2010年主龙类古生物学
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本条目记录了2010年描述的各种主龙类化石的新分类群,以及2010年发现的与主龙类相关的其他重大发现和事件。主龙类包括鸟类(唯一现存的恐龙类群)和鳄鱼类爬行动物,还包括所有已灭绝的恐龙、已灭绝的鳄鱼近亲和翼龙类。主龙类古生物学是对这些动物的科学研究,尤其是它们所存在于的大约11,700年前的全新世之前的时期。2010年在古生物学领域涉及了与主龙类相关的各种重大进展。
新命名的镶嵌踝类
[编辑]中文名及学名 | 状态 | 命名人 | 时期 | 单位 | 发现地 | 注释 | 图集 |
---|---|---|---|---|---|---|---|
Baurusuchus albertoi[1] |
有效 |
||||||
Crocodylus anthropophagus[2] |
有效 |
捕食早期原始人的角鳄 |
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Cerrejonisuchus[3] |
有效 |
具有通才进食策略的森林鳄。它长到大约7英尺长。 |
|||||
Diplocynodon elavericus[4] |
有效 |
始新世晚期 |
|||||
Eoneustes[5] |
有效 |
Teleidosaurus gaudryi分离建立的一个新属 Metriorhynchus bathonicus是黎明泳鳄属的第二个物种。 |
|||||
Gracilineustes[5] |
有效 |
Metriorhynchus leedsi分离建立的一个新属 Metriorhynchus acutus是纤泳鳄属的第二个物种。 |
|||||
Krabisuchus[6] |
有效 |
始新世晚期 |
早期的短吻鳄。 | ||||
Pakasuchus[7] |
有效 |
||||||
Pravusuchus[8] |
有效 |
一种植龙。 |
|||||
Stagonolepis olenkae[9] |
有效 |
卡尼期晚期 |
|||||
有效 |
最初被描述为Theriosuchus属的一种; Tennant, Mannion & Upchurch (2016)将其归入Sabresuchus属。[11] |
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Torvoneustes[12] |
有效 |
启莫里期 |
Dakosaurus carpenteri分离建立的一个新属 |
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Tsoabichi[13] |
有效 |
早期的凯门鳄。 |
新命名的恐龙型类基群
[编辑]中文名及学名 | 状态 | 命名人 | 时期 | 单位 | 发现地 | 注释 | 图集 |
---|---|---|---|---|---|---|---|
Asilisaurus[14] |
有效 |
新命名的非鸟类恐龙
[编辑]- Benson、Carrano和Brusatte发表了一个新的异特龙类兽脚类动物科,新猎龙科(Neovenatoridae)。[15]
- Rauhut、Milner和Moore-Fay发表了一个暴龙类兽脚类动物科,原角鼻龙科(Proceratosauridae)。[16]
中文名及学名 | 状态 | 命名人 | 发现年 | 时期 | 单位 | 发现地 | 注释 | 图集 |
---|---|---|---|---|---|---|---|---|
Aardonyx[17] |
有效 |
|||||||
Abydosaurus[18] |
有效 |
|||||||
Ajkaceratops[19] |
有效 |
|||||||
Archaeoceratops yujingziensis[20] |
有效 |
?阿普第期–阿尔布期 |
古角龙属的第二个物种 |
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Arkharavia[21] |
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Atsinganosaurus[22] |
有效 |
一种泰坦巨龙类恐龙 |
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Austrocheirus[23] |
有效 |
2002[23] |
马斯特里赫特期 |
|||||
Banji[24] |
有效 |
马斯特里赫特期 |
一种偷蛋龙类恐龙,头骨上有横纹嵴。 |
|||||
Barilium[25] |
有效 |
凡蓝今期早期 |
Iguanodon dawsoni分离建立的一个新属 |
|||||
Beishanlong[26] |
有效 |
阿普第期-阿尔布期 |
新民堡群 |
一种巨型的似鸟龙类恐龙 |
||||
Bistahieversor[27] |
有效 |
|||||||
Blasisaurus[28] |
有效 |
马斯特里赫特期晚期 |
||||||
Bolong[29] |
