河北泥河湾"Pliopentalagus nihewanensis"分类地位的再思考

自20世纪60年代,欧亚大陆晚新生代地层中陆续发现了p3由5个主要褶沟组成的兔类化石,并先后建立了上新五褶兔(Pliopentalagus Gureev et Konkova,1964)和三裂齿兔(Tris- chizolagus Radulesco et Samson,1967)两属。近年,在中国安徽淮南大居山新生代晚期不同时代的洞穴、裂隙堆积物中发现了保存相当完整,数量颇多的上新五褶兔的材料。笔者在研究大居山新洞早上新世的上新五褶兔时, 将其与欧亚大陆该属内的已知种和三裂齿兔的各种进行了详细比较,发现产自河北省阳原县泥河湾盆地晚上新世稻地组的Pliopentalagus nihewanensis Cai,1989被指定为上新五褶兔值得商榷。Pliopentalagus nihewanensis的材料仅有1枚p3(GMC V 2008-1)和两枚中间颊齿(p4 或ml,GMC V 2008-2及m2,V 2008-3)。正型标本p3的中前褶沟(AR)中央、后外褶沟和后内褶沟后壁釉质层具有小褶曲,这些形态确实与上新五褶兔的特征有些相似。但褶曲的发育程度明显比上新五褶兔的弱;另外,其齿冠舌侧后缘向后内突出,后外褶沟和后内褶沟较平直并近与齿纵轴垂直,后外褶沟与后内褶沟深度相近等而与上新五褶兔也有所不同。褶沟的釉质层在两枚中间颊齿中较平直,与上新五褶兔显然也有较大的区别。就该p3而言,可以认为它属于一枚釉质构造极简单的上新五褶兔的前臼齿,也可以认为是釉质构造很复杂的三裂齿兔的p3。研究表明,在上新五褶兔和三裂齿兔的系统演化过程中,其颊齿褶沟釉质层的构造有越来越复杂的趋向。作为上新世较晚期的“Pliopentalagus nihewanensis”的p3,指定为上新五褶兔显然有悖于该属釉质构造在地史中越来越复杂的演化事实,而指定为三裂齿兔则正好与该属釉质构造的演化趋势相符(Averianov and Tesakov,1997)。另外,从共生动物群和动物的生活习性看,安徽淮南发现的上新五褶兔与大量现代东洋界特有的类型共生(如Tupaiidae、Platacanthomyidae等),上新五褶兔的后裔——现生的日本琉球奄美黑兔(Pentalagus)的栖息地为温暖、湿润的多山环境;而目前发现的三裂齿兔共生动物群所指示的是干凉的稀树草原环境,与上新五褶兔的生态环境有所不同。含“Pliopentalagus nihewanensis”的晚上新世稻地动物群主要由典型的古北界属种(如Mesosiphneus paratingi、Mimomys orientalis、Germanomys cf. G.weileri、Chardinomys nihewanicus及Ochotona spp.等)组成,而未见典型的东洋界成员。这种温带相对干旱的草原环境,显然与中国发现的上新五褶兔及其后裔的生存环境很不一样。因此,笔者认为“泥河湾上新五褶兔”应归入三裂齿兔属,正名泥河湾三裂齿兔Trischizolagus nihe—wanensis(Cai,1989)。种征订正为:p3具有较复杂的形态构造;中前褶沟具衍生的中央小褶曲, 后外褶沟和后内褶沟后壁釉质层褶曲相对发育。该种以这些基本特征而不同于欧亚大陆的已知种(如T.dumitrescuae、T.mirificus等),它可能代表该属的一个进步类型。     

安徽上新五褶兔两新种及淮南上新五褶兔化石(英文)

