GEOLOGICA CARPATHICA, AUGUST 2008, 59, 4, 295—306
www.geologicacarpathica.sk
An apatite-rich enclave in the High Tatra granite (Western
Carpathians): petrological and geochronological study
ALEKSANDRA GAWĘDA
University of Silesia, Faculty of Earth Sciences, Będzińska st. 60, 41-200 Sosnowiec, Poland; gaweda@us.edu.pl
(Manuscript received June 25, 2007; accepted in revised form March 14, 2008)
Abstract: A mafic, coarse-grained apatite-rich enclave found in the High Tatra granite, Western Carpathians, is an
ultrapotassic rock with mixed (mantle-crustal) geochemical and mineralogical signatures. A U-Pb zircon age dates the
intrusion at 345 ± 5.1 Ma. Zircon cores preserve ages of 361 ± 7.6 Ma and 391 ± 4.6 Ma. The apatite-rich rock could be
interpreted as a cumulate material related to common Tatra granite of comparable age (360—340 Ma). This rock, of very
unusual mineralogy, is an atypical cumulate formed in rocks of granitoid composition.
Key words: Variscan, High Tatra Mts, petrology, apatite-rich cumulate, U-Pb zircon dating.
Introduction
Granites usually contain enclaves of various origins. Some are
co-genetic with the host granite magma (autoliths), some are
mingled magmas of more basic types, others are restite and
many show no genetic links (xenoliths). All enclaves are a
record of the hidden history of the granite they are enclosed in.
The role of mafic magma in granite plutonism was underlined
in the first half of the XX
th
century and is still under active in-
vestigation (Pitcher 1997; Vincenzo & Rocchi 1999; Barbarin
2005). The rock- and mineral chemistry of mafic enclaves car-
ries information about the source, origin and evolution of the
mantle contribution to the processes involved in granitoid
magmatism and also about the source mantle, existing beneath
the crust at the time of magma generation.
Phosphorus-rich magmatic rocks are not a common lithology
in the Earth’s crust. Apatite-rich lamprophyres related to peralu-
minous, post-collisional, 1.8 Ga granitoid intrusions occur in
the Fennoscandian Shield (Konopelko et al. 1998; Eklund et al.
1998). Enclaves of biotite-apatite rocks in early Variscan
(368 Ma) granites have been described from the Achala
Batholith, Argentina; these are interpreted as cumulates (Dorais
et al. 1997). Internal structures of granitoid rocks (sensu lato)
resembling depositional features and interpreted as a result of
accumulation of early-formed crystals (cumulates) are relatively
scarce and restricted to magmas rich in water and flourine, low-
ering the melt viscosity (Collins et al. 2006).
In this paper, new data from an apatite-rich mafic enclave
from the High Tatra granite are presented. They help to define
and constrain a poorly known magmatic episode in the
Variscan history of the Tatra Mountains, a part of the Central
Western Carpathians.
Geological setting and sampling
The Tatra Mountains crystalline core is composed of four
petrographic types of granitoids: common Tatra granodiorite-
tonalite (360—340 Ma), Goryczkowa Granite (356 Ma),
quartz-diorite (341 Ma) and the youngest High Tatra granite
(314 Ma) (Kohút & Janák 1994; Poller et al. 2001; Gawęda et
al. 2005; Burda & Klötzli 2007). All intrude a metamorphic
envelope outcropping mainly in the western part of the Tatra
massif (Fig. 1).
The eastern part of the Tatra Mts (High Tatra Mts) is com-
posed of two main types of granite – a meso-Variscan S-type
(340—360 Ma) and a late-Variscan hybrid I/S-type (ca.
314 Ma). The latter is rich in various types of enclaves includ-
ing metasedimentary xenoliths, diorites (mafic precursors),
mafic magmatic enclaves (MME), schlieren and felsic blobs
(Pawlica 1918; Janák 1993; Gawęda 2005; Gawęda et al.
2005; Gawęda 2007a,b). Two basic petrographic types, biotite
monzogranite and porphyritic granite, were distinguished
among the High Tatra type (Gawęda 2007b). All of the granite
pulses, differing in age and chemistry, form one composite,
polygenetic pluton. The granite components of the pluton
show VAG (Volcanic Arc Granites) geochemical characteris-
tics and isotopic signatures that suggest continuous melting of
heterogeneous metasediments during subduction of oceanic
crust under the continental wedge and during which interac-
tion with mantle melts was significant (Poller et al. 2001;
Gawęda 2007b).
In the upper part of the Batyżowiecka (Batizovská) Valley,
at about 1950 m on the western slopes of Gerlach Mt, a ca.
0.9 m enclave of mela-syenite with numerous K-feldspar phe-
nocrysts was discovered in the porphyritic variety of the High
Tatra granite (Figs. 1, 2a). The contact between the mafic en-
clave and the leucocratic porphyritic granite is sharp. The maf-
ic enclave, the host granite, their contact zone and different
petrographical types of granites (including quartz diorites)
were sampled over the distance of ca. 100 m.
Analytical methods
Microscopic observations were made using a BX-60 Olym-
pus microscope at the Faculty of Earth Sciences, University of
Silesia, Sosnowiec, Poland. Microprobe analyses of minerals
296
GAW
Ę
DA
and BSE photographs were carried out on a CAMECA SX-
100 electron microprobe in the Inter-Institution Laboratory of
Microanalysis of Minerals and Synthetic Substances, Warsaw,
using sets of natural and synthetic standards. Major and trace
elements were analysed by XRF and ICP-MS at the ACME
Analytical Laboratories, Vancouver, Canada.
87
Sr/
86
Sr and
143
Nd/
144
Nd isotopic ratios were measured using a VG sector
54 mass spectrometer at the Department of Geochronology,
Institute of Geological Sciences, Polish Academy of Sciences,
Warsaw. Values of
87
Sr/
86
Sr were normalized to SRM 987
(
87
Sr/
86
Sr = 0.710266 ± 17, n = 5). Values of
143
Nd/
144
Nd were
normalized to JNd-1 (
143
Nd/
144
Nd = 0.512107 ± 15, n = 10).
Zircons crystals were separated using standard techniques in-
volving crushing, hydrofracturing, washing, Wilfley table,
magnetic separator and handpicking at the Institute of Geolog-
ical Sciences, Polish Academy of Sciences, Kraków. 75 zircon
grains were selected for morphological studies by (SEM). Zir-
con and apatite morphology (SEM), their internal structures
(CL) as well as 7 zircons selected for dating were imaged by
SEM and CL using a FET Philips XL 30 electron microscope
(15kV and 1nA) at the University of Silesia, Sosnowiec.
