Abstract
Amber is an exceptional organic mineral found all over the world that occasionally contains fossilised organisms. The physical and chemical characteristics of amber pose a challenge when looking for microfossils, such as microfungi. However, also, macrofungi are rarely found in amber, probably because of their ephemeral nature. Yet, in the course of this review, 137 records of non-lichnenised fungi and 182 of lichens were found, the earliest reaching back to the eighteenth century. The findings range from the Carboniferous (ca. 310 Ma) to the Upper Miocene (ca. 10 Ma). About 10% were macrofungi, the rest microfungi (Ascomycetes, Deuteromycetes) or lichens. Identification poses problems due to the fragmentary remains which, as a rule, are inaccessibly entombed in fossilised resin. Most non-lichenised taxa per Ma were, according to this review, recovered from Neogene deposits, whilst lichens showed a marked diversity surge during the Palaeogene. Overall, the record of fungal fossils in amber seems to mirror the diversity patterns through deep time. Nevertheless, the few records from the Palaeozoic and the Lower to Mid-Mesozoic call for the development of additional tools for detection and identification.
Similar content being viewed by others
References
Alekseev V, Alekseev P (2016) New approaches for reconstruction of the ecosystem of an Eocene amber forest. Biol Bull 43(1):75–86
Anderson KB (1994) The nature and fate of natural resins in the geosphere—IV. Middle and Upper Cretaceous amber from the Taimyr Peninsula, Siberia—evidence for a new form of polylabdanoid of resinite and revision of the classification of Class I resinites. Organic Geochemistry 21 (2):209–212
Andrée K (1951) Der Bernstein. Franckh’sche Verlagshandlung, Stuttgart
Antoine P-O, De Franceschi D, Flynn JJ, Nel A, Baby P, Benammi M, Calderón Y, Espurt N, Goswami A, Salas-Gismondi R (2006) Amber from western Amazonia reveals Neotropical diversity during the middle Miocene. Proc Natl Acad Sci 103(37):13595–13600
Ascaso C, Wierzchos J, Speranza M, Gutiérrez JC, González AM, de los Ríos A, Alonso J (2005) Fossil protists and fungi in amber and rock substrates. Micropaleontology 51(1):59–72
Azar D (1997) A new method for extracting plant and insect fossils from Lebanese amber. Palaeontology 40(4):1027–1060
Bachmayer F (1962) Fossile Pilzhyphen im Flyschharz des Steinbruches im Höbersbachtal bei Gablitz in Niederösterreich. Ann Naturhist Mus Wien:47–49
Bachofen-Echt A (1949) Der Bernstein und seine Einschlüsse. Springer-Verlag, Wien
Bąk M, Natkaniec-Nowak L, Drzewicz P, Czapla D (2016) Ambrosiella-like fungi in fossil resin from Jambi Province in Sumatra Island—possible phoretic organisms interacted with invaded insects. Paper presented at the 17th Czech-Slovak-Polish Palaeolontological Conference, Warsaw,
Baniya CB, Solhøy T, Gauslaa Y, Palmer MW (2010) The elevation gradient of lichen species richness in Nepal. Lichenologist 42(1):83–96
Beimforde C, Schmidt AR (2011) Microbes in resinous habitats: a compilation from modern and fossil resins. In: Reitner J, Quéric N-V, Arp G (eds) Advances in stromatolite geobiology. Springer, pp 391–407
Beimforde C, Schäfer N, Dörfelt H, Nascimbene PC, Singh H, Heinrichs J, Reitner J, Rana RS, Schmidt AR (2011) Ectomycorrhizas from a Lower Eocene angiosperm forest. New Phytol 192(4):988–996
Berbee ML, Taylor JW (2010) Dating the molecular clock in fungi - how close are we? Fungal Biology Reviews 24:1–16
Berkeley MJ (1848) XXXIX.—On three species of mould detected by Dr. Thomas in the amber of East Prussia. Ann Mag Nat Hist 2(12):380–383
Boenigk J, Wodniok S, Glücksman E (2015) Biodiversity and earth history. Springer, Berlin Heidelberg
Boucot AJ, Poinar Jr GO (2011) Fossil behavior compendium. CRC Press,
Bresinsky A, Körner C, Kadereit JW, Neuhaus G, Sonnewald U (2008) Lehrbuch der Botanik, 36. edition. Spektrum Akademischer Verlag, Heidelberg
