R-L categories correct, but text here does not match final assessment. Updated version will be published in IUCN´s Red List June or Nov 2019.
Gloioxanthomyces vitellinus is a European species growing mainly in seminatural grasslands, mostly in lowlands near the coasts (an oceanic species). The habitat is strongly declining due to changing agricultural practices, development projects and pollution. We assume a total habitat loss of more than 50% over the last 50 years (approximately three generations: one generation is assumed to be about 17 years). Habitat quality has also become impaired and the decline in population size over this time could be even higher, strengthening the assumption of a population decline of >50%. This decline in habitat is ongoing and expected to continue over the next 50 years. GBIF (2019) lists about 500 occurrences. The species is assumed to have a population of more than 20000 mature individuals. At a global scale (i.e. Europe) the decline is assumed to be on the average >50% in 50 years (past, present and future). The species meets the threshold for EN (A2c+3c+4c).
Gloioxanthomyces vitellinus (Fr.) Lodge, Vizzini, Ercole & Boertm. is a European species which belongs in the new genus Gloioxanthomyces, close to the N American species G. nitidus (Lodge et al. 2013). There is an epitype selected from Sweden (Lodge et al. 2013, cf. Bergelin 2012). GBIF occurences of G. vitellinus in N America should be G. nitidum, and other non-European occurences in GBIF are also doubtful (cf. Lodge et al. 2013), and will not be further treated here. In some European countries there is probably confusion with Chromosera (Hygrocybe) citrinopallida (A.H. Sm. & Hesler) Vizzini & Ercole which is mostly an alpine species; this species e.g. lack a viscid/slimy lamellae edge and has completely different spores (Boertmann 1990). The central European interpretation of H. vitellina is apparently sometimes Hygrocybe ceracea (Boertmann 2010). Synonymes: Hygrophorus vitellinus Fr., Hygrocybe vitellina (Fr.) P. Karst., Hygrocybe luteolaeta Arnolds.
This is a species of old seminatural grasslands in coastal/lowland parts of NW Europe (especially coastal Scandinavia, Netherlands, Germany and UK). It occurs in areas with rapid changes in land use, in a habitat which is strongly declining due to changing agricultural practices, development projects and pollution. There is also a serious decrease in quality of the remaining habitats.It is redlisted in most countries where it occurs.
Non-European occurences are excluded (see Taxonomic remarks). The largest populations are in NW Europe (especially UK, Netherlands, Germany, Sweden, Denmark and Norway) and with more scattered occurences in the rest of western and central Europe. The absence from Finland and most of eastern Europe, and the high frequency in North Sea areas, suggest a coastal distribution which could be caused by frost intolerance. The species has a striking coastal distribution in western Norway, in areas where january-february mean temperatures are >-1°C (Jordal & Gaarder 2002, Wollan et al. 2008). This is consistent with the occurence in the outermost SW coast of Sweden (Bergelin 2012), also consistent with a january mean temperature >-1°C. The coastal distribution could be caused by frost intolerance (Jordal & Gaarder 2002). The eastern boundary of distribution is not clear due to lack of data. Confusion with Chromosera citrinopallida or Hygrocybe ceracea can possibly explain GBIF occurences in some inland/alpine/continental parts of Europe. Information from some countries and localities should therefore be verified by microscopy or by DNA.
GBIF (2019) lists about 500 occurrences, which is probably too many due to confusion with other species. The total population probably exceeds 20 000 mature individuals but is decreasing in all known countries of occurence, caused by disappearance of small scale farming and traditional ways of grassland management, especially in coast/lowland areas. Griffith et al. (2013) estimated a habitat loss of 90% over the last 75 years for the CHEG-fungi (grassland fungi of the groups Clavariaceae, Hygrocybe s.l., Entoloma and Geoglossaceae) as a whole in Western Europe (i.e. loss in seminatural grasslands, based on available information). According to the Food and Agriculture Organization of the United Nations (FAO 2006), the area of grasslands in the EU declined by 12.8% over 13 years (1990-2003). The habitat quality of seminatural grasslands is also declining, strengthening the population decline. More than 75% of the grasslands habitats are in an unfavourable conservation status (http://ec.europa. eu/environment/nature/knowledge/ rep_habitats/index_en.htm#csa). Since the species occurs in the coast/lowland parts of Europe, we assume a total population decline for the species of >50% over the last 50 years. This trend is expected to continue in the future.