Zircons were dated by LA-ICP-MS at the Geochronology
Laboratory, Institute of Geology, University of Vienna. Zir-
con
206
Pb/
238
U and
207
Pb/
206
Pb ages were determined using a
193 nm solid state Nd-YAG laser (NewWave UP193-SS) cou-
pled to a multi-collector ICP-MS (Nu Instruments HR). Spot
analyses were 15—25 µm in diameter. Line widths for rastering
were 10—15 µm with a rastering speed of 5 µm/sec. The calcu-
lated
206
Pb/
238
U and
207
Pb/
206
Pb intercept values were correct-
ed for mass discrimination from analyses of standards 91500
(Wiedenbeck et al. 1995) and Plešovice (Slama et al. 2006)
measured during the analyses using a standard bracketing
method. The correction involves regression of standard mea-
surements by a quadratic function. A common Pb correction
was applied to the final data using the apparent
207
Pb/
206
Pb
age and the Stacey-Kramers (1975) Pb evolution model. The
Fig. 1. Simplified geological map of the Tatra Mts massif with the location of the apatite-rich enclave sampling point (compilation after Kohút
& Janák 1994; Gawęda et al. 2005). 1 – metamorphic cover, 2 – anatectic leucogranites, 3 – common Tatra granite, 4 – High Tatra granite,
5 – Goryczkowa granite, 6 – sedimentary cover, 7 – main faults: a – identified, b – assumpted, 8 – sampling point.
Fig. 2. Photos of apatite-rich enclave: a – Field photograph of the
apatite-rich enclave. Geological hammer as a scale. b – Micropho-
tograph of the apatite-rich enclave. Note the quartz grains, mantled
by mica and titanite. Abbreviations: Kfs – K-feldspar, Pl – pla-
gioclase, Qtz – quartz, Bt – biotite, Ap – apatite, Tnt – titan-
ite, Ms – muscovite.
297
PETROLOGICAL AND GEOCHRONOLOGICAL STUDY OF THE HIGH TATRA GRANITE (WESTERN CARPATHIANS)
Sample No. G2-05 G1g-05 Mkn-05 G12g-05 G9d-05 CTG
1 2 3 4 5 6
Pl
6.13
51.35
38.68
37.25
46.18 60.30
Kfs
39.77 13.37 33.14 29.10 – 20.90
Qtz
4.37
18.56
16.42
19.65
6.73 16.60
Bt/Chl
30.77
9.63
6.05
7.00
41.99 1.40
Ms
4.49
2.91
4.05
4.60
0.70 0.40
Ep
0.10
–
0.96
1.00
0.65 0.25
Np+tnt
0.57
1.84
0.35
0.43
1.35 0.02
Ap
13.74
1.77
0.25
0.70
1.90 0.10
Zrn/Mnz
0.04
0.60
0.10
0.27
0.50 0.03
Table 1: Modal analyses of the apatite-rich enclave and the surround-
ing granitoid rocks. 1 – apatite-rich enclave, 2, 3, 4 – porphyritic
varieties of High Tatra type granites, 5 – quartz diorite, 6 – an ex-
ample of common Tatra type granite.
Component
Bt1c Bt1m Bt4c Bt4m Bt4r Ms1c Ms2c Ms2m
Ms2r
SiO
2
35.01 34.86 34.83 34.97 35.66 44.94 44.97 45.06 44.96
TiO
2
3.26 2.48 3.33 3.12 3.08 1.63 1.70 1.31 1.62
Al
2
O
3
16.84 15.72 16.84 16.93 17.02 31.51 31.48 31.80 31.37
Cr
2
O
3
0.05 0.01 0.02 0.02 0.03 0.04 0.00 0.00 0.00
FeO
21.54 23.53
22.04 22.78 22.57 4.36 4.18 4.25 4.36
MgO
8.74 8.43 7.79 8.07
7.9
0.85 0.81 0.78 0.88
MnO
0.39 0.22 0.36 0.34 0.29 0.03 0.00 0.00 0.04
Na
2
O
0.14 0.04 0.07 0.09 0.09 0.48 0.45 0.46 0.42
K
2
O
9.4
8.88
9.17 9.22 9.28 10.37 10.42 10.30 10.37
BaO
0.00 0.04 0.06 0.02 0.19 0.12 0.04 0.14 0.06
Total
95.37 94.21 94.51 95.56 96.11 94.33 94.06 94.09 94.08
Si
5.414 5.497 5.44 5.421 5.484 6.174 6.184 6.192 6.187
Al
IV
2.586 2.503 2.56 2.579 2.516 1.826 1.816 1.808 1.813
Al
VI
0.483 0.419 0.539 0.514 0.569 3.275 3.286 3.342 3.275
Ti
0.380 0.294 0.391 0.364 0.356 0.168 0.176 0.135 0.168
Cr
0.006 0.001 0.003 0.002 0.004 0.004 0.000 0.000 0.000
Fe
2.785 3.103 2.878 2.952 2.903 0.501 0.481 0.488 0.502
Mg
2.016 1.981 1.814 1.864 1.811 0.174 0.167 0.159 0.180
Mn
0.051 0.030 0.048 0.044 0.038 0.003 0.000 0.000 0.005
Na
0.041 0.013 0.022 0.026 0.026 0.128 0.120 0.123 0.113
K
1.854 1.786 1.828 1.823 1.822 1.817 1.829 1.805 1.821
Ba
0.000 0.003 0.004 0.001 0.011 0.006 0.002 0.007 0.003
fm
0.574 0.607 0.607 0.608 0.612 0.739 0.742 0.754 0.731
Table 2: Microanalyses of biotite (Bt) and muscovite (Ms) with their crystal-chemical formu-
las (22 O
2—
) from the mela-syenite enclave. fm = Fe/(Fe + Mg + Mn); c – core, m – margin.
final U/Pb ages were calculated at 1
σ standard deviation us-
ing the Isoplot/Ex program – version 3.00 (Ludwig 2003).
Petrography and mineral characteristics
The porphyritic mafic enclave shows minor secondary alter-
ation (insignificant biotite chloritization) only in the 5 mm
thick contact zone. The enclosing porphyritic K-feldspar gran-
itoid is also slightly altered near the contact. The composition
of the host granitoid changes from K-feldspar syenogranite in
the 1 m contact zone to the porphyritic, K-feldspar-rich
monzogranite with quartz diorite enclave at about 50 m from
the contact and to biotite monzogranite further out. There is no
indication of cooling against the granite in the enclave and no
mineralogical zoning, but the narrow (about 1 cm) fine-
grained margin is noticeable inside the granite.
