edu/fosrec/)
Oleh
DAFTAR ISI
1. Sampling
2. Sampel
3. Metoda Preparasi
4. Peralatan Praktikum
5. Glossary
6. Morfologi Foraminifera
7. Kunci Identifikasi Genus dan Species Plangton Umur Plistosen - Resen
8. Kunci Identifikasi Genus dan Species Plangton Umur Kenozoikum
9. Kunci Identifikasi Genus dan Species Plangton Umur Mesozoikum
10. Kisaran Umur Beberapa Marker Plangton
Plangton
11. Kunci Identifikasi Genus Bentonik
12. Diskripsi Beberapa Genus Foraminifera Plangton
13. Diskripsi Beberapa Genus Foraminifera Bentonik yang Kosmopolitan di Endapan
Neogen
14. Foraminifera Besar
15. Kisaran Umur Beberapa Marker Foraminifera
Foraminifera Besar
16. Kunci Identifikasi Genus Kelompok Fusulinid.
17 Penyajian Data
18. Interpretasi Umur
19. Interpretasi Lingkungan Pengendapan
21. Non-Foraminifera
22. Accessory Mineral
Accessory Mineral
PANDUAN PRAKTIKUM
MIKROFOSIL FORAMINIFERA
1. S ampli
ampling
ng
Sistematika pengambilan sampel untuk analisa fosil foraminifera
f oraminifera secara umum ada dua cara
yaitu :
a. spot sampling
spot sampling ;
b. sistematic sampling
sistematic sampling .
Sample bisa berasal dari permukaan (surface outcrop) atau dari hasil pemboran.
2. S ample
ample
Ada empat macam sample yang dikenal yaitu:
- Outcrop (sample lapangan)
- Dicth Cutting
- Sidewall Core
Sidewall Core (SWC)
- Core
Masalah dalam interpretasi dapat disebabkan adanya fosil yang tidak in situ bisa karena
reworked (rombakan) atau displace/contaminant
displace/contaminant . . Beberapa hal yang dapat menyebabkan
kontaminasi adalah:
a. caving: yaitu material yang berasal dari lapisan yang lebih tinggi dalam suatu sumur
pemboran, material tersebut dapat dikenali dari ciri litologi yang sama yang telah terlihat
diatasnya dalam satu sumur.
b. Recirculation: recirculation ini terjadi akibat adanya material/microfossil dari batuan yang
telah dibor yang kemudian ikut masuk kembali ke sumur bersama aliran lumpur pemboran
dan kemudian berkontaminasi
berkontaminasi dengan
dengan sampel
sampel yang ada.
c. Lost circulation material : kontaminasi berasal dari material pengisi rongga sumur pada
waktu terjadi lost circulation
d. Cement: semen untuk casing juga dapat mengandung foram yang dapat mengakibatkan
kontaminasi
e. Drilling mud
Dari empat macam sjenis sampel dicth cutting merupakan sampel yang mempunyai karakter
yang berbeda (banyak mengandung contaminat) sehingga berbeda pula dalam
interpretasinya. Sampel dari outcrop, swc atau core akan memberikan gambaran lebih baik
mengenai assosiasi
assosiasi fosil yang sebenarnya (in situ) dibanding ditch cutting.
Jenis litologi juga harus diperhatikan dalam interpretasi, misal batupasir dilihat dari
mekanisme sedimentasinya jenis batuan ini merupakan hasil tranportasi, sehingga fosil yang
berasosiasi dengan batupasir harus dilihat dengaan hati-hati.
3. Metoda Preparasi
The techniques used to prepare and concentrate samples for examination vary according
to rock type (composition and grain size), how hard or resistant the sediment or rock is,
how abundant the foraminifera are, and how they are preserved within the sediment matrix.
The discussions that follow focus on sediment types that can be disaggregated in order to
free the foraminiferal tests. This would include sands, silts and clays, and the
t he rock types
produced when these sediments are hardened (sandstones, siltstones and shales,
respectively). For the hard limestone usually can be examination using thin section.
Foraminifera can be recovered from bulk sediment samples, although their presence or
absence in any given sample often cannot be established until after processing. The
sampling strategy is simply to collect bags of sediments/sedimentary
sediments/sedimentary rocks that can later be
broken down and processed for foraminifera. Another approach is to process sediment
contained within larger fossils that one might
m ight collect. For example, the fossil shells of marine
snails and clams are often filled with the same sediment that surrounds them. Processing
these sediment fillings may yield foraminifera. Processing samples in the laboratory will
require a source of running water, a sieve, a funnel and some filter paper, and perhaps
detergents or chemicals to help disaggregate the sediments.
Precautionary Note: Make sure that labeling is carefully and accurately transcribed at every
step. A mislabeled sample has little, if any, scientific value.
a. Pencucian (Washing)
The object of all techniques described below is to isolate microfossils, in this case
foraminifera, from the sediment grains that surround them.Unconsolidated sediment and
some soft rocks will break down after soaking
soak ing in water for a few
f ew hours, whereas harder rocks
may first require crushing and then boiling. The rule of thumb here is to utilize the simplest
and easiest technique that will provide the desired results. If simple soaking is all that is
required to disaggregate the sediment, then forego more involved techniques. Regardless
of which technique you utilize, initially breaking the sediment or rock into fragments several
mm in maximum dimension, or slightly larger, will speed the process.
Hydrogen Peroxide (H2O2) Method — If your sample is more resistant, additional
treatments may be required to breakit down. Soaking and, if necessary, boiling in a dilute
solution of hydrogen peroxide is an effective means of breaking down such samples (kadar
peroksida yang digunakan jangan lebih dari 15 persen).
The steps in the H2O2 method are:
1) air-dry sample for several days or oven-dry sample for 24 hours at about 45°C;
2) place sample in 500-ml or 1000-ml pyrex beaker;
3) add fifteen percent hydrogen peroxide solution (volume of solution should be 2 to 3
times that of sample being processed);
4) gently agitate and let soak for 24 hours at room temperature or in oven at about 45°C
(stir occasionally and keep covered to prevent contamination);
5) heat solution containing sample for 15 to 20 minutes, stirring frequently and taking care
that the solution does not boil over;
6) wash sample over No. 230 U. S. Standard Sieve as described earlier;
7) if sample is not disaggregated, transfer it back into beaker and repeat steps 3 through 6;
8) wash sample over No. 18 U.S. Standard Sieve (1-mm openings) and No. 230 U.S.
Standard Sieve, trapping coarser material on the No. 18 sieve and the sand fraction
containing foraminifera on the No. 230 sieve (a coarse screen of the proper mesh size,
available at any hardware store, can substitute for the No. 18 sieve);
9) dry and examine any material retained on the No. 18 sieve (not likely to be forams but
may include other fossils of interest);
10) transfer sample retained on No. 230 sieve to filter paper;
11) air-dry or oven-dry sample at 45°C;
12) transfer dried material to labeled vial for storage.
float the foraminifera in order to separate them from other sediment grains. The only reason
this works is because foraminifera, with their hollow chambers, have an effective density
much less than solid sediment grains of comparable size. If the foraminifera are filled with
sediment or secondary mineral material, they will not float.
Soap Float — One of the simplest ways to concentrate foraminiferal tests is to employ a
soap float. Here the detergent is not of the low sudsing variety (such as Quaternary O), but
rather a standard detergent or soap that produces a sudsy froth. The processed sample is
added in small increments to a solution of soap and distilled water. With frequent agitation,
the foraminifera become suspended in the surface froth while solid sediment particles such
as quartz grains sink to the bottom of the container. The froth can be periodically decanted
onto a No. 230 sieve and washed in a gentle stream of water to eliminate the suds. What
remains will be a concentration of foraminiferal tests, perhaps with some very fine sands of
nonbiogenic origin. This residue can be dried and examined under the microscope.
Other techniques can provide an even cleaner separation, but many involve the use of
chemicals that are extremely hazardous. For example, bromoform and carbon tetrachloride
have been widely used to concentrate foraminiferal tests by f loating. However, both are
carcinogenic and must be used under a fume hood. The fumes are toxic and the chemicals
can be absorbed through the skin. Consequently, use of these chemicals to concentrate
foram tests is not recommended. The use of another, safer chemical to accomplish the
same sort of separation is described below.
You need to pick a set number of forams from the tray. In scientific studies 300 specimens
(if the number of preserved foram are avaliable) are usually picked. There is nothing magic
in this number. It is an arbitrary stopping point above which additional rare species are
encountered more and more infrequently. Make sure that you pick a representative suite of
specimens. That is, do not pick only large specimens, or only small ones, or only pretty
ones. The best way to do this is to mark your picking tray with a numbered grid. Then use a
random numbers table to select a square. Pick all the specimens from that square and then
select a second square. Continue this process until your target number is reached and the
specimens have been transferred to a gum tragacanth-coated cardboard slide.
b. Sayatan tipis
Sayatan tipis umumnya ditujukan untuk pengamatan foram besar. Sayatan tersebut dapat
berasal dari sayatan batuan ataupun individu foram besar. Untuk batuan yang sangat
kompak (indurated) biasanya juga diamati dengan membuat sayatan tipis.
Ada beberapa cara untuk membuat sayatan pada individu foram besar:
4. Peralatan Praktikum:
- Mikroskop (reflected dan/atau transmited lights) + lampunya. Mikroskop jenis reflected light
digunakan untuk mengamati sampel hasil pencucian, sedang yang transmited light untuk
pengamatan sampel dalam bentuk sayatan tipis.
