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core  usr 

"76 3^  U  Southwestern  Pine  Tip  Moth  Damage 

to  Ponderosa  Pine  Reproduction 

v 


Abstract 


Lessard,  Gene,  and  Daniel  T.  Jennings. 

1976.  Southwestern  pine  tip  moth  damage  to  ponderosa  pine 
reproduction.  USDA  For.  Serv.  Res.  Pap.  RM-168,  8  p. 
Rocky  Mt.  For.  and  Range  Exp.  Stn.,  Fort  Collins,  Colo. 
80521. 

The  southwestern  pine  tip  moth  deforms  young  pines  by 
mining  growth  tips.  Deformities,  recognizable  several  years  after 
initial  attack,  are  categorized  as  prune,  crook,  fork,  posthorn, 
bush,  and  spiketop.  Combinations  of  deformities — crook/prune, 
bush/crook — are  prevalent  at  Chevelon,  Arizona. 

As  tree  height  increases,  tip  moth  damage  decreases. 
Deformities  causing  the  greatest  reduction  in  height  growth  also 
occur  most  frequently.  Only  7  percent  of  the  5,012  whorls 
examined  escaped  tip  moth  damage;  89  percent  had  a  signifi- 
cant height  growth  loss  of  from  13  to  40  percent. 

Keywords:  Pinus  ponderosa,  Rhyacionia  neomexicana.  insect 
damage. 


USDA  Forest  Service 
Research  Paper  RM-168 


May  1976 


ft  \?C^ 

Southwestern  Pine  Tip  Moth  Damage 
to  Ponderosa  Pine  Reproduction  ^ 

Gene  Lessard1  and  Daniel  T.  Jennings2 


Entomologist,  Division  of  State  and  Private  Forestry,  Southwestern  Region,  USDA  Forest 
Service,  Albuquerque,  New  Mexico. 
2 

Research  Entomologist,  Rocky  Mountain  Forest  and  Range  Experiment  Station,  located  at 
Station's  Research  Work  Unit  at  Albuquerque,  in  cooperation  with  University  of  New  Mexico; 
Station's  central  headquarters  is  maintained  at  Fort  Collins,  in  cooperation  with  Colorado  State 
University. 


Contents 


Page 


Introduction   1 

Methods  1 

Results  and  Discussion  3 

Types  of  Deformities   3 

Frequency  of  Deformities  6 

Effect  on  Tree  Growth   8 

Literature  Cited  8 


Southwestern  Pine  Tip  Moth  Damage 
to  Ponderosa  Pine  Reproduction 


Introduction 

Tip-  and  shoot-feeding  insects  damage  trees  by 
injuring  or  destroying  the  apical  meristems  or  new 
growth  centers.  One  such  insect,  the  southwestern 
pine  tip  moth  {Rhyacionia  neomexicana  (Dyar)), 
attacks  and  damages  ponderosa  pine  (Pinus  ponder- 
osa Laws.)  in  the  central  and  southern  Rockies, 
midwestern  Plains,  and  the  Southwest.  This  tip  moth 
and  related  species  are  important  pests  threatening 
the  establishment  and  growth  of  pine  reproduction. 

Larvae  of  R.  neomexicana  pass  through  five 
instars  and  have  three  distinctive  feeding  stages:  (1) 
a  needle-mining  stage  before  new  shoots  are  at- 
tacked, (2)  a  pitch-tent  stage  when  new  needles  on 
expanding  shoots  are  severed  and  mined,  and  (3)  a 
shoot-mining  stage  that  often  destroys  the  entire  new 
shoot  (Jennings  1975).  Both  terminal  and  lateral 
shoots  in  upper  and  midcrowns  of  young  pines  are 
susceptible  to  attack.  Destruction  of  these  shoots  not 
only  reduces  height  growth,  but  also  deforms  sub- 
sequent tree  growth  form. 

