short time (high average force), but its pulling or pushing impact on propulsion and load could still be less than the other leg if the latter had lower forces for a longer time (low average force). In such cases, calculating the weight-specific leg impulses becomes crucial in pinpointing mechanical functions of individual legs, where a positive weight-specific impulse in the direction of progression (fore–aft) indicates the function of a motor, and a negative weight-specific impulse indicates the function of a brake.

List of symbols and abbreviations
BW
body weight
CoM
centre of mass
GRF
ground reaction force
i
slope i = {(±60 deg, steep), (±30 deg, moderate), (0 deg, level locomotion)}
Jlk
weight-specific leg impulse Embedded Image[GRF Flk integrated over the time of foot contact for each leg and direction divided by body weight (body mass m times the local acceleration of free fall g=9.81 m s–2)]
k
direction k={(x, fore–aft, direction of progression), (y, lateral, left–right), (z, normal to the substrate)}
l
leg number l={(1, front), (2, middle), (3, hind)}
tll
normalised double support duration for each leg pair from the touchdown of one tripod composition (left front leg L1, right middle leg R2, left hind leg L3) to the subsequent lift-off of the other tripod composition (R1, L2, R3) normalised by the stride duration of the middle legs

Thus, in order to study mechanical functions of individual hexapod legs over inclined locomotion, the present study has focused on how the alternating tripod gait, the GRF and the weight-specific leg impulses of the desert ant C. fortis changed on different slopes. Because the load carrying functions of the leg pairs have been studied for vertical climbing weaver ants on a smooth surface (Endlein and Federle, 2015), where the front legs used more pulling forces in climbing upward and the hind legs used more pulling forces in climbing downward, it was hypothesised that for the transition between level locomotion and vertical climbing, the front legs of C. fortis would exert pulling forces as the dominant motor on upslopes whereas the hind legs would exert pulling forces as the dominant brake on downslopes.

MATERIALS AND METHODS

Animals

A C. fortis colony with more than 600 ants from Tunisia near Menzel Chaker was housed in a formicarium. A 60 W daylight lamp was installed to illuminate one half of the formicarium from 07:00 h to 19:00 h. The temperature of the formicarium was kept at around 28°C. The ants were fed with honey, water and insects ad libitum. The experiments were performed between October 2012 and March 2013 at Friedrich Schiller University Jena.

Data acquisition

We used the same experimental setup and procedure as previously published by our work group (Reinhardt and Blickhan, 2014a,b). For each set of measurements, one ant was randomly taken from the formicarium with a plastic tube (diameter 12 mm, length 150 mm) and repeatedly placed at the start of a 90 mm long running track. The running track was covered with graph paper and confined to a width of 25 mm and a height of 30 mm.

A custom-built three-dimensional 4×4 mm force platform with resolvable forces Fx=5.4 μN, Fy=2.9 μN and Fz=10.8 μN (Reinhardt and Blickhan, 2014b) was fixed in the middle of the track and also covered with graph paper. It was designed based on PVC/semiconductor strain gauges KSP-3-120-F2-11 (Kyowa, Tokyo, Japan) and used to record the GRF of single steps of the moving ants. The signals received by the force platform were amplified by a data acquisition system (MGCplus, Hottinger Baldwin Messtechnik, Darmstadt, Germany) and collected by a computer with a sampling frequency of 1200 Hz. The natural frequencies of the force platform with the graph paper attached were measured to be fx=380 Hz, fy=279 Hz and fz=201 Hz. The force data could not be used to identify the dragging length because the dragging forces were smaller than the resolvable forces and the ants could drag their legs off the force platform.

A Photron Fastcam SA3 (San Diego, CA, USA) camera with a frequency of 500 Hz was used to record the dorsal view of the ants. The sagittal view was captured by the same camera objective via glass prisms functioning as a 45 deg mirror. MATLAB R20015b (The MathWorks, Natick, MA, USA) and DigitizingTools 20160711 (Hedrick, 2008) were used for motion tracking.

The body masses of the ants were measured with a precision scale (±0.1 mg, ABS 80-4, Kern & Sohn, Germany) directly after each single leg force signal was recorded. After each set of measurements, the investigated ant was isolated in a separate box and only placed back into the formicarium at the end of every measurement day.

Data selection

A total of 893 trials with GRF measurements and video sequences were recorded. In the first round of data screening, we excluded trials in which the ants stopped, changed direction or touched the force platform with their gasters. Trials in which the ants dragged their hind legs were not excluded from the dataset.

Subsequently, we took the first 15 force and kinematic measurements for each set of legs (front legs, middle legs, hind legs) and slope (steep=±60 deg, moderate=±30, level locomotion=0 deg) for further data analysis. Altogether, 225 different strides from 225 different runs were selected.

Data analysis

MATLAB 8.6.0 R20015b and R 3.3.1 (R Foundation for Statistical Computing, Vienna, Austria) were used for data analysis. Petiole and tarsi trajectories and the GRF were calculated over one stride cycle, i.e. consecutive touchdowns of the same leg, and adjusted to the average direction of progression through rotational transformation in the frontal x–y plane. The force signals were smoothed with a Savitzky–Golay filter of polynomial order 0 and frame length 5. All signals were normalised to the body weight and the mean stepping pattern for every slope (45 strides per slope). The GRF are given as arithmetic means and standard deviations unless stated otherwise.

