Diesel & Sour Diesel... Chem... TRUE Lineage/Story

[reservationlabs]

would that mean a sister to Chemdog91 and Diesel, confused between F1 and S1, understand thinking without MSS genes.

That would mean that a cutting of '91 Chemdog hermied and pollenated itself thus producing seeds, those seeds were popped and thus OG Kush was born. Just my thoughts.

 

[MadBuddhaAbuser]

Hey guys, just a quick question from someone who doesn't know much about breeding.

What is the difference between the original strain, say Sour Diesel, and the backcrossed version of it like Sour Diesel IBL?

I've always wondered because it seems confusing to me. A strain that is backcrossed with it's own genetics (doesn't IBL mean "inbred backcross line"?) I would think would produce the same genetics. Can someone please help me clear up my confusion? There's gotta be something I'm missing...

Thanks a bunch!

Ernest

its the same "strain", but won't match the originalclone exactly, at least consistently. When referring to a specific clone, it is more of a "sport" representation of the "strain" itself. An accidental pollination of a room almost certainly produced more than 1 seed. But we are to believe to ECSD to have been the best.

IBL means "In-Bred Line"


a little breedin readin from Chimera-

you’ve just discovered the biggest myth (IMNSHO) of marijuana breeding- it is a mistake that almost EVERYONE makes (including many of the most respected breeders!).

Backcrossing will not stabilize a strain at all- it is a technique that SHOULD be used to reinforce or stabilize a particular trait, but not all of them.

For e.g.- G13 is a clone, which I would bet my life on is not true breeding for every, or even most traits- this means that it is heterozygous for these traits- it has two alleles (different versions of a gene). No matter how many times you backcross to it, it will always donate either of the two alleles to the offspring. This problem can be compounded by the fact that the original male used in the cross (in this case hashplant) may have donated a third allele to the pool- kinda makes things even more difficult!

So what does backcrossing do?
It creates a population that has a great deal of the same genes as the mother clone. From this population, if enough plants are grown, individuals can be chosen that have all the same traits as the mother, for use in creating offspring that are similar (the same maybe) as the original clone.
Another problem that can arise is this- there are three possibilities for the expression of a monogenic (controlled by one gene pair) trait.

We have dominant, recessive, and co-dominant conditions.

In the dominant condition, genotypically AA or Aa, the plants of these genotypes will look the same (will have the same phenotype, for that trait).

Recessive- aa will have a phenotype

Co-dominant- Aa- these plants will look different from the AA and the aa.

A perfect example of this is the AB blood types in humans:

Type A blood is either AA or AO
Type B blood is either BB or BO
Type AB blood is ONLY AB
Type O blood is OO.

In this case there are three alleles (notated A, B, and O respectively).

If the clone has a trait controlled by a co-dominant relationship- i.e. the clone is Aa (AB in the blood example) we will never have ALL plants showing the trait- here is why:

Suppose the clone mother is Aa- the simplest possibility is that the dad used contributes one of his alleles,
let us say A. That mean the boy being use for the first backcross is either AA or Aa. We therefore have two possibilities:

1) If he is AA- we have AA X Aa- 50% of the offspring are AA, 50% are Aa. (you can do the punnett square to prove this to yourself).

In this case only 50% of the offspring show the desired phenotype (Aa genotype)!

2) If the boy being used is Aa- we have Aa X Aa (again do the punnett square) this gives a typical F2 type segregation- 25% AA, 50% Aa, and 25% aa.
This shows that a co-dominant trait can ONLY have 50% of the offspring showing the desired trait (Aa genotype) in a backcross.

If the phenotype is controlled by a dominant condition- see example #1- all 100% show the desired phenotype, but only 50% will breed true for it.

If the phenotype is controlled by a recessive condition- see example #2- only 25% will show the desired phenotype, however if used for breeding these will all breed true if mated to another aa individual.

Now- if the original dad (hashplant) donates an 'a' allele, we only have the possibilities that the offspring, from which the backcross boy will be chosen, will be either Aa or aa.
For the Aa boy, see #2.
For the aa boy (an example of a test cross, aa X Aa) we will have:
50% aa offspring (desired phenotype), and 50% Aa offspring.

Do you see what is happening here? Using this method of crossing to an Aa clone mother, we can NEVER have ALL the offspring showing the desired phenotype! Never! Never ever ever! Never!! LOL

The ONLY WAY to have all the offspring show a Aa phenotype is to cross an AA individual with an aa individual- all of the offspring from this union will be the desired phenotype, with an Aa genotype.

Now, all of that was for a Aa genotype for the desired phenotype. It isn't this complicated if the trait is AA or aa. I hope this causes every one to re-evaluate the importance of multiple backcrosses- it just doesn't work to stabilize the trait!