The medium-grained enclave (size of rock-forming miner-
als fall in the range of 2—8 mm) is composed of K-feldspar
porphyrocrysts ( ~ 30 mm), biotite, apatite, albite, quartz and
muscovite (Table 1). The accessories ( < 1%) are monazite, xe-
notime, epidote-allanite, zircon, magnetite-ilmenite-rutile in-
tergrowths, titanite, chlorite and calcite. The Mafic Index (MI
= biotite + apatite + opaque minerals + titanite + epidote) is
ca. 45 % (Gawęda 2006). A weak fabric is defined by Kfs
megacrysts and biotite-apatite alignment (Fig. 2b).
The Kfs euhedral porphyrocrysts show normal zoning in
BaO content from 1.86—0.91 wt. % (0.035—0.024 Ba a.p.f.u.)
in cores to 0.75—0.43 wt. % (0.014—0.008 Ba a.p.f.u.) at rims
(Fig. 3). Inclusions of albitic plagioclase, and falls in Ba con-
tent, emphasise the zoning of the host-feldspar (Fig. 3). The
matrix plagioclase is also albite (Ab
93
An
5
Or
2
—Ab
97
An
3
). Bi-
otite (fm = 0.644—0.598, Ti = 0.39—0.36 a.p.f.u.) is weakly
zoned with a slight drop in Ti content from core to rim (Ta-
ble 2). In general, the biotite chemistry compares with that of
the enclosing granite (Fig. 4). The TiO
2
content of the dis-
persed muscovite flakes in the range 1.3—1.7 wt. %, and fm in
the range 0.731—0.754 (Table 2) both reflect the magmatic
character of the white mica (Monier & Robert 1986). They are
chemically and optically homogeneous.
Two types of apatite (0.2—2 mm ) were identified: Ap
1
–
unzoned isometric clear apatite crystals (Figs. 2b, 5a,c;
Table 3a) and prevailing Ap
2
– xenomorphic crystals with a
patchy internal structure marked by differences in Fe, Y, Na
and Mg contents and with inclusions of HREE-rich xenotime
and zircon (Fig. 5a,b,d; Table 3b), poiki-
loblastically intergrown with biotite
flakes.
Zircons, from 15—100
µm in size, oc-
cur as inclusions in Ap
1
, in biotite and in
opaque minerals. In the classification of
Pupin (1980), the zircon morphologies
are widely distributed with populations
typical of high-temperature mantle-de-
rived magmas (J
1—2
), lower-temperature
crustal-derived magmas (S
6—7
—S
16—17
) and
mixtures of both (S
21—24
, Figs. 6, 7). Zir-
con inclusions in apatite are of J
1
type
only (Fig. 5d,e). All of the zircon crystals
have cores with Zr/Hf ~ 43—55 and rims
with Zr/Hf ~ 19.5—42 (Fig. 7; Table 4).
Zoned euhedral epidotes show transi-
tions from allanite cores to REE-bearing
epidote at the rims (Table 5), as is typical
of magmatic epidote crystals. Secondary
zoizite + titanite fringes the overgrow the
REE-epidote (Table 5). Unzoned Ce-
monazite crystals (Table 3b) occur as in-
clusions in biotite, apatite and opaque
minerals, locally the decomposition of
monazite and formation of REE-epidote
is observed. Opaque minerals occur as
aggregates of intergrown ilmenite, mag-
netite and rutile in varying proportions
Ø
298
GAW
Ę
DA
(Table 6) and suggest the decomposition of an original ul-
vöspinel under oxidizing conditions. The opaque crystals host
tiny inclusions of calcite and are overgrown by titanite coro-
nas. The titanite may be a product of secondary reaction be-
tween Ti-rich opaque minerals and calcite.
Whole-rock geochemistry
The rock is characterized by low SiO
2,
and a very high P
2
O
5
reflecting the high apatite content (Table 7). However, it is
quartz (3.60) and corundum (4.34) normative (Gawęda 2006)
as biotite is the main rock-forming aluminosilicate and prima-
ry muscovite is present. Petrographical observations (i.e. man-
tling of the quartz by micas and titanite, Fig. 2b) suggest that the
quartz could have been physically wedged into the enclave.
The Fe
2
O
3
, TiO
2
, Ba, Rb, total REE, Zr, Hf, Y contents are
high and that of Sr moderate (Table 6; Fig. 8a,b,c,d). REE
fractionation, dominated by HREE fractionation, is weak
(Ce
N
/Yb
N
= 3.16; Table 7). The rock is characterized by a pro-
nounced negative Eu anomaly (Eu/Eu* = 0.354; Table 7; Fig. 9)
and a low Sr/Sr* value (Sr/Sr* = Sr
N
/
√[Ce
N
×Nd
N
] = 0.135), es-
pecially when compared to the other Tatra granitoids (com-
pare Table 7 and Gawęda 2007b). The ASI index (ASI = Al/
[Ca + K + Na—3.33P]) recalculated against the molecular P
2
O
5
content equals 1.499 and the sample plots in the peraluminous
field of Maniar & Piccoli (1989), while without correction to
phosphorus the sample is metaluminous (ASI = 0.837). As the
rock is corundum normative and magmatic micas are volu-
metrically important components the first value is considered
here. The K
2
O/Na
2
O ratio is equal to 3.93, so the rock can be
classified as ultrapotassic (Fig. 8e). The agpaitic index
([K
2
O + Na
2
O]/Al
2
O
3
[molar]) is 0.61. Sr prevails over Rb (Rb/
Sr = 0.467) and Nd over Th (Nd/Th = 6.526; Fig. 8d). Zr/Hf at
32.41 is typical of most crustal rocks.
Fig. 3. Cs and Ab distribution profiles in alkali feldspar phenocryst.
Scale in micrometers.
Fig. 4. Plot of biotite composition in the Ti [a.p.f.u.]/fm space. For
comparison biotites from porphyritic granites, monzogranites and
diorites were used.
Fig. 5. Examples of
SEM and BSE images
of apatite and zircon.
a – BSE image of
isometric Ap
1
(analyt-
ical points of apatite 1
& 2) and xenomorphic
Ap
2
(point 3), inter-
grown with biotite
(grey). b – BSE im-
age of xenomorphic
Ap
2
with patchy inter-
nal structure (analyti-
cal points 4—7 ade-
quate to analyses in
Table 3a) and dissolu-
tion embayments. c –
SEM image of Ap
1
.
d – SEM image of
hipidiomorphic Ap2
with zircon inclusion
(pointed by arrow).
e – SEM image of J2
zircon crystal.
