Predictions & Data for this entry
|ab|| 4 ||3.669 ||(0.08263)||d||age at birth||HarvHarv1994|
|tj|| 5 ||5.123 ||(0.02461)||d||time since birth at pupation||HarvHarv1994|
|te|| 10 ||11.66 ||(0.1656)||d||time since pupation at emergence||HarvHarv1994|
|am||36.5 ||36.3 ||(0.005465)||d||life span as imago||HarvHarv1994|
|Wd0||1.87e-07 ||1.877e-07 ||(0.003585)||g||initial eggs dry weight||HarvHarv1994|
|Wdb||6.9e-05 ||6.956e-05 ||(0.008131)||g||dry weight at hatch||HarvHarv1994|
|Wdj||0.00477 ||0.004451 ||(0.06689)||g||dry weight at pupation||HarvHarv1994|
|Wde||0.00175 ||0.002491 ||(0.4236)||g||dry weight at emergence||HarvHarv1994|
|Uni-variate data |
|Dataset||Figure||(RE)||Independent variable||Dependent variable||Reference|
|tWd ||see Fig. 1 ||(0.2628)||time since hatch||larva dry weight||HarvHarv1994|
|tWdj ||see Fig. 2 ||(0.1132)||time since pupation||pupa dry weight||HarvHarv1994|
|tN ||see Fig. 3 ||(0.02629)||time since emergence||cum # of eggs||HarvHarv1994|
| Pseudo-data at Tref|
|Data||Generalised animal||Venturia canescens||Unit||Description|
|v ||0.02 ||0.04624||cm/d||energy conductance|
|kap ||0.8 ||0.6646||-||allocation fraction to soma|
|kap_R ||0.95 ||0.04195||-||reproduction efficiency|
|p_M || 18 ||19.79||J/d.cm^3||vol-spec som maint|
|k_J ||0.002 ||0.002||1/d||maturity maint rate coefficient|
|kap_G ||0.8 ||0.7731||-||growth efficiency|
V. canescens is a koinobiont parasitoid wasp, i.e. allows its host to continue development after parasitism. (ref: HarvHarv1994)
It has hydrophic eggs, meaning that they take up nutrients in the embryo-stage. (ref: HarvHarv1994)
This species does not host-feed, so host access is just for oviposition. (ref: HarvHarv1994)
This entry is discussed in LlanMarq2015 (ref: LlanMarq2015)
Hydrophic egg is modelled as a new maturity level E_Hx, which preceeds birth
E_Hx is treated as birth, while at E_Hb uptake switches from absorbtion to feeding
All parasitoid data is from host (moth Plodia interpunctella) that was infected at instar 5
Assimilation by imago is assumed to cover maintenance costs
J. A. Harvey, I. F. Harvey, and D. J. Thompson.
Flexible larval growth allows use of a range of host sizes by a
Ecology, 75:1420--1428, 1994.
Dynamic Energy Budget theory for metabolic organisation.
Cambridge Univ. Press, Cambridge, 2010.
A. L. Llandres, G. M. Marques, J. Maino, S. A. L. M. Kooijman, M. R. Kearney,
and J. Casas.
A dynamic energy budget for the whole life-cycle of holometabolous
Ecological Monographs, 85:353--371, 2015.
Bibtex file with references for this entry
Ana Lopez Llandres, Bas Kooijman, 2013/07/18 (last modified by Bas Kooijman
refer to this entry as: AmP Venturia canescens version 2016/03/18 bio.vu.nl/thb/deb/deblab/add_my_pet/