[dinosaur] Early Paleocene condylarths from Bolivia + Asmodochelys, new Cretaceous marine turtle + more

Ben Creisler <[email protected]> Thu, 19 Dec 2019 15:41:02 -0800
Newsgroups gmane.science.dinosaurs.general
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Ben [email protected]=0A=0ARecent non-dino papers:=0A=0AFree p=
df:=0A=0A=0AChristian de MUIZON, Guillaume BILLET & Sandrine LADEV=C3=88ZE =
(2019)=0ANew remains of kollpaniine "condylarths" (Panameriungulata) from t=
he early=0APalaeocene of Bolivia shed light on hypocone origins and molar p=
roportions=0Aamong ungulate-like placentals.=0AGEODIVERSITAS 41(25): 841-87=
4=0Adoi: https://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__doi.org_10.=
5252_geodiversitas2019v41a25&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0=
H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzk=
cVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3DhzhwbLzDGgoXUQImErbQH8eguHHGsH89JGKfu=
VIm0qU&e=3D .=0Ahttps://urldefense.proofpoint.com/v2/url?u=3Dhttp-3A__geodi=
versitas.com_41_25&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_=
gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3H=
zxj2Z1u56KA5zd06Xe0C5Do&s=3DLUYyqVQTOpxy3H-dkUpgAEJZ1kwZdFjhEGd_x8zGp94&e=
=3D=20=0Ahttps://urldefense.proofpoint.com/v2/url?u=3Dhttp-3A__sciencepress=
.mnhn.fr_en_periodiques_geodiversitas_41_25&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVI=
gvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI=
&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3DTh2mq86hVem1uLDKGAnXdl=
kEWr_E2-54t8diQGxag5Q&e=3D=20=0A=0AFree pdf:=0Ahttps://urldefense.proofpoin=
t.com/v2/url?u=3Dhttp-3A__sciencepress.mnhn.fr_sites_default_files_articles=
_pdf_g2019v41a25.pdf&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfn=
c_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv=
3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3D3YpYUQVPlX_dAQifiE1qI9flj05akm_B49V1UxxDRtc&e=
=3D=20=0A=0AThe description of new specimens of kollpaniines =E2=80=9Ccondy=
larths=E2=80=9D from=0ATiupampa (early Palaeocene of Bolivia) represents a =
significant addition to=0Athe knowledge of the earliest fauna of South Amer=
ican ungulates. Several=0Apartial mandibles and maxillae of Molinodus suare=
zi and Simoclaenus=0Asylvaticus are described. The morphology of the lower =
premolars of=0AMolinodus, being associated to lower molars, is established =
and a previous=0Areferral of an isolated p4 is rejected. A maxilla of Simoc=
laenus reveals=0Athe morphology of the so far unknown P1-4 of this taxon an=
d allows a=0Adiscussion on the development of the protocone in Palaeocene =
=E2=80=9Ccondylarths=E2=80=9D.=0AThe subvertical maxilla-premaxilla suture =
and the vertical implantation of=0Athe P1/p1 confirm the shortness of the s=
nout of Simoclaenus, whereas the=0Aprocumbency of the p1 of Molinodus indic=
ates a longer rostrum. The upper=0Amolars of Molinodus confirm the presence=
 of a tendency to duplication of=0Athe protocone, which is regarded as the =
incipient development of a=0Apseudohypocone. The various patterns of format=
ion of a hypocone (or=0Apseudohypocone) are considered and, among other Sou=
th American Native=0AUngulates, a protocone-derived pseudohypocone (i.e. Mo=
linodus-like) is=0Ahypothesized in Lamegoia, Raulvaccia, and notoungulates,=
 whereas a=0Apostcingulum-derived, hypocone is present in didolodontids and=
 litopterns.=0A=0A=0A=0A=3D=3D=3D=3D=3D=3D=0A=3D=3D=3D=3D=3D=3D=0A=0AFree p=
df:=0A=0ANicholas R. Friedman, Eliot T. Miller, Jason R. Ball, Haruka Kasug=
a,=0AVladim=C3=ADr Reme=C5=A1 and Evan P. Economo (2019)=0AEvolution of a m=
ultifunctional trait: shared effects of foraging ecology=0Aand thermoregula=
tion on beak morphology, with consequences for song=0Aevolution.=0AProceedi=
ngs of the Royal Society B 286: 20192474.=0Adoi: https://urldefense.proofpo=
int.com/v2/url?u=3Dhttps-3A__doi.org_10.1098_rspb.2019.2474&d=3DDwIFaQ&c=3D=
clK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCK=
Hn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3D6XcIvS=
LHf6l2tk_NC6QKxK64Xm3rsJuhx8iUnVWBvYU&e=3D=20=0Ahttps://urldefense.proofpoi=
nt.com/v2/url?u=3Dhttps-3A__royalsocietypublishing.org_doi_full_10.1098_rsp=
b.2019.2474&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3D=
Ry_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u=
56KA5zd06Xe0C5Do&s=3DmKhFkfVX_v7a4l4_ExXKqKCOJAB-vR_EwYFyyLgf9i4&e=3D=20=0A=
=0AFree pdf:=0Ahttps://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__royal=
societypublishing.org_doi_pdf_10.1098_rspb.2019.2474&d=3DDwIFaQ&c=3DclK7kQU=
TWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1=
CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3DtYnJMG3EIsCV9=
y-IMbJJi319iIahx9iNuERvnZWdvi8&e=3D=20=0A=0AWhile morphological traits are =
often associated with multiple functions, it=0Aremains unclear how evolutio=
n balances the selective effects of different=0Afunctions. Birds' beaks fun=
ction not only in foraging but also in=0Athermoregulating and singing, amon=
g other behaviours. Studies of beak=0Aevolution abound, however, most focus=
 on a single function. Hence, we=0Aquantified relative contributions of dif=
ferent functions over an=0Aevolutionary timescale. We measured beak shape u=
sing geometric=0Amorphometrics and compared this trait with foraging behavi=
our, climatic=0Avariables and song characteristics in a phylogenetic compar=
ative study of=0Aan Australasian radiation of songbirds (Meliphagidae). We =
found that both=0Aclimate and foraging behaviour were significantly correla=
ted with the beak=0Ashape and size. However, foraging ecology had a greater=
 effect on shape,=0Aand climate had a nearly equal effect on size. We also =
found that=0Aevolutionary changes in beak morphology had significant conseq=
uences for=0Avocal performance: species with elongate-shaped beaks sang at =
higher=0Afrequencies, while species with large beaks sang at a slower pace.=
 The=0Aevolution of the avian beak exemplifies how morphological traits can=
 be an=0Aevolutionary compromise among functions, and suggests that special=
ization=0Aalong any functional axis may increase ecological divergence or=
=0Areproductive isolation along others.=0A=0A=3D=3D=3D=3D=3D=3D=3D=3D=3D=3D=
=3D=3D=0AFree pdf:=0A=0ANicholas M. A. Crouch and Roberta Mason-Gamer (2019=
)=0AMass estimation of extinct taxa and phylogenetic hypotheses both influe=
nce=0Aanalyses of character evolution in a large clade of birds (Telluraves=
