Data

Arthropod Energy & Nutrients

Terrestrial Ecosystem Research Network
Potter, Tamara ; Stannard, Hayley ; Greenville, Aaron ; Dickman, Chris
Viewed: [[ro.stat.viewed]] Cited: [[ro.stat.cited]] Accessed: [[ro.stat.accessed]]
ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=info:doi10.4227/05/5ab9a8bfa60bd&rft.title=Arthropod Energy & Nutrients&rft.identifier=10.4227/05/5ab9a8bfa60bd&rft.publisher=Terrestrial Ecosystem Research Network&rft.description=The lesser hairy­footed dunnart (Sminthopsis youngsoni, Dasyuridae) is a generalist marsupial insectivore in arid Australia, but consumes wolf spiders (Lycosa spp., Lycosidae) disproportionately often relative to their availability. Here, we tested whether lycosids have relatively high energy or nutrient contents compared to other invertebrates, and hence whether these aspects of food quality can explain selective predation of lycosids by S.youngsoni. Energy, lipid and protein composition of representatives of 10 arthropod families that are eaten by S. youngsoni in the Simpson Desert were ascertained using microbomb calorimetry, chloroform-methanol extraction and Dumas combustion. Differences between invertebrate groups were assessed using separate analyses of variance (ANOVAs) and appropriate post-hoc tests. These analyses were performed using this data.Determining energy and nutrient content of arthropods : [1] Collection of invertebrates. Study specimens were collected at Main Camp, Ethabuka Reserve in the north-eastern Simpson Desert, Queensland during five field trips in April, July and October 2016, and May and October 2017. Specimens from several arthropod Orders Araneae (including Lycosidae), Blattodea, Coleoptera, Orthoptera, and Scorpiones were collected from the Main Camp site for compositional analysis. Only arthropods known to be eaten by dunnarts were sampled. Arthropods were live-captured in vertebrate pitfall traps set on 16 permanent trapping grids, or through opportunistic diurnal searches to capture grasshoppers and katydids (Caelifera and Tettigoniidae, respectively), using a hat as a net. Hand-sampling was also undertaken over several nights covering an area of ~3 ha around Main Camp, using a spotlight (Fenix TK35) to locate eyeshine, and capture nocturnal arthropods such as arachnids (Lycosidae, Miturgidae). Captured arthropods were immediately placed into individual plastic vials or snap-lock bags to minimise water loss. [2] Preparation for energy and nutrient analyses Given the absence of any detailed identification key for Simpson Desert arthropods, collected specimens were identified to Order or Family (Coleoptera and Araneae). As lycosids were the focus of the study, two distinct morphospecies were also identified based on size (leg-span) and colouration. At the University of Sydney specimens were weighed to an accuracy of 0.0001 g before being dried for 72 h in an oven set to 60 C. Following this, they were weighed a final time before being ground into a powder using a mortar and pestle to get samples as homogeneous as possible. [3] Determining energy content A Phillipson Oxygen Microbomb Calorimeter was used to determine energy content of arthropods. Calorimetric assays require pellets weighing 0.01-0.02 g, so ~0.015 g (mean SE; 0.016 0.0003 g) of dried sample was combusted in 100 % oxygen. This process was repeated twice per sample and averaged for increased accuracy. A benzoic ash standard was used to calibrate the calorimeter every 10th sample and, after combustion, pellets were re-weighed to obtain the ash content and the known energy density of benzoic acid (i.e., 26.393 kJ g-1), was used to calculate the energy content of each arthropod sample in kJ per gram. [4] Nutrient content Total lipids were extracted using a chloroform-methanol-water (1:1:1, by volume) mixture. In summary, this method involved homogenising the tissue in the chloroform-methanol-water mixture before centrifuging and separating the resulting pellet. This process was repeated a second time and the lower chloroform phase was left to evaporate over 24-72 h before being re-weighed. Total lipid content was calculated gravimetrically as the difference in mass before and after the extraction method was applied. This process was repeated three times for each sample, and these triplicates were averaged to obtain a single value per sample.Total arthropod protein content was ascertained via the Dumas combustion technique using a LECO FP628 machine. Samples weighing 0.2 g were placed in the analyser and combusted to produce carcass nitrogen content. Crude protein was then calculated by multiplying the nitrogen value by a standard factor of 6.25.Progress Code: completedMaintenance and Update Frequency: notPlanned&rft.creator=Potter, Tamara &rft.creator=Stannard, Hayley &rft.creator=Greenville, Aaron &rft.creator=Dickman, Chris &rft.date=2018&rft.edition=1&rft.coverage=The study was undertaken around Main Camp site on Ethabuka Reserve, north-western Simpson Desert, Queensland. IBRA region: Simpson Desert (Simpson Strzelecki Dunefields)&rft.coverage=northlimit=-23.54228; southlimit=-23.74104; westlimit=138.40768; eastLimit=138.75649; projection=EPSG:3577&rft_rights=Creative Commons Attribution 4.0 International Licence http://creativecommons.org/licenses/by/4.0&rft_rights=TERN services are provided on an as-is and as available basis. Users use any TERN services at their discretion and risk. They will be solely responsible for any damage or loss whatsoever that results from such use including use of any data obtained through TERN and any analysis performed using the TERN infrastructure. <br />Web links to and from external, third party websites should not be construed as implying any relationships with and/or endorsement of the external site or its content by TERN. <br /><br />Please advise any work or publications that use this data via the online form at https://www.tern.org.au/research-publications/#reporting&rft_rights=Please cite this dataset as {Author} ({PublicationYear}). {Title}. {Version, as appropriate}. Terrestrial Ecosystem Research Network. Dataset. {Identifier}.&rft_rights=(C)2018 University of Sydney. Rights owned by University of Sydney.&rft_subject=biota&rft_subject=CONSUMER BEHAVIOR&rft_subject=EARTH SCIENCE&rft_subject=HUMAN DIMENSIONS&rft_subject=SOCIAL BEHAVIOR&rft_subject=ARTHROPODS&rft_subject=BIOLOGICAL CLASSIFICATION&rft_subject=ANIMALS/INVERTEBRATES&rft_subject=SPECIES PREDATION&rft_subject=BIOSPHERE&rft_subject=ECOLOGICAL DYNAMICS&rft_subject=SPECIES/POPULATION INTERACTIONS&rft_subject=Behavioural Ecology&rft_subject=BIOLOGICAL SCIENCES&rft_subject=ECOLOGY&rft_subject=Terrestrial Ecology&rft_subject=Conservation and Biodiversity&rft_subject=ENVIRONMENTAL SCIENCES&rft_subject=ENVIRONMENTAL SCIENCE AND MANAGEMENT&rft_subject=field species name (Unitless)&rft_subject=Unitless&rft_subject=1 km - < 10 km or approximately .01 degree - < .09 degree&rft_subject=biannual&rft_subject=Lycosa&rft_subject=Sminthopsis_youngsoni&rft_subject=Arid ecology&rft_subject=Behavioural Ecology&rft_subject=Molecular Ecology&rft_subject=Predator-Prey Interactions&rft.type=dataset&rft.language=English Access the data

