scholarly journals Time‐lapse camera trapping as an alternative to pitfall trapping for estimating activity of leaf litter arthropods

2017 ◽  
Vol 7 (18) ◽  
pp. 7527-7533 ◽  
Author(s):  
Rachael A. Collett ◽  
Diana O. Fisher
Keyword(s):  
Leaf Litter ◽  
Time Lapse ◽  
Camera Trapping ◽  
Pitfall Trapping

Pits or pictures: a comparative study of camera traps and pitfall trapping to survey small mammals and reptiles

2019 ◽  
Vol 46 (2) ◽  
pp. 104 ◽  
Author(s):  
Shannon J. Dundas ◽  
Katinka X. Ruthrof ◽  
Giles E. St.J. Hardy ◽  
Patricia A. Fleming
Keyword(s):  
Community Composition ◽  
Small Mammals ◽  
Survey Methods ◽  
Infrared Camera ◽  
Camera Traps ◽  
Camera Trapping ◽  
Survey Method ◽  
Pitfall Traps ◽  
Pitfall Trapping ◽  
Trapping Methods

Context Camera trapping is a widely used monitoring tool for a broad range of species across most habitat types. Camera trapping has some major advantages over other trapping methods, such as pitfall traps, because cameras can be left in the field for extended periods of time. However, there is still a need to compare traditional trapping methods with newer techniques. Aims To compare trap rates, species richness and community composition of small mammals and reptiles by using passive, unbaited camera traps and pitfall traps. Methods We directly compared pitfall trapping (20-L buried buckets) with downward-facing infrared-camera traps (Reconyx) to survey small reptiles and mammals at 16 sites within a forested habitat in south-western Australia. We compared species captured using each method, as well as the costs associated with each. Key results Overall, we recorded 228 reptiles, 16 mammals and 1 frog across 640 pitfall trap-nights (38.3 animal captures per 100 trap-nights) compared to 271 reptiles and 265 mammals (for species likely to be captured in pitfall traps) across 2572 camera trap nights (20.8 animal captures per 100 trap-nights). When trap effort is taken into account, camera trapping was only 23% as efficient as pitfall trapping for small reptiles (mostly Scincidae), but was five times more efficient for surveying small mammals (Dasyuridae). Comparing only those species that were likely to be captured in pitfall traps, 13 species were recorded by camera trapping compared with 20 species recorded from pitfall trapping; however, we found significant (P<0.001) differences in community composition between the methods. In terms of cost efficacy, camera trapping was the more expensive method for our short, 4-month survey when taking the cost of cameras into consideration. Conclusions Applicability of camera trapping is dependent on the specific aims of the intended research. Camera trapping is beneficial where community responses to ecosystem disturbance are being tested. Live capture of small reptiles via pitfall trapping allows for positive species identification, morphological assessment, and collection of reference photos to help identify species from camera photos. Implications As stand-alone techniques, both survey methods under-represent the available species present in a region. The use of more than one survey method improves the scope of fauna community assessments.

Ecology and conservation of the northern hopping-mouse (Notomys aquilo)

2016 ◽  
Vol 64 (1) ◽  
pp. 21 ◽  
Author(s):  
Rebecca L. Diete ◽  
Paul D. Meek ◽  
Christopher R. Dickman ◽  
Luke K.-P. Leung
Keyword(s):  
Conservation Status ◽  
Species Conservation ◽  
Camera Traps ◽  
Camera Trapping ◽  
Home Ranges ◽  
Pitfall Trapping ◽  
Sandy Substrate ◽  
Live Trapping ◽  
Eucalypt Woodland ◽  
Abundance And Distribution