Damage  is  generally  greater  on  young  ponderosa 
pines  less  than  6  to  8  feet  tall.  Seedlings  less  than  1 
foot  in  height  may  be  attacked  the  same  year  they  are 
planted  (Jennings  1975).  Large,  open  areas  with 
numerous  small  trees,  such  as  naturally  seeded  or 
planted  burns,  seem  most  vulnerable  to  persistent 
infestations. 

Working  with  the  related  European  pine  shoot 
moth,  R.  buoliana  (Schiff.),  Heikkenen  (1960) 
grouped  tree  damage  into  the  following  categories: 
pruning,  crook,  fork,  posthorn,  bush,  and  spiketop. 
Descriptions  of  these  damage  categories  on  red  pine, 
Pinus  resinosa  Ait.,  are  given  by  Heikkenen  (1960), 
Talerico  and  Heikkenen  (1962),  Miller  and  Schallau 
(1963),  and  Miller  (1967).  Similar  types  of  damage 
are  found  on  ponderosa  pine  due  to  feeding  by  R. 
neomexicana. 

In  1956,  a  devastating  forest  fire,  the  Dudley  Fire, 
burned  21,000  acres  of  ponderosa  pine  on  the 
Chevelon  Ranger  District,  Apache-Sitgreaves 
National  Forest,  about  45  miles  south  of  Winslow, 
Arizona.  Most  of  the  Dudley  Burn  reseeded  natural- 
ly with  ponderosa  pine,  but  large  open  areas  were 
subsequently  planted  with  ponderosa  planting  stock. 
The  young  seedlings,  both  natural  and  planted,  soon 
became  infested  with  tip  moths.  Surveys  conducted 
by  entomologists  with  the  Forest  Insect  and  Disease 
Management  Branch,  Southwestern  Region,  USDA 
Forest  Service,  showed  that  few  seedlings  escaped 


damage.  In  1966,  38  percent  of  the  seedlings 
examined  were  damaged  by  tip  moths.3  By  1969,  this 
percentage  had  increased  to  82.4 

Although  tip  moths  are  continuing  (1975)  to 
damage  young  pines  at  Chevelon,  there  is  some 
indication  that  thinning  naturally  seeded  areas  allows 
the  remaining  trees  to  grow  beyond  the  height 
susceptible  to  tip  moth  attack.  The  smaller  planta- 
tion trees,  including  those  under  heavy  grass  compe- 
tition, are  still  being  heavily  damaged. 

In  1975,  studies  were  initiated  to  obtain  informa- 
tion on  how  the  tip  moth  affects  ponderosa  pine 
regeneration  in  the  Southwest.  These  studies  were 
designed  to  determine  the  nature  and  extent  of 
damage  and  resultant  deformities  to  ponderosa  pine 
reproduction  at  Chevelon.  This  paper  summarizes  (1) 
the  types  of  tree  deformities  found,  (2)  how  frequent- 
ly each  type  occurs,  and  (3)  their  possible  effects  on 
tree  growth  rates. 

Methods 

In  1968,  fifteen  100-acre  study  plots  were  estab- 
lished on  the  Dudley  Burn.5  Most  of  the  plots  were 
located  in  naturally  seeded  areas,  and  were  originally 
established  to  determine  the  effectiveness  of  chemical 
treatments  for  controlling  tip  moths.  Additional 
study  plots  were  established  the  same  year  in  planted 
areas  of  the  George,  Loop,  and  Hatchery  Burns,  on 
the  Chevelon  Ranger  District.  Within  each  study 
plot  on  the  Dudley  Burn,  25  subplots  of  variable  size 
(only  10  subplots  on  the  George,  Loop,  and  Hatchery 
Burns)  were  systematically  established.  The  10  trees 
nearest  subplot  center  were  then  chosen  and  perma- 
nently tagged. 

Tip  moth  survey,  1966,  Chevelon  Ranger  District, 
Sitgreaves  National  Forest.  15  p.  (Unpubl.  rep.  on  file  at 
Southwest.  Reg.,  USDA  For.  Serv.,  Albuquerque,  N.M.) 

