I’ll look at it again. It was definitely on healthy live bark.
Juliet
There is a good scatter of the Caloplaca “cerina” (yellow-disked broad-margined boiled eggs) fruit at various points along the branch, but also this little group, apparently with “cerina” to the right and startling orange, narrow-margined “pyracea” fruit in the middle. The smaller greener-yellow fruit to the left might be cerinella. I am loathe to section it as it is such an attractive specimen for the juxtaposition, though I’d be prepared to do so if it could usefully demonstrate anything – a pyracea look-alike, maybe? Any thoughts please?
Juliet
I’m so pleased that you think it looks good for L chlarotera s. str, though. Thanks.
Juliet
I’ve had another look at my specimen assuming it is glaucellum. The ring of pruine is visible on a few of the aps.
Measuring the asci is tricky, because mature aps just squash to a mess of spores, so here is one where the head is just starting to swell.
Asci length measured 39-42 microns.
The spores are so variable in length and shape I can’t see how to pick the normal range.
Can anyone give me guidance on observing spore ornamentation, please.
Juliet
I had gone through all the lichenicolous fungi listed in LGBI3, picture matching with photos available on the net (not very scientific, but it often works!) and came up with Nectriopsis physciicola too. However, then I read the fungi.myspecies description which says “Ascospores 14-18 (-22.5) x 5.5-8 µm (slightly wider in KOH), broadly ellipsoidal, the ends rounded, hyaline, smooth, with a single ± median septum.”
Given the consistently larger spore size – greater than 20 microns – I thought mine could well be something else.
Unless anyone has further thoughts I’ll record it as Nectriopsis physciicola but add a Record note that the spores were larger, with a reference to this post.
The blue colour of your specimen also sounds right.
With my specimen, I was concerned about the friesiana/caerulea split, and was plumping for caerulea because I could see no brown pigments. I can’t really make out the colour in your section, so a different shot with the condenser aperture more open would be helpful.
But having said all that, I have little experience with Bacidinas so I hope some one else comments too!
Juliet
I cannot see any septation in my photos. I followed the key as you suggested, Maxine, which got me fairly securely to Psammina simplex, though I really wish I had more material to recheck. Put it down to experience.
Juliet
I’ve just been out to check and the sclerotia are only just starting to form this year, and not on many infections yet. I’m expecting there to be huge quantities of them by February.
Juliet
It answers well enough to Neonectria ilicis, though the spores are rarely larger than 17x7um and I didn’t observe any browning of the most mature spores. Also, it was growing on a lovely big strong grey-shiny branch (though on a veteran holly) that didn’t look sick at all. I’ll have to keep an eye on it as well as looking for further examples.
I’ll iRecord it as Neonectria ilicis, referencing this forum.
Paul Cannon says it would probably have had more views if I had put it in the Ascomycetes area. Should it be moved?
Herewith some more photos, and thanks for all your help.
Juliet
Juliet
I have retained four specimens of M elegantula from that branch, collected on 29 December 2023. Of these, two had almost lost their red fluorescence on 31 December and two still showed good fluorescence. Today, 2 January 2024, one of the specimens that was fluorescent two days ago is now barely fluorescent, the other still shows red fluorescence, but not strikingly so. I’ll rewet them all at some point and see what happens.
How useful is UV as a field tool for identification, I wonder. Is it only red fluorescence I need to be wary of?
Happy New Year
Juliet
Happy Christmas
Juliet
Juliet