The northern hopping-mouse (Notomys aquilo) is a cryptic and enigmatic rodent endemic to Australia’s monsoonal tropics. Focusing on the insular population on Groote Eylandt, Northern Territory, we present the first study to successfully use live traps, camera traps and radio-tracking to document the ecology of N. aquilo. Searches for signs of the species, camera trapping, pitfall trapping and spotlighting were conducted across the island during 2012–15. These methods detected the species in three of the 32 locations surveyed. Pitfall traps captured 39 individuals over 7917 trap-nights. Females were significantly longer and heavier, and had better body condition, than males. Breeding occurred throughout the year; however, the greatest influx of juveniles into the population occurred early in the dry season in June and July. Nine individuals radio-tracked in woodland habitat utilised discrete home ranges of 0.39–23.95 ha. All individuals used open microhabitat proportionally more than was available, and there was a strong preference for eucalypt woodland on sandy substrate rather than for adjacent sandstone woodland or acacia shrubland. Camera trapping was more effective than live trapping at estimating abundance and, with the lower effort required to employ this technique, it is recommended for future sampling of the species. Groote Eylandt possibly contains the last populations of N. aquilo, but even there its abundance and distribution have decreased dramatically in surveys over the last several decades. Therefore, we recommend that the species’ conservation status under the Environment Protection and Biodiversity Conservation Act 1999 be changed from ‘vulnerable’ to ‘endangered’.

scholarly journals Improving Terrestrial Squamate Surveys with Camera-Trap Programming and Hardware Modifications

Animals ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 388 ◽  
Author(s):  
D. J. Welbourne ◽  
A. W. Claridge ◽  
D. J. Paull ◽  
F. Ford
Keyword(s):  
Focal Length ◽  
Time Lapse ◽  
Camera Trap ◽  
Camera Traps ◽  
Camera Trapping ◽  
Infrared Sensor ◽  
Vertebrate Fauna ◽  
The World ◽  
Lens Focal Length

Camera-traps are used widely around the world to census a range of vertebrate fauna, particularly mammals but also other groups including birds, as well as snakes and lizards (squamates). In an attempt to improve the reliability of camera-traps for censusing squamates, we examined whether programming options involving time lapse capture of images increased detections. This was compared to detections by camera-traps set to trigger by the standard passive infrared sensor setting (PIR), and camera-traps set to take images using time lapse in combination with PIR. We also examined the effect of camera trap focal length on the ability to tell different species of small squamate apart. In a series of side-by-side field comparisons, camera-traps programmed to take images at standard intervals, as well as through routine triggering of the PIR, captured more images of squamates than camera-traps using the PIR sensor setting alone or time lapse alone. Similarly, camera traps with their lens focal length set at closer distances improved our ability to discriminate species of small squamates. With these minor alterations to camera-trap programming and hardware, the quantity and quality of squamate detections was markedly better. These gains provide a platform for exploring other aspects of camera-trapping for squamates that might to lead to even greater survey advances, bridging the gap in knowledge of this otherwise poorly known faunal group.

Estimating macropod grazing density and defining activity patterns using camera-trap image analysis

2018 ◽  
Vol 45 (8) ◽  
pp. 706 ◽  
Author(s):  
Helen R. Morgan ◽  
Guy Ballard ◽  
Peter J. S. Fleming ◽  
Nick Reid ◽  
Remy Van der Ven ◽  
...  
Keyword(s):  
Vegetation Change ◽  
Activity Patterns ◽  
Time Lapse ◽  
Camera Trap ◽  
Camera Traps ◽  
Camera Trapping ◽  
Absolute Abundance ◽  
Deposition Rates ◽  
Pellet Counts ◽  
Density Methods