Also- that was all for a monogenic trait! What if the trait is controlled by a polygenic interaction or an epistatic interaction- it gets EVEN MORE complicated? AARRGH!!!!

Really, there is no need to do more than 1 backcross. From this one single backcross, as long as we know what we are doing, and grow out enough plants to find the right genotypes, we can succeed at the goal of eventually stabilizing most, if not all of the desired traits.

The confusion arises because we don't think about the underlying biological causes of these situations- to really understand this; we all need to understand meiosis.

We think of math-e.g. 50% G13, 50% hashplant

Next generation 50% G13 x 50% g13hp or (25% G13, 25%HP)

We interpret this as an additive property:
50% G13 + 25% G13 +25% HP = 75% G13 and 25% hashplant

This is unfortunately completely false- the same theory will apply for the so called 87.%% G13 12.5% HP next generation, and the following 93.25% G13, 6.25% HP generation; we'd like it to be true as it would make stabilizing traits fairly simple, but it JUST DOESN'T work that way. The above is based on a mathematical model, which seems to make sense- but it doesn't- we ignore the biological foundation that is really at play.

I hope this was clear, I know it can get confusing, and I may not have explained it well enough- sorry if that is the case, I'll try to clear up any questions or mistakes I may have made.

Have fun everyone while making your truebreeding varieties, but just remember that cubing (successive backcrosses) is not the way to do it!

-Chimera

 

[CalcioErba2004]

Sorry so late,

Here is Apoth Chem 91 done by Natagonnaworrie:

I'm under the impression OG has nothing to do with Chem/Diesel. I have a cut that predates '91...

 

[Natagonnaworrie]

Stumbled over here and thought i'd throw up a few.

I love this garden. There is a light of the Apoth '91 Chem and light of legit ECSD.

SD


SD


Chem


Chem


i'm not saying anything but they do look similar and both are 100% legit

 

[KITCHA]

I've always thought ecsd and 91 have the small non serrated leaves in the buds, they look like little tongues, not many other strains have this.

 

[Forest20]

...I've always wondered because it seems confusing to me. A strain that is backcrossed with it's own genetics (doesn't IBL mean "inbred backcross line"?)...

From my understanding It meant.. Incomplete Breeding Line or (Rudimentary)

 

[JOJO420]

Sour Apple

Sour Apple

I have smoked a cross of the original Diesel crossed with AK47, it was fantastic,

I have something close,the SOUR Apple. I was told the Sour Apple is SourD x AK-47.. I have Sour Apple x Headband and Sour Apple x Purps..
https://www.icmag.com/modules/Journal/viewentry.php?journalid=1024

 

[Harpo]

I "personally" believe OG Kush to be a S1 of '91 Chemdog. But that is my thought.

I only get to play with seeds.

I grew out a pack of Orgnkid's S1 og kush back in 06. Frosty as hell. Finished bud structure, density and plant shape was very similar to Rez's Chemdog IBL. Although not as dense. No fuel smell or taste.

I have a couple questions to those of you lucky folks like Natagonnaworrie who can get clones of the real deal stuff.

What does the real deal OG kush smell and taste like? Is there a fuel smell or taste? Does it smell or taste anything like the real deal Chemdog?

 

[MilitantUK]

its the same "strain", but won't match the originalclone exactly, at least consistently. When referring to a specific clone, it is more of a "sport" representation of the "strain" itself. An accidental pollination of a room almost certainly produced more than 1 seed. But we are to believe to ECSD to have been the best.

IBL means "In-Bred Line"


a little breedin readin from Chimera-

heres the update from Chimera!

Wow that is painful for me to read.... I must have been pretty stoned when I wrote that, now years ago. I'm glad at least that it's info that has spread a little knowledge and perspective into the community over the years.. I do however need to re-write it...

Here's a snipet on backcrossing from the breeding chapter I wrote for Jorge's most recent version of the bible.

Backcross Breeding –
A type of breeding that involves repeated crossing of progeny with one of the original parental genotypes; cannabis breeders most often cross progeny to the mother plant. This parent is known as the recurrent parent. The non-recurrent parent is called the donor parent. More widely, any time a generation is crossed to a previous generation, it is a form of backcross breeding. Backcross breeding has become one of the staple methods clandestine cannabis breeders use, mainly because it is a simple, rapid method when using greenhouses or grow
rooms, and requires only small populations. The principle goal of backcross breeding is to create a population of individuals derived mainly from the genetics of one single parent (the recurrent parent).

The donor parent is chosen based on a trait of interest that the recurrent parent lacks; the idea is to introgress this trait into the backcross population, such that the new population is comprised mainly of genetics from the recurrent parent, but also contains the genes responsible for the trait of interest from the donor parent.