近年,作者在安徽淮南大居山陆续发现了数量很多的上新五褶兔化石,其中包括保存较完整的数十个头骨及上百个下颌骨,均产自新洞、无名洞及铁四局洞穴、裂隙堆积,分别记述为大居山上新五褶兔Pliopentalagus dajushanensis sp.nov.和安徽上新五褶兔Pl.anhuiensis sp.nov.两新种。淮南地区的晚新生代洞穴和裂隙堆积十分发育,其中常含有丰富的脊椎动物化石,而且在时、空分布上有一定的规律。区内洞穴和裂隙堆积垂直分布至少有6个水平层,最高的第6层海拔高度为160 m(如大居山老洞),第5层(如大居山新洞、无名洞)及第4层(如大居山铁四局洞穴)的海拔高度分别为130 m和90 m,属于新近纪,常含有丰富的上新五褶兔化石;第3层为第四纪早期(如大居山西裂隙),未见上新五褶兔,代之出现丝绸兔(Sericolagus sp.),第2层为中更新世(如大顶山西裂隙),出现野兔(Lepus sp.)。迄今为止,安徽淮南地区共发现了3种上新五褶兔化石,即淮南上新五褶兔Pl.huainanensis (金昌柱,2004)、大居山上新五褶兔Pl.dajushanensis sp.nov.及安徽上新五褶兔Pl. anhuiensis sp.nov.,至少涉及了3个不同地质时期的动物群:一为Pl.huainanensis,Kowalskia neimengensis,Adcrocuta eximia等代表的老洞晚中新世动物群,二为Pl.dajushanensis sp.nov.和Promimomys asiaticus等代表的新洞早上新世动物群,三为Pl.anhuiensis sp.nov.和Kowalskia yinanensis所代表的晚上新世动物群。淮南地区发现的3种上新五褶兔地史分布较连续,演化特征明显,它们构成上新五褶兔连续的进化系列。从晚中新世至晚上新世,淮南大居山上新五褶兔体型从小变大;p3较原始的釉岛状后内褶沟逐渐向舌侧开放(晚中新世种Pl. huainanensis的后内褶沟均为釉岛状,早上新世种Pl.dajushanensis为83.9%,晚上新世种Pl. anhuiensis为33.3%);p4-m2的前外褶沟逐渐退化,其下跟座舌侧的釉质层越来越变细。依性状分析,安徽发现的3种上新五褶兔化石与日本琉球奄美黑兔(Pentalagus furnessi)具有密切的亲缘关系,但从日本奄美黑兔的p4-m2完全缺失前外褶沟、颊齿褶沟釉质层的褶曲异常复杂等衍生性状看,上新五褶兔和奄美黑兔的系统演化关系较为复杂,尚有待发现更多早更新世的材料进一步探讨。     

新疆准噶尔盆地北缘中中新世兔形类新材料

在新疆准噶尔盆地北线中中新世索索泉组顶部和哈拉玛盖组底部发现4枚尺寸较大、具有齿根的高齿冠兔形类牙齿（P2、2p3和p4／m1／m2）－,曾被鉴定为Amphilagus。研究表明,它们不是Amphilagus,而是与中亚的Desmatoloagus、欧洲的Amphilagus和对Titanomys及北美的Hesperolagomys、Gripholagomys和Russellagus都较亲近的一个属。命名为新属新种准噶尔褶齿兔Plicalagusjunggarensis。其主要特征是：p3冠面三角形,外褶沟的深度为齿宽的1／2,其后壁釉质层具小褶皱。     

河北秦皇岛柳江盆地中更新世野兔一新种

在河北秦皇岛柳江盆地山羊寨附近中更新世洞穴堆积中发现一种小型野兔化石:秦皇岛兔Lepus qinhuangdaoensis sp.nov.,该种以其个体小、p3后外褶沟深达内侧齿缘或贯穿整个齿冠面、部分标本p3具有釉岛及前内褶沟等特征区别于其他已知种。它是迄今为止所知的体形最小的野兔。     

山西忻州中新世鼠兔科化石

本文记述了山西忻州发现的跑兔属—新种.该种以个体较小, P~2 较简单,无前沟, M~2 后叶无后突, P_3 小,无前内沟与前外沟等特征与属型种 B. forsythmajori 相区别,命名为杨胡跑兔 B. yanghuensis sp. nov..新种在进化水平上较属型种稍原始,但两者显示出较近的系统关系.根据 B. yanghuensis sp. nov. 的进化水平,推断其地质时代可能为中中新世早期,约相当于欧洲 Orleanian 期.     

江苏泗洪下草湾中中新世脊椎动物群──9.鼠兔科(哺乳纲,兔形目)

江苏泗洪松林庄、双沟和郑集早中新世（山旺期,约与欧洲新第三纪陆相哺乳动物分带MN4相当）的新种泗洪跳兔Alloptoxsihongensissp.nov.是迄今为止该属中出现最早、个体最小的种。该种已有较明显的形态分化。主要表现在p3上。p3在形态和大小上可分为两类。第一美个体较大,珐琅质厚度分化较明显,个别p3的下后尖前端已呈圆钝的角状,具有两个前外沟。第二类个体较小,珐琅质厚度分化较差,下后尖前端浑圆,仅具一个前外沟。由于对Alloptox的系统进化尚无足够的了解,现将其作为同一个种处理。根据上下齿列尤其是p3的形态分析,推测Alloptox可能由晚渐新世的Sinolagomysulungurensis或与其相近的鼠兔进化而来。     