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TERN services are provided on an "as-is" and "as available" basis. Users use any TERN services at their discretion and risk. They will be solely responsible for any damage or loss whatsoever that results from such use including use of any data obtained through TERN and any analysis performed using the TERN infrastructure.
Web links to and from external, third party websites should not be construed as implying any relationships with and/or endorsement of the external site or its content by TERN.

Please advise any work or publications that use this data via the online form at https://www.tern.org.au/research-publications/#reporting

Please cite this dataset as {Author} ({PublicationYear}). {Title}. {Version, as appropriate}. Terrestrial Ecosystem Research Network. Dataset. {Identifier}.

(C)2018 University of Sydney. Rights owned by University of Sydney.

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Brief description

The lesser hairy­footed dunnart (Sminthopsis youngsoni, Dasyuridae) is a generalist marsupial insectivore in arid Australia, but consumes wolf spiders (Lycosa spp., Lycosidae) disproportionately often relative to their availability. Here, we tested whether lycosids have relatively high energy or nutrient contents compared to other invertebrates, and hence whether these aspects of food quality can explain selective predation of lycosids by S.youngsoni. Energy, lipid and protein composition of representatives of 10 arthropod families that are eaten by S. youngsoni in the Simpson Desert were ascertained using microbomb calorimetry, chloroform-methanol extraction and Dumas combustion. Differences between invertebrate groups were assessed using separate analyses of variance (ANOVAs) and appropriate post-hoc tests. These analyses were performed using this data.