).=0AProceedings of the Royal Society B 286: 20191745=0Adoi: https://urldef=
ense.proofpoint.com/v2/url?u=3Dhttps-3A__doi.org_10.1098_rspb.2019.1745&d=
=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGo=
f_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C=
5Do&s=3D-6ccg4mxlp203FKMAtxJ7ClqiIT-T6WFWiFEb8_OCK0&e=3D=20=0Ahttps://urlde=
fense.proofpoint.com/v2/url?u=3Dhttps-3A__royalsocietypublishing.org_doi_pd=
f_10.1098_rspb.2019.1745&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7=
CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoW=
trRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3DfczKnH8MXTr4-dZpp5XBjMewbxcydbXrRpkYxAobs=
Y8&e=3D=20=0A=0AFree pdf:=0Ahttps://urldefense.proofpoint.com/v2/url?u=3Dht=
tps-3A__royalsocietypublishing.org_doi_pdf_10.1098_rspb.2019.1745&d=3DDwIFa=
Q&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZ=
gecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3D=
fczKnH8MXTr4-dZpp5XBjMewbxcydbXrRpkYxAobsY8&e=3D=20=0A=0AIncorporating exti=
nct taxa in phylogenetic comparative methods is rapidly=0Abecoming invaluab=
le in studies of character evolution. An increasing number=0Aof studies hav=
e evaluated the effects of extinct taxa, and different=0Anumbers of extinct=
 taxa, on model selection and parameter estimation. Body=0Amass is a well-s=
tudied phenotype, but individual mass estimates may vary=0Adramatically dep=
ending on the particular measurement used. Here, we perform=0Aan analysis o=
f body mass evolution in a large clade of principally arboreal=0Abirds, inc=
orporating 76 extinct species. We evaluate how different methods=0Afor esti=
mating body mass of extinct taxa, and different phylogenetic=0Ahypotheses, =
affect our understanding of the rate and pattern of body mass=0Aevolution. =
Our results show that model selection can vary dramatically=0Adepending on =
the phenotypic and phylogenetic hypothesis used in the=0Areconstruction. Ev=
en small changes in phenotype estimates can lead to=0Adifferent model selec=
tion and, as a result, affect the inferred=0Aevolutionary history. The best=
-fit models support an increase in the rate=0Aof evolution following the K=
=E2=80=93Pg boundary, with variation accumulating=0Alinearly through the Ce=
nozoic. These results provide additional insight=0Ainto the application of =
comparative models of evolution, as well as the=0Aevolutionary history of o=
ne of the most spectacular vertebrate radiations.=0A=0A=3D=3D=3D=3D=0A=0AGe=
rald Mayr (2020)=0AComparative morphology of the avian maxillary bone (os m=
axillare) based on=0Aan examination of macerated juvenile skeletons.=0AActa=
 Zoologica 101 (1): 24-38=0Adoi:  https://urldefense.proofpoint.com/v2/url?=
u=3Dhttps-3A__doi.org_10.1111_azo.12268&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0=
NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=
=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3DxrZZa8jyUNVmTcFY8cL8RyEC=
RebmYwb4E93s8BGBcBA&e=3D=20=0Ahttps://urldefense.proofpoint.com/v2/url?u=3D=
https-3A__onlinelibrary.wiley.com_doi_abs_10.1111_azo.12268&d=3DDwIFaQ&c=3D=
clK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCK=
Hn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3Dq-TpEs=
3avZg-4o27GU1xqAP-pCnwRjqlyBlB4UwQD3s&e=3D=20=0A=0A=0AFor the first time, i=
solated maxillary bones of juvenile neornithine birds=0Aare examined and co=
mpared. Contrary to the anatomical terminology currently=0Aemployed, the av=
ian maxillare exhibits five rather than four processes. In=0Aaddition to th=
e praemaxillary, jugal, nasal, and maxillopalatine processes,=0Aall palaeog=
nathous and many neognathous birds also have a palatine process.=0AThe occu=
rrence of these processes is, however, variable across different=0Aclades a=
nd only few taxa exhibit a pentaradiate maxillare with all five=0Aprocesses=
. Within Neognathae, a great morphological variability exists in=0Athe shap=
e of the maxillopalatine process, which is more easily studied in=0Ajuvenil=
e individuals, in which the bones of the beak and palate are not=0Aco=E2=80=
=90ossified. In some Neognathae, a caudally facing recess is situated in=0A=
the junction of the maxillopalatine and jugal processes, which is likely to=
=0Abe homologous to the pneumatic recess of palaeognathous birds. Several=
=0Aderived morphologies of potential phylogenetic significance for the=0Ach=
aracterization of neognathous clades are identified and major=0Amorphologic=
al transformations in the lineage leading towards modern birds=0Aare highli=
ghted.=0A=0A=3D=3D=3D=3D=3D=0A=3D=3D=3D=3D=3D=0A=0AFree pdf:=0A=0AAsmodoche=
lys parhami gen. et sp. nov.=0A=0AAndrew D. Gentry, Jun A. Ebersole and Cai=
tlin R. Kiernan (2019)=0AAsmodochelys parhami, a new fossil marine turtle f=
rom the Campanian=0ADemopolis Chalk and the stratigraphic congruence of com=
peting marine turtle=0Aphylogenies.=0ARoyal Society Open Science 6: 191950=
=0Adoi: https://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__doi.org_10.1=
098_rsos.191950&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&=
r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj=
2Z1u56KA5zd06Xe0C5Do&s=3D7YwCdLES5-E7nh73Q7qG8frosjn8-Ucw27_l0aEWzYQ&e=3D=
=20=0Ahttps://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__royalsocietypu=
blishing.org_doi_10.1098_rsos.191950&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5=
BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3Dtu=
wKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3D584Og6Dzt1LUOOrf_F7fFgsKwhgQe=
G-zCpJCTuaVs98&e=3D=20=0A=0AFree pdf:=0Ahttps://urldefense.proofpoint.com/v=
2/url?u=3Dhttps-3A__royalsocietypublishing.org_doi_pdf_10.1098_rsos.191950&=
d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmG=
of_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0=
C5Do&s=3DAMLy_zrf0k-7nvzeEOxNxqHhiJX_kSoPTDMmCObL1KU&e=3D=20=0A=0A=0AResolv=
ing the phylogeny of sea turtles is uniquely challenging given the=0Ahigh p=
otential for the unification of convergent lineages due to systematic=0Ahom=
oplasy. Equivocal reconstructions of marine turtle evolution=0Asubsequently=
 inhibit efforts to establish fossil calibrations for molecular=0Adivergenc=
e estimates and prevent the accurate reconciliation of=0Abiogeographic or p=
alaeoclimatic data with phylogenetic hypotheses. Here we=0Adescribe a new g=
enus and species of marine turtle, Asmodochelys parhami,=0Afrom the Upper C=
ampanian Demopolis Chalk of Alabama and Mississippi, USA=0Arepresented by t=
hree partial shells. Phylogenetic analysis shows that A.=0Aparhami belongs =