Population Trend: Decreasing
Gloioxanthomyces vitellinus is an indicator of mycologically rich but nutrient-poor, semi-natural grassland (a member of the waxcap grassland assemblage), often on acid soil. This habitat, which may be of low conservation concern for its plant and animal diversity, is rapidly disappearing due to changes in land use (see Threats). In Norway, most localities of the species are in seminatural grasslands or grassy/mossy spots in coastal Calluna heath (N=74; 90,5% in seminatural grasslands, only 1.4% in forests; Jordal et al. 2016), and similar patterns are found in other countries. Boertmann (2010) also mentions occurrences in fixed dunes, moist soil in Salix scrubs and once in a forest bog. Waxcaps are currently regarded as forming a biotrophic relationship with plants but the details remain unclear (Halbwachs et al. 2018). The fruit bodies are short-lived (weeks), but the mycel is suspected to be longlived; >50-100 years.
Habitat destruction and abandoning are the main threats to seminatural grasslands. The most important process is probably withgrowing due to ceased grazing/mowing of old seminatural grasslands as part of intensification of agriculture. Further modern cultivation methods like use of fertilizers, pesticides and plowing. Also some places changed land use with the construction of roads, industrial areas, settlements etc. Decline is expected to continue, as the areas of seminatural grasslands are of little economic importance in modern agriculture. Most waxcap grasslands are among types redlisted as VU, EN or CR in the EU red list of habitats (Jansen et al. 2016). The quality of habitats is also decreasing. More than 75% of the grassland habitats in EU are in an unfavourable conservation status, according to draft data provided by Member States under Article 17 of the Habitats Directive.
Site protection and management of habitats are very important conservation actions. The habitats should be protected against destruction due to intensification of agriculture or development plans. The maintaining of seminatural grasslands demands yearly grazing or mowing. If grazing by heavy animals destroys part of the soil, light animals like sheep should be recommended. Habitat conservation by governmental support to traditional agricultural practices is most important, this exists in many countries to maintain extensive areas of agricultural areas, and should be extended to larger areas than today.
Further ecological research is needed to clarify the nutrient strategy of waxcaps. Management plans are needed. Habitat trends should be monitored.
The species is not known to be used.
Artdatabanken Sweden 2019. Artfakta Gloioxanthomyces vitellinus http://artfakta.artdatabanken.se/taxon/4399
Artsdatabanken Norway 2019. https://www.artsdatabanken.no/Rodliste
Bergelin K 2012. Kromvaxskivling (Hygrocybe vitellina) funnen i Sverige. Svensk Mykologisk Tidskrift 33:2–8. [in Swedish; Hygrocybe vitellina found in Sweden]
Boertmann, D. 1990. The identity of Hygrocybe vitellina and related species. Nord. J. Bot. 10:311-317.
Boertmann, D. 2010. The genus Hygrocybe. Fungi of Northern Europe 1. 2nd revised edition. Danish Mycological Society, Copenhagen.
Boertmann D 2012. Update on Hygrocybe nitida. Omphalina 3(1): 12–13.
Food and Agricultural Organisation of the United Nations 2006. FAO Statistical Yearbook. – FAOSTAT.