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
7
Catatan
Untuk mengambil (picking) dan menempelkan pada slide jangan memakai lem, tetapi
dengan cara membasahi kuas dengan ludah (dengan cara ujung kuas dikulum dalam mulut).
Kalau menggunakan lem akan susah untuk membolak-balik fosil bila sudah kering (fosil akan
pecah dan lubang2 akan tertutup, sedangkan air tidak akan menempelkan fosil dengan kuat
(mudah lepas)). Penggunaan jarum akan membuat fosil pecah atau loncat. Selama
membolak-balik fosil gunakan kuas yang sudah dibasahi supaya fosil tidak loncat dan tektur
dinding kelihatan. Pewarna digunakan untuk melihat tektur dinding atau lubang apertur.
5. GLOSSARY
Flange : platelike marginal extention along chambers (misal pada Sphaeroidinella) atau
batas apertur yang tinggi karena pembentukan apertural lip (misal pada
Hantkenina)
Flap : suatu dinding kamar yang tak berpori yang merupakan perpanjangan atau
tambahan kamar, terletak diluar dari struktur yang ada dan berada diatas atau
sepanjang apertur utama
Flush : bercampur, bentuk suatu permukaan yang menerus
Globular: bentuk yang membundar
Hemispherical: inflated pada satu sisi, sisi yang berlawanan datar
Hispid : ditutupi oleh spine (duri) yang halus, pendek seperti rambut
Infralaminal : bukaan sepanjang tepi dari struktur accesory (misal: bulla)
Involute : overlap yang sangat kuat, putaran kamar berikutnya seluruhnya melingkkupi
putaran sebelumnya)
Keel : bagian dari peripheri dinding kamar yang menebal seperti punggungan dan tidak
berpori
Lamellar wall: test-wall built of layers of calcite or aragonite formed at consecutive instars
and covering exposed surfaces of previously formed test. Wall generally
possessing true pores. Most lamellar genera are bilamellar and some primarily
multilamellar
Limbate : menunjuk pada batas atau tepi kamar yang menebal, umumnya pada suture,
bisa juga suatu tinggian
Lip : batas yang tinggi/menebal dari apertur, bisa hanya pada satu sisi apertur ataupun
mengelilinginya
Lobate : suatu bentuk yang arcuate
Ovate : bentuk seperti telur bila dipotong secara vertical
Planispiral: terputar pada satu bidang datar
Pustule : tonjolan-tonjolan kecil, mempunyai pusat cekungan akibat duri-duri yang
menyatu
Pseudocarina (pseudo keel): bagian perpheri dari dinding kamar yang berlobang-lobang,
menebal seperti punggunagan
Reticulate: seperti jaring, menunjuk pada ornamen berupa punggungan ( ridge) pada suatu
permukaan cangkang
Robus : kokoh, kuat
Rugose : ornamentasi kasar yang tak beraturan, bisa berupa punggungan
Sensu lato: dalam arti luas, menunjuk pada nama taxon dalam arti luas.
Sensu stricto: dalam arti sempit
Spinose : permukaan cangkanya mempunyai duri-duri halus yang memanjang
Spiral side (dorsal): bagian sisi evolute dari suatu test yang terputar trochospiral
Stellate : berbentuk seperti bintang
Streptospiral: suatu perubahan dari putaran trochospiral dimana bidang coiling selalu
berganti. (terputar seperti putaran benang bola)
Sutura : garis yang menghubungkan dua kamar atau antara dua putaran
Test : shell (cangkang) atau tulang penutup, bisa berupa sisa-sia buangan, gelatin,
chitinous, dinding yang padat, gampingan, aglutinant, silicieoous, atau kombinasi
dua atau lebih dari bahan diatas
Taxa : bentuk jamak dari taxon
Tegillum: suatu penutup bidang umbilcal pada cangkang planktonik foraminifera (seperti
pada Globotruncana), teridiri dari suatu pemanjangan kamar (seperti suatu lip yang
memanjang/menerussampai umbilicus) yang menutupi seluruh apertur utama,
sepanjang tepinya bisa jadi mempunyai lobang bukaan yang kecil-kecil.
Triform : tersusun oleh tiga macan susunan kamar = awal triserial kemudian biserial
selanjutnya menjadi uniserial, dll.
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
10
6. Morfologi Foraminifera
Test (Shell)/Cangkang Foraminifera
Test atau cangkang foraminifera bisa terdiri dari sebuah kamar atau beberapa kamar yang
berukuran umumnya kurang dari 1 mm (kecuali foraminifera dari beberapa kelompok
Rotaliina dan Fusuliina) dan masing-masing kamar terhubungkan oleh sebuah bukaan
(foramen) atau beberapa bukaan (foramina). Batas antar kamar disebut sutura dan
mempunyai satu atau lebih lobang bukaan yang di sebut apertur. Foramina sering kali
termodifikasi dan berbeda dengan apertur
Berikut ini beberapa hal penting mengenai morfology test foraminifera. istilah-istilah bisa
dilihat di glossary.
1. The basic building block of foraminifera tests consists of a cavity with a surrounding wall
called a chamber .
2. Although a few species consist of only a single chamber, most species are multi-
chambered.
3. The simplest multi-chambered arrangement is a single linear series forming a uniserial
test. Internally the chambers are separated by walls called septa.
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
11
4. Externally a line or junction forms where the septa meet the chamber walls. This
external line formed between two chambers is called a suture.
5. In addition to a uniserial arrangement, biserial and triserial chamber arrangements are
common.
6. Instead of forming a straight series of chambers, some foraminifera coil. Each volution
in a coil (through 360 degrees) is called a whorl.
7. If the test coils in a single plane (that is, the chambers are centered on the plane), the
coil is called planispiral. Because of the bilateral symmetry, both sides of the test will
appear identical.
8. If the test coils in a spire, like a snail, the coil is called trochospiral. A raised area in the
center of a coil is called an umbo and a depression, an umbilicus. A test in which
earlier chambers become enveloped by later ones is called involute. One in which
chambers from a previous whorl are visible is called evolute. In many trochospiral
forms the spiral side is evolute and the umbilical side is involute. Some foraminifera add
their chambers in several planes.
9. A common arrangement in which five chambers are visible is called quinqueloculine.
10. Some Major evolutionary trends in coiling include Triserial to biserial to uniserial.
However, some lineages have reversable trends (e.g. Unilocular to multichambered to
unilocular)
B. Gampingan (Calcareous):
Dinding gampingan ini umumnnya terdiri dari kristal-kristal kalsit dan aragonit, mempunyai
berbagai susunan/struktur yang berbeda satu sama lain, antara lain:
- porcelin ( dimiliki oleh Suboder Miliolina):
di mikroskop yang reflected: milky while (seperti porselen Cina)
di mikroskop yang transmited: amber colour (light brown)
Contoh: Quinqueloculina, Spiroloculina, Pyrgo.
Dinding dari jenis hyaline dapat terdiri dari satu atau beberapa lapis, macamnya (Gambar
3):
non-laminar (= non-lamellar, meskipun sebenarnya istilah ini kurang tepat) : bila kamar
berikutnya (kamar baru) langsung nempel diatas kamar sebelumnya (tidak ada dinding
kamar yang dilingkupi dengan dinding kamar sebelumnya)
multilaminar bila dinding masing-masing kamar mempunyai beberapa lapisan, bisa berupa:
monolamelar: masing-masing kamar terdiri dari satu lapisan
bilamelar: masing-masing dinding kamar mempunyai konstruksi dasar yang terdiri dari
dua lapisan
Penting untuk diperhatikan adalah jumlah kamar, terutama jumlah kamar pada putaran
terakhir, bila kamar-kamarnya terputar.
(Brasier, 1980)
(Brasier, 1980)
6.4 Apertur:
Apertur merupakan suatu lubang bukaan pada cangkang foraminifera, bukaan ini
merupakan tempat dimana tubuh protoplasm berhubungan/mempunyai akses kebagian
exterior (Gambar 7,8,9,10 &11).
jenis: primer, sekunder, aksesori dan modifikasinya
jumlah: single , multiple
posisi: interomarginal, marginal, umbilical, extraumbilical, sutural, terminal, areal, basal,
peripheral.
bentuk: slit atau loop-like, low arch, hig arch, irregular, straight, phialine (bentuk leher
botol), radiate, denritik, rounded, dll
modifikasi: apertual lip, flap, portici, tegilla, apertural teeth (valvular tooth, simple toth,
bifid tooth, flattened tooth) , bulla, umbilical bos
Gambar 7 Apertur utama (primary aperture) foraminifera (Loeblich & Tappan, 1964)
1a 1b 1c 1d
Gambar 8 Macam-macam apertur tambahan (1-6) dan apertur aksesori (7-11) (Loeblich &
Tappan, 1964)
Gambar 9 Bentuk dan macam modifikasi apertur pada foraminifera (flap, tooth, flang, lip,
bulla, tegilla) (Loeblich & Tappan, 1964)
6.5 Sutura:
Sutura merupakan pertemuan antar kamar atau antar putaran, dapat dibedakan dari
bentuknya, apakah : lurus (straight), arcuate (lengkung), sinusous (bergelombang) dan
karakternya: flush, depresed, incised, beaded. Seringkali sutura foraminifera menebal dan
biasa disebut sebagai limbate.