Context When measuring grazing impacts of vertebrates, the density of animals and time spent foraging are important. Traditionally, dung pellet counts are used to index macropod grazing density, and a direct relationship between herbivore density and foraging impact is assumed. However, rarely are pellet deposition rates measured or compared with camera-trap indices. Aims The aims were to pilot an efficient and reliable camera-trapping method for monitoring macropod grazing density and activity patterns, and to contrast pellet counts with macropod counts from camera trapping, for estimating macropod grazing density. Methods Camera traps were deployed on stratified plots in a fenced enclosure containing a captive macropod population and the experiment was repeated in the same season in the following year after population reduction. Camera-based macropod counts were compared with pellet counts and pellet deposition rates were estimated using both datasets. Macropod frequency was estimated, activity patterns developed, and the variability between resting and grazing plots and the two estimates of macropod density was investigated. Key Results Camera-trap grazing density indices initially correlated well with pellet count indices (r2=0.86), but were less reliable between years. Site stratification enabled a significant relationship to be identified between camera-trap counts and pellet counts in grazing plots. Camera-trap indices were consistent for estimating grazing density in both surveys but were not useful for estimating absolute abundance in this study. Conclusions Camera trapping was efficient and reliable for estimating macropod activity patterns. Although significant, the relationship between pellet count indices and macropod grazing density based on camera-trapping indices was not strong; this was due to variability in macropod pellet deposition rates over different years. Time-lapse camera imagery has potential for simultaneously assessing herbivore foraging activity budgets with grazing densities and vegetation change. Further work is required to refine the use of camera-trapping indices for estimation of absolute abundance. Implications Time-lapse camera trapping and site-stratified sampling allow concurrent assessment of grazing density and grazing behaviour at plot and landscape scale.

Artificial water ponds and camera trapping of tortoises, and other vertebrates, in a dry Mediterranean landscape

2016 ◽  
Vol 43 (7) ◽  
pp. 533 ◽  
Author(s):  
J.-M. Ballouard ◽  
X. Bonnet ◽  
C. Gravier ◽  
M. Ausanneau ◽  
S. Caron
Keyword(s):  
Low Cost ◽  
Cost Effective ◽  
Time Lapse ◽  
Camera Trapping ◽  
Mediterranean Landscape ◽  
Mediterranean Habitats ◽  
Freshwater Ponds ◽  
Large Numbers ◽  
Hot Environments ◽  
Lapse Function

Context Mediterranean areas offer a mosaic of favourable microhabitats to reptiles (e.g. open zones, thorny bushes) and are considered as biodiversity hotspots for these organisms. However, in these dry and hot environments, reptiles remain sheltered most of the time. They generally escape observation, posing difficulties to perform inventories. Trap sampling or rock-turning surveys commonly used to detect reptiles entail important logistical constraints, may perturb fragile microhabitats, and are not appropriate for chelonians. Alternative simple and cost-effective methods are desired. Aims We tested the efficiency of camera trapping in a dry Mediterranean landscape, notably to detect threatened Hermann’s tortoises. We tested whether small artificial freshwater ponds could attract animals in the field of view of the cameras to increase detectability. We also tested whether sand tracks survey around ponds could improve the method. Methods We used a small number of cameras with ponds (5 in 2011, 7 in 2012), thereby maintaining low logistical costs. We randomly filled three ponds and emptied three ponds every 7 days. We set the time-lapse function of each camera with an interval of 5 min and inspected the sand tracks every 2 or 3 days. We used information from 39 radio-tracked tortoises to better estimate the detectability performances of the camera–pond system. Key results This technique was effective to detect tortoises (n = 348 observations) and five other reptiles (among the 11 species present in the study area). Large numbers of birds and mammals were observed (n = 4232, n = 43 species at least), thereby increasing the biodiversity list of the surveyed area. We detected 28% of the radio-tracked tortoises present in the monitored area. Filled ponds were more attractive and sand track survey completed camera monitoring. Conclusions Camera trapping associated with small ponds represent a useful tool to perform rapid inventories of the fauna in Mediterranean habitats, especially to detect the emblematic Hermann’s tortoise and other cryptic reptiles (e.g. snakes). Implications The low cost–efficiency ratio of this method allows performing multiple counting surveys, and thus may help collect robust data necessary to justify the protection of key habitats that are coveted by property developers.

The Impact of Fire and Increasing Time After Fire Upon Heleioporus Eyrei, Limnodynastes Dorsalis and Myobatrachus Gouldii (Anura: Leptodactylidae) in Banksia Woodland Near Perth, Western Australia.

