Predictions & Data for this entry
Model: abp | climate: A, C, D | migrate: | phylum: |
COMPLETE = 3.5 | ecozone: TH, TPi | food: biCii | class: |
MRE = 0.302 | habitat: 0iTh, 0iTf, 0iTi, 0iTs, 0iTg | gender: D | order: |
SMSE = 0.110 | embryo: Th | reprod: O | family: |
Zero-variate data
Data | Observed | Predicted | (RE) | Unit | Description | Reference |
---|---|---|---|---|---|---|
ahT21 | 5 | 4.896 | (0.0208) | d | age at hatch | Sund1966 |
teT21 | 8.5 | 7.644 | (0.1007) | d | time since pupation at emergence | Sund1966 |
RiT21 | 12.52 | 20.04 | (0.6005) | #/d | maximum reprod rate | Sund1966 |
ahT25 | 2.42 | 3.165 | (0.3078) | d | age at hatch | OmkaSriv2003 |
t1T25 | 1.72 | 1.753 | (0.01938) | d | duration of instar 1 | OmkaSriv2003 |
t2T25 | 1.64 | 1.545 | (0.05789) | d | duration of instar 2 | OmkaSriv2003 |
t3T25 | 1.84 | 1.697 | (0.07761) | d | duration of instar 3 | OmkaSriv2003 |
t4T25 | 2.75 | 2.211 | (0.1959) | d | duration of instar 4 | OmkaSriv2003 |
teT25 | 3.55 | 4.941 | (0.3918) | d | time since pupation at emergence | OmkaSriv2003 |
tR125 | 8.2 | 6.625 | (0.1921) | d | pre-oviposition period | OmkaSriv2003 |
RiT25 | 25.27 | 31.01 | (0.2268) | #/d | maximum reprod rate | OmkaSriv2003 |
Ww1T25 | 0.00226 | 0.001841 | (0.1855) | g | wet weight of instar 1 | OmkaSriv2003 |
Ww2T25 | 0.00555 | 0.004417 | (0.2041) | g | wet weight of instar 2 | OmkaSriv2003 |
Ww3T25 | 0.01063 | 0.01088 | (0.02321) | g | wet weight of instar 3 | OmkaSriv2003 |
Ww4T25 | 0.01979 | 0.0338 | (0.7078) | g | wet weight of instar 4 | OmkaSriv2003 |
WwjT25 | 0.01505 | 0.05202 | (2.456) | g | wet weight of pupa | OmkaSriv2003 |
WweT25 | 0.04063 | 0.03344 | (0.177) | g | wet weight of female imago after emergence | OmkaSriv2003 |
ahT23 | 3.8 | 3.931 | (0.03435) | d | age at hatch | ObryOrr1990 |
t1T23 | 3.1 | 2.178 | (0.2976) | d | duration of instar 1 | ObryOrr1990 |
t2T23 | 2.2 | 1.919 | (0.1278) | d | duration of instar 2 | ObryOrr1990 |
t3T23 | 2.4 | 2.108 | (0.1217) | d | duration of instar 3 | ObryOrr1990 |
t4T23 | 5.4 | 2.746 | (0.4914) | d | duration of instar 4 | ObryOrr1990 |
teT23 | 6.3 | 6.136 | (0.02596) | d | time since pupation at emergence | ObryOrr1990 |
WweT23 | 0.0377 | 0.03344 | (0.1131) | g | wet weight of female imago after emergence | ObryOrr1990 |
L1eT23 | 0.765 | 0.7655 | (0.0007008) | cm | body length of female imago after emergence | ObryOrr1990 |
L2eT23 | 0.591 | 0.5711 | (0.03364) | cm | body width female imago after emergence | ObryOrr1990 |
ahT28 | 3 | 2.299 | (0.2337) | d | age at hatch | SingSing1993 |
t1T28 | 1.76 | 1.274 | (0.2763) | d | duration of instar 1 | SingSing1993 |
t2T28 | 1.8 | 1.122 | (0.3765) | d | duration of instar 2 | SingSing1993 |
t3T28 | 2.4 | 1.233 | (0.4863) | d | duration of instar 3 | SingSing1993 |
t4T28 | 3.15 | 1.606 | (0.4901) | d | duration of instar 4 | SingSing1993 |
teT28 | 6.68 | 3.589 | (0.4627) | d | time since pupation at emergence | SingSing1993 |
tR128 | 6.66 | 4.812 | (0.2774) | d | pre-oviposition period | SingSing1993 |
RiT28 | 47.62 | 42.69 | (0.1036) | #/d | maximum reprod rate | SingSing1993 |
aemT28 | 26.74 | 24.5 | (0.08395) | d | life span of female imago | SingSing1993 |