Gambar 12. Macam-macam ornamen pada foraminifera (Loeblich & Tappan, 1964)
(Catatan: Hati-hati dalam penggunaan parameter identifikasi terkait variasi pada tahap
ontogeni dan juga pengaruh oleh lingkungan)
6.7 Umbilicus
Parameter lain yang sering digunakan untuk deskripsi adalah umbilicus yaitu axial area
yang mana dari sisi ini kamar2 tampak memencar (radiate). Umbilicus bisa tertutup (closed
: terlihat hanya sebagai titik dimana sutura bertemu) atau narrowly deep ( bentuk seperti
pinhole: lubang kecil dan panjang) bentuk2 tersebut umumnya dimiliki oleh yang mempunyai
putaran ketat; bentuk lain dari umbilicus adalah terbuka.
Ada juga peneliti yang memakai parameter ini untuk identifikasi misal, Saito dkk. 1981. Pada
permukaan test dilihat apakah non spinose atau spinose, misal: spines, spine bases,
granules, pustules
6. 9 Ukuran:
Termasuk ukuran diameter dan panjang atau tinggi. Jika mungkin ukuran dari proloculus
dan kecepatan peningkatan ukuran dan diameter kamar serta putaranya.
Catatan:
Berikut ini adalah urutan parameter yang digunakan untuk kriteria klasifikasi dalam
urutan hirarkinya:
Sejauh ini paramenter 1 s/d 4 adalah yang paling penting didalam taxonomi
foraminifera (dalam panduan ini, parameter 6.1 s/d 6.9). Parameter/unsur-unsur
tersebut harus diperhatikan dalam mengamati atau mendiskripsi fosil foraminifera,
terutama pada foraminifera kecil. Pengamatan pada foraminifera besar lebih komplek
meskipun pada dasarnya parameternya hampir sama.
Dalam mendiskripsi suatu fosil hendaknya mengikuti aturan tertentu (lihat contoh
diskripsi) dan usahakan sejelas mungkin.
tertekan (depressed). Apertur umbilical, ditutupi oleh triangular f lap (gigi) dari material yang
tak berpori. Umbilicus terbuka dan dalam, dengan apertural teeth dari kamar sebelumnya
kelihatan didalamnya. Dindingnya cancelate halus. Diameter dan tingginya 0.45 sampai 0.75
mm.
7. Kunci untuk identifikasi genus dan species umur Pli stosen- Resen
(Saito et. all. 1981)
I. Test surface rough under light microscope (spine, spine bases, granules, pustuloses):
A. Spine visible on living or well-preserved specimens; spine-bases on most specimens,
located interporate area [Hastigerinnidae; Globigerinidae]
1. Spines or spine bases restricted to distal end of chambers [Hastigerinidae]
a. globular to subglobular chamberss, planispiral coiling [Hastigerina], species:H.
pelagica, parapelagica
b. clavate chambers, streptospiral coiling [Hastigerinopsis], species: H.
digitiformans
2. Spines or spine baseson all portion of test wall [Globigerinidae]
a. primary aperture only
a.1 radially elongate chambers
low trochospire: [Globigerinella], species: G. adamsi, aequilateralis, calida
mediumtrochospire or streptosspire [Bella], species: B. digitata
a.2 globular or sperical chambers [Globigerina], species: G. antartica,
bernudezi, bulloides, decoraperta, falconensis, quinquiloba, umbilicata
b. suplementary aperture present
b.1 sperical to subbglobular chambers
singgle spherical chambers [Orbulina], species O universa, suturalis
subglobular chambers [Sphaeroidinella], sspecies: S. dehiscens,
excavata
subglobular - spherical chambers [Globigerinoides], species:
conglobatus, elongatus, fistulosus, obliquus, pyramidalis, ruber, sacculifer
B. Pustules or granules visible under light microscope on test surface, no spines or
spine bases [ globorotalidae]
1. Surface granular, coarsely pitted
a. pustules present only near aperture
Apertural tooth present [Globoquadrina], species: G. conglomerata,
pseudofoiliata
No apertural tooth [Globorotaloides], species: G.hexagona
b. pustules not prominent (generally with apertural tooth) [Neogloboquadrina]
low to medium trochospire; species N. asonoi, blowi, eggeri, humerosa,
pachyderma, pseudohumerosa, himiensis
medium to high trochospire, species: dutertrei
2. Surface pustulate
a. peripheral keel absent
Singular pustules [Globorotalia], species: hirsuta, inflata, oceanica, scitula,
tosaensis, hessi, ronda;
Multiple pustules[Neocarinina], species: N. blowi
b. peripheral keel present [Globorotalia (keeled)], species: frimbiata, flexuosa,
menardii, tumida, pertenuis, theyeri, truncatulinoides, cultrata ungulata, viola
1. trochospiral coiling
a. primary aperture with bulla
strongly inflated chambers [Globigerinita], species: glutinata, iota, uvula,minuta
weakly inflated subglobular or radial elongated chambers [Turborotalita],
species: humilis
b. primary aperture extraumbilical [Berggrenia], species: praepumilio, pumilio,
riedeli
c. sutural aperture [Candeina], species: nitida
2. biserial coiling [Streptochilus], species: tokelauae
4. Test pada putaran awal trochospiral, putaran akhir atau kamar akhir melingkupi
sebagian atau seluruh kamar putaran sebelumnya
4.1 tanpa bulla
4.1.1 seperti globigerina, putaran akhir atau kamar akhir melingkupi sebagian
umbilical dengan aperture tambahan pada sutura melingkupi umbilical ruang =
Globigerapsis
4.1.2 seperti globigerinoides dengan kamar akhir mempunyai aperture tambahan
pada sutura yang melingkupi umbilical ruang = Orbulinoides atau
Praeorbulina
4.1.3 seperti globigerina dengan kamar akhir seluruh atau hampir seluruhnya
melingkupi kamar pada putaran sebelumnya; aperture sepanjang sutura dan
aerial aperture pada kamar akhir = Orbulina
4.2 dengan bulla
4.2.1 seperti globigerina, putaran akhir atau kamar akhir membulat menutupi
umbilicus, mempunyai aperture tambahan pada sutura yang ditutupi oleh bulla
sempit ( tiap bulla punya lubang infralaminal) = Globigerinatheka
4.2.2 seperti globigerinatheka, sutura lebih tak teratur; aperture multiple tersebar
pada kamar akhir yang ditutupi oleh bulla; bulla appressed, bervariasi menutupi
sebagian besar test , tiap bulla mempunyai lubang infralaminal (infralaminal
aperture) sepanjang tepi-tepinya = Globigerinatella
4.3 dengan atau tanpa bulla
putaran awal seperti globigerina, putaran akhir terdiri 2 atau 3 kamar yang berpukan
erat, stuktur dinding komplek terdiri dari lebih satu lapisan kulit meterial.
aperture slit-like atau iregular
4.3.1 hanya punya satu apertuer = Sphaeroidinellopsis
4.3.2 punya dua atau lebih apertur = Sphaeroidinella
5. Test pada putaran awal trochospiral menjadi streptospiral pada putaran akhir; pada
putaran awal umbilicus terbuka, pada putaran akhir tanpa ada umbilicus =
Pulleniatina
1. Test trochospiral
1.1 primary aperture umbilical-extraumbilical
1.1.1-with sutural suplementary apertures at umbilical: (Rotaliporinae):
-chamber sperical, without keel : Ticinella
-with keel : Rotalipora
1.1.2-without suplementary aperture at umbilical
-without keel: (Hedbergellinae)
-with lip
-without relict aperture at spiral side: Hedbergella
-with relict aperture at spiral side: Loeblichella
-with tegilla and infralaminal ap. acc.: Globotruncanella
-with 1 or 2 keel (composed of : pustules and/or imbrication):
(Marginotruncaninae)
-radial sutura, depressed at umbilical side
- with lip or portici
- 1 keel : Praeglobotruncana
- 2 keel : Dicarinella
- with tegila and infra and intralaminal aperture
accesory:Abathomphalus
-sutura sigmoid at umbilical side, 2 keel : Marginotruncana
3. Test planispiral
-Primary aperture equatorial bordered by a lip, with relict aperture:
- with keel: Planomalina
- without keel:
-chambers globular to ovate: Globigerinelloides
-chambers radial-ellongate : Hastigerinoides
Globorotalia truncatulinoides
Globorotalia tosaensis
Globigerinoides fistulosus
Sphaeroidinellopsis seminulina
Globigerina apertura
Globigerina nepenthes
Sphaeroidinellopsis subdehiscens
Globorotalia margaritae
Globigerina venezuelana
Globorotalia merotumida
Globorotalia pleisotumida
Globorotalia paralenguaensis
Globoquadrina baroemoenensis
Globorotalia continuosa
Globorotalia siakensis
Globorotalia druyii
Globigerinoides subquadratus
Cassigerinella chipolensis
Globorotalia mayeri
Globorotalia praefohsi
Globorotalia praemenardi praemenardi
Globorotalia peripheroacuta
Globorotalia peripheroronda
Globorotalia archeomenardii
Globorotalia birnageae
Praeobrulina transitoria
Globigerinoides sicanus
Globigerinoide diminitus
Globigerinatella insueta
Globigerinoides altiaperturus
Globigerinita unicava
Globigerinita dissimilis
Globigerina binaiensis
P19 P20 P21 P22 N4 N5 N6 N7 N8 N9 N10 N11 N12 N13 N14 N15 N16 N17 N18 N19 N20 N21 N22 N23
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
32
Globorotalia kugleri
Globigerina angulisuturalis
Globigerina tripartita
Globigerina sellii
lobigerina gortanii
lobigerina galavisi
Globigerinoides conglobatus
Globorotalia humerosa
Globorotalia acostaensis
Globigerinoides elongatus
Globigerinoides ruber
P19 P20 P21 P22 N4 N5 N6 N7 N8 N9 N10 N11 N12 N13 N14 N15 N16 N17 N18 N19 N20 N21 N22 N23
73. a. Periphery with a fimbriate keel, aperture at the periphery, oval, on a short neck
andwith a distinct lip
...................................................................................................................... Siphonina
b. If not, please going to .......................................................................................... 74)
74. a. Imperforate field above umbilicus ....................................................................... 75)
b. No imperforate field above umbilicus ................................................................. 77)
75. a. Chamber extentions into the umbilical area ......................................................... 76)
b. No chamber extentions into the umbilical area ........................................... Baggina
76. a. Extention of last chamber (apertural lip) almost completely covering umbilical
region,large imperforate field above umbilicus
.................................................................... Cancris
b. Broad chambers flaps projecting over the umbilicus (if not broken off); flaps of
previous chambers often remain partially visible, imperforate field above umbilicus not
always distinct . Valvulineria
77. a. Umbilical surface with irregular granules along the (often excavated) sutures and
over the umbilical region; often with an umbilical plug which is broken up in adult
specimens ..........78)
b. Less irregular ventral surface ............................................................................... 79)
78. a. Three prominent spines spines radiating from the test test ....................................