to the ctenochelyids, an extinct group that shares=0Acharacteristics with b=
oth pan-chelonioids and pan-cheloniids. In addition=0Ato supporting Ctenoch=
elyidae as a sister taxon of Chelonioidea, our=0Aanalysis places Protostegi=
dae outside of the Chelonioidea crown group and=0Arecovers Allopleuron hofm=
anni as a stem dermochelyid. Gap excess ratio=0A(GER) results indicate a st=
rong stratigraphic congruence of our=0Aphylogenetic hypothesis; however, th=
e highest GER value is associated with=0Athe phylogenetic hypothesis of mar=
ine turtles which excludes Protostegidae=0Afrom the Cryptodira crown group.=
 Ancestral range estimations derived from=0Aour phylogeny imply a European =
or North American origin of Chelonioidea in=0Athe middle-to-late Campanian,=
 approximately 20 Myr earlier than current=0Amolecular divergence studies s=
uggest.=0A=0ANews:=0A=0Ahttps://urldefense.proofpoint.com/v2/url?u=3Dhttps-=
3A__www.uab.edu_news_research_item_10991-2D75-2Dmillion-2Dyear-2Dold-2Dsea-=
2Dturtle-2Dfossil-2Ddiscovery-2Dis-2Da-2Dnew-2Dgenus-2Dand-2Dspecies-2Dthat=
-2Dsheds-2Dlight-2Don-2Dthe-2Devolution-2Dof-2Dits-2Dmodern-2Drelatives&d=
=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGo=
f_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C=
5Do&s=3DAEf4Di8XAIfMY1Tj16BMEh7V6fdnToILvxS06bA0mbk&e=3D=20=0A=0A=3D=3D=3D=
=3D=3D=0A=0AChristian A. Perez-Martinez, Julia L. Riley & Martin J. Whiting=
 (2019)=0AUncovering the function of an enigmatic display: antipredator beh=
aviour in=0Athe iconic Australian frillneck lizard.=0ABiological Journal of=
 the Linnean Society, blz176=0Adoi: https://urldefense.proofpoint.com/v2/ur=
l?u=3Dhttps-3A__doi.org_10.1093_biolinnean_blz176&d=3DDwIFaQ&c=3DclK7kQUTWt=
AVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJ=
gFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3DqbdIGcRzVsIUMR8z=
tO-nnWg1FqoDB54LL67_9IowWbc&e=3D=20=0Ahttps://urldefense.proofpoint.com/v2/=
url?u=3Dhttps-3A__academic.oup.com_biolinnean_advance-2Darticle-2Dabstract_=
doi_10.1093_biolinnean_blz176_5679583&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU=
5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3Dt=
uwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3Dfk5Av9sCtxAsqc2IOWrOmKxPQ6jy=
c-RNTs27wIxP5zg&e=3D=20=0A=0A=0AWhen faced with a predator, some animals en=
gage in a deimatic display to=0Astartle the predator momentarily, resulting=
 in a pause or retreat, thereby=0Aincreasing their chance of escape. Frilln=
eck lizards (Chlamydosaurus=0Akingii) are characterised by a large, pronoun=
ced frill that extends from=0Athe base of the head to beyond the neck and, =
when displayed, can be up to=0Asix times the width of the head. We used beh=
avioural assays with a model=0Aavian predator to demonstrate that their dis=
play conforms to deimatic=0Adisplay theory. First, juveniles and adults dep=
loyed the frill in=0Aencounters with a model predator. Second, the display =
revealed three colour=0Apatches (white and red=E2=80=93orange patches on th=
e frill; yellow mouth palate)=0Athat facilitate a transition from a cryptic=
 to a conspicuous state as=0Aperceived by a raptor visual system. Third, th=
e display was performed with=0Amovements that amplified its effect. The fri=
ll area was larger in males=0Athan in females, which suggests that the fril=
l might also be co-opted for=0Amale=E2=80=93male contests. If future resear=
ch confirms a role of the frill in male=0Aagonistic interactions, frillneck=
 lizards will be a rare case in which a=0Astructure has a dual function in =
a deimatic display and a sexually selected=0Asignal.=0A=0A=3D=3D=3D=0A=0AS.=
 L. Cross, M. D. Craig, S. Tomlinson & P. W. Bateman (2019)=0AI don=E2=80=
=99t like crickets, I love them: invertebrates are an important prey=0Asour=
ce for varanid lizards.=0AJournal of Zoology (advance online publication)=
=0Adoi: https://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__doi.org_10.1=
111_jzo.12750&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=
=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2=
Z1u56KA5zd06Xe0C5Do&s=3Da6bqFxR1V5oFPyT9T8SCjihZj44rfIdJ60m8Ia21TPA&e=3D=20=
=0Ahttps://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__zslpublications.o=
nlinelibrary.wiley.com_doi_10.1111_jzo.12750&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOV=
Igvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9S=
I&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3DS3zPFHFxQIXH0Z2IzyBgR=
kYrBtlpyFs2sB3WBdltImg&e=3D=20=0A=0ATemporary free link:=0A=0Ahttps://urlde=
fense.proofpoint.com/v2/url?u=3Dhttps-3A__zslpublications.onlinelibrary.wil=
ey.com_doi_epdf_10.1111_jzo.12750-3Fshared-5Faccess-5Ftoken-3D1BV8rHPdsd87A=
Q3GQ4MlMota6bR2k8jH0KrdpFOxC64uwLBj3N-2DLtlBdbO6inBCBSVZ-2DPYvEnbxaWuA2055R=
Wb5wKACmeEED6-2DXYk3Jbi-5F7DComDFOJBge1aifJSRv9-5F&d=3DDwIFaQ&c=3DclK7kQUTW=
tAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CY=
JgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3Dgg9GfiJaf5LwfW0=
XjSmEE6UclTsIrdyQyLIWTRaEuG8&e=3D=20=0A=0A=0AMinimal annual rainfall in ari=
d environments results in low productivity=0Aecosystems with fluctuating fo=
od availability. Large mammalian predators=0Athat require frequent consumpt=
ion of vertebrate prey tend to be less=0Aabundant in desert environments; h=
owever, such environments often support=0Anumerous large=E2=80=90bodied car=
nivorous reptiles. Diet is a fundamental component=0Aof an animal=E2=80=99s=
 ecology, and we explore the diets of three coexisting,=0Asympatric Varanus=
 species occurring in arid Australia: V. tristis, V.=0Agouldii and V. panop=
tes. We hypothesized that the diet of varanids living=0Ain arid environment=
s would primarily consist of relatively abundant=0Ainvertebrate prey, and t=
hat vertebrate prey items would largely be limited=0Ato opportunistically c=
onsumed mammalian carrion and small reptilian=0Aspecies. All three Varanus =
species had high dietary overlap and broad,=0Ageneralist diets. Invertebrat=
e prey, particularly Orthoptera, were key to=0Athe diets of all three speci=
es. Vertebrate prey was infrequently consumed=0Aby all three Varanus specie=
s; however, when consumed, tended to comprise=0Asmall reptilian species and=
 mammalian carrion. Unlike large mammalian=0Apredators, varanids can surviv=
e on invertebrate prey and infrequent feeds=0Aand can aestivate when condit=
ions become unfavourable, contributing to=0Atheir success in arid environme=
nts.=0A=0A=3D=3D=3D=0A=3D=3D=3D=0A=0AYuewu Sun,  Xiang Li,  Quanyou Liu,  M=
