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1 The literature on , and earliest dinoflagellate cysts: supplement 4 2 3 James B. Riding 4 5 British Geological Survey, Environmental Science Centre, Keyworth, Nottingham NG12 6 5GG, United Kingdom 7 8 CONTACT James B. Riding email [email protected] 9 10 ABSTRACT 11 Since the publication of four compilations issued between 2012 and 2019, 93 further 12 published contributions on Triassic, Jurassic and earliest Cretaceous (Berriasian) 13 dinoflagellate cysts from Africa, North America, South America, the Arctic, Australasia, East 14 Europe, West Europe, the Middle East and Russia have been discovered in the literature, or 15 were issued in the last 12 months (i.e. between February 2018 and January 2019). Of these, 16 55 were published during 2018 and 2019, making this period a very productive one. These 17 studies are mostly on the Late Triassic and Early Jurassic of Europe. All the 93 items are 18 listed herein with digital object identifier (doi) numbers where available, as well as a 19 description of each item as a string of keywords. Publications on West Europe comprise 20 31.2% of the total, and items on Africa, the Arctic, Australasia, East Europe and Russia are 21 also significant (15.1%, 6.5%, 7.5%, 9.7% and 14.0% respectively). The least well- 22 represented regions are North America, South America and the Middle East (2.2%, 1.1% and 23 1.1% respectively). 24 25 KEYWORDS dinoflagellate cysts; earliest Cretaceous (Berriasian); Jurassic; literature 26 analysis and compilation; Triassic; worldwide 27 28 29 1. Introduction 30 The literature on Triassic to earliest Cretaceous (Berriasian) dinoflagellate cysts is extensive, 31 and was listed and reviewed by Riding (2012, 2013, 2014, 2019). These four papers cited 32 1347, 94, 89 and 266 publications respectively, with each citation followed by keywords 33 detailing the scope of each of the 1796 studies. The reviews provided by Riding (2014, 2019) 34 were substantially more interpretive than those in Riding (2012, 2013); the former two papers 1

35 reviewed and summarised each of the major publications listed. During the 12 months since 36 the completion of Riding (2019), i.e. between February 2018 and January 2019, the author 37 has compiled a further 93 relevant articles. Of these, 55 are recently published papers; the 38 other 38 were previously overlooked. Thirty of the 93 items are considered to be of 39 substantial scientific significance. The total of 55 articles published between February 2018 40 and January 2019 makes this one of the most productive periods on this topic in recent years. 41 The 93 articles are largely on the Late Triassic and Early Jurassic of Europe 42 (Tables 1, 2), and are listed in Appendix 1 of the Supplementary data. Papers on West Europe 43 are most numerous (29), and comprise 31.2% of the overall total (Table 1). By contrast, 44 Riding (2012, 2013, 2014, 2019) noted a substantial bias towards the Late Jurassic of Europe. 45 Publications on Africa, the Arctic, Australasia, East Europe and Russia are also numerous 46 (15.1%, 6.5%, 7.5%, 9.7% and 14.0% respectively; Table 1). Finally, relatively low 47 proportions of articles are on North America, South America and the Middle East (2.2%, 48 1.1% and 1.1% respectively; Table 1). In this compliation, six formally unpublished PhD 49 theses are listed (e.g. Ruckwied 2009, Baranyi 2018, Correia 2018); these are all freely 50 available online and the respective web addresses are quoted. 51 52 2. Regional review and synthesis 53 In this section, brief commentaries/reviews of selected articles from the 93 publications listed 54 in Appendix 1 of the Supplementary data are presented. These items are from nine of the 14 55 geographical subdivisions in Riding (2019). In the present compilation, there are no relevant 56 single-region publications from Central America, Antarctica, Southeast Asia, China and the 57 Indian subcontinent. Each contribution in Appendix 1 of the Supplementary data is referred 58 to at least one of these 14 regions; furthermore, ‘multi-region’ and ‘no geographical focus’ 59 are also options (Table 1). 60 The publication by Mangerud et al. (2019) is a good example of the latter two 61 categories. This article is a global synthesis of the available literature on Triassic 62 dinoflagellate cysts; it reviewed data from Arabia, the present Arctic region, Europe, Oceania 63 and South America. It is clear that, with the exception of Sahulidinium ottii in one well in 64 offshore Australia, dinoflagellate cyst body fossils first appeared during the Late Triassic. 65 The Norian–Rhaetian genus Rhaetogonyaulax appears to be a cosmopolitan pioneer taxon. 66 There was migration into many formerly land-locked regions during the Rhaetian, and most 67 Triassic dinoflagellate cyst taxa became extinct at the end-Triassic event. Other examples of 68 ‘multi-region’ and ‘no geographical focus’ papers include Boersma et al. (1987), Lindstrom 2

69 et al. (2017), Londeix (2018) and Penaud et al. (2018). All dinoflagellate cysts and other 70 palynomorph taxa at and below species level mentioned in this paper are listed in Appendix 2 71 of the Supplementary data with full author citations. 72 73 74 2.1. Africa 75 This compilation includes 14 single-region contributions from East and North Africa, 76 including five that are deemed especially significant (Appendix 1 of the Supplementary data). 77 The highlights of this research are outlined in the next two subsections. 78 79 2.1.1. East Africa 80 In this synthesis, four single-region contributions on Ethiopia and Tanzania in East Africa are 81 considered. Msaky (2008) is a thesis on the Bajocian to Cenomanian palynology of coastal 82 Tanzania, and is available online. The thesis was published as Msaky (2011a, 2011b), and 83 these major publications were reviewed by Riding (2019). 84 The palynofloras of the Pindiro Group (Triassic to Lower Jurassic) of southern 85 Tanzania were studied by Hudson and Nicholas (2014). These authors reported the 86 dinoflagellate cysts Dapcodinium priscum, Sahulidinium ottii, Scriniocassis sp. cf. S. weberi 87 and Sverdrupiella sp. from the Mbuo Formation (Hudson and Nicholas 2014, p. 59). This 88 assemblage was interpreted as being Late Triassic in age. The presence of Dapcodinium 89 priscum and Sverdrupiella sp. is consistent with this age determination. However, 90 Sahulidinium ottii and Scriniocassis sp. cf. S. weberi are indicative of the Middle Triassic and 91 the late Pliensbachian to Aalenian respectively (Helby et al. 1987, Riding and Thomas 1992). 92 If confirmed, this report would be the first record of Sahulidinium ottii since this species was 93 first described by Stover & Helby (1987). Nannoceratopsis pellucida was recorded from the 94 Mihambia Formation by Hudson and Nicholas (2014, p. 65). The Mihambia Formation was 95 interpreted as being Toarcian to Aalenian in age. Either the interpreted age, or the 96 identification of Nannoceratopsis pellucida appears to be erroneous because the range base of 97 this species in both hemispheres is (Riding et al. 1985, Riding et al. 2010). It 98 should be noted that the ‘probable reworked dinoflagellate’ figured by Hudson and Nicholas 99 (2014, fig. 3.5M) is an indeterminate palynomorph, and has no demonstrable dinoflagellate 100 affinity. 101 Smelror et al. (2018) is a relatively short paper on the Upper Jurassic and Lower 102 Cretaceous palynostratigraphy of the Kipatimu, Mitole, Nalwehe and Kihuluhulu formations 3

103 of the onshore Mandawa Basin in southeastern coastal Tanzania. The authors concluded that 104 the four formations span the –Tithonian to Aptian–Albian interval. Jurassic and 105 earliest Cretaceous dinoflagellate cysts were recorded only from the Mitole Formation, and 106 these were interpreted as being of Oxfordian to Berriasian age. They include Canningia 107 reticulata, Circulodinium distinctum, Cribroperidinium spp., Dingodinium jurassicum, 108 Kaiwaradinium scruttinum and Systematophora areolata. This assemblage is significantly 109 reminiscent of the Late Jurassic and Early Cretaceous of Gondwana (Helby et al. 1987, 110 Riding et al. 2010). Sample WP232-5-14 from the Mitole Formation contains a marine 111 palynoflora reminiscent to the Dingodinium jurassicum-Kilwacysta assemblage of Schrank 112 (2005), and is indicative of a correlation with the Trigonia smeei Bed of Tendaguru Hill in 113 southeastern Tanzania. 114 115 116 2.1.2. North Africa 117 Ten single-region contributions on North Africa are included herein. Nine of the articles are 118 on northern Egyptian material, which reflects the intense hydrocarbon exploration and 119 production activity in this region. One contribution (Jaydawi et al. 2016) is a study of 120 Moroccan material. 121 Aboul Ela and Tahoun (2010) documented the stratigraphical palynology of the 122 to Lower Cretaceous (Bathonian–Callovian to Albian) of the Mango-1 and 123 Til-1 offshore wells, northern Sinai, Egypt. Based on 174 samples of ditch cuttings, the 124 authors established 11 informal dinoflagellate cyst zones which were correlated with other 125 successions in Egypt and surrounding Tethyan areas. Five of these zones cover the 126 Bathonian–Callovian to ?Berriasian interval. A major depositional hiatus between the late 127 and the ?Berriasian was identified, and was attributed to a major sea-level fall 128 associated with the Cimmerian orogenic event (Aboul Ela and Tahoun 2010, figs 2, 3). The 129 samples yielded diverse and rich marine and terrestrial palynofloras. This paper focuses 130 entirely on biostratigraphy, and the ranges of all the palynomorphs were given in non- 131 quantitative range charts (Aboul Ela and Tahoun 2010, p. 90–98). The Jurassic dinoflagellate 132 cyst associations appear to be substantially similar in content and distribution to their 133 European counterparts; for example Cribroperidinium? longicorne, Ctenidodinium 134 continuum, Gonyaulacysta jurassica, Korystocysta pachyderma and Systematophora areolata 135 were recorded.

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136 Ied and Ibrahim (2010) studied the Jurassic and Early Cretaceous palynology of the 137 Almaz-1 well in northern Egypt. This contribution focused mostly on miospores, but some 138 dinoflagellate cysts were recorded from the Bajocian–Callovian to the Barremian. These 139 include Ctenidodinium sellwoodii, Gonyaulacysta jurassica, Pareodinia ceratophora and 140 Systematophora penicillata (see Ied and Ibrahim 2010, p. 10). A very similar 141 biostratigraphical paper on the Middle Jurassic to Early Cretaceous (Callovian–Albian) of the 142 Kabrit-1 well drilled west of Cairo in northeastern Egypt was published by Ied and Lashin 143 (2016). They recorded dinoflagellate cysts from the entire succession examined, including 144 Cribroperidinium spp., Dichadogonyaulax? pannea, Gonyaulacysta jurassica, Lithodinia 145 jurassica, Pareodinia prolongata and Systematophora areolata (see Ied and Lashin 2016, fig. 146 2). This assemblage is similar to floras from eastern North America and Europe. 147 Tahoun et al. (2012) undertook a study of the Middle Jurassic to Upper Cretaceous 148 succession of the Alamein-IX well in northern Egypt. In this study, zone 5, which comprises 149 the Masajid Formation, was interpreted as being of Callovian to possibly Kimmeridgian age 150 (Tahoun et al. 2012, p. 68, fig. 3). This interpretation was based on the presence of 151 Acanthaulax sp. cf. A. crispa, Amphorulacysta? dodekovae, Epiplosphaera reticulospinosa, 152 Lithodinia jurassica, Meiourogonyaulax reticulata and Sentusidinium spp. This assemblage 153 appears to be somewhat biostratigraphically ambiguous; however, the presence of 154 Amphorulacysta? dodekovae and Epiplosphaera reticulospinosa strongly suggests a late 155 Oxfordian to early Kimmeridgian age (Feist-Burkhardt and Wille 1992, fig. 2). 156 Gentzis et al. (2018) published a study on the petroleum prospectivity of the 157 Matruh Basin, North Western Desert, Egypt. The dinoflagellate cysts Ctenidodinium 158 sellwoodii, Korystocysta gochtii, Mancodinium semitabulatum, Nannoceratopsis gracilis 159 Rhynchodiniopsis cladophora and Systematophora penicillata were recorded from the Wadi 160 Natrun, Khattatba and Masajid formations. The two discrete intervals represented by these 161 formations were interpreted as being of Toarcian–Aalenian and ?late Bathonian–Oxfordian 162 (Gentzis et al. 2018, fig. 4). Some photographs were presented, although the images of 163 Nannoceratopsis gracilis (Gentzis et al. 2018, pl. 1/1, 2) are not clearly of that species. 164 The stratigraphical palynology of the Middle and Upper Jurassic (Bathonian– 165 Oxfordian) strata of the South Sallum well, North Western Desert, Egypt was studied by 166 Mostafa et al. (2018). This interval yielded relatively diverse dinoflagellate cyst 167 asssociations, and these were comprehensively illustrated (Mostafa et al. 2018, pls 2–5). Two 168 dinoflagellate cyst biozones were recognised. These are the Dichadogonyaulax sellwoodii – 169 Wanaea acollaris – Wanaea digitata Assemblage Zone, interpreted as Bathonian–Callovian 5

170 in age, and the Amphorula dodekovae Interval Zone which was deemed to be Callovian– 171 Oxfordian. Note that the species Amphorula dodekovae is now questionably accommodated 172 in Amphorulacysta? (see Williams and Fensome 2016, p. 139). Included in the 173 Dichadogonyaulax sellwoodii – Wanaea acollaris – Wanaea digitata Assemblage Zone were 174 Ctenidodinium ornatum, Impletosphaeridium varispinosum, Korystocysta spp., 175 Mendicodinium groenlandicum, Pareodinia prolongata and Wanaea digitata. By comparison 176 with Europe, this interval is most likely to be entirely Callovian in age (e.g. Poulsen and 177 Riding 2003). The index taxon for the Amphorula dodekovae Interval Zone was first 178 described from the Kimmeridgian and its range was determined as late Oxfordian to early 179 Kimmeridgian (Zotto et al. 1987; Feist-Burkhardt and Wille 1992, fig. 2). Mostafa et al. 180 (2018) interpreted this biozone as being of Callovian–Oxfordian age. However the presence 181 of Amphorulacysta? dodekovae, Compositosphaeridium? polonicum, Endoscrinium 182 galeritum, Gonyaulacysta jurassica and Neuffenia willei is strongly suggestive that it is 183 entirely of Oxfordian age (Riding 1984a, Riding and Thomas 1992). The biostratigraphical 184 significance of selected Berriasian dinoflagellate cysts from northern Egypt was discussed in 185 a review paper by Tahoun and Ied (2018). Sparse and low diversity dinoflagellate cyst 186 associations were recorded from the Tithonian to Albian strata penetrated by the Minqar-IX 187 well, northern Egypt by Mahmoud et al. (2019). 188 The paper by Jaydawi et al. (2016) is a major and well-illustrated contribution on 189 the Callovian to Kimmeridgian dinoflagellate cyst biostratigraphy of the petroliferous 190 Essaouira Basin in the Marrakesh–Safi region of central-western Morocco. These authors 191 examined three boreholes. An early Callovian assemblage which includes Ctenidodinium 192 combazii, Ctenidodinium cornigerum and Impletosphaeridium varispinosum was encountered 193 in the MKL-110 borehole. Further material was studied from the NDK-2 and NDK-3 194 boreholes. A rich late Callovian flora containing Ctenidodinium continuum, Ctenidodinium 195 ornatum and Wanaea thysanota was recovered in the latter borehole. The NDK-2 well 196 yielded established marker species such as Cribroperidinium? longicorne, Egmontodinium 197 polyplacophorum, Gonyaulacysta centriconnata, Scriniodinium crystallinum, 198 Systematophora areolata and Trichodinium scarburghense, indicative of the interval from the 199 Callovian–Oxfordian transition to the Kimmeridgian. 200 201 202 2.2. Sub-Arctic North America

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203 The only relevant single-region publication on sub-Arctic North America issued between 204 February 2018 and January 2019 is that by Dodsworth and Eldrett (2018). These authors 205 recorded the reworking of low numbers of Chytroeisphaeridia chytroeides, ?Gonyaulacysta 206 jurassica, ?Rhynchodiniopsis cladophora and Scriniodinium spp. into the Upper Cretaceous 207 (Cenomanian–Turonian) Bridge Creek Member (Greenhorn Formation) near Pueblo, 208 Colorado, USA. These Middle to Late Jurassic forms are part of an extensive suite of 209 allochthonous palynomorphs of to middle Cretaceous age (Dodsworth and 210 Eldrett 2018, p. 9, 10). 211 Additionally, one older single-region contribution was also discovered. This is by 212 van Helden (1987), and comprises a short article in a newsletter designed to encourage 213 research on the Jurassic palynology of Alberta and Saskatchewan in western Canada. This 214 author reported that the Nordegg, Poker Chip and Rock Creek formations of Alberta, and the 215 Shaunavon and Vanguard formations in Saskatchewan contain abundant and diverse Jurassic 216 dinoflagellate cyst assemblages. It was noted that detailed study of these floras would help 217 the understanding of both the biostratigraphy and palaeoecology of the region. Van Helden 218 (1987) expressed surprise that the palynology of these lithostratigraphical units had not been 219 studied by contemporary palynologists in Canada, and recommended that this open field of 220 research be advanced. 221 222 223 2.3. South America 224 Only one publication is included here on South America. This is Olivera et al. (2018), which 225 is a report of the pollen grain Shanbeipollenites proxireticulatus from the Vaca Muerta 226 Formation of the Neuquén Basin, Argentina and its associated palynomorphs, including 227 dinoflagellate cysts. Shanbeipollenites proxireticulatus was previously reported from the 228 Upper Jurassic of Tanzania (Schrank 2004). The material in this study was interpreted as 229 being of ?Berriasian–Valanginian age based on the overall palynoflora which includes 230 Meiourogonyaulax bulloidea, Sentusidinium villersense and Systematophora penicillata 231 (Olivera et al. 2018, figs 4, 5). 232 233 234 2.4. The Arctic

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235 Six recent single-region contributions from the Arctic are considered in this subsection. Four 236 of these are from Arctic Russia, one of which (Nikitenko et al. 2018a) is considered to be 237 especially significant (Appendix 1 of the Supplementary data). 238 The Lower Jurassic through Upper Cretaceous (Hettangian–Turonian) 239 biostratigraphy and lithostratigraphy of the New Siberian Islands and adjacent areas of 240 continental Arctic Siberia was studied by Nikitenko et al. (2017), who defined three 241 depositional series with important reference sections. These strata have been substantially 242 deformed. Despite the substantial structural complications, however, Nikitenko et al. (2017) 243 demonstrated the applicability of these successions for correlation in the continental shelf east 244 of the Laptev Sea and in the west of the East Siberian Sea. These authors used ammonites, 245 bivalves, foraminifera, miospores and ostracods, in addition to dinoflagellate cysts. Nikitenko 246 et al. (2018b) is a closely related study and involves an investigation of the same sections that 247 were studied by Nikitenko et al. (2017). Nikitenko et al. (2018b) comprises a detailed 248 examination of the micropalaeontology (dinoflagellate cysts, foraminifera, miospores and 249 ostracods) and Hettangian and Pliensbachian organic geochemistry of the Hettangian to 250 Turonian reference sections of the New Siberian Islands. A scheme of Boreal standard 251 biozones was erected that have regional applicability in northern Siberia. Kashirtsev et al. 252 (2018) involves a study based on organic geochemistry on the Oxfordian to Valanginian 253 succession of the Nordvik Peninsula, western Anabar Bay, Arctic Russia. A comprehensive 254 biostratigraphy has been developed for this succession including seven dinoflagellate cyst 255 zones (Kashirtsev et al. 2018, fig. 2). 256 By far the most significant publication on the Arctic region in this review is that by 13 257 Nikitenko et al. (2018a). This work details the biostratigraphy, geochemistry (δ CTOC), 258 palaeoecology and sedimentology of the Middle Jurassic to Lower Cretaceous (Bathonian– 259 Valanginian) succession of the Olenek section in the Anabar-Lena region of Arctic Russia. 260 The emphasis is on the uppermost Jurassic and Lower Cretaceous (Tithonian [=Volgian] to 261 Valanginian) Buolkalakh and Iaedaes formations (Nikitenko et al. 2018a, fig. 3). Detailed 262 range data was gathered for ammonites, dinoflagellate cysts, foraminifera and miospores 263 (Nikitenko et al. 2018a, figs 6–9). Five ‘dinocyst local zones’ were recognised: 1 – the 264 Cometodinium whitei, Epiplosphaera gochtii, Gonyaulacysta eisenackii ‘dinocyst local 265 zone’; 2 – the Bourkidinium sp. ‘dinocyst local zone’; 3 – the Gochteodinia villosa ‘dinocyst 266 local zone’; 4 – the Batioladinium varigranosum, Occisucysta tentorium ‘dinocyst local 267 zone’; and 5 – the Cyclonephelium cuculliforme, Batioladinium reticulatum ‘dinocyst local 268 zone’ (Nikitenko et al. 2018a, fig. 7). Numbers 1 to 4 of these ‘zones’ cover the ?uppermost 8