299
PETROLOGICAL AND GEOCHRONOLOGICAL STUDY OF THE HIGH TATRA GRANITE (WESTERN CARPATHIANS)
Sample
Xen 1
Xen 2
Mon 1
P
2
O
5
35.13 35.01 29.60
Y
2
O
3
44.19
43.12
0.00
La
2
O
3
0.03
0.06
13.71
Ce
2
O
3
0.03
0.15
29.09
Pr
2
O
3
0.07
0.04
3.25
Nd
2
O
3
0.43
0.70
12.67
Sm
2
O
3
0.57
0.72
2.31
Gd
2
O
3
2.66
2.85
1.51
Er
2
O
3
4.09
3.73
0.12
Dy
2
O
3
4.89
4.89
0.32
Ho
2
O
3
1.20
0.84
0.09
Yb
2
O
3
2.97
2.97
0.00
Lu
2
O
3
0.71
0.73
0.00
Fe
2
O
3
0.24
0.00
0.00
Tb
2
O
3
0.52
0.50
0.10
SiO
2
0.15
0.16
0.20
UO
2
0.67
0.69
0.18
ThO
2
0.00
0.10
4.33
PbO
0.00
0.00
0.03
Total 98.552 97.238 97.51
Apatite
Ap 1
Ap 2
Analysis
No.
1 2 3 4 5 6 7
P
2
O
5
42.54 40.69 42.03 42.48 40.14 42.91 41.91
SiO
2
0.02 0.03 0.00 0.03 0.01 0.02 0.00
SO
2
0.00 0.04 0.02 0.01 0.05 0.03 0.05
ThO
2
0.00 0.00 0.06 0.09 0.00 0.03 0.08
Fe
2
O
3
0.09 0.21 0.24 0.01 0.12 0.06 0.14
Y
2
O
3
0.15 0.11 0.23 0.24 0.34 0.17 0.19
La
2
O
3
0.02 0.01 0.18 0.24 0.03 0.01 0.01
Ce
2
O
3
0.03 0.05 0.04 0.11 0.17 0.00 0.16
Nd
2
O
3
0.13 0.10 0.00 0.01 0.15 0.00 0.16
Gd
2
O
3
0.02 0.03 0.05 0.10 0.07 0.00 0.01
CaO
54.52 55.17 54.43 54.76 55.23 55.52 55.20
MnO
0.14 0.19 0.22 0.14 0.31 0.00 0.14
SrO
2
0.03 0.04 0.02 0.01 0.04 0.02 0.08
Na
2
O
0.06 0.06 0.15 0.11 0.18 0.07 0.10
H
2
O
0.00 0.00 0.00 0.05 0.00 0.00 0.06
F
2.71 3.63 3.25 2.12 3.90 2.43 2.12
Cl
0.03 0.04 0.04 0.02 0.04 0.01 0.02
Total 100.41
100.40
100.73
100.26
100.78 101.26
100.43
Table 3: a – Selected microanalyses of apatite. b – Selected xe-
notime and monazite microanalyses.
Sample
Zr1(c1) Zr1(c2) Zr1(m) Zr1(r) Zr2(c) Zr2(m) Zr3(c1) Zr3(c2) Zr3(m)
SiO
2
31.98 31.91 31.13 32.15 31.92 31.98 32.15 31.27
32.18
ZrO
2
65.65 65.75 65.00 64.08 65.28 65.04 66.08 65.49
65.71
HfO
2
1.04
1.08
1.35
2.87
1.18
2.17
1.08
1.32
1.92
UO
2
0.09
0.05
0.05
0.22
0.10
0.10
0.05
0.06
0.08
Y
2
O
3
0.54
0.47
0.32
0.12
0.43
0.16
0.46
0.22
0.11
Yb
2
O
3
0.14
0.11
0.05
0.08
0.11
0.05
0.11
0.03
0.08
CaO
0.26
0.00
0.14
0.37
0.18
0.18
0.00
0.17
0.00
Total
99.69 99.37 98.04 99.89 99.21 99.68 99.92 98.55 100.09
Si
0.989
0.989
0.981
0.996
0.991
0.991
0.991
0.981
0.992
Zr
0.990
0.994
0.999
0.969
0.989
0.983
0.993
1.002
0.988
Hf
0.009
0.010
0.012
0.025
0.011
0.019
0.010
0.012
0.017
U
0.001
0.000
0.000
0.002
0.001
0.001
0.000
0.000
0.001
Y
0.009
0.008
0.005
0.002
0.007
0.003
0.008
0.004
0.002
Yb
0.001
0.001
0.001
0.001
0.001
0.001
0.001
0.000
0.001
Ca
0.009
0.000
0.005
0.012
0.006
0.006
0.000
0.006
0.000
Zr/Hf
55.108 53.151 42.034 19.493 48.299 26.167 53.418 43.316
29.879
a
b
Table 4: Microanalyses of zircon crystals and their crystal-chemical formulae.
U-Pb zircon dating and isotope geochemistry
U-Pb dating of 7 zircon crystals representing both J and S
morphological types (Fig. 7) reveal three generations of ages.
The oldest age of 391 ± 4.6 Ma (Fig. 10a; Table 8a) was found
in zircon cores and one mantle. Two zircon mantles and one
core provide an age of 361 ± 7.6 Ma (Fig. 10b; Table 8b). Zir-
con rims, and one core with magmatic zoning, yielded the
youngest age of 345 ± 5.1 Ma (Fig. 10c; Table 8c). One homo-
geneous inner core was dated to ca. 700 Ma and one core with
oscillatory zonation to ca. 430 Ma (Table 8d).
The apatite
87
Sr/
86
Sr can be considered to be the rock initial
ratio as apatite contains little or no Rb, assuming no isotopic
disturbances occurred (Tsuboi & Suzuki 2003). The apatite
87
Sr/
86
Sr value of 0.707620, lower than whole-rock IR
Sr
345
87
Sr/
86
Sr ratio (Table 9) suggests either a mixed mantle/crust-
Fig. 6. The position of zircon crystals morphology on Pupin’s
(1980) typological diagram.
300
GAW
Ę
DA
al origin for the rock or, perhaps, some disturbance of a prima-
ry value. A three point errorchron based on apatite, Kfs and
the host whole rock suggests an age of 312 ± 530 Ma
(IR
Sr
312
= 0.70740). The rock is characterized by an IR
Nd
345
value of 0.511901,
ε
Nd
345
and crustal residence age
T
DM
= 1.341 (Table 9). It is worth mentioning that both the Sr
and Nd isotopic characteristics of the apatite rock resemble
those found in most Variscan granitoid rocks (Kohút et al.
1999).