ingda Zhang,  Peng Li,  Rui Zhang  &=0AXiao Shi (2019)=0AIn search of the i=
nland Carnian Pluvial Event: Middle=E2=80=93Upper Triassic=0Atransition pro=
file and U=E2=80=93Pb isotopic dating in the Yanchang Formation in=0AOrdos =
Basin, China=0AGeological Journal (advance online publication)=0Adoi: https=
://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__doi.org_10.1002_gj.3691&d=
=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGo=
f_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C=
5Do&s=3DlMOd_kCLHVkWpHn2k9fxRaOPNUe-NEx3jqxKB4mMcXc&e=3D=20=0Ahttps://urlde=
fense.proofpoint.com/v2/url?u=3Dhttps-3A__onlinelibrary.wiley.com_doi_10.10=
02_gj.3691&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DR=
y_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u5=
6KA5zd06Xe0C5Do&s=3DNjZXTJpSW_dv3yCi1f33fiqbqCmEk_ZL12YIGnprDBU&e=3D=20=0A=
=0A=0AThe Carnian Pluvial Event (CPE) in the early Late Triassic is a globa=
l=0Aclimate change. The CPE is not only recorded in the ocean but also on t=
he=0Acontinent. It has been well=E2=80=90documented in the marine environme=
nts in Tethys=0Aand boreal areas. However, it is less reported for the terr=
estrial. As a=0Aglobal precipitation event, the CPE on the supercontinent P=
angaea is=0Arelated directly to the sudden increase in argillaceous transpo=
rtation in=0Athe marine carbonate platform. Here, we report a chronological=
 study of the=0AYunmeng profile in south=E2=80=90eastern Ordos Basin, China=
 where the continuous=0Alacustrine deposits developed with several tuff int=
erlayers. Laser Ablation=0AInductively Coupled Plasma Mass Spectrometry (LA=
=E2=80=90ICP=E2=80=90MS) U=E2=80=93Pb isotopic=0Adating of zircons from thr=
ee bentonite samples show weighted mean ages of=0A234.1 =C2=B1 2.4 Ma, 234.=
8 =C2=B1 2.1 Ma, and 236.0 =C2=B1 1.7 Ma, respectively. Based on=0Athe revi=
ew of isotopic dating, sedimentary and palaeontological=0Acharacteristics o=
f the Triassic Yanchang Formation, the Middle and Upper=0ATriassic boundary=
 is located at the bottom of Chang 7 oil layer (YC7) in=0Athe Yanchang Form=
ation at the Yunmeng profile in the Ordos Basin.=0ATherefore, the Yunmeng p=
rofile provides a potential case for understanding=0Athe inland CPE and mig=
ht link the terrestrial and oceanic systems in the=0ACarnian.=0A=0A=3D=3D=
=3D=3D=0A=0AFree pdf:=0A=0AKyle W. Meyer, Sierra V. Petersen, Kyger C Lohma=
nn, Joel D. Blum, Spencer=0AJ. Washburn, Marcus W. Johnson, James D. Gleaso=
n, Aaron Y. Kurz & Ian Z.=0AWinkelstern  (2019)=0ABiogenic carbonate mercur=
y and marine temperature records reveal global=0Ainfluence of Late Cretaceo=
us Deccan Traps.=0ANature Communications 10, Article number: 5356=0Adoi: ht=
tps://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__doi.org_10.1038_s41467=
-2D019-2D13366-2D0&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_=
gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3H=
zxj2Z1u56KA5zd06Xe0C5Do&s=3DZQfb8RPQu_8qa5DhsuHZAFak-V6HhaROuYrhKBWsK00&e=
=3D=20=0Ahttps://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__www.nature.=
com_articles_s41467-2D019-2D13366-2D0&d=3DDwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU=
5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&m=3Dt=
uwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&s=3Dh5vVSTlvdHjJFL-UC8UcqKO9uTVY=
z5dOaAvkfuf4I_M&e=3D=20=0AFree pdf:=0Ahttps://urldefense.proofpoint.com/v2/=
url?u=3Dhttps-3A__www.nature.com_articles_s41467-2D019-2D13366-2D0.pdf&d=3D=
DwIFaQ&c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&r=3DRy_mO4IFaUmGof_Y=
l9MyZgecRCKHn5g4z1CYJgFW9SI&m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do=
&s=3DamQfPfbSBSjKeRj0LvFWTWG6a-07Ke2HxJKFop9FK0Q&e=3D=20=0A=0A=0AThe climat=
e and environmental significance of the Deccan Traps large=0Aigneous provin=
ce of west-central India has been the subject of debate in=0Apaleontologica=
l communities. Nearly one million years of semi-continuous=0ADeccan eruptiv=
e activity spanned the Cretaceous-Paleogene boundary, which=0Ais renowned f=
or the extinction of most dinosaur groups. Whereas the=0AChicxulub impactor=
 is acknowledged as the principal cause of these=0Aextinctions, the Deccan =
Traps eruptions are believed to have contributed to=0Aextinction patterns a=
nd/or enhanced ecological pressures on biota during=0Athis interval of geol=
ogic time. We present the first coupled records of=0Abiogenic carbonate clu=
mped isotope paleothermometry and mercury=0Aconcentrations as measured from=
 a broad geographic distribution of marine=0Amollusk fossils. These fossils=
 preserve evidence of simultaneous increases=0Ain coastal marine temperatur=
es and mercury concentrations at a global=0Ascale, which appear attributabl=
e to volcanic CO2 and mercury emissions.=0AThese early findings warrant fur=
ther investigation with additional records=0Aof combined Late Cretaceous te=
mperatures and mercury concentrations of=0Abiogenic carbonate.=0A=

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<div dir=3D"ltr"><div><br></div><div>Ben Creisler</div><div><a href=3D"mail=
to:[email protected]" target=3D"_blank">[email protected]</a></div><div=
><br></div><div>Recent non-dino papers:<br></div><div><br></div><div>Free p=
df:</div><div><br></div><div><br></div><div>Christian de MUIZON, Guillaume =
BILLET &amp; Sandrine LADEV=C3=88ZE (2019)<br>New remains of kollpaniine &q=
uot;condylarths&quot; (Panameriungulata) from the early Palaeocene of Boliv=
ia shed light on hypocone origins and molar proportions among ungulate-like=
 placentals.<br>GEODIVERSITAS 41(25): 841-874<br>doi: <a href=3D"https://ur=
ldefense.proofpoint.com/v2/url?u=3Dhttps-3A__doi.org_10.5252_geodiversitas2=
019v41a25&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_g=
I&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVo=
WtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3DhzhwbLzDGgoXUQImErbQH8eguHHGsH89JGKf=
uVIm0qU&amp;e=3D">https://doi.org/10.5252/geodiversitas2019v41a25</a>. <a h=
ref=3D"https://urldefense.proofpoint.com/v2/url?u=3Dhttp-3A__geodiversitas.=
com_41_25&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_g=
I&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVo=
WtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3DLUYyqVQTOpxy3H-dkUpgAEJZ1kwZdFjhEGd_=
x8zGp94&amp;e=3D">http://geodiversitas.com/41/25</a> <br><a href=3D"https:/=
/urldefense.proofpoint.com/v2/url?u=3Dhttp-3A__sciencepress.mnhn.fr_en_peri=
odiques_geodiversitas_41_25&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5B=
OUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp=
;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3DTh2mq86hVem1uLDKGA=
nXdlkEWr_E2-54t8diQGxag5Q&amp;e=3D">http://sciencepress.mnhn.fr/en/periodiq=
ues/geodiversitas/41/25</a></div><div><br>Free pdf:<br><a href=3D"https://u=
rldefense.proofpoint.com/v2/url?u=3Dhttp-3A__sciencepress.mnhn.fr_sites_def=
ault_files_articles_pdf_g2019v41a25.pdf&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAV=
EOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1C=
YJgFW9SI&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3D3YpYUQ=
VPlX_dAQifiE1qI9flj05akm_B49V1UxxDRtc&amp;e=3D">http://sciencepress.mnhn.fr=
/sites/default/files/articles/pdf/g2019v41a25.pdf</a><br><br>The descriptio=
n of new specimens of kollpaniines =E2=80=9Ccondylarths=E2=80=9D from Tiupa=
mpa (early Palaeocene of Bolivia) represents a significant addition to the =
knowledge of the earliest fauna of South American ungulates. Several partia=
l mandibles and maxillae of Molinodus suarezi and Simoclaenus sylvaticus ar=
e described. The morphology of the lower premolars of Molinodus, being asso=
ciated to lower molars, is established and a previous referral of an isolat=
ed p4 is rejected. A maxilla of Simoclaenus reveals the morphology of the s=
o far unknown P1-4 of this taxon and allows a discussion on the development=
 of the protocone in Palaeocene =E2=80=9Ccondylarths=E2=80=9D. The subverti=
cal maxilla-premaxilla suture and the vertical implantation of the P1/p1 co=
nfirm the shortness of the snout of Simoclaenus, whereas the procumbency of=
 the p1 of Molinodus indicates a longer rostrum. The upper molars of Molino=
dus confirm the presence of a tendency to duplication of the protocone, whi=
ch is regarded as the incipient development of a pseudohypocone. The variou=
s patterns of formation of a hypocone (or pseudohypocone) are considered an=
d, among other South American Native Ungulates, a protocone-derived pseudoh=
ypocone (i.e. Molinodus-like) is hypothesized in Lamegoia, Raulvaccia, and =
notoungulates, whereas a postcingulum-derived, hypocone is present in didol=
odontids and litopterns.<br></div><div><br></div><div><br></div><div><br></=
div>=3D=3D=3D=3D=3D=3D<div>=3D=3D=3D=3D=3D=3D</div><div><br><div>Free pdf:<=
/div><div><br>Nicholas R. Friedman, Eliot T. Miller, Jason R. Ball, Haruka =
Kasuga, Vladim=C3=ADr Reme=C5=A1 and Evan P. Economo (2019)<br>Evolution of=
 a multifunctional trait: shared effects of foraging ecology and thermoregu=
lation on beak morphology, with consequences for song evolution.<br>Proceed=
ings of the Royal Society B 286: 20192474.<br>doi: <a href=3D"https://urlde=
fense.proofpoint.com/v2/url?u=3Dhttps-3A__doi.org_10.1098_rspb.2019.2474&am=
p;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy=
_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z=
1u56KA5zd06Xe0C5Do&amp;s=3D6XcIvSLHf6l2tk_NC6QKxK64Xm3rsJuhx8iUnVWBvYU&amp;=
e=3D">https://doi.org/10.1098/rspb.2019.2474</a><br><a href=3D"https://urld=
efense.proofpoint.com/v2/url?u=3Dhttps-3A__royalsocietypublishing.org_doi_f=
ull_10.1098_rspb.2019.2474&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BO=
UHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;=
m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3DmKhFkfVX_v7a4l4_ExX=
KqKCOJAB-vR_EwYFyyLgf9i4&amp;e=3D">https://royalsocietypublishing.org/doi/f=
ull/10.1098/rspb.2019.2474</a></div><div><br>Free pdf:<br><a href=3D"https:=
//urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__royalsocietypublishing.org=
_doi_pdf_10.1098_rspb.2019.2474&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0=
NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI=
&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3DtYnJMG3EIsCV9y=
-IMbJJi319iIahx9iNuERvnZWdvi8&amp;e=3D">https://royalsocietypublishing.org/=
doi/pdf/10.1098/rspb.2019.2474</a><br><br>While morphological traits are of=
ten associated with multiple functions, it remains unclear how evolution ba=
lances the selective effects of different functions. Birds&#39; beaks funct=
ion not only in foraging but also in thermoregulating and singing, among ot=
her behaviours. Studies of beak evolution abound, however, most focus on a =
single function. Hence, we quantified relative contributions of different f=
unctions over an evolutionary timescale. We measured beak shape using geome=
tric morphometrics and compared this trait with foraging behaviour, climati=
c variables and song characteristics in a phylogenetic comparative study of=
 an Australasian radiation of songbirds (Meliphagidae). We found that both =
climate and foraging behaviour were significantly correlated with the beak =
shape and size. However, foraging ecology had a greater effect on shape, an=
d climate had a nearly equal effect on size. We also found that evolutionar=
y changes in beak morphology had significant consequences for vocal perform=
ance: species with elongate-shaped beaks sang at higher frequencies, while =
species with large beaks sang at a slower pace. The evolution of the avian =
beak exemplifies how morphological traits can be an evolutionary compromise=
 among functions, and suggests that specialization along any functional axi=
s may increase ecological divergence or reproductive isolation along others=
.<br><br>=3D=3D=3D=3D=3D=3D=3D=3D=3D=3D=3D=3D<br>Free pdf:</div><div><br>Ni=
cholas M. A. Crouch and Roberta Mason-Gamer (2019)<br>Mass estimation of ex=
tinct taxa and phylogenetic hypotheses both influence analyses of character=
 evolution in a large clade of birds (Telluraves).<br>Proceedings of the Ro=
yal Society B 286: 20191745<br>doi: <a href=3D"https://urldefense.proofpoin=
t.com/v2/url?u=3Dhttps-3A__doi.org_10.1098_rspb.2019.1745&amp;d=3DDwMFaQ&am=
p;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl=
9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C=
5Do&amp;s=3D-6ccg4mxlp203FKMAtxJ7ClqiIT-T6WFWiFEb8_OCK0&amp;e=3D">https://d=
oi.org/10.1098/rspb.2019.1745</a><br><a href=3D"https://urldefense.proofpoi=
nt.com/v2/url?u=3Dhttps-3A__royalsocietypublishing.org_doi_pdf_10.1098_rspb=
.2019.1745&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_=
gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcV=
oWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3DfczKnH8MXTr4-dZpp5XBjMewbxcydbXrRpk=
YxAobsY8&amp;e=3D">https://royalsocietypublishing.org/doi/pdf/10.1098/rspb.=
2019.1745</a></div><div><br>Free pdf:<br><a href=3D"https://urldefense.proo=