......................... ........... Asterorotalia
Asterorotalia
b. Well developed secondary openings along the chamber sutures at the ventral side,
outside the umbilical region ..............................................................................................
Buccella
c. No prominent spines or distinct secondary openings ..................... Amonia or Rotalia
79. a. Test with secondary chambers, chambers, or chambers split up into segments segments .................... 80)
b. If not, please going to .......................................................................................... 83)
80. a. Test a high trochospiral with several chambers in each whorl, each chamber divided
by an infolding of the wall; one triangular secondary aperture at the dorsal side
(between the last two chambers, where internal partition meets chamber suture)
................................................................... 81)
b. Large biconvex multi chambered from (more then ten chambers to whorl) basal slit-
like aperture surrounded by a granulate area, chambers on ventral side split up into
chamberlets.. Amphistegina
c. Test with secondary chambers at the ventral side forming a stelliform pattern, less
than ten chambers to whorl
..................................................................................................... 82)
81. a. Primary aperture one elongate loop-shaped opening extending up up face of final
chamber Robertina
b. Primary aperture consisting of two t wo divergent slits,one up face of final chamber, and
one aperture of previous whorl ....................................................................................
Robertinoides
82. a. Convex ventral side, dorsal dorsal side almost flat, no umbilical plug ............ Asterigerina
b. Convex dorsal side, ventral side almost flat, no umbilical plug ......... Asterigerinata
83. a. Test with flaplike structures (imperforate) in in the umbilical region ...................... 84)
b. If not, please going to .......................................................................................... 88)
84. a. Concavo-convex form, chambers lunate, last chamber chamber at the ventral side occupies a
large part of the test, distinct flap with aprtural openings at both of it, aperture of earlier
chambers remain open
.................................................................................................................. Neoconorbia
b. If not please going to ........................................................................................... 85)
85. a. The umbilicus is open .......................................................................................... 86)
b. The umbilicus is closed by flap-like structures (if not broken off) ....... ................. 87)
86. a. Distinct flaps in umbilicus, primary aperture a basal arch near the periphery
.Rosalina
b. Very small flaps in umbilicus, primary aperture a low slit restricted to mid -portion of
the apertural face (Gyroidina) or extending from periphery to umbilicus
....(Gyroidinoides)
87. a. Extensions of basal portions of the chambers into the umbilicus, flusing and totally
closing the umbilicus .....................................................................................Discorbis
b. Broad chambers flaps projecting over the umbilicus ............................ Valvulineria
88. a. Secondary apertures developed outside the umbilicus umbilicus region .............................. 89)
b. No secondary apertures outside the umbilicus region ......................................... 91)
89. a. Secondary aperture at the periphery, over the complete breath of the chambers .......
Hoeglundina
b. Secondary aperture only at the ventral side, along the chamber sutures, outside the
umbilical region
......................................................................................................................... Bucella
c. Primary aperture bipartitioned, or two separate openings, one part of basal split, the
other part a split extending up the apertural face
................................................................. Osangularia
d. Secondary apertures dorsal or dorsal as well as ventral ....................................... 90)
90. a. Secondary apertures at the dorsal side at the junction of spiral and chamber sutures,
at the ventral side at the mid-point of the sinuate sutures
.................................................. Oridorsalis
b. Only one secondary aperture at the dorsal of the test, triangular, at the basis of the
last chamber
................................................................................................................................. 91)
91. a. Test with a prominent plug in the umbilicus ........................................
...................................... .. Gavelinopsis
b. No umbilical plug ................................................................................................... 92)
92. a. Test distincly planoconvex, last chamber ventrally occuping occuping most of the
test......Lamarckiana
b. If not, please going to .......................................................................................... 93)
93. a. Primary aperture a vertical elongate slit up chamber face ................................................................ ...... 94)
b. Primary aperture arch-like ................................................................................... 95)
c. Primary aperture bipartitioned, or two separate openings, one part a basal split,
theother part a split extending up the apertural face
................................................................. Osangularia
d. Primary aperture a basal split extending from periphery to umbilicus .. Gyroidinoides
94. a. Aperture near and and parallel to periphery
periphery ...............................................
.............................. ................. Epistominella
b. Aperture umbilical, elongate slit, in a groove, extending up face of final chamber on
umbilical side ..................................................................................Ceratobulimina
c. Aperture a low slit restricted to the mid-portion mid -portion of the apertural face, very flaps in
umbilicus .......................................................................................................
Gyroidina
95. a. Aperture a basal split, laying in an unfolded unfolded area ....................................
................................ .... Alabamina
Alabamina
b. Aperture not in an unfolded area ................................................................ Eponides
c. If not, please going to ........................................................................................... 96)
96. a. Test subglobular, chambers hemisphaerical, hemisphaerical, strongly embracing, aperture an arch-
likeslit, near suture
................................................................................................................. Sphaeroidina
b. Test in early stage trochospiral, alter with numerous chambers forming a discoidal di scoidal
test . Planorbulina.
Ammonia : test calcareous, low trochospiral 3-4 putaran, suture slightly curved, thicknes,
depressed on umbilical side, umbilical surface with irregular granulanes along suture
and over umbilical region, umbilicus with open umbilical fissure and plug.
Anomalinella: test planispiral involute; lenticular; wall coarse perfotare with peripheral keel;
aperture low, rounded interomarginal arch, bordered by lip.
Anomallina: test low trochospiral or nearly planispiral; spiral side with umbonal bos, oppsite
site with depressed umbilicus; aperture interomarginal equatorial opening extending to
umbilical side.
Asterorotalia: test trochospiral, biconvex, with 3 prominent slender spine radiating from test,
margin carinate.
Bigenerina: early test biserial become uniserial, wall aglutinanted; aperture terminal
rounded.
Bolivina: biserial, retral processes, aperture narrow elongate loop up chamber face with
toothplate
Bulimina: triserial, aperture bentuk koma
Cancris: test trochospiral; biconvex; elongated and auriculte in shape; chamber rapidly
enlarging; may have peripheral keel and apertural lip. ( differs from Baggina in being
more elongated, evolute in spiral side, keeled and in having an open umbilicus and an
apertural lip)
Cassidulina: biserial terputar; lenticular; aperture elongated slit curve pararel to anterior
margin of chamber with narrow lip
Cellanthus: seperti elphidium tetapi mempunyai biumbilical bos
Cibicides: low trochospiral; dorsal flat; umbilical convex; peripheri angular with keel
Cyclamina: test palnispiral involute; wall aglutinant; wall and septa strongly labyrinthic;
aperture equatorial slit and numerous pore scatered over face.
Dentalina: test elongate; arcuate; uniserial; suture oblique; aperture radiate, terminal
Discorbis: test trochospiral biconvex; plano-convex; flatened on umbilical side; periphery
angled; umbilical with flap; primary aperture extraumbilical, secondary sutural opening
at opposide of chamber flap
Elpidium: test planispiral involute; chamber numerous with retral processes; wall
calcareous; surface commonly with groves or ridges pararelling periphery.
Fissurina: test rounded or ovate in outline; compressed trigonal or tetragonal in section, and
may keeled, surface smooth, costate, beaded; aperture slitlike to oval or rounded
Florilus: test planispiral bbut may be asymetrical, involute; chambers increasing rapidly in
breadth and thickness resulting in flaring test; aperture narrow equatorial opening.
Frondicularia: test elongated or palmae; flatened; chamber low broad and equitant; suture
strongly arched or angled at center of test; aperture terminal radiate may have short
neck.