269 Kimmeridgian–Lower Volgian to uppermost Tithonian/Volgian–lower Boreal Berriasian 270 interval. The ages of the five ‘dinocyst local zones’ from the Olenek section were calibrated 271 to the current geological time scale via correlations with 11 coeval studies throughout the 272 northern and southern hemispheres (Nikitenko et al. 2018a, fig. 11). 273 The only other single-region publications on the Arctic reviewed herein are those by 274 Felix and Burbridge (1977) and Rismyhr et al. (2018). Felix and Burbridge (1977) 275 established a new species of pteridophytic spore, Ricciisporites umbonatus, from the Upper 276 Triassic (Carnian–Norian) of the Sverdrup Basin, Arctic Canada. This comprehensive study 277 and it included details of the associated palynomorphs, including common occurrences of the 278 dinoflagellate cysts Sverdrupiella baccata, Sverdrupiella manicata, Sverdrupiella 279 ornaticingulata, Sverdrupiella septentrionalis and Sverdrupiella usitata in the borehole 280 successions that were examined. Dinoflagellate cysts proved absent in the outcrop samples 281 that were studied (Felix and Burbridge 1977, table 1). Sverdrupiella usitata is the most 282 prominent species throughout the boreholes sections studied. The genus Sverdrupiella is 283 therefore highly characteristic of the Norian of boreholes drilled in the Canadian Arctic 284 (Bujak and Fisher 1976). 285 Rismyhr et al. (2018) provided a major study of the palynology, sedimentology and 286 sequence stratigraphy of the Carnian to Callovian strata of western central Spitsbergen, 287 Svalbard. Ten composite assemblage zones (CAZs) were established, of which the six for the 288 Norian to Callovian interval are based on dinoflagellate cysts (Rismyhr et al. 2018, fig. 3). 289 The principal focus of this study was the Knorringfjellet Formation (Wilhelmøya Subgroup), 290 in which three sequences were identified. Sequence 1 is Norian, and is characterised by the 291 Rhaetogonyaulax arctica and Heibergella spp. CAZs. Nannoceratopsis senex gives its name 292 to a Toarcian CAZ which is equivalent to Sequence 2. The Brentskardhaugen Bed is a highly 293 condensed deposit of late Toarcian–early Aalenian age. It is assigned to the Phallocysta 294 eumekes CAZ, and was assigned to Sequence 2 by Rismyhr et al. (2018). 295 296 297 2.5. Australasia 298 Seven single-region contributions from Australasia are listed in Appendix 1 of the 299 Supplementary data in this review. Zhang Wangping & Grant-Mackie (2001) described the 300 palynology of the Late Triassic and Early Jurassic (Norian–Sinemurian) of New Zealand. 301 This paper is chiefly on miospores, although the authors also reported undifferentiated

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302 acritarchs and dinoflagellate cysts from various lithostratigraphical units of the Hokonui Hills 303 and southwestern Kawhia. 304 The remaining six single-region studies are from Australia. Jones & Nicoll (1984) and 305 Dixon et al. (2012) are short papers on the Late Triassic (Carnian–Norian) of the North West 306 Shelf of Australia. Both mention dinoflagellate cysts briefly. Dixon et al. (2012) worked on 307 the Upper Mungaroo Formation from the offshore Carnarvon Basin. These authors recorded 308 Dapcodinium spp. from marginal marine to tidally influenced facies, and Hebecysta balmei 309 and Rhaetogonyaulax spp. from open-marine settings. The paper by Paumard et al. (2018) is 310 also on material from the North West Shelf of Australia. In this multidisciplinary study the 311 authors examined the sedimentary architecture and sediment partitioning in the Barrow 312 Group (Tithonian–Valanginian) of the Northern Carnarvon Basin. Offshore well data were 313 integrated to establish a seismic stratigraphy of this economically important unit. The authors 314 related seven third-order seismic sequences to the eustatic and tectonic history of the 315 depocentre, and calibrated these sequences using the Pseudoceratium iehiense to 316 Systematophora areolata dinoflagellate cyst zones of Helby et al. (1987). 317 However, the most significant Australasian contribution listed herein is by Wainman 318 et al. (2018a). This paper is on the latest Jurasssic (Tithonian) palynology of the Indy 3 well 319 in the western Surat Basin, Queensland, southeastern Australia. These authors discovered 320 low-diversity dinoflagellate cysts and colonial algae in the Walloon Coal Measures (Injune 321 Creek Group). The Walloon Coal Measures were previously believed to be entirely 322 nonmarine. The study showed that either a brief marine transgression is represented by this 323 unit, or that these planktonic palynomorphs were freshwater forms and thus represent a rare 324 report of pre-Cretaceous nonmarine dinoflagellate cysts. These records are coincident with an 325 interval of high global sea level hence the former scenario appears to be the best explanation. 326 The new dinoflagellate cyst species described by Wainman et al. (2018a) are Moorodinium 327 crispa and Skuadinium fusum, and they also described the colonial alga Palambages pariunta 328 as new. Moorodinium crispa and Skuadinium fusum are small, thin-walled proximate cysts 329 from a thin (ca. 2 m) unit interpreted as a possible upper estuarine deposit (Wainman et al. 330 2018a, pls 1, 2). This interpretation, together with the high dominance and low species 331 richness nature of the assemblage, is consistent with a freshwater setting. Wainman et al. 332 (2018a) provided the palynological basis for a wider study of the Middle–Upper Jurassic 333 Walloon Coal Measures of the Surat Basin (Wainman and McCabe 2018, Wainman et al. 334 2018b). 335 10

336 337 2.6. East Europe 338 None of the nations generally considered to comprise this region are in the Arctic Circle, so 339 the prefix ‘sub-Arctic’ is superfluous in this case. Nine single-region items concerning 340 Bulgaria, Hungary, Poland and Slovakia in East Europe are listed in Appendix 1 of the 341 Supplementary data. Two of these publications are deemed to have substantial significance. 342 Three multi-authored papers written in Bulgarian detail the Jurassic (Sinemurian– 343 Tithonian) lithostratigraphy of northeastern Bulgaria (Sapunov et al. 1985, 1986a, 1986b). 344 Specifically, the Dobrič, Drinovo, Esenica, Ginci, Javorec, Kalojan, Ozirovo, Polaten, 345 Provadija, Sultanci and Tiča formations were considered in this set of contributions, all in the 346 same journal. The material studied is from numerous deep, continuously cored, boreholes 347 drilled as part of a partially successful petroleum exploration campaign throughout northern 348 Bulgaria. In Sapunov et al. (1985), the four formations considered are treated separately in 349 ascending stratigraphical order. By contrast in Sapunov et al. (1986a, 1986b), the 350 lithostratigraphy was described borehole-by-borehole. Throughout each of these three papers, 351 integrated biostratigraphy based on brachiopods, calpionellids, molluscs and palynomorphs 352 was included. Selected occurrences of dinoflagellate cysts, especially in Sapunov et al. 353 (1986a), were provided by the late Lilia Dodekova, who was one of the co-authors. No 354 photographs or range charts were provided. 355 The paper by Bóna (1995) is a major work on the Upper Triassic 356 palynostratigraphy of a large coal-bearing basin around Pécs, in the Mecsek Mountains of 357 southern Hungary. Only ‘dinoflagellate indet.’ was recovered from the lowermost Mecsek 358 Coal formations (Rhaetian) (Bóna 1995, table 2; pl. 8/17). This specimen is very poorly- 359 preserved, but appears to be referable to Rhaetogonyaulax rhaetica. This author also reported 360 questionable specimens of Hystrichosphaeridium magnum from the Karolinavölgy Sandstone 361 and the lowermost Mecsek Coal formations, which are of Norian and Rhaetian age 362 respectively (Bóna 1995, table 2; pl. 8/16; pl. 9/2, 3, 6). The original authorship of the 363 spinose species Hystrichosphaeridium magnum was not provided by Bóna (1995) and was 364 not located by the present author. Only one of the two specimens illustrated of 365 Hystrichosphaeridium magnum appears to have possible dinoflagellate cyst affinity (Bóna 366 1995, pl. 8/16). This specimen is a chorate form with an apparent apical archaeopyle and may 367 be refereable to Beaumontella. 368 As part of an unpublished, PhD thesis mainly focussed on miospores from 369 southwestern England, Hungary and the southwestern USA, Baranyi (2018) analysed 11

370 borehole material from the the Veszprém Marl Formation (Carnian) of the southern 371 Transdanubian Range, western Hungary and recorded ‘dinocyst indet.’ and Heibergella sp. 372 (see Baranyi 2018, pl. 12/10, 11). These records are within the Carnian Pluvial Episode, and 373 are highly unusual in that most Triassic dinoflagellate cyst occurrences are Norian–Rhaetian 374 (Mangerud et al. 2019, fig. 2). 375 The dissertation by Ruckwied (2009) on the palynology of the Rhaetian and 376 Hettangian strata of the northwestern Tethyan Realm of Hungary and northern Slovakia 377 aimed to investigate biostratigraphy, palaeoclimate and palaeoecology. The principal thrust of 378 this contribution is on miospores. However Ruckwied (2009) reported Dapcodinium priscum 379 and Rhaetogonyaulax rhaetica from the Rhaetian and Hettangian of the Furkaska section in 380 the Tatra Mountains of northern Slovakia (see also Ruckwied and Götz 2009). Ruckwied 381 (2009) did not record dinoflagellate cysts from the successions investigated in Hungary. 382 The prominent Hungarian palynologist Mária Sütőné Szentai produced a 383 compilation of all the genera and species of to Holocene organic-walled 384 microplankton reported from Hungary since 1957 (Sütőné Szentai 2018). This compendium 385 was an alphabetical listing of all published post-Silurian records of palynomorphs excluding 386 miospores. By far the largest section of this book is on dinoflagellate cysts (Sütőné Szentai 387 2018, p. 11–111). Every species recorded from Hungary is included; the holotype and the 388 stratigraphical range are also given. The main papers on Triassic and Early Jurassic 389 dinoflagellate cysts from Hungary included in this compilation are Bóna (1995), Bucefalo 390 Palliani et al. (1997) and Baranyi et al. (2016). 391 392 393 2.7. Sub-Arctic West Europe 394 A total of 29 single-region contributions on the Triassic, Jurassic and earliest Cretaceous of 395 sub-Arctic West Europe are covered in this review, and 12 of these are considered to be 396 considerably impactful (Appendix 1 of the Supplementary data). This section is subdivided 397 into three subsections based on the stratigraphical coverage of the items. 398 399 2.7.1. Triassic and Early Jurassic 400 Seven articles summarised here are focused on the Triassic and Early Jurassic interval. The 401 paper by Karle (1984) involves a detailed study of the palynology of the Triassic–Jurassic 402 boundary at Fonsjoch, western Austria. This author recorded Rhaetogonyaulax rhaetica from 403 the Rhaetian. This species is especially common in the middle and upper Rhaetian, and the 12

404 range top is immediately below a prominent limestone bed which underlies the Pre-Planorbis 405 Beds at the Triassic–Jurassic transition (Karle 1984, fig. 3). 406 The published PhD dissertation by Holstein (2004) details the palynofacies, 407 palynology and sequence stratigraphy of the Kössen Beds (Upper Triassic, Norian–Rhaetian) 408 of the Eiberg and Mörtlbachgraben sections in the Northern Calcareous Alps of northern 409 Austria. The palynofloras are dominated by miospores, but the dinoflagellate cysts 410 Dapcodinium priscum and Rhaetogonyaulax rhaetica were recognised. This author asserted 411 that Dapcodinium priscum preferred high-energy, shallow-water settings, and 412 Rhaetogonyaulax rhaetica had a preference for deep-water, low-energy palaeoenvironments. 413 A wide-ranging and multidisciplinary study on the Triassic–Jurassic boundary by 414 Lindström et al. (2017) includes descriptions of palynofloras from several localities in 415 Austria, Denmark, England and Germany. The range top of the last, last common and last 416 consistent occurrences (LO, LCO and LCON respectively) of Rhaetogonyaulax rhaetica 417 were used as a reliable regional markers. The LCO and LCON of this prominent and 418 cosmopolitan species are consistently within, or immediately below and above, the extinction 419 phase in the late Rhaetian. However, Rhaetogonyaulax rhaetica apparently became extinct 420 (LO) during the post-extinction phase in Austria and England (Lindström et al. 2017, fig. 12). 421 Juncal et al. (2018) involves a multidisciplinary study of the and Triassic 422 of the Paris Basin in central France. These authors reported Dapcodinium priscum and 423 Rhaetogonyaulax rhaetica from the uppermost Rhaetian of the Sancerre-Couy 1 borehole, 424 within their SC-4 assemblage. Schneebeli-Hermann et al. (2018) provided a very detailed 425 study of the palynology of the Norian, Rhaetian and Sinemurian strata of northern 426 Switzerland, distinguishing five informal palynomorph associations. The main emphasis was 427 on miospores, but nine dinoflagellate cyst taxa were recognised from the Rhaetian and 428 Sinemurian (Schneebeli-Hermann et al. 2018, figs 2, 5). These include Beaumontella langii, 429 Dapcodinium priscum, Rhaetogonyaulax rhaetica and ?Suessia swabiana; the greatest 430 dinoflagellate cyst diversity is in the Rhaetian (Schneebeli-Hermann et al. 2018, figs 2, 5). 431 As part of a major multidisciplinary paper on the cores recovered by the 432 Schandelah Scientific Drilling Project in northern Germany, van de Schootbrugge et al. 433 (2018) investigated the palynology of an important Rhaetian to Toarcian succession. Full 434 details of the palynomorphs recovered were not given, but these authors illustrated major 435 bioevents and figured significant dinoflagellate cyst, miospore taxa (van de Schootbrugge et 436 al. 2018, fig. 3, pl. 1). The authors recognised the Early Jurassic Dapcodinium priscum, 437 Liasidium variabile and Nannoceratopsis dinoflagellate cyst zones. 13

438 Several contributions on the Early Jurassic palynology of the Lusitanian Basin in 439 western Portugal were published recently by Vânia Correia and her co-authors (Appendix 1 440 of the Supplementary data). These are all associated with the author’s PhD thesis (Correia 441 2018), and the most significant is Correia et al. (2018). This paper is on the 442 palynostratigraphy of the Lower Jurassic strata of this important Iberian depocentre. Correia 443 et al. (2018) documented the Sinemurian to Toarcian palynomorph biostratigraphy based on 444 six localities, with the principal emphasis being on dinoflagellate cysts. The Sinemurian 445 proved devoid of dinoflagellate cysts. By contrast the Pliensbachian and Toarcian are 446 characterised by the presence of the genera Luehndea, Mancodinium, Mendicodinium, 447 Nannoceratopsis and Scriniocassis. Luehndea was apparently made extinct by the Toarcian 448 Oceanic Anoxic Event (T-OAE). This event proved substantially more intense in the 449 Lusitanian Basin than elsewhere in southern Europe, and the recovery of phytoplankton was 450 protracted in this basin. Correia et al. (2018) proposed a biozonation for the late 451 Pliensbachian and Toarcian, comprising the Luehndea spinosa and Mendicodinium 452 microscabratum dinoflagellate cyst zones. The zones were subdivided into subzones (Correia 453 et al. 2018, fig. 15). 454 455 2.7.2. Middle Jurassic 456 In this subsection, four items focused on the Middle Jurassic are documented. A major study 457 on the palynology of the Middle Jurassic Ravenscar Group, from the Cleveland Basin, 458 northeastern Yorkshire, northern England, was undertaken by Hogg (1993). This unpublished 459 PhD thesis focussed on outcrops of the Cloughton, Scarborough, Scalby and Cornbrash 460 formations (Bajocian–Bathonian) in the Scarborough area of North Yorkshire. The emphasis 461 was on miospores, but diverse dinoflagellate cyst floras were also recovered and 30 genera 462 were recognised (Hogg 1993, p. 121–137, fig. 4.6, pls 17–23). Three new species were 463 informally introduced. Furthermore, Ambonosphaera calloviana and Tabulodinium senarium 464 were reported from the UK for the first time. Hogg (1993) determined that much of the Long 465 Nab Member of the Scalby Formation is of latest Bathonian (Clydoniceras discus ammonite 466 zone) age. This work refined the biostratigraphical results of Riding and Wright (1989), who 467 reported a Bathonian (undifferentiated) age. Hogg (1993, p. 179–190) discussed the 468 dinoflagellate cyst biostratigraphy of the Scarborough and Scalby formations in some detail, 469 comparing his results with previous studies such as those by Riding and Wright (1989) and 470 Gowland and Riding (1991). The sequence stratigraphy of the successions investigated was 471 also analysed. 14

472 Powell et al. (2018, appendix B) documented the palynology of two samples from 473 the Kellaways Sand Member (Lower Callovian) of Burythorpe Sand Quarry, North 474 Yorkshire, UK. Sample 2 was relatively rich in dinoflagellate cysts and five specimens were 475 illustrated (Powell et al. 2018, fig. 12). 476 The early Mesozoic phytoplankton radiation was investigated by Wiggan et al. 477 (2018). The coccolithophores and dinoflagellates radiated substantially during the Bajocian 478 (~170–168 Ma). Wiggan et al. (2018) described and interpreted a dominance of the genus 479 Dissiliodinium in the mid-latitudes, followed by the explosive evolutionary expansion of the 480 dinoflagellate family Gonyaulacaceae. The latter phenomenon was viewed as being strongly 481 influenced by increases in sea level and changes in ocean gateways, and possibly related to 482 the Mesozoic Marine Revolution. The key dinoflagellate cyst data in Wiggan et al. (2018) 483 were from an important borehole succession in southern Germany initially published by 484 Wiggan et al. (2017). 485 Correia et al. (2019) presents part of the senior author’s PhD study (Correia 2018), 486 providing an account of the palynostratigraphy of the Cabo Mondego and Póvoa de Lomba 487 formations (uppermost Toarcian–Bathonian) at Cabo Mondego and São Gião in the northern 488 Lusitanian Basin. The succession at Cabo Mondego includes the Global Stratotype Section 489 and Point (GSSP) for the Bajocian. The samples from Cabo Mondego were by far the most 490 palynologically productive. Here the uppermost Toarcian to lowermost Bajocian succession 491 produced low diversity dinoflagellate cyst associations dominated by Nannoceratopsis. 492 Within the Witchellia laeviuscula ammonite zone, the assemblages become markedly more 493 diverse, reflecting the intra-Bajocian global evolutionary explosion of dinoflagellates. This 494 predominantly involved the family Gonyaulacaceae, and was apparently strongly linked to 495 sea-level rise (Wiggan et al. 2017, 2018). The upper part of the Lower Bajocian and much of 496 the Upper Bajocian were not sampled by Correia et al. (2019, fig. 2); however the trend of 497 increasing dinoflagellate cyst diversity continued through the Bajocian–Bathonian transition. 498 It is clear from Correia et al. (2019) that the Middle Jurassic dinoflagellate cyst species 499 richnesses in the Arctic region and the Boreal Realm are substantially higher than in southern 500 Europe. This may be because more northerly palaeolatitudes were a phytoplankton-diversity 501 hotspot during the Mesozoic, that the the recovery from the Toarcian Oceanic Anoxic Event 502 (T-OAE) was more protracted in the Iberian region, or that regional palaeogeographical 503 factors controlled dinoflagellate diversity in the Lusitanian Basin. 504 505 2.7.3. Middle Jurassic to Early Cretaceous inclusive 15