丹江库区晚新生代三种兔形类化石

记述了丹江库区周围发现的三种兔形类化石：产在丹江二级阶地基座岩层中的淅川跳兔（新种）Alloptoxxichuanwnsissp．nov．个体小,形态较早中新世中期的A．minor原始,其时代可能是早中新世早期,同时详细讨论了Alloptox的进化和分类;发现于台子山林场裂隙堆积物中的进步上新五褶兔（新种）Pliopentalagusprogressivussp.nov.个体为该属已知各种中最大者,形态较已知种更接近于现生的Pentalagus,它的时代可能为上新世末或更新世初;产于郧县曲远河口汉水Ⅳ级阶地的复齿拟鼠兔Ochotonoidescomplicidens与蓝田金丝猴发现于同一阶地,推测其时代为早更新世晚期。     

内蒙古四子王旗大庙中新世的真角鹿一新种(英文)

描述了内蒙古四子王旗大庙中中新世化石地点(DM01)产出的真角鹿一新种:高枝真角鹿Euprox altus sp.nov.。新种具真正的角节,角节之上一定高度的两个分枝,长的角柄;牙齿低冠,上臼齿的前附尖和中附尖发育,新棱和齿带存在;p4的下后尖发育,下次凹存在;下臼齿具古鹿褶。这些特征可作为其归入真角鹿属Euprox的依据。Euprox altus最主要的特征是其分叉起始位置比属内其他种的高。分叉起始位置的标志是角基的突然变宽,它不同于分叉的位置,可作为一个新的鉴定特征。角冠表面纵向分布不均的沟棱、更低冠的牙齿、P4原尖后棱上的脊、p4不明显的下前凹和不是很发育的下三角凹、下臼齿上发育较弱的古鹿褶等特征都是新种区别于属内其他种的重要特征。Euprox altus所指示的可能是温暖湿润的生活环境,与大庙现在干旱、恶劣的景象截然不同。     

中国异痂蝗属一新种(直翅目,斑翅蝗科)

记述采自新疆北部地区异痂蝗属1新种,即黑翅异痂蝗Bryodemalla nigripennis sp.nov.,新种区别于属内所有已知种为:1)前胸背板沟后区两侧具3条侧隆线;2)后翅除基部淡红色外其余部分全黑色;3)后足股节外侧上下隆线均具细齿。模式标本保存于陕西师范大学动物研究所。     

中国沟芫菁属分类研究及一新种记述(鞘翅目,芫菁科)

总结中国沟芫菁属Hycleus Latreille,1817并记述1新种:毛背沟芫菁Hycleus dorsetiferus sp.nov.及1新组合:多毛沟芫菁Hycleus hirtus(Tan,1992)comb.nov.。新种模式标本保存在河北大学博物馆。提供了中国已知种类的分种检索表。     

安徽淮南大居山的早更新世反刍类

继在安徽淮南大居山发现晚中新世老洞哺乳动物群和新洞早上新世哺乳动物群后,1998年在老洞西侧又发现了西裂隙哺乳动物群。据对所出土的化石标本所作的整理研究,大居山西裂隙的反刍类动物化石有4个种：狍后麂Metacervulus capmolinus、山西轴鹿Axis shan- sius、布氏真枝角鹿Eucladoceros boulei和半牛未定种Hemibos?sp．,全部为绝灭种。它们所指示的地质年代为早更新世早期;所显示的动物群面貌为带有北方色彩的南、北方过渡带特色;所反映的生态环境为北温带森林景观,山谷间有少量密林,山脚下有局部草地。反刍类中山西轴鹿的标本数量最多,说明这个种是大居山西裂隙动物群中的优势种群。西裂隙动物群中的反刍类化石的另一个特点是未成年个体占有较大的比例,与河流冲击扇沉积中的动物年龄结构有很大的差别,也许指示大居山西裂隙是食肉动物存储和食用它们猎物的场所或这些反刍类的天然陷阱。     

安徽淮南大居山早更新世猪化石

继在安徽淮南大居山发现晚中新世老洞哺乳动物群和新洞早上新世哺乳动物群后,1998年在老洞西侧又发现了西裂隙哺乳动物群。记述了西裂隙动物群中的李氏野猪(Sus ly- dekkeri),并对李氏野猪的地理与地层分布进行了综述,对李氏野猪与其近亲之间的关系进行了探讨。李氏野猪主要分布于华北、东北和江南,最早出现在下更新统下部,最晚可延续到上更新统底部。李氏野猪与早更新世分布在长江以南的裴氏猪(S.peii)、早更新世和中更新世分布在欧洲和中东的斯氏猪(S.strozzii)之间的关系很可能是地理亚种或仅仅是形态种,晚更新世以后分布于欧亚大陆的野猪(S.scrofa)是它们的直接后裔。     