Gyroidina: test trochospiral, planoconvex; periphery rounded to subtruncate; primary
aperture a low interomarginal slit restricted to mid-portion of apertural face bordered by
narrow lip.
Haplophragmoides: test planispiral involute; wall aglutinanted; aperture equatorial slit.
Heterolepa: test trochospiral, planoconve; periphery bluntly angled, may have keel; slowly
enlargering chamber; aperture interomarginal slitlike at extraumblical to peripheri on
spiral side.
Hoeglundina: test trochospiral, lenticular, perpheri angular to carinete; umbilical area
closed; suture thickened may be elevated; aperture lateromarginal opening pararelling
pheriphery on umbilical side.
6. Foram Besar
Disebut Foram besar karena ukuranya berkisar antara 600 mikron - 20 cm. Hidupnya biasa
bersimbion dengan diatom atau algae serta mempunyai struktur kamar internal yang
komplek sehingga identifikasi foram besar umumnnya hanya bisa dilakukan dengan
mengamati sayatan tipis (thin section) menggunakan mikroskop transmited light. Kadang
beberapa genus hanya bisa dibedakan hanya dengan jenis sayatan tertentu. Parameter
yang penting diperhatikan untuk pembeda adalah: bentuk dan ukuran test, putaran
test/cangkang, posisi dan susunan kamar embrionik, kamar neanik, kamar lateral, kamar
median, tebal atu tipis dinding cangkang, bentuk dinding, septa, cord, alar prolongation, pilar,
Sebagian besar foram besar masuk dalam kelompok Rotaliina dan Fusulinina serta
beberapa dari Miliolid. Berikut ini pembahasan secara garis besar identifikasi genus-genus
penting dalam stratigrafi foram besar Tersier di Indonesia. (disarikan dari Paul Baumann,
1971, gambar2 dari berbagai sumber), dan sistematika identifikasi kelompok Fusulinid
(diambil dari Sundharovat & Nogami, 1972).
Test flattened smooth or ornamented. Three to four whorls present, height or whorls
increasing rapidly as added.V involute or evolute.
Subgenera
Operculina S. str : evolute
Operculinella : involute
Operculinoides : intermediate form between Operculinella and Nummulites
These terms as no more in use.
Evolution
Operculina evolves into different other groups and is therefore an important form regarding
the phylogeny of larger Foraminifera.
Operculina - Nummulites
Operculina - Heterostegina - Cycloclypeus
Operculina - Heterostegina - Spiroclypeus
A relationship was found between factor E and time. E is increasing from Eocene to Recent.
Same E = same age. See v.d. Vlerk & Bannink, 1969.
Species determination
There is no use for the time being to distinguish different species as the stratigraphic value
of these forms is still very doubtful. The method based on the measuring of E is difficult and
very time consuming.
Remarks
Often it is difficult to make the difference between Numulites and Operculina. However
Operculina has only 3 - 4 whorls 'which increase very rapidly in height. Nummulites has
mostly more than 4 whorls, increasing very slowly.
Evolution,
Ontogeny:
3 stages observable in arrangement of the spire of the B- form
- inner primitive part: spire and septa regular, spire narrow
- middle part: spire broad, often irregular
- terminal part : narrow spire
The spire of the A-form-is less differentiated than that of the B-form.
Phylogeny:
- same stages as in ontogeny : Primitive forms with regular spire (lower Ta).
- change in ornamentation : smooth forms may evolve into pillared ones. Radiate septal
structure evolves into sinuate - meandrine - semireticulate reticulate.
N. pengaronensis: adiate ridges, about 40, extending from the center to the periphery,
forming a small umbo in the center; about 12 whorls.
N.gizehensis : Septal structure neandrine, ver-y flat form, one side flatter than the other,
pillars mostly on septal filaments. Pillar heads only on the border of the test clearly
visible. most.forms between 2 - 3 cm.
N.javanus : is considered as younger synonym. It might be a little thicker than the typical N.
gizehensis.
N variolarius one of the smallest Nummulites,, centrally arranged pillars, radiate ridges, 3 -
5 whorls.
N.semiglobulus small to middle in size., distinct central pillar, straight to slightly curved
ornamentation thick walls sharp edges.
Evolution
Ontogeny: same as in Nummulites,
Phylogeny : similar to that of Nummulites.
General trends: increase in size of A end B forms. Increase in size of macrosperic embryonic
apparatus
2. A.spira - group: pillarheads forming distinct, spirelly arranged ridge on the surface, large
form. Spiral well visible from the outside.
Evolution
Ontogeny: 3 stages,
-Embryonic stage (Protoconch + Deuteroconch)
-Operculina stage (chambers not subdivided)
-Heterostegina stage (chambers subdivided)
Phylogeny :
Polyphyletic, several times during the Tertiary, species of Operculina evolve into
Heterostegina by developing secondary septa. Two groups are important in Indonesia.
Species determination
Heterostegina praecursor - bantamensis group: Ancestral group of cycloclypeus. Test thin,
with pillars like early Cycloclypeus spp.
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
40
Remarks - Besides these forms a lot of other Heterostegina species are known in different
regions of the world.
Subgenera
Cycloclypeus s. str.: smooth Radiocycloclypeus with radii
Katacycloclypeus with one., two or more annuli
Evolution
Ontogeny: 3 stages
- Embryonic stage : (Proto + Deuteroconch)
- Nepionic stage (spirally arranged chambers)
a) Operculina substage : (chambers not yet divided)
b) Heterostegina substage : (chambers divided)
- Neanic stage : cyclically arranged chambers.
Phylogeny :
Good example for the biogenetic law of Haeckel: Operculina - Heterostegina - Cycloclypeus
immediate ancestral forms.
H. bantamensis (without umbonal pillar) to C. oppenoorthi
H. praecursor (with umbonal pillar) to C. koolhoveni .
general trends :
- reduction of Heterostegina like arranged chambers
- size of proloculus increasing
- development of forms without pillars
- chamber walls become thicker, multilayered (axial section).
Species determination
Three main criteria: - surface features
- number nepionic whorls
- number of nepionic septa
Species see "determination table for Cycloclypeuis”
Evolution
Most probably polyphyletic out of Heterostegina. Eocene Spiroclypeus spp. evolve from
another Heterostegina group than Oligo-Miocene forms. Latter ones seem to have evolved
from Heterostegina borneensis.
Lateral chambers : two kinds
- subdivided alat prolongations
- chambers formed by cavities in the side walls (Spiroclypeus lateral chamber)
Species determination
S. vermicularis : characterized by lateral chambers of vermicular outline in tangential section,
pustulate.
S. pleurocentralis : very small and thin oval form. Umbo lies very strongly exentrically. Thick
lateral walls., few and long, irregular lateral chambers, pustulate Synonym S. yabei
S. tidoenganensis-: larger than S pleurocentralis, more lateral chambers, less flattened,
pustulate.
S. margaritatus: round form, lateral, chambers becoming shorter. Intermediate form to
reticulate forms.
S. leupodi : reticulate, smaller than 2 cm, round. Lateral chambers are uniform in shape and
size. Synonym : S. wolfgangi, S,. higginsi ?
S. orbitoideus: reticulate, largest Spiroclypeus, up to 4 cm. These forms bear considerable
resemblance to Lepidocyclina.
Remarks
Genera Asterocyclina and Aktinocyclina
belong to the same family and are closely
related to the genus Discocyclina.
Aktinocyclina : radial ribs formed by lateral
chambers, only one layer of equatorial
chambers,pl-13.
Asterocyclina : radial ribs are formed by
multilayered equatorial chambers, pl-13.
Species determination
Complicated as a number of different
description of the same species exist. The
following features are important to identify
a species
- macrosperic embryonic apparatus
- equatorial chambers (size arrangement)
Some authors consider this classification as unsuitable and showed that the arrangement of
protoconch and deuteroconch was not strictly constant within one species. It is however,
still customary to speak of Lepidocyclina with nephrolepidine, trybliolepidine etc. embryonic
apparatus.
Evolution
Ontogeny: very similar to Miogypsina, 3 stages:
- embryonic apparatus
- nepionic stage
- neanic stage (equatorial chambers)
Neanic stage equatorial chambers are of different shapes: lozenge, arcuate ogival spatulate,,
hexagonal, depending on stolon system Pl-14. It is even possible that one species has two
different stolonsystems and therefore different kinds of equatorial chambers.
Species determination
One method to get the relative age of Lepidocyclina method by van der Vlerk (1968) using
the degree of curvature, pl-14 (only for nephro lepidine forms suitable; proved in E.Java,
Madura and elsewhere.
After Adams (1970) not suitable in N. Kalimantan. Some easily recognizable species:
Nephrolepidine-forms :
L.(N.) isolepidinoides: small forms, often with small pillars. Equal to subequal embryonic
chambers. Wall between Protoconch and Deuteroconch straight to almost straight.
Polygonal arrangement of equatorial chambers.
L.(N.) parva : like L. isolepiainoides but distinctly nephro-, lepidine and larger.
L. (N) borneensis resembles L. perva but is almost twice as large. Equatorial chambers
cyclically arranged. Some larger nepionic chambers around the embryonic apparatus
are present, showing a tendency towards pliolepidine forms, pl..14.
L. (N.) tournoueri : is exactly the same f om, but does not show the larger embryonic
chambers.