506 In this subsection, the six remaining substantial papers exclusively on West Europe are 507 discussed. The works involved range from the Middle Jurassic to Early Cretaceous. Heunisch 508 and Luppold (2018) present an important study of the Middle Jurassic to earliest Cretaceous 509 (Callovian–Berriasian) micropalaeontological biostratigraphy of two boreholes drilled in the 510 Lower Saxony Basin of northern Germany. It is a technical report with the 511 micropalaeontology of selected intervals in the Eulenflucht-1 and Wendhausen-6 boreholes 512 described one-by-one. In the palynology subsections, age-diagnostic dinoflagellate cysts such 513 as Compositosphaeridium? polonicum, Dingodinium tuberosum, Gonyaulacysta jurassica, 514 Hystrichosphaerina? orbifera, Muderongia simplex subsp. microperforata, Nannoceratopsis 515 pellucida, Pareodinia brevicornuta, Systematophora areolata and Systematophora 516 penicillata are mentioned (Heunisch and Luppold 2018, pl. 3). 517 An overview of the Middle Jurassic to Early Cretaceous (Bathonian–Barremian) 518 basin evolution in the Central Graben area of the North Sea (representing the Danish, Dutch 519 and German sectors) was presented by Verreussel et al. (2018). This study was entirely based 520 on the correlations of wells that have been analysed for palynology (Verreussel et al. 2018, 521 fig. 2). These authors recognised four intervals that they termed tectonostratigraphical 522 megasequences (TMS). Each TMS represents a distinct phase of basin evolution; for example 523 TMS-1 reflects the onset of basin rifting and the rift climax occurred during this phase. It was 524 characterised by thick mud deposition. 525 A study focussed on the Oxfordian/Kimmeridgian boundary beds in the Flodigarry 526 Shale Member (Staffin Bay Formation) of the Isle of Skye, northwestern Scotland, was 527 undertaken by Barski (2018). This unit is notable because it includes a proposed Global 528 Stratotype Section and Point (GSSP) for the base of the Kimmeridgian. Barski (2018) studied 529 seven samples from the Ringsteadia pseudocordata and Pictonia baylei ammonite zones, and 530 presented quantitative data (Barski 2018, table 1). The author recognised a eutrophication 531 event in the lowermost Kimmeridgian. Furthermore, Barski (2018) noted that the range bases 532 of sparse Emmetrocysta sarjeantii, Perisseiasphaeridium pannosum and Senoniasphaera 533 jurassica can be used as markers for the base of the Kimmeridgian. 534 Turner et al. (2018) is a major study by on the comprehensive stratigraphy of the 535 Upper Jurassic and Lower Cretaceous of the Arctic and Europe, and it included palynological 536 analysis of the Kimmeridgian to Berriasian of the Norwegian Continental Shelf. These 537 authors integrated carbon isotope, cyclostratigraphical, dinoflagellate cyst and gamma ray 538 data to effect interregional correlations throughout this important interval. Turner et al. (2018, 539 fig. 2) calibrated the palynological data from the Barents and North seas to the the current 16

540 geological time scale using ammonite-dated dinoflagellate cyst studies such as Riding and 541 Thomas (1992) and Poulsen and Riding (2003). 542 Schneider et al. (2018) undertook a detailed study of the micropalaeontology and 543 palynology of the Jurassic–Cretaceous transition (Tithonian–Berriasian) in the Lower Saxony 544 Basin of northern Germany. This study is based mainly on miospores, but the authors noted 545 the regional correlative significance of the range bases of Batioladinium pomum, 546 Cantulodinium speciosum, Muderongia simplex subsp. microperforata, Muderongia simplex 547 and Pseudoceratium pelliferum in the Berriasian (Schneider et al. 2018, fig. 2). 548 Stanley Duxbury continued his extensive research into dinoflagellate cysts from 549 the Lower Cretaceous of the North Sea and surrounding areas that began with Duxbury 550 (1977). Duxbury (2018) is a major study of the Berriasian to lower Hauterivian marine 551 palynostratigraphy of the Speeton Clay and Valhall formations of the Central North Sea and 552 northeastern England based on 1131 samples. The biozonation of Duxbury (2001) is 553 substantially refined. Duxbury (2018) is dominated by a systematic section with taxonomic 554 novelties including one new genus and 21 new species. 555 556 557 2.8. The Middle East 558 The one single-region contribution on the Middle East herein is the article by Eshet (1990). 559 This author studied the Permian and Triassic successions of 11 boreholes drilled throughout 560 Israel. Eshet (1990) erected seven interval zones for the Early Permian to Late Triassic. Only 561 one dinoflagellate cyst zone, the Rhaetogonyaulax rhaetica Zone (VII; Norian–Rhaetian), 562 was established. The base of this zone was defined by the range bases of post-Carnian 563 miospores, and the top by the range top of Rhaetogonyaulax rhaetica and other dinoflagellate 564 cysts (i.e. Heibergella asymmetrica, Noricysta fimbriata, Suessia swabiana and Sverdrupiella 565 spp.). Two distinct palynofacies are present in this zone, one with dinoflagellate cysts and the 566 other devoid of these marine palynomorphs. The Rhaetogonyaulax rhaetica Zone is restricted 567 to the coastal plain in the extreme west of Israel; elsewhere the Norian–Rhaetian has been cut 568 out by a regional unconformity. Its reference section is within the Shefaiym Formation, 569 between 4860 m and 4495 m in the Ga’ash 2 Borehole, northwestern Israel (Cousminer 1981; 570 Eshet 1990, fig. 1). The age interpretation of Norian–Rhaetian is based on the ranges of the 571 dinoflagellate cysts Rhaetogonyaulax rhaetica and Suessia swabiana (see Visscher & 572 Brugman 1981) and foraminifera. 573 17

574 575 2.9. Sub-Arctic Russia 576 Twelve single-region articles on sub-Arctic Russia are compiled in this review, six of which 577 are deemed to be highly significant (Appendix 1 of the Supplementary data). Three of these 578 are on sub-Arctic West Russia, i.e. west of the Ural Mountains, and the remaining nine are on 579 southwestern Russia. The most significant of these contributions are detailed below in two 580 subsections. 581 582 2.9.1. Sub-Arctic West Russia 583 The unpublished PhD thesis by Smith (1999), available online, details the palynostratigraphy 584 of the Tithonian (Volgian) to Valanginian strata of the important Volgian lectostratotype 585 successions at Gorodische and Kashpir, near Ulyanovsk, southwestern Russia. The key 586 findings were later incorporated into Harding et al. (2011). Another noteworthy article based 587 on the Upper Kimmeridgian and Tithonian strata of Gorodische is Pestchevitskaya (2018). 588 This author focussed on the distinctive camocavate dinoflagellate cyst genus Dingodinium. 589 The genus was emended, with the archaeopyle interpreted as of combination type 590 (apical/anterior intercalary), and the tabulation partiform (Pestchevitskaya 2018, fig. 2). 591 Pestchevitskaya (2018) thus placed Dingodinium into the family Cladopyxiaceae. She 592 compiled the Middle Jurassic to the latest Cretaceous stratigraphical ranges of the genus 593 worldwide, and discussed the morphologies of 12 species of Dingodinium (Pestchevitskaya 594 2018, figs 1, 3). Pestchevitskaya (2018) identified Dingodinium albertii, Dingodinium 595 jurassicum and Dingodinium tuberosum from Gorodische, and established the new species 596 Dingodinium nequeas. In another publication Dzyuba et al. (2018) discussed the ranges of 597 dinoflagellate cysts, mainly identified only at the generic level, from the Tithonian– 598 Berriasian (Volgian–Ryazanian) of a fossiliferous succession exposed on the banks of the 599 Maurynya River in the Northern Ural Mountains of West Siberia. 600 601 2.9.2. Southwestern Russia (the Caspian Sea, the Caucasus Mountains and Crimea) 602 The discussion of articles on the Caspian Sea, the Caucasus Mountains and Crimea is placed 603 in the subsection on sub-Arctic Russia herein for purely geographical and pragmatic reasons. 604 This strategy has absolutely no political significance whatsoever. 605 The remaining nine items from sub-Arctic Russia, all recently published, are based 606 on material from southwestern Russia. Arkadiev et al. (2018) is a biostratigraphical and 607 magnetostratigraphical synthesis of the Jurassic–Cretaceous boundary beds of the Crimean 18

608 Mountains. Tithonian and Berriasian strata are well-developed and highly fossiliferous 609 throughout this region. The authors summarised research on ammonites, calpionellids, 610 dinoflagellate cysts, foraminifera and ostracods from Tithonian to lowermost Valanginian 611 strata across Crimea, and correlated these fossil records with magnetostratigraphy. Two 612 subdivisions based on dinoflagellate cysts were recognised. These are the ‘beds with 613 Amphorula expirata’ (now Amphorulacysta? expirata) and the ‘beds with Phoberocysta 614 neocomica’ of latest Tithonian–earliest Berriasian and earliest Berriasian–latest Berriasian 615 age respectively. The range bases of Ctenidodinium elegantulum, Phoberocysta neocomica 616 and Spiniferites spp. define the boundary between these two informal biozones; these 617 bioevents are within the Tirnovella occitanica ammonite zone (Arkadiev et al. 2018, fig. 21). 618 The short paper by Goryacheva and Ruban (2018) is on the Pliensbachian and 619 Toarcian palynology of the Sjuk River valley in the northwestern Caucasus, where the 620 authors identified Nannoceratopsis senex. Another short article by Goryacheva et al. (2018) 621 is on the palynology of a sandstone representing a reportedly deep marine setting in the upper 622 part of the Bagovskaja Formation from the River Belaja, south of Guzeripl in the northern 623 Arkhyz-Guzereplskaja area, Western Caucasus region. This unit is Toarcian in age, based on 624 ammonites recovered from its lowermost beds. Goryacheva et al. (2018) reported a 625 dinoflagellate cyst assemblage dominated by Nannoceratopsis. The most abundant species is 626 Nannoceratopsis spiculata. Less common forms include Nannoceratopsis plegas, 627 Nannoceratopsis senex, Phallocysta eumekes and Susadinium faustum. Goryacheva et al. 628 (2018) interpreted this association as being of late Toarcian age. 629 Mitta et al. (2017) provided an integrated palaeontological study of the Middle 630 Jurassic (Bajocian–Bathonian) of the Bolshoi Zelenchuk River Basin in the Northern 631 Caucasus region. Samples were collected from the uppermost Bajocian and lowermost 632 Bathonian (Parkinsonia parkinsoni and Zigzagiceras zigzag ammonite zones) part of the 633 Djangura Formation from localities 8, 11, 12 and 25 of Mitta et al. (2017, fig. 2). The authors 634 examined ammonites, dinoflagellate cysts, foraminifera, miospores and ostracods from this 635 succession. The five productive samples yielded moderately diverse dinoflagellate cyst 636 associations. Prominent species recorded throughout include Aldorfia aldorfensis, 637 Chytroeisphaeridia chytroeides, Ctenidodinium sellwoodii, Korystocysta gochtii, 638 Meiourogonyaulax caytonensis, Nannoceratopsis gracilis, Nannoceratopsis spiculata and 639 Valensiella ovulum. Mitta et al. (2017) recognised two informal zones. The uppermost 640 Bajocian was termed ‘beds with Rynchodiniopsis? regalis’, the nominate species being 641 confined to this interval. The most prominent dinoflagellate cysts are Ctenidodinium 19

642 sellwoodii and Dissiliodinium spp. The presence of Acanthaulax aff. crispa (as 643 Cribroperidinium aff. crispum) is indicative of the late Bajocian (Wiggan et al. 2017). 644 However, Mitta et al. (2017) also recorded Nannoceratopsis dictyambonis from this interval. 645 This species, characteristic of the latest Toarcian to early Bajocian interval (Riding 1984a, 646 1984b; Wiggan et al. 2017), may thus be reworked. The overlying lowermost Bathonian was 647 assigned to ‘beds with Ctenidodinium sellwoodii’, named after one of the dominant species. 648 The dinoflagellate cysts of this interval are substantially similar to those from the underlying 649 interval. Only six range bases were observed in the ‘beds with Ctenidodinium sellwoodii’, 650 including that of Ctenidodinium continuum. 651 Mitta et al. (2018) is a companion paper to that of Mitta et al. (2017). The former is 652 an important biostratigraphical study of the Upper Bajocian Djangura Formation from the 653 banks of the Kyafar River, a tributary of the Bolshoi Zelenchuk River, Karachay-Cherkessia, 654 Northern Caucasus, southwestern Russia. The material is all from the Rarecostites subarietis 655 ammonite subzone of the Parkinsonia parkinsoni ammonite zone. Ten samples were 656 examined, and all yielded substantial proportions of dinoflagellate cysts in relatively diverse 657 associations (Mitta et al. 2018, fig. 6). The samples are dominated by Dissiliodinium spp. 658 Furthermore, the following species were found throughout: Aldorfia aldorfensis; 659 Chytroeisphaeridia chytroeides; Ctenidodinium continuum; Ctenidodinium sellwoodii; 660 Durotrigia daveyi; Korystocysta spp.; Meiourogonyaulax caytonensis; Meiourogonyaulax 661 valensii; Nannoceratopsis gracilis; Nannoceratopsis senex; Nannoceratopsis spiculata; 662 Pareodinia ceratophora; Pareodinia prolongata; Rhynchodiniopsis? regalis; Sentusidinium 663 spp.; Tubotuberella spp.; and Valensiella ovulum. The following are also present, but rather 664 less consistently: Endoscrinium galeritum; Kalyptea stegasta; Leptodinium sp.; 665 Nannoceratopsis dictyambonis; Nannoceratopsis raunsgaardii; Pareodinia halosa; 666 Phallocysta elongata; and Wanaea acollaris (see Mitta et al. 2018, fig. 6, pl. V). The authors 667 assigned the entire succession that they studied to the ‘beds with Meiourogonyaulax valensii, 668 Rhynchodiniopsis? regalis’ (Mitta et al. 2018, fig. 7). Many of the dinoflagellate cyst taxa 669 recovered by Mitta et al. (2018) are entirely consistent with the latest Bajocian age 670 determined by ammonites and other fossils. These marker taxa include Aldorfia aldorfensis, 671 Ctenidodinium continuum, Ctenidodinium sellwoodii, Dissiliodinium spp., Durotrigia daveyi, 672 Kalyptea stegasta, Korystocysta spp., Leptodinium sp., Meiourogonyaulax caytonensis, 673 Meiourogonyaulax valensii, Rhynchodiniopsis? regalis, Tubotuberella spp. and Wanaea 674 acollaris (see for example Riding and Thomas 1992, Wiggan et al 2017).

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675 As in Mitta et al. (2017), Mitta et al. (2018), identified apparent reworking of 676 dinoflagellate cysts. The diversity of the species involved is considerable, comprising 677 Nannoceratopsis dictyambonis, Nannoceratopsis raunsgaardii, Nannoceratopsis gracilis, 678 Nannoceratopsis senex and Phallocysta elongata. The presence of these taxa is clearly 679 stratigraphically incompatible with a latest Bajocian age and reflects stratigraphical recycling 680 of Upper Pliensbachian to Early Bajocian strata. The range bases of Nannoceratopsis gracilis 681 and Nannoceratopsis senex are late Pliensbachian, and these species are common throughout 682 the Toarcian and earliest Bajocian interval (e.g. Morgenroth 1970, Poulsen 1996, Riding et al. 683 1999, Correia et al. 2018, Correia et al. 2019). The allochthonous species with the shortest 684 ranges are Nannoceratopsis dictyambonis and Phallocysta elongata, forms that are 685 characteristic of the latest Toarcian to earliest Bajocian (Riding 1984b, 1994). 686 The earliest Cretaceous (Berriasian) dinoflagellate cysts from the Uruh section in 687 the North Caucasus, southwestern Russia were reported in a short contribution in Russian by 688 Shurekova (2018). The article is well-illustrated and a semiquantitative range chart was 689 presented (Shurekova, 2018, p. 283–285). The author distinguished the Phoberocysta 690 neocomica and Systematophora cf. palmula dinoflagellate cyst zones which are broadly 691 equivalent to the Tirnovella occitanica and Fauriella boissieri ammonite zones. The species 692 Systematophora palmula is now known as Palaecysta palmula. 693 694 3. Conclusions 695 In a literature search from February 2018 to January 2019, 55 new publications pertaining to 696 Triassic to earliest Cretaceous dinoflagellate cysts were discovered, and are compiled herein 697 together with 38 older items which were not covered by Riding (2012, 2013, 2014, 2019). 698 These 93 papers are based on material from Africa, North America, South America, the 699 Arctic, Australasia, East Europe, West Europe, the Middle East and Russia. Thirty of them 700 are deemed herein to be significantly impactful and are asterisked in Appendix 1 of the 701 Supplementary data. All 93 contributions are listed in Appendix 1 of the Supplementary data, 702 and most are on the Late Triassic and Early Jurassic of Europe (Tables 1, 2). This may be due 703 to substantial recent interest in the Triassic–Jurassic transition, and the situation differs from 704 previous compilations which demonstrated greater focus on the Late Jurassic of Europe 705 (Riding 2012, 2013, 2014, 2019). Papers based on West Europe comprise 31.2% of the total, 706 and publications on Africa, the Arctic, Australasia, East Europe and Russia are also 707 significant (15.1%, 6.5%. 7.5%, 9.7% and 14.0% respectively). The least well-represented

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708 regions are North America, South America and the Middle East (2.2%, 1.1% and 1.1% 709 respectively; Table 1). 710 711 Acknowledgements 712 This paper is respectfully dedicated to the memories of David J. Batten (UK; 1943–2019), 713 Lilia D. Dodekova (Bulgaria; 1934–2016), Lanny H. Fisk (USA; 1944–2018), Alan F. 714 Hibbert (UK; 1938–2018), Peter A. Hochuli (Switzerland; 1946–2018), Vera I. Ilyina 715 (Russia; 1930–2018), Louis James (‘Lou’) Maher Jr. (USA; 1933–2018), Norman J. Norton 716 (USA; 1933–2017), W.H. Eberhard Schulz (Germany; 1931–2017), Edwin G. ‘Ted’ Spinner 717 (UK; 1938–2018) and John Utting (Canada; 1940–2018), eleven highly distinguished 718 palynologists who very sadly passed away recently. I extend thanks to the staff of the BGS 719 Library for their help in obtaining several articles for this compilation. Constructive, helpful 720 and perceptive comments from Robert A. Fensome (Geological Survy of Canada) and an 721 anonymous reviewer substantially improved this contribution. This paper is published with 722 the approval of the Executive Director, British Geological Survey (NERC). 723 724 Disclosure statement 725 The author has no potential conflict of interest. 726 727 Notes on contributor 728 JAMES B. RIDING is a geologist/palynologist with the British Geological Survey (BGS) in 729 Nottingham, UK. He undertook the MSc in palynology at the University of Sheffield and, 730 several years later, Jim was awarded a PhD by the same institution. During 2004, Jim gained 731 a DSc from the University of Leicester, where he did his Bachelor’s degree in geology. His 732 interests include the Mesozoic–Cenozoic palynology of the world, palaeoenvironmental 733 palynology, palynomorph floral provinces, forensic palynology, preparation techniques, the 734 history of palynology, and the morphology, systematics and taxonomy of dinoflagellate cysts. 735 Jim is a past President of AASP – The Palynological Society, and became Managing Editor 736 in 2004. 737 738 739 References 740

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1104 1105 van Helden BG. 1987. Dinocysts from the Jurassic of Saskatchewan and Alberta: an open 1106 field for research. Canadian Association of Palynologists Newsletter 10.1:12–14. 1107