Discussion
The origin of the apatite-rich rock and its systematic position
Low SiO
2
and high CaO contents reflect the high apatite
content. The high Al
2
O
3
content and peraluminous character
of the rock are due to the high contents of biotite and musco-
vite; both minerals are peraluminous—biotite because of its
significant siderophyllite component. The modal and chemi-
Component Al-ep9 Al-ep10 Al-ep11 Al-ep12 Al-ep16 Al-ep13 Al-ep14 Al-ep15 Ep-r-1 Ep-r-2
rim mantle
core
mantle rim secondary
SiO
2
33.75
32.63
33.32
32.6
31.98
32.89
33.85
34.89
37.32
37.45
TiO
2
0.1
0.19
0.12
0.17
0.22
0.13
0.06
0.11
0.01
0.04
Al
2
O
3
19.35 18.06 19.08 18.06 17.65 18.69 19.98 20.36 21.66 22.09
P
2
O
5
0.63
0.07
0.42
0.19
0.38
0.05
0.19
0.21
0.29
0.56
FeO
12.59 13.65 12.97 13.46 12.82 12.75 12.34 13.03 14.01 13.65
MnO
0.79
1.18
0.7
0
0.87
0.87
0.54
0.79
0.58
0.19
0.11
MgO
0.18
0.22
0.19
0.22
0.26
0.20
0.15
0.14
0.00
0.00
CaO
14.91 12.83
14.6
0
13.2
0
12.19
14.16
15.61
17.1
22.66
22.59
SrO
0.00
0.00
0.00
0.00
0.00
0.00
0.00
0.00
0.18
0.33
La
2
O
3
2.10
3.21
2.18
3.20
3.77
3.00
1.59
1.67
0.04
0.00
Ce
2
O
3
5.08
7.11
5.50
6.90
8.84
7.11
4.32
3.66
0.08
0.00
Pr
2
O
3
0.62
0.81
0.61
0.71
0.97
0.75
0.53
0.41
0.03
0.00
Nd
2
O
3
2.40
2.74
2.92
3.10
3.70
2.70
2.24
1.72
0.04
0.08
Sm
2
O
3
0.65
0.54
0.66
0.59
0.74
0.64
0.61
0.32
0.02
0.04
Gd
2
O
3
0.44
0.48
0.48
0.50
0.43
0.40
0.72
0.50
0.07
0.14
ThO
2
0.01
0.19
0.21
0.14
0.10
0.00
0.14
0.08
0.02
0.12
V
2
O
3
0.00
0.00
0.00
0.03
0.01
0.01
0.00
0.01
0.03
0.03
Total
93.60 93.91 93.96 93.94 94.93 94.02 93.12 94.79 96.66 97.22
Si
6.169
6.166
6.144
6.15
6.089
6.151
6.180
6.193
6.219
6.180
Ti
0.014
0.027
0.016
0.024
0.032
0.018
0.008
0.015
0.002
0.005
Al
4.168
4.022
4.146
4.016
3.960
4.119
4.300
4.259
4.255
4.296
Fe
1.924
2.156
2.000
2.124
2.041
1.995
1.883
1.935
1.952
1.884
Mn
0.122
0.190
0.109
0.138
0.140
0.085
0.123
0.087
0.027
0.015
Mg
0.050
0.063
0.051
0.061
0.075
0.055
0.041
0.037
0.000
0.001
Ca
2.920
2.596
2.884
2.669
2.487
2.836
3.053
3.252
4.046
3.993
Sr
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.018
0.032
La
0.142
0.223
0.148
0.222
0.264
0.207
0.107
0.109
0.002
0.000
Ce
0.340
0.492
0.371
0.476
0.616
0.487
0.289
0.238
0.005
0.000
Pr
0.041
0.056
0.041
0.049
0.067
0.051
0.035
0.027
0.002
0.000
Nd
0.157
0.185
0.192
0.209
0.252
0.180
0.146
0.109
0.002
0.005
Sm
0.041
0.035
0.042
0.038
0.049
0.041
0.038
0.019
0.001
0.002
Gd
0.027
0.030
0.029
0.031
0.027
0.025
0.044
0.030
0.004
0.007
Th
0.001
0.008
0.009
0.006
0.004
0.000
0.006
0.003
0.001
0.004
Table 5: Selected microanalyses of epidotes and their crystal-chemical formulae (25 O
2—
).
Sample sp1 Ilm1 sp2 Ilm2 sp3 Ilm3 sp4
FeO
31.06 41.35 30.71 40.87 31.3 40.85 30.73
Fe
2
O
3
66.37 4.04 55.6 3.77 66.52 4.49 67.8
MnO
0.05 3.87 0.64 4.65 0.00 4.18 0.07
MgO
0.00 0.06 0.00 0.06 0.04 0.06 0.00
Cr
2
O
3
0.07 0.00 0.05 0.00 0.07 0.00 0.06
V
2
O
5
0.81 0.00 0.41 0.00 0.47 0.00 0.43
Nb
2
O
5
0.24 0.01 0.15 0.00 0.21 0.00 0.06
TiO
2
1.81 50.46 11.32 50.81 1.38 50.24 1.03
Total
100.41 99.78 98.88 100.16 99.99 99.82 100.18
Fe
+2
0.986 0.875 0.975 0.862 0.994 0.865 0.975
Fe
+3
1.896 0.077 1.588 0.072 1.900 0.086 1.937
Mn
+2
0.002 0.083 0.019 0.100 0.000 0.090 0.002
Mg
+2
0.000 0.002 0.000 0.002 0.002 0.002 0.000
Cr
+3
0.002 0.000 0.002 0.000 0.002 0.000 0.002
V
+5
0.020 0.000 0.010 0.000 0.012 0.000 0.011
Nb
+5
0.005 0.001 0.003 0.000 0.004 0.000 0.001
Ti
+4
0.052 0.960 0.323 0.964 0.039 0.957 0.029
Table 6: Selected microanalyses of magnetite (sp) and ilmenite (Il)
and their crystal-chemical formulae (for 4 O
2—
and 3 O
2—
respectively).
Notice: sp2 and Ilm2 are not in equilibrium
301
PETROLOGICAL AND GEOCHRONOLOGICAL STUDY OF THE HIGH TATRA GRANITE (WESTERN CARPATHIANS)
Table 7: Whole-rock analyses of major and trace elements in the
apatite-rich enclave (G2-05), the selected granitoids (G1g-05, Mkn-
05, G12g-05) and quartz-diorite enclave (G9d-05). T
Zr
– tempera-
ture calculated according to Watson & Harrison (1983) procedure.
CTG – an example of common Tatra granite.
Sample
No.