Breton G (2007) La bioaccumulation de microorganismes dans l’ambre: analyse comparée d’un ambre cénomanien et d’un ambre sparnacien, et de leurs tapis algaires et bactériens. Comptes Rendus Palevol 6(1–2):125–133
Breton G (2012) L'ambre des Corbières (Aude - France). Société d'Etudes Scientifiques de l'Aude, Carcassonne
Breton G, Tostain F (2005) Les microorganismes de l’ambre cénomanien d’Écommoy (Sarthe, France). Comptes Rendus Palevol 4(1–2):31–46
Breton G, Gauthier C, Vizcaino D (1999) Land and freshwater microflora in a Sparnacian amber from the Corbières (South France): first observations. Estudios del museo de Ciencias Naturales de alava 14 (2)
Breton G, Bilotte M, Eychenne G L’ambre campanien du Mas d’Azil (Ariège, France): gisement, micro-inclusions, taphonomie. Annales de Paléontologie, 2013. vol 4. Elsevier, pp 317–337
Breton G, de Lourdes S-SM, Vega FJ (2014) Filamentous micro-organisms, inorganic inclusions and pseudo-fossils in the Miocene amber from Totolapa (Chiapas, Mexico): taphonomy and systematics. Bol Soc Geol Mex 66(1):199–214
Caspary R, Klebs RHE (1907) Die Flora des Bernsteins und anderer fossiler Harze des ostpreussischen Tertiärs. Königlich Geologische Landesanstalt,
Conwentz H (1890) Monographie der baltischen Bernsteinbäume. Commissions-Verlag von Wilhelm Engelmann, Leipzig
de Lara NOT, Marcati CR (2016) Cambial dormancy lasts 9 months in a tropical evergreen species. Trees 30(4):1331–1339
Divakar PK, Crespo A, Wedin M, Leavitt SD, Hawksworth DL, Myllys L, McCune B, Randlane T, Bjerke JW, Ohmura Y et al (2015) Evolution of complex symbiotic relationships in a morphologically derived family of lichen-forming fungi. New Phytol 208(4):1217–1226
Dörfelt H, Schäfer U (1998) Fossile Pilze in Bernstein der alpischen Trias. Zeitschrift für Mykologie 64:141–152
Dörfelt H, Schmidt AR (2005) A fossil Aspergillus from Baltic amber. Mycol Res 109(8):956–960
Dörfelt H, Striebich B (2000) Palaeocybe striata, ein neuer fossiler Pilz in Bernstein des Tertiär. ZMykol 66:27–34
Fahn A, Werker E, Ben-Tzur P (1979) Seasonal effects of wounding and growth substances on development of traumatic resin ducts in Cedrus libani. New Phytol 82(2):537–544
Girard V, Adl SM (2011) Amber microfossils: on the validity of species concept. Comptes Rendus Palevol 10(2–3):189–200
Girard V, Schmidt AR, Struwe S, Perrichot V, Breton G, Néraudeau D (2009) Taphonomy and palaeoecology of mid-Cretaceous amber-preserved microorganisms from southwestern France. Geodiversitas 31(1):153–162
Goeppert HR, Berendt GC (1845) Der Bernstein und die in ihm befindlichen Pflanzenreste der Vorwelt. Nicolaische Buchhandlung, Berlin
Gothan W, Weyland H (1964) Lehrbuch der Paläobotanik. Akademie-Verlag, Berlin
Graham A (1962) The role of fungal spores in palynology. J Paleontol 36(1):60–68
Green OR (2001) Preparation of amber specimens containing fossils. In: A manual of practical laboratory and field techniques in palaeobiology. Springer Netherlands, Dordrecht, pp 234–241. https://doi.org/10.1007/978-94-017-0581-3_23
Green OR (2014) A manual of practical laboratory and field techniques in palaeobiology. Springer Science & Business Media,
Gregory PH (1973) Microbiology of the atmosphere, 2nd edition. John Wiley & Sons, New York
Grimaldi DA, Bonwich E, Delannoy M, Doberstein S (1994) Electron microscopic studies of mummified tissues in amber fossils. American Museum novitates; no. 3097
Grimaldi DA, Engel MS, Nascimbene PC (2002) Fossiliferous Cretaceous amber from Myanmar (Burma): its rediscovery, biotic diversity, and paleontological significance. Am Mus Novit 3361:1–71
Grüß J (1931) Die Urform des Anthomyces Reukaufii und andere Einschlüsse in den Bernstein durch Insekten verschleppt. Wochenschr Brau 22:1–6
Guimarães JTF, Nogueira ACR, Bandeira Cavalcante Da Silva Jr J, Lima Soares J, Silveira R (2013) Fossil fungi from Miocene sedimentary rocks of the central and coastal Amazon region, North Brazil. J Paleontol 87(3):484–492
Halbwachs H, Bässler C (2015) Gone with the wind—a review on basidiospores of lamellate agarics. Mycosphere 6:78–112