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1108 Verreussel RMCH, Bouroullec R, Munsterman DK, Dybkjær K, Geel CR, Houben AJP, 1109 Johannessen PN, Kerstholt-Boegehold SJ. 2018. Stepwise basin evolution of the Middle 1110 Jurassic–Early Cretaceous rift phase in the Central Graben area of Denmark, Germany and 1111 The Netherlands. In: Kilhams B, Kukla PA, Mazur S, McKie T, Mijnlieff HF, van Ojik K. 1112 (editors). Mesozoic Resource Potential in the Southern Permian Basin. Geological Society, 1113 London, Special Publications No. 469, doi: 10.1144/SP469.23. 1114 1115 Visscher H, Brugman WA. 1981. Ranges of selected palynomorphs of the Alpine Triassic of 1116 Europe. Review of Palaeobotany and Palynology 34:115–128. 1117 1118 Wainman CC, McCabe PJ. 2018. Evolution of the depositional environments of the Jurassic 1119 Walloon Coal Measures, Surat Basin, Queensland, Australia. Sedimentology, doi: 1120 10.1111/sed.12548. 1121 1122 Wainman CC, Mantle DJ, Hannaford C, McCabe PJ. 2018a. Possible freshwater 1123 dinoflagellate cysts and colonial algae from the Upper Jurassic of the Surat Basin, Australia. 1124 Palynology, doi: 10.1080/01916122.2018.1451785. 1125 1126 Wainman CC, Hannaford C, Mantle D, McCabe PJ. 2018b. Utilizing U–Pb CA-TIMS dating 1127 to calibrate the Middle to Late Jurassic spore-pollen zonation of the Surat Basin, Australia to 1128 the geological time-scale. Alcheringa 42:402–414. 1129 1130 Wiggan NJ, Riding JB, Franz M. 2017. Resolving the Middle Jurassic dinoflagellate 1131 radiation: The palynology of the Bajocian of Swabia, southwest Germany. Review of 1132 Palaeobotany and Palynology 238:55–87. 1133 1134 Wiggan NJ, Riding JB, Fensome RA, Mattioli E. 2018. The Bajocian (Middle Jurassic): a 1135 key interval in the early Mesozoic phytoplankton radiation. Earth-Science Reviews 180:126– 1136 146. 1137 1138 Williams GL, Fensome RA. 2016. Fossil dinoflagellates: nomenclatural proposals in 1139 anticipation of a revised DINOFLAJ database. Palynology 40:137–143. 1140

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1141 Zhang Wangping, Grant-Mackie JA. 2001. Late Triassic–Early Jurassic palynofloral 1142 assemblages from Murihiku strata of New Zealand, and comparisons with China. Journal of 1143 the Royal Society of New Zealand 31:575–683. 1144 1145 Zotto M, Drugg WS, Habib D. 1987. Kimmeridgian dinoflagellate stratigraphy in the 1146 southwestern North Atlantic. Micropaleontology 33:193–213. 1147 1148 1149 Display material captions: 1150 1151 Table 1. A breakdown of the 93 publications on Triassic to earliest Cretaceous dinoflagellate 1152 cysts compiled herein, based on the nine relevant geographical regions (i.e. Africa, North 1153 America, South America, the Arctic, Australasia, East Europe, West Europe, the Middle East 1154 and Russia) and the initial letter of the family name of the first author. The number in the 1155 geographical region cell refers to the number of relevant published items on that area alone. 1156 An ellipsis (…) indicates a zero return for that particular parameter. 1157 1158 Table 2. A breakdown of of the 93 publications on Triassic to earliest Cretaceous (Berriasian) 1159 dinoflagellate cysts compiled herein, subdivided into Triassic, Early Jurassic, Middle 1160 Jurassic, Late Jurassic, Jurassic–Cretaceous transition, investigations comprising three or 1161 more of the previous intervals and studies with no stratigraphical focus, and reworking. Some 1162 latitude and pragmatism is used in this compilation; for example, if a publication is on the 1163 Berriasian and Valanginian it is classified as covering the Jurassic–Cretaceous transition. One 1164 item may be counted twice (e.g. if it spans the Oxfordian to Berriasian), but not three times. 1165 An ellipsis (…) indicates a zero return for that particular parameter. 1166 1167 1168 SUPPLEMENTARY DATA 1169 1170 Appendix 1. List of Literature 1171 1172 Ninety-three contributions on Triassic to earliest Cretaceous dinoflagellate cysts issued after 1173 the publication of Riding (2012, 2013, 2014, 2019), together with papers encountered after 1174 these compilations were made, are listed in alphabetical/chronological order below. The 35

1175 reference citation format used is much the same as in Riding (2013, 2014, 2019), which was 1176 slightly modified from Riding (2012). Digital object identifier (doi) numbers are included 1177 where these are available. The 30 papers which are deemed to be of major significance are 1178 asterisked. The language in which a paper was written in is indicated if it is not in English. A 1179 synthesis of the scope of each item is given as a string of keywords in parentheses after each 1180 citation. These keywords attempt to comprehensively summarise the principal subject matter, 1181 age range, major geographical region(s) and country/countries. A distinction is made between 1182 publications that present new data (‘primary data’), and those that compile, review or 1183 summarise existing datasets (‘compilation’). A significant number of abstracts are listed here; 1184 these are denoted by the word ‘summary’ in the keyword string. If the author(s) have 1185 included photographs, occurrence charts and a zonal breakdown, these are indicated 1186 respectively in the keywords. For the purpose of this work, the world is subdivided into 14 1187 major geographical regions. These are Africa, Central America, North America, South 1188 America, Antarctica, the Arctic, Southeast Asia, Australasia, China, East Europe, West 1189 Europe, the Indian subcontinent, the Middle East and Russia (Table 1). The regional 1190 assignments of any disputed territories, for example of Crimea, are merely for internal 1191 consistency and geographical pragmatism, and have no political significance whatsoever. 1192 1193 1194 A 1195 1196 *ABOUL ELA, N.M., and TAHOUN, S.S. 2010. Dinoflagellate cyst stratigraphy of the 1197 subsurface Middle–Upper Jurassic/Lower Cretaceous sequence in North Sinai, Egypt. Fifth 1198 International Conference on the Geology of the Tethys Realm, 2nd–7th January 2010, South 1199 Valley University, Quena, Luxor, Egypt, 85–115. 1200 (acritarchs; biostratigraphy; biozonation; calcareous nannofossils; correlation; eustasy; 1201 foraminifera; foraminiferal test linings; fungal spores; hiatus; lithostratigraphy; pollen-spores; 1202 tectonics; primary data; occurrence charts; photographs; Middle Jurassic–Early Cretaceous 1203 [Bathonian–Albian]; North Africa [Mango-1 and Til-1 wells, offshore northern Sinai Basin, 1204 Egypt]) 1205 1206 *ARKADIEV, V., GUZHIKOV, A., BARABOSHKIN, E., SAVELIEVA, J., 1207 FEODOROVA, A., SHUREKOVA, O., PLATONOV, E., and MANIKIN, A. 2018.

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1208 Biostratigraphy and magnetostratigraphy of the upper Tithonian–Berriasian of the Crimean 1209 Mountains. Cretaceous Research, 87: 5–41 (doi: 10.1016/j.cretres.2017.07.011). 1210 (acritarchs; ammonites; belemnites; biostratigraphy; brachiopods; calpionellids; correlation; 1211 foraminifera; magnetostratigraphy; ostracods; prasinophytes; stratigraphical synthesis; 1212 Tethyan palaeogeography; primary data; photographs; latest Jurassic–Early Cretaceous 1213 [Tithonian–Valanginian]; sub-Arctic Russia [Crimean Mountains from Feodosiya to 1214 Sevastopol, Crimea, southwestern Russia) 1215 1216 ARKADIEV, V.V., BARABOSHKIN E.Yu., GUZHIKOV, A.Yu., BARABOSHKIN, E.E., 1217 SHUREKOVA, O.V., and SAVELIEVA, Yu.N. 2018. Tirnovella occitanica zone 1218 (Berriasian) of the Eastern Crimea. In: Baraboshkin E.Yu., Lipnitskaya, T.A., and Guzhikov, 1219 A.Yu. (editors). Cretaceous system of Russia and near abroad: problems of stratigraphy and 1220 paleogeography. Proceedings of the Ninth All-Russian Conference, Belgorod State National 1221 Research University, Belgorod, September 17th–21st, 2018. Polyterra Publishing House, 1222 Belgorod, ISBN 978-5-98242-250-7, 32–38 (in Russian with an English abstract). 1223 (ammonites; biostratigraphy; biozonation; magnetostratigraphy; ostracods; pollen-spores; 1224 Tirnovella occitanica zone; summary; earliest Cretaceous [Berriasian]; sub-Arctic Russia 1225 [Zavodskaya Balka section, eastern Crimea, southwestern Russia]) 1226 1227 1228 B 1229 1230 BARABOSHKIN, E.Yu., SHTUN, S.Yu., GUZHIKOV, A.Yu., KUZNETZOV, A.B., 1231 FEODOROVA, A.A., SHUREKOVA, O.V., and SMIRNOV, M.V. 2018. Sedimentology 1232 and stratigraphy of the Jurassic-Cretaceous boundary interval of the carbonate ramp of the 1233 Northern Caspian. In: Baraboshkin E.Yu., Lipnitskaya, T.A., and Guzhikov, A.Yu. (editors). 1234 Cretaceous system of Russia and near abroad: problems of stratigraphy and 1235 paleogeography. Proceedings of the Ninth All-Russian Conference, Belgorod State National 1236 Research University, Belgorod, September 17th–21st, 2018. Polyterra Publishing House, 1237 Belgorod, ISBN 978-5-98242-250-7, 54–58 (in Russian with an English abstract). 1238 (biostratigraphy; correlation; palaeoecology; palaeomagnetism; sedimentology; stable 1239 isotopes; summary; latest Jurassic–earliest Cretaceous [Tithonian–Berriasian]; sub-Arctic 1240 Russia [the Khvalynskaya-5 and Sarmatskaya-3 wells, northern Caspian Sea, offshore 1241 southwestern Russia]) 37

1242 1243 BARANYI, V. 2018. Vegetation dynamics during the Late Triassic (Carnian–Norian): 1244 Response to climate and environmental changes inferred from palynology. Unpublished PhD 1245 thesis, University of Oslo, Norway, 164 p., ISSN 1501-7710 (available online at: 1246 https://www.duo.uio.no/handle/10852/61940). 1247 (biostratigraphy; carbon isotope analysis; clay mineralogy; correlation; floral evolutionary 1248 history; Carnian Pluvial Episode; Mid-Norian Climate Shift; lithostratigraphy [the Chinle and 1249 Veszprém Marl formations and the Mercian Mudstone Group]; palaeoclimatology; 1250 palaeoecology; Sub-Boreal and Tethyas realms; taphonomy; terrestrial ecosystems; Late 1251 Triassic [Carnian–Norian]; multi-region: sub-Arctic North America [Petrified Forest National 1252 Park, Arizona, southwestern USA]; East Europe [southern Transdanubian Range, western 1253 Hungary]; sub-Arctic West Europe [Wessex Basin, southwestern England]) 1254 1255 *BARSKI, M. 2018. Dinoflagellate cyst assemblages across the Oxfordian/Kimmeridgian 1256 boundary (Upper Jurassic) at Flodigarry, Staffin Bay, Isle of Skye, Scotland - a proposed 1257 GSSP for the base of the Kimmeridgian. Volumina Jurassica, 16: 51–62 (doi: not available in 1258 Oct 18). 1259 (ammonites; biostratigraphy; bloom of zygnemataceous chlorophycean alga [?Spirogyra]; 1260 correlation; eutrophication event [“green tide”]; lithostratigraphy [Flodigarry Shale Member, 1261 Staffin Bay Formation]; palynofacies; proposed Global Stratotype Section and Point (GSSP); 1262 primary data; quantitative occurrence chart; photographs; Late Jurassic [Oxfordian– 1263 Kimmeridgian]; sub-Arctic West Europe [foreshore sections at Flodigarry, Trotternish 1264 Peninsula, Isle of Skye, northwestern Scotland]) 1265 1266 BARTH, G., PIEŃKOWSKI, G., ZIMMERMANN, J., FRANZ, M., and KUHLMANN, G. 1267 2018. Palaeogeographical evolution of the Lower Jurassic: high-resolution biostratigraphy 1268 and sequence stratigraphy in the Central European Basin. In: Kilhams, B., Kukla, P.A., 1269 Mazur, S., McKie, T., Mijnlieff, H.F., and van Ojik, K. (editors). Mesozoic Resource 1270 Potential in the Southern Permian Basin. Geological Society, London, Special Publications, 1271 469, doi: 10.1144/SP469.8. 1272 (ammonites; ammonite biozones; basin evolution; biofacies; biostratigraphy; Central 1273 European Basin; correlation; Dapcodinium priscum; Liasidium variabile; Luehndea spinosa; 1274 palaeoecology; palaeogeography; palaeontology; pollen-spores; sedimentary architecture; 1275 sequence stratigraphy; compilation; Late Triassic–Middle Jurassic [Norian–Callovian]; multi- 38

1276 region: East Europe [Poland]; sub-Arctic West Europe [Denmark; England, France, 1277 Germany]) 1278 1279 BOERSMA, M., BRUGMAN, W.A., and VELD, H. 1987. Triassic palynomorphs: index to 1280 genera and species. LPP Special Services, No. 1987-02, 228 p. Laboratory of Palaeobotany 1281 and Palynology (LPP), State University of Utrecht, The Netherlands. 1282 (acritarchs; genera; index; megaspores; miscellaneous palynomorphs [e.g. fungal spores]; 1283 pollen-spores; species; compilation; Triassic [undifferentiated]; no specific geographical 1284 focus) 1285 1286 BÓNA, J. 1995. Palynostratigraphy of the Upper Triassic formations in the Mecsek Mts 1287 (Southern Hungary). Acta Geologica Hungarica, 38(4): 319–354. 1288 (acritarchs; algae; biostratigraphy; coal exploration boreholes; foraminiferal test linings; 1289 hiatuses; lithostratigraphy [Kantavár, Karolinavölgy Sandstone and lowermost Mecsek Coal 1290 formations]; pollen-spores; primary data; occurrence charts; photographs; Late Triassic 1291 [Carnian–Rhaetian]; East Europe [Pécs region, Mecsek Mountains, southern Hungary]) 1292 1293 1294 C 1295 1296 *CORREIA, V.D.P.F. 2018. Jurassic dinoflagellate cyst biostratigraphy of the Lusitanian 1297 Basin, west-central Portugal, and its relevance to the opening of the North Atlantic and 1298 petroleum geology. Unpublished PhD thesis, Universidade do Algarve, Portugal, xxxii + 283 1299 p. 1300 (acritarchs; ammonite biozones; biostratigraphy; biozonation; correlation; diversity; 1301 foraminiferal test linings; geochemistry; lithostratigraphy; palaeobiology; palaeoecology; 1302 palaeogeography; palynomorph fluorescence; petroleum geology; pollen-spores; 1303 prasinophytes; provincialism; regional geology; tectonic history; thermal alteration index 1304 [TAI]; Toarcian Oceanic Anoxic Event [T-OAE]; primary data; occurrence charts; 1305 photographs; Early–Middle Jurassic [Sinemurian–Callovian]; sub-Arctic West Europe 1306 [Lusitanian Basin, western-central Portugal]) 1307 1308 CORREIA, V.F., RIDING, J.B., FERNANDES, P., DUARTE, L.V., and PEREIRA, Z. 2016. 1309 The palaeobiological response of dinoflagellate cysts to the Toarcian Oceanic Anoxic Event 39

1310 (T-OAE), in the Lusitanian Basin, Portugal. Twelfth International Conference on 1311 Paleoceanography (ICP 12), Utrecht, The Netherlands, August 29th–September 2nd 2016, p. 1312 108. 1313 (abundance and diversity fluctuations; Luehndea spinosa; palaeoenvironmental change; 1314 Toarcian Oceanic Anoxic Event (T-OAE); recovery; summary; Early Jurassic [Toarcian]; 1315 sub-Arctic West Europe [Maria Pares, Peniche, Vale das Fontes, Lusitanian Basin, western- 1316 central Portugal) 1317 1318 CORREIA, V.F., RIDING, J.B., FERNANDES, P., DUARTE, L.V., and PEREIRA, Z. 2017. 1319 The response of dinoflagellate cysts to the Toarcian Oceanic Anoxic Event (T-OAE) in the 1320 Lusitanian Basin. In: XV Encuentro de Jóvenes Investigadores en Paleontología (XV EJIP), 1321 19–22 April 2017, Pombal, Portugal. Libro de Resúmenes, 113-117. 1322 (abundance and diversity; Luehndea spinosa; palaeobiology; palaeoceanography; Toarcian 1323 Oceanic Anoxic Event (T-OAE); recovery; summary; photographs; Early Jurassic [Toarcian]; 1324 sub-Arctic West Europe [Maria Pares, Peniche, Vale das Fontes, Lusitanian Basin, western- 1325 central Portugal) 1326 1327 CORREIA, V.F., RIDING, J.B., HENRIQUES, M.H., FERNANDES, P., and PEREIRA, Z. 1328 2017. The dinoflagellate cysts of the Bajocian GSSP (Middle Jurassic) at Cabo Mondego, 1329 Lusitanian Basin, Portugal. Eleventh International Conference on Modern and Fossil 1330 Dinoflagellates (DINO 11), Bordeaux, France, 17th–21st July 2017, p. 52. 1331 (ammonites; biostratigraphy; diversity; evolutionary radiation; Global Stratotype Section and 1332 Point (GSSP); Mesozoic Marine Revolution; summary; Early–Middle Jurassic [Toarcian– 1333 Bajocian]; sub-Arctic West Europe [Cabo Mondego, Lusitanian Basin, western-central 1334 Portugal]) 1335 1336 CORREIA, V.F., RIDING, J.B., DUARTE, L.V., FERNANDES, P., and PEREIA, Z. 2018. 1337 An overview of the Lower Jurassic dinoflagellate cyst biostratigraphy in the Lusitanian 1338 Basin, Portugal. In: Vaz, N., and Sá, A.A. (editors). Yacimientos paleontológicos 1339 excepcionales en la península Ibérica. Cuadernos Del Museo Geominero, No. 27: 335–342. 1340 Instituto Geológico y Minero de España, Madrid. ISBN 978-84-9138-066-5. 1341 (ammonite biozones; biostratigraphy; diversity; summary; occurrence chart; photographs; 1342 Early Jurassic [Sinemurian–Toarcian]; sub-Arctic West Europe [Brenha, Fonte Coberta,

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1343 Maria Pares, Peniche, São Pedro de Moel and Val das Fontes, Lusitanian Basin, western 1344 central Portugal]) 1345 1346 CORREIA, V.F., RIDING, J.B., DUARTE, L.V., FERNANDES, P., and PEREIA, Z. 2018. 1347 Lower Jurassic dinoflagellate cysts throughout the Toarcian Oceanic Anoxic Event (T-OAE) 1348 in the Lusitanian Basin, Portugal. In: Silva, R.L., Duarte, L.V., and Sêco, S. (editors). Second 1349 International Workshop on the Toarcian Oceanic Anoxic Event, Coimbra, Portugal, 1350 September 6–9, 2018. Abstracts Volume, 33–34. ISBN: 978-989-98914-6-3. 1351 (abundances; diversity; palaeoecology; palaeogeography; recovery; Toarcian Oceanic Anoxic 1352 Event (T-OAE); summary; photographs; Early Jurassic [Pliensbachian–Toarcian]; sub-Arctic 1353 West Europe [Fonte Coberta, Maria Pares, Peniche, Lusitanian Basin, western central 1354 Portugal]) 1355 1356 *CORREIA, V.F., RIDING, J.B., DUARTE, L.V., FERNANDES, P., and PEREIRA, Z. 1357 2018. The Early Jurassic palynostratigraphy of the Lusitanian Basin, western Portugal. 1358 Geobios, 51(6): 537–557 (doi: 10.1016/j.geobios.2018.03.001). 1359 (acritarchs; ammonite biozones; biostratigraphy; biozonation; diversity; foraminiferal test 1360 linings; pollen-spores; prasinophytes; regional geology; Toarcian Oceanic Anoxic Event (T- 1361 OAE); primary data; occurrence charts; photographs; Early Jurassic [Sinemurian–Toarcian]; 1362 sub-Arctic West Europe [Brenha, Fonte Coberta, Maria Pares, Peniche, São Pedro de Moel 1363 and Val das Fontes, Lusitanian Basin, western central Portugal]) 1364 1365 *CORREIA, V.F., RIDING, J.B., HENRIQUES, M.H., FERNANDES, P., PEREIRA, Z., 1366 and WIGGAN, N.J. 2019. The Middle Jurassic palynostratigraphy of the northern Lusitanian 1367 Basin, Portugal. Newsletters on Stratigraphy, 52(1): 73–96 (doi: 10.1127/nos/2018/0471). 1368 (acritarchs; ammonite biozones; archaeopyle types; biostratigraphy; diversity; eustasy; 1369 evolutionary radiation of the family Gonyaulaceae; foraminiferal test linings; Global 1370 Stratotype Section and Point (GSSP); lithostratigraphy (Cabo Mondego and Póvoa de Lomba 1371 formations); palaeobiology; palaeogeography; regional geology; pollen-spores; 1372 prasinophytes; Toarcian Oceanic Anoxic Event (T-OAE); primary data; quantitative 1373 occurrence charts; photographs; Early–Middle Jurassic [Toarcian–Bathonian]; sub-Arctic 1374 West Europe [Cabo Mondego and São Gião, northern Lusitanian Basin, western central 1375 Portugal]) 1376 41