The GRF signals were extrapolated with the assumptions that: (1) the GRF did not change over multiple stride cycles, i.e. straight locomotion and constant speed; and (2) left and right leg GRF were mirrored in the lateral direction and equal in the normal and fore–aft direction, i.e. bilateral symmetry of GRF and tripod symmetry of the ant body. As a result, the GRF signals were periodic.

The weight-specific leg impulses were approximated numerically using the trapezoidal sum method with partitions of equal size Δt=1200–1 s of the GRF over the whole ground contact duration.

The Wilcoxon rank sum test with Bonferroni correction was used to compare the measurements.

RESULTS

Actuation on upslopes

On the moderate upslope, the primary motors of C. fortis (Fig. 1A, Table 1) were found to be the middle and hind legs as J1x(30 deg)<J2x(30 deg) and J1x(30 deg)<J3x(30 deg), where J is the weight-specific leg impulse (both P<0.001). Pushing forces by the hind legs dominated over pulling forces by the front legs, where the CoM was mostly above the tarsi (Fig. 2D). On the steep upslope, the primary motor became the front legs as J1x(60 deg)>J2x(60 deg) and J1x(60 deg)>J3x(60 deg) (both P<0.001). Pulling forces by the front legs above the CoM dominated over pushing forces by the hind legs below the CoM (Fig. 2E). The front legs exhibited the highest amplitude of the mean GRF at approximately F1x(60 deg)≈0.5 BW≈120 μN (Fig. 3A).

Fig. 1.
  • Download figure
  • Open in new tab
  • Download powerpoint
Fig. 1.

Weight-specific leg impulses of Cataglypis fortis at different slopes. Results are grouped by the direction of the impulses [(A) fore–aft; (B) lateral; (C) normal] and by the type of leg (front, middle and hind leg). The central lines of the Tukey boxplots are the medians and the edges of the boxes are the 25th and 75th percentiles (N=15 strides for each subset). Asterisks indicate significant differences between slopes (*P≤0.05; **P≤0.01; ***P≤0.001; n.s., not significant; two-sided Wilcoxon rank sum test with Bonferroni correction).

View this table:
  • View inline
  • View popup
  • Download powerpoint
Table 1.

Inter-leg comparisons of the weight-specific leg impulses

Fig. 2.
  • Download figure
  • Open in new tab
  • Download powerpoint
Fig. 2.

Mean ground reaction force (GRF) vectors of C. fortis with mean stepping patterns at different slopes. (A) Steep downslope; (B) moderate downslope; (C) level locomotion; (D) moderate upslope; and (E) steep upslope. The direction of progression x is from left to right. Blue, green and red arrows indicate the mean GRF vectors of left front leg, right middle leg and left hind leg, respectively. GRF and tarsus trajectories are plotted in the sagittal (x–z plane) and dorsal views (x–y plane) in body-fixed coordinate systems with the origins in the centres of mass (CoM). The solid grey/black lines in the x–y plane represent the measured/mean tarsus trajectories during the ground contacts from touchdowns to lift-offs (tarsus motions from right to left). The dashed and dotted black triangles represent the mean area of the supporting tripods during the mean temporal mid-stance of the right and left middle legs, respectively. The orange lines in the x–z plane show the mean thorax length and orientation. The black asterisks represent the locations of the CoM, which were calculated near the thorax–petiole joint at 20% of the thorax length (McMeeking et al., 2012). The distance between the two asterisks represents the mean displacement of the ants for one stride cycle. The black contours represent individual sample ants on respective slopes during the temporal mid-stances of the right middle leg. All means were calculated from 15 strides per leg pair and slope, resulting in 225 strides in total.

Fig. 3.
  • Download figure
  • Open in new tab
  • Download powerpoint
Fig. 3.

GRF of C. fortis over time. (A) Fore–aft direction; (B) lateral direction; and (C) normal direction. Mean GRF with standard deviations (grey shaded areas) over time and percentage of the stride cycle of the middle legs (N=15 strides for each subset). The subplots are grouped by slope and leg pair (left front leg L1, right middle leg R2, left hind leg L3). The GRF signals are normalised to the mean stepping pattern of each slope (N=45 strides for each subset) and to the body weight (BW) (Table 3). The vertical green shaded areas mark the mean double support durations of the middle legs (Fig. 6).

In the sagittal view (x–z plane), the mean GRF vectors of the hind legs pointed along the tibia axis towards the gaster on both the moderate and steep upslopes (Fig. 2D,E). In the dorsal view (x–y plane), they pointed into the area of the supporting tripod towards the CoM, whereas front and middle leg GRF vectors pointed out of the supporting tripod frame. All legs pushed outwards on the moderate upslope (Fig. 2D), but a directional change in the lateral GRF occurred for the front legs on the steep upslope as they started pulling inwards (Fig. 2E). The GRF standard deviations were observed to increase on the steep slopes for all leg pairs (Fig. 3A).

The shapes of the GRF over time changed remarkably from the moderate to steep upslope for the front and hind legs in the normal direction. Whereas front leg GRF diminished on the steep upslope, hind leg GRF changed from a triangular shape on the moderate upslope to a trapezoidal shape with longer double support durations on the steep upslope.

