The introduction of the first citation explains it a little bit:

> DNA has limited chemical stability and decays without the enzymatic repair mechanisms of living cells [18]. Following cell death, nucleases start to cleave the DNA into fragments [19] and during decomposition, the DNA is digested by micro-organisms [18,20]. In determining long-term DNA decay, it is believed that hydrolysis of amino groups accelerates the loss of purine residues (depurination), resulting in strand cleavage [21,22]. This random DNA fragmentation generates a characteristic negative exponential correlation between DNA fragment length and number of molecules (figure 1a) [23,24,26,27].

To be fair, many of those processes are things that I would presume halt at some point in an isolated chemical environment.

Also, what kind of breakdown? If segments up to a certain sizer were stable, that would be enough to reconstruct a full genome of the sequencers were sensitive enough and the final segments long enough.

Thanks! I even clicked on the link and read every sentence that had "half" in it but didn't see anything... didn't expect it to be somewhere else in the introduction haha.

As a general rule, it's safe to assume every word in the abstract of a paper is significant.

> As a general rule, it's safe to assume every word in the abstract of a paper is significant.

...what? The sentence quote above was from the introduction, not the abstract. Nothing in the abstract answered my question of why a stable structure like that of DNA should undergo disintegration. (Did you read the abstract yourself?)

DNA has a half life, but the real question here is how being trapped in amber would affect that half life. So there may be more - or less - than one would expect if the DNA would be in some other environment. At a guess the time span involved is long enough that no matter how this would be influenced there still would not be any usable DNA fragments.

Another question is what sort of artifacts would sequencing material in amber produce. Considering the quality of data from formaldehyde fixed paraffin embedded (FFPE) samples I think it would be quite a struggle

All exponential decay processes have half-lifes - or rather, half-life is a metric that describes the scale of an exponential decay rate.

https://en.wikipedia.org/wiki/Exponential_decay

This link might help answer your questions. Also, half-life in this context is just referring to how long it takes the number phosphodiesterase linkages (bonds holding the DNA backbone together) to decrease by 1/2. Half-life can refer to other types of decay as well :-)

https://www.nature.com/news/dna-has-a-521-year-half-life-1.1...

Everything has a half-life. Even plain old protons have a theoretical half-life of of 10^31 to 10^36 years.

https://en.wikipedia.org/wiki/Proton_decay

Proton decay is not a feature of the standard model, it comes from other theories with far less experimental evidence behind them; by no means at this point can we say that protons "have" a half-life.