1377 1378 D 1379 1380 DARWISH, M., EL-ARABY, A., ABU KHADRAH, A.M., and HUSSEIN, H.M. 2004. 1381 Sedimentary facies models and organic geochemical aspects of the Upper Jurassic–Lower 1382 Cretaceous sequences in northern Sinai. Sixth International Conference on Geochemistry, 1383 Alexandria University, Egypt, 15th to 16th September 2004, 183–208. 1384 (correlation; foraminifera; lithofacies analysis; lithostratigraphy; organic geochemistry; 1385 palaeogeography; palynofacies; petroleum geology; compilation; Middle Jurassic–Early 1386 Cretaceous [Callovian–Aptian]; North Africa [offshore and onshore northern Sinai, Egypt]) 1387 1388 DIXON, M., MORGAN, R., GOODALL, J., and VAN DEN BERG, M. 2012. Higher- 1389 resolution palynostratigraphy of the Norian–Carnian (Triassic) Upper Mungaroo Formation, 1390 offshore Carnarvon Basin (extended abstract). APPEA 2012 Journal and Conference 1391 Proceedings (13th–16th May 2012 Adelaide, South Australia), 3 p. 1392 (biostratigraphy; biozonation; correlation; freshwater algae; lithostratigraphy [Mungaroo 1393 Formation]; palaeoecology; petroleum geology; pollen-spores; subdividing species into sub- 1394 types; summary; photographs; Late Triassic [Carnian–Norian]; Australasia [offshore 1395 Carnarvon Basin, Western Australia]) 1396 1397 DODSWORTH, P., and ELDRETT, J.S. 2018. A dinoflagellate cyst zonation of the 1398 Cenomanian and Turonian (Upper Cretaceous) in the Western Interior, United States. 1399 Palynology, doi: 10.1080/01916122.2018.1477851. 1400 (biostratigraphy; biozonation; chemostratigraphy; correlation; Global Stratotype Section and 1401 Point (GSSP); lithostratigraphy [Bridge Creek Member, Greenhorn Formation]; pollen- 1402 spores; reworking; primary data; occurrence chart; photographs; reworked Middle and Late 1403 Jurassic [undifferentiated] into the Late Cretaceous [Cenomanian–Turonian]; sub-Arctic 1404 North America [Rock Canyon anticline outcrop, west of Pueblo, Colorado, USA]) 1405 1406 *DUXBURY, S. 2018. Berriasian to lower Hauterivian palynostratigraphy, U.K. onshore and 1407 Outer Moray Firth. Micropaleontology, 64(3): 171–252. 1408 (ammonites; bioevents; biostratigraphy; biozonation; caving; correlation; 1409 evolution/evolutionary trends; inter- and intra-species trends; lithostratigraphy [Speeton Clay 1410 and Valhall formations]; palaeoecology; pollen-spores; reworking; taxonomy; primary data; 42

1411 photographs; Early Cretaceous [Berriasian–Hauterivian]; sub-Arctic West Europe [Blocks 1412 14/26a and 20/01, Golden Eagle Field, Outer Moray Firth, Central North Sea; coastal 1413 outcrops at Speeton, Filey Bay, North Yorkshire, northeastern England]) 1414 1415 DZYUBA, O.S., PESTCHEVITSKAYA, E.B., URMAN, O.S., SHURYGIN, B.N., 1416 ALIFIROV, A.S., IGOLNIKOV, A.E., and KOSENKO, I.N. 2018. The Maurynya section, 1417 West Siberia: a key section of the Jurassic–Cretaceous boundary deposits of shallow marine 1418 genesis. Russian Geology and Geophysics, 59: 864–890 (doi: 10.1016/j.rgg.2018.07.010). 1419 (acritarchs; ammonites; belemnites; biodiversity; biostratigraphy; biozonation; bivalves; 1420 Boreal Realm; brachiopods; eustasy; gastropods; geochemistry (carbon, oxygen and 1421 strontium isotopes, and elemental analysis); green algae [prasinophytes and Zygnemataceae]; 1422 Jurassic–Cretaceous boundary; landscape/vegetation dynamics; palaeobathymetry; 1423 palaeoclimate; palaeoecology; palaeotemperature; pollen-spores; shallow water deposition; 1424 primary data; semiquantitative occurrence charts; photographs; latest Jurassic–earliest 1425 Cretaceous [Tithonian–Berriasian]; sub-Arctic Russia [Maurynya River outcrop section, 1426 south of Tolya, northern Ural Mountains, West Siberia]) 1427 1428 1429 E 1430 1431 *ESHET, Y. 1990. Paleozoic–Mesozoic palynology of Israel. I. Palynological aspects of the 1432 Permian–Triassic succession in the subsurface of Israel. Geological Survey of Israel Bulletin, 1433 81, 73 p. 1434 (ammonites; biostratigraphy; biozonation; boreholes; conodonts; correlation; foraminifera; 1435 foraminiferal test linings; fungal spores; Ga’ash 2 borehole; hiatus; lithostratigraphy (Sa’ad to 1436 Shefaiym formations); ostracods; palaeoclimate cycles; palaeoclimatology; palaeoecology; 1437 palynofacies; petroleum geology; pollen-spores; regional geology; reworking; scolecodonts; 1438 sedimentology; thermal maturity; primary data; occurrence charts; photographs; Early 1439 Permian–Late Triassic [Asselian–Sakmarian to Norian–Rhaetian]; Middle East [Israel]) 1440 1441 1442 F 1443

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1444 FEIST-BURKHARDT, S., HOLSTEIN B., and GÖTZ, A.E. 2002. Phytoplankton diversity 1445 and distribution patterns in the Triassic: the dinoflagellate cysts of the upper Rhaetian 1446 Koessen Beds (Northern Calcareous Alps, Austria). The Palaeontology Newsletter, No. 51: 1447 92 (abstract). 1448 (Calcareous Alps; cyclic sedimentation; diversity; Koessen Beds; palaeoecology; Wanneria 1449 listeri; summary; Late Triassic [Rhaetian]; sub-Arctic West Europe [Eiberg, near Kufstein, 1450 Northern Calcareous Alps, Austria]) 1451 1452 FELIX, C.J., and BURBRIDGE, P.P. 1977. A new Ricciisporites from the Triassic of Arctic 1453 Canada. Palaeontology, 20(3): 581–587. 1454 (biostratigraphy; bivalves; boreholes and outcrops; correlation; Heiberg and Schei Point 1455 formations; pollen-spores; Ricciisporites umbonatus; Sverdrupiella spp.; taxonomy; primary 1456 data; occurrence chart; Late Triassic [Carnian–Norian]; Arctic Canada [Borden, Melville and 1457 Prince Patrick islands, Sverdrup Basin]) 1458 1459 1460 G 1461 1462 GENTZIS, T., CARVAJAL-ORTIZ, H., DEAF, A., and TAHOUN, S.S. 2018. Multi-proxy 1463 approach to screen the hydrocarbon potential of the Jurassic succession in the Matruh Basin, 1464 North Western Desert, Egypt. International Journal of Coal Geology, 190: 29–41 (doi: 1465 10.1016/j.coal.2017.12.001). 1466 (biostratigraphy; geochemistry; hydrocarbon generation potential; Khattatba and Masajid 1467 formations; petroleum geology; pollen-spores; reservoir and source rocks; Rock-Eval 1468 pyrolysis; total organic carbon [TOC]; vitrinite reflectance; Wadi Natrun Formation; primary 1469 data; photographs; Early–Late Jurassic [Toarcian–Oxfordian]; North Africa [Matruh Basin, 1470 North Western Desert, northern Egypt]) 1471 1472 GOODWIN, M.B., CLEMENS, W.A., HUTCHISON, J.H., WOOD, C.B., ZAVADA, M.S., 1473 KEMP, A., DUFFIN, C.J., and SCHAFF, C.R. 1999. Mesozoic continental vertebrates with 1474 associated palynostratigraphic dates from the northwestern Ethiopian plateau. Journal of 1475 Vertebrate Paleontology, 19(4): 728–741 (doi: 10.1080/02724634.1999.10011185). 1476 (acritarchs; ammonites; biogeography; biostratigraphy; Ethiopian northwestern high plateau; 1477 Leptodinium acneum; Mugher Mudstone Formation; palaeoecology; palaeogeography; 44

1478 pollen-spores; vertebrate migration; vertebrate palaeontology; primary data; latest Jurassic 1479 [Tithonian]; East Africa [Aleltu River Valley, north of Addis Ababa, Ethiopia]) 1480 1481 GORYACHEVA, A.A., and RUBAN, D.A. 2018. New palynological data from the Lower 1482 Jurassic deposits of the northwestern Caucasus. Bulletin of Udmurt University, Series 1483 Biology, Earth Sciences, 28(3) (short communications): 321–324 (in Russian with an English 1484 abstract). 1485 (biostratigraphy; Nannoceratopsis senex; palaeoclimate; palaeovegetation; pollen-spores; 1486 sandstones; primary data; photographs; Early Jurassic [Pliensbachian–Toarcian]; sub-Arctic 1487 Russia [Sjuk River valley, north of the Dakh Crystalline Massif, Republic of Adygeja, 1488 northwestern Caucasus]) 1489 1490 *GORYACHEVA, A.A., ZORINA, S.O., RUBAN, D.A., ESKIN, A.A., NIKASHIN, K.I., 1491 GALIULLIN, B.M., MOROZOV, V.P., MIKHAILENKO, A.V., NAZARENKO, O.V., and 1492 ZAYATS, P.P. 2018. New palynological data for Toarcian (Lower Jurassic) deep-marine 1493 sandstones of the Western Caucasus, southwestern Russia. Geologos, 24(2): 127–136 (doi: 1494 10.2478/logos-2018-0012). 1495 (acritarchs; biostratigraphy; chlorophytes; lithostratigraphy [Bagovskaja Formation]; 1496 Nannoceratopsis spiculata; pollen-spores; regional geology; sandstone; X-ray diffraction 1497 [XRD] of minerals; primary data; photographs; Early Jurassic [Toarcian]; sub-Arctic Russia 1498 [west bank of the River Belaja south of Guzeripl, northern Arkhyz-Guzereplskaja area, 1499 Western Caucasus, southwestern Russia]) 1500 1501 1502 H 1503 1504 HEILMANN-CLAUSEN, C., and THOMSEN, E. 1995. Barremian–Aptian dinoflagellates 1505 and calcareous nannofossils in the Ahlum 1 Borehole and the Otto Gott Clay Pit, Sarstedt, 1506 Lower Saxony Basin, Germany. In: Kemper, E. (editor). Die Wende Barrême/Apt 1507 Untersuchungen an Profilen des Borealgebietes. Geologisches Jahrbuch Reihe A, 141: 257– 1508 365. 1509 (ammonite and belemnite zones; biostratigraphy; calcareous nannofossils; correlation; 1510 Ctenidodinium combazii; Jurassic reworking; Lower Saxony Basin; Nannoceratopsis plegas; 1511 Nannoceratopsis triceras; taxonomy; Wanaea acollaris; primary data; occurrence charts; 45

1512 photographs; Early Jurassic–Early Cretaceous [Early and Middle Jurassic reworking into 1513 Barremian–Aptian]; sub-Arctic West Europe [Ahlum 1 Borehole and the Otto Gott Clay Pit, 1514 east of Hannover, northern Germany]) 1515 1516 *HEUNISCH, C., and LUPPOLD, F.W. 2018. 3. Mitteljura bis Unterkreide in den 1517 Bohrungen Eulenflucht 1 und Wendhausen 6 – litho- und biostratigraphische Ergebnisse 1518 [Middle Jurassic to Lower Cretaceous in the Eulenflucht 1 and Wendhausen 6 boreholes – 1519 litho- and biostratigraphical results]. In: Fischer, K., Herrendorf, G., Heunisch, C., Luppold, 1520 F.W., Meinsen, J., Possin, W., Schwarz, C., and Thomas, M. Neue Erkenntnisse zu Quartär, 1521 Jura und Unterkreide in Niedersachsen [New results on the Quaternary, Jurassic and Lower 1522 Cretaceous in Lower Saxony]. GeoBerichte, 31: 40–85. Landesamt fur Bergbau, Energie und 1523 Geologie (LBEG), Hannover, Germany, ISSN 1864-6891 and 1864-7529 (in German). 1524 (acritarchs; biostratigraphy; calcareous nannofossils; core photographs; foraminifera; 1525 freshwater algae; lithostratigraphy; ostracods; prasinophytes; trace fossils; Wealden type 1526 facies; primary data; occurrence chart; photographs; Middle Jurassic–earliest Cretaceous 1527 [Callovian–Berriasian]; sub-Arctic West Europe [the Eulenflucht-1 and Wendhausen-6 1528 boreholes, Lower Saxony Basin, northern Germany]) 1529 1530 *HOGG, N.M. 1993. A palynological investigation of the Scalby Formation (Ravenscar 1531 Group, Middle Jurassic) and adjacent strata from the Cleveland Basin, north east Yorkshire. 1532 Unpublished PhD thesis, University of Sheffield, UK, 233 p. plus two appendices, 23 plates 1533 and six enclosures (available online at: http://etheses.whiterose.ac.uk/14604/1/576086.pdf). 1534 (acritarchs; biostratigraphy; botanical keys; Chlorophyceae; Cleveland Basin; cluster 1535 analysis; correlation; dispersed and in-situ pollen and spores; informal taxonomy; 1536 lithostratigraphy [Cloughton, Scarborough, Scalby and Cornbrash formations]; megaspores; 1537 palaeobotany; palaeoclimate; palaeoecology; plant macrofossils; prasinophytes; Ravenscar 1538 Group; sequence stratigraphy; primary data; quantitative occurrence charts; photographs; 1539 Middle Jurassic [Bajocian–Bathonian]; sub-Arctic West Europe [Cloughton Wyke, Crook 1540 Ness, Gristhorpe Bay, White Nab and Yons Nab, near Scarborough, and Saltergate and 1541 Talbot Wood, north of Pickering, North Yorkshire, northeastern England]) 1542 1543 *HOLSTEIN, B. 2004. Palynologische Untersuchungen der Kössener Schichten (Rhät, 1544 Alpine Obertrias). Jahrbuch der Geologischen Bundesanstalt, 144(3/4): 261–365 (in German 1545 with an English abstract). 46

1546 (acritarchs; biostratigraphy; correlation; foraminiferal test linings; Kössen Beds; 1547 lithostratigraphy; macrofossils; palaeoclimatology; palaeoecology; palynofacies; pollen- 1548 spores; prasinophytes; sequence stratigraphy; statistics; systematics; primary data; 1549 quantitative occurrence charts; photographs; Late Triassic [Norian–Rhaetian]; sub-Arctic 1550 West Europe [Eiberg near Kufstein and Mörtlbachgraben near Salzburg, Northern Calcareous 1551 Alps, northern central Austria]) 1552 1553 HUDSON, W.E., and NICHOLAS, C.J. 2014. The Pindiro Group (Triassic to Early Jurassic 1554 Mandawa Basin, southern coastal Tanzania): Definition, palaeoenvironment, and 1555 stratigraphy. Journal of African Earth Sciences, 92: 53–67 (doi: 1556 org/10.1016/j.jafrearsci.2014.01.005). 1557 (basin evolution; biofacies; correlation; evaporites; foraminifera; lithostratigraphy; 1558 palaeoecology; petroleum geology; Mandawa Basin; Mbuo, Mihambia and Nondwa 1559 formations; ostracods; palaeoecology; palaeogeography; Pindiro Group; pollen-spores; 1560 regional geology; reworking; sedimentology; tectonic rifting of Gondwana; compilation; 1561 photographs; Late Triassic–Middle Jurassic [undifferentiated]; East Africa [southern coastal 1562 Tanzania]) 1563 1564 1565 I 1566 1567 IED, I.M., and IBRAHIM, N. 2010. Jurassic – Early Cretaceous palynomorphs in Almaz -1 1568 Well, north Western Desert, Egypt. Bulletin of the Faculty of Science, Zagazig University, 1569 Egypt, 32: 115–133. 1570 (acritarchs; Almaz-1 well; biostratigraphy; biozonation; foraminiferal test linings; fungal 1571 spores; lithostratigraphy; palaeoclimate; palaeoecology; pollen-spores; primary data; 1572 occurrence chart; photographs; Early Jurassic–Early Cretaceous [undifferentiated– 1573 Bajocian/Callovian–Barremian]; North Africa [west of Alexandria, north Western Desert, 1574 northern Egypt]) 1575 1576 IED, I.M., and LASHIN, G.M.A. 2016. Palynostratigraphy and paleobiogeography of the 1577 Jurassic – Lower Cretaceous succession in Kabrit-1 well, northeastern Egypt. Cretaceous 1578 Research, 58: 69–85 (doi: 10.1016/j.cretres.2015.09.011).