Braking on downslopes

Hind legs were used as the primary braking unit for both the moderate and steep downslopes as J3x(–30 deg)<J2x(–30 deg)<0 (P<0.05), J3x(–30 deg)<J1x(–30 deg)<0 (P<0.01), J3x(–60 deg)<J2x(–60 deg)<0 (P<0.001) and J3x(–60 deg)<J1x(–60 deg)<0 (P<0.001) (Fig. 1A, Table 1). Pulling forces by the hind legs above the CoM dominated over pushing forces by the front and middle legs below the CoM (Fig. 2A,B). The hind legs on the steep downslope had the strongest mean GRF at approximately F3x(–60 deg)≈–0.5 BW≈–120 μN (Fig. 3A).

In the sagittal view, braking forces of the front legs pointed along the tibia axis towards the head (Fig. 2A,B). In the dorsal view, they pointed into the area of the supporting tripod towards the thorax.

Similar to the shift in direction in the lateral GRF of the front legs on the steep upslope, the hind legs started pulling strongly inwards on the steep downslope (Figs 1A, 2A).

Direction dependency

A comparison of impulses on the steep upslope against the steep downslope for the same leg pair revealed that front legs pulled more strongly on the steep upslope than they pushed on the steep downslope (Fig. 1A) as |J1x(60 deg)|>|J1x(–60 deg)| (P<0.001). Similarly, hind leg pulling impulses were stronger on the steep downslope than pushing impulses on the steep upslope as |J3x(–60 deg)|>|J3x(60 deg)| (P<0.05).

Front–hind leg symmetry

The GRF vectors of the front legs on upslopes (Fig. 4, dark blue arrows) were compared against those of the hind legs on downslopes (light red arrows). At the same time, the GRF vectors of the front legs on downslopes (light blue arrows) were also compared against those of the hind legs on upslopes (dark red arrows). Even though the starting points of the GRF vectors were more distal for the hind legs than for the front legs, it was observed that the GRF vectors of the front legs on the steep upslope and those of the hind legs on the steep downslope (Fig. 4A,B) had similar magnitudes but opposite directions along the body (x) axis, and vice versa. Such symmetry was also evident on moderate slopes (Fig. 4C,D), although there was slight deviation in the direction of the GRF vectors of the hind legs in the lateral direction on the moderate downslope.

Fig. 4.
  • Download figure
  • Open in new tab
  • Download powerpoint
Fig. 4.

Comparison of the mean GRF vectors on upslopes and downslopes in C. fortis. (A) Steep slopes, sagittal view; (B) steep slopes, dorsal view; (C) moderate slopes, sagittal view; and (D) moderate slopes, dorsal view. The mean GRF vectors (N=15 strides for each subset) are plotted in a space-fixed coordinate system for the left front legs (blue, L1), the right middle legs (green, R2) and the left hind legs (red, L3). Darker colours indicate the GRF on upslopes whereas lighter colours indicate the GRF on downslopes. The grey crosses represent the positions of the ground contacts of individual tarsi for all the strides (N=15 strides for each subset). The black crosses represent the mean positions with standard deviations of the grey crosses. The black dots illustrate the positions of petioles during temporal midstance of the right middle legs. The grey shaded contours represent sample ants during the temporal mid-stance of the right middle leg. The direction of progression is from left to right.

In the fore–aft direction, front and hind legs exhibited supportive mechanical functions during inclined locomotion as sgn[J1x(i)]=sgn[J3x(i)] for i={±60 deg, ±30 deg} and contrary mechanical functions for level locomotion as sgn[J1x(0 deg)]≠sgn[J3x(0 deg)]. While the distribution of the body weight in the normal direction was nearly equal for level locomotion among the three leg pairs, it was shifted mostly to the hind leg on the steep upslope and to the front and middle legs on the steep downslope (Figs 1C, 2A–E).

Dragging hind leg

The hind legs were dragged behind the ants in numerous measurements. In order to distinguish aerial phases from dragging, we set the maximum height of uncertainty to 0.4 mm, which was twice the magnitude of the measuring accuracy. The number of lift-offs was counted and the dragging length for each slope was calculated (Fig. 5A, Table 2). The median dragging length ranged from 2.2 mm (moderate upslope) to 5.6 mm (steep downslope) and constituted 26% to 82% of the step length depending on the slope. Most of the dragging across the whole swing phase occurred on the steep downslope, which was observed in 67% of all steep downslope strides.

Fig. 5.
  • Download figure
  • Open in new tab
  • Download powerpoint
Fig. 5.

Hind leg dragging and change of body height in C. fortis. (A) Dragging hind leg in the sagittal view. The dragging lengths are defined as the distances between the locations of touchdowns and the intersections of the hind leg tarsus trajectories (grey lines, N=75 strides) with the dashed horizontal line at twice the measurement accuracy z=2×0.2 mm. The red line highlights an example tarsus trajectory. The black bold horizontal line represents the location of the force plate. (B) Body height at different slopes. Body height was defined as the distance between the CoM and the substrate. The locations of the CoM were calculated near the thorax–petiole joint at 20% of the of the thorax length (McMeeking et al., 2012). Asterisks indicate significant differences between slopes (***P≤0.001; n.s., not significant; two-sided Wilcoxon rank sum test with Bonferroni correction; N=45 per subset).