1992 ◽  
Vol 19 (2) ◽  
pp. 169 ◽  
Author(s):  
MJ Bamford
Keyword(s):  
Leaf Litter ◽  
Western Australia ◽  
Vegetation Density ◽  
Potential Prey ◽  
Pitfall Trapping ◽  
Burnt Areas ◽  
The Impact

Banksia woodland is a seasonally arid and fire-prone environment. Although a seemingly inhospitable environment for frogs, seven species were recorded in pitfall-trapping carried out in six areas of Banksia woodland near Perth from April 1983 to March 1986. These areas had different fire histories, ranging from recently burnt to unburnt for 23 years. One of the areas was burnt during the course of the study. Three species made up 95% of captures, viz. Heleioporus eyrei, Limnodynastes dorsalis and Myobatrachus gouldii. Annual numbers of captures of H. eyrei were not greatly affected by fire or increasing time after fire. L. dorsalis and, to a lesser extent, M. gouldii were caught in greater numbers in long-unburnt areas than in recently burnt areas. Variation in the abundance of L. dorsalis and M. gouldii with time after fire did not appear to be related to changes in leaf litter and vegetation density, or to the abundance of invertebrates as potential prey.

Ultrastructure of melanocyte-keratinocyte interactions and pigment transfer in vitro

1978 ◽  
Vol 36 (2) ◽  
pp. 650-651
Author(s):  
Raul I. Garcia ◽  
Evelyn A. Flynn ◽  
George Szabo
Keyword(s):  
Direct Injection ◽  
Skin Pigmentation ◽  
Freeze Fracture ◽  
Pigment Granule ◽  
Time Lapse ◽  
Ultrastructural Level ◽  
Lanthanum Tracer ◽  
A Cell

Skin pigmentation in mammals involves the interaction of epidermal melanocytes and keratinocytes in the structural and functional unit known as the Epidermal Melanin Unit. Melanocytes(M) synthesize melanin within specialized membrane-bound organelles, the melanosome or pigment granule. These are subsequently transferred by way of M dendrites to keratinocytes(K) by a mechanism still to be clearly defined. Three different, though not necessarily mutually exclusive, mechanisms of melanosome transfer have been proposed: cytophagocytosis by K of M dendrite tips containing melanosomes, direct injection of melanosomes into the K cytoplasm through a cell-to-cell pore or communicating channel formed by localized fusion of M and K cell membranes, release of melanosomes into the extracellular space(ECS) by exocytosis followed by K uptake using conventional phagocytosis. Variability in methods of transfer has been noted both in vivo and in vitro and there is evidence in support of each transfer mechanism. We Have previously studied M-K interactions in vitro using time-lapse cinemicrography and in vivo at the ultrastructural level using lanthanum tracer and freeze-fracture.

High-voltage Electron Microscopy of astroglial cell whole mounts

1986 ◽  
Vol 44 ◽  
pp. 316-317
Author(s):  
J.N. Turner ◽  
W.G. Shain ◽  
V. Madelian ◽  
R.A. Grassucci ◽  
D.L. Forman
Keyword(s):  
Electron Microscopy ◽  
High Voltage ◽  
Time Lapse ◽  
Astroglial Cells ◽  
High Voltage Electron Microscopy ◽  
Rat Glioma ◽  
Voltage Electron ◽  
High Voltage Electron ◽  
Nervous System Function ◽  
Beta Adrenergic Agonist

Homogeneous cultures of astroglial cells have proved useful for studying biochemical, pharmacological, and toxicological responses of astrocytes to effectors of central nervous system function. LRM 55 astroglial cells, which were derived from a rat glioma and maintained in continuous culture, exhibit a number of astrocyte properties (1-3). Stimulation of LRM 55s and astrocytes in primary cell cultures with the beta-adrenergic agonist isoproterenol results in rapid changes of morphology. Studies with time lapse video light microscopy (VLM) and high-voltage electron microscopy (HVEM) have been correlated to changes in intracellular levels of c-AMP. This report emphasizes the HVEM results.