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1579 (biostratigraphy; biozonation; Kabrit-1 well; lithostratigraphy; palaeoecology; 1580 palaeogeography; pollen-spores; provincialism; primary data; occurrence charts; 1581 photographs; Middle Jurassic–Early Cretaceous [Callovian–Albian]; North Africa [south of 1582 Bitter Lake, north Eastern Desert, northeastern Egypt]) 1583 1584 1585 J 1586 1587 *JAYDAWI, S., HSSAIDA, T., BENBOUZIANE, A., MOUFLIH, M., and CHAKOR 1588 ALAMI, A. 2016. Datation par les kystes de dinoflagellés des formations jurassiques 1589 (Callovien–Kimméridgien) du bassin d’Essaouira (Marge atlantique marocaine). 1590 [Dinoflagellate cyst dating of the Jurassic (Callovian–Kimmeridgian) Formations in the 1591 Essaouira Basin (Moroccan Atlantic Margin)]. Bulletin de l’Institut Scientifique, Rabat, 1592 Section Sciences de la Terre, No. 38: 127–148 (e-ISSN 2458-7184) (in French with an 1593 English abstract and summary). 1594 (biostratigraphy; petroleum geology; regional geology; primary data; occurrence charts; 1595 photographs; Middle–Late Jurassic [Callovian–Kimmeridgian]; North Africa [boreholes 1596 MKL-110, NDK-2 and NDK-3, Essaouira Basin, central western Morocco]) 1597 1598 JONES, P.J., and NICOLL, R.S. 1984. Late Triassic conodonts from Sahul Shoals No. 1, 1599 Ashmore Block, northwestern Australia. BMR Journal of Australian Geology and 1600 Geophysics, 9(4): 361–364. 1601 (biostratigraphy; conodonts [Epigondolella primitia]; correlation; compilation; Late Triassic 1602 [Carnian–Norian]; Australasia [Sahul Shoals No. 1 well, Ashmore Block, offshore Bonaparte 1603 Basin, North West Shelf, Timor Sea, Australia]) 1604 1605 JUNCAL, M.A., BOURQUIN, S., BECCALETTO, L., and DIEZ, J.B. 2018. New 1606 sedimentological and palynological data from the Permian and Triassic series of the 1607 Sancerre-Couy core, Paris Basin, France. Geobios, 51(6): 517–535 (doi: 1608 10.1016/j.geobios.2018.06.007). 1609 (acritarchs; biostratigraphy; biozonation; Dapcodinium priscum; depositional 1610 environments/facies analysis; lithostratigraphy; Plaesiodicton mosellanum; pollen-spores; 1611 regional geology; Rhaetogonyaulax rhaetica; sedimentology; sequence stratigraphy; well-log 1612 analysis; primary data; non-quantitative occurrence chart; photographs; Permian 48

1613 [undifferentiated] and Middle–Late Triassic [Ladinian–Rhaetian]; sub-Arctic West Europe 1614 [Sancerre-Couy-1 borehole, Paris Basin, near Nevers, central France]) 1615 1616 1617 K 1618 1619 KARLE, U. 1984. Palynostratigraphische Untersuchung eines Rhät/Lias-Profils am Fonsjoch, 1620 Achensee (Nördliche Kalkalpen, Österreich) [Palynostratigraphical investigation of a Rhaeto- 1621 Lias-Profile at the Fonsjoch (Northern Limestone Alps, Austria)]. Mitteilungen der 1622 Österreichischen Geologischen Gesellschaft, 77: 331–353 (in German with an English 1623 abstract). 1624 (acritarchs; ammonite [Psiloceras planorbis]; biostratigraphy; biozonation; lithostratigraphy; 1625 Northern Limestone Alps; palaeoecology; pollen-spores; Rhaetogonyaulax rhaetica; primary 1626 data; semi-quantitative occurrence chart; photographs; latest Triassic–earliest Jurassic 1627 [Rhaetian–Hettangian]; sub-Arctic West Europe [Fonsjoch, western Austria]) 1628 1629 KASHIRTSEV, V.A., NIKITENKO, B.L., PESHCHEVITSKAYA, E.B., and FURSENKO, 1630 E.A. 2018. Biogeochemistry and microfossils of the Upper Jurassic and Lower Cretaceous, 1631 Anabar Bay, Laptev Sea. Russian Geology and Geophysics, 59: 386–404 (doi: 1632 10.1016/j.rgg.2017.09.004). 1633 (ammonites; biostratigraphy; eustasy; foraminifera; lithostratigraphy; macrofossils; molecular 1634 biomarkers; organic geochemistry; ostracods; palaeobathymetry; palaeoecology; 1635 palaeoceanography; pollen-spores; prasinophytes; radiolaria; sedimentology; source rock 1636 potential; trace fossils; primary data; Late Jurassic–Early Cretaceous [Oxfordian– 1637 Valanginian]; Arctic Russia [outcrops A32 and 33, Cape Urdyuk-Khaya, Nordvik Peninsula, 1638 western Anabar Bay, Laptev Sea]) 1639 1640 1641 L 1642 1643 LINDSTRÖM, S., VAN DE SCHOOTBRUGGE, B., HANSEN, K.H., PEDERSEN, G.K., 1644 ALSEN, P., THIBAULT, N., DYBKJÆR, K., BJERRUM, C.J., and NIELSEN, L.H. 2017. A 1645 new correlation of Triassic–Jurassic boundary successions in NW Europe, Nevada and Peru, 1646 and the Central Atlantic Magmatic Province: A time-line for the end-Triassic mass 49

1647 extinction. Palaeogeography, Palaeoclimatology, Palaeoecology, 478: 80–102 (doi: 1648 10.1016/j.palaeo.2016.12.025). 1649 (acritarchs; ammonite zonation; biostratigraphy; Central Atlantic Magmatic Province 13 1650 [CAMP]; correlation; end-Triassic mass extinction; eustasy; geochemistry (δ CTOC); 1651 geochronology; hiatuses; lithostratigraphy; methane release; pollen-spores; prasinophytes; 1652 Rhaetogonyaulax rhaetica; sedimentology; seismic activity; Triassic–Jurassic boundary; 1653 primary data; occurrence charts; latest Triassic–earliest Jurassic [Rhaetian–Hettangian]; 1654 multi-region: North America [New York Canyon, Nevada, USA]; South America [Pucara 1655 Basin, Peru]; sub-Arctic West Europe [Austria, Denmark, England, Germany]) 1656 1657 LONDEIX, L. 2018. Quantitative biostratigraphical ranges of some late Cenozoic species of 1658 the dinoflagellate genus Spiniferites and taxonomic considerations. Palynology, 42 1659 Supplement 1: 203–220 (doi: 10.1080/01916122.2018.1465740). 1660 (Achomosphaera; databases; generic genome; Gonyaulax spinifera complex; index of 1661 stratigraphical abundance [ISA]; morphology; motile dinoflagellates; palaeoecology; 1662 phylogeny; quantitative biostratigraphy; Spiniferites; compilation; occurrence charts; 1663 photographs; Late Jurassic [Oxfordian]–Holocene; no specific geographical focus) 1664 1665 1666 M 1667 1668 MAHMOUD, M.S., DEAF, A.S., TAMAM, M.A., and KHALAF, M.M. 2019. Revised 1669 (miospores-based) stratigraphy of the Lower Cretaceous succession of the Minqar-IX well, 1670 Shushan Basin, north Western Desert, Egypt: Biozonation and correlation approach. Journal 1671 of African Earth Sciences, 151: 18–35 (doi: 10.1016/j.jafrearsci.2018.11.019). 1672 (biostratigraphy; biozonation; correlation; foraminiferal test linings; freshwater algae; 1673 lithostratigraphy [Alam El-Bueib, Alamein and Kharita formations]; palaeogeography; 1674 palaeooceanography; petroleum geology; pollen-spores; regional geology; Shushan Basin; 1675 primary data; quantitative occurrence chart; photographs; Late Jurassic–Early Cretaceous 1676 [Kimmeridgian–Tithonian to Albian]; North Africa [Minqar-IX well, north Western Desert, 1677 northern Egypt]) 1678

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1679 *MANGERUD, G., PATERSON, N.W., and RIDING, J.B. 2019. The temporal and spatial 1680 distribution of Triassic dinoflagellate cysts. Review of Palaeobotany and Palynology, 261: 1681 53–66 (doi: 10.1016/j.revpalbo.2018.11.010). 1682 (biostratigraphy; diversity; end-Triassic extinction; evolution; palaeogeography; Pangaea; 1683 provincialism; literature review; occurrence chart; Middle Triassic–earliest Jurassic 1684 [Ladinian–Hettangian]; multi-region: South America; Arctic; Australasia; East and West 1685 Europe; Middle East) 1686 1687 *MITTA, V.V., SAVELIEVA, Yu.N., FEODOROVA, A.A., and SHUREKOVA, O.V. 2017. 1688 Biostratigraphy of the Bajocian–Bathonian Boundary Beds in the Basin of the Bolshoi 1689 Zelenchuk River (Northern Caucasus). Stratigraphy and Geological Correlation, 25(6): 607– 1690 626 (doi: 10.1134/S0869593817060065). (The original Russian text was published during 1691 2017 in Stratigrafiya, Geologicheskaya Korrelyatsiya, 25(6): 30–49). 1692 (ammonites; ammonite biozones; biostratigraphy; biozonation; Djangura Formation; 1693 foraminifera; ostracods; pollen-spores; primary data; semi-quantitative occurrence chart; 1694 photographs; Middle Jurassic [Bajocian–Bathonian]; sub-Arctic Russia [Bolshoi Zelenchuk 1695 (Karachay-Cherkessia) Basin, Northern Caucasus, southwestern Russia]) 1696 1697 *MITTA, V.V., SAVELIEVA, YU.N., FEDOROVA, A.A., and SHUREKOVA, O.V. 2018. 1698 Ammonites, microfauna, and palynomorphs from the lower part of the Upper Bajocian 1699 Parkinsoni Zone of the basin of the Bolshoi Zelenchuk River, Northern Caucasus. 1700 Stratigraphy and Geological Correlation, 26(5): 552–570 (doi: 1701 10.1134/S0869593818050040). (the original Russian text was published during 2018 in 1702 Stratigrafiya, Geologicheskaya Korrelyatsiya, 26(5): 49–67). 1703 (acritarchs; ammonites [Rarecostites subarietis ammonite subzone of the Parkinsonia 1704 parkinsoni ammonite zone]; biostratigraphy; biozonation; foraminifera, foraminiferal test 1705 linings; lithostratigraphy [Djangura Formation]; ostracods, pollen-spores; primary data; 1706 occurrence chart; photographs; Middle Jurassic [Bajocian]; sub-Arctic Russia [banks of the 1707 Kyafar River, Bolshoi Zelenchuk River, Karachay-Cherkessia, Northern Caucasus, 1708 southwestern Russia]) 1709 1710 *MOSTAFA, T.F., EL SOUGHIER, M.I., and MAKLED, W.A. 2018. Middle–Upper 1711 Jurassic palynology of the South Sallum well, North Western Desert, Egypt. Egyptian 1712 Journal of Petroleum, doi: 10.1016/j.ejpe.2018.06.002. 51

1713 (biostratigraphy; biozonation; ditch cuttings; lithostratigraphy [Khatatba and Masajid 1714 formations]; palaeoclimate; palaeoecology; pollen-spores; primary data; semi-quantitative 1715 occurrence chart; photographs; Middle–Late Jurassic [Bathonian–Oxfordian]; North Africa 1716 [South Sallum well, North Western Desert, northwestern Egypt]) 1717 1718 *MSAKY, E.S. 2008. Middle Jurassic–earliest Late Cretaceous palynofloras, coastal 1719 Tanzania. Unpublished PhD Thesis, University of Queensland, Brisbane, Australia, 198 p. 1720 (available online at: https://espace.library.uq.edu.au/view/UQ:178439). 1721 (biostratigraphy; biozonation; correlation; cosmopolitanism/provincialism; Elaterates [pollen] 1722 province; informal taxonomy; Kipatimi Formation; Makonde and Mkindani beds; 1723 palaeoecology; palaeogeography; palynofacies; petroleum geology; pollen-spores; 1724 quantitative bioevents; regional geology; systematics; primary data; occurrence charts; 1725 photographs; Middle Jurassic–earliest Late Cretaceous [Bajocian–Cenomanian]; East Africa 1726 [coastal Tanzania]) 1727 1728 1729 N 1730 1731 NIKITENKO, B.L., DEVYATOV, V.P., LEBEDEVA, N.K., BASOV, V.A., 1732 GORYACHEVA, A.A., PESTCHEVITSKAYA, E.B., and GLINSKIKH, L.A. 2017. Jurassic 1733 and Cretaceous stratigraphy of the New Siberian Archipelago (Laptev and East Siberian 1734 Seas): facies zoning and lithostratigraphy. Russian Geology and Geophysics, 58(12): 1478– 1735 1493 (doi: 10.1016/j.rgg.2017.11.012). 1736 (biostratigraphy; foraminifera; lithofacies zones; lithostratigraphy; macrofossils; ostracods; 1737 pollen-spores; primary data; Early Jurassic–Cretaceous [Hettangian–Turonian]; Arctic Russia 1738 [New Siberian Islands Archipelago, East Siberian and Laptev seas]) 1739 1740 NIKITENKO, B.L., DEVYATOV, V.P., LEBEDEVA, N.K., BASOV, V.A., FURSENKO, 1741 E.A., GORYACHEVA, A.A., PESHCHEVITSKAYA, E.B., GLINSKIKH, L.A., and 1742 KHAFAEVA, S.N. 2018. Jurassic and Cretaceous biostratigraphy and organic matter 1743 geochemistry of the New Siberian Islands (Russian Arctic). Russian Geology and 1744 Geophysics, 59: 168–185 (doi: 10.1016/j.rgg.2018.01.014). 1745 (ammonites; biostratigraphy; biozonation; bivalves; foraminifera; lithostratigraphy; 1746 ostracods; pollen-spores; molecular biomarkers; organic geochemistry; petroleum geology; 52

1747 primary data; Early Jurassic–Late Cretaceous [Hettangian–Turonian]; Arctic Russia [New 1748 Siberian Islands Archipelago, East Siberian and Laptev seas]) 1749 1750 *NIKITENKO, B.L., PESTCHEVITSKAYA, E.B., and KHAFAEVA, S.N. 2018. High- 1751 resolution stratigraphy and palaeoenvironments of the Volgian–Valanginian in the Olenek 1752 key section (Anabar-Lena region, Arctic East Siberia, Russia). Revue de Micropaléontologie, 1753 61(3–4): 271–312 (doi: 10.1016/j.revmic.2018.07.001). 1754 (acritarchs; ammonites; biostratigraphy; biozonation; Boreal Realm; correlation; 13 1755 foraminifera; geochemistry (δ CTOC); lithostratigraphy [Buolkalakh, Chekurovka and 1756 Iaedaes formations]; palaeoclimatology; palaeoecology; pollen-spores; prasinophytes; 1757 sedimentology; shallow water deposition; Volgian and Boreal Berriasian; primary data; semi- 1758 quantitative occurrence chart; photographs; Middle Jurassic–Early Cretaceous [Bathonian– 1759 Valanginian]; Arctic Russia [Outcrop O14, Olenek section, Anabar-Lena region, eastern 1760 Siberia, northeastern Russia]) 1761 1762 1763 O 1764 1765 OLIVERA, D.E., MARTÍNEZ, M.A., ZAVALA, C., OTHARÁN, G., MARCHAL, D., and 1766 KÖHLER, G. 2018. The gymnosperm pollen Shanbeipollenites proxireticulatus Schrank 1767 from the Vaca Muerta Formation (Upper Jurassic–Lower Cretaceous), Neuquén Basin, 1768 Argentina. Cretaceous Research, 90: 120–130 (doi: 10.1016/j.cretres.2018.04.003). 1769 (biomes; biostratigraphy; Cycadales/Bennettitales/Ginkgoales; lithostratigraphy [Vaca 1770 Muerta Formation]; palaeoclimate; palaeogeography; pollen-spores; prasinophytes; 1771 Shanbeipollenites proxireticulatus [pollen]; volcanic activity; primary data; semiquantitative 1772 occurrence chart; photographs; Early Cretaceous [?Berriasian–Valanginian]; South America 1773 [Mallin Quemado, north of Zapala, Neuquén Basin, central western Argentina]) 1774 1775 1776 P 1777 1778 PAUMARD, V., BOURGET, J., PAYENBERG, T., AINSWORTH, R.B., GEORGE, A.D., 1779 LANG, S., POSAMENTIER, H.W., and PEYROT, D. 2018. Controls on shelf-margin 1780 architecture and sediment partitioning during a syn-rift to post-rift transition: Insights from 53

1781 the Barrow Group (Northern Carnarvon Basin, North West Shelf, Australia). Earth-Science 1782 Reviews, 177: 643–677 (doi:10.1016/j.earscirev.2017.11.026). 1783 (biostratigraphy; biozonation; clinoforms; eustasy; lithostratigraphy [Barrow Group]; 1784 regional geology; rift tectonics; sedimentary architecture; sediment thickness maps; seismic 1785 stratigraphy; sequence stratigraphy; shelf margin depositional setting; latest Jurassic–Early 1786 Cretaceous [Tithonian–Valanginian]; Australasia [Northern Carnarvon Basin, North West 1787 Shelf, offshore Western Australia]) 1788 1789 PENAUD, A., HARDY, W., LAMBERT, C., MARRET, F., MASURE, E., SERVAIS, T., 1790 SIANO, R., WARY, M., and MERTENS, K.N. 2018. Dinoflagellate fossils: Geological and 1791 biological applications. Revue de Micropaléontologie, 61(3/4): 235–254 (doi: 1792 10.1016/j.revmic.2018.09.003). 1793 (acritarchs; biostratigraphy; dinoflagellate cyst-motile stage relationships; DNA; 1794 geographical distributions; history of research; living dinoflagellates; palaeoecology; 1795 palaeogeography; palaeoceanography; primary productivity; transfer functions; literature 1796 review; occurrence chart; photographs; no geographical and stratigraphical focus) 1797 1798 PESTCHEVITSKAYA, E.B. 2017. Preliminary data on the palynostratigraphy and biofacies 1799 of the transitional Jurassic–Cretaceous interval in the Maurynya section (Northern Urals). In: 1800 Zakharov, V.A., Rogov, M.A., and Shchepetova E.V. (editors). Jurassic System of Russia: 1801 Problems of stratigraphy and рaleogeography. Seventh all-Russian Conference. Moscow, 1802 September 18th–22nd, 2017. Scientific materials. Russian Academy of Sciences, Moscow, p. 1803 156–161 (in Russian with an English abstract). 1804 (acritarchs; biostratigraphy; biozonation; correlation; palaeoecology; prasinophytes; 1805 summary; latest Jurassic–earliest Cretaceous [Tithonian–Berriasian (=Volgian–Ryazanian]; 1806 sub-Arctic Russia [Maurynya River outcrop section, south of Tolya, Northern Ural 1807 Mountains, West Siberia]) 1808 1809 *PESTCHEVITSKAYA, E.B. 2018. Morphology, systematics, and stratigraphic significance 1810 of the dinocyst genus Dingodinium. Paleontological Journal, 52(6): 682–696 (doi: 1811 10.1134/S0031030118060084). (Originally Russian text published in Paleontologicheskii 1812 Zhurnal, 6: 94–106, 2018). 1813 (archaeopyle; biostratigraphy; Dingodinium; family Cladopyxiaceae [suborder 1814 Cladopyxiineae]; morphology; partiform tabulation pattern; taxonomy; primary data and 54

1815 compilation; line drawings; photographs; occurrence chart; Late Jurassic [Kimmeridgian– 1816 Tithonian]; sub-Arctic Russia [Gorodishche, Volga River, near Ulyanovsk, southwestern 1817 Russia]) 1818 1819 PETERSEN, H.I., LINDSTRÖM, S., THERKELSEN, J., and PEDERSEN, G.K. 2013. 1820 Deposition, floral composition and sequence stratigraphy of uppermost Triassic (Rhaetian) 1821 coastal coals, southern Sweden. International Journal of Coal Geology, 116–117: 117–134 1822 (doi: 10.1016/j.coal.2013.07.004). 1823 (acritarchs; coal; eustasy; fire; lithostratigraphy [Bjuv Member]; Lunnomidinium scaniense; 1824 organic geochemistry; palaeoclimate; palaeoecology; palynofacies; peat-forming 1825 environments; pollen-spores; Rhaetogonyaulax rhaetica; sedimentology; sequence 1826 stratigraphy; vegetational analysis/dynamics; Triassic–Jurassic boundary; primary data; 1827 occurrence charts; photographs; latest Triassic [Rhaetian]; sub-Arctic West Europe [Lunnom 1828 and Norra Albert quarries, Höganäs and Danish basins, Scania, southern Sweden]) 1829 1830 PIEŃKOWSKI, G., and WAKSMUNDZKA, M. 2009. Palynofacies in Lower Jurassic 1831 epicontinental deposits of Poland – tool to interpret sedimentary environments. Episodes, 1832 32(1): 21–32. 1833 (acritarchs; charcoal; Dapcodinium priscum; palaeoclimate; palaeoecology; palaeogeography; 1834 palynofacies; pollen-spores; sedimentology; sequence stratigraphy; primary data; 1835 photographs; Early Jurassic [Hettangian–Toarcian]; East Europe [Poland]) 1836 1837 PIEŃKOWSKI, G., NIEDŹWIEDZKI, G., and WAKSMUNDZKA, M. 2012. 1838 Sedimentological, palynological, and geochemical studies of the terrestrial Triassic–Jurassic 1839 boundary in northwestern Poland. Geological Magazine, 149(2): 308–332 (doi: 1840 10.1017/S0016756811000914). 1841 (biostratigraphy; correlation; Dapcodinium priscum; geochemistry; Kamién Pomorski IG-1 1842 borehole; lithostratigraphy; palaeoclimate; palaeogeography; pollen-spores; Rhaetogonyaulax 1843 rhaetica; sedimentology; sequence stratigraphy; compilation; latest Triassic–earliest Jurassic 1844 [Rhaetian–Hettangian]; East Europe [near Szczecin, Pomerania, northwestern Poland]) 1845 1846 POWELL, J.H., RAWSON, P.F., RIDING, J.B., and FORD, J.R. 2018. Sedimentology and 1847 stratigraphy of the Kellaways Sand Member (Lower Callovian), Burythorpe, North

