I can see a variety of mitochondrial states. Definitively there is a degradatio process. the ones on the right ade edematized and on the left seem very dense. With little information is difficult to say more. In my experience, swelled mitochondria tend to be present in zones of heavy metabolic activity where reactive oxigen species generate at a high rate. On the first look I dont see autophagosomes, at least not well developed ones. I would lean more towards necrosis beacuse of all the celular debris and I cant see the full cell structure so it looks like the membrane is fractured.

The text of your question shows that you are a beginner morphologist. Remember for the future: in any presentation of a microscopic image, first indicate the staining method and the amount of magnification. In the form you submitted, the answer to your question is impossible, since you did not specify the method of staining microscopic preparations. In the most general terms, I agree with Héctor Osorio-Vega answer, but specifying the method of staining can clarify a lot.

仅从此图无法看出是否有自噬，建议结合蛋白水平的改变进行确认.

It is not possible to see if there is autophagy from this graph alone, and it is recommended to confirm the change in the level of the binding protein.

Right part / margin of image: IHMO remnants of a necrotic cell (debris within decomposed /disrupted cell outlining, I can [edited: cannot!] see any cell membrane structures). It might be that the part on the right side originally was part of the cellular remnant on the left margin...there - at places - one could imagine the presence of membraneous structures. So not only all the questions from Alexey Orlovsky (staining, image magnification) matter, but also the specimen itself (tissue, human, animal; vital physiological / experimental state?) and, naturally, your handling the tissue until, as well as your actual specimen preparation specifically matters too. IMHO it might be you've applied a special preparation regimen (esp. first fixation, or during dehydration, or section staining too) since some neutral lipid vacuoles as well as IMF's(?) and 'extra- / intercellular matrix' (albumin?, collagen?) are shown nicely e-dense....(therfore it would be of interest too to get the info about the whole specimen preparation steps. Thank you in advance for giving clues to the readers of your question.

perhaps could you try in parrallel the effect of deferroxamine (100 µM) during the death process. It could give you an indication