有效 |
一种禽龙类恐龙 |
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Chromogisaurus[30] |
有效 |
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Chuxiongosaurus[31] |
有效 |
一种原蜥脚类恐龙 |
||||||
Coahuilaceratops[32] |
有效 |
坎帕期 |
||||||
Concavenator[34] |
有效 |
鲨齿龙科,在臀部附近有一个尖的、驼峰状的嵴,在尺骨上有突起,可能是羽毛球状突起。 |
||||||
Cruxicheiros[35] |
有效 |
1960年代早期[35] |
下巴通期 |
|||||
Diabloceratops[36] |
有效 |
坎帕期中期 |
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Duriatitan[37] |
有效 |
泰坦巨龙类恐龙 |
||||||
Fruitadens[38] |
有效 |
1970年代晚期[38] |
下提通期 |
|||||
Fukuititan[39] |
有效 |
上巴列姆期 |
一种泰坦巨龙类恐龙 |
|||||
Geminiraptor[40] |
有效 |
?下巴列姆期 |
雪松山组 |
一种伤齿龙类恐龙 |
||||
Glishades[41] |
有效 |
坎帕期 |
鸭嘴龙类的基群 |
|||||
Haplocheirus[42] |
有效 |
2004[43] |
已知最原始的阿瓦拉慈龙类恐龙。 |
|||||
Hippodraco[44] |
有效 |
上巴列姆期-阿普第期 |
雪松山组 |
禽龙类的基群 |
||||
Hypselospinus[25] |
有效 |
凡蓝今期早期 |
威尔顿群 |
Iguanodon fittoni分离建立的一个新属 |
||||
Ignavusaurus[45] |
次异名 |
赫塘期 |
艾略特组 |
最初被解释为一个独特的蜥脚类基群,但现在似乎是一个被错误识别的幼年大椎龙标本。 |
||||
Iguanacolossus[44] |
有效 |
?下巴列姆期 |
雪松山组 |
禽龙类的基群 |
||||
Jeyawati[46] |
有效 |
鸭嘴龙类的基群 |
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Kayentavenator[47] |
有效 |
坚尾龙类的基群 |
||||||
Kileskus[48] |
有效 |
巴通期 |
一种暴龙类恐龙 |
|||||
Kosmoceratops[49] |
有效 |
坎帕期晚期 |
一种开角龙类恐龙 |
|||||
Kukufeldia[50] |
有效 |
1848 |
上巴列姆期 |
威尔顿群 |
禽龙类的基群,之前被归入Iguanodon anglicus |
ñ | ||
Linheraptor[51] |
有效 |
坎帕期 |
一种驰龙类恐龙 |
|||||
有效 |
早白垩世 |
一种真蜥脚类恐龙 |
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Machairasaurus[53] |
有效 |
晚白垩世 |
巴彦满达呼组 |
|||||
Medusaceratops[54] |
有效 |
坎帕期 |
||||||
Mojoceratops[56] |
有效 |
坎帕期晚期 |
一种长角的开角龙类恐龙 |
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Ojoceratops[57] |
有效 |
晚白垩世 |
一种开角龙类恐龙 |
|||||
Paludititan[58] |
有效 |
马斯特里赫特期 |
一种泰坦巨龙类 |
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Panamericansaurus[59] |
有效 |
坎帕期-马斯特里赫特期 |
||||||
Pneumatoraptor[60] |
有效 |
桑托期 |
切赫巴尼奥组 |
一种小型的类似鸟类的近鸟类,估计身长略超过两英尺。 |
||||
Proplanicoxa[61] |
有效 |
巴列姆期晚期 |
禽龙类的基群 |
|||||
Psittacosaurus gobiensis[62] |
有效 |
下白垩世 |
鹦鹉嘴龙属的第九或十一个物种 |
|||||
Rahiolisaurus[63] |
有效 |
|
马斯特里赫特期 |
一种阿贝力龙类恐龙 |
||||
Rubeosaurus[64] |
有效 |
坎帕期 |
双麦迪逊组 |
Styracosaurus ovatus分离建立的一个新属 |
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Sanjuansaurus[65] |
有效 |
卡尼期晚期 |
伊斯基瓜拉斯托组 |
一种艾雷拉龙类恐龙 |
||||
Seitaad[66] |
有效 |
2005[67] |
普林斯巴期 |