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1848 Yorkshire, UK. Proceedings of the Yorkshire Geological Society, 62(1): 36–49 (doi: 1849 10.1144/pygs2017-402). 1850 (acritarchs; ammonites; biostratigraphy; correlation; foraminiferal test linings; Kellaways 1851 Formation; Kellaways Sand Member; macrofossils; palaeogeography; sedimentology; 1852 thickness variations; trace fossils; palynofacies; pollen spores; primary data; occurrence data; 1853 photographs; Middle Jurassic [Callovian]; sub-Arctic West Europe [Burythorpe Quarry, near 1854 Malton, Howardian Hills, North Yorkshire, northern England]) 1855 1856 1857 R 1858 1859 *RISMYHR, B., BJÆRKE, T., OLAUSSEN, S., MULROONEY, M.J., and SENGER, K. 1860 2018. Facies, palynostratigraphy and sequence stratigraphy of the Wilhelmøya Subgroup 1861 (Upper Triassic–Middle Jurassic) in western central Spitsbergen, Svalbard. Norwegian 1862 Journal of Geology, doi: 10.17850/njg001. 1863 (acritarchs; algae; biostratigraphy; biozonation; carbon dioxide sequestration; condensation; 1864 correlation; facies analysis/associations; lithostratigraphy [Brentskardhaugen Bed; 1865 Wilhelmøya Subgroup;De Geerdalen, Knorringfjellet and Agardhfjellet formations; Kapp 1866 Toscana Group]; pollen-spores; provenance; regional geology; reworking; sedimentology; 1867 sequence stratigraphy; trace fossils; primary data; Late Triassic–Middle Jurassic [Carnian– 1868 Callovian]; Arctic [western central Spitsbergen, Svalbard]) 1869 1870 *RUCKWIED, K. 2009. Palynology of Triassic/Jurassic boundary key sections of the NW 1871 Tethyan Realm (Hungary and Slovakia). Unpublished PhD dissertation, Technischen 1872 Universität Darmstadt, Germany, 95 p. plus 4 plates and 4 appendices. (available online at: 1873 http://tuprints.ulb.tu-darmstadt.de/1359/). 1874 (biostratigraphy; biozonation; botanical affinities; Central Atlantic Magmatic Province 1875 (CAMP); clay mineralogy; Dapcodinium priscum; diversity; end Triassic mass extinction; 1876 foraminiferal test linings; lithofacies; palaeoclimate; palaeoecology; palaeogeography; 1877 palynofacies; Pangaea; pollen-spores; prasinophytes; Rhaetogonyaulax rhaetica; spore spike; 1878 sporomorph ecogroups; stable isotope geochemistry; statistics; Tethyan Realm; primary data; 1879 occurrence charts; photographs; latest Triassic–earliest Jurassic [Rhaetian–Hettangian]; East 1880 Europe [Csövár, northern Hungary, the Mecsek Mountains, southern Hungary and the Tatra 1881 Mountains, northern Slovakia]) 56

1882 1883 1884 S 1885 1886 SAPUNOV, I.G., TCHOUMATCHENCO, P.V., DODEKOVA, L.D. and ČERNJAVSKA, 1887 S.P. 1985. Contribution to the formal lithostratigraphic scheme related to the Middle Jurassic 1888 deposits from north-east Bulgaria. Review of the Bulgarian Geological Society, 46(2): 144– 1889 152 (in Bulgarian with an English abstract). 1890 (ammonites; biostratigraphy; bivalves; boreholes; brachiopods; correlation; Dobrič, Kalojan, 1891 Provadija and Sultanci formations; lithostratigraphy; pollen-spores; sedimentology; primary 1892 data; Middle–Late Jurassic [Aalenian–Callovian/Tithonian]; East Europe [northeastern 1893 Bulgaria]) 1894 1895 *SAPUNOV, I., TCHOUMATCHENCO, P., BABURKOV, I., BAKALOVA, D., 1896 DODEKOVA, L., ZHELEVA, C., NIKOLOVA, M. and ČERNJAVSKA, S. 1986. The 1897 Jurassic System in the new boreholes in the area of Provadija. Review of the Bulgarian 1898 Geological Society, 47(2): 103–120 (in Bulgarian with an English abstract).

1899 (ammonites; biostratigraphy; bivalves; boreholes; brachiopods; calpionellids; correlation; 1900 Esenica, Polaten, Provadija, Sultanci and Tiča formations, eustasy; lithostratigraphy; pollen- 1901 spores; sedimentology; primary data; Early–Late Jurassic [Sinemurian–Tithonian]; East 1902 Europe [Provadija, northeastern Bulgaria])

1903 1904 SAPUNOV, I., TCHOUMATCHENCO, P., BÂRDAROV, S., VAVILOVA, M., 1905 DODEKOVA, L., KITOV, P. and ČERNJAVSKA, S. 1986. Stratigraphy of Jurassic rocks 1906 from the borehole sections between the villages of Resen, Veliko Târnovo area and Konak, 1907 Târgovište area. Review of the Bulgarian Geological Society, 47(3): 26–42 (in Bulgarian with 1908 an English abstract). 1909 (ammonites; biostratigraphy; bivalves; boreholes; brachiopods; correlation; Drinovo, Esenica, 1910 Ginci, Javorec, Ozirovo and Tiča formations; eustasy; lithostratigraphy; pollen-spores; 1911 sedimentology; trace fossils; primary data; Early–Late Jurassic [Sinemurian–Tithonian]; East 1912 Europe [Târgovište and Veliko Târnovo areas, northeastern Bulgaria]) 1913

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1914 *SCHNEEBELI-HERMANN, E., LOOSER, N., HOCHULI, P.A., FURRER, H., 1915 REISDORF, A.G., WETZEL, A., and BERNASCONI, S.M. 2018. Palynology of Triassic– 1916 Jurassic boundary sections in northern Switzerland. Swiss Journal of Geosciences, 111, 99– 1917 115 (doi: 10.1007/s00015-017-0286-z). 1918 (acritarchs; biostratigraphy; biozonation; boreholes and outcrops; correlation; end-Triassic 1919 mass extinction; eustasy; foraminiferal test linings; lithostratigraphy [Klettgau and Staffelegg 1920 formations]; palaeoecology; pollen-spores; regional geology; primary data; quantitative 1921 occurrence chart; photographs; Late Triassic–Early Jurassic [Norian–Sinemurian]; sub-Arctic 1922 West Europe [Adlerberg, Chilchzimmersattel and Weiach, northern Switzerland]) 1923 1924 SCHNEIDER, A.C., and KÜRSCHNER, W.M. 2016. Pollen und Sporen als Indikatoren für 1925 den Klimawandel an der Jura/Kreide-Grenze. Palynologische Untersuchungen an einem 1926 Bohrprofil im Nordosten von NRW. [Pollen and spores as indicators for climate change at the 1927 Jurassic/Cretaceous boundary. Palynological investigations on a drilling profile in 1928 northeastern NRW]. ScriptumOnline., Geowissenschaftlich Arbeitsergebnisse aus Nordrhein- 1929 Westfalen, 1, 26 p. Geologischer Dienst NRW, Krefeld, ISSN 2510-1331 (available online at: 1930 https://www.gd.nrw.de/pr_shop_scriptumonline_01_2016-09.php) (in German with an 1931 English abstract). 1932 (biostratigraphy; freshwater algae; Jurassic-Cretaceous boundary; lithostratigraphy [Münder 1933 Formation and Bückeberg Group]; Lower Saxony Basin; organic geochemistry; ostracods; 1934 palaeoclimatology; palaeoecology; palynofacies; petroleum prospectivity; pollen-spores; 1935 regional geology; Wealden type facies; primary data; photographs; latest Jurassic–earliest 1936 Cretaceous [Tithonian–Berriasian]; sub-Arctic West Europe [the Husen 1/08 borehole, 1937 southwest of Hannover, northern Germany]) 1938 1939 SCHNEIDER, A.C., HEIMHOFER, U., HEUNISCH, C., and MUTTERLOSE, J. 2018. 1940 From arid to humid – The Jurassic–Cretaceous boundary interval in northern Germany. 1941 Review of Palaeobotany and Palynology 255: 57–69 (doi: 10.1016/j.revpalbo.2018.04.008). 1942 (biostratigraphy; correlation; freshwater algae; Jurassic–Cretaceous boundary; 1943 lithostratigraphy [Münder Formation and Bückeberg Group]; palaeoclimatology; 1944 palaeoecology; pollen-spores; vegetational dynamics; Wealden type facies; primary data; 1945 photographs; quantitative occurrence charts; latest Jurassic–earliest Cretaceous [Tithonian– 1946 Berriasian]; sub-Arctic West Europe [boreholes C-1 and Eulenflucht-1 (E-1), west of 1947 Hannover, Lower Saxony Basin, northern Germany]) 58

1948 1949 SCHNEIDER, A.C., HEIMHOFER, U., HEUNISCH, C., and MUTTERLOSE, J. 2018. The 1950 Jurassic–Cretaceous boundary interval in non-marine strata of northwest Europe – New light 1951 on an old problem. Cretaceous Research, 87: 42–54 (doi: 10.1016/j.cretres.2017.06.002). 1952 (acritarchs; biostratigraphy; calcareous nannofossils; correlation; eustacy; freshwater algae; 1953 Jurassic–Cretaceous boundary; lithostratigraphy [Münder Formation and Bückeberg Group]; 1954 ostracods; palaeoclimatology; palaeoecology; pollen-spores; provincialism; Purbeck and 1955 Wealden type facies; regional geology; primary data; photographs; latest Jurassic–earliest 1956 Cretaceous [Tithonian–Berriasian]; sub-Arctic West Europe [boreholes 1/08 Husen (H-1), 1957 “core-1” (C-1), Eulenflucht-1 (E-1) and Isterberg 1001 (I-1), west of Hannover, Lower 1958 Saxony Basin, northern Germany]) 1959 1960 SELKOVA, L.A. 2017. Palynological characteristics in Jurassic sediments of the Yarenga oil 1961 shale region (north-east of the Russian plate). In: Zakharov, V.A., Rogov, M.A., and 1962 Shchepetova E.V. (editors). Jurassic System of Russia: Problems of stratigraphy and 1963 рaleogeography. Seventh all-Russian Conference. Moscow, September 18th–22nd, 2017. 1964 Scientific materials. Russian Academy of Sciences, Moscow, p. 199–200 (in Russian with an 1965 English abstract). 1966 (acritarchs; biostratigraphy; pollen-spores; prasinophytes; reworking; summary; Middle and 1967 Late Jurassic [Callovian and Kimmeridgian]; sub-Arctic Russia [Yarenga oil shale region, 1968 Timan-Northern Ural Region, Komi Republic]) 1969 1970 SHUREKOVA, O.V. 2018. The Berriasian dinocysts of the section Uruh (North Caucasus). 1971 In: Baraboshkin, E.Yu., Lipnitskaya, T.A., and Guzhikov, A.Yu. (editors). Cretaceous system 1972 of Russia and near abroad: problems of stratigraphy and paleogeography. Proceedings of 1973 the Ninth All-Russian Conference, Belgorod State National Research University, Belgorod, 1974 September 17th–21st, 2018. Polyterra Publishing House, Belgorod, ISBN 978-5-98242-250- 1975 7, 282–286 (in Russian with an English abstract). 1976 (acritarchs; biostratigraphy; biozonation; correlation; summary of primary data; semi- 1977 quantitative range chart; photographs; earliest Cretaceous [Berriasian]; sub-Arctic Russia 1978 [Uruh, Crimean Mountains, North Caucasus, southwestern Russia]) 1979 1980 SMELROR, M., FOSSUM, K., DYPVIK, H., HUDSON, W., and MWENEINDA, A. 2018. 1981 Late Jurassic–Early Cretaceous palynostratigraphy of the onshore Mandawa Basin, 59

1982 southeastern Tanzania. Review of Palaeobotany and Palynology, 258: 248–255 (doi: 1983 10.1016/j.revpalbo.2018.09.001). 1984 (acritarchs; biostratigraphy; biozonation; correlation; Dingodinium jurassicum-Kilwacysta 1985 assemblage; eustasy; freshwater algae; fungal palynomorphs; lithostratigraphy [the Kipatimu, 1986 Mitole, Nalwehe and Kihuluhulu formations]; palaeoecology; pollen-spores; prasinophytes; 1987 regional geology; primary data; photographs; Late Jurassic–Early Cretaceous [Oxfordian– 1988 Tithonian to Aptian–Albian]; East Africa [Mandawa Basin, southeastern coastal Tanzania]) 1989 1990 *SMITH, G.A. 1999. Palynology of the Jurassic/Cretaceous boundary interval in the Volga 1991 Basin, Russia. Unpublished PhD Thesis, University of Bristol, UK, 527 p. (available online 1992 at: https://research-information.bristol.ac.uk/en/theses/palynology-of-the-jurassiccretaceous- 1993 boundary-interval-in-the-volga-basin-russia(a981fc30-fa69-4cf5-aae5-7290d2a489df).html). 1994 (acritarchs; biostratigraphy; diversity; Jurassic–Cretaceous boundary; informal taxonomy; 1995 palynofacies; pollen-spores; prasinophytes; regional stratigraphical synthesis; sedimentology; 1996 total organic carbon [TOC]; Volgian lectostratotype; primary data; occurrence charts; 1997 photographs; latest Jurassic–Early Cretaceous [Tithonian–Valanginian]; sub-Arctic Russia 1998 [Gorodische and Kashpir, Ulyanovsk region, Volga River Basin, western Russia]) 1999 2000 STANLEY, G., and VAN DE SCHOOTBRUGGE, B. 2018. Chapter 2. The evolution of the 2001 coral-algal symbiosis and coral bleaching in the geologic past. In: van Oppen, M.J.H., and 2002 Lough, J.M. (editors). Coral Bleaching. Patterns, processes, causes and consequences. 2003 Second Edition. Ecological Studies 233: 9–26. Springer, Cham, Switzerland (doi: 2004 10.1007/978-3-319-75393-5_2). 2005 (Beaumontella langii; coral bleaching; ecology; evolution; fossil and modern coral reefs; 2006 modern corals; photosymbiosis; Suessia swabiana; Symbiodinium; review; photographs; 2007 occurrence chart; Late Triassic–Early Jurassic [Carnian–Toarcian]; multi-region: North 2008 Africa [Libya]; Australasia [northwestern Australia]; sub-Arctic West Europe [Austria, 2009 southwestern Germany, southern Sweden]) 2010 2011 SUAN, G., SCHÖLLHORN, I., SCHLÖGL, J., SEGIT, T., MATTIOLI, E., LÉCUYER, C., 2012 and FOUREL, F. 2018. Euxinic conditions and high sulfur burial near the European shelf 2013 margin (Pieniny Klippen Belt, Slovakia) during the Toarcian oceanic anoxic event. Global 2014 and Planetary Change, 170: 246–259 (doi: 10.1016/j.gloplacha.2018.09.003).

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2015 (acritarchs; ammonites; biogeochemical cycles; calcareous nannofossils; correlation; euxinia; 2016 foraminiferal test linings; inorganic and organic geochemistry; palaeoceanography; 2017 palaeogeography; palynofacies; Pieniny Klippen Belt; pollen-spores; prasinophytes; pyrite 2018 framboid size; regional geology; scolecodonts; Tethyan Realm; Toarcian Oceanic Anoxic 2019 Event [T-OAE]; primary data; Early Jurassic [Toarcian]; East Europe [Zázrivá, northwestern 2020 Slovakia]) 2021 2022 SÜTŐNÉ SZENTAI, M. 2018. Taxon-list of Silurian to Holocene organic-walled 2023 microplankton from Hungary (1957–2017). [Szervesvázú microplankton fajok listája 2024 Magyarországról, a szilurtól a holocénig (1957–2017)]. e-Acta Naturalia Pannonica, 18, 203 2025 p. (doi: 10.24369/eANP.2018.18.1). 2026 (acritarchs; biostratigraphy; biozonations; Botryococcus; chitinozoa; chlorophytes; 2027 foraminiferal test linings; graptolites; history of research; incertae sedis; organic-walled 2028 microplankton; prasinophytes; scolecodonts; testate amoebae [formerly thecamoebians]; 2029 zooplankton; compilation of genera and species; Silurian [undifferentiated]–Holocene; East 2030 Europe [Hungary]) 2031 2032 2033 T 2034 2035 TAHOUN, S.S., IBRAHIM, M.I.A., and KHOLEIF, S. 2012. Palynology and 2036 paleoenvironments of Middle Jurassic to Cenomanian successions, Alamein-IX well, north 2037 Western Desert, Egypt. Revista Española de Micropaleontología, 44(1–3): 57–78. 2038 (biostratigraphy; biozonation; correlation; hiatus; lithostratigraphy; miscellaneous 2039 palynomorphs; palaeoecology; pollen-spores; primary data; occurrence charts; photographs; 2040 Middle Jurassic–Late Cretaceous [Callovian–Oxfordian and Barremian–Cenomanian]; North 2041 Africa [Alamein-IX well, northern Western Desert, Egypt]) 2042 2043 TAHOUN, S.S., and IED, I.M. 2018. A Cretaceous dinoflagellate cyst palynozonation of 2044 northern Eygpt. Palynology, doi: 10.1080/01916122.2018.1449029. 2045 (biostratigraphy; boreholes; correlation; last occurrence datums (LODs); regional 2046 biozonation; Tethys; review/synthesis; occurrence chart; Late Jurassic–Late Cretaceous 2047 [undifferentiated–Maastrichtian]; North Africa [northern Egypt]) 2048 61

2049 *TURNER, H.E., BATENBURG, S.J., GALE, A.S., and GRADSTEIN, F.M. 2018. The 2050 Kimmeridge Clay Formation (Upper Jurassic–Lower Cretaceous) of the Norwegian 2051 Continental Shelf and Dorset, UK: a chemostratigraphic correlation. Newsletters on 2052 Stratigraphy, doi: 10.1127/nos/2018/0436. 2053 (biostratigraphy; carbon cycle perturbations; carbon isotope excursions; chemostratigraphy; 2054 chronostratigraphy; correlation; cyclostratigraphy; gamma ray logs; geochemistry; 2055 lithostratigraphy [Kimmeridge Clay Formation]; pollen-spores; wavelet analyses; primary 2056 data; occurrence chart; Late Jurassic–Early Cretaceous [Oxfordian–Valanginian]; multi- 2057 region: Arctic [Barents Sea; Arctic Russia; Svalbard]; East Europe [Brodno, Slovakia]; sub- 2058 Arctic West Europe [Dorset, southern England; North Sea, offshore Norway]) 2059 2060 2061 V 2062 2063 *VAN DE SCHOOTBRUGGE, B., RICHOZ, S., PROSS, J., LUPPOLD, F.W., HUNZE, S., 2064 WONIK, T., BLAU, J., MEISTER, C., VAN DER WEIJST, C.M.H., SUAN, G., 2065 FRAGUAS, A., FIEBIG, J., HERRLE, J.O., GUEX, J., LITTLE, C.T.S., WIGNALL, P.B., 2066 PÜTTMANN, W., and OSCHMANN, W. 2018. The Schandelah Scientific Drilling Project: 2067 A 25-million year record of Early Jurassic palaeo-environmental change from northern 2068 Germany. Newsletters on Stratigraphy, doi: 10.1127/nos/2018/0259, 48 p. 2069 (ammonites; ammonite zones; benthic foraminifera; biostratigraphy; biozonation; black 2070 shales; calcareous nannofossils; carbon cycle perturbations; chemostratigraphy; correlation; 13 18 2071 end-Triassic extinction; eustasy; geochemistry [δ Corg; δ O]; geophysical downhole 2072 logging; glendonites; hydrocarbon seepage; lithostratigraphy; marine anoxia; ostracods; 2073 palaeoecology; pollen-spores; reworking; sedimentology; seismic activity; taxonomy; 2074 primary data; photographs; latest Triassic–Early Jurassic [Rhaetian–Toarcian]; sub-Arctic 2075 West Europe [Schandelah-1 borehole, Lehre, Landkreis Helmstedt, Lower Saxony, northern 2076 Germany]) 2077 2078 VAN ELDIJK, T.J.B., WAPPLER, T., STROTHER, P.K., VAN DER WEIJST, C.M.H., 2079 RAJAEI, H., VISSCHER, H., and VAN DE SCHOOTBRUGGE, B. 2018. A Triassic- 2080 Jurassic window into the evolution of Lepidoptera. Science Advances, 4(1): e1701568 (doi: 2081 10.1126/sciadv.1701568), 7 p. (includes online supplementary material) (available online at: 2082 http://advances.sciencemag.org/content/advances/4/1/e1701568.full.pdf). 62