L. (N.) inflata (A-form)/L.acuta (B-fom) One large pillar in the center. Earliest forms small
and thin more evolved ones thicker and larger.
L. (N. ) angulosa : Several pillars arranged around the center. L. (N.) verrucosa is here
considered as younger synonym. The latter may shows more curved roofs of the lateral
chambers in axial sections. L. ( N.) verbeeki belongs to this group, too. However, it is
much flatter.
L. (N.) ferreroi : 3-6 eccentrically arranged pillars in the corners of the polygonal test. No
pillars in the center.
L. (N. ) crucifera : four rays with pillars, ranging from the border to the center of the test.
L.(N.) sumatrensis (A-fom)/L. dekroesi (B-form) form with subglobose central boss and small
peripheral flanges, pl. 14. There are 3 types
L.(N.) sumstrensis inornata
L.(N.) sumetrensis minor
L. (N) , sumtrensis umbilicata
L.(N.) minor is smaller than L. (N) inornata These forms show often a slight tendency to get
pillars at the surface.
L.(N.) morgani : exactly the same as the sumatrensis group but with very strong pillars all
over the surface,pl.14.
L.(N.) flexuosa :border often with flexuosa peripheral flange. Numerous thick pustules
regulary distributed over the whole surface. Large form, microspheric.
Eulepidine forms
L. (E.) dilatata : large form (3-4 cm) , with polygonal pillars and polygonal net-work on the
surface and in tangential section. Equatorial chambers cyclically arranged and
hexagonal or spatulate. A - and B
L.(E.) formosa : Synonyms: (E.) ephippioides; (E.) weberi; (E.) undosa; (E.) richthofeni; (E.)
planata : no pillars, swollen to saddle shaped central boss., often even flat, equatorial
section shows often hyperbolical shape. Wall masses dense, lateral chambers round
in a tangential section, pl-1,4.
L.(E.) papuaensis : with pillars like (E.) diletata but less thick chamber wells
Wall thickness of Deuteroconch:
papuaensis dilatata
70 u 190 u
Thickness of roofs of lateral chambers
papuaensis dilatata 1
15 u 50 - 70 u
Trybliolepidine forms
L.(T. ) rutteni : largest T., often with small pillars. very loose network of lateral chambers at
the surface,
L.(T.) radiata : like (T.) rutteni but stellate. L. (T.) rutteni stellata is here considered as a
younger synonym. L. (N.) martini seems to be the nephrolepidine ancestral form of L.
(T.) radiate. The nomenclature of eulepidine and pliolepidine stellate forms is still
doubtful.
L. (T.) orientalis : small form., occasionally pillars.Relatively large embryonic apparatus, pl.
14. L. (T.) talahabensis is here considered as younger synonym.
Pliolepidine forms :
These forms show a large embryont surrounded by a thick wall enclosing one large chamber
and from four to ten smaller peripheral chambers, the wall between which are relatively thin.
This group derives most probably from a form like L.(N.) borneensis.
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
42
L.(P) irregularis: very irregular axial outline. L.(P.) fijiensis is a younger synonym.
L. (P. ) luxurians no pillars
L. (P.) stigteri with pillars
Subgenera:
Miogypsina s.str : with lateral chambers embryonic apparatus completely eccentrically
situated
Miogypsinoides Yabe.& Hanzawa : as Miogyptina but without lateral chambers
Miolepidocyclina Silvestri : embryonic apparatus not completely eccentrically situated
Evolution:
Ontogeny 3 different stages: 1. Embryonic stage (Protoconch + Deuteroconch)
2. Nepionic stage (peri-embryonic chambers)
3. Neanic stage (equatorial chambers)
Remarks: Microspheric forms are very rare, they seem to follow the same evolutionary
trends, which are hardly visible, however.
Species:
complanata and borneensis-type after Another method for the determination of
number of spirally arranged chambers. Miogypsina s.str was, worked out by
For Ms. and for M. valid Drooger and consists in measuring the
Ms. complanatus 25 - 17 degree of symeetry of both protoconchal
Ms. formosensis 17 - 13 nepionic spirals.
Ms. bantamensis 13 - 10
Ms. dehaarti less than 10 Remarks :- In the borneensis-type group
M. borneensis 7-9 intermediate forms between
M. thecideaeformis Rutten about 5 Miogypsiza and Mioypsinoides
can be found. e.g. Miogypsina
ecuadorensis-type: M. bispiralis (former primitive; Miogypsinoides
M. kotoi var. bispiralis) primitive , both names can be
bifida - type : 2-3 spirals : M. kotoi found in publications
(including M. kotoi var. digitata) - Size and pillars of the forms
indonesiensis-type M. indonesiensis With depend mainly on environment.
very advanced s-)iral-s and large pillars Forms in turbulent water
:M.tuberosa develop stronger pillars.
Evolution
Deriving from Assilina by thickening of the walls
Species determination
7 easily recognizable species in axial section:
,Pellatispira madaraszi Spirally arranged form might represent the end form of
pillars forming a distinct ridge. the Pellatispira evolution.
P.orbitoidea fFat, lenticular, sharp edges in P.crassicolumnata Very thick pillars, thin
axial outline radial canals. Often intemediate forms
R. rutteni Cone shaped pillars, strongly to P. rutteni and P. provalei.
developed on surface. Embryonic
apparatus often very large. 6.11 Genus Biplanispira Umbgrove,
P. inflata Very thick form, ratio 3 2 to 1 no 1937
edges, rounded axia 1 outline. Like Pellatispira, secondary chambers are
P . glabra like P. inflata but with pillars. formed in the adult stage. They are
P.irregularis Very irregular form concerning arranged. in.two layers,
internal features, and external Evolution
features, canals irregular, too. This Ontogeny: 2 stages,
-Pellatispira stage
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
44
-Biplanispira stage
Phylogeny
out of Pellatispira
Species determination
Only by using shape of axial outline, see
bellow. There are many intermediate forms.
Phylogeny
polyphyletic, very complicated. still doubtful. Relationship to Miliolidae, still visible in early
ontogenic stage of B-forms
General trends:
small to large
round to long
regular to'irregular
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
44
Species determination
Only in two sections possible: equatorial section and axial section (more specific characters)
Almost 100 different species are known with different stratigraphical distribution These forms
are not yet very important for the stratigraphy in Indonesia.
Evolution
Ontogeny : similar to Fasciolites
Phylogeny: not well known
Species determination
Borelis pygmaeus cigar shaped
B. melo : small spherical form
B. pulchrus : cigar shaped (Pleistocene -
Recent)
Cigar shaped, long. Only one canal is present (preseptal canal). External apertures are
arranged in three rows, but may increase to five near the poles. Secondary chamberlets
(attics) above the primary chambers. Septula are arranged continuously.
Evolution
Out of Flosculinella. Intermediate formwas formerly called. Alveolinella borneensis or-
Flosculinella borneensis. It might be a younger synonym of A. fennemai .
Species determination
The genus may be represented by only one valid species A. quoyi, A. borneensis, A.
fennemai as mentioned early representatives of Alveolinella have never been described or
figured sufficiently.
Evolution
Ontogeny : first quinqueloculine later
triloculine. Microspheric forms have more
chambers.
Wall consists of two parts :
- relatively thick inner layer with alveoli
(blind ending cavities)
- a very thin, non alveolate outer skin
which is pitted externally
This skin is very delicate and therefore
often lost.
Species determination
Based on the arrangement and shape of the alveoli. In Indonesia., three different species
were found. A. striata and A. howchini which are frequent, and A. asmariensis which is rather
rare.
A. striata : simple alveolip widely spaced, 6-10 in the last chamber (equatorial section)
A.asmariensis : simple alveoli, closely spaced, 15-20 in the last chamber (equatorial section)
A. howchini : complex alveoli
Remarks : a lot of intermediate forms of these species can be found.
Evolution
Ontogeny: similar to Lepidocyclina, 3 stages
1. Embryonic apparatus (Protoconch and Deuteroconch)
2. Nepionic chambers
3. Neanic chambers: imbricate and radially arranged
Phylogeny: doubtful.
Species determination
two different forms are known in the Indo-Pacific region
H. minima without pillars
H. bikinensis : with pillars and thick walls
Baculogypsina spaerulata
Asterorotalia pulchella gr.
Calcarina spengleri
Cycloclypeous spp.
Lepidocyclina (N) spp.
Lepidocyclina (T) radiata
Lepidocyclina (N) ferreroi
Lepidocyclina (N) inflata
Lepidocyclina (N) sumatraensis
Katacycloclypeous anulatus
Austrorillina spp.
Austrorillina howchini
Borelis melo melo
Miogypsna spp.
Flosculinella spp.
Flosculinella bontangesis
Cycloclypeous eidae
Miogypsinoides spp.
Flosculinella globulosa
Spiroclypeous spp.
Lepidocyclina (E) spp.
Borelis pygmeous
Austrotrillina sriata
Austrotrillina asmariensis
Pararotalia mecatepecennsis
Heterostegina borneensiss
Pellatispira spp.
Biplanispira spp.
Discocyclina spp.
Asterocyclina spp.
Alveolina spp.
Assilina spp.
Praealveolina spp.
Subalveolina spp.
Ovalvulina spp.