Measurement of spontaneous neuronal membrane activity by time lapse confocal microscopy

1995 ◽  
Vol 53 ◽  
pp. 972-973
Author(s):  
R H. Selinfreund ◽  
A. H. Cornell-Bell
Keyword(s):  
Membrane Potential ◽  
Confocal Microscopy ◽  
Patch Clamp ◽  
Electrical Activity ◽  
Time Lapse ◽  
Neuronal Firing ◽  
Neuronal Membrane ◽  
Pituitary Cells ◽  
Patch Clamp Recording ◽  
Spontaneous Electrical Activity

Cellular electrophysiological properties are normally monitored by standard patch clamp techniques . The combination of membrane potential dyes with time-lapse laser confocal microscopy provides a more direct, least destructive rapid method for monitoring changes in neuronal electrical activity. Using membrane potential dyes we found that spontaneous action potential firing can be detected using time-lapse confocal microscopy. Initially, patch clamp recording techniques were used to verify spontaneous electrical activity in GH4\C1 pituitary cells. It was found that serum depleted cells had reduced spontaneous electrical activity. Brief exposure to the serum derived growth factor, IGF-1, reconstituted electrical activity. We have examined the possibility of developing a rapid fluorescent assay to measure neuronal activity using membrane potential dyes. This neuronal regeneration assay has been adapted to run on a confocal microscope. Quantitative fluorescence is then used to measure a compounds ability to regenerate neuronal firing.The membrane potential dye di-8-ANEPPS was selected for these experiments. Di-8- ANEPPS is internalized slowly, has a high signal to noise ratio (40:1), has a linear fluorescent response to change in voltage.

Five-Dimensional Microscopy using Widefield-Deconvolution: Practical Considerations and Biological Applications

1996 ◽  
Vol 54 ◽  
pp. 268-269
Author(s):  
W.F. Marshall ◽  
K. Oegema ◽  
J. Nunnari ◽  
A.F. Straight ◽  
D.A. Agard ◽  
...  
Keyword(s):  
Confocal Microscopy ◽  
High Speed ◽  
Laser Scanning ◽  
Ccd Camera ◽  
Image Plane ◽  
Time Lapse ◽  
Laser Scanning Confocal Microscopy ◽  
Three Dimensions ◽  
Excitation Light ◽  
Cooled Ccd

The ability to image cells in three dimensions has brought about a revolution in biological microscopy, enabling many questions to be asked which would be inaccessible without this capability. There are currently two major methods of three dimensional microscopy: laser-scanning confocal microscopy and widefield-deconvolution microscopy. The method of widefield-deconvolution uses a cooled CCD to acquire images from a standard widefield microscope, and then computationally removes out of focus blur. Using such a scheme, it is easy to acquire time-lapse 3D images of living cells without killing them, and to do so for multiple wavelengths (using computer-controlled filter wheels). Thus, it is now not only feasible, but routine, to perform five dimensional microscopy (three spatial dimensions, plus time, plus wavelength).Widefield-deconvolution has several advantages over confocal microscopy. The two main advantages are high speed of acquisition (because there is no scanning, a single optical section is acquired at a time by using a cooled CCD camera) and the use of low excitation light levels Excitation intensity can be much lower than in a confocal microscope for three reasons: 1) longer exposures can be taken since the entire 512x512 image plane is acquired in parallel, so that dwell time is not an issue, 2) the higher quantum efficiently of a CCD detect over those typically used in confocal microscopy (although this is expected to change due to advances in confocal detector technology), and 3) because no pinhole is used to reject light, a much larger fraction of the emitted light is collected. Thus we can typically acquire images with thousands of photons per pixel using a mercury lamp, instead of a laser, for illumination. The use of low excitation light is critical for living samples, and also reduces bleaching. The high speed of widefield microscopy is also essential for time-lapse 3D microscopy, since one must acquire images quickly enough to resolve interesting events.

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