2083 (biostratigraphy; evolution; evolutionary radiation; flowering plants; Glossata; insect-plant 2084 interactions; Lepidoptera (butterflies and moths); lepidopteran wing scales; Lunnomidinium 2085 scaniense; mass extinction; pollen-spores; primary data; quantitative selective occurrence 2086 chart; latest Triassic–Early Jurassic [Rhaetian–Sinemurian]; sub-Arctic West Europe 2087 [Schandelah-1 well, near Braunschweig, Lower Saxony, northern Germany]) 2088 2089 VAN HELDEN, B.G. 1987. Dinocysts from the Jurassic of Saskatchewan and Alberta: an 2090 open field for research. Canadian Association of Palynologists (CAP) Newsletter, 10(1): 12– 2091 14. 2092 (biostratigraphy; Botryococcus; foraminiferal test linings; lithostratigraphy; palaeoecology; 2093 petroleum geology; plant fossils; pollen-spores; scolecodonts; research proposal; Jurassic 2094 [undifferentiated]; sub-Arctic North America [Alberta and Saskatchewan, western Canada]) 2095 2096 *VERREUSSEL, R.M.C.H., BOUROULLEC, R., MUNSTERMAN, D.K., DYBKJÆR, K., 2097 GEEL, C.R., HOUBEN, A.J.P., JOHANNESSEN, P.N., and KERSTHOLT-BOEGEHOLD, 2098 S.J. 2018. Stepwise basin evolution of the Middle Jurassic–Early Cretaceous rift phase in the 2099 Central Graben area of Denmark, Germany and The Netherlands. In: Kilhams, B., Kukla, 2100 P.A., Mazur, S., McKie, T., Mijnlieff, H.F., and van Ojik, K. (editors). Mesozoic Resource 2101 Potential in the Southern Permian Basin. Geological Society, London, Special Publications, 2102 No. 469, doi: 10.1144/SP469.23, 36 p. 2103 (ammonite zones; basin evolution/history; biostratigraphy; chronostratigraphy; correlations; 2104 electric logs; lithostratigraphy; palaeoecology; palaeoceanography; petroleum geology; 2105 pollen-spores; sedimentary architecture and facies; sedimentology; structural geology; 2106 tectonic extension and rifting; tectonostratigraphical mega-sequences (TMS); compilation; 2107 Middle Jurassic–Early Cretaceous [Bathonian–Barremian]; sub-Arctic West Europe [Danish- 2108 Dutch-German Central Graben, North Sea]) 2109 2110 VISSCHER, H., and BRUGMAN, W.A. 1981. Ranges of selected palynomorphs of the 2111 Alpine Triassic of Europe. Review of Palaeobotany and Palynology, 34(1): 115–128 2112 (doi.org/10.1016/0034-6667(81)90069-5). 2113 (acritarchs; ammonites; biostratigraphy; informal taxonomy; pollen-spores; Rhaetogonyaulax 2114 rhaetica; Suessia swabiana; Tethyan Realm; compilation; occurrence charts; photographs; 2115 Triassic–earliest Jurassic [Induan–Hettangian]; multi-region: East Europe and sub-Arctic

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2116 West Europe [The Alpine region, i.e. Austria; Germany, Hungary, Italy and the former 2117 Yugoslavia]) 2118 2119 2120 W 2121 2122 WAINMAN, C.C., and McCABE, P.J. 2018. Evolution of the depositional environments of 2123 the Jurassic Walloon Coal Measures, Surat Basin, Queensland, Australia. Sedimentology, doi: 2124 10.1111/sed.12548, 50 p. 2125 (acritarchs; allocyclicity; biostratigraphy; boreholes; chronostratigraphy; coalbed methane; ; 2126 colonial alga; correlation; estuarine, freshwater-brackish dinoflagellate cysts; marine and 2127 terrestrial [fluviolacustrine] facies analysis; eustasy; isopach maps; lithostratigraphy; 2128 palaeoclimatology; palaeodrainage patterns; palaeogeography; regional geology; 2129 sedimentology; sequence stratigraphy; Walloon Coal Measures [Injune Creek Group]; 2130 uranium–lead [U–Pb] dating; wireline log analysis; primary data; photographs; Late Jurassic 2131 [Oxfordian–Tithonian]; Australasia [Surat Basin, Queensland, eastern Australia]) 2132 2133 WAINMAN, C.C., HANNAFORD, C., MANTLE, D., and McCABE, P.J. 2018. Utilizing 2134 U–Pb CA-TIMS dating to calibrate the Middle to Late Jurassic spore-pollen zonation of the 2135 Surat Basin, Australia to the geological time-scale. Alcheringa, 42(3): 402–414 (doi: 2136 10.1080/03115518.2018.1457179). 2137 (acritarchs; biostratigraphy; biozonation; boreholes; correlation; economic geology; fungi; 2138 geochronology; Moorodinium; pollen-spores; regional geology; Skuadinium; tuff horizons; 2139 uranium–lead chemical abrasion thermal ionization mass spectroscopy [U–Pb CA-TIMS] 2140 dating; Walloon Coal Measures [Injune Creek Group]; primary data; photographs; Middle– 2141 Late Jurassic [Bathonian–Tithonian]; Australasia [Surat Basin, Queensland, eastern 2142 Australia]) 2143 2144 *WAINMAN, C.C., MANTLE, D.J., HANNAFORD, C., and McCABE, P.J. 2018. Possible 2145 freshwater dinoflagellate cysts and colonial algae from the Upper Jurassic of the Surat Basin, 2146 Australia. Palynology, doi: 10.1080/01916122.2018.1451785, 12 p. 2147 (acritarchs; biostratigraphy; colonial alga; freshwater-brackish dinoflagellate cysts; 2148 morphology; palaeoecology; pollen-spores; sea levels; sedimentology; taxonomy; uranium– 2149 lead [U–Pb] dating; Walloon Coal Measures [Injune Creek Group]; primary data; occurrence 64

2150 chart; photographs; Late Jurassic [Tithonian]; Australasia [Indy 3 well, western Surat Basin, 2151 Queensland, southeastern Australia]) 2152 2153 WALLEY, R., BOOMER, I., and HARRINGTON, G. 2017. Palynological record of 2154 changing environments across the Triassic–Jurassic boundary interval in Northern Ireland. 2155 The Micropalaeontological Society Annual Conference 2017, 15th–16th November 2017, The 2156 Natural History Museum, London, Programme and Abstracts Volume, p. 68. 2157 (acritarchs; biostratigraphy; palaeoecology; regression-transgression; spore-pollen; 2158 sporomorph eco-grouping; statistics; summary; latest Triassic–earliest Jurassic [Rhaetian– 2159 Hettangian]; sub-Arctic West Europe [Carnduff-1 Borehole, near Larne, Northern Ireland]) 2160 2161 *WIGGAN, N.J., RIDING, J.B., FENSOME, R.A., and MATTIOLI, E. 2018. The Bajocian 2162 (Middle Jurassic): a key interval in the early Mesozoic phytoplankton radiation. Earth- 2163 Science Reviews, 180: 126–146 (doi:10.1016/j.earscirev.2018.03.009). 2164 (ammonites; belemnites; biological productivity; bivalves; bryozoan; carbon isotope 2165 geochemistry; coccolithophores; continental weathering; Dissiliodinium; diversity; evolution; 2166 evolutionary radiation; fish; Gonyaulacaceae; Mesozoic Marine Revolution; nutrient flux; 2167 palaeoclimate; palaeoecology; palaeogeography; palaeoceanography; phytoplankton; 2168 planktonic foraminifera; sea level; sequence stratigraphy; Watznaueria; compilation; 2169 occurrence charts; photographs; Middle Jurassic [Aalenian–Bathonian]; sub-Arctic West 2170 Europe [no specific geographical focus]) 2171 2172 WILLEMS, C.J.L., VONDRAK, A., MUNSTERMAN, D.K., DONSELAAR, M.E., and 2173 MIJNLIEFF, H.F. 2017. Regional geothermal aquifer architecture of the fluvial Lower 2174 Cretaceous Nieuwerkerk Formation – a palynological analysis. Netherlands Journal of 2175 Geosciences – Geologie en Mijnbouw, 96(4): 319–330 (doi: 10.1017/njg.2017.23) (includes 2176 online supplementary material). 2177 (aquifers; biostratigraphy; boreholes; correlation; downhole logging; fluvial sandstones; 2178 geothermal groundwaters and heat; lateral thickness variability; Nieuwerkerk Formation; 2179 pollen-spores; sedimentary architecture; seismic interpretation; sequence stratigraphy; 2180 sporomorph eco-grouping; tectonic activity; primary data; Early Cretaceous 2181 [Berriasian/Ryazanian–Barremian]; sub-Arctic West Europe [West Netherlands Basin, The 2182 Netherlands]) 2183 65

2184 WILLIAMS, G., FENSOME, R., MILLER, M., and BUJAK, J. 2018. Microfossils: 2185 Palynology. In: Sorkhabi, R. (editor). Encyclopedia of Petroleum Geoscience, doi: 2186 10.1007/978-3-319-02330-4_146-1, 15 p. 2187 (acritarchs; biostratigraphy; chitinozoa; evolution; Gonyaulacysta jurassica; history of study; 2188 miscellaneous palynomorphs; morphology; palaeoclimatology; palaeoecology; 2189 palaeogeography; palynofacies; palynology; pollen-spores; preparation techniques; 2190 photographs; review article; no specific geographical or stratigraphical focus) 2191 2192 2193 Z 2194 2195 ZHANG WANGPING, and GRANT-MACKIE, J.A. 2001. Late Triassic–Early Jurassic 2196 palynofloral assemblages from Murihiku strata of New Zealand, and comparisons with 2197 China. Journal of the Royal Society of New Zealand, 31(3): 575–683 (doi: 2198 10.1080/03014223.2001.9517668). 2199 (assemblage zones; biostratigraphy; correlations with China; lithostratigraphy; Murihiku 2200 Terrane; pollen-spores; systematics; Triassic–Jurassic boundary; primary data; occurrence 2201 charts; photographs; Late Triassic–Early Jurassic [Norian–Sinemurian]; Australasia 2202 [Awakino Gorge, southwestern Auckland, Hokonui Hills, Southland, and southwestern 2203 Kawhia, New Zealand]) 2204 2205 2206 Appendix 2. List of palynomorph species and subspecies 2207 2208 This Appendix alphabetically lists all valid, formally-defined palynomorph taxa below 2209 generic level which are mentioned in this contribution with full author citations. This listing 2210 largely comprises dinoflagellate cysts, together with colonial alga and miospores; these are 2211 given separately below. References to the majority of the author citations for the 2212 dinoflagellate cysts can be found in Williams et al. (2017). Note that the proposals of Correia 2213 et al. (2017, p. 93, appendix 2) regarding the taxonomy of Nannoceratopsis gracilis and 2214 Nannoceratopsis senex are followed herein. 2215 2216 Dinoflagellate cysts: 2217 Acanthaulax crispa (Wetzel 1967) Woollam & Riding 1983 66

2218 Aldorfia aldorfensis (Gocht 1970) Stover & Evitt 1978 2219 Ambonosphaera calloviana Fensome 1979 2220 Amphorulacysta? dodekovae (Zotto et al. 1987) Williams & Fensome 2016 2221 Amphorulacysta? expirata (Davey 1982) Williams & Fensome 2016 2222 Batioladinium pomum Davey 1982 2223 Batioladinium reticulatum Stover & Helby 1987 2224 Batioladinium varigranosum (Duxbury 1977) Davey 1982 2225 Beaumontella langii (Wall 1965) Below 1987 2226 Canningia reticulata Cookson & Eisenack 1960 2227 Cantulodinium speciosum Alberti 1961 2228 Chytroeisphaeridia chytroeides (Sarjeant 1962) Downie & Sarjeant 1965 2229 Circulodinium distinctum (Deflandre & Cookson 1955) Jansonius 1986 2230 Cometodinium whitei (Deflandre & Courteville 1939) Stover & Evitt 1978 2231 Compositosphaeridium? polonicum (Górka 1965) Lentin & Williams 1981 2232 Cribroperidinium? longicorne (Downie 1957) Lentin & Williams 1985 2233 Ctenidodinium combazii Dupin 1968 2234 Ctenidodinium continuum Gocht 1970 2235 Ctenidodinium cornigerum (Valensi 1947) Jan du Chêne et al. 1985 2236 Ctenidodinium elegantulum Millioud 1969 2237 Ctenidodinium ornatum (Eisenack 1935) Deflandre 1938 2238 Ctenidodinium sellwoodii (Sarjeant 1975) Stover & Evitt 1978 2239 Cyclonephelium cuculliforme (Davies 1983) Århus 1992 2240 Dapcodinium priscum Evitt 1961 2241 Dichadogonyaulax? pannea (Norris 1965) Sarjeant 1969 2242 Dingodinium albertii Sarjeant 1966 2243 Dingodinium jurassicum Cookson & Eisenack 1958 2244 Dingodinium tuberosum (Gitmez 1970) Fisher & Riley 1980 2245 Dingodinium nequeas Pestchevitskaya 2018 2246 Durotrigia daveyi Bailey 1987 2247 Endoscrinium galeritum (Deflandre 1938) Vozzhennikova 1967 2248 Egmontodinium polyplacophorum Gitmez & Sarjeant 1972 2249 Emmetrocysta sarjeantii (Gitmez 1970) Stover & Evitt 1978 2250 Epiplosphaera gochtii (Fensome 1979) Brenner 1988 2251 Epiplosphaera reticulospinosa Klement 1960 67

2252 Gochteodinia villosa (Vozzhennikova 1967) Norris 1978 2253 Gonyaulacysta centriconnata Riding 1983 2254 Gonyaulacysta eisenackii (Deflandre 1938) Górka 1965 2255 Gonyaulacysta jurassica (Deflandre 1938) Norris & Sarjeant 1965 2256 Hebecysta balmei (Stover & Helby 1987) Below 1987 2257 Heibergella asymmetrica Bujak & Fisher 1976 2258 Hystrichosphaerina? orbifera (Klement 1960) Stover & Evitt 1978 2259 Impletosphaeridium varispinosum (Sarjeant 1959) Islam 1993 2260 Kaiwaradinium scruttinum Backhouse 1987 2261 Kalyptea stegasta (Sarjeant 1961) Wiggins 1975 2262 Korystocysta gochtii (Sarjeant 1976) Woollam 1983 2263 Korystocysta pachyderma (Deflandre 1938) Woollam 1983 2264 Luehndea spinosa Morgenroth 1970 2265 Liasidium variabile Drugg 1978 2266 Lithodinia jurassica Eisenack 1935 2267 Mancodinium semitabulatum Morgenroth 1970 2268 Meiourogonyaulax bulloidea (Cookson & Eisenack 1960) Sarjeant 1969 2269 Meiourogonyaulax caytonensis (Sarjeant 1959) Sarjeant 1969 2270 Meiourogonyaulax reticulata Dodekova 1975 2271 Meiourogonyaulax valensii Sarjeant 1966 2272 Mendicodinium groenlandicum (Pocock & Sarjeant 1972) Davey 1979 2273 Mendicodinium microscabratum Bucefalo Palliani et al. 1997 2274 Moorodinium crispa Wainman et al. 2018 2275 Muderongia simplex Alberti 1961 2276 Muderongia simplex Alberti 1961 subsp. microperforata Davey 1982 2277 Nannoceratopsis dictyambonis Riding 1984 2278 Nannoceratopsis gracilis Alberti 1961 2279 Nannoceratopsis plegas Drugg 1978 2280 Nannoceratopsis pellucida Deflandre 1938 2281 Nannoceratopsis raunsgaardii Poulsen 1996 2282 Nannoceratopsis senex van Helden 1977 2283 Nannoceratopsis spiculata Stover 1966 2284 Neuffenia willei Brenner & Dürr 1986 2285 Noricysta fimbriata Bujak & Fisher 1976 68

2286 Occisucysta tentorium Duxbury 1977 2287 Palaecysta palmula (Davey 1982) Williams & Fensome 2016 2288 Pareodinia brevicornuta Kunz 1990 2289 Pareodinia ceratophora Deflandre 1947 2290 Pareodinia prolongata Sarjeant 1959 2291 Pareodinia halosa (Filatoff 1975) Prauss 1989 2292 Perisseiasphaeridium pannosum Davey & Williams 1966 2293 Phallocysta elongata (Beju 1971) Riding 1994 2294 Phallocysta eumekes Dörhöfer & Davies 1980 2295 Phoberocysta neocomica (Gocht 1957) Millioud 1969 2296 Pseudoceratium iehiense Helby & May in Helby 1987 2297 Pseudoceratium pelliferum Gocht 1957 2298 Rhaetogonyaulax arctica (Wiggins 1973) Stover & Evitt 1978 2299 Rhaetogonyaulax rhaetica (Sarjeant 1963) Loeblich Jr. & Loeblich III 1968 2300 Rhynchodiniopsis cladophora (Deflandre 1938) Below 1981 2301 Rynchodiniopsis? regalis (Gocht 1970) Jan du Chêne et al. 1985 2302 Sahulidinium ottii Stover & Helby 1987 2303 Scriniocassis weberi Gocht 1964 2304 Scriniodinium crystallinum (Deflandre 1938) Klement 1960 2305 Senoniasphaera jurassica (Gitmez & Sarjeant 1972) Lentin & Williams 1976 2306 Sentusidinium villersense (Sarjeant 1968) Sarjeant & Stover 1978 2307 Skuadinium fusum Wainman et al. 2018 2308 Suessia swabiana Morbey 1975 2309 Susadinium faustum (Bjaerke 1980) Lentin & Williams 1985 2310 Sverdrupiella baccata Bujak & Fisher 1976 2311 Sverdrupiella manicata Bujak & Fisher 1976 2312 Sverdrupiella ornaticingulata Bujak & Fisher 1976 2313 Sverdrupiella septentrionalis Bujak & Fisher 1976 2314 Sverdrupiella usitata Bujak & Fisher 1976 2315 Systematophora areolata Klement 1960 2316 Systematophora penicillata (Ehrenberg 1843 ex Ehrenberg 1865) Sarjeant 1980 2317 Tabulodinium senarium Dodekova 1990 2318 Trichodinium scarburghense (Sarjeant 1964) Williams et al. 1993 2319 Valensiella ovulum (Deflandre 1947) Eisenack 1963 69

2320 Wanaea acollaris Dodekova 1975 2321 Wanaea digitata Cookson & Eisenack 1958 2322 Wanaea thysanota Woollam 1982 2323 2324 Colonial alga: 2325 Palambages pariunta Wainman et al. 2018 2326 2327 Miospores: 2328 Ricciisporites umbonatus Felix & Burbridge 1977 2329 Shanbeipollenites proxireticulatus Schrank 2004 2330 2331 2332 References 2333 2334 Correia VF, Riding JB, Fernandes P, Duarte LV, Pereira Z. 2017. The palynology of the 2335 lower and middle Toarcian (Lower Jurassic) in the northern Lusitanian Basin, western 2336 Portugal. Review of Palaeobotany and Palynology 237:75–95. 2337 2338 Riding JB. 2012. A compilation and review of the literature on Triassic, Jurassic, and earliest 2339 Cretaceous dinoflagellate cysts. American Association of Stratigraphic Palynologists 2340 Contributions Series No. 46, 119 p. plus CD ROM. 2341 2342 Riding JB. 2013. The literature on Triassic, Jurassic and earliest Cretaceous dinoflagellate 2343 cysts: supplement 1. Palynology 37:345–354. 2344 2345 Riding JB. 2014. The literature on Triassic, Jurassic and earliest Cretaceous dinoflagellate 2346 cysts: supplement 2. Palynology 38:334–347. 2347 2348 Riding JB. 2019. The literature on Triassic, Jurassic and earliest Cretaceous dinoflagellate 2349 cysts: supplement 3. Palynology 43:104–150. 2350 2351 Williams GL, Fensome RA, MacRae RA. 2017. The Lentin and Williams index of fossil 2352 dinoflagellates. 2017 edition. American Association of Stratigraphic Palynologists 2353 Contributions Series 48, 1097 p. 70

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