蜥脚形恐龙的基群 |
||||
Sellacoxa[61] |
有效 |
凡蓝今期早期 |
威尔顿群 |
禽龙类的基群 |
||||
Sinoceratops[68] |
有效 |
上白垩世 |
尖角龙亚科的基群 |
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Tatankaceratops[69] |
有效 |
马斯特里赫特期 |
一种开角龙类恐龙 |
|||||
Texacephale[70] |
有效 |
上坎帕期 |
厚头龙类的基群 |
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Tianyuraptor[71] |
有效 |
早白垩世 |
义县组 |
一种短臂的驰龙类恐龙 |
||||
Tonganosaurus[72] |
有效 |
早侏罗世 |
一种马门溪龙类恐龙 |
|||||
Torilion[61] |
次异名 |
凡蓝今期中期 |
||||||
Utahceratops[49] |
有效 |
坎帕期晚期 |
凯帕罗维茨组 |
一种开角龙类恐龙 |
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Vagaceratops[49] |
有效 |
坎帕期晚期 |
恐龙公园组 |
Chasmosaurus irvinensis分离建立的一个新属 |
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Wadhurstia[61] |
次异名 |
凡蓝今期早期 |
德赫斯特黏土组 |
|||||
Willinakaqe[73] |
有效 |
|
坎帕期晚期-马斯特里赫特期早期 |
艾伦组 |
||||
Xiongguanlong[74] |
有效 |
阿普第期-阿尔布期 |
新民堡群 |
一种暴龙类恐龙 |
||||
Xixianykus[75] |
有效 |
坎帕期 |
||||||
Xixiasaurus[76] |
有效 |
坎帕期 |
马家村组 |
一种伤齿龙类恐龙 |
||||
Xixiposaurus[77] |
有效 |
下侏罗世 |
下禄丰组 |
一种原蜥脚类恐龙 |
||||
Zhuchengceratops[78] |
有效 |
上白垩世 |
王氏群 |
一种纤角龙类恐龙 |
||||
Zuolong[79] |
有效 |
牛津期 |
石树沟组 |
虚骨龙类的基群 |
新命名的鸟类
[编辑]中文名及学名 | 状态 | 新颖性 | 命名人 | 时期 | 单位 | 发现地 | 注释 | 图集 |
---|---|---|---|---|---|---|---|---|
有效 |
Sp. nov. |
上新世晚期 |
||||||
有效 |
Gen. nov. et Sp. nov. |
中新世早期或中期 |
鸭科的一个基础成员。这是新属的模式种。 |
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有效 |
Sp. nov. |
中新世中期 |
澳大利亚: |
|||||
Balaur bondoc [83] |
有效 |
Gen. nov. et Sp. nov. |
一种四趾、两指鸟类。 |
|||||
Bauxitornis mindszentyae [84] |
有效 |
Gen. nov. et Sp. nov. |
||||||
有效 |
Sp. nov. |
中新世早期 |
MN 4c |
德国: |
鸬鹚科,可能是Borvocarbo的一种。 |
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Camptodontus yangi [86] |
有效 |
Gen. nov. et Sp. nov. |
九佛堂组 |
一种长翼鸟科的反鸟类, 这是新属的模式种。 |
||||
有效 |
Sp. nov. |
西班牙: |
||||||
有效 |
Gen. nov. et Sp. nov. |
美国: |
鼠鸟科的一个种。这是新属的模式种。 |
|||||
Confuciusornis jianchangensis [89] |
Disputed |
Sp. nov. |
九佛堂组 |
从一具骨骼中发现的一种孔子鸟。被Wang, O'Connor & Zhou (2018)判定为圣贤孔子鸟(Confuciusornis sanctus)的次异名。[90] |
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有效 |
Sp. nov. |
上新世晚期 |
MN 15-16 |
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有效 |
Sp. nov. |
中新世晚期;上新世晚期 |
MN 13; MN 16 |
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有效 |
Gen. nov. |
始新世早期 |
美国: 怀俄明州; 英国: |
以Primobucco olsoni为模式种的新属。 |