18. Mature shell larger, inflated fusiform to subcylindrical, composed 14-22 volutions, 9-15
mm long and 3-8 mm wide. Spirotheca very thin. Septula bar-shaped to somewhat
pendant-shape, 2 or 3 axial septula present in inner volutions, 3-5 in outer volutions, 1 or
2 secondary traverse septula present. Parachomata very small .........................
Lepidolina
19. Keriotheca present .............................................................. ...................... see 20
absent ................................................................ ...................... see 29
20. Septa fluting limited to axia 1 region .................................... ...................... see 21
more or lest intense throught volution ............. ...................... see 24
21. Shell smal to medium, fussiform ......................................... ...................... see 22
medium to large, subsphaerical ................................ ...................... see 23
22. Mature shell, composed 5-10 volutions, 3-10 mm long and 2-5 mm wide. Proloculus
small, shell expanded slowly. Septa fluted weakly in axial region. Chomata developed
strongly, but replaced by Pseudochomata sometimes in outer volution ........
Triticites
23. Mature shell highly inflated fusiform to sphaerical, composed 6-8 volutions, 8-15 mm
long and 6-14 mm wide. Proloculus small, inner 2 or 3 volutions coiled tightly, following
expanded rapidly. Septa fluted weakly in axial region. Chomata distict only in inner
volution.. .................................................................................. Pseudoschwagerina
24. Septa fluted widely and irregulary ........................................ ...................... see 25
narrowly and highly ......................................... ...................... see 26
25. Mature shell medium to large, inflated to elongated fusiform, composed 5-8 volutions, 6-
15 mm long and 3-6 mm wide. Proloculus moderate to larger, shell colied rather slowly.
Chomata indistinct, replaced by pseudochomata in outer volution ................ .......
Pseudofusulina
26. Shell small to medium, fusiform ............................................ ...................... see 27
medium to large, subcylindrical .................................. ...................... see 28
27. Mature shell more or lest inflated fusiform, composed 6-9 volutions, 5-11 mm long and
3-5 mm wide. Proloculus small, shell expanded rather slowly. Spirotheca relatively thin.
Septa fluted regulary and highly. Chomata usualy indistinct replaced by pseudochomata
in outer volution.......... ............................................................. ......... Schwagerina
28. Mature shell elongated fusiform to cylindrycal, large in size. Proloculus medium to larger,
shell expanded rather rapidly. Spirotheca thin. Septa fluted highly and regulary. Chomata
indisstinct in almost all volution ............................................. .............Parafusulina
29. Diaphanotheca absent ......................................................... ...................... see 30
present ........................................................ ...................... see 33
30. Shell rhomboidal to sperical ................................................ ...................... see 31
ellipsoidal to fusiform .................................................. ...................... see 32
31. Mature shell minute, provided with umbilicated axial region and short of coiling,
composed 4-7 volutions, 0.5-2 mm long and wide. Spirotheca composed of tectum and
tectoria. Septa unfluted. Chomata heavy, hallf-circular to ribbon-likke . ........ ..........
Pseudostaffela
32. Mature shell small, composed of 4-7 volutions. 1-3 mm long and 0.5-2 mm wide.
Proloculus minute to small, inner 1 or 2 volutions usually umbilicated. Spirotheca thin.
composed of tectum and tectoria, but diaphanotheca sometimes seen in outer volutions.
Chomata formed strongly .......................................................Profusulinella
33. Septa fluted only in axial regions ............................................................ . .... see 34
throughout volution ........................................................ . .... see 35
34 Mature shell small to medium, elipsoidal to fusiform, composed of 6-9 volutions, 1.5-4.5
mm long and 0.5-3.5 mm wide. Proloculus small to moderate. Diaphanotheca observed
clearly in outer volutions.. Septa fluted usually only in axial regions.. Chomata heavy,
gradually decreasing in development from middle to outer volutions .......Fusulinella
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
59
Dalam suatu analisa foram untuk menginterpretasi umur dan lingkungan pengendapan suatu
sampel, memerlukan data genus maupun species yang sudah diidentifikasi/dianalisa. Ada
beberapa macam metoda analisa:
a. analisa kualitatif : hanya mencatat suatu taxon ada atau tidak
b. analisa semi kualitatif: mencatat hasil pengamatan dalam interval tertentu dan
direpresentasikan dengan simbol tertentu (misal: 1-3= jarang (o), 4-10 = sedikit (+), 11-
25=banyak (I), > 25 = melimpah (IIII)).
c. analisa kuantitatif: disini semua kehadiran fosil diidentifikasi dan masing-masing taxon
dihitung jumlahnya. Ada beberapa cara/teknik dalam analisa kuantitatif yang bisa
digunakan dalam menghitung jumlah fosil, misal dengan membagi sampel dengan
microspliter atau dengan menggunakan menggunakan tray yang ada grit-nya.
Perhitungan bisa dilakukan secara absolut (dihitung jumlah riilnya) atau menggunakan
teknik hitungan 300 (sampel di bagi-bagi sampai kira-kira jumlahnya 300, dan jumlah
tersebutlah yang dihitung secara riil.
Penentuan macam analisa mana yang dipakai tergantung dari tujuan kita menganalisa
sampel tersebut. Bila hanya untuk menentukan umur maka analisa bisa secara kualitatif,
tetapi bila kita ingin juga menentukan lingkungan pengendapan maka setidaknya analisa
harus semi-kuantitatif. Untuk keperluan tertentu misalnya dalam studi event stratigraphy,
sikuen stratigrafi maka cara terbaik adalah dengan analisa kuantitatif.
Setelah selesai diidentifikasi biasanya taxa dikelompokan paling tidak dalam dua kelompok
yaitu plangton dan bentos, tetapi yang lebih umum terutama di dunia industri adalah
mengelompokan dalam 5 kelompok foram yaitu plangton, calcareous bentonik, miliolid,
foram besar, arenaceous dan dan 1 kelompok non foram.
Meskipun tidak ada cara penyajian data yang baku tetapi beberapa contoh berikut ini yang
sering dipakai.
O + I o o o o +
o + + o + o +
o o o o + I + o o o
+ + o o +
o o o + +
Penyajian data dari hasil analisa semi-kuantitatif dari data field sample atau outcrop
Secara garis besar ada tiga metoda dalam penentuan umur, dimana m etoda yang digunakan
tergantung dari jenis contoh yang dianalisa.
1. single sample (bisa Cutting atau outcrop Sampel.)
penentuan umur diperoleh dengan cara mencari overlap antara FAD dan LAD taxon2
tertentu (marker). pada outcrop: Problem yang mungkin ditemui adalah adanya fosil
rombakan. Fosil rombakan akan dikenali dari LAD-nya yang relatif lebih tua dari FAD marker.
(lihat gambar). sedangakan pada dicth cutting: penentuan umur lebih sulit, biasanya batas
atasnya ditentukan dari LAD marker yang paling tua. Tetapi hal ini akan sulit bila kita juga
menemui adanya fosil rombakan. Analisa biofacies akan sangat membantu dalam
menginterpretasi umurnya.
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A P B S P O G G P G G G G G C G G G G G G G B
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N 17
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Bila sampel A merupakan sampel lapangan atau core atau SWC, maka umur sampel
tersebut adalah N12, dengan demikian kehadiran Globorotalia. archeomenardii dan Gr.
peripheroronda adalah sebagai fosil rombakan. Sedangkan bila sampel A adalah sampel
jenis ditch cutting maka umurnya adalah tidak lebih muda dari N 10 (LAD dari Gr.
archeomenardii).
BIOSTRATIGRAFI
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N - H 3 Globorotalia tosaensis toenuitheca
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2: Zona Globorotalia tosaensis tosaensis dan/atau lebih muda
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a. Quantitative: Species diversity (i.e. alpha index), M-R-T Ternary diagram, similarity,
dominance:
Agglutinated foraminifera can be classified into four morphogroups and these have a
distinctive distribution in modern environments:
Berikut ini adalah penjelasan singkat, sebagai dasar dalam menginterpretasi lingkungan
pengendapan beradasarkan asosiasi formainiferanya (diambil dari Rawenda dkk, 1983.
Robertson Research Indonesia)
Studies of recent foraminiferal ecology have provided numerous distinct criteria by which
many depositional environments can be characterised and which can be applied to fossil
assemblages from sedimentary rocks. Some of the main variables can be summarised as
follows:
1. The total number of species and of individuals increases away from the shoreline,
and with increasing depth of water, to maximum values on the outer shelf and in
the upper bathyal zone.
2. Porcelaneous forms show their present diversity in shallow, nearshore
environments.
3. Arenaceous foraminifers with simple interior wall structure become dominant in
shallow waters or in intertidal areas. The percentage occurrence of these
arenaceous forms reaches a maximum near the effluence of rivers.
4. Calcareous foraminiferal tests become smaller and thinner near sources of fresh
water. In carbonate rich environments, tests may reach a large size and be very
robust.
5. The percentage occurrence of the most common species in a foraminiferal
population relates to the variability of the environment. As marginal marine
conditions are approached, environmental parameters become more pronounced
resulting in a tendency towards single species dominance in the most
unfavourable environments.
6. Planktonic forms occur most abundantly within the outer shelf and deeper water.
Under ideal sedimentation contitions, especially in clastic deposit, planktonic
foraminifers can show a more or less regular increase in abundance with depth.