The effect of cave microclimate on winter roosting behaviour in the bat,Miniopterus schreibersii blepotis

The microclimate at Thermocline Cave (lat, 30° 45′S, long, 149° 43′E) was investigated by measuring air temperature and relative humidity at five stations on 18 occasions from September 1971 to December, 1973. The activity, body weight and roosting sites of the bat Miniopterus schreibersii blepotis in the cave were recorded on each visit. Relative humidity in the cave was generally high and paralleled temperature. The cave exhibited a range of temperatures from 9 to 19.5°C but bats selected roosting sites only in a part of this range. During the autumn when the bats arrived and were feeding, their body weights were low, and they roosted in a domed area at the rear of the cave with a temperature of 19.5°C. As they became less active and body weight increased they moved to cooler parts (9.5-11°C) towards the front of the cave and underwent periods of torpor, in one case lasting for at least 12 days. From July to September body weight decreased. The bats became more active in September and most had left the cave by October. It appears that M.s. blepotis can detect temperature differences of 1°C. They used this ability to select cold areas with stable high humidity in Thermocline Cave to under go periods of winter torpor.     

北京房山十渡西太平洞晚更新世哺乳动物化石

北京市房山区十渡镇西太平村发现的动物化石是首次在该镇辖区发现的更新世化石。动物群由6目、15科、22属的22种组成,以岩羊、香麝及鼯鼠等为主,为典型的北方山区动物群。该动物群的时代为晚更新世晚期,~(14)C年代为距今29335～37350年,与山顶洞及田园洞动物群基本同期。西太平洞动物群中有76%的种曾出现于周口店田园洞动物群,而只有38%的种曾出现于山顶洞。目前在此发现的可鉴定到种的化石材料均可归入现生种,但其中有23%的种已经在北京地区消失,消失属种以大中型动物为主。在该地点发现的西伯利亚飞鼠和复齿鼯鼠材料是首次在华北地区发现的此类化石记录。该地点是我国北方地区已报道的第四纪化石点中含香麝和岩羊材料最丰富的地点之一。在国内有关文献中,岩羊化石的分类命名一直没有得到统一,这次发现的新材料,有利于澄清该类化石的分类命名问题。     

A Mass Burial of Fossil Lions (Carnivora,Felidae, <Emphasis Type="Italic">Panthera</Emphasis> (<Emphasis Type="Italic">Leo</Emphasis>) <Emphasis Type="Italic">ex gr. fossilis-spelaea</Emphasis>) from Eurasia

The vertebrate fauna from the cave deposits in Imanai Cave in the Southern Urals (53°02′ N, 56°26′E) has been studied. It contains 715 bones that belonged to at least 11 individuals of fossil lion (Panthera (Leo) ex gr. fossilis-spelaea). It has been established that this is one of the largest Eurasian burial sites of fossil lions. The bones were accumulated due to the natural death of animals inside the cave. The age and sex estimations have shown that at least six adult males and five adult females died there. According to the accompanying fauna, radiocarbon, geochemical, and mineralogical analyses and archaeological finds, the interval of the lion bone accumulation is determined as the first half to middle of Late Pleistocene (OIS 5–3).     

A New Mass Burial of Cave Bears (Carnivora,Ursidae, Ursus kanivetz,Vereshchagin, 1973) from the Middle Urals

Doklady Biological Sciences - Remains of a cave bear were studied from a new locality in the Prokoshev Cave in the Middle Urals (58°13´ N, 58°12´ E). Bones from all regions of...     

Leporids as a potential resource for predators (hominins,mammalian carnivores,raptors): An example of mixed contribution from level III of Teixoneres Cave (MIS 3, Barcelona,Spain)

Apart from humans, other predators can take part in creating bone accumulations by generating waste materials that may have been mixed with those produced by hominids and leading to the formation of palimpsests. This is discussed here in the case of Middle Paleolithic leporid assemblages, to which carnivores have frequently contributed. Level III of Teixoneres Cave (MIS 3) is a sample that can be used to address the origin of leporid assemblages in archaeological contexts. Applying an archaeozoological and taphonomical methodology has made it possible to state that the assemblage of leporids in the site has been generated by a mix of contributions, in which small mammal carnivores and nocturnal raptors seem to play an important role, together with occasional hominid inputs. The aim of this paper is to present new data about Neanderthal activities at this site and support the hypothesis related to short-term human occupations in the cave.     

