Veles
Arachnobaron
- Joined
- Jul 20, 2017
- Messages
- 404
The frequency and availability of food matters quite a bit, to quote a study done by Benjamin N Philip's and Cara Shillington:It means supplying a near constant influx of food to increase growth, while increasing temps to maximize metabolism....but it applies to cold blooded animals, reptiles most specifically, as they have linear growth....ts do not....they grow much much differently.
Every t, regardless of size, has a certain amount of time needed before being physically ready to molt..only warmer temps can decrease this, and there is a point at which too warm past a certain point decreases the effect...as every t has its optimal temp for growth. Its much easier really to lengthen this time with cooler temps than to shorten it significantly with warmer temps.
So, for example... a 2" B. vagans may need 120 days minimum to be physically ready to molt. And that same t may need 20 crickets to be nutritionally plump and ready....when the nutritional needs are met first, it doesnt effect that 120 day period it physically needed, so it just fasts until that 120 days is met and the t can molt.
To maximize growth in ts, one merely needs to plump the t in conjunction with that necessary 120 day period (or whatever that period may be).
One could feed those 20 crickets in a month...its still going to need the next 90 to be physically ready to molt...so it just fasts for the next 3 months....yes, maximizing growth, but....
I could feed those 20 crickets one every 6 days and have it plumped in conjunction with that 120 days, still maximize growth and never deal with a significant fasting period....showing zero advantage to this percieved power feeding schedule.
This is even more dramatic with larger, slow growing species as they may molt once every 2 years or more..., so even needing more food than that 2 incher, its still wont need to be fed but once or twice a month over that time to maximize growth rates.
Now, growing a t faster will shorten a males life, but have little effect on female longevity....why is simple if you understand tarantula growth....
Males have a limited number of molts before maturing...usually 9-11....so get them through those molts quicker, or as fast as possible, means faster maturity, and shorter life.....females on tbe other hand, do not have a limited number of molts, so their maturity may come faster, but because molts arent limited, longevity is barely effected, if at all.
And the one done by H. L. Contreras and T. J. Bradley implies that metabolism can be fastened up via oxygen levels, increased oxygen levels alongside frequent feedings would keep high metabolic rates, high metabolic rate=faster development of an organism=faster moltingSpiders typically exhibit very low resting metabolic rates (RMR) and altered feeding behaviors as mechanisms to survive extended periods of limited food availability. We examined the effect of different periods of food deprivation on RMR and foraging activities in the Hispaniolan giant tarantula (Phormictopus cancerides (Latreille, 1806)) (Araneae: Theraphosidae). Juvenile tarantulas were separated into two feeding groups and fed once either every 5 or 30 days. Monthly feeding trials were preceded by RMR measurements. During feeding trials, we compared differences between the two groups in (i) prey capture frequency, (ii) time to prey capture, (iii) locomotory activity, and (iv) the predator’s prey detection distance. Metabolic rates increased for the well-fed group but remained constant for individuals fed once a month. Time to prey capture decreased for food-limited individuals and the proportion of individuals that ate during each feeding trial was significantly higher in the 30-day group. Conversely, results for locomotory activity and detection distances were inconclusive.
The majority of scientific papers on the subject of respiratory patterns in insects have dealt with the discontinuous gas-exchange cycle (DGC). The DGC is characterized by the release of bursts of CO2from the insect, followed by extended periods of spiracular closure. Several hypotheses have been put forward to explain the evolutionary origin and physiological function of this unusual respiratory pattern. We expand upon one of these (the oxidative damage hypothesis) to explain not only the occurrence of the DGC but also the mechanistic basis for the transition to two other well-characterized respiratory patterns: the cyclic pattern and the continuous pattern. We propose that the specific pattern employed by the insect at any given time is a function of the amount of oxygen contained in the insect at the time of spiracular closure and the aerobic metabolic rate of the insect. Examples of each type of pattern are shown using the insect Rhodnius prolixus. In addition, contrary to the expectations deriving from the hygric hypothesis, it is demonstrated that the DGC does not cease in Rhodnius in humid air.