G2-05 G1g-05 Mkn-05
G12g-05
G9d-05 CTG
SiO
2
48.89 62.9
64.74 66.66 61.07 75.62
TiO
2
1.23 0.65 0.52 0.58 0.77 0.11
Al
2
O
3
16.21 18.87 17.78 17.04 17.91 13.48
Fe
2
O
3
7.98 3.23 3.19 3.61 5.89 0.67
MnO
0.11 0.02 0.04 0.05 0.09 0.01
MgO
2.7
1.92 1.23 1.13 2.73 0.13
CaO
7.21 1.67 1.48 2.41 3.33 0.94
Na
2
O
1.67 4.71 3.88 4.49 4.31 3.07
K
2
O
6.57 3.56 5.14 2.39 2.33 5.10
P
2
O
5
5.08 0.25 0.32 0.28 0.36 0.15
LOI
2.00 2.30 1.60 1.50 1.3 0.90
C(tot)
0.04 0.15 0.02 0.05 0.01 0.03
S(tot)
0.01 0.01 0.01 0.01 0.01 0.01
Total
99.7
100.24 99.95 100.2 100.11 100.18
ASI
1.499 1.301 1.228 1.199 0.821 0.957
Sr
384.3
319.5
445.4
499.6 735.2 370.1
Ba
2538.5
1093.7
2421.9
705.7 681.9 1477.4
Rb
179.6
91.9
110.4
73.2 107.5 131.4
Th
25.1
15.9
9.3
9.9 2
0.4
U
8.7
1.7
1.8
2.6 19.3 1.0
Cr
20.5
20.6
23
103
47.9 48.0
V
125
59
48
126
115
9.0
Zr
440.8
205.8
159.1
143.8 122
41.7
Hf
13.6
6.0
4.2
3.9 3.6 1.5
Y
401.1
16.8
20
26.1 22
5.1
Nb
19.7
8.5
8.8
11.3 8.6 2.7
Ta
1.0
0.5
0.5
0.8 0.6 0.3
La
105.70 49.70 14.20 39.90 17
4.40
Ce
266.60 104.60 29.40 84.90 65.6 9.20
Pr
36.90 11.98 3.36 10.37 129.6 1.12
Nd
163.80 42.80 12.20 41.00 14.13 4.10
Sm
54.10 8.50 3.00 9.40 50.6 1.20
Eu
6.78 1.69 0.69 1.56 8.6 0.59
Gd
63.48 5.89 2.98 7.78 1.58 0.94
Tb
12.23 0.91 0.66 1.35 6.01 0.18
Dy
72.06 3.99 4.58 7.65 0.84 0.99
Ho
14.07 0.56 0.96 1.49 4.24 0.18
Er
35.49 1.36 3.00 4.29 0.72 0.47
Tm
4.64 0.20 0.44 0.64 1.91 0.08
Yb
23.27 1.15 2.49 3.70 0.3 0.39
Lu
3.00 0.19 0.37 0.57 1.62 0.09
Eu/Eu* 0.354 0.730 0.657 0.600 0.672 1.698
(Ce/Yb)
N
3.157 25.061 12.950 11.655 22.042 6.500
T
Zr
[ºC] 752 822 797 801 754 695
Fig. 7. CL and SEM images of zircon crystals used for U-Pb dating.
Analytical lines and points marked not to scale.
cal composition of the apatite-rich rock cannot, in any case,
represent liquid, so it cannot be interpreted as a microgranular
enclave. There are a number of ways in which the enclave
rock may have originated. It may be (a) restite, (b) cumulate,
(c) recrystallized metasediment or (d) magmatic rock unrelat-
ed to the host granite. The lack of a negative Ce-anomaly and
the high REE, Ba, Zr, Y and Hf contents (Table 8) tell against
it being a P-rich metasediment (see Dorais et al. 1997). More-
over, there is no field and mineralogical evidence that the en-
clave was a metasomatized country rock. The negative Eu
anomaly and the high LILE content are atypical of restite. On
the other hand, a magmatic origin is supported by the internal
structures of minerals (zonation).
302
GAW
Ę
DA
The high REE content, the flat chondrite-normalized pat-
tern and the high HFSE content combined with low SiO
2
(Table 8) could point to a mantle derivation or to its origin as
a cumulate. The undepleted HREE rule out residual garnet in
the source. The source similar to MORB can also be exclud-
ed as partial melting would give HREE-depleted, fractionat-
ed magmas. The prevalence of Nd over Th (Fig. 8d) is also
indicative for mantle-derived rocks. The strong negative Eu
anomaly, and the high Cr/Ni (4.1), low Zr and Nb contents
suggest a mantle fractionate or a related cumulate rock. A
low Sr/Sr* value indicates relative Sr depletion analogous to
that of Eu; both suggest feldspar fractionation with a plagio-
clase-rich residue.
The low transitional-metal content, the high LILE concen-
tration, and the high La/Nb (22.64) open the possibility of
the rock being a crustal melt. The prevalence of Fe over Mg
is also atypical of mantle derivatives as is the high Al
2
O
3
content (Table 7). The extreme P
2
O
5
, enrichment, high P
2
O
5
/
TiO
2
and high LILE content have been noted as typical of
low fraction lithospheric mantle melts (Backer & Wyllie
1992). With only one sample, any fractional pattern calcula-
tions are impossible.
As a magmatic rock, the apatite-rich enclave can be classi-
fied as quartz mela-syenite (IUGS classification) or apatite-
rich mela-syenodiorite (TAS classification – Le Maitre et
al. 1989). The rock plots in the shoshonitic field in contrast
to the calc-alkaline and high-K calc-alkaline host granitoid
suites (Fig. 8d).
Fig. 8. Selected Harker diagrams of the apatite-rich enclave, diorites and host High Tatra granites.
Fig. 9. Chondrite-normalized (C1 chondrite, after Sun & Mc Donough
1989) REE patterns of the apatite-rich enclave, host granitoids and
metapelitic xenoliths. Symbols explanations: G2-05 – apatite-rich
enclave, G1g-05 – porphyritic granite from the contact, Mkn-96
and G12g-04 – porphyritic granites 9 m and 20 m from the con-
tact, G4m-05 – monzogranite from the Upper Batizovská Valley,
G9d-05 – quartz diorite from the Upper Batizovská Valley. Grey
area cover the quartz-diorites C1-normalized REE values.
303
PETROLOGICAL AND GEOCHRONOLOGICAL STUDY OF THE HIGH TATRA GRANITE (WESTERN CARPATHIANS)
Table 8: LA ICP-MS isotope data from zircon grains from apatite-rich enclave. For the loca-
tion of the analytical points (sample numbers) see Fig. 7. U and Pb concentrations were not de-
termined because sample weighing was not possible.
Isotope
parameter G2-05 G9d-05 G12g-04 CTG
Rb [ppm]
179.6 107 73.2 111.3
Sr [ppm]
384.3
735.2 499.6 370.1
87
Sr/
86
Sr WR
0.713624±11
0.707074±11 0.709021 0.711642
87
Rb/
86
Sr WR
1.352949
0.421059 0.423972 0.886077
87
Sr/
86
Sr Ap
0.707620±11
– – –
87
Sr/
86
Sr Kfs
0.710478±21
– – –
87
Rb/
86
Sr Kfs
0.680109
– – –
IR
Sr
345
0.706980 0.705006 0.707126 0.707038
Sm [ppm]
54.1
8.6 6.7 1.2
Nd [ppm]
163.8
50.6 32.1 4.1
143
Nd/
144
Nd WR
0.512463±5
0.512472±8 0.512360±13 0.512410±28
147
Sm/
144
Nd
0.199678
0.102753 0.126188 0.176948
143
Nd/
144
Nd Ap
0.512618±15
– – –
IR
Nd
345
0.511901 0.512103 0.511944 0.511894
ε
Nd
345
–3.548 0.902 –2.318 –3.580
T
DM
[Ga]
1.341 0.989 1.242 1.353
Table 9: Isotopic analyses of apatite-rich rock, its mineral separates and comparable rock-types.
