Net cost of transport by burrowing and metabolic rate measurements for a selection of mammalian fossorial and semifossorial species
. | Mass (g) . | . | NCOTb . | . | MR (ml O2 min−1) . | . | . | |||
---|---|---|---|---|---|---|---|---|---|---|
. | Burrowing . | Basal . | (kJ m−1) . | (J g−0.67 m−1) . | Burrowing . | Basal . | Reference . | |||
Heterocephalus glaber | 31.5 | 32.0 | 2.3 | 230 | 1.76 | 0.34 | 1, 2, 3 | |||
Notomys alexis* | 33.0 | 33.0 | 7.1 | 684 | 3.70 | 0.67 | This study | |||
Georychus capensis | 113.0 | 195.0 | 1.8 | 76 | 6.42 | 1.93 | 4, 5 | |||
Thomomys bottae | 150.0 | 143.0 | 6.4 | 224 | 10.3 | 2.00 | 6 | |||
Cryptomys damarensis | 152.1 | 138.0 | 2.0 | 68 | 7.68 | 1.31 | 3, 7, 8, 9 | |||
Octoaon degus* | 203.0 | 193.0 | 22.6 | 2.84 | 10, 11, 12 | |||||
Thomomys talpoides | 300.0 | 106.8 | 19.6 | 2.37 | 13, 14, 15 |
. | Mass (g) . | . | NCOTb . | . | MR (ml O2 min−1) . | . | . | |||
---|---|---|---|---|---|---|---|---|---|---|
. | Burrowing . | Basal . | (kJ m−1) . | (J g−0.67 m−1) . | Burrowing . | Basal . | Reference . | |||
Heterocephalus glaber | 31.5 | 32.0 | 2.3 | 230 | 1.76 | 0.34 | 1, 2, 3 | |||
Notomys alexis* | 33.0 | 33.0 | 7.1 | 684 | 3.70 | 0.67 | This study | |||
Georychus capensis | 113.0 | 195.0 | 1.8 | 76 | 6.42 | 1.93 | 4, 5 | |||
Thomomys bottae | 150.0 | 143.0 | 6.4 | 224 | 10.3 | 2.00 | 6 | |||
Cryptomys damarensis | 152.1 | 138.0 | 2.0 | 68 | 7.68 | 1.31 | 3, 7, 8, 9 | |||
Octoaon degus* | 203.0 | 193.0 | 22.6 | 2.84 | 10, 11, 12 | |||||
Thomomys talpoides | 300.0 | 106.8 | 19.6 | 2.37 | 13, 14, 15 |
NCOTb, net cost of transport by burrowing; MR, metabolic rate.
All digging measurements were obtained in damp sand or sandy loam. NCOTb data are presented as whole animal measurements (J m−1) and normalised to burrow cross-sectional area(∞Mb2/3)(Vleck, 1979).
References: 1 (McNab,1966); 2 (Withers and Jarvis,1980); 3 (Lovegrove,1989); 4 (Du Toit et al.,1985); 5 (Lovegrove,1987); 6 (Vleck,1979); 7 (Lovegrove,1986); 8 (Lovegrove,1988); 9 (Bennett et al.,1992); 10 (Bozinovic and Novoa,1997); 11 (Ebensperger and Bozinovic, 2000); 12 (Arends and McNab, 2001); 13 (Bradley et al., 1974); 14 (Gettinger,1975); 15 (Andersen and Macmahon, 1981).
Species are semi-fossorial, the remainder are fossorial.