4Buffam,  Paul  E.  1969.  Results  of  the  1969  evaluation 
of  the  southwestern  pine  tip  moth  trend  study  plots. 
Sitgreaves  National  Forest,  Chevelon  Ranger  District, 
Region  3.  4  p.  (Off.  Rep.,  on  file  at  Southwest.  Reg., 
USDA  For.  Serv.,  Albuquerque,  N.M.) 

5Buffam,  P.  £.,  and  C.  J.  Germain.  1968.  Helicopter 
application  of  Cygon  (dimethoate)  for  control  of  the 
southwestern  pine  tip  moth,  Rhyacionia  neomexicana 
[Dyar).  Results-Pilot  Control  Study,  Sitgreaves  National 
Forest,  Chevelon  District,  Region  3.  8  p.  (Off.  Rep.,  on 
file  at  Southwest.  Reg.,  USDA  For.  Serv.,  Albuquerque, 
N.M.) 


1 


Since  1968,  Forest  Insect  and  Disease  Manage- 
ment entomologists  have  measured  height  growth 
and  determined  tip  moth  infestation  trends  on  the 
George,  Loop,  Hatchery,  and  nine  of  the  Dudley 
Burn  plots  (fig.  1).  Because  these  observations  and 
measurements  provide  infestation  and  tree-growth 
histories  for  individually  tagged  trees,  these  same 
trees  were  examined  for  tip  moth-caused  deformities. 

Tagged  natural  and  planted  trees  were  measured 
and  examined  for  deformities  in  September-October 


1975.  By  this  time,  R.  neomexicana  larvae  had 
completed  their  shoot  feeding.  Tree  heights  were 
measured  with  telescoping  12-foot  poles.  Heights 
were  measured  to  the  nearest  inch  from  the  upper- 
most shoot,  regardless  of  intrawhorl  position,  to 
ground  level.  For  example,  if  the  terminal  shoot  was 
destroyed  by  tip  moth  feeding,  a  lateral  shoot 
generally  assumed  dominance.  Height  of  this  upper- 
most shoot  aboveground  determined  tree  height. 


CHEVELON  RANGER  DISTRICT 
APACHE -SITGREAVES  NATIONAL  FOREST 

Location  of  southwestern 
™  pine  tip  moth  plots 

□  Lookouts 

i  scale 

0   12   3  4 


A- 


Chevelon 
Work  Center 


M0G0LL0N 
MESA 

George^  Burn 

Dutch 
Jo< 

Loop  Burn 


Ohaccy 


6 

\Dudley 
Lake 


Dudley  Burn^ 


Jarts  ) 
Crossing  / 

M0G0LL0N 


Hatchery 
Burn 


( 


PLATEAU 


Figure  1.  — Location  of  study  plots  on  the 
Dudley,  Loop,  George,  and  Hatchery 
Burns. 


RIM 


2 


Individual  whorls  within  trees  were  examined  for 
deformities  and  measured  for  internodal  growth, 
starting  at  the  crown  apex  and  working  downward 
toward  the  base  of  the  tree.  Small  trees  were 
examined  for  three  or  four  whorls;  larger  trees  for 
five  or  six  and  occasionally  seven  whorls.  For 
analysis,  the  type  and  percentage  of  each  deformity 
was  determined  for  each  10  inches  of  tree  height. 
Mean  height  growth  following  each  type  of  deformity 
was  then  determined  from  the  internodal  measure- 
ments. 


Results  and  Discussion 

Types  of  Deformities 

The  deformities  found  on  ponderosa  pine  due  to 
feeding  by  R.  neomexicana  are  summarized  as  fol- 
lows: 

Prune:  one  or  more  lateral  buds  killed,  resulting  in 
fewer  branches  per  whorl;  no  crook  in  main 
stem  (fig.  2). 