View this table:
  • View inline
  • View popup
  • Download powerpoint
Table 2.

Dragging hind leg measurements

Total GRF over time

In order to ensure the validity of the measurements, the total GRF over time was calculated for all six legs on all slopes (Table 3). In the ideal case, the total GRF in the normal direction should oscillate at around a mean of 1 BW for level locomotion, Embedded Image BW at ±30 deg slope, and 2–1 BW at ±60 deg slope. However, the calculated total GRF over multiple stride cycles was 0.03 BW (moderate downslope) to 0.10 BW (level locomotion) lower than the ideal case. This could be attributed to the dragging hind leg (Fig. 4, Table 2), which could have generated pulling or pushing forces during the dragging phase.

View this table:
  • View inline
  • View popup
  • Download powerpoint
Table 3.

Mean of total GRF

Kinematics

Temporal parameters such as ground contact duration and running speed were highly variable across all slopes (Table 4). For example, the standard deviations of the contact durations of the middle legs increased from 11 ms for level locomotion to 29 ms on the steep downslope. The mean speed ranged from 54±10 mm s–1 (steep upslope) to 87±17 mm s–1 (level locomotion). The duty factor of the middle legs lay between 62±9% (moderate downlsope) and 72±7% (steep downslope). The body height (CoM–substrate distance; Table 4, Fig. 5B) ranged from 2.4±0.4 mm (steep downslope) to 3.8±0.7 mm (level locomotion).

View this table:
  • View inline
  • View popup
  • Download powerpoint
Table 4.

Kinematic parameters

Touchdowns and lift-offs of the tripod composition occurred almost simultaneously on the moderate slopes and level locomotion. However, the tarsi of the left hind legs touched down and lifted off the ground later than the right middle legs and left front legs on the steep slopes, and vice versa (Fig. 3). The normalised double support durations (Fig. 6) increased significantly for the front (P<0.001) and hind legs (P<0.001) from level locomotion to the steep upslope and for the middle legs from level locomotion to the steep slopes (P<0.01).

Fig. 6.
  • Download figure
  • Open in new tab
  • Download powerpoint
Fig. 6.

Normalised double support durations for each leg pair at different slopes in C. fortis. The double support durations of the (A) front legs, (B) middle legs and (C) hind legs were normalised by the stride durations of the middle legs (N=45 strides for each subset). The central lines of the Tukey boxplots are the medians and the edges of the boxes are the 25th and 75th percentiles. Asterisks indicate significant differences between slopes (**P≤0.01; ***P≤0.001; n.s., not significant; two-sided Wilcoxon rank sum test with Bonferroni correction).

DISCUSSION

Motor and brake functions

Similar to the findings about vertically climbing weaver ants on a smooth surface, where a larger proportion of body weight was carried by the legs above the CoM (Endlein and Federle, 2015), our measurements showed that the front legs rose above the CoM and became the primary motor (positive weight-specific leg impulse in the direction of progression) on the steep upslope. The hind legs maintained their position above the CoM and kept their function as the primary braking leg pair (negative weight-specific leg impulse in the direction of progression) on both the moderate and steep downslopes. While the dominant braking function of the hind legs on downslopes corresponded with our hypothesis, the front legs did not act as the primary motor on the moderate upslope, probably because the tarsi did not rise above the CoM adequately (Fig. 2). Therefore, we deduced that the position of the tarsi relative to the CoM could be the main factor in determining the individual leg pairs as the primary motor or brake during inclined locomotion.

This suggested that the tarsi of the front legs could act as the main suspension point of the supporting tripod on the steep upslope and the tarsi of the hind legs could act as the main suspension point on downslopes. If the hind legs were used as the primary motor on the steep upslope, the main suspension point would be below the CoM, thereby causing instability. Further stability could be achieved by the dragging hind leg. Under risky situations such as moving down the steep slope where most of the dragging across the whole swing phase was observed, the dragging leg could form a temporary quadrangle configuration or hook onto protruding objects for abrupt braking.

Direction dependency and shear loading

The front and hind legs also showed direction-dependent GRF and weight-specific impulses. For the front legs, the fore–aft pulling impulses (motor function) on the steep upslope were higher than their pushing impulses (brake function) on the steep downslope. For the hind legs, the fore–aft pulling impulses (brake function) on the steep downslope were higher than their pushing impulses (motor function) on the steep upslope. In the lateral direction, the front legs changed from pushing outwards to pulling inwards from the moderate to the steep upslope, whereas the hind legs changed from pushing outwards to pulling inwards from the moderate to the steep downslope.

Higher pulling forces over pushing forces were observed in other Hexapoda as well, including stick insects, cockroaches and ants (Bullock et al., 2008; Clemente and Federle, 2008; Endlein and Federle, 2015). Close examination of the silhouettes of the typical tarsus of Cataglyphis, hornets and weaver ants (Frantsevich and Gorb, 2004; Endlein and Federle, 2008) revealed that the claws of their front legs were curved against the direction of progression, but those of their hind legs were curved towards the direction of progression. As such, the action of pulling for both the front and hind legs would be able to help the ants interlock their claws better with the surface asperities of our substrate. This could be of special importance for Cataglyphis considering the granular surface of their desert habitat.

