The free-living nematode Caenorhabditis elegans
is the predominant model organism in biological research, being used by a huge number of laboratories worldwide. Many researchers have evaluated life-history traits of C. elegans
in investigations covering quite different aspects such as ecotoxicology, inbreeding depression and heterosis, dietary restriction/supplement, mutations, and ageing. Such traits include juvenile growth rates, age at sexual maturity, adult body size, age-specific fecundity/mortality, total reproduction, mean and maximum lifespan, and intrinsic population growth rates. However, we found that in life-cycle experiments care is needed regarding protocol design. Here, we test a recently developed method that overcomes some problems associated with traditional cultivation techniques. In this fast and yet precise approach, single individuals are maintained within hanging drops of semi-fluid culture medium, allowing the simultaneous investigation of various life-history traits at any desired degree of accuracy. Here, the life cycles of wild-type C. elegans
strains N2 (Bristol, UK) and MY6 (Münster, Germany) were compared at 20°C with 5 × 109Escherichia coli
as food source.
High-resolution life tables and fecundity schedules of the two strains are presented. Though isolated 700 km and 60 years apart from each other, the two strains barely differed in life-cycle parameters. For strain N2 (n = 69), the intrinsic rate of natural increase (rm
), calculated according to the Lotka equation, was 1.375, the net reproductive rate (R0
) 291, the mean generation time (T) 90 h, and the minimum generation time (Tmin
) 73.0 h. The corresponding values for strain MY6 (n = 72) were rm
= 1.460, R0
= 289, T = 84 h, and Tmin
= 67.3 h. Peak egg-laying rates in both strains exceeded 140 eggs d-1
. Juvenile and early adulthood mortality was negligible. Strain N2 lived, on average, for 16.7 d, while strain MY6 died 2 days earlier; however, differences in survivorship curves were statistically non-significant.
We found no evidence that adaptation to the laboratory altered the life history traits of C. elegans
strain N2. Our results, discussed in the light of earlier studies on C. elegans
, demonstrate certain advantages of the hanging drop method in investigations of nematode life cycles. Assuming that its reproducibility is validated in further studies, the method will reduce the inter-laboratory variability of life-history estimates and may ultimately prove to be more convenient than the current standard methods used by C. elegans