3 


Crook:  a  departure  from  straightness,  resulting  Posthorn:  a  severe  crook  resulting  from  larval 

from  complete  or  partial  destruction  of  the  feeding  on  only  one  side  of  the  terminal  shoot; 

terminal  shoot.  Miller  (1967,  p.  13)  lists  four  feeding  stops  before  the  shoot  is  killed  and  the 

types.  Lateral  generally  assumes  dominance  over  injured  leader  bends  at  the  point  of  attack  (fig. 

damaged  terminal;  loss  of  form  depends  on  5). 
degree  of  crook  and  number  of  lateral  shoots 
that  continue  height  growth  (fig.  3). 

Fork:  two  or  more  laterals  assume  dominance  (fig. 

4).  Forking  may  follow  bushing  (Talerico  and  Bush:  an  increase  in  the  normal  number  of 

Heikkenen  1962);  one  ultimate  effect  of  forking  branches  at  a  whorl;  adventitious  buds  produce 

may  be  a  crook,  if  a  competing  branch  becomes  multiple  shoots  after  destruction  of  terminal  and 

dominant.  lateral  shoots  (fig.  6). 


4 


Spiketop:  insect  attack  kills  the  terminal  but 
adventitious  buds  do  not  develop,  resulting  in  a 
dead  top  (fig.  7). 


Frequency  of  Deformities 

We  examined  a  total  of  5,012  whorls  for  tree 
deformities  caused  by  tip  moths  (table  1).  Only  7 


Table  1 . --D i str i but  ion  of  southwestern  pine  tip  moth  tree  deformities,  by  whorl  level 


Damage 
Category 


Whorl  level 


Total 

  or 

7  average 


Observat  ions 


919 


919 


905 


Number 
828 


664 


488 


289 


5012 


Percent 

SINGLE: 

Norma  1 

1  1 

0 

5 

0 

6 

0 

5.1 

6 

6 

6 

4 

13 

5 

7 

0 

Bush 

15 

3 

6 

3 

6 

8 

4.2 

7 

8 

9 

2 

10. 

0 

8 

4 

Crook 

8 

2 

9 

8 

9 

7 

10.5 

10 

5 

7 

8 

6 

9 

9 

3 

Prune 

21 

0 

15 

0 

12 

5 

17.9 

18 

4 

21 

1 

18 

3 

17 

it 

Fork 

1 

2 

2 

8 

1 

9 

1.9 

1 

5 

1 . 

8 

1 . 

7 

1 

9 

Sp  i  ketop 

1 

1 

0 

0 

0 

0 

0.0 

0 

0 

0 

0 

0 

0 

0 

2 

Posthorn 

1 

0 

0 

0 

0 

2 

0.0 

0 

3 

0 

2 

0. 

0 

0 

4 

DOUBLE: 


Prune/crook 

25 

4 

3^ 

7 

31 

7 

34 

3 

33 

3 

32 

6 

28 

0 

31 

6 

Bush/crook 

14 

1 

21 

8 

27 

2 

23 

2 

20 

2 

18 

2 

21 

1 

21 

0 

Prune/fork 

0 

9 

2 

5 

2 

2 

1 

8 

1 

0 

1 

8 

0 

3 

1 

7 

Bush/fork 

0 

5 

1 

2 

1 

6 

1 

0 

0 

2 

0 

8 

0. 

0 

0 

9 

Posthorn/fork 

0 

0 

0 

0 

0 

1 

0 

0 

0 

0 

0. 

0 

0 

0 

0 

0 

Posthorn/bush 

0 

5 

0. 

3 

0 

0 

0 

0 

0 

0 

0 

0 

0. 

0 

0 

2 

Posthorn/prune 

0 

2 

0 

1 

0 

0 

0. 

1 

0 

0 

0 

0 

0. 