Foreningen til svampekundskabens fremme 2019. Danmarks svampeatlas. https://svampe.databasen.org/
GBIF 2019. Hygrocybe vitellina/Gloioxanthomyces vitellinus. https://www.gbif.org/species/2538488; https://www.gbif.org/species/8390574
German Mycological Society 2019. Pilzen Deutschlands: Hygrocybe vitellina. http://www.pilze-deutschland.de/organismen/hygrocybe-vitellina-fr-p-karst-1879-1
Grifﬁth, G. W., Gamarra, J. P., Holden, E. M., Mitchel, D., Graham, A., Evans, D. A., et al. (2013) The international conservation importance of welsh ’waxcap’ grasslands. Mycosphere 4: 969–984. http://mycosphere.org/pdf/MC4_5_No10.pdf
Halbwachs H, Easton GL, Bol R, Hobbie EA, Garnett MH, Peršoh D, Dixon L, Ostle N, Karasch P & Grifﬁth GW, 2018. Isotopic evidence of biotrophy and unusual nitrogen nutrition in soil-dwelling Hygrophoraceae. Environmental Microbiology 20 (10), 3573–3588 doi:10.1111/1462-2920.14327
Janssen, JAM, J.S. Rodwell, M. García Criado, S. Gubbay, T. Haynes, A. Nieto, N. Sanders, F. Lan-ducci, J. Loidi, A. Ssymank, T. Tahvanainen, M. Valderrabano, A. Acosta, M. Aronsson, G. Arts, F. Attorre, E. Bergmeier, R.-J. Bijlsma, F. Bioret, C. Biţă-Nicolae, I. Biurrun, M. Calix, J. Capelo, A. Čar-ni, M. Chytrý, J. Dengler, P. Dimopoulos, F. Essl, H. Gardfjell, D. Gigante, G. Giusso del Galdo, M. Hájek, F. Jansen, J. Jansen, J. Kapfer, A. Mickolajczak, J.A. Molina, Z. Molnár, D. Paternoster, A. Piernik, B. Poulin, B. Renaux, J.H.J. Schaminée, K. Šumberová, H. Toivonen, T. Tonteri, I. Tsiripidis, R. Tzonev and M. Valachovič, (2016). European Red List of habitats. Part 2, terrestrial and freshwater habitats. European Union, Luxembourg. http://ec.europa.eu/environment/nature/knowledge/pdf/terrestrial_EU_red_list_report.pdf
Jordal, J.B. & Gaarder, G. 2002. Hygrocybe vitellina (Fr.) P.Karst. (sensu Boertmann 1990) - en oseanisk sopp. Blyttia 60:195-202. [in Norwegian; Hygrocybe vitellina – an oceanic fungus] http://www.jbjordal.no/publikasjoner/Hygrocybe vitellina Blyttia 2002.pdf
Jordal, J.B., Evju, M., Gaarder, G., 2016. Habitat specificity of selected grassland fungi in Norway. Agarica 37: 5-32. http://www.jbjordal.no/publikasjoner/Habitat_specificity_Jordal_et_al2016.pdf
Lodge D.J., Padamsee M., Matheny P.B., Aime M.C., Cantrell S.A., Boertmann D., Kovalenko A., Vizzini A., Dentinger B.T.M., Kirk P.M., Ainsworth A.M., Moncalvo J.-M., Vilgalys R., Larsson E., Lücking R., Griffith G.W., Smith M.E., Norvell L.L., Desjardin D.E., Redhead S.A., Ovrebo C.L., Lickey E.B., Ercole E., Hughes K.W., Courtecuisse R., Young, A., Binder M., Minnis A.M., Lindner D.L., Ortiz-Santana B., Haight J., Læssøe T., Baroni T.J.,
Geml J., Hattori T. (2014). Molecular phylogeny, morphology, pigment chemistry and ecology in Hygrophoraceae (Agaricales). Fungal Diversity 64:1-99. https://www.researchgate.net/publication/258508783_Molecular_phylogeny_morphology_pigment_chemistry_and_ecology_in_Hygrophoraceae_Agaricales
NBN Atlas 2019. Hygrocybe vitellina. https://species.nbnatlas.org/species/NBNSYS0000037585
NMV Verspreidingsatlas Paddenstoelen 2019. Hygrocybe vitellina. https://www.verspreidingsatlas.nl/0059350
Wollan AK, Bakkestuen V, Kauserud H, Gulden G, Halvorsen R 2008. Modelling and predicting fungal distribution patterns using herbarium data. Journal of Biogeography 35: 2298–2310. https://doi.org/10.1111/j.1365-2699.2008.01965.x