The presence of direction-dependent attachment structures could also enhance shear loading of the opposing tarsi of the ants. Just as shear loading of the opposing toes or legs enabled geckos to hang from the ceiling (Autumn, 2006) and spiders to make use of the collective effect of their hairy foot pads (Wohlfart et al., 2014), it could also help the ants to move on steep surfaces. The increase in the normalised durations of double support phases from level locomotion to steep slopes in the experiment implied that the forces in the lateral direction acted longer against each other on steep slopes (Fig. 3B). Thus, by changing their temporal gait kinematics, the ants could engage their opposing tarsal hair structures and probably adjust their whole-body adhesion force to move on steep surfaces.

Coordination and navigation

The changes in the weight-specific leg impulses as well as the changes of the magnitudes and directions of the GRF over time and different slopes could imply that the ants employed different coordination programs in their extensor–flexor system on different slopes. For example, the front legs switched from pushing to pulling laterally between the moderate and steep upslope, whereas the hind legs switched from pushing to pulling laterally between the moderate and steep downslope. This showed that the participating muscles and their interactions could have changed with the slope.

Such changes could further provide insights into the mechanisms behind hexapod navigation. Cataglyphis were found to employ odometry during inclined locomotion (Wittlinger et al., 2006; Wohlgemuth et al., 2001), and it has been suggested that both odometry and gravity perception could play a key role in their three-dimensional path integration. However, the primary receptors in gravity perception for Formica, the hair fields located on the body joints (Markl, 1962, 1974), were not necessary for path integration of Cataglyphis (Wittlinger et al., 2007), neither was the monitoring of the thorax–coxae joint angles. Instead, force sensors such as muscular strain sensors and campaniform sensilla could provide idiothetic cues for three-dimensional path integration (Seidl and Wehner, 2008). Such sense organs exhibited orientation-dependent directional sensitivity (Zill and Moran, 1981) and have been observed in other hexapods such as cockroaches (e.g. McIver, 1975; Moran et al., 1971; Pringle, 1938; Ridgel et al., 2000) and stick insects (e.g. Schmitz, 1993; Zill et al., 2013).

Even though we could not verify the involvement of proprioceptors in path integration directly from the results, it was clear that the strain on the attachment structures and leg segments has changed on different slopes because of the changes in the magnitudes and directions of the GRF. If similar patterns of GRF changes could be observed on a different substrate or with another ant species, it would be possible to hypothesise that ants triggered a relatively consistent motor program with respect to the angle of the slope, where the cuticular structures were affected more by the slope of the substrate than its roughness or stiffness. As such, the bending of leg segments or tarsi during inclined locomotion could probably be discussed together with odometry in three-dimensional path integration of C. fortis.

Conclusions

In the analysis of mechanical functions of the individual legs of desert ants on different slopes, our experimental data showed that the tarsi of the hind legs were above the CoM and acted as the main brake on both the moderate and steep downslopes, whereas the main motor changed from the middle and hind legs at the moderate upslope to the front legs at the steep upslope after the tarsi of the front legs rose above the CoM. This suggested that the need to maintain stability during inclined locomotion always constituted the shift of the main motor/brake towards the leg pair above the CoM. This finding varied slightly from our hypothesis about the mechanical function of the front legs, which we initially surmised to be the main motor on both the moderate and steep upslopes.

The increased double support durations on steep slopes probably enhanced shear loading of the opposing tarsal hair structures to ensure better adhesion on steep surfaces. In addition, the notable change of the weight-specific leg impulses from pushing laterally on the moderate slopes to pulling laterally on the steep slopes illustrated the flexibility of the extensor–flexor system, which could serve as another potential mechanism for the path integration of the desert ants.

Acknowledgements

We would like to thank C. Bühlmann (Max Planck Institute for Chemical Ecology Jena) for lending us a Cataglyphis fortis colony, S. Cai for proofreading, and C. Leonhardt, Y. Sutedja and R. Schälike for motion tracking.

FOOTNOTES

  • Competing interests

    The authors declare no competing or financial interests.

  • Author contributions

    T.W. made substantial contributions to the execution and interpretation of the findings being published, as well as the drafting and revision of the article. L.R. and R.B. made substantial contributions to the design and execution of the findings being published.

  • Funding

    This work was funded by Deutsche Forschungsgemeinschaft [BL 236/20-1 to R.B.].

  • Data availability

    Data are available from the Dryad Digital Repository (Wöhrl et al., 2017): http://dx.doi.org/10.5061/dryad.j4594.