ahT24 | 3.56 | 3.526 | (0.009648) | d | age at hatch | FaroZhu2020 |
t1T24 | 2 | 1.953 | (0.02337) | d | duration of instar 1 | FaroZhu2020 |
t2T24 | 2 | 1.721 | (0.1394) | d | duration of instar 2 | FaroZhu2020 |
t3T24 | 2.47 | 1.891 | (0.2345) | d | duration of instar 3 | FaroZhu2020 |
t4T24 | 2.29 | 2.463 | (0.07575) | d | duration of instar 4 | FaroZhu2020 |
teT24 | 4.17 | 5.504 | (0.32) | d | time since pupation at emergence | FaroZhu2020 |
tR124 | 3.26 | 7.38 | (1.264) | d | pre-oviposition period | FaroZhu2020 |
RiT24 | 30.21 | 27.83 | (0.07864) | #/d | maximum reprod rate | FaroZhu2020 |
aemT24 | 48.16 | 37.57 | (0.22) | d | life span of female imago | FaroZhu2020 |
pA1T27 | 2.502e+04 | 1.858e+04 | (0.2574) | J/g.d | dry-weight-specific assimilation rate at instar 1 | Sing1976 |
pA2T27 | 2.983e+04 | 1.858e+04 | (0.3772) | J/g.d | dry-weight-specific assimilation rate at instar 2 | Sing1976 |
pA3T27 | 3.72e+04 | 1.858e+04 | (0.5005) | J/g.d | dry-weight-specific assimilation rate at instar 3 | Sing1976 |
pA4T27 | 3.732e+04 | 1.858e+04 | (0.5021) | J/g.d | dry-weight-specific assimilation rate at instar 4 | Sing1976 |
pAeT27 | 4.916e+04 | 3.496e+04 | (0.2888) | J/g.d | dry-weight-specific assimilation rate of imago | Sing1976 |
tjT25 | 8.9 | 7.207 | (0.1902) | d | time since hatch at pupation | KaluHode2004 |
WweT252 | 0.0388 | 0.03344 | (0.1382) | g | wet weight of female imago after emergence | KaluHode2004 |
Ww0 | 0.000187 | 0.001213 | (5.485) | g | initial wet weight of an egg | ChatNaz2020 |
Wwj | 0.0424 | 0.05202 | (0.2268) | g | wet weight of fresh pupa | Baye2024 |
Ww14d | 0.039 | 0.03344 | (0.1426) | g | wet weight of female imago after emergence (14 d old) | Baye2024 |
Ww21d | 0.0659 | 0.0692 | (0.05006) | g | wet weight of older female imago (21 d old) | Baye2024 |
L114d | 0.769 | 0.7655 | (0.004504) | cm | body length of female imago after emergence (14 d old) | Baye2024 |
L214d | 0.588 | 0.5711 | (0.02871) | cm | body width of female imago after emergence (14 d old) | Baye2024 |
Wwj2 | 0.0415 | 0.05202 | (0.2534) | g | wet weight of fresh pupa | Baye2024 |
Ww14d2 | 0.0359 | 0.03344 | (0.06861) | g | wet weight of female imago after emergence (14 d old) | Baye2024 |
Ww24d | 0.0658 | 0.0692 | (0.05166) | g | wet weight of older female imago (24 d old) | Baye2024 |
L114d2 | 0.72 | 0.7655 | (0.06324) | cm | body length of female imago after emergence (14 d old) | Baye2024 |
L214d2 | 0.552 | 0.5711 | (0.03463) | cm | body width of female imago after emergence (14 d old) | Baye2024 |
L124d | 0.756 | 0.7655 | (0.01261) | cm | body length of female imago after emergence (24 d old) | Baye2024 |
L224d | 0.555 | 0.5711 | (0.02904) | cm | body width of female imago after emergence (24 d old) | Baye2024 |
Uni- and bivariate data
Data | Figure | Independent variable | Dependent variable | (RE) | Reference |
---|---|---|---|---|---|
tWwB1 | ![]() ![]() | time since birth | wet weight | (0.2073) | Baye2024 |
tWwB2 | ![]() ![]() | time since birth | wet weight | (0.1294) | Baye2024 |
tWwf1 | ![]() ![]() | time since birth | wet weight | (0.2106) | Blac1967 |
tWwf2 | ![]() ![]() | time since birth | wet weight | (0.2125) | Blac1967 |
tWwf3 | ![]() ![]() | time since birth | wet weight | (0.1673) | Blac1967 |