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Dasornis abdoun [93] |
有效 |
Sp. nov. |
一种远洋鸟 |
|||||
有效 |
Gen. nov. et Sp. nov. |
伊普雷斯期 |
绿河组 |
美国: |
雀形目,Zygodactylidae科,这是新属的模式种。 |
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有效 |
Sp. nov. |
上新世晚期 |
MN 16 |
佛法僧科的一新种 |
||||
Flexomornis howei [96] |
有效 |
Gen. nov. et Sp. nov. |
美国: |
一种反鸟类。这是新属的模式种。 |
||||
有效 |
Sp. nov. |
上新世晚期 |
阿尔厄格拉姆 |
|||||
有效 |
Sp. nov. |
上新世晚期 |
MN 15-16 |
|||||
有效 |
Sp. nov. |
上新世晚期 |
MN 17 |
鹰科兀鹫属的一新种。 |
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Hollanda luceria [98] |
有效 |
Gen. nov. et Sp. nov. |
坎帕期 |
一种掠食性地面鸟类,因具有不寻常的后肢而为人所知。这是新属的模式种。 |
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Huoshanornis huji [99] |
有效 |
Gen. nov. et Sp. nov. |
早白垩世 |
九佛堂组 |
一种反鸟类。这是新属的模式种。 |
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Inkayacu paracasensis [100] |
有效 |
Gen. nov. et Sp. nov. |
始新世晚期 |
一种企鹅。这是新属的模式种。 |
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Intiornis inexpectatus [101] |
有效 |
Gen. nov. et Sp. nov. |
坎帕期 |
一种鸟龙鸟科的反鸟类。这是新属的模式种。 |
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有效 |
Gen. nov. et Sp. nov. |
中新世早期 |
刺鹩科,这是新属模式种。 |
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有效 |
Gen. nov. et Sp. nov. |
白垩翼鸟科,这是新属的模式种。 |
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有效 |
Comb. nov. |
晚白垩世 |
美国: |
由Agnolin, 2010将Cimolopteryx minima转移到的一个新属,Lamarqueavis。[103] |
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Lamarqueavis petra [105] |
有效 |
Comb. nov. |
晚白垩世 |
兰斯组 |
美国: |
由Agnolin, 2010将Cimolopteryx petra转移到的一个新属,Lamarqueavis。[103] |
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Leptoptilos robustus [106] |
有效 |
Sp. nov. |
更新世晚期 |
鹳科的新种 |
||||
Longicrusavis houi [107] |
有效 |
Gen. nov. et Sp. nov. |
红山鸟科,这是新属的模式种。 |
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有效 |
Gen. nov. et Sp. nov. |
中新世中期 |
雉科,这是新属的模式种。 |
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有效 |
Gen. nov. et Sp. nov. |
中新世早期 |
鹭科,这是新属的模式种。 |
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有效 |
Gen. nov. et Sp. nov. |
渐新世晚期/中新世早期 |
德国: |
鹦鹉科,这是新属的模式种。 |
||||
有效 |
Gen. nov. et Sp. nov. |
始新世早期 |
这是新属的模式种。它是一种种系发生位置不确定的鸟类;它可能是鸻形目的近亲,[111]或者雀形目和已灭绝的Zygodactylidae科的近亲。[112]可能类似于Pumiliornis tessellatus。[112][113] |
|||||
有效 |