  • Received January 14, 2016.
  • Accepted February 7, 2017.
  • © 2017. Published by The Company of Biologists Ltd
http://www.biologists.com/user-licence-1-1/

References

  1. ↵
    1. Autumn, K.
    (2006). Properties, principles, and parameters of the gecko adhesive system. In Biological Adhesives (ed. A. M. Smith and J. A. Callow), pp. 225-256. Berlin, Heidelberg: Springer.
  2. ↵
    1. Bohn, H. F.,
    2. Thornham, D. G. and
    3. Federle, W.
    (2012). Ants swimming in pitcher plants: kinematics of aquatic and terrestrial locomotion in camponotus schmitzi. J. Comp. Physiol. A 198, 465-476. doi:10.1007/s00359-012-0723-4
    OpenUrlCrossRefPubMed
  3. ↵
    1. Bullock, J. M. R.,
    2. Drechsler, P. and
    3. Federle, W.
    (2008). Comparison of smooth and hairy attachment pads in insects: friction, adhesion and mechanisms for direction-dependence. J. Exp. Biol. 211, 3333-3343. doi:10.1242/jeb.020941
    OpenUrlAbstract/FREE Full Text
  4. ↵
    1. Clemente, C. J. and
    2. Federle, W.
    (2008). Pushing versus pulling: division of labour between tarsal attachment pads in cockroaches. Proc. R. Soc. B 275, 1329-1336. doi:10.1098/rspb.2007.1660
    OpenUrlAbstract/FREE Full Text
  5. ↵
    1. Cruse, H.
    (1976). The function of the legs in the free walking stick insect, Carausius morosus. J. Comp. Physiol. A 112, 235-262. doi:10.1007/BF00606541
    OpenUrlCrossRef
  6. ↵
    1. Endlein, T. and
    2. Federle, W.
    (2008). Walking on smooth or rough ground: passive control of pretarsal attachment in ants. J. Comp. Physiol. A 194, 49-60. doi:10.1007/s00359-007-0287-x
    OpenUrlCrossRefPubMedWeb of Science
  7. ↵
    1. Endlein, T. and
    2. Federle, W.
    (2015). On heels and toes: how ants climb with adhesive pads and tarsal friction hair arrays. PLoS ONE 10, e0141269. doi:10.1371/journal.pone.0141269
    OpenUrlCrossRef
  8. ↵
    1. Frantsevich, L. and
    2. Gorb, S.
    (2004). Structure and mechanics of the tarsal chain in the hornet, Vespa crabro (Hymenoptera: Vespidae): implications on the attachment mechanism. Arthropod. Struct. Dev. 33, 77-89. doi:10.1016/j.asd.2003.10.003
    OpenUrlCrossRefPubMedWeb of Science
  9. ↵
    1. Full, R. J.,
    2. Blickhan, R. and
    3. Ting, L. H.
    (1991). Leg design in hexapedal runners. J. Exp. Biol. 158, 369-390.
    OpenUrlAbstract/FREE Full Text
  10. ↵
    1. Gravish, N.,
    2. Monaenkova, D.,
    3. Goodisman, M. A. D. and
    4. Goldman, D. I.
    (2013). Climbing, falling, and jamming during ant locomotion in confined environments. Proc. Natl. Acad. Sci. USA 110, 9746-9751. doi:10.1073/pnas.1302428110
    OpenUrlAbstract/FREE Full Text
  11. ↵
    1. Günther, M. and
    2. Weihmann, T.
    (2012). Climbing in hexapods: a plain model for heavy slopes. J. Theoret. Biol. 293, 82-86. doi:10.1016/j.jtbi.2011.10.011
    OpenUrlCrossRefPubMed
  12. ↵
    1. Hedrick, T. L.
    (2008). Software techniques for two- and three-dimensional kinematic measurements of biological and biomimetic systems. Bioinspir. Biomim. 3, 34001. doi:10.1088/1748-3182/3/3/034001
    OpenUrlCrossRef
  13. ↵
    1. Kaspari, M. and
    2. Weiser, M. D.
    (1999). The size-grain hypothesis and interspecific scaling in ants. Funct. Ecol. 13, 530-538. doi:10.1046/j.1365-2435.1999.00343.x
    OpenUrlCrossRef
  14. ↵
    1. Linsenmair, K. E. and
    2. Pfeiffer, M.
    (1998). Polydomy and the organization of foraging in a colony of the Malaysian giant ant Camponotus gigas (Hym./Form.). Oecologia 117, 579-590. doi:10.1007/s004420050695
    OpenUrlCrossRefWeb of Science
  15. ↵
    1. Markl, H.
    (1962). Borstenfelder an den Gelenken als Schweresinnesorgane bei Ameisen und anderen Hymenopteren. Z. vergl. Physiol. 45, 475-569. doi:10.1007/BF00342998
    OpenUrlCrossRef
  16. ↵
    1. Markl, H.
    (1974). The perception of gravity and of angular acceleration in invertebrates. In Handbook of Sensory Physiology. Vestibular System Part 1: Basic Mechanisms (ed. H. H. Kornhuber), pp. 17-74. Berlin, Heidelberg: Springer.
  17. ↵
    1. McIver, S. B.
    (1975). Structure of cuticular mechanoreceptors of arthropods. Annu. Rev. Entomol. 20, 381-397. doi:10.1146/annurev.en.20.010175.002121
    OpenUrlCrossRefPubMed
  18. ↵
    1. McMeeking, R. M.,
    2. Arzt, E. and
    3. Wehner, R.
    (2012). Cataglyphis desert ants improve their mobility by raising the gaster. J. Theor. Biol. 297, 17-25. doi:10.1016/j.jtbi.2011.12.003
    OpenUrlCrossRefPubMed
  19. ↵
    1. Moran, D. T.,
    2. Chapman, K. M. and
    3. Ellis, R. A.
    (1971). The fine structure of cockroach campaniform sensilla. J. Cell Biol. 48, 155-173. doi:10.1083/jcb.48.1.155