tWwf4 | ![]() ![]() | time since birth | wet weight | (0.107) | Blac1967 |
tWwf5 | ![]() ![]() | time since birth | wet weight | (0.1304) | Blac1967 |
tWwf6 | ![]() ![]() | time since birth | wet weight | (0.157) | Blac1967 |
tL1 | ![]() ![]() | time since birth | larval length | (0.1034) | Baye2024 |
tL12 | ![]() ![]() | time since birth | larval length | (0.07806) | Baye2024 |
tL2 | ![]() ![]() | time since birth | larval width | (0.1742) | Baye2024 |
tL22 | ![]() ![]() | time since birth | larval width | (0.1156) | Baye2024 |
TRi | ![]() | temperature | maximum reprod rate | (0.6016) | XiaWerf1999 |
Tab | ![]() | temperature | age at hatch | (0.2031) | TrilFrei1996 |
Team | ![]() | temperature | mean imago life span | (0.3408) | XiaWerf1999 |
Tte | ![]() | temperature | pupal development time | (0.1537) | TrilFrei1996 |
Ttj | ![]() | temperature | larval development time | (0.3554) | TrilFrei1996 |
Pseudo-data at Tref = 20°C
Data | Generalised animal | Coccinella septempunctata | Unit | Description |
---|---|---|---|---|
v | 0.02 | 0.04927 | cm/d | energy conductance |
p_M | 18 | 47.83 | J/d.cm^3 | vol-spec som maint |
k_J | 0.002 | 0.002 | 1/d | maturity maint rate coefficient |
k | 0.3 | 0.184 | - | maintenance ratio |
kap | 0.8 | 0.7945 | - | allocation fraction to soma |
kap_G | 0.8 | 0.8083 | - | growth efficiency |
kap_R | 0.95 | 0.95 | - | reproduction efficiency |
Discussion
- For now, this entry focuses only on females
- It is assumed that energetic investment in the reproduction buffer takes place during the imago stage (synovigeny) because (a) imagos still feed on live prey, and (b) the wet weight of total reproductive output exceeds the adult female wet weight by a lot (making reproductive investment only during the larval phase implausible)
- Since ovary development takes place after emergence in the female imago, we assume an additional maturation phase after emergence
- Pupation is triggered by a maturity threshold at the end of the larval growth phase
- The phase from pupation until emergence is modeled analogous to the model variants hex and hax
- During the final maturation phase after emergence, the imago feeds, does not grow, and all energy not needed for maintenance goes to maturity
- Puberty is reached at the end of the final maturation phase after emergence
- At puberty the imago still feeds, and does not grow, and all energy not needed for maintenance goes to egg production (like in the abp model)
- Due to the above considerations, the model can be thought of as an extension of the abp model with an added pupa and a preoviposition phase
- Whenever studies reported the pre-pupa duration, here it was added to the pupa phase due to functional similarity (neither feeding nor growth take place)
- Not all developmental studies reported the pre-pupa duration, meaning that it was either included in the larval or the pupal duration; however since the pre-pupa phase was always very short, the resulting uncertainty is considered tolerable
Facts
- Development of ovaries takes place after emergence in the female imago (Ref: PhooObry1995)
- Imagos continue feeding on aphids (Ref: JalaReit2019)
Bibliography