Comb. nov. |
更新世晚期 |
美国: |
鸱鸮科,Strix brea分离建立的新属,这是新属的模式种。 |
||||
有效 |
Sp. nov. |
中新世早期 |
班诺克本组 |
火烈鸟目, Palaelodidae科的新种 |
||||
Pelagornis chilensis [116] |
有效 |
Sp. nov. |
中新世 |
具有大翼展的远洋鸟 |
||||
有效 |
Gen. nov. et Sp. nov. |
始新世中期 |
梅塞尔坑、MP 11 |
德国: |
今颚类的成员。这是新属的模式种。 |
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有效 |
Sp. nov. |
上新世晚期 |
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Presbyornis mongoliensis [118] |
有效 |
Sp. nov. |
古新世晚期 |
纳拉布拉格斯维塔的本巴姆成员 |
||||
有效 |
Gen. nov. et Sp. nov. |
渐新世晚期/中新世早期 |
MN 2a、威斯巴登组、美因茨盆地 |
德国: |
秧鸡科,这是新属的模式种。 |
|||
Shenqiornis mengi [119] |
有效 |
Gen. nov. et Sp. nov. |
阿普第期 |
一种反鸟类,这是新属的模式种。 |
||||
Shenshiornis primita [120] |
有效 |
Gen. nov. et Sp. nov. |
阿普第期 |
九佛堂组 |
杂食鸟科(或叫会鸟科)的物种, 这是新属的模式种。 |
|||
Vastanavis cambayensis [121] |
有效 |
Sp. nov. |
伊普雷斯期 |
瓦斯坦鸟科的物种,鹦形目基群。 |
||||
Zhongjianornis yangi [122] |
有效 |
Gen. nov. et Sp. nov. |
阿普第期 |
九佛堂组 |
有喙的鸟类基群 |
新命名的翼龙
[编辑]中文名及学名 | 状态 | 命名人 | 时期 | 单位 | 发现地 | 注释 | 图集 |
---|---|---|---|---|---|---|---|
Aetodactylus[123] |
有效 |
仅从部分下颌骨才知道的鸟掌翼龙类动物。 |
|||||
Alanqa[124] |
有效 |
仅从前上颚和下颚的五个碎片以及可能的颈椎骨中获知的神龙翼龙科动物。 |
|||||
Archaeoistiodactylus[125] |
有效 |
||||||
Darwinopterus[127] |
有效 |
髫髻山组 |
|||||
Darwinopterus linglongtaensis[128] |
有效 |
髫髻山组 |
达尔文翼龙属的第二个物种 |
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Dawndraco[129] |
争议 |
一种翼龙。模式种是Dawndraco kanzai。Martin-Silverstone et al. (2017) 认为该物种是Pteranodon sternbergi的次异名。[130] |
|||||
Faxinalipterus[131] |
有效 |
||||||
Fenghuangopterus[132] |
有效 |
中侏罗世 |
髫髻山组 |
最早的掘颌翼龙亚科物种。 |
|||
Geosternbergia maiseyi[129] |
有效 |
科尼亚克期晚期 - 坎帕期早期 |
|||||
Kunpengopterus[128] |
有效 |
晚侏罗世 |
髫髻山组 |
悟空翼龙科。模式种为K. sinensis。 |
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Prejanopterus[133] |
有效 |
下阿普第期 |
|||||
Sericipterus[134] |
有效 |
牛津期 |
翼展近六英尺的喙嘴翼龙类翼龙。 |
||||
Zhenyuanopterus[135] |
有效 |
注释
[编辑]参考资料
[编辑]- ^ Paulo Miranda Nascimento; Hussam Zaher. A new species of Baurusuchus (Crocodyliformes, Mesoeucrocodylia) from the Upper Cretaceous of Brazil, with the first complete postcranial skeleton described from the family Baurusuchidae (PDF). Papéis Avulsos de Zoologia. 2010, 50 (21): 323‑361 [14 January 2011]. doi:10.1590/s0031-10492010002100001. (原始内容存档 (PDF)于2015-09-24).
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