fpoint.com/v2/url?u=3Dhttps-3A__royalsocietypublishing.org_doi_pdf_10.1098_=
rspb.2019.1745&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CS=
fnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_im=
zkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3DfczKnH8MXTr4-dZpp5XBjMewbxcydbX=
rRpkYxAobsY8&amp;e=3D">https://royalsocietypublishing.org/doi/pdf/10.1098/r=
spb.2019.1745</a><br><br>Incorporating extinct taxa in phylogenetic compara=
tive methods is rapidly becoming invaluable in studies of character evoluti=
on. An increasing number of studies have evaluated the effects of extinct t=
axa, and different numbers of extinct taxa, on model selection and paramete=
r estimation. Body mass is a well-studied phenotype, but individual mass es=
timates may vary dramatically depending on the particular measurement used.=
 Here, we perform an analysis of body mass evolution in a large clade of pr=
incipally arboreal birds, incorporating 76 extinct species. We evaluate how=
 different methods for estimating body mass of extinct taxa, and different =
phylogenetic hypotheses, affect our understanding of the rate and pattern o=
f body mass evolution. Our results show that model selection can vary drama=
tically depending on the phenotypic and phylogenetic hypothesis used in the=
 reconstruction. Even small changes in phenotype estimates can lead to diff=
erent model selection and, as a result, affect the inferred evolutionary hi=
story. The best-fit models support an increase in the rate of evolution fol=
lowing the K=E2=80=93Pg boundary, with variation accumulating linearly thro=
ugh the Cenozoic. These results provide additional insight into the applica=
tion of comparative models of evolution, as well as the evolutionary histor=
y of one of the most spectacular vertebrate radiations.<br></div><div><br><=
/div><div>=3D=3D=3D=3D</div><div><br><div>Gerald Mayr (2020)<br>Comparative=
 morphology of the avian maxillary bone (os maxillare) based on an examinat=
ion of macerated juvenile skeletons.<br>Acta Zoologica 101 (1): 24-38<br>do=
i: =C2=A0<a href=3D"https://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__=
doi.org_10.1111_azo.12268&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOU=
HhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=
=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3DxrZZa8jyUNVmTcFY8cL8=
RyECRebmYwb4E93s8BGBcBA&amp;e=3D" target=3D"_blank">https://doi.org/10.1111=
/azo.12268</a><br><a href=3D"https://urldefense.proofpoint.com/v2/url?u=3Dh=
ttps-3A__onlinelibrary.wiley.com_doi_abs_10.1111_azo.12268&amp;d=3DDwMFaQ&a=
mp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Y=
l9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0=
C5Do&amp;s=3Dq-TpEs3avZg-4o27GU1xqAP-pCnwRjqlyBlB4UwQD3s&amp;e=3D" target=
=3D"_blank">https://onlinelibrary.wiley.com/doi/abs/10.1111/azo.12268</a><b=
r><br><br>For the first time, isolated maxillary bones of juvenile neornith=
ine birds are examined and compared. Contrary to the anatomical terminology=
 currently employed, the avian maxillare exhibits five rather than four pro=
cesses. In addition to the praemaxillary, jugal, nasal, and maxillopalatine=
 processes, all palaeognathous and many neognathous birds also have a palat=
ine process. The occurrence of these processes is, however, variable across=
 different clades and only few taxa exhibit a pentaradiate maxillare with a=
ll five processes. Within Neognathae, a great morphological variability exi=
sts in the shape of the maxillopalatine process, which is more easily studi=
ed in juvenile individuals, in which the bones of the beak and palate are n=
ot co=E2=80=90ossified. In some Neognathae, a caudally facing recess is sit=
uated in the junction of the maxillopalatine and jugal processes, which is =
likely to be homologous to the pneumatic recess of palaeognathous birds. Se=
veral derived morphologies of potential phylogenetic significance for the c=
haracterization of neognathous clades are identified and major morphologica=
l transformations in the lineage leading towards modern birds are highlight=
ed.<br><br>=3D=3D=3D=3D=3D</div><div><div>=3D=3D=3D=3D=3D</div><div><br></d=
iv><div>Free pdf:</div><div><br></div><div>Asmodochelys parhami gen. et sp.=
 nov.</div><div><br>Andrew D. Gentry, Jun A. Ebersole and Caitlin R. Kierna=
n (2019)<br>Asmodochelys parhami, a new fossil marine turtle from the Campa=
nian Demopolis Chalk and the stratigraphic congruence of competing marine t=
urtle phylogenies.<br>Royal Society Open Science 6: 191950<br>doi: <a href=
=3D"https://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__doi.org_10.1098_=
rsos.191950&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc=
_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkc=
VoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3D7YwCdLES5-E7nh73Q7qG8frosjn8-Ucw27=
_l0aEWzYQ&amp;e=3D" target=3D"_blank">https://doi.org/10.1098/rsos.191950</=
a><br><a href=3D"https://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__roy=
alsocietypublishing.org_doi_10.1098_rsos.191950&amp;d=3DDwMFaQ&amp;c=3DclK7=
kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCK=
Hn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=
=3D584Og6Dzt1LUOOrf_F7fFgsKwhgQeG-zCpJCTuaVs98&amp;e=3D" target=3D"_blank">=
https://royalsocietypublishing.org/doi/10.1098/rsos.191950</a></div><div><b=
r>Free pdf:<br><a href=3D"https://urldefense.proofpoint.com/v2/url?u=3Dhttp=
s-3A__royalsocietypublishing.org_doi_pdf_10.1098_rsos.191950&amp;d=3DDwMFaQ=
&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof=
_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06X=
e0C5Do&amp;s=3DAMLy_zrf0k-7nvzeEOxNxqHhiJX_kSoPTDMmCObL1KU&amp;e=3D" target=
=3D"_blank">https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.191950<=
/a></div><div><br></div><div><br>Resolving the phylogeny of sea turtles is =
uniquely challenging given the high potential for the unification of conver=
gent lineages due to systematic homoplasy. Equivocal reconstructions of mar=
ine turtle evolution subsequently inhibit efforts to establish fossil calib=
rations for molecular divergence estimates and prevent the accurate reconci=
liation of biogeographic or palaeoclimatic data with phylogenetic hypothese=
s. Here we describe a new genus and species of marine turtle, Asmodochelys =
parhami, from the Upper Campanian Demopolis Chalk of Alabama and Mississipp=
i, USA represented by three partial shells. Phylogenetic analysis shows tha=
t A. parhami belongs to the ctenochelyids, an extinct group that shares cha=