0 

0 

1 

6 


percent  of  the  whorls  were  categorized  as  normal, 
that  is,  without  damage  and  having  a  complement  of 
at  least  three  lateral  branches  (fig.  8).  Most  whorls 
(55  percent)  had  a  combination  of  two  kinds  of 
deformity,  such  as  crook/prune  or  prune/fork;  38 
percent  had  only  one  kind. 

The  crook,  bush/crook,  prune,  and  prune/crook 
categories  accounted  for  about  79  percent  of  the 
deformities.  The  remaining  categories  made  up  14 
percent  of  the  total  whorls  examined,  of  which  only  5 
percent  were  forks,  posthorns,  and  spiketops.  In 
contrast,  Talerico  and  Heikkenen  (1962)  found  that 


most  European  pine  shoot  moth  damage  resulted  in 
forking,  and  that  most  forks  were  an  outgrowth  of 
bushing.  From  60  to  90  percent  of  the  red  pine  trees 
they  sampled  had  forks. 

As  tree  height  increased,  especially  above  61 
inches,  tip  moth  damage  decreased  (table  2).  Dis- 
tribution of  damage  by  10-inch  height  classes  indi- 
cates that  as  tree  height  increases:  (1)  percentage  of 
normal  and  bush  whorls  increases;  (2)  percentage  of 
crook,  bush/crook,  prune/crook  and  prune/fork 
decreases;  and  (3)  percentage  of  prune  remains 
about  the  same.  These  percentages  possibly  reflect 


Table  2. --Percent  deformity,  by  tree  height  class  and  damage  category 
Damage  Tree  height  class  ( i nches) 

Category  1-10      11-20     21-30  M-50     51-60     61-70     71-80     81-90  91-100 


Percent 


Normal 

l.k 

k 

7 

6.5 

9 

0 

7 

1 

7 

3 

8 

0 

9 

7 

14.9 

13 

9 

Bush 

2.7 

8 

0 

7.6 

8 

3 

8 

2 

8 

3 

7 

h 

10 

1 

12.9 

20 

3 

Crook 

3-9 

7 

k 

8.7 

9 

h 

10 

8 

1 1 

3 

13 

0 

1  1 

2 

9.8 

8 

9 

Bush/crook 

25-9 

18 

9 

20.8 

21 

1 

21 

7 

23 

0 

21 

5 

20 

h 

19-6 

16 

5 

Prune 

13.6 

19 

8 

16.0 

15 

9 

17 

2 

17 

7 

19 

3 

16 

2 

H.9 

25 

3 

Prune/crook 

kk.3 

37 

5 

3*».0 

32 

h 

29 

6 

27 

5 

25 

8 

25 

0 

2k. 2 

1 1 

k 

Prune/fork 

3-9 

1 . 

6 

2.3 

0 

7 

1 . 

1 

1 

2 

1 

1 

1 

2 

0.5 

0 

0 

7 


height  preferences  by  ovipositing  females.  Fewer  eggs 
are  deposited  on  upper  crown  needles  more  than  6  to 
8  feet  aboveground;  consequently,  larger  trees  sus- 
tain less  tip  moth  damage. 

Effect  on  Tree  Growth 

Three  distinct  deformity  classes  were  established 
on  the  basis  of  analysis  of  variance  and  multiple 
range  tests  (table  3).  Mean  internodal  height  growth 
was  significantly  different  (P<.05)  between  each  of 
the  deformity  classes,  but  no  differences  were  found 
within  classes:  Class  I,  normal  and  bush;  Class  II, 
crook  and  bush/crook;  and,  Class  III,  prune, 
prune/crook,  and  prune/fork.  Deformities  not  in- 
cluded in  these  three  classes  were  infrequently 
observed. 


Table  3- "Mean  internodal  height  growth,  by 
deformity  class2 


Type  of 
deform  i  ty , 
by  class 

Mean 
internodal 

Stan- 
da  rd 

Observa- 

height 
growth 

dev  i  - 
at  ion 

t  i  ons 

Inches 

Number 

CLASS  1: 

Normal    (no  damage) 

7.5 

3 

3 

1 3k 

Bush 

7.6 

k 

2 

165 

CLASS   1 1 : 

Crook 

3 

2 

3H 

Bush/crook 

6.5 

8. 