Henkels JF, Zimmermann CF (1744) Kleine mineralogische, und chymische Schriften: nebst einer Vorrede von den Bergwerks-Wissenschaften zur Vermehrung der Cameral-Nutzungen. Friedrich Hekel, Dresden/Leipzig
Hibbett D (2017) Major events in the evolution of fungi. In: Losos JB, Baum DA, Futuyma DJ et al (eds) . Princeton University Press, The Princeton guide to evolution, pp 152–158
Hibbett D, Grimaldi D, Donoghue M (1995) Cretaceous mushrooms in amber. Nature 377(6549):487
Hibbett D, Grimaldi D, Donoghue M (1997) Fossil mushrooms from Miocene and Cretaceous ambers and the evolution of Homobasidiomycetes. Am J Bot 84(7):981–981
Hibbett DS, Binder M, Wang Z, Goldman Y (2003) Another fossil agaric from Dominican amber. Mycologia 95(4):685–687
Holt EA, Bradford R, Garcia I (2015) Do lichens show latitudinal patterns of diversity? Fungal Ecol 15:63–72. https://doi.org/10.1016/j.funeco.2015.03.004
Horton TR (2017) Spore dispersal in ectomycorrhizal fungi at fine and regional scales. In: Tedersoo L (ed) Biogeography of mycorrhizal symbiosis. Springer, pp 61–78
Kaasalainen U, Schmidt AR, Rikkinen J (2017) Diversity and ecological adaptations in Palaeogene lichens. Nature plants 3(5):17049
Kaasalainen U, Heinrichs J, Renner MA, Hedenäs L, Schäfer-Verwimp A, Lee GE, Ignatov MS, Rikkinen J, Schmidt AR (2018) A Caribbean epiphyte community preserved in Miocene Dominican amber. Earth and environmental science transactions of the royal society of Edinburgh 107(2–3):321–331
Kalgutkar R, Sigler L (1995) Some fossil fungal form-taxa from the Maastrichtian and Palaeogene ages. Mycol Res 99(5):513–522
Kappen L (1973) Response to extreme environments. In: Ahmadjian V, Hale ME (eds) The lichens. Academic Press, New York & London, pp 311–380
Kettunen E, Grabenhorst H, Gröhn C, Dörfelt H, Sadowski E-M, Rikkinen J, Schmidt AR (2015) The enigmatic hyphomycete Torula sensu Caspary revisited. Rev Palaeobot Palynol 219:183–193
Kettunen E, Schmidt AR, Diederich P, Grabenhorst H, Rikkinen J (2016) Lichen-associated fungi from Paleogene amber. New Phytol 209(3):896–898
Kettunen E, Schmidt AR, Diederich P, Grabenhorst H, Rikkinen J (2017) Diversity of lichen-associated filamentous fungi preserved in European Paleogene amber. Earth and Environmental Science Transactions of The Royal Society of Edinburgh 107(2–3):311–320
Kettunen E, Sadowski E-M, Seyfullah LJ, Dörfelt H, Rikkinen J, Schmidt AR (2018) Caspary’s fungi from Baltic amber: historic specimens and new evidence. Papers in Palaeontology. https://doi.org/10.1002/spp2.1238
Khattab A, Levetin E (2008) Effect of sampling height on the concentration of airborne fungal spores. Ann Allergy Asthma Immunol 101(5):529–534
King R (2006) Amber (Part 1). Geol Today 22(6):232–237
King R (2007) Amber (part 2). Geol Today 23(2):74–77
Krings M, Taylor TN, Harper CJ (2017) Early fungi—evidence from the fossil record. In: Dighton J, White JF (eds) The fungal community—its organization and role in the ecosystem, 4th edition. CRC Press, Boca Raton, pp 37–51
Krumbiegel G, Krumbiegel B (1994) Bernstein - Fossile Harze aus aller Welt. Goldschneck Verlag, Weinstadt
Labandeira CC (2014) Amber. The Paleontological Society Papers 20:163–216. https://doi.org/10.1017/S1089332600002850
Lak M, Néraudeau D, Nel A, Cloetens P, Perrichot V, Tafforeau P (2008) Phase contrast X-ray synchrotron imaging: opening access to fossil inclusions in opaque amber. Microsc Microanal 14(3):251–259
Langenheim R Jr, Smiley C, Gray J (1960) Cretaceous amber from the Arctic coastal plain of Alaska. Geol Soc Am Bull 71(9):1345–1356
Leelawatanasuk T, Wathanakul P, Paramita S, Sutthirat C, Sriprasert B, Bupparenoo P (2013) The characteristics of amber from Indonesia. Aust Gemmol 25(4):142–145
Lin C-P, Huang J-P, Wu C-S, Hsu C-Y, Chaw S-M (2010) Comparative chloroplast genomics reveals the evolution of Pinaceae genera and subfamilies. Genome biology and evolution 2:504–517
