Culturing Photeros annecohenae - Revision history

128.111.227.119: /* Notes on culture and signals */

2016-03-04T18:00:28Z

‎Notes on culture and signals

128.111.227.119: /* Notes on culture and signals */

2016-03-04T17:59:11Z

‎Notes on culture and signals

128.111.227.158: /* Notes on culture and signals */

2016-02-29T20:59:22Z

‎Notes on culture and signals

128.111.227.119: /* Notes on culture and signals */

2016-02-29T20:55:58Z

‎Notes on culture and signals

128.111.227.119: /* Notes on culture and signals */

2016-02-29T20:48:51Z

‎Notes on culture and signals

128.111.227.119: /* Notes on culture and signals */

2016-02-29T20:41:49Z

‎Notes on culture and signals

128.111.227.119: /* Notes on culture and signals */

2016-02-24T18:11:44Z

‎Notes on culture and signals

128.111.227.119: /* Notes on culture and signals */

2016-02-24T17:56:05Z

‎Notes on culture and signals

128.111.227.119: /* Notes on culture and signals */

2016-02-24T17:55:07Z

‎Notes on culture and signals

128.111.227.119: /* Notes on signals */

2016-02-24T17:54:33Z

‎Notes on signals

← Older revision		Revision as of 18:00, 4 March 2016
Line 32:		Line 32:

	* '''Monday February 29''' - Saw no signals in ~10 minutes from 5:00-5:10. Now, Kessil lights are on, which are leaking a bit into dark room. Their timing may have changed.		* '''Monday February 29''' - Saw no signals in ~10 minutes from 5:00-5:10. Now, Kessil lights are on, which are leaking a bit into dark room. Their timing may have changed.
		+
		+	* '''Thursday May 3''' - Copepods seem less numerous. Cyanobacteria (red) is growing a lot. Might be that leaving excess food in tank is changing chemistry. WIll try to remove food after feeding.

← Older revision		Revision as of 17:59, 4 March 2016
Line 30:		Line 30:

	* '''Sunday February 28''' - Saw 1 signal after cueing. Only watched for ~10 minutes from 6:30-6:40.		* '''Sunday February 28''' - Saw 1 signal after cueing. Only watched for ~10 minutes from 6:30-6:40.
		+
		+	* '''Monday February 29''' - Saw no signals in ~10 minutes from 5:00-5:10. Now, Kessil lights are on, which are leaking a bit into dark room. Their timing may have changed.

@@ Line 27: / Line 27: @@
 * '''Friday February 26''' - Did not see signals this day, but came in later (~8:30 pm)
-* '''Saturday February 27''' - Saw several signal after cuing. Only watched for ~10 minutes. Signals were at ~6:00pm. Then turned on lights to check aquarium and feed. At 6:30, checked with Natasha for signals, but saw none.
+* '''Saturday February 27''' - Saw several signal after cueing. Only watched for ~10 minutes. Signals were at ~6:00pm. Then turned on lights to check aquarium and feed. At 6:30, checked with Natasha for signals, but saw none.
-* '''Sunday February 28''' - Saw 1 signal after cuing. Only watched for ~10 minutes from 6:30-6:40.
+* '''Sunday February 28''' - Saw 1 signal after cueing. Only watched for ~10 minutes from 6:30-6:40.

← Older revision		Revision as of 20:55, 29 February 2016
Line 20:		Line 20:

	* '''Monday February 15''' - Checked for signals with Craig and Craig (aquarium guys). Saw 1-2 constant glowing ostracods, but no signals.		* '''Monday February 15''' - Checked for signals with Craig and Craig (aquarium guys). Saw 1-2 constant glowing ostracods, but no signals.
		+
		+	* '''Monday February 22''' - Day after full moon saw first signal in about a week.
		+
		+	* '''Tuesday February 23''' - Saw some signals again
		+
		+	* '''Friday February 26''' - Did not see signals this day, but came in later (~8:30 pm)
		+
		+	* '''Saturday February 27''' - Saw several signal after cuing. Only watched for ~10 minutes. Signals were at ~6:00pm. Then turned on lights to check aquarium and feed. At 6:30, checked with Natasha for signals, but saw none.
		+
		+	* '''Sunday February 28''' - Saw 1 signal after cuing. Only watched for ~10 minutes from 6:30-6:40.

@@ Line 15: / Line 15: @@
 * '''Saturday February 3''' - Saw ''signals'' for the first time. With prospective student Sarah Solie and visiting student John Kirwan, we viewed the aquarium after the graduate student symposium dinner. At about 10 pm, we saw multiple vertical displays.
 * '''Through February 13''' - Saw signals on multiple days after lights out. Each time I looked, I saw signals.
 * '''Monday February 15''' - Checked for signals with Craig and Craig (aquarium guys). Saw 1-2 constant glowing ostracods, but no signals.

← Older revision		Revision as of 20:41, 29 February 2016
Line 14:		Line 14:

	* '''Saturday February 3''' - Saw ''signals'' for the first time. With prospective student Sarah Solie and visiting student John Kirwan, we viewed the aquarium after the graduate student symposium dinner. At about 10 pm, we saw multiple vertical displays.		* '''Saturday February 3''' - Saw ''signals'' for the first time. With prospective student Sarah Solie and visiting student John Kirwan, we viewed the aquarium after the graduate student symposium dinner. At about 10 pm, we saw multiple vertical displays.
		+
		+
		+	* '''Through February 13''' - Saw signals on multiple days after lights out. Each time I looked, I saw signals.
		+
		+	* '''Monday February 15''' - Checked for signals with Craig and Craig (aquarium guys). Saw 1-2 constant glowing ostracods, but no signals.