racteristics with both pan-chelonioids and pan-cheloniids. In addition to s=
upporting Ctenochelyidae as a sister taxon of Chelonioidea, our analysis pl=
aces Protostegidae outside of the Chelonioidea crown group and recovers All=
opleuron hofmanni as a stem dermochelyid. Gap excess ratio (GER) results in=
dicate a strong stratigraphic congruence of our phylogenetic hypothesis; ho=
wever, the highest GER value is associated with the phylogenetic hypothesis=
 of marine turtles which excludes Protostegidae from the Cryptodira crown g=
roup. Ancestral range estimations derived from our phylogeny imply a Europe=
an or North American origin of Chelonioidea in the middle-to-late Campanian=
, approximately 20 Myr earlier than current molecular divergence studies su=
ggest.<br><br></div><div>News:</div><div><br><a href=3D"https://urldefense.=
proofpoint.com/v2/url?u=3Dhttps-3A__www.uab.edu_news_research_item_10991-2D=
75-2Dmillion-2Dyear-2Dold-2Dsea-2Dturtle-2Dfossil-2Ddiscovery-2Dis-2Da-2Dne=
w-2Dgenus-2Dand-2Dspecies-2Dthat-2Dsheds-2Dlight-2Don-2Dthe-2Devolution-2Do=
f-2Dits-2Dmodern-2Drelatives&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5=
BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&am=
p;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3DAEf4Di8XAIfMY1Tj1=
6BMEh7V6fdnToILvxS06bA0mbk&amp;e=3D">https://www.uab.edu/news/research/item=
/10991-75-million-year-old-sea-turtle-fossil-discovery-is-a-new-genus-and-s=
pecies-that-sheds-light-on-the-evolution-of-its-modern-relatives</a></div><=
/div><div><br></div><div>=3D=3D=3D=3D=3D</div><div><br></div><div>Christian=
 A. Perez-Martinez, Julia L. Riley &amp; Martin J. Whiting (2019)<br>Uncove=
ring the function of an enigmatic display: antipredator behaviour in the ic=
onic Australian frillneck lizard.<br>Biological Journal of the Linnean Soci=
ety, blz176<br>doi: <a href=3D"https://urldefense.proofpoint.com/v2/url?u=
=3Dhttps-3A__doi.org_10.1093_biolinnean_blz176&amp;d=3DDwMFaQ&amp;c=3DclK7k=
QUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKH=
n5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=
=3DqbdIGcRzVsIUMR8ztO-nnWg1FqoDB54LL67_9IowWbc&amp;e=3D" target=3D"_blank">=
https://doi.org/10.1093/biolinnean/blz176</a><br><a href=3D"https://urldefe=
nse.proofpoint.com/v2/url?u=3Dhttps-3A__academic.oup.com_biolinnean_advance=
-2Darticle-2Dabstract_doi_10.1093_biolinnean_blz176_5679583&amp;d=3DDwMFaQ&=
amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_=
Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe=
0C5Do&amp;s=3Dfk5Av9sCtxAsqc2IOWrOmKxPQ6jyc-RNTs27wIxP5zg&amp;e=3D" target=
=3D"_blank">https://academic.oup.com/biolinnean/advance-article-abstract/do=
i/10.1093/biolinnean/blz176/5679583</a><br><br><br>When faced with a predat=
or, some animals engage in a deimatic display to startle the predator momen=
tarily, resulting in a pause or retreat, thereby increasing their chance of=
 escape. Frillneck lizards (Chlamydosaurus kingii) are characterised by a l=
arge, pronounced frill that extends from the base of the head to beyond the=
 neck and, when displayed, can be up to six times the width of the head. We=
 used behavioural assays with a model avian predator to demonstrate that th=
eir display conforms to deimatic display theory. First, juveniles and adult=
s deployed the frill in encounters with a model predator. Second, the displ=
ay revealed three colour patches (white and red=E2=80=93orange patches on t=
he frill; yellow mouth palate) that facilitate a transition from a cryptic =
to a conspicuous state as perceived by a raptor visual system. Third, the d=
isplay was performed with movements that amplified its effect. The frill ar=
ea was larger in males than in females, which suggests that the frill might=
 also be co-opted for male=E2=80=93male contests. If future research confir=
ms a role of the frill in male agonistic interactions, frillneck lizards wi=
ll be a rare case in which a structure has a dual function in a deimatic di=
splay and a sexually selected signal.<br></div><div><br></div><div>=3D=3D=
=3D</div><div><br></div><div>S. L. Cross, M. D. Craig, S. Tomlinson &amp; P=
. W. Bateman (2019)<br>I don=E2=80=99t like crickets, I love them: inverteb=
rates are an important prey source for varanid lizards.<br>Journal of Zoolo=
gy (advance online publication)<br>doi: <a href=3D"https://urldefense.proof=
point.com/v2/url?u=3Dhttps-3A__doi.org_10.1111_jzo.12750&amp;d=3DDwMFaQ&amp=
;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9=
MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5=
Do&amp;s=3Da6bqFxR1V5oFPyT9T8SCjihZj44rfIdJ60m8Ia21TPA&amp;e=3D">https://do=
i.org/10.1111/jzo.12750</a><br><a href=3D"https://urldefense.proofpoint.com=
/v2/url?u=3Dhttps-3A__zslpublications.onlinelibrary.wiley.com_doi_10.1111_j=
zo.12750&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI=
&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVoW=
trRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3DS3zPFHFxQIXH0Z2IzyBgRkYrBtlpyFs2sB3WB=
dltImg&amp;e=3D">https://zslpublications.onlinelibrary.wiley.com/doi/10.111=
1/jzo.12750</a></div><div><br></div><div>Temporary free link:</div><div><br=
></div><div><a href=3D"https://urldefense.proofpoint.com/v2/url?u=3Dhttps-3=
A__zslpublications.onlinelibrary.wiley.com_doi_epdf_10.1111_jzo.12750-3Fsha=
red-5Faccess-5Ftoken-3D1BV8rHPdsd87AQ3GQ4MlMota6bR2k8jH0KrdpFOxC64uwLBj3N-2=
DLtlBdbO6inBCBSVZ-2DPYvEnbxaWuA2055RWb5wKACmeEED6-2DXYk3Jbi-5F7DComDFOJBge1=
aifJSRv9-5F&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc=
_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkc=
VoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3Dgg9GfiJaf5LwfW0XjSmEE6UclTsIrdyQyL=
IWTRaEuG8&amp;e=3D">https://zslpublications.onlinelibrary.wiley.com/doi/epd=
f/10.1111/jzo.12750?shared_access_token=3D1BV8rHPdsd87AQ3GQ4MlMota6bR2k8jH0=
KrdpFOxC64uwLBj3N-LtlBdbO6inBCBSVZ-PYvEnbxaWuA2055RWb5wKACmeEED6-XYk3Jbi_7D=
ComDFOJBge1aifJSRv9_</a></div><div><br><br>Minimal annual rainfall in arid =
environments results in low productivity ecosystems with fluctuating food a=
vailability. Large mammalian predators that require frequent consumption of=
 vertebrate prey tend to be less abundant in desert environments; however, =
such environments often support numerous large=E2=80=90bodied carnivorous r=
eptiles. Diet is a fundamental component of an animal=E2=80=99s ecology, an=
d we explore the diets of three coexisting, sympatric Varanus species occur=
ring in arid Australia: V. tristis, V. gouldii and V. panoptes. We hypothes=