Lodge DJ, Ammirati J, O'Dell TE, Mueller GM, Huhndorf SM, Wang C-J, Stokland JN, Schmit JP, Ryvarden L, Leacock PR, Mata M, Umaña L, Wu Q, Czederpiltz DL (2004) Terrestrial and lignicolous macrofungi. In: Mueller GM, Bills GF, Foster MS (eds) Biodiversity of fungi: inventory and monitoring methods. Academic Press, pp 127–172
Lorrey AM, Boswijk G, Hogg A, Palmer JG, Turney CSM, Fowler AM, Ogden J, Woolley J-M (2018) The scientific value and potential of New Zealand swamp kauri. Quat Sci Rev 183:124–139. https://doi.org/10.1016/j.quascirev.2017.12.019
Lücking R, Nelsen MP (2018) Ediacarans, protolichens, and lichen-derived Penicillium: a critical reassessment of the evolution of lichenization in fungi. In: Harper CJ, Cúneo NR, Rothwell GW (eds) Krings M. Elsevier, Transformative paleobotany, pp 551–590
Lumbsch HT, Rikkinen J (2017) Evolution of lichens. In: Dighton J, White JF (eds) The fungal community—its organization and role in the ecosystem, 4th Edition. CRC Press, pp 53–62
Martín-González A, Wierzchos J, Gutiérrez JC, Alonso J, Ascaso C (2009) Microbial Cretaceous park: biodiversity of microbial fossils entrapped in amber. Naturwissenschaften 96(5):551–564
Masuch G (1993) Biologie der Flechten. Quelle und Meyer, Heidelberg & Wiesbaden
Mazur N, Nagel M, Leppin U, Bierbaum G, Rust J (2014) The extraction of fossil arthropods from Lower Eocene Cambay amber. Acta Palaeontol Pol 59(2):455–459
Menge A (1858) Beitrag zur Bernsteinflora. Schriften der Naturforschenden Gesellschaft in Danzig 5:1–18
Murray AP, Edwards D, Hope JM, Boreham CJ, Booth WE, Alexander RA, Summons RE (1998) Carbon isotope biogeochemistry of plant resins and derived hydrocarbons. Org Geochem 29(5–7):1199–1214
Mustoe GE (1985) Eocene amber from the Pacific Coast of North America. GSA Bull 96(12):1530–1536. https://doi.org/10.1130/0016-7606(1985)96<1530:EAFTPC>2.0.CO;2
Naglik B, Kosmowska-Ceranowicz B, Natkaniec-Nowak L, Drzewicz P, Dumańska-Słowik M, Matusik J, Wagner M, Milovsky R, Stach P, Szyszka A (2018) Fossilization history of fossil resin from Jambi Province (Sumatra, Indonesia) based on physico-chemical studies. Minerals 8(3):95
Nel P, Schmidt AR, Bässler C, Nel A (2012) Fossil thrips of the family Uzelothripidae suggest 53 million years of morphological and ecological stability. Acta Palaeontol Pol 58:609–614
Nicholas CJ, Henwood AA, Simpson M (1993) A new discovery of early Cretaceous (Wealden) amber from the Isle of Wight. Geol Mag 130(6):847–850. https://doi.org/10.1017/S0016756800023207
Pampaloni L (1902) Resti organici nel disolide di Melilli in Sicilia. In: Canavari M (ed) Palaeontographia Italica. Museo Geologico della R. Università di Pisa, Pisa, pp 121–130
Peñalver E, Delclòs X (2010) Spanish amber. In: Penney D (ed) Biodiversity of fossils in amber from the major world deposits. Siri Scientific Press, Manchester, pp 299–303
Peñalver E, Delclos X, Soriano C (2007) A new rich amber outcrop with palaeobiological inclusions in the Lower Cretaceous of Spain. Cretac Res 28(5):791–802
Penney D (2010) Biodiversity of fossils in amber from the major world deposits. Siri Scientific Press,
Penney D, Green DI (2010) Introduction, preparation, study & conservation of amber inclusions. In: Penney D (ed) Biodiversity of fossils in amber from the major world deposits. Siri Scientific Press, Manchester, pp 5–21
Penney D, Preziosi RF (2010) On inclusions in subfossil resins (copal). In: Penney D (ed) Biodiversity of fossils in amber from the major world deposits. Siri Scientific Press, Manchester, pp 299–303
Penney D, Wadsworth C, Green DI, Kennedy SL, Preziosi RF, Brown TA (2013) Extraction of inclusions from (sub) fossil resins, with description of a new species of stingless bee (Hymenoptera: Apidae: Meliponini) in Quaternary Colombian copal. Paleontological Contributions 7:1–6
Perrichot V, Boudinot B. F., Cole J, Delhaye-Prat V, Esnault J, Al E (2016) African fossiliferous amber: a review. Paper presented at the 7th International Conference on Fossil Insects, Arthropods and Amber, Edinburgh, 2016-04-21
Pirozynski K (1976) Fossil fungi. Annu Rev Phytopathol 14(1):237–246
Poinar Jr GO (1992) Life in amber. Stanford University Press.