    OpenUrlAbstract/FREE Full Text
  20. ↵
    1. Pringle, J.
    (1938). Proprioception in insects I. A new type of mechanical receptor from the palps of the cockroach. J. Exp. Biol. 15, 101-113.
    OpenUrlAbstract
  21. ↵
    1. Reinhardt, L. and
    2. Blickhan, R.
    (2014a). Level locomotion in wood ants: evidence for grounded running. J. Exp. Biol. 217, 2358-2370. doi:10.1242/jeb.098426
    OpenUrlAbstract/FREE Full Text
  22. ↵
    1. Reinhardt, L. and
    2. Blickhan, R.
    (2014b). Ultra-miniature force plate for measuring triaxial forces in the micronewton range. J. Exp. Biol. 217, 704-710. doi:10.1242/jeb.094177
    OpenUrlAbstract/FREE Full Text
  23. ↵
    1. Ridgel, A. L.,
    2. Frazier, S. F.,
    3. DiCaprio, R. A. and
    4. Zill, S. N.
    (2000). Encoding of forces by cockroach tibial campaniform sensilla: implications in dynamic control of posture and locomotion. J. Comp. Physiol. A 186, 359-374. doi:10.1007/s003590050436
    OpenUrlCrossRefPubMed
  24. ↵
    1. Schmitz, J.
    (1993). Load-compensating reactions in the proximal leg joints of stick insects during standing and walking. J. Exp. Biol. 183, 15-33.
    OpenUrlAbstract/FREE Full Text
  25. ↵
    1. Seidl, T. and
    2. Wehner, R.
    (2008). Walking on inclines: how do desert ants monitor slope and step length. Front. Zool. 5, 1-15. doi:10.1186/1742-9994-5-8
    OpenUrlCrossRefPubMed
  26. ↵
    1. Wahl, V.,
    2. Pfeffer, S. E. and
    3. Wittlinger, M.
    (2015). Walking and running in the desert ant Cataglyphis fortis. J. Comp. Physiol. A 201, 645-656. doi:10.1007/s00359-015-0999-2
    OpenUrlCrossRefPubMed
  27. ↵
    1. Weihmann, T. and
    2. Blickhan, R.
    (2009). Comparing inclined locomotion in a ground-living and a climbing ant species: sagittal plane kinematics. J. Comp. Physiol. A 195, 1011-1020. doi:10.1007/s00359-009-0475-y
    OpenUrlCrossRefPubMed
  28. ↵
    1. Went, F. W.
    (1968). The size of man. Am. Sci. 56, 400-413.
    OpenUrlPubMedWeb of Science
  29. ↵
    1. Wittlinger, M.,
    2. Wehner, R. and
    3. Wolf, H.
    (2006). The ant odometer: stepping on stilts and stumps. Science 312, 1965-1967. doi:10.1126/science.1126912
    OpenUrlAbstract/FREE Full Text
  30. ↵
    1. Wittlinger, M.,
    2. Wolf, H. and
    3. Wehner, R.
    (2007). Hair plate mechanoreceptors associated with body segments are not necessary for three-dimensional path integration in desert ants, Cataglyphis fortis. J. Exp. Biol. 210, 375-382. doi:10.1242/jeb.02674
    OpenUrlAbstract/FREE Full Text
  31. ↵
    1. Wöhrl, T.,
    2. Reinhardt, L. and
    3. Blickhan, R.
    (2017). Data from: Propulsion in hexapod locomotion: how do desert ants traverse slopes? Dryad Digital Repository. http://dx.doi.org/10.5061/dryad.j4594
  32. ↵
    1. Wohlfart, E.,
    2. Wolff, J. O.,
    3. Arzt, E. and
    4. Gorb, S. N.
    (2014). The whole is more than the sum of all its parts: collective effect of spider attachment organs. J. Exp. Biol. 217, 222-224. doi:10.1242/jeb.093468
    OpenUrlAbstract/FREE Full Text
  33. ↵
    1. Wohlgemuth, S.,
    2. Ronacher, B. and
    3. Wehner, R.
    (2001). Ant odometry in the third dimension. Nature 411, 795-798. doi:10.1038/35081069
    OpenUrlCrossRefPubMed
  34. ↵
    1. Yanoviak, S. P.,
    2. Dudley, R. and
    3. Kaspari, M.
    (2005). Directed aerial descent in canopy ants. Nature 433, 624-626. doi:10.1038/nature03254
    OpenUrlCrossRefPubMedWeb of Science
  35. ↵
    1. Zill, S. N. and
    2. Moran, D. T.
    (1981). The exoskeleton and insect proprioception. I. Responses of tibial campaniform sensilla to external and muscle-generated forces in the American cockroach, Periplaneta americana. J. Exp. Biol. 91, 1-24.
    OpenUrlAbstract/FREE Full Text
  36. ↵
    1. Zill, S. N.,
    2. Chaudhry, S.,
    3. Büschges, A. and
    4. Schmitz, J.
    (2013). Directional specificity and encoding of muscle forces and loads by stick insect tibial campaniform sensilla, including receptors with round cuticular caps. Arthropod. Struct. Dev. 42, 455-467. doi:10.1016/j.asd.2013.10.001
    OpenUrlCrossRefPubMed
  37. ↵
    1. Zollikofer, C. P. E.
    (1994a). Stepping patterns in ants – influence of body morphology. J. Exp. Biol. 192, 107-118.
    OpenUrlAbstract/FREE Full Text
  38. ↵
    1. Zollikofer, C. P. E.
    (1994b). Stepping patterns in ants – influence of load. J. Exp. Biol. 192, 119-127.
    OpenUrlAbstract/FREE Full Text
  39. ↵
    1. Zollikofer, C. P. E.
    (1994c). Stepping patterns in ants – influence of speed and curvature. J. Exp. Biol. 192, 95-106.
    OpenUrlAbstract/FREE Full Text
View Abstract
Previous ArticleNext Article
Back to top
Previous ArticleNext Article