The backcross method is a suitable scheme for adding new desirable traits to a mostly ideal, relatively true-breeding genotype. When embarking on a backcross breeding plan, the recurrent parent should be a highly acceptable or nearly ideal genotype (for example, an existing commercial cultivar or inbred line). The ideal traits considered for introgression into the new seed line should be simply inherited and easily scored for phenotype. The best donor parent must possess the desired trait, but should not be seriously deficient in other traits. Backcross line production is repeatable, if the same parents are used.

Backcross breeding is best used when adding simply inherited dominant traits that can easily be identified in the progeny of each generation (example 1). Recessive traits are more difficult to select for in backcross breeding, since their expression is masked by dominance in each backcross to the recurrent parent. An additional round of open pollination or sib-mating is needed after each backcross generation, to expose homozygous-recessive plants. Individuals showing the recessive condition are selected from F2 segregating generations and backcrossed to the recurrent parent (see example 2).

Example 1– Backcrossing: Incorporating a dominant trait

Step1– Recurrent Parent × Donor Parent
|
V
F1 Hybrid generation

Step 2 – Select desirable plants showing dominant trait, and hybridize selected plants to recurrent parent. The generation produced is denoted BC1 (some cannabis breeders break from botanical convention and denote this generation Bx1. BC1= Bx1).

Step 3 – Select plants from BC1 and hybridize with the recurrent parent; the resulting generation is denoted BC2.

Step 4 – Select plants from BC2 and hybridize with the recurrent parent; the resulting generation is denoted BC3.
.

Example 2 Backcrossing: Incorporating a recessive trait

Step1– Recurrent Parent × Donor Parent
|
V
F1 Hybrid generation

Step 2 – Select desirable plants, and create an F2 population via full sib-mating.

Step 3 – Select plants showing the desired recessive trait in the F2 generation, then hybridize selected F2-recessive plants to the recurrent parent. The generation produced is denoted BC1.

Step 3 – Select plants from BC1, and create a generation of F2 plants via sib-mating; the resulting generation can be denoted BC1F2

Step 4 – Select desirable BC1F2 plants showing the recessive condition, and hybridize with the recurrent parent; the resulting generation is denoted BC2.

Step 5 – Select plants from BC2, and create an F2 population via sib-mating; denote the resulting generation BC2F2.

Step 6 – Select plants showing the recessive condition from the BC2F2 generation, and hybridize to the recurrent parent; the resulting generation is denoted BC3.

Step 7 – Grow out BC3, select and sib-mate the most ideal candidates to create an F2 population, where plants showing the recessive condition are then selected and used as a basis for a new inbred, or open-pollinated seed line.

This new generation created from the F2 is a population that consists of, on average, ~93.7% of genes from the recurrent parent, and only ~6.3% of genes leftover from the donor parent. Most importantly, one should note that since only homozygous-recessives were chosen for mating in the BC3F2 generation, the entire resulting BC3F3 generation is homozygous for the recessive trait, and breeds true for this recessive trait. Our new population meets our breeding objective. It is a population derived mainly from the genetics of the recurrent parent, yet breeds true for our introgressed recessive trait.


Backcross derived lines are expected to be well-adapted to the environment in which they will be grown, which is another reason backcrossing is often used by cannabis breeders who operate indoors. Indoor grow rooms are easily replicated all over the world, so the grower is able to grow the plants in a similar environment in which they were bred. Progeny therefore need less extensive field-testing by the breeder across a wide range of environments.

If two or more characters are to be introgressed into a new seed line, these would usually be tracked in separate backcross programs, and the individual products would be combined in a final set of crosses after the new populations have been created by backcrossing.

The backcross scheme has specific drawbacks, however. When the recurrent parent is not very true-breeding, the resulting backcross generations segregate, and many of the traits deemed desirable to the line fail to be reproduced reliably. Another limitation of the backcross is that the “improved” variety differs only slightly from the recurrent parent (e.g., one trait). If multiple traits are to be introgressed into the new population, other techniques such as inbreeding or recurrent selection may be more rewarding.

Hope that's a little more clear......
Respectfully,
-Chimera

 

[BudZad7]

Chemdawg Colorado cut...

Chemdawg Colorado cut...

Need info about the Best way to fert the 91 chemdog in flower...use PBPG, bud blood in 10 day transition, then PBPB+Big Bud powder
for weeks 2-6, then PBPB/soil+ Overdrive last 2weeks, then use FinalPhase for flush 7days,then plain ro water for the end.

does chemdog 91 like chem ferts better???? thanks for info, or direct me to an answer......

 

[mg75]

Hello all !!! This is a very helpful thread....Also Nice Pics !!!!


My question is what is the flowering length of weeks for Chemdawg ??
Also Sour Diesel ???? For Maximum effect!!!

that will depend on your environment, CO2 use, nutrients, medium, lighting choice, and pre/post 12/12 dark period. all can be manipulated...
oh, and it also depends on your preferred effect... up or down.

70-77 days is usually a good marker for SD harvests.