Poinar GO Jr (2001) Fossil puffballs (Gasteromycetes: Lycoperdales) in Mexican amber. Hist Biol 15(3):219–222
Poinar GO Jr (2003) Coelomycetes in Dominican and Mexican amber. Mycol Res 107(1):117–122
Poinar GO Jr (2014a) Bird’s nest fungi (Nidulariales: Nidulariaceae) in Baltic and Dominican amber. Fungal biology 118(3):325–329
Poinar GO Jr (2014b) Xylaria antiqua sp. Nov.(Ascomycota: Xylariaceae) in Dominican amber. Journal of the Botanical Research Institute of Texas 8(1):145–149
Poinar GO Jr (2016a) A Mid-Cretaceous ectoparasitic fungus, Spheciophila adercia gen et sp. nov, attached to a wasp in Myanmar amber. Fungal Genet Biol 6(2):1–4
Poinar GO Jr (2016b) Fossil fleshy fungi (“mushrooms”) in Amber. Fungal Genom Biol 6(142):2
Poinar GO Jr (2016c) A gilled mushroom, Gerontomyces lepidotus gen. et sp. nov. (Basidiomycota: Agaricales), in Baltic amber. Fungal biology 120(9):1090–1093
Poinar GO Jr (2017a) Developmental stages of the fungus, Synaptomitus orchiphilus, in the germinating seed, Mycophoris elongatus (Orchidaceae), in Dominican amber. Hist Biol:1–5. doi:https://doi.org/10.1080/08912963.2017.1411352
Poinar GO Jr (2017b) Two new genera, Mycophoris gen. nov. (Orchidaceae) and Synaptomitus gen. nov. (Basidiomycota) based on a fossil seed with developing embryo and associated fungus in Dominican amber. Botany 95(1):1–8
Poinar GO Jr (2018) A mid-Cretaceous pycnidia, Palaeomycus epallelus gen. et sp. nov., in Myanmar amber. Historical biology Doi https://doi.org/10.1080/08912963.2018.1481836:1-4
Poinar GO Jr, Buckley R (2007) Evidence of mycoparasitism and hypermycoparasitism in Early Cretaceous amber. Mycol Res 111(4):503–506
Poinar GO Jr, Hess R (1985) Preservative qualities of recent and fossil resins: electron micrograph studies on tissue preserved in Baltic amber. Journal of Baltic Studies 16(3):222–230
Poinar GO Jr, Poinar R (1999) The amber forest: a reconstruction of a vanished world. Princeton University Press, Princeton
Poinar GO Jr, Singer R (1990) Upper Eocene gilled mushroom from the Dominican Republic. Science 248(4959):1099–1101
Poinar GO Jr, Thomas G (1982) An entomophthoralean fungus from Dominican amber. Mycologia 74(2):332–334
Poinar GO Jr, Thomas G (1984) A fossil entomogenous fungus from Dominican amber. Experientia 40(6):578–579
Poinar GO Jr, Waggoner BM, Bauer U-C (1993) Terrestrial soft-bodied protists and other microorganisms in Triassic amber. Science 259(5092):222–224
Poinar GO Jr, Peterson E, Platt J (2000) Fossil Parmelia in new world amber. Lichenologist 32(3):263–269
Poinar GO Jr, da Silva AD, Baseia IG (2014) A gasteroid fungus, Palaeogaster micromorpha gen. & sp. nov. (Boletales) in Cretaceous Myanmar amber. Journal of the Botanical Research Institute of Texas 8(1):139–143
Poinar GO Jr, Alderman S, Wunderlich J (2015) One hundred million year old ergot: psychotropic compounds in the Cretaceous? Palaeodiversity 8:13–19
Poinar GO Jr, Vega FE (2019) A mid-Cretaceous trichomycete, Priscadvena corymbosa gen. et sp. nov., in Burmese amber. Fungal Biology. https://doi.org/10.1016/j.funbio.2019.02.007
Ponomarenko AG (2016) Insects during the time around the Permian—Triassic crisis. Paleontol J 50(2):174–186. https://doi.org/10.1134/s0031030116020052
Rikkinen J, Poinar G (2002) Yeast-like fungi in Dominican amber. Karstenia 42:29–32
Rikkinen J, Poinar GO Jr (2001) Fossilised fungal mycelium from Tertiary Dominican amber. Mycol Res 105(7):890–896