Lineage

Determining energy and nutrient content of arthropods : [1] Collection of invertebrates. Study specimens were collected at Main Camp, Ethabuka Reserve in the north-eastern Simpson Desert, Queensland during five field trips in April, July and October 2016, and May and October 2017. Specimens from several arthropod Orders Araneae (including Lycosidae), Blattodea, Coleoptera, Orthoptera, and Scorpiones were collected from the Main Camp site for compositional analysis. Only arthropods known to be eaten by dunnarts were sampled. Arthropods were live-captured in vertebrate pitfall traps set on 16 permanent trapping grids, or through opportunistic diurnal searches to capture grasshoppers and katydids (Caelifera and Tettigoniidae, respectively), using a hat as a net. Hand-sampling was also undertaken over several nights covering an area of ~3 ha around Main Camp, using a spotlight (Fenix TK35) to locate eyeshine, and capture nocturnal arthropods such as arachnids (Lycosidae, Miturgidae). Captured arthropods were immediately placed into individual plastic vials or snap-lock bags to minimise water loss. [2] Preparation for energy and nutrient analyses Given the absence of any detailed identification key for Simpson Desert arthropods, collected specimens were identified to Order or Family (Coleoptera and Araneae). As lycosids were the focus of the study, two distinct morphospecies were also identified based on size (leg-span) and colouration. At the University of Sydney specimens were weighed to an accuracy of 0.0001 g before being dried for 72 h in an oven set to 60 C. Following this, they were weighed a final time before being ground into a powder using a mortar and pestle to get samples as homogeneous as possible. [3] Determining energy content A Phillipson Oxygen Microbomb Calorimeter was used to determine energy content of arthropods. Calorimetric assays require pellets weighing 0.01-0.02 g, so ~0.015 g (mean SE; 0.016 0.0003 g) of dried sample was combusted in 100 % oxygen. This process was repeated twice per sample and averaged for increased accuracy. A benzoic ash standard was used to calibrate the calorimeter every 10th sample and, after combustion, pellets were re-weighed to obtain the ash content and the known energy density of benzoic acid (i.e., 26.393 kJ g-1), was used to calculate the energy content of each arthropod sample in kJ per gram. [4] Nutrient content Total lipids were extracted using a chloroform-methanol-water (1:1:1, by volume) mixture. In summary, this method involved homogenising the tissue in the chloroform-methanol-water mixture before centrifuging and separating the resulting pellet. This process was repeated a second time and the lower chloroform phase was left to evaporate over 24-72 h before being re-weighed. Total lipid content was calculated gravimetrically as the difference in mass before and after the extraction method was applied. This process was repeated three times for each sample, and these triplicates were averaged to obtain a single value per sample.Total arthropod protein content was ascertained via the Dumas combustion technique using a LECO FP628 machine. Samples weighing 0.2 g were placed in the analyser and combusted to produce carcass nitrogen content. Crude protein was then calculated by multiplying the nitrogen value by a standard factor of 6.25.

Progress Code: completed
Maintenance and Update Frequency: notPlanned

Notes

Credit
We at TERN acknowledge the Traditional Owners and Custodians throughout Australia, New Zealand and all nations. We honour their profound connections to land, water, biodiversity and culture and pay our respects to their Elders past, present and emerging.
Purpose
The lesser hairy­footed dunnart (Sminthopsis youngsoni) is a common generalist insectivore in arid Australia that consumes wolf spiders (Lycosa spp.) disproportionately often relative to their availability. This study aimed to uncover the underlying mechanisms that drive this observed pattern of selective predation.

Created: 2016-04-16

Issued: 2018-03-27

Modified: 2024-05-12

Data time period: 2016-04-16 to 2017-10-30

This dataset is part of a larger collection

Click to explore relationships graph

138.75649,-23.54228 138.75649,-23.74104 138.40768,-23.74104 138.40768,-23.54228 138.75649,-23.54228

138.582085,-23.64166

text: The study was undertaken around Main Camp site on Ethabuka Reserve, north-western Simpson Desert, Queensland. IBRA region: Simpson Desert (Simpson Strzelecki Dunefields)