← Older revision		Revision as of 18:11, 24 February 2016
Line 11:		Line 11:
	* '''Tuesday February 2''' - At KU in incubator. Trevor and Todd went through individuals to clean up tubes and culture dishes. We did not notice any parasites, but also did not look particularly carefully.		* '''Tuesday February 2''' - At KU in incubator. Trevor and Todd went through individuals to clean up tubes and culture dishes. We did not notice any parasites, but also did not look particularly carefully.

−	* '''Wednesday February 3''' - Todd took ostracods in 50 ml ~~conicals~~ from KU to UCSB. Kept them warm in inside coat pocket on the plane. Arrived fairly late to UCSB - put ostracods into 30 gallon aquarium with Belizean plants. Transferred ostracods by floating conical tubes in the water for ~30 minutes, then gradually mixing aquarium water.	+	* '''Wednesday February 3''' - Todd took ostracods in 50 ml conical tubes from KU to UCSB. Kept them warm in inside coat pocket on the plane. Arrived fairly late to UCSB - put ostracods into 30 gallon aquarium with Belizean plants. Transferred ostracods by floating conical tubes in the water for ~30 minutes, then gradually mixing aquarium water. The LED grow lights for the plants was set to 12:12 from about 6 am to 6 pm.
		+
		+	* '''Saturday February 3''' - Saw ''signals'' for the first time. With prospective student Sarah Solie and visiting student John Kirwan, we viewed the aquarium after the graduate student symposium dinner. At about 10 pm, we saw multiple vertical displays.

← Older revision		Revision as of 17:56, 24 February 2016
Line 1:		Line 1:
		+	= Thallassia bed notes =
		+
		+
	=Notes on culture and signals=		=Notes on culture and signals=
	* '''Saturday January 30''' - Trevor trapped animals at Carrie Bow, Belize. He placed them in 50 ml eppendorf tubes, and kept them warm in his pockets on the plane.		* '''Saturday January 30''' - Trevor trapped animals at Carrie Bow, Belize. He placed them in 50 ml eppendorf tubes, and kept them warm in his pockets on the plane.

@@ Line 1: / Line 1: @@
 =Notes on culture and signals=
-* Saturday January 30 - Trevor trapped animals at Carrie Bow, Belize. He placed them in 50 ml eppendorf tubes, and kept them warm in his pockets on the plane.
+* '''Saturday January 30''' - Trevor trapped animals at Carrie Bow, Belize. He placed them in 50 ml eppendorf tubes, and kept them warm in his pockets on the plane.
-* Sunday January 31 - Ostracods arrive in Kansas. Trevor kept them warm in bed over night!
+* '''Sunday January 31''' - Ostracods arrive in Kansas. Trevor kept them warm in bed over night!
-* Monday February 1 - Ostracods placed in culture plates in an incubator at KU. Water changed using Instant Ocean.
+* '''Monday February 1''' - Ostracods placed in culture plates in an incubator at KU. Water changed using Instant Ocean.
-* Tuesday February 2 - At KU in incubator. Trevor and Todd went through individuals to clean up tubes and culture dishes. We did not notice any parasites, but also did not look particularly carefully.
+* '''Tuesday February 2''' - At KU in incubator. Trevor and Todd went through individuals to clean up tubes and culture dishes. We did not notice any parasites, but also did not look particularly carefully.
-* Wednesday February 3 - Todd took ostracods in 50 ml conicals from KU to UCSB. Kept them warm in inside coat pocket on the plane. Arrived fairly late to UCSB - put ostracods into 30 gallon aquarium with Belizean plants. Transferred ostracods by floating conical tubes in the water for ~30 minutes, then gradually mixing aquarium water.
+* '''Wednesday February 3''' - Todd took ostracods in 50 ml conicals from KU to UCSB. Kept them warm in inside coat pocket on the plane. Arrived fairly late to UCSB - put ostracods into 30 gallon aquarium with Belizean plants. Transferred ostracods by floating conical tubes in the water for ~30 minutes, then gradually mixing aquarium water.

← Older revision		Revision as of 17:54, 24 February 2016
Line 1:		Line 1:
−	=Notes on signals=	+	=Notes on culture and signals=
		+	* Saturday January 30 - Trevor trapped animals at Carrie Bow, Belize. He placed them in 50 ml eppendorf tubes, and kept them warm in his pockets on the plane.
		+
		+	* Sunday January 31 - Ostracods arrive in Kansas. Trevor kept them warm in bed over night!
		+
		+	* Monday February 1 - Ostracods placed in culture plates in an incubator at KU. Water changed using Instant Ocean.
		+
		+	* Tuesday February 2 - At KU in incubator. Trevor and Todd went through individuals to clean up tubes and culture dishes. We did not notice any parasites, but also did not look particularly carefully.
		+
		+	* Wednesday February 3 - Todd took ostracods in 50 ml conicals from KU to UCSB. Kept them warm in inside coat pocket on the plane. Arrived fairly late to UCSB - put ostracods into 30 gallon aquarium with Belizean plants. Transferred ostracods by floating conical tubes in the water for ~30 minutes, then gradually mixing aquarium water.