Rikkinen J, Poinar GO Jr (2008) A new species of Phyllopsora (Lecanorales, lichen-forming Ascomycota) from Dominican amber, with remarks on the fossil history of lichens. J Exp Bot 59(5):1007–1011
Rikkinen J, Schmidt AR (2018) Morphological convergence in forest microfungi provides a proxy for Paleogene forest structure. In: Krings M, Harper CJ, Cúneo NR, Rothwell GW (eds) Transformative Paleobotany. Elsevier, pp 527–549
Rikkinen J, Meinke SKL, Grabenhorst H, Gröhn C, Kobbert M, Wunderlich J, Schmidt AR (2018) Calicioid lichens and fungi in amber—tracing extant lineages back to the Paleogene. Geobios 51(5):469–479
Rossi W, Kotrba M, Triebel D (2005) A new species of Stigmatomyces from Baltic amber, the first fossil record of Laboulbeniomycetes. Mycol Res 109(3):271–274
Rust J, Singh H, Rana RS, McCann T, Singh L, Anderson K, Sarkar N, Nascimbene PC, Stebner F, Thomas JC (2010) Biogeographic and evolutionary implications of a diverse paleobiota in amber from the early Eocene of India. Proc Natl Acad Sci 107(43):18360–18365
Ryberg M, Matheny PB (2011) Asynchronous origins of ectomycorrhizal clades of Agaricales. Proceedings of the Royal Society of London B: Biological Sciences:rspb20112428
Sadowski E-M, Beimforde C, Gube M, Rikkinen J, Singh H, Seyfullah LJ, Heinrichs J, Nascimbene PC, Reitner J, Schmidt AR (2012) The anamorphic genus Monotosporella (Ascomycota) from Eocene amber and from modern Agathis resin. Fungal biology 116(10):1099–1110
Sadowski E-M, Schmidt AR, Kunzmann L, Gröhn C, Seyfullah LJ (2016) Sciadopitys cladodes from Eocene Baltic amber. Bot J Linn Soc 180(2):258–268
Sadowski E-M, Schmidt AR, Seyfullah LJ, Kunzmann L (2017) Conifers of the “Baltic Amber Forest” and their Palaeoecological significance (Stapfia 106), vol 106. Stapfia. Oberösterreichisches Landesmuseum, Linz
Saint Martin J-P, Saint Martin S (2018) Exquisite preservation of a widespread filamentous microorganism in French Cretaceous ambers: crucial for revising a controversial fossil. Comptes Rendus Palevol 17(7):415–434
Saint Martin S, Saint Martin J-P, Girard V, Grosheny D, Néraudeau D (2012) Filamentous micro-organisms in Upper Cretaceous amber (Martigues, France). Cretac Res 35:217–229
Schmidt A (2003) Das fossile Harz von Schliersee (Bayerische Alpen) und seine Mikroinklusen. Doctoral thesis, Friedrich-Schiller-Universität, Jena
Schmidt AR, Dörfelt H (2007) Evidence of Cenozoic Matoniaceae from Baltic and Bitterfeld amber. Rev Palaeobot Palynol 144(3–4):145–156
Schmidt AR, Ragazzi E, Coppellotti O, Roghi G (2006) A microworld in Triassic amber. Nature 444(7121):835
Schmidt AR, Dörfelt H, Perrichot V (2007) Carnivorous fungi from Cretaceous amber. Science 318(5857):1743–1743
Schmidt AR, Dörfelt H, Perrichot V (2008) Palaeoanellus dimorphus gen. et sp. nov. (Deuteromycotina): a Cretaceous predatory fungus. Am J Bot 95(10):1328–1334
Schmidt AR, Perrichot V, Svojtka M, Anderson KB, Belete KH, Bussert R, Dörfelt H, Jancke S, Mohr B, Mohrmann E (2010) Cretaceous African life captured in amber. Proc Natl Acad Sci 107(16):7329–7334
Schmidt AR, Beimforde C, Seyfullah LJ, Wege S-E, Dörfelt H, Girard V, Grabenhorst H, Gube M, Heinrichs J, Nel A (2013a) Amber fossils of sooty moulds. Rev Palaeobot Palynol 200:53–64
Schmidt AR, Dörfelt H, Grabenhorst H, Tuovila H, Rikkinen J (2013b) Fungi of the Bitterfeld amber forest. Exkursf und Veröfftl DGG 249:54–60