G2-05 – apatite rich enclave, G9d-05 – quartz—diorite enclave, G12g-04 – porphyritic variety
of High Tatra type granite, CTG – an example of common Tatra granite. Errors are given in 2
σ.
Time of the apatite-rich rock for-
mation
U-Pb zircon dating provides dif-
ferent Variscan ages. Zircons crys-
tallized early enough to be included
in biotite and apatite. In the context
of the geological history of the Tatra
Mts massif, cores yielding 391 Ma
and some older exceptions possibly
reflect the metamorphic events and/
or partial melting episodes in the
Tatra Massif (Fig. 10a,b; Burda
2006, 2007; Gawęda 2007b). The
concordant age of 361 Ma is in ac-
cordance with both the common
Tatra granite age (Poller et al. 2000)
and the age of Western Carpathians
Variscan
granite
magmatism
(365 Ma; Kohút et al. 1999) as well
as with the partial melting processes
in the Western Tatra Mts (Burda
2006, 2007). The concordant age
from the zircon rims (345 Ma;
Fig. 10c) compares closely with a U-
Pb zircon age for quartz diorites
(341 Ma; Poller et al. 2001), a WR
Rb-Sr isochron age for Western
Tatra pegmatites (ca. 345 Ma;
Gawęda 1995) and a K-Ar age for
shear-zone muscovite (ca. 343 Ma;
Deditius 2004).
The Rb-Sr three-point errochron
age of ca. 312 Ma, and a zircon low-
er intercept U-Pb age of 314 ± 4 Ma
for the High Tatra granite intrusion
(Poller et al. 2001), are consistent
with 300—330 Ma Ar-Ar age of
Variscan uplift of the High Tatra Mts
(Janák 1994) and 298—318 K-Ar ages
of shearing (Deditius 2004) and,
presumably, final cooling of the
Tatra crystalline massif.
Temperature and pressure determi-
nations
The thermometer of Watson &
Harrison (1983), based on rock Zr
content, applied for the apatite-rich
rock, provided a temperature of
752
°C without correction for Ca in
apatite, while after correction the
calculated temperature increased to
890
°C. For the other Tatra granitoid
rocks the temperature intervals are
as follows: 822—797
°C for the Kfs-
rich pophyritic granites, 806—736
°C
for the biotite monzogranites and
304
GAW
Ę
DA
822—753
°C for the quartz diorites (Gawęda 2007b), and the
correction for Ca in apatite is insignificant. As the rock chemi-
cal and mineralogical composition cannot be interpreted in
terms of liquid, both temperatures are of doubtful meaning.
For the apatite-rich rock, calculation of the Mt-Ilm exsolu-
tion (Spencer & Lindsley 1981) gave a temperature of exsolu-
tion in the range 680—668
°C in a growing oxygen fugacity re-
gime (log
10
fO
2
= —16). The latter temperature range is similar
to earlier determinations for the High Tatra granitoids
(Grabowski & Gawęda 1999).
The flat REE profile of the enclave constrains the depth of
melt origin. High-pressure (22—32 kbar) melts in equilibrium
Fig. 10.
206
Pb/
238
U versus
207
Pb/
235
U Concordia plots for the analy-
sed zircon grains from apatite-rich enclave. 1 – concordia plot for
391 ± 4.6 Ma zircon cores, 2 – concordia plot for 361 ± 7.6 Ma zircon
core and mantles, 3 – concordia plot for 345 ± 5.1 Ma zircon rims.
with an eclogitic residue show highly fractionated HREE de-
pletion with low Yb contents, whereas low-pressure ( ~ 8 kbar)
melts with no residual garnet show weakly fractionated REE
patterns (Luais & Hawkesworth 1994) similar to that of the
enclave (Fig. 9). Magmatic zoned epidote with allanitic cores
(Table 4), that crystallized after biotite but before quartz and K-
feldspar, suggests a pressure > 6—8 kbar. The temperature of the
crystal mush for the given P did not exceed 740—775
°C for
H
2
O > 9 wt. % (Schmidt & Poli 2004). Assuming the high con-
centration of volatiles in the magma, suggested by the lack of
“dry” minerals and the presence of biotite as the predominant
mafic mineral, the higher temperature limit can be approved
(Schmidt & Poli 2004), covering temperatures revealed by Mt-
Ilm geothermometer, conspicuously consistent with zircon ther-
mometry. Biotite chemical zoning, although weak, means
growing oxygen fugacity as Ti is incorporated into oxides.
The presence of allanite-epidote also suggests the changes
in Ca activity in the melt as monazite crystallization typifies
low-Ca activity conditions, and allanite presence, high Ca ac-
tivity (Broska et al. 2000). Possibly, early apatite (Ap
1
) crys-
tallization lowered the Ca activity enabling monazite crystalli-
zation, and Ap
2
maintained it so. Afterwards, the remaining
Ca was used for allanite formation during more oxidizing con-
ditions while plagioclase is almost pure albite (Petrík & Bros-
ka 1994).
The zoned K-feldspars, and changes in barium content, can
be interpreted in terms of magma mixing and/or changing par-
ent-magma temperatures, water contents, crystallization of ad-
ditional minerals, etc. (Long & Luth 1986; Słaby et al. 2002).
As barium diffusivity in alkali feldspars is very low, zoning is
usually a primary feature. No features such as perthite coars-
ening identify the influence of post-magmatic fluids in the
subsolidus stage (see Brown & Parsons 1989). The perturba-
tions observed in the analysed profile (Fig. 3) may reflect
changes in the crystallization path due, in the main, to falling
water contents – favouring crystallization of the plagioclase
now trapped as inclusions in the Kf megacrysts. Increased Ba
in Kf near each albite inclusion could reflect increasing water
contents in the magma and/or new mantle magma input. After
the Ba decrease to the margin, the Kf megacryst rims show re-
newed Ba-enrichment (up to 0.029 a.p.f.u., 1.58 wt. % BaO
– see Fig. 3). This may represent crystallization from a resid-
uum rich in water, and in Ba.
The calculated temperature interval of 700—800
°C is the
crystallization temperature of most of the rock-forming sili-
cates in the apatite-rich enclave as oxygen fugacity increased.