0 

783 

CLASS  III: 

Prune 

5-5 

3. 

1 

520 

Prune/c  rook 

5.0 

2 

9 

1229 

Prune/fork 

h.5 

2 

0 

59 

1 Internodal   growth  following  each  deformity 
cl ass . 

2Classes  are  significantly  different  at  P<.05. 


Mean  internodal  height  growth  following  fork  (6.1 
inches)  was  significantly  different  from  Class  I 
deformities,  but  not  from  Class  II  or  III  deformities. 
Also,  no  differences  were  found  following  posthorn 
(6.8  inches)  or  bush/fork  (6.3  inches),  or  between 
these  two  damage  categories  and  all  other  damage 
categories. 

Height  growth  following  crook  and  bush/crook 
was  significantly  less  than  that  following  the  normal 
internode.  Pruning  and  combinations  of  prune/fork 


and  prune/crook  produced  even  greater  departures 
from  normal.  Reduced  height  growth  following  crook 
is  probably  a  function  of  the  severity  of  the  crook. 
Although  pruning  causes  no  departure  from  straight- 
ness,  loss  of  height  growth  may  be  a  function  of 
reduced  photosynthetic  area  necessary  for  terminal 
growth. 

Only  7  percent  of  the  5,012  whorls  examined 
escaped  tip  moth  damage;  89  percent  of  the  whorls 
had  a  significant  height  growth  loss  of  from  13  to  40 
percent.  Although  we  have  no  data  on  long-term 
effects  of  the  southwestern  pine  tip  moth  on  pon- 
derosa  pine,  Miller  (1967)  found  that  red  pine 
eventually  outgrows  crook  and  bush  deformities. 
In  the  Southwest,  ponderosa  pines  taller  than  6  to  8 
feet  are  less  susceptible  to  attack  by  the  southwestern 
pine  tip  moth.  Some  deformities  probably  persist  as 
the  tree  matures,  however,  and  may  appear  later  as 
defects  in  merchantable  trees.  Ffolliott  and  Barger 
(1967)  quantified  some  stem  features,  including 
crook  and  fork,  that  reduce  quality  of  southwestern 
ponderosa  pine.  Perhaps  some  of  these  defects  may 
be  attributed  to  earlier  tip  moth  infestations. 


Literature  Cited 

Ffolliott,  Peter  F.,  and  Roland  L.  Barger. 

1967.  Occurrence  of  stem  features  affecting  qual- 
ity of  cutover  southwestern  ponderosa  pine.  U.S. 
For.  Serv.  Res.  Pap.  RM-28,  11  p.  Rocky  Mt. 
For.  and  Range  Exp.  Stn.,  Fort  Collins,  Colo. 
Heikkenen,  Herman  John. 

1960.  The  identification  and  dating  of  past  attacks 
of  the  European  pine  shoot  moth  on  red  pine. 
J.  For.  58:380-384. 
Jennings,  Daniel  T. 

1975.  Life  history  and  habits  of  the  southwestern 
pine  tip  moth,  Rhyacionia  neomexicana  (Dyar) 
(Lepidoptera:  Olethreutidae).   Ann.  Entomol. 
Soc.  Am.  68:597-606. 
Miller,  William  E. 

1967.  The  European  pine  shoot  moth — ecology 
and  control   in  the  Lake  States.    For.  Sci. 
Monogr.  14,  72  p. 
Miller,  William  E.,  and  Con  H.  Schallau. 

1963.  Problems  in  identifying  old  European  pine 
shoot  moth  damage.  J.  For.  61:677-678. 
Talerico,  Robert  L.,  and  H.  J.  Heikkenen. 

1962.   Stem  injury  to  young  red  pine  by  the 
European  pine  shoot  moth.  J.  For.  60:403-406. 


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