7. Arenaceous taxa with labyrinthic wall structures occurs most abundantly in
bathyal or deeper waters. In sediments deposited below the calcium carbonate
compensation depth (CCD) these forms may become dominant since the
calcareous shells of other foraminifers are dissolved.
Fossil sandy beaches can be recognised by poorly preserved abraded specimens. However,
due to continuous transport of the tests after death many small or thin-shelled specimens
may be destroyed, and foraminifers are sometimes completely absent from an exposed
beach sand. A further complication in determining an ancient sandy beach is, that many
alochnous forms may have been washed in.
Species diversity is highest in hyposaline marshes, although the general diversity is low. The
hyposaline marshes are characterised by the predominance of arenaceous species
(Miliammina sp., Ammotiurn sp., Trochammina inflata) and rotalids (Elphidium spp.) and the
absence of miliolids.
Normal marine marshes are inhabited by dominantly arenaceous species with minor miliolids
(Quinqueloculina) and rotalids (Elphidium spp., Ammonia beccarii).
In hypersaline marshes the percentage of arenaceous species, miliolids and rotalids is about
equal. Typical cosmopolitan marsh species are:
Ammotium salsum
Areno parrella mexicana
Miliammina fusca
Trochammina macrescens
T. polystoma
The lithology of a marsh deposit consists of dark grey highly organic clay and silt, containing
abundant roots and other in determining an ancient plant debris. This can often help marsh
deposit. Pyrite is common, due to the reducing conditions.
Haplophragmoides salsun
Haplophragmoides wilberti
Miliammina pariaensis
Arenoparella mexicana
Trochammina laevigata
Rotalids predominate in tidal flat assemblages, miliolids are rare to absent, and arenaceous
species not common.
2d. Estuaries
An estuary is the wide mouth of a river or arm of.the sea where the tide meets the river
currents, or flows and ebbs.
Estuaries are hyposaline in character, and can be subdivided into an upper part, subject to
the greatest freshwater influence and a lower part connected with the sea. This differences
in salinity is reflectedinthe faunas of both parts:
2e. Lagoons
A lagoon is a shallow lake or sheet of water, connected with the sea or a river. Coastal
lagoons are shallow water bodies, running parallel to the coast, and connected to the sea
with an outlet. They are separated from the sea by sand bars or barrier islands.
Based on the amount of seawater entering through the inlet, and the amount of freshwater
contributed by river, the following subdivision of lagoons can be made:
2f. Deltas
With respect to foraminiferal assemblages deltas require special comments since in these
environments certain species behave abnormally,especially within the prodelta region.
C) Prodelta
The prodelta consists -of the smooth, steep slope seaward of the edge of the delta front
platform, marked by an abrupt slope break at the 5 meter isobath. The outer limit of the
prodelta appears to coincide with the 60-70m,isobath.
It is important to mention the "delta effect" (e.g. Pflum & Frerichs, 1976), that is,a variable
upper depth limit of certain species. They call these species heterobathyal species, as
opposed to isobathyal species (which have a more or less consistant upper depth limit). It
is possible to distinguish delta elevated and delta depressed species. Delta elevated species
are species with a shallower upper depth limit in the delta area. (For instance Sigmoilopsis
schlwnbergeri and Martinotiella occidentalis). Delta depressed species have a lower upper
depth limit in a delta area. Examples are Pullenia quinqueloba, Melonls barleeanus,
Hoglundina elegans and Bulimina aculeata.
3. Marine Environments
A widely used tool for distinguishin- marine environments is the planktonic/benthonic ratio.
In general it is believed that increasindepth will imply an increase in the percentage of
planktonic species. The system was developed initially by Grimsdale and van Morkhoven
(1955) who found that it lacked the precision that they had hoped for. They suggested the
following relationship:
Bearing these points in mind, and also noting the distribution of calcareous benthonic,
arenaceous and larger foraminifers the following marine environments may be characterised:
3a.Inner Shelf (low tide -20m) inner neritic, shallow inner sublittoral.
This environment has its lower boundary at the base of the turbulent zone. Within this depth
range many sub-environments can be recognised, depending on wave energy, substratum
etc., and hence many different populations can be found. Characteristic for inner shelf
environments is the low species diversity, with one or two species dominating the faunas.
Planktonic foraminifers may occur in frequencies of 0-20%. Larger foraminifera such as
Operculina and Amphistegina may be locally abundant, other forms may be abundant only
in carbonate sediments.
The following taxa are typical of inner shelf environments. It must be stressed that this is not
a complete list and that the taxa indicated are not restricted to this environment.
Southeast Asia
Planorbulinella sp. Chrysalidinella limbatum
Massilina sp. Asterorotatia spp.
Cibicides tobatulus Cymbaloporetta squamosa
Pseudorotatia spp. Bacutogypsina sphaerulata
Cellan thus craticulatus Amphistegina lessonii
Loxostom limbatum Ammonia spp.
Elphidium spp.
Planktonic foraminifers can make up 20-30% of the total assemblages, but their diversity is
low, and restricted to forms such as Globigerinoides spp. and Globigerina bulloides.
The lower boundary of this zone is the shelf edge. The species diversity in this environment
is high. Planktonic foraminifera make up to 40-80% of the total assemblages and their
diversity is high (moreless 20 species in recent samples). Larger foraiainifera are absent.
Most of the calcareous benthic species of the deep middle shelf are present.
Species diversity and abundance is usually very high in this environment. The planktonic
percentage increases to 50-95%. Robust arenaceous species such as Martinotiella
comminis, Karreriella sp., Tritaxilina sp., Dorothia and Haplophragmoides sp. occur
frequently.
Isobathyal (-cosmopolitan) species with their highest depth limit within zone are as follows:
Bolivina albatrossi
Bulimina striate mexicana ) highest
Chilostomell,a oozina ) occurrence
Eponides reguza ) at 200m
Gyroidina altiformis cushmani )
Discorbis transluucens
Uvigerina peregrina
Bulimina acuzeala
Bulimina rostrata alazanensis ) highest
Osangularia rugosa ) occurrence
Uvigerina peregrina dirupta ) at 300m
Uvigerina peregrina mediterranea
Cibicides kullenbergi )
Cibicides rugosus )
Eponides polilus ) highest
Oriidorsalis tener umbonatus ) occurrence
Osangularia culter ) at 700 - 800 m
Pleurostomella bolivinoides )
Isobathyal (cosmopolitan) species with their highest'depth limit within zone are as follows:
Assemblages from this depth are generally rare and little-diverse. The calcium carbonate
compensation level (40OOm-5500m) causes the solution of calcareous tests below this
depth. Consequently, the faunas below 4000-5500m, will consist of large, simple arenaceous
species such as Ammodiscus sp., Rhabdamina sp. and Rathysiphon sp.
Above the calcium carbonate compensation level the calcarous benthic fauna from the
bathyal environments, and thick walled, solution resistant planktonics ( Sphaeroidinellopsis
sp., Globorotalia spp.) are still present.
15. NON-FORAM
A. MIKROFOSIL NON FORAM
(some part taken from: Pamela J. W. Gore Department of Geology, Georgia Perimeter
College Clarkston, GA 30021)
15.1 . PROTISTS (unicellular organisms)
A. Animal-like protists
RADIOLARIA
Geologic range: Cambrian to Recent
Shell composition: Silica (amorphous, opaline silica)
Size: 0.1 - 2.0 mm
Significance: Useful in biostratigraphy; they accumulate to form
radiolarian ooze on the abyssal plain.
Morphology: Microscopic spiny globes with large, lace-like pores, or
helmet-shaped (or space-ship shaped) with large, lace-like pores.
Very transparent and glassy.
Environment: Marine only; planktonic.
Radiolaria
B. Plant-like protists
1. DIATOMS
Geologic range: Cretaceous to Recent
Shell composition: Silica
Size: Most are 0.05 - 0.02 mm (some up to 1 mm)
Significance: Useful in biostratigraphy and paleoenvironmental
interpretation; major constituent of diatomite or diatomaceous
earth; an integral part of the food chain (phytoplankton). Most
abundant phytoplankton in the modern ocean.
Morphology: "Pillbox" shape, consisting of two valves (shells) which
may be circular, triangular, or elongate. Circular forms have radial
ornamentation. Elongate forms have transverse markings. They
are covered with pores.
Environment: Both marine and non-marine. Planktonic or attached.
Diatoms
Ostracodes
2. CONODONTS (Phylum unknown)
Geologic range: Cambrian to Late Triassic. Conodonts are extinct,
and the organism from which they came is not known with
certainty.
Composition: Phosphate (calcium fluorapatite)
Size: Most are 0.5 - 1.5 mm (some up to 10 mm, and some as
small as 0.1 mm)
Significance: Useful in biostratigraphy and marine
paleoenvironmental interpretation; their color is a good indicator
of the temperature to which the enclosing rock has been
subjected (this is important in determining whether oil or gas
may be present in the rock).
Morphology: Parts of a larger organism which resemble cone-
shaped teeth, or consisting of bars with rows of tooth-like
denticles, or irregular knobby plates called platforms.
Environment: Marine, free-swimming.
Conodonts
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999
66
Sponge spicules
B. OTHER FOSSILS
15.8 Sepulid
15.9 Pteropod/Gastropod
15.10 Otolith
15.11 Fish teeth
Dirangkum oleh: Khoiril Anwar M
Lab. Mikropaleontologi, Jurusan Teknik Geologi ITB
1999