Schmidt AR, Kaulfuss U, Bannister JM, Baranov V, Beimforde C, Bleile N, Borkent A, Busch A, Conran JG, Engel MS, Harvey M, Kennedy EM, Kerr PH, Kettunen E, Kiecksee AP, Lengeling F, Lindqvist JK, Maraun M, Mildenhall DC, Perrichot V, Rikkinen J, Sadowski E-M, Seyfullah LJ, Stebner F, Szwedo J, Ulbrich P, Lee DE (2018) Amber inclusions from New Zealand. Gondwana Res 56:135–146. https://doi.org/10.1016/j.gr.2017.12.003
Schöller H (1997) Flechten: Geschichte, Biologie, Systematik, Ökologie, Naturschutz und kulturelle Bedeutung: Begleitheft zur Ausstellung" Flechten-Kunstwerke der Natur". Waldemar Kramer, Frankfurt a. M
Schönborn W, Dörfelt H, Foissner W, Krienitz L, Schäfer U (1999) A fossilized microcenosis in Triassic amber. J Eukaryot Microbiol 46(6):571–584
Selosse M-A, Brundrett M, Dearnaley J, Merckx VS, Rasmussen F, Zettler LW, Rasmussen HN (2017) Why Mycophoris is not an orchid seedling, and why Synaptomitus is not a fungal symbiont within this fossil. Botany 95(9):865–868
Sendel N (1742) Historia succinorum corpora aliena involventium et naturae opere pictorum et caelatorum. Apud Io. Fridericum Gleditschium, Leipzig
Seyfullah LJ, Beimforde C, Dal Corso J, Perrichot V, Rikkinen J, Schmidt AR (2018) Production and preservation of resins–past and present. Biol Rev 93:1684–1714
Sidorchuk EA (2013) A new technique for preparation of small-sized amber samples with application to mites. Paper presented at the proceedings of the 6th International Congress on Fossil Insects, Arthropods and Amber, Byblos/Lebanon,
Signor PW (1990) The geologic history of diversity. Annu Rev Ecol Syst 21(1):509–539
Smith J (1896) On the discovery of fossil microscopic plants in the fossil amber of the Ayrshire coal-field. Trans Geol Soc Glasgow 10(2):318–322
Smith RD, Ross AJ (2017) Amberground pholadid bivalve borings and inclusions in Burmese amber: implications for proximity of resin-producing forests to brackish waters, and the age of the amber. Earth and Environmental Science Transactions of the Royal Society of Edinburgh 107(2–3):239–247
Speranza M, Wierzchos J, Alonso J, Bettucci L, Martín-González A, Ascaso C (2010) Traditional and new microscopy techniques applied to the study of microscopic fungi included in amber. In: Méndez-Vilas A, Díaz J (eds) Microscopy: science, technology, application and education. Formatex Research Center, Badajoz, pp 1135–1145
Stankiewicz BA, Poinar HN, Briggs DE, Evershed RP, Poinar GO Jr (1998) Chemical preservation of plants and insects in natural resins. Proc R Soc Lond B Biol Sci 265(1397):641–647
Stubblefield SP, Taylor TN (1988) Recent advances in palaeomycology. New Phytol 108(1):3–25
Stubblefield SP, Miller CE, Taylor TN, Cole GT (1985) Geotrichites glaesarius, a conidial fungus from Tertiary Dominican amber. Mycologia 77(1):11–16
Sung G-H, Poinar GO Jr, Spatafora JW (2008) The oldest fossil evidence of animal parasitism by fungi supports a Cretaceous diversification of fungal–arthropod symbioses. Mol Phylogenet Evol 49(2):495–502. https://doi.org/10.1016/j.ympev.2008.08.028
Taylor TN, Krings M (2010) Paleomycology: the rediscovery of the obvious. Palaios 25(5):283–286
Taylor TN, Krings M, Taylor EL (2014) Fossil Fungi. Elsevier Science, London
Taylor TN, Krings M, Taylor EL (2015) Fungal diversity in the fossil record. In: McLaughlin DJ, Spatafora JW (eds) Systematics and evolution, 2nd edition. Springer, Berlin/Heidelberg, pp 259–278