This Issue

Keywords

  • Alternating Tripod Gait
  • Attachment
  • Ground reaction force
  • Impulse
  • Navigation
  • Stability

 Download PDF

Email

Thank you for your interest in spreading the word on Journal of Experimental Biology.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Propulsion in hexapod locomotion: how do desert ants traverse slopes?
(Your Name) has sent you a message from Journal of Experimental Biology
(Your Name) thought you would like to see the Journal of Experimental Biology web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
Research Article
Propulsion in hexapod locomotion: how do desert ants traverse slopes?
Toni Wöhrl, Lars Reinhardt, Reinhard Blickhan
Journal of Experimental Biology 2017 220: 1618-1625; doi: 10.1242/jeb.137505
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
Citation Tools
Research Article
Propulsion in hexapod locomotion: how do desert ants traverse slopes?
Toni Wöhrl, Lars Reinhardt, Reinhard Blickhan
Journal of Experimental Biology 2017 220: 1618-1625; doi: 10.1242/jeb.137505

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Alerts

Please log in to add an alert for this article.

Sign in to email alerts with your email address

Article navigation

  • Top
  • Article
    • ABSTRACT
    • INTRODUCTION
    • MATERIALS AND METHODS
    • RESULTS
    • DISCUSSION
    • Acknowledgements
    • FOOTNOTES
    • References
  • Figures & tables
  • Info & metrics
  • PDF

Related articles

Cited by...

More in this TOC section

  • Early developmental stages of native populations of Ciona intestinalis under increased temperature are affected by local habitat history
  • Three auditory brainstem response (ABR) methods tested and compared in two anuran species
  • Differing thermal sensitivities of physiological processes alter ATP allocation
Show more RESEARCH ARTICLE

Similar articles

Subject collections

  • Comparative biomechanics of movement

Other journals from The Company of Biologists

Development

Journal of Cell Science

Disease Models & Mechanisms

Biology Open

Advertisement

Meet the Editors at SICB Virtual 2021

Reserve your place to join some of the journal editors, including Editor-in-Chief Craig Franklin, at our Meet the Editor session on 17 February at 2pm (EST). Don’t forget to view our SICB Subject Collection, featuring relevant JEB papers relating to some of the symposia sessions.


2020 at The Company of Biologists

Despite 2020's challenges, we were able to bring a number of long-term projects and new ventures to fruition. As we enter a new year, join us as we reflect on the triumphs of the last 12 months.


The Big Biology podcast

JEB author Christine Cooper talks to Big Biology about her research. In this fascinating JEB sponsored podcast she tells us how tough zebra finches adjust their physiology to cope with extreme climate events. 


Developmental and reproductive physiology of small mammals at high altitude

Cayleih Robertson and Kathryn Wilsterman focus on high-altitude populations of the North American deer mouse in their review of the challenges and evolutionary innovations of pregnant and nursing small mammals at high altitude.


Read & Publish participation extends worldwide

“Being able to publish Open Access articles free of charge means that my article gets maximum exposure and has maximum impact, and that all my peers can read it regardless of the agreements that their universities have with publishers.”

Professor Roi Holzman (Tel Aviv University) shares his experience of publishing Open Access as part of our growing Read & Publish initiative. We now have over 60 institutions in 12 countries taking part – find out more and view our full list of participating institutions.

Articles

  • Accepted manuscripts
  • Issue in progress
  • Latest complete issue
  • Issue archive
  • Archive by article type
  • Special issues
  • Subject collections
  • Interviews
  • Sign up for alerts

About us

  • About JEB
  • Editors and Board
  • Editor biographies
  • Travelling Fellowships
  • Grants and funding
  • Journal Meetings
  • Workshops
  • The Company of Biologists
  • Journal news

For Authors

  • Submit a manuscript
  • Aims and scope
  • Presubmission enquiries
  • Article types
  • Manuscript preparation
  • Cover suggestions
  • Editorial process
  • Promoting your paper
  • Open Access
  • Outstanding paper prize
  • Biology Open transfer

Journal Info

  • Journal policies
  • Rights and permissions
  • Media policies
  • Reviewer guide
  • Sign up for alerts

Contact

  • Contact JEB
  • Subscriptions
  • Advertising
  • Feedback

 Twitter   YouTube   LinkedIn

© 2021   The Company of Biologists Ltd   Registered Charity 277992