Upper Pleistocene Panthera leo spelaea (Goldfuss, 1810) remains from the Bilstein Caves (Sauerland Karst) and contribution to the steppe lion taphonomy,palaeobiology and sexual dimorphism

Remains of the steppe lion Panthera leo spelaea (Goldfuss) from historical digs in the Bilstein Caves of Warstein (Sauerland, NW Germany) are described. Their age seems to be from the Early Weichselian periods (Upper Pleistocene). Whereas the Bilstein cave was inhabited by cave bears at that time only a few hyena prey remains, were most likely imported into the cave entrance by hyenas. Bite and crush marks on a few bones of Bison priscus, Bos primigenius, Cervus elaphus, a rhinoceros Coelodonta antiquitatis vertebra and even several chewed cave bear bones prove the hyena presence which is similar to other caves in the Sauerland hyena den cave rich region. Additionally some larger wolves subspecies Canis lupusspelaeus bones were found, but only few Crocuta crocuta spelaea remains are present. After taphonomic comparisons to six other hyena and cave bear den caves of northern Germany, this cave can be classified as a cave bear den, which was briefly used by hyenas only for food storage or commuting or cave bear predation site in one part of the Cave. The lion material refers at least to one young adult lioness, one more adult female and two male lions; therefore, at minimum, the remains of four adult individuals are represented. The absence of juvenile lion material, in contrast to cave bear cub remains in the Bilstein Caves, proves that P. leo spelaea did not use this and all other caves in the region to raise their cubs. The bone material from the Bilstein Caves would prove the same hyena-lion antagonism conflict being recently proven for the Perick Caves, Balve Cave or Martins Cave well. Other situations in caves such as the Keppler Cave and the Bilstein Cave initially show the more complex taphonomic situation of lion remains in European caves, especially in cave bear dens, where they seem to have hunted periodically cave bears, such as it is already proven for hyenas in the Sauerland Karst and other caves of Europe.     

The Crocuta crocuta spelaea (Goldfuss 1823) population and its prey from the Late Pleistocene Teufelskammer Cave hyena den besides the famous Paleolithic Neandertal Cave (NRW,NW Germany)

Remains from at least seven individuals of the Late Pleistocene Ice Age spotted hyena Crocuta crocuta spelaea (Goldfuss, 1823) from the Teufelskammer Cave in the Neandertal valley (North Rhine-Westphalia, northwest Germany) are described. The small cave was a well-frequented hyena den of the Early to Middle Late Pleistocene which was only 100 m from the famous small Feldhofer Cave, where the first Neandertal human skeleton was found. The high amount of hyena bone material (37%) and its strongly chewed and incomplete prey remains of the mixed mammoth steppe and boreal forest megafauna prove one more of 11 recently known hyena den caves in the Rhenish Massif. Hyenas and cave bears have used the cave, but Neandertal humans lived possibly not at the same time in the same valley. Although hyenas occupied mainly the smaller caves such as the Teufelskammer Cave, humans preferred large portal cave entrances such as in the Neandertal valley with the Small Feldhofer Cave.     

An Ice Age spotted hyena Crocuta crocuta spelaea (Goldfuss 1823) population,their excrements and prey from the Late Pleistocene hyena den of the Sloup Cave in the Moravian Karst,Czech Republic

A Late Pleistocene spotted hyena Crocuta crocuta spelaea (Goldfuss 1823) population from the cave bear den Sloup Cave, Moravia (Czech Republic) consists of mainly adult/senior and few cub/juvenile remains and coprolites, and 139 prey bones. Hyenas used the Nicová Cave branch that is connected to the entrance area mainly as a communal den site. Prey bone damage is most visible on the imported woolly rhinoceros remains. The partly excavated prey bone accumulation consists of a single woolly mammoth Mammuthus primigenius (Blumenbach 1799) tooth (2%), mainly Coelodonta antiquitatis (Blumenbach 1807) remains (16%), 4% Bos primigenius (Bojanus 1827) and 1% each of Megaloceros giganteus (Blumenbach 1799) and Rangifer tarandus (Linnaeus 1758). The other carnivores such as Panthera leo spelaea (Goldfuss 1810), Gulo gulo (Linnaeus 1758) and Canis lupus (Linnaeus 1758) subsp. are less represented (1–3%). Wolverines might have been imported also as prey remains, whereas wolves also possibly used this cave on a short-term basis, whereas steppe lions seem to have preyed upon cave bears deeper in the cave periodically, where even skeletons of P. leo spelaea were found in the Elisabeth Cave part.