ized that the diet of varanids living in arid environments would primarily =
consist of relatively abundant invertebrate prey, and that vertebrate prey =
items would largely be limited to opportunistically consumed mammalian carr=
ion and small reptilian species. All three Varanus species had high dietary=
 overlap and broad, generalist diets. Invertebrate prey, particularly Ortho=
ptera, were key to the diets of all three species. Vertebrate prey was infr=
equently consumed by all three Varanus species; however, when consumed, ten=
ded to comprise small reptilian species and mammalian carrion. Unlike large=
 mammalian predators, varanids can survive on invertebrate prey and infrequ=
ent feeds and can aestivate when conditions become unfavourable, contributi=
ng to their success in arid environments.<br></div><div><br></div><div>=3D=
=3D=3D</div><div>=3D=3D=3D</div><div><br></div><div>Yuewu Sun, =C2=A0Xiang =
Li, =C2=A0Quanyou Liu, =C2=A0Mingda Zhang, =C2=A0Peng Li, =C2=A0Rui Zhang =
=C2=A0&amp; Xiao Shi (2019)<br>In search of the inland Carnian Pluvial Even=
t: Middle=E2=80=93Upper Triassic transition profile and U=E2=80=93Pb isotop=
ic dating in the Yanchang Formation in Ordos Basin, China<br>Geological Jou=
rnal (advance online publication)<br>doi: <a href=3D"https://urldefense.pro=
ofpoint.com/v2/url?u=3Dhttps-3A__doi.org_10.1002_gj.3691&amp;d=3DDwMFaQ&amp=
;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9=
MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5=
Do&amp;s=3DlMOd_kCLHVkWpHn2k9fxRaOPNUe-NEx3jqxKB4mMcXc&amp;e=3D" target=3D"=
_blank">https://doi.org/10.1002/gj.3691</a><br><a href=3D"https://urldefens=
e.proofpoint.com/v2/url?u=3Dhttps-3A__onlinelibrary.wiley.com_doi_10.1002_g=
j.3691&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&a=
mp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVoWtr=
Rv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3DNjZXTJpSW_dv3yCi1f33fiqbqCmEk_ZL12YIGnp=
rDBU&amp;e=3D" target=3D"_blank">https://onlinelibrary.wiley.com/doi/10.100=
2/gj.3691</a><br><br><br>The Carnian Pluvial Event (CPE) in the early Late =
Triassic is a global climate change. The CPE is not only recorded in the oc=
ean but also on the continent. It has been well=E2=80=90documented in the m=
arine environments in Tethys and boreal areas. However, it is less reported=
 for the terrestrial. As a global precipitation event, the CPE on the super=
continent Pangaea is related directly to the sudden increase in argillaceou=
s transportation in the marine carbonate platform. Here, we report a chrono=
logical study of the Yunmeng profile in south=E2=80=90eastern Ordos Basin, =
China where the continuous lacustrine deposits developed with several tuff =
interlayers. Laser Ablation Inductively Coupled Plasma Mass Spectrometry (L=
A=E2=80=90ICP=E2=80=90MS) U=E2=80=93Pb isotopic dating of zircons from thre=
e bentonite samples show weighted mean ages of 234.1 =C2=B1 2.4 Ma, 234.8 =
=C2=B1 2.1 Ma, and 236.0 =C2=B1 1.7 Ma, respectively. Based on the review o=
f isotopic dating, sedimentary and palaeontological characteristics of the =
Triassic Yanchang Formation, the Middle and Upper Triassic boundary is loca=
ted at the bottom of Chang 7 oil layer (YC7) in the Yanchang Formation at t=
he Yunmeng profile in the Ordos Basin. Therefore, the Yunmeng profile provi=
des a potential case for understanding the inland CPE and might link the te=
rrestrial and oceanic systems in the Carnian.</div><div><br>=3D=3D=3D=3D</d=
iv><div><br></div><div>Free pdf:</div><div><br></div><div>Kyle W. Meyer, Si=
erra V. Petersen, Kyger C Lohmann, Joel D. Blum, Spencer J. Washburn, Marcu=
s W. Johnson, James D. Gleason, Aaron Y. Kurz &amp; Ian Z. Winkelstern =C2=
=A0(2019)<br>Biogenic carbonate mercury and marine temperature records reve=
al global influence of Late Cretaceous Deccan Traps.<br>Nature Communicatio=
ns 10, Article number: 5356<br>doi: <a href=3D"https://urldefense.proofpoin=
t.com/v2/url?u=3Dhttps-3A__doi.org_10.1038_s41467-2D019-2D13366-2D0&amp;d=
=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO=
4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u5=
6KA5zd06Xe0C5Do&amp;s=3DZQfb8RPQu_8qa5DhsuHZAFak-V6HhaROuYrhKBWsK00&amp;e=
=3D" target=3D"_blank">https://doi.org/10.1038/s41467-019-13366-0</a> <br><=
a href=3D"https://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__www.nature=
.com_articles_s41467-2D019-2D13366-2D0&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVE=
OVIgvi0NU5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CY=
JgFW9SI&amp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3Dh5vVSTl=
vdHjJFL-UC8UcqKO9uTVYz5dOaAvkfuf4I_M&amp;e=3D" target=3D"_blank">https://ww=
w.nature.com/articles/s41467-019-13366-0</a><br>Free pdf:<br><a href=3D"htt=
ps://urldefense.proofpoint.com/v2/url?u=3Dhttps-3A__www.nature.com_articles=
_s41467-2D019-2D13366-2D0.pdf&amp;d=3DDwMFaQ&amp;c=3DclK7kQUTWtAVEOVIgvi0NU=
5BOUHhpN0H8p7CSfnc_gI&amp;r=3DRy_mO4IFaUmGof_Yl9MyZgecRCKHn5g4z1CYJgFW9SI&a=
mp;m=3DtuwKU_imzkcVoWtrRv3Hzxj2Z1u56KA5zd06Xe0C5Do&amp;s=3DamQfPfbSBSjKeRj0=
LvFWTWG6a-07Ke2HxJKFop9FK0Q&amp;e=3D" target=3D"_blank">https://www.nature.=
com/articles/s41467-019-13366-0.pdf</a><br><br><br>The climate and environm=
ental significance of the Deccan Traps large igneous province of west-centr=
al India has been the subject of debate in paleontological communities. Nea=
rly one million years of semi-continuous Deccan eruptive activity spanned t=
he Cretaceous-Paleogene boundary, which is renowned for the extinction of m=
ost dinosaur groups. Whereas the Chicxulub impactor is acknowledged as the =
principal cause of these extinctions, the Deccan Traps eruptions are believ=
ed to have contributed to extinction patterns and/or enhanced ecological pr=
essures on biota during this interval of geologic time. We present the firs=
t coupled records of biogenic carbonate clumped isotope paleothermometry an=
d mercury concentrations as measured from a broad geographic distribution o=
f marine mollusk fossils. These fossils preserve evidence of simultaneous i=
ncreases in coastal marine temperatures and mercury concentrations at a glo=
bal scale, which appear attributable to volcanic CO2 and mercury emissions.=
 These early findings warrant further investigation with additional records=
 of combined Late Cretaceous temperatures and mercury concentrations of bio=
genic carbonate.<br><br><br><br></div></div></div></div>=0A=

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