Tedersoo L, Bahram M, Põlme S, Kõljalg U, Yorou NS, Wijesundera R, Ruiz LV, Vasco-Palacios AM, Thu PQ, Suija A, Smith ME, Sharp C, Saluveer E, Saitta A, Rosas M, Riit T, Ratkowsky D, Pritsch K, Põldmaa K, Piepenbring M, Phosri C, Peterson M, Parts K, Pärtel K, Otsing E, Nouhra E, Njouonkou AL, Nilsson RH, Morgado LN, Mayor J, May TW, Majuakim L, Lodge DJ, Lee SS, Larsson K-H, Kohout P, Hosaka K, Hiiesalu I, Henkel TW, Harend H, Guo L-d, Greslebin A, Grelet G, Geml J, Gates G, Dunstan W, Dunk C, Drenkhan R, Dearnaley J, De Kesel A, Dang T, Chen X, Buegger F, Brearley FQ, Bonito G, Anslan S, Abell S, Abarenkov K (2014) Global diversity and geography of soil fungi. Science 346(6213). https://doi.org/10.1126/science.1256688
Thiel V, Lausmaa J, Sjövall P, Ragazzi E, Seyfullah LJ, Schmidt AR (2016) Microbe-like inclusions in tree resins and implications for the fossil record of protists in amber. Geobiology 14(4):364–373. https://doi.org/10.1111/gbi.12180
Thomas GM, Poinar GO Jr (1988) A fossil Aspergillus from Eocene Dominican amber. J Paleontol:141–143
Traverse A (2008) Paleopalynology 2nd edition. Springer, Dordrecht
Tripathi S (2012) The systematics and evolutionary perspectives of fossil fungi. In: Misra J, Tewari J, Deshmukh S (eds) Systematics and evolution of fungi. pp 15–27
Tripp EA, Lendemer JC, Barberán A, Dunn RR, Fierer N (2016) Biodiversity gradients in obligate symbiotic organisms: exploring the diversity and traits of lichen propagules across the United States. J Biogeogr 43(8):1667–1678
Tuovila H, Schmidt AR, Beimforde C, Dörfelt H, Grabenhorst H, Rikkinen J (2013) Stuck in time—a new Chaenothecopsis species with proliferating ascomata from Cunninghamia resin and its fossil ancestors in European amber. Fungal Divers 58(1):199–213
Urbański T, Molak W (1984) Chemistry of Baltic amber. Part VII*. Chemistry 32(1–2):3–8
Varga T, Krizsán K, Földi C, Dima B, Sánchez-García M, Sánchez-Ramírez S, Szöllősi GJ, Szarkándi JG, Papp V, Albert L, Andreopoulos W, Angelini C, Antonín V, Barry KW, Bougher NL, Buchanan P, Buyck B, Bense V, Catcheside P, Chovatia M, Cooper J, Dämon W, Desjardin D, Finy P, Geml J, Haridas S, Hughes K, Justo A, Karasiński D, Kautmanova I, Kiss B, Kocsubé S, Kotiranta H, LaButti KM, Lechner BE, Liimatainen K, Lipzen A, Lukács Z, Mihaltcheva S, Morgado LN, Niskanen T, Noordeloos ME, Ohm RA, Ortiz-Santana B, Ovrebo C, Rácz N, Riley R, Savchenko A, Shiryaev A, Soop K, Spirin V, Szebenyi C, Tomšovský M, Tulloss RE, Uehling J, Grigoriev IV, Vágvölgyi C, Papp T, Martin FM, Miettinen O, Hibbett DS, Nagy LG (2019) Megaphylogeny resolves global patterns of mushroom evolution. Nature Ecology & Evolution. https://doi.org/10.1038/s41559-019-0834-1
Wolfe AP, Tappert R, Muehlenbachs K, Boudreau M, McKellar RC, Basinger JF, Garrett A (2009) A new proposal concerning the botanical origin of Baltic amber. Proc R Soc Lond B Biol Sci 276(1672):3403–3412
Acknowledgements
I sincerely thank Heinrich Dörfelt (Jena/Germany) for his valuable comments on the manuscript. For the provision of electronic images, I am indebted to David S. Hibbett (Worcester/ Massachusetts) and George Poinar Jr. (Corvallis/Oregon), and again to George Poinar Jr. for our fruitful dialogue.
Author information
Authors and Affiliations
Corresponding author
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
ESM 1
(PDF 569 kb)
Rights and permissions
About this article
Cite this article
Halbwachs, H. Fungi trapped in amber—a fossil legacy frozen in time. Mycol Progress 18, 879–893 (2019). https://doi.org/10.1007/s11557-019-01498-y
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11557-019-01498-y