The Mt-Ilm geothermometry (680—668
°C) could reflect cool-
ing on intrusion of the crystal mush and the decomposition of
primary opaque mineral phases. The assumed pressure (6—
8 kbar) is at the higher end for the hybrid quartz diorite mag-
ma range (4—6 kbar; Gawęda et al. 2005). The enclave crystal-
lization and cooling temperatures compare with those of the
surrounding granites (Gawęda 2007b). Thus, the cooling his-
tory of the hosting granite may have been the key influence.
Speculative model of the apatite-rich magma formation
The apatite, which is the rock-forming mineral in the rock in
question, is a carrier of both F and P, elements significantly
305
PETROLOGICAL AND GEOCHRONOLOGICAL STUDY OF THE HIGH TATRA GRANITE (WESTERN CARPATHIANS)
lowering the magma viscosity. Fluorine and phosphorus en-
richment could allow formation of a cumulate, typical rather
of basic and alkaline rocks (Collins et al. 2006). Here the term
cumulate is used without defining the specific process of its
formation. That could be both crystal sorting caused by gravi-
ty or during magma flow in the stress field. The last possibility
is supported by the oriented fabric of the apatite-rich rock and
the presence of tectosilicates (micas).
The hybrid character of the apatite rock suggests some simi-
larities with quartz diorites of roughly the same age (ca.
341 Ma; compare data and discussion in Gawęda et al. 2005).
However, the differences in
ε
Nd
345
and in T
DM
values point out
the different source of both rock-types (compare: Table 9 and
Poller et al. 2001). The processes like cumulate formation or
fractional crystallization could not change the isotopic charac-
teristics of the magma. On the selected Harker diagrams
(Fig. 8a,b,c) diffuse trends links the apatite-rich enclave rather
to common Tatra granites then to quartz diorites. However, it
must be noted that most of the quartz-diorites occur as xeno-
liths in younger (ca. 314 Ma) High Tatra granites and were
subjected to secondary recrystallization (see Gawęda et al.
2005). Moreover, the linear trends typically produced by mix-
ing/mingling and fractional crystallization processes could be
easily destroyed if cumulates were produced early and more
evolved liquids were mingled/mixed with the magmas differ-
ing in origin and chemistry (Collins et al. 2006).
Both the IR
Sr
345
and the apatite
87
Sr/
86
Sr ratios (0.706980
and 0.707620 adequately) could suggest at least mixed (I/S)
origin (Table 9). As the apatite
87
Sr/
86
Sr ratio is higher then
IR
Sr
345
either system disturbance or the “foreign” character of
apatite in the rock can be suggested. The whole-rock Rb-Sr
isotopic system may have been easily disturbed by a younger
episode or may not be representative of the real whole-rock
value if the enclave size (and consequently the sample) is
small. Another possibility is the assumption that during filter
pressing of the cumulate material the squeezed melt was
mixed and isotopically equilibrated with more mafic magma.
The presence of a large amount of interstitial liquid might influ-
ence the equilibration between the enclave and the host magma
(Elburg 1996). In fact, apatite Ap
2
crystals, showing deep disso-
lution embayments and irregular internal zoning (Fig. 5a,b),
could be interpreted in terms of magma mixing regime (Słaby
& Martin 2008). The incoherence between the U-Pb zircon dat-
ing (last marked episode at 345 Ma) and the Rb-Sr errorchrone
point out that more then one process affected the isotope system
and diffusion played an important role (Elburg 1996).
The measured apatite
143
Nd/
144
Nd ratio is lower than that in
the whole-rock sample, but higher than IR
Nd
345
(Table 9). Be-
cause of the slow diffusion the LREE are thought to be less
sensitive to secondary processes than Rb-Sr system (Pin et al.
1990). The calculated
ε
Nd
345
value of —3.548 (Table 9) would
imply a crustal provenance for the enclave. As both
ε
Nd
345
and
the calculated T
DM
model age of the enclave (1.341 Ga, Ta-
ble 9) are similar to those calculated for common Tatra gran-
ites (sample CGT, Table 9, Gawęda, in print), and also fall in
the interval stated for typical West Carpathian Variscan gran-
ites (Kohút et al. 1999) it is possible that the enclave material
was in a crustal environment for a long time or it is genetically
linked with it.
Assuming the genetic link between the common Tatra gran-
ite (360—340 Ma) and apatite-rich cumulate the U-Pb age of
361 Ma, found in selected zircon grains (one core with mag-
matic zonation and 2 mantles) together with 345 Ma zircon
rims, can mirror one prolonged magmatic process. Such a
long time span for a magmatic activity marks either the mag-
ma convection in the chamber and/or the replenishment by the
mafic magma pulses, forming together the prolonged magma
crystallization and formation of the hybrid features. Such a
conclusion is consistent with the presence of two MME types,
representing two mingling episodes (Gawęda, in print). The
presence of the cumulate enclave, showing features of both
crustal- and mantle-derived magma influence, shed new light
on the origin and history of meso-Variscan granitoid magma-
tism, till now assumed to be purely S-type.
Concluding remarks
1. Chemical and mineralogical signatures suggest that the
apatite-rich enclave has a hybrid character with similarities to
the ca. 360—340 Ma common Tatra granite. It can reasonably
be interpreted as the cumulate fraction, formed by the crystal
accumulation, possibly during magma flow.
2. The present enclave mineralogy is a result of mostly mag-
matic processes (magma mixing/mingling), and changes in
water content, calcium activity and oxygen fugacity, usually
occurring during magma mixing.
3. The P-T history of the rock was partly overprinted by the
younger High Tatra granite. Petrographical and geochemical
data suggest that the temperature reached 740—775
°C 8 kbar
at the base of the crystal-mush layer.
4. The ca. 361—345 Ma hybrid apatite-rich rock is a unique
feature of the geology of the Tatra Mts massif that spans a his-
tory of the meso-Variscan magmatism.
Acknowledgments: R. Piwkowski and E. Lichota, Tatra
guides, are thanked for help during climbing, field work and
sample transportation. Dr P. Dzierżanowski and Mrs. L. Jeżak
helped with microprobing and E. Teper with zircon imaging.
Dr J. Burda did the zircon dating in Vienna University. Prof.
U. Klötzli provided the Lam-Tool computer program for U-Pb
data correction and plotting. Prof. J.A. Winchester (Keele
University, GB) and Dr P.S. Kennan (University College
Dublin, Ireland) are thanked for English corrections and for
discussions during the investigation. The work gained sub-
stantially from advice from Prof. B. Bonin, Prof. E. Słaby and
from reviewer’s comments by Dr I. Broska, Dr I. Petrík and
Prof. R. Kryža. Polish Ministry of Sciences and Education
Grant No